The Human Gastric Pathogen Helicobacter pylori and Its Association with Gastric Cancer and Ulcer Disease
With the momentous discovery in the 1980's that a bacterium, Helicobacter pylori, can cause peptic ulcer disease and gastric cancer, antibiotic therapies and prophylactic measures have been successful, only in part, in reducing the global burden of these diseases. To date, ~700,000 deaths worldwide are still attributable annually to gastric cancer alone. Here, we review H. pylori's contribution to the epidemiology and histopathology of both gastric cancer and peptic ulcer disease. Furthermore, we examine the host-pathogen relationship and H. pylori biology in context of these diseases, focusing on strain differences, virulence factors (CagA and VacA), immune activation and the challenges posed by resistance to existing therapies. We consider also the important role of host-genetic variants, for example, in inflammatory response genes, in determining infection outcome and the role of H. pylori in other pathologies—some accepted, for example, MALT lymphoma, and others more controversial, for example, idiopathic thrombocytic purpura. More recently, intriguing suggestions that H. pylori has protective effects in GERD and autoimmune diseases, such as asthma, have gained momentum. Therefore, we consider the basis for these suggestions and discuss the potential impact for future therapeutic rationales.
After a long history of discoveries on the pathology and bacterial colonization of the gastric mucosa starting in the beginning of the last century , the gastroenterologist Barry Marshall and the pathologist Robin Warren, in the 1980’s, fulfilled Koch’s postulates for the association between gastritis and the human gastric pathogen Helicobacter pylori [1–3]. This decisive demonstration substantially changed our views of the microbiology and pathology of the human stomach and resulted in Marshall and Warren receiving the 2005 Nobel Prize in Physiology and Medicine.
Marshall and Warren’s discovery founded the concept that infection with H. pylori , and not (if at all, very indirectly) stress, can lead to a variety of upper gastrointestinal disorders (Figure 1) such as gastric inflammation (gastritis), peptic ulcer disease (10%–20%), distal gastric adenocarcinoma (1%-2%), and gastric mucosal-associated lymphoid tissue (MALT) lymphoma (<1%) [4–7]. These insights not only dramatically improved the management and therapy of gastric diseases but also provided an invaluable key for deeper insights into the pathogenesis of chronic infections. Moreover, during the past 20 years of research, the initially tentative association between persistent H. pylori infection and the development of gastric cancer has been well established [8–10], prompting the International Agency for Research on Cancer to classify H. pylori as a type I carcinogen .
While the prevalence of H. pylori is decreasing in the Western world, it still constitutes a significant medical burden in less industrialized countries, with constant higher infection rates and a more widespread distribution. The challenge now is to fill in the remaining gaps in our knowledge such as transmission routes as well as genetic preconditions and, as antibiotic resistance increases, develop preventative strategies, including improved hygiene conditions and vaccination.
Here, we review the role of H. pylori in severe human gastric disease such as peptic disease and gastric cancer, with an emphasis on clinical aspects and molecular pathogenesis.
2. Evolution and Epidemiology
The relationship between H. pylori and the human race began around 100,000 years ago. Phylogenetic simulations predict that the bacterium spread from East Africa over the same time scale as anatomically modern humans. The close association is underlined by observations showing that key patterns of bacterial genetic diversity are mirrored in the migration and ethnic origins of the human host . By genotyping different strains collected from all over the world, the migration of humans into North America and the Pacific Area has been tracked [13, 14]. Because a variety of gastric Helicobacter species can also be found in mammals besides humans , it is speculated that Helicobacter species are, in general, ancestral in mammals, and we may have already been infected by ancestors of the present H. pylori strains prior to our evolution towards modern mankind .
It is estimated that half of the world’s population is infected with H. pylori ; however, infection prevalence shows large geographical variations (Figure 2). For example, in several emerging nations and developing countries including India, Saudi Arabia, and Vietnam, more than 80% of the human population is infected. Infections in these regions are characterized by rapid acquisition even at a young age [17–19]. By contrast, the prevalence of H. pylori in industrialized countries is generally less than 40% and considerably lower in children than in adults . H. pylori acquisition most frequently appears during early childhood , indicating that the decreased prevalence with age is largely due to a birth cohort effect rather than to new infections. The prevalence of H. pylori is inversely correlated with socioeconomic status, in particular in relation to family income levels, hygiene, and housing conditions . This may be the reason why the prevalence of H. pylori in the industrialized world is significantly declining, whereas infection rates in developing countries remain relatively constant. Moreover, the widespread use of antibiotics may have accelerated the progressive decrease of H. pylori infection during childhood in developed countries. The elimination of H. pylori from the population by improved hygiene, housing conditions, and antibiotic treatment also strongly correlates with a decrease in gastric cancer worldwide .
Although the association between H. pylori and severe human disease has been established, the exact mechanisms of H. pylori acquisition are still unknown (Figure 3). Gastro-oral (e.g., exposure to vomit) and fecal-oral routes from human to human are posited as the primary means of transmission . Indeed, H. pylori isolates from children and their mothers often have the same genotype [24, 25], supporting the notion that infection primarily occurs during childhood via close contact to family members (e.g., via premastication of food by parents). Other transmission routes, including exposure to contaminated food or water [26–28] or via domestic animals such as cats and sheep [29, 30] are also thought to play a role. To date, no conclusive evidence of predominant transmission by any of these routes has been established.
5. Colonization and Persistence
The majority of colonizing H. pylori reside within the gastric mucus and do not directly interact with host cells. Although H. pylori was long considered to be an extracellular bacterium, recent studies have provided evidence that H. pylori occasionally enters epithelial cells via a zipper-like mechanism [31–35]. Despite causing numerous gastric environmental changes and eliciting a host immune response, H. pylori can persistently colonize the human stomach for long periods . This is in stark contrast to most other commonly ingested microbes, which cannot successfully colonize the stomach due to its manifold microbicidal properties.
6. Mechanisms to Escape Low pH
One of the most efficient biological barriers against bacterial infection is the acidic pH (<2) of the gastric lumen. However, the mucus layer overlying gastric epithelial cells exhibits a pH gradient, ranging from about pH 2 at the luminal surface to between 5 and 6 at the epithelial surface . To avoid the bactericidal activity of acid, H. pylori produces substantial amounts of cytosolic and cell surface-associated urease. Urease is highly conserved in different H. pylori strains and transiently buffers the acidic environment by converting urea into ammonia and carbon dioxide [18, 38]. H. pylori has evolved several other strategies to minimize exposure to the low pH in the gastric lumen (see Figure 4). The bacteria remain within the mucus in close proximity to the epithelial surface where the pH is nearly neutral. The spiral cell shape of Helicobacter, which is based on specific cross-linkages of the peptidoglycan layer, supports a screw-like movement which facilitates motility within the viscous mucus layer and enhances colonization efficiency [39, 40]. To rapidly reach and remain in the mucus layer, H. pylori uses polar flagella [41, 42]. Interestingly, null mutants defective in the production of flagella are unable to colonize gnotobiotic piglets but grow normally in vitro . Consistent with the importance of functional flagella, control of directed movement by chemotactic responses is also essential for successful colonization . Intriguingly, during infection of Mongolian gerbils H. pylori orient themselves via the pH gradient in the mucus, remaining mainly within 25 μm of the epithelial surface and thereby avoiding acidic distal regions . A specific chemoreceptor, encoded by the tlpB gene, seems to be involved as mutants can swim but do not avoid acidic regions .
7. Adhesion to Epithelial Cells
Only ~20% of H. pylori present in the gastric mucosa are adhered to the surface of epithelial cells with a majority exhibiting a tropism for intercellular junctions and, occasionally, for deeper intercellular spaces [47, 48]. Adherence is mediated by a subset of H. pylori-encoded autotransporter proteins (e.g., BabA, SabA, AlpA, AlpB, HopZ, and OipA) exposed on the bacterial cell surface. However, no individual molecule has been shown to be essential, indicating redundancy of adhesive mechanisms [49–52]. Additionally, expression of individual adhesins differs between strains and is variable within a single strain over time, leading to dynamic adaption capacities via on/off switching of gene expression, gene inactivation, or recombination [53–55].
8. Manipulation of the Immune System
H. pylori can persist for long time periods within the host without being extinguished by the immune system or by the frequent gastric environmental changes. Interactions of H. pylori with host epithelial surfaces are thought to elicit effective escape mechanisms, often causing cellular damage and inflammation. For example, intimate adherence via SabA has been shown to enhance inflammatory responses, which are assumed to facilitate access to essential nutrients released from damaged host cells . Although direct evidence is lacking that inflammation is beneficial for H. pylori , the hypothesis still remains intriguing given that infection always elicits inflammation, regardless of symptoms. In addition, the delivery of cytotoxin associated antigen A (CagA), a key virulence factor, into the host cell via the type four secretion system (T4SS), depolarizes the epithelial cell to exploit the apical cell surface for use as a replicative niche and to obtain nutrients which are normally delivered to the basolateral side .
In general terms, immunity does not seem to exert a decisive influence on the establishment of an infection, as immune-compromised patients do not exhibit higher colonization rates . Besides, adherence and the concomitant delivery of toxins, H. pylori possess a range of mechanisms to attenuate and manipulate the immune response, for example, the bacteria preferentially induce a T-helper cell 1 [Th1] type-based response, classified as typical cell mediated immunity, essential for the fight against intracellular pathogens . H. pylori also expresses lipopolysaccharide (LPS) with a very low endotoxic and immunobiological activity compared to LPS of other Gram-negative bacteria  that can antagonize signaling mediated by the innate immune receptor, toll-like receptor 4 (TLR4) . This antagonistic feature is based on specific modifications of the lipid A component  and strain-dependent expression of LPS O-antigens that are structurally related to Lewis blood group antigens found on human cells . This molecular mimicry is not only involved in autoimmune responses but could also allow H. pylori LPS to evade recognition by the innate immune system . The incorporation of cholesterol and its subsequent glycosylation in the H. pylori membrane  as well as the coating of the bacterium with host molecules such as plasminogen  might represent additional mechanisms of antigenic camouflage. Moreover, H. pylori flagella, structures which are normally recognized via the innate immune receptor TLR5, evoke only a very weak immune response due to a modified N-terminal TLR5 recognition site [67–69]. Other mechanisms by which H. pylori triggers the host immune system are based on bacterial factors that directly target host immune cells; for example, the vacuolating cytotoxin (VacA), which is encoded in the genome of all H. pylori strains, inhibits the nuclear translocation of the transcription factor nuclear factor of activated T-cells (NFAT), thereby blocking T-cell proliferation of CD4+ cells . VacA also inhibits the proliferation of B-cells and CD8+ cells  and is able to disrupt the normal function of macrophages by either inducing apoptosis  or interrupting phagosomal maturation . Bacterial arginase and γ-glutamyl transferase show similar functions in altering the normal function of T-cells [74, 75], while arginase and VacA additionally downregulate the expression of inducible nitric oxide synthase [76, 77].
9. Genetic Diversity and Variation
H. pylori exhibits a remarkable allelic diversity and genetic variability, typically involving endogenous (point) mutations and recombination, which result in every infected person carrying a distinct strain [78, 79]; however, differences between relatives are minimal . Allelic diversity is promoted by a significantly higher mutation rate than found in many other bacteria , which may also explain the rapid development of high-level resistance to commonly used antibiotics such as clarithromycin. High mutation rates are most likely due to the lack of a complete DNA mismatch repair system (mutS1/MutL/mutH) and several enzymes involved in base excision repair [82, 83]. A large repertoire of hyper-mutable genes frequently undergoes length changes as a consequence of slipped-strand mispairing-mediated mutagenesis, leading to numerous subpopulations within any large population . Each of these subpopulations carry a specific combination of active and inactive phase-variable genes; for instance, LPS biosynthesis and outer membrane encoding genes, which allow H. pylori to rapidly adapt to environmental changes [85, 86]. High natural competence for DNA uptake in combination with one of the highest intergenomic recombination rates found amongst pathogenic bacteria  also contributes to the high genomic variability between H. pylori isolates. Moreover, recent work has demonstrated that genetic exchange induced by damage of bacterial DNA contributes to persistence of H. pylori in its host . Interestingly, a recent microarray analysis identified a large number of genes not previously associated with infection as essential for colonization of mice . The majority of gene products were hypothetical, indicating that many other unknown bacterial factors may be required for colonization.
10. Gastric Cancer and Ulcers: Mutually Exclusive Pathologies?
10.1. Gastric Cancer
Although many H. pylori-associated diseases including peptic ulcer, gastric cancer, and MALT lymphoma only develop decades after infection (Figure 5), their medical burden is tremendous. Gastric cancer is one of the most common forms of cancer, with approximately 700,000 to 900,000 new cases diagnosed every year, and the second leading cause of cancer-related deaths worldwide . Survival rates are very low, ranging from 15% if diagnosed during later stages of the disease to 65% if diagnosed early. Incidence rates vary widely geographically, and, in general, more males than females are affected [50% lower incidence]. Although high-risk areas in Japan, China, Eastern Europe, and certain Latin America countries still remain , incidence rates worldwide have been declining for several decades .
Gastric adenocarcinomas are mainly divided into two histologically distinct forms, diffuse-type gastric adenocarcinoma, and intestinal-type adenocarcinoma (Lauren classification) each exhibiting different epidemiological and pathophysiological features . Diffuse-type gastric adenocarcinoma is found predominantly in younger people, with no gender bias. It consists of individually infiltrating neoplastic cells that do not form glandular structures and are not associated with intestinal metaplasia . The more prevalent form of gastric adenocarcinoma is called intestinal-type adenocarcinoma, which usually occurs in elderly people, predominates in men, and progresses through a well-defined chain of histological events, typically starting with a transition from normal mucosa to chronic gastritis, followed by atrophic gastritis and intestinal metaplasia which finally ends in dysplasia and adenocarcinoma . H. pylori significantly increases the risk of developing both cancer types. We focus here mainly on the association between H. pylori and intestinal-type adenocarcinoma as the mechanisms of disease progression are better characterized as compared to diffuse-type gastric adenocarcinoma. Gastric cancers are also classified by their localization within the stomach: the most important distinction being between cardia (the proximal part of the stomach) and noncardia. H. pylori is the strongest risk factor for the development of non-cardia (distal) gastric cancer.
10.2. Peptic Ulcer Disease
Due to the high morbidity and mortality rates associated with peptic ulcer disease, which comprises both gastric and duodenal ulcers, this disease is regarded as a major medical threat. In most Western countries, morbidity from duodenal ulcer is more common than from gastric ulcer, even though the mortality rate is higher for gastric ulcer. In Japan, morbidity and mortality rates are generally higher for gastric ulcer than for duodenal ulcer . Both ulcer types are defined as mucosal defects with a diameter of at least 0.5 cm penetrating through the muscularis mucosa. Whereas gastric ulcers mainly occur along the lesser curvature of the stomach, at the transition from corpus to antrum , duodenal ulcers can be normally detected in the duodenal bulb, or even with the pylorus. As with gastric cancer, recent epidemiological studies show a sharp decline in the incidence of ulcer disease , a direct consequence of the disease association with H. pylori and the now-possible effective antibiotic medication. Although the identification of H. pylori and its association with ulcer development completely changed the prevailing concept of “no acid, no ulcer”, nonsteroidal anti-inflammatory drugs (NSAIDs) and low-dose aspirin are also an increasingly important cause of ulcers, even in H. pylori-negative patients .
11. What Makes the Difference between Cancer and Ulcer?
Although both gastric cancer and peptic ulcer disease are associated with H. pylori infection, mechanistically they appear to have entirely different origins and outcomes (Figure 6). Gastric adenocarcinomas are malignant tumors which arise from uncontrolled proliferation of the epithelial cell layer and are accompanied by hypochlorhydria (low-acid secretion). The tumors mainly occur in the gastric antrum, body, or, to a lesser extent, in the fundus and originate from the inflammation of the entire stomach (pangastritis). By contrast, a peptic ulcer is a sore on the lining of the stomach (gastric ulcer) or duodenum (duodenal ulcer; DU) and originates from a disruption of normal wound-healing processes of the epithelial layer. Whereas acid secretion in duodenal ulcer is increased (hyperchlorhydria), gastric ulcers develop in low acid concentrations, as also observed with gastric cancer. This discrepancy is also due to the differences in the origin of prior inflammation, that is, predominantly in the antrum in cases of duodenal ulcer, but involving the entire stomach in cases of gastric ulcer . While gastric cancer and duodenal ulcer can be easily discriminated from one other, gastric ulcer more closely resembles gastric cancer in localization and outcome. This relationship is also reflected in the observation that gastric cancer often occurs in patients with a history of gastric ulcers but hardly ever in patients with recent duodenal ulcers . Moreover, gastric ulcer and gastric cancer patients are characterized by reduced acid secretion, corpus-predominant pangastritis, and an accelerated progression towards atrophic gastritis and intestinal metaplasia. The differences in gastric cancer and duodenal ulcer are also mirrored in their worldwide prevalence, but not cooccurrence (Figure 7). Duodenal ulcer incidence is mainly concentrated in South Asia (e.g., India) and West Africa, whereas gastric cancer is mainly prevalent in Middle Asia and Middle Africa. Interestingly, some African (and Indian) populations have a high prevalence of H. pylori but low incidence of H. pylori- associated diseases, termed the “African enigma” . One possible hypothesis posited for this anticorrelation is that enteric helminth infection in developing countries can attenuate H. pylori- induced atrophy and premalignant lesion by modulating the Th1-driven immune response to bacterial infection [102, 103].
12. H. pylori Virulence Determinants
12.1. Strain Variations Trigger the Pathogenic Outcome of H. pylori Infections
The phenomenon that most H. pylori-infected patients develop no complications other than chronic active gastritis led to the notion that some strains may be more virulent than others. In fact, early investigations indicated that the severity of pathogenic outcome was correlated with the strain’s ability to induce strong morphological changes, vacuolization and degeneration of in vitro cultured cells . Because H. pylori can colonize the entire gastric epithelium, clinical outcomes are mainly dependent on the pattern of chronic inflammation induced. Therefore, bacterial factors involved in H. pylori-induced inflammatory responses constitute risk factors for both gastric cancer and peptic ulcer. Despite the wide genetic diversity of H. pylori hampering the search for bacterial factors involved in pathogenesis, several genomic loci encoding virulence factors, such as the cag pathogenicity island (cagPAI), the toxin VacA, and the Bab2 adhesin, have been strongly associated with an increased risk of developing gastric cancer and peptic ulcer disease [105, 106]. Like disease prevalence, the distribution of these genomic loci varies geographically. While the VacA-encoding gene can be found in all strains, albeit with various allelic combinations, only 60–70% of all Western strains carry cagPAI. In contrast, cagPAI is present in 95–100% of all Asian strains. The bab2 gene is present in around 85% of all strains.
12.2. The cag Island and the Virulence Factor CagA
One of the most important strain-specific determinants influencing H. pylori-mediated pathogenesis is cagPAI. This horizontally acquired genomic locus of approximately 40 kb contains 31 genes [83, 107] that encode a T4SS. It was first detected while searching for the genomic localization of the bacterial protein CagA, a marker for H. pylori-associated diseases . The cagA gene, located at the 3′ end of cagPAI, encodes the only known bacterial effector protein translocated by the T4SS into host cells. The T4SS forms a membrane protrusion, often inaccurately referred to as a needle-like structure [109, 110]: it is not comparable to the static form of a bacterial type 3 secretion system [T3SS], which truly resembles an injection syringe . CagA is often detected on the surface of the T4SS; it becomes translocated into epithelial cells and to a lesser extent into hematopoietic cells [112, 113]. Intriguingly, CagA has also been detected on the surface of outer membrane vesicles (OMVs) secreted by H. pylori . The interdependence of T4SS function, OMV formation, and CagA translocation likely remains an interesting area of future investigation.
Surface-exposed integrin molecules act as host cell receptors which permit the successful delivery of CagA and, thus, play a key role in T4SS functionality. In this context, CagL, a T4SS component, was proposed to have an important function by mediating binding between β1α5 integrins and its RGD-domain . Although contradictory data have been published , recent observations could support the CagL-integrin interaction concept by showing that CagL activates the integrin-binding molecule ADAM17 via mediating its dissociation from β-1integrin . Accordingly, ADAM17 inhibits the expression of the gastric H+, K+-ATPase α subunit via the transcription factor nuclear factor κB (NF-κB). Since the H+, K+-ATPase α subunit is involved in acid secretion, these data demonstrate a T4SS-dependent molecular mechanism for hypochlorhydria and indicate that the influence of cagPAI on the development of gastric cancer and gastric ulcer is more pronounced than on the induction of duodenal ulcer (Figure 8). Additional cag-encoded proteins (CagA, CagI and CagY) have been shown to bind β1-integrin in order to induce conformational changes of integrin heterodimers which enable CagA translocation . Since integrins are not located at the apical membrane but are expressed at the basolateral side, H. pylori would have to reach the basolateral surface to efficiently activate the T4SS. Moreover, in addition to the normal expected apical niche, viable bacteria have been observed within paracellular spaces and the gastric lamina propria . Accordingly, H. pylori induces the shedding of E-cadherin to disrupt adherence junction complexes in a CagA-independent manner , enabling bacteria to enter the basolateral side of formerly closed epithelial cell layers (Figure 8).
The status of CagA as a marker of pathogenic disease resulted from the observation that patients with elevated antibody titers against CagA showed higher incidences of both peptic ulcers  and gastric adenocarcinoma [120, 121]. The association of CagA with gastric cancer was cemented by subsequent work showing that the expression of CagA in transgenic mice leads to gastric epithelial cell proliferation and the development of gastric adenocarcinoma . Data showing CagA-dependent attenuation of apoptosis in Mongolian gerbils  and that CagA-induced blockage of endocytosis mediated the downregulation of the proliferation controlling epidermal growth factor receptor (EGFR)  further support the hypothesis that CagA has oncogenic features. CagA can also provoke proinflammatory responses  and activate the signal transducer and activator of transcription 3 (STAT3) pathway, thought to play a role in gastric cancerogenesis (Figure 8) . Nevertheless, strains lacking cagPAI, which consequently do not express CagA, have also been found in patients with peptic ulcers or gastric cancer, albeit at lower frequencies. The mechanisms by which CagA mediates gastric human disease are still not fully understood. Future work is required to unravel the complex but extremely efficient manipulation of important host cell signaling cascades facilitated by this multifunctional protein.
Recent investigations have shown that surface-exposed CagA interacts with externalized phosphatidylserine to initiate its entry into host cells . Following its injection into epithelial cells, CagA undergoes tyrosine phosphorylation [128, 129], mediated by the nonreceptor tyrosine kinases Src  and Abl , two well-known oncoproteins (Figure 8). Phosphorylation is tightly controlled by H. pylori in a time-dependent manner; Src is only activated during initial stages of infection (0.5–2 h) , whereas Abl is strongly activated at late infection time points (2–8 h) . Phosphorylation takes place at specific C-terminal Glu-Pro-Ile-Tyr-Ala (EPIYA) sequence motifs of CagA which can vary in number in a strain-dependent manner [134, 135]. Four EPIYA-sites—A, B, C, D—have been identified. The EPIYA-A and EPIYA-B motifs are distributed worldwide, whereas the EPIYA-C motif is more prominent in strains from Western countries (e.g., Europe, Australia, North America) and some Asian countries (Malaysia and India). EPIYA-D sequence motifs are mainly present in East Asian CagA (Japan, China, and Korea) and are linked to the development of gastric cancer .
It is not only the sequence motif but also the number and variation of phosphorylation sites that determine the pathogenic potential of CagA. Elevated phosphorylation, caused by an increase in number of EPIYA sites, leads to enhanced binding of another oncoprotein, the tyrosine phosphatase SHP-2. After binding to CagA, SHP-2 is functionally deregulated . CagA recruits and activates SHP-2 in a phosphorylation-dependent manner and induces a Ras-independent response which leads to dramatic morphological changes of the host cell, reflected by a strong actin polymerization and cellular elongation (Figure 9), termed the “hummingbird” phenotype . Expression of EPIYA-A and EPIYA-B sites correlate with the ability of CagA to bind the tyrosine kinase Csk, which in turn inhibits Src-dependent CagA-phosphorylation, thereby, attenuating the induction of cellular elongation by the CagA-SHP-2 complex . These contradictory functions of different EPIYA sites highlight the complex and multifunctional role of CagA in H. pylori-mediated disease. That CagA interacts with a surprisingly high number of host cell signaling factors further complicates the elucidation of CagA function. Interactions can be phosphorylation dependent or independent, and interaction partners range from kinases to adaptor molecules . In addition to CagA-independent interactions reported by Weydig and colleagues , a phosphorylation-independent interaction between Zonula occludens-1 (ZO-1), a junctional adhesion molecule, and CagA was shown to contribute to an alternative mechanism of epithelial layer disruption . The CagA-ZO-1 association was closely linked to an ectopic assembly of tight junction components at the site of bacterial attachment which altered the composition and function of the apical junctional complex (see Figure 8).
Binding between CagA and the PAR1/MARK kinase complex, which has an essential role in the maintenance of epithelial cell polarity (Figure 8), has also been shown to be phosphorylation independent . Association with CagA inhibits PAR1 kinase activity leading to the dissociation of PAR1 from the membrane causing junctional and polarity defects. These effects are dependent on conserved amino acid motifs at the C-terminus of CagA, termed the CagA multimerization (CM) domain . The binding of PAR1 by the CM domain mediates the dimerization of CagA, thereby, strengthening the bond between CagA and SHP-2. The functional relevance of this association has been further corroborated by cocrystallography analysis of CagA, showing that the C-terminal CM domain blocks PAR1 function by occupying the substrate-binding site of PAR1 . Thus, the CagA-PAR1 association not only causes polarity defects but also promotes the morphogenic response induced via the interaction of CagA and SHP-2.
Another host cell factor potentially influencing cancerogenic responses in conjunction with CagA is the ubiquitously expressed protein β-catenin (Figure 8). While membrane bound β-catenin is an important component of adherence junctions, cytoplasmic β-catenin is a downstream signaling molecule of the WNT signal transduction pathway. Upon dissociation of the inhibitory β-catenin-interaction partner GSK3β, β-catenin is translocated into the nucleus where it induces the transcription of target genes involved in cancerogenesis . After translocation, CagA induces nuclear accumulation and functional activation of β-catenin via the disruption of the membrane-bound E-cadherin/β-catenin complex [146–148]. H. pylori infection was also shown to lead to AKT dependent, but CagA-independent, β-catenin activation through phosphorylation (Figure 8) and subsequent inactivation of the β-catenin inhibitor GSK3β .
Studies of CagA-host cell interactions have provided many fundamental insights into the molecular mechanisms by which H. pylori induces potentially cancerogenic host cell responses; however, the mechanisms underlying the association of CagA with ulceration remain elusive. It has neither been postulated nor shown that CagA could promote a delay in wound healing or an inhibition of cell proliferation. By contrast, VacA could inhibit proliferation, whereas undialyzed H. pylori blocked both wound healing and cell proliferation, indicating the existence of CagA- and VacA-independent mechanisms leading to the promotion of ulcer development . Future work is undoubtedly required to solve the remaining conundrums.
12.3. The cag Island and the Delivery of Peptidoglycan
Besides CagA translocation, the T4SS is also involved in the production of chemokines, such as interleukin-8 (IL-8). This process is mediated by the combinatorial activation of the host cell transcription factors NF-κB  and AP-1, the latter activated by the MAPK pathway [152, 153]. MAPK phosphorylation and activation of AP-1 are dependent on the intracellular pattern recognition factor NOD-1 (nucleotide-binding oligomerization domain-containing protein 1) , which is known to recognize universal bacterial components such as peptidoglycan. Indeed, peptidoglycan was suggested to be translocated into the host cell in a T4SS-dependent manner , thereby, inducing the activation of NF-κB via NOD-1 (Figure 8). Delivery is mediated via cholesterol-rich microdomains (lipid rafts) of the host cell plasma membrane . Delivery of peptidoglycan, however, can also occur independently of the TFSS, instead mediated by bacterial OMVs which enter human gastric epithelial cells via lipid rafts . This mechanism provides an explanation for the varying dependency of IL-8 secretion in different epithelial cell lines on the T4SS . The cell-line specificity of TFSS-independent IL-8 secretion could be due to variations in the composition of lipid raft associated receptors, enabling TFSS-dependent peptidoglycan delivery and/or OMV-mediated peptidoglycan translocation.
Both CagA and peptidoglycan seem to be responsible for the induction of a T4SS-dependent proinflammatory response, although the ability of CagA to mediate IL-8 expression is not identical for all CagA-expressing strains [125, 158]. Observations that CagA and NOD-1 accumulate in a novel type of intracellular host cell structure enforce the model that CagA and peptidoglycan can induce immune-inflammatory and proliferative responses in the gastric epithelium with potential pathologic relevance . Recent work, however, shows that the deletion of the bacterial deacetylase HP0310, which is required for normal synthesis of peptidoglycan, results in an increased delivery of CagA into host cells , indicating that even in the absence of peptidoglycan H. pylori retains the ability to initiate a proinflammatory response.
12.4. Vacuolating Toxin VacA
H. pylori VacA is a paradigmatic type-V-secreted bacterial toxin that contributes to the establishment of successful infection and virulence in multiple ways. Similar to CagA, it has been shown to be responsible for epithelial ulceration . VacA was initially identified through its ability to cause vacuolation in cultured epithelial cells . VacA-induced vacuoles are positive for marker proteins of the late endocytic compartment, including Rab7 [162, 163], LAMP1, and Lgp110 . It is supposed that VacA induces the formation of large vacuoles after its internalization into endosomal structures, where it forms anion-selective channels, subsequently leading to swelling of VacA-containing endosomal compartments . Although vacuolation is readily observed in vitro, it does not seem to occur in vivo .
The VacA amino acid sequence shares no similarities with other prokaryotic or eukaryotic proteins, and although all strains contain vacA, their sequences vary remarkably. vacA alleles are distinguished by differences in the 5′region (s-region) and midregion (m-region). Strains possessing s1m1 type alleles are associated with an increased risk of peptic ulceration and gastric carcinoma as compared to strains harboring other allelic forms, for example, s2m2 [166, 167]. In countries with high rates of distal cancer, such as Colombia and Japan, most H. pylori strains contain the more pathogenic vacA allele types . In vivo experimental studies have corroborated the association, reporting mucosal injury and gastric inflammation after the administration of large quantities of VacA into the stomachs of mice  and demonstrating, using isogenic wild-type and vacA-null mutant strains that VacA contributes to severe gastritis in gerbils .
Monomeric 88 kDa VacA molecules are secreted into the extracellular space  via type V secretion  where they self-assemble into water-soluble oligomeric structures to form anion-selective membrane channels. However, VacA can also remain associated with the bacterial membrane as a biologically active molecule and can be taken up by the host cell in a contact-dependent mechanism . The mature form can undergo specific proteolytic cleavage to yield the functionally different subunits, p33 and p55 . The p33 domain contains a hydrophobic sequence that is involved in pore formation [175, 176] and vacuolating cytotoxin activity , whereas the p55 fragment contains cell-binding domains . VacA can bind multiple epithelial cell surface molecules, including the transmembrane protein receptor-type tyrosine protein phosphatase-ζ (PTPRZ1) , fibronectin , EGFR , CD18 on T-cells  as well as various lipids  and sphingomyelin .
Besides its ability to induce the vacuolation of epithelial cells in vitro, VacA can also stimulate apoptosis (Figure 8), a process restricted to the more pathogenic allelic combination s1m1 . The p34 VacA subunit modulates mitochondrial membrane permeability  by a mechanism dependent on toxin channel activity, ultimately resulting in cytochrome c release and the subsequent activation of caspase 3 . Since VacA mutants that are defective in forming membrane channels fail to elicit cytochrome c release, it seems likely that VacA-mediated alterations of mitochondria are based on the formation of VacA channels in the mitochondrial membrane . In stark contrast to VacA, CagA exhibits antiapoptotic features , leading to the hypothesis that these two key virulence factors may have antagonistic functions. Indeed, CagA has been shown to inhibit VacA-induced apoptosis  and reduce vacuolation of epithelial cells, while VacA can inhibit CagA-mediated cellular elongation . Within the latter scenario, active VacA exerts its inhibitory impact by interfering with signaling pathways known to be crucial for cell scattering and elongation, for example, the EGFR pathway . The opposing behavior of these two key virulence factors is even more fascinating because cagPAI-positive strains are most likely to possess the more toxic s1 forms of VacA, whereas cagPAI-negative strains generally harbor nontoxic s2 forms. This is not due to genetic linkage as the gene loci are not close to each other. The antagonistic properties of VacA and CagA could represent a strategy to protect the ecological niche of H. pylori against its own bacterial virulence factors, which are initially needed for colonization but later have detrimental consequences for the human host. Moreover, the immunosuppressive properties of VacA may play an important role in enabling H. pylori to persistently colonize the human host.
12.5. Additional Virulence Attributes
Besides cagPAI, CagA, and VacA, other bacterial virulence effectors are known to trigger H. pylori-mediated gastric disease. The duodenal ulcer-promoting gene A (dupA), encoding a VirB4 ATPase homolog, is associated with an increased risk of developing duodenal ulcer but a reduced risk of gastric atrophy and gastric cancer . Recent work indicates this could be due to dupA-mediated induction of proinflammatory cytokine secretion by mononuclear cells .
Another gene implicated in peptic ulcer disease is iceA1, albeit with considerable geographic differences in expression . The gene encodes a CATG-recognizing restriction endonuclease with significant sequence homology to nlaIIIR, an endonuclease of Neisseria lactamica [195, 196], and is induced by bacterial adherence to the gastric epithelium .
The Hop protein family member, bacterial outer membrane protein OipA (HopH) has also been identified as a potential disease-promoting factor. Like vacA, the oipA gene is present in all H. pylori strains, but its expression is modified by phase variation, caused by variable numbers of CT dinucleotide repeats in the 5′region. OipA was originally identified as a proinflammatory response-inducing protein, but may also serve as an adhesin . Its expression correlates with increased in vitro and in vivo production of IL-8  and, more recently, OipA has been shown to be involved in the activation of the focal adhesion kinase (FAK) and cytoskeletal reorganization, resulting in an altered morphological host cell phenotype . Other adhesins of the Hop protein family such as SabA (HopP) and BabA (HopS) are also categorized as bacterial virulence factors since they mediate bacterial adherence to the host and thus influence pathogenesis.
12.6. Host Cell Determinants of H. pylori Pathogenesis
It has become apparent that not only the pathogen but also host genetics play an important role in determining the clinical manifestation of H. pylori infections. Indeed, host genetic polymorphisms affecting expression levels of important genes involved in pathogenicity have been demonstrated to influence susceptibility and severity of H. pylori infection. In general, genetic polymorphisms in proinflammatory genes tend to increase the risk of gastric cancer, as demonstrated for IL-1, a potent proinflammatory cytokine and the most prominent inhibitor of gastric acid secretion . IL-1 is encoded by a gene cluster containing the polymorphic IL-1B (IL-1 cytokine-encoding gene) and IL-RN (IL-1 receptor antagonist encoding gene) encoding genes. Several polymorphisms, such as IL-1B*-31C, lead to the expression of large quantities of IL-1β and a subsequent reduction in acid secretion . Reduced acid secretion is linked to corpus-predominant colonization by H. pylori , which results in pangastritis formation of atrophic gastritis and thus an increased risk of gastric cancer and gastric ulcer disease [202–207]. Similar effects have been described for polymorphisms in other inflammation-associated genes, for example, the genes encoding tumor necrosis factor alpha (TNF-α) and IL-10. Distinct TNF-α polymorphisms lead to increased TNF-α expression, which influences, in concert with IL-1, gastrin production and thus acid production by parietal cells . In addition to alterations in acid production, cancer patients carrying the IL1B-511T/T genotype show significantly higher methylation levels of specific genes than patients with other genotypes. This leads to the assumption that the L1B-511T/T allele is associated with enhanced hypermethylation of multiple CpG island loci, which might contribute to an increase in the risk of gastric cancer in H. pylori-infected individuals . Similar to specific IL-1 genotypes, these TNF-α polymorphisms are, therefore, strongly linked to H. pylori infection and increased risk of gastric cancer [202, 210, 211]. In addition, specific IL-10 haplotypes lead to higher cytokine expression levels, thereby, shifting the balance towards an anti-inflammatory host cell [202, 212–214]; this is associated with the colonization of more virulent H. pylori strains . By contrast, specific IL-10 haplotypes actually induce lower IL-10 expression levels, favoring proinflammatory responses and an associated increased risk of gastric cancer. Polymorphisms in other gene types may also influence H. pylori-induced disease; for instance, a specific allelic variant of the TLR-9 promoter gene sequence creates a potential NF-κB binding site that increases the transcriptional activity of the gene . Since altered NF-κB activation is associated with premalignant gastric changes, this genotype could also be involved in H. pylori-mediated gastric cancer. Moreover, genes encoding IL-8 and NOD1 have also been shown to be associated with H. pylori-induced duodenal ulcer and gastritis . Interestingly, the number of polymorphisms seems to influence the clinical outcome dramatically. Whereas single polymorphisms of genes involved in proinflammatory responses may increase the risk of cancer development only two- to threefold, the presence of multiple genotypes increases the risk further [205, 218].
13. Beyond Peptic Ulceration and Gastric Cancer
13.1. MALT Lymphoma
All H. pylori-infected persons have a significantly increased risk for the development of gastric MALT lymphoma . Accordingly, the majority of MALT lymphoma patients are H. pylori positive . In very rare cases, a monoclonal population of B-cells arises from this mucosal tissue and proliferates to form a MALT lymphoma via chronic T-cell driven antigenic stimulation. The incidence of MALT lymphoma in H. pylori-infected patients is estimated to occur in less than 1% of H. pylori-positive subjects , but due to diagnostic controversies, based on difficult histological interpretations, and the rarity of this disorder, no exact figures are known. In contrast to gastric cancer, where the “point of no return” often abolishes successful treatment of adenocarcinoma via the eradication of H. pylori , the eradication of the bacteria in MALT patients can lead to complete remission in 60%–80% of patients with stage 1 low-grade gastric MALT lymphoma [221–224]. However, 10–35% of patients in complete remission after H. pylori eradication showed recurrent disease, necessitating the implementation of mandatory long-term follow-up examinations . Recurrence in specific patients could be due to the presence of at [11; 18] (q21; q21) translocation, which is associated with API2-MALT1 fusion. API2 is involved in apoptosis, and the latter resembles a caspase-like protein. The gene fusion leads to the suppression of apoptosis, and several studies have shown that MALT-lymphoma patients with this translocation do not or only rarely respond to H. pylori eradication [226, 227]. Despite these caveats, H. pylori eradication has been designated as the first choice treatment in the Maastricht III Consensus Report .
The development of gastroesophageal reflux disease (GERD) has long been considered to be independent of H. pylori as it occurred at the same frequency in H. pylori-positive and -negative patients . An intriguing, albeit controversial, role for H. pylori has emerged from observations that the bacterium’s prevalence was low in GERD patients , and that the incidence of GERD increased after H. pylori eradication , suggesting that the bacteria play a protective role. Moreover, H. pylori-induced corpus gastritis has been shown to reduce acid secretion and thus prevent patients from contracting GERD . Conflicting evidence exists, however, demonstrating that H. pylori eradication has no impact on either the new cases of GERD  or the worsening of preexisting cases when treatment has been withdrawn during disease remission. This inverse correlation between H. pylori and GERD, if it exists, warrants further study before sound scientific conclusions can be made.
13.3. Extra-Gastrointestinal Disease
A putative role for H. pylori in the development of idiopathic thrombocytic purpura (ITP) was first described by Gasbarrini and colleagues . Subsequent studies showed that platelet counts in patients with ITP returned to normal levels after the eradication of H. pylori [235, 236]. In addition, anti-CagA antibody titers have been shown to be significantly decreased in patients responsive to H. pylori eradication therapy in comparison to nonresponsive patients, implicating CagA in ITP pathogenesis .
A number of studies have also demonstrated a link between the pathogen and iron deficiency anaemia (IDA), another extragastrointestinal disease. The prevalence of H. pylori was highly increased in patients with unexplained IDA, and patients showed normal haemoglobin levels after H. pylori eradication therapies . Interestingly, despite normal serum transferrin and iron levels, soluble transferring receptor (sTFR) was significantly elevated in H. pylori-infected children, suggesting that sTFR is a more reliable indicator of iron status than serum iron or ferritin.
Similar to GERD, a negative correlation between H. pylori and disorders such as asthma, allergy, and atopic disease has been postulated. In general, H. pylori prevalence and asthma as well as allergic diseases show an inverse association ; in children not predisposed to atopy, an inverse correlation between H. pylori and eczema has been observed . Furthermore, due to the observations that diminished exposure to microbes during childhood leads to an increase of atopic disease , the debate regarding whether H. pylori should always be eradicated upon diagnosis has been heightened.
14. Diagnosis and Treatment
Diagnostic tests for H. pylori are generally divided into two categories: invasive and noninvasive. Invasive tests comprise the histological examination of gastric specimens. Noninvasive tests are based on peripheral samples such as blood, breath, stools, urine, and saliva, in order to detect antibodies, bacterial antigens, or urease activity. The choice of a specific test always depends on local experience and clinical settings, but usually a combination of two methods is often recommended since, for example, the detection of H. pylori-specific antibodies does not ultimately reflect a current infection.
Although H. pylori is sensitive to a wide range of antibiotics in vitro, they all fail when applied as monotherapy in vivo. Therefore, a combined therapeutic strategy is used, usually including two antibiotics (clarithromycin, combined with amoxicillin or metronidazole) and either a bismuth compound or a proton pump inhibitor (PPI). Rarely, quadruple therapies are used in which the bismuth compound and PPI are used in combination with two antibiotics. The use of these drugs has resulted in effective therapies, with eradication rates over 80%. During the past several years, however, resistant bacteria have been detected constantly [242, 243], leading to the search for alternative drugs and treatment strategies.
In the past decade, much effort has been devoted to the development of vaccination strategies. Based on the successful elimination of Helicobacter felis after mucosal immunization of mice with urease , the focus of much research has been the induction of a humoral or Th2-driven immune response. To date, however, effective vaccination has only been observed in animal models and no human vaccine trial has been successful . The failure to replicate the success of the vaccine in humans may be due to differences in H. pylori-specific immune responses or anatomical differences of the stomach. For instance, one of the main surface bacterial virulence factors, cagPAI, is usually switched off in mice.
Vaccines and antibiotics are not the only ways to prevent and cure H. pylori infection or H. pylori-associated disease. H. pylori-positive individuals infected with helminths have standard levels of H. pylori colonization rates and gastritis patterns, but they develop significantly less H. pylori-associated disease [246, 247]. These are intriguing observations that might result in low-dose administration of immunomodulating agents to H. pylori-positive patients, which have the same consequences as enteric helminth infections.
Another approach is the application of probiotics. There is convincing evidence that H. pylori is killed by Lactobacilli both in vitro and to a limited extent in vivo [248–250]. Furthermore, Lactobacilli show a positive impact on some H. pylori therapy-related side effects, and recent studies suggest that Lactobacilli supplements could be effective in increasing eradication rates .
15. Closing Remarks
The discovery that the world’s most common bacterial infection is clearly associated with the development of severe human gastric disease signaled a medical revolution that has already significantly reduced the incidence of one major human disorder (duodenal ulcer disease) and also promises to decrease a global lethal malignancy (gastric cancer). The great leaps forward in understanding the mechanisms of H. pylori pathogenesis are redefining our understanding of bacterial ecology and homeostasis; however, we are still a long way away from completely understanding how H. pylori is associated with the host and the development of disease. Elucidating this conundrum faces a number of challenges that require a combination of global and more focused, in-depth analyses. Monitoring the epigenetic changes occurring during infection, alongside more detailed analyses of the H. pylori-induced adaptive and innate immune responses may help to decipher the reasons for the failure of current vaccines. Given the increased incidence of antibiotic resistance, discovery of so far unknown bacterial virulence factors may potentially facilitate the development of new drugs. Moreover, in light of accumulating data showing that H. pylori infection could be beneficial for humans, we may need to rethink the commonly used medical approaches to treat H. pylori infections.
J. R. Warren, “Unidentified curved bacilli on gastric epithelium in active chronic gastritis,” Lancet, vol. 1, no. 8336, pp. 1273–1275, 1983.View at: Google Scholar
B. J. Marshall, J. A. Armstrong, D. B. McGechie, and R. J. Glancy, “Attempt to fulfil Koch's postulates for pyloric campylobacter,” Medical Journal of Australia, vol. 142, no. 8, pp. 436–439, 1985.View at: Google Scholar
A. Nomura, G. N. Stemmermann, P. H. Chyou, I. Kato, G. I. Perez-Perez, and M. J. Blaser, “Helicobacter pylori infection and gastric carcinoma among Japanese Americans in Hawaii,” New England Journal of Medicine, vol. 325, no. 16, pp. 1132–1136, 1991.View at: Google Scholar
J. Parsonnet, G. D. Friedman, and D. P. Vandersteen, “Helicobacter pylori infection and the risk of gastric carcinoma,” New England Journal of Medicine, vol. 325, no. 16, pp. 1127–1131, 1991.View at: Google Scholar
L. E. Hansson, L. Engstrand, and O. Nyren, “Helicobacter pylori infection: independent risk indicator of gastric adenocarcinoma,” Gastroenterology, vol. 105, no. 4, pp. 1098–1103, 1993.View at: Google Scholar
P. J. Hu, H. M. Mitchell, Y. Y. Li, M. H. Zhou, and S. L. Hazell, “Association of Helicobacter pylori with gastric cancer and observations on the detection of this bacterium in gastric cancer cases,” American Journal of Gastroenterology, vol. 89, no. 10, pp. 1806–1810, 1994.View at: Google Scholar
World Health Organisation, “Schistosomes, liver flukes and Helicobacter pylori. IARC Working Group on the Evaluation of Carcinogenic Risks to Humans. Lyon, 7–14 June 1994,” IARC Monographs on the Evaluation of Carcinogenic Risks to Humans / World Health Organization, International Agency for Research on Cancer, vol. 61, pp. 1–241, 1994.View at: Google Scholar
M. A. Al-Moagel, D. G. Evans, and M. E. Abdulghani, “Prevalence of Helicobacter (formerly Campylobacter) pylori infection in Saudia Arabia, and comparison of those with and without upper gastrointestinal symptoms,” American Journal of Gastroenterology, vol. 85, no. 8, pp. 944–948, 1990.View at: Google Scholar
D. Y. Graham, M. F. Go, and D. J. Evans, “Review article: urease, gastric ammonium/ammonia, and Helicobacter pylori—the past, the present, and recommendations for future research,” Alimentary Pharmacology and Therapeutics, vol. 6, no. 6, pp. 659–669, 1992.View at: Google Scholar
K. D. Crew and A. I. Neugut, “Epidemiology of gastric cancer,” World Journal of Gastroenterology, vol. 12, no. 3, pp. 354–362, 2006.View at: Google Scholar
R. A. Feldman, A. J. P. Eccersley, and J. M. Hardie, “Epidemiology of Helicobacter pylori: acquisition, transmission, population prevalence and disease-to-infection ratio,” British Medical Bulletin, vol. 54, no. 1, pp. 39–53, 1998.View at: Google Scholar
H. Malaty, H. M. T. El-Zimaity, R. M. Genta, R. A. Cole, and D. Y. Graham, “High-dose proton pump inhibitor plus amoxycillin for the treatment or retreatment of Helicobacter pylori infection,” Alimentary Pharmacology and Therapeutics, vol. 10, no. 6, pp. 1001–1004, 1996.View at: Google Scholar
R. M. Peek and M. J. Blaser, “Helicobacter pylori and gastrointestinal tract adenocarcinomas,” Nature Reviews Cancer, vol. 2, no. 1, pp. 28–37, 2002.View at: Google Scholar
Y. Yamaoka, D. H. Kwon, and D. Y. Graham, “A M(r) 34000 proinflammatory outer membrane protein (OipA) of Helicobacter pylori,” Proceedings of the National Academy of Sciences of the United States of America, vol. 97, no. 13, pp. 7533–7538, 2000.View at: Google Scholar
K. J. Goodman, P. Correa, H. J. Tenganá Aux et al., “Helicobacter pylori infection in the Colombian Andes: a population-based study of transmission pathways,” American Journal of Epidemiology, vol. 144, no. 3, pp. 290–299, 1996.View at: Google Scholar
R. J. Hopkins, P. A. Vial, and C. Ferreccio, “Seroprevalence of Helicobacter pylori in chile: vegetables may serve as one route of transmission,” Journal of Infectious Diseases, vol. 168, no. 1, pp. 222–226, 1993.View at: Google Scholar
J. G. Fox, “Non-human reservoirs of Helicobacter pylori,” Alimentary Pharmacology and Therapeutics, Supplement, vol. 9, no. 2, pp. 93–103, 1995.View at: Google Scholar
A. Özbek, E. Özbek, H. Dursun, Y. Kalkan, and T. Demirci, “Can Helicobacter pylori invade human gastric mucosa?: an in vivo study using electron microscopy, immunohistochemical methods, and real-time polymerase chain reaction,” Journal of Clinical Gastroenterology, vol. 44, no. 6, pp. 416–422, 2010.View at: Publisher Site | Google Scholar
N. J. Talley, J. E. Ormand, C. A. Frie, and A. R. Zinsmeister, “Stability of pH gradients in vivo across the stomach in Helicobacter pylori gastritis, dyspepsia, and health,” American Journal of Gastroenterology, vol. 87, no. 5, pp. 590–594, 1992.View at: Google Scholar
J. V. Solnick, C. Josenhans, S. Suerbaum, L. S. Tompkins, and A. Labigne, “Construction and characterization of an isogenic urease-negative mutant of Helicobacter mustelae,” Infection and Immunity, vol. 63, no. 9, pp. 3718–3721, 1995.View at: Google Scholar
G. Geis, H. Leying, S. Suerbaum, U. Mai, and W. Opferkuch, “Ultrastructure and chemical analysis of Campylobacter pylori flagella,” Journal of Clinical Microbiology, vol. 27, no. 3, pp. 436–441, 1989.View at: Google Scholar
S. Suerbaum, “The complex flagella of gastric Helicobacter species,” Trends in Microbiology, vol. 3, no. 5, pp. 168–170, 1995.View at: Google Scholar
K. A. Eaton, S. Suerbaum, C. Josenhans, and S. Krakowka, “Colonization of gnotobiotic piglets by Helicobacter pylori deficient in two flagellin genes,” Infection and Immunity, vol. 64, no. 7, pp. 2445–2448, 1996.View at: Google Scholar
D. J. McGee, M. L. Langford, E. L. Watson, J. E. Carter, Y. T. Chen, and K. M. Ottemann, “Colonization and inflammation deficiencies in Mongolian gerbils infected by Helicobacter pylori chemotaxis mutants,” Infection and Immunity, vol. 73, no. 3, pp. 1820–1827, 2005.View at: Publisher Site | Google Scholar
L. A. Noach, T. M. Rolf, and G. N. J. Tytgat, “Electron microscopic study of association between Helicobacter pylori and gastric and duodenal mucosa,” Journal of Clinical Pathology, vol. 47, no. 8, pp. 699–704, 1994.View at: Google Scholar
A. Bäckström, C. Lundberg, D. Kersulyte, D. E. Berg, T. Borén, and A. Arnqvist, “Metastability of Helicobacter pylori bab adhesin genes and dynamics in Lewis b antigen binding,” Proceedings of the National Academy of Sciences of the United States of America, vol. 101, no. 48, pp. 16923–16928, 2004.View at: Publisher Site | Google Scholar
J. V. Solnick, L. M. Hansen, N. R. Salama, J. K. Boonjakuakul, and M. Syvanen, “Modification of Helicobacter pylori outer membrane protein expression during experimental infection of rhesus macaques,” Proceedings of the National Academy of Sciences of the United States of America, vol. 101, no. 7, pp. 2106–2111, 2004.View at: Publisher Site | Google Scholar
C. Petersson, M. Forsberg, M. Aspholm et al., “Helicobacter pylori SabA adhesin evokes a strong inflammatory response in human neutrophils which is down-regulated by the neutrophil-activating protein,” Medical Microbiology and Immunology, vol. 195, no. 4, pp. 195–206, 2006.View at: Publisher Site | Google Scholar
R. Battan, M. C. Raviglione, A. Palagiano et al., “Helicobacter pylori infection in patients with acquired immune deficiency syndrome,” American Journal of Gastroenterology, vol. 85, no. 12, pp. 1576–1579, 1990.View at: Google Scholar
A. Muotiala, I. M. Helander, L. Pyhala, T. U. Kosunen, and A. P. Moran, “Low biological activity of Helicobacter pylori lipopolysaccharide,” Infection and Immunity, vol. 60, no. 4, pp. 1714–1716, 1992.View at: Google Scholar
A. P. Moran, B. Lindner, and E. J. Walsh, “Structural characterization of the lipid A component of Helicobacter pylori rough- and smooth-form lipopolysaccharides,” Journal of Bacteriology, vol. 179, no. 20, pp. 6453–6463, 1997.View at: Google Scholar
B. J. Appelmelk, I. Simoons-Smit, R. Negrini et al., “Potential role of molecular mimicry between Helicobacter pylori lipopolysaccharide and host Lewis blood group antigens in autoimmunity,” Infection and Immunity, vol. 64, no. 6, pp. 2031–2040, 1996.View at: Google Scholar
S. K. Lee, A. Stack, E. Katzowitsch, S. I. Aizawa, S. Suerbaum, and C. Josenhans, “Helicobacter pylori flagellins have very low intrinsic activity to stimulate human gastric epithelial cells via TLR5,” Microbes and Infection, vol. 5, no. 15, pp. 1345–1356, 2003.View at: Publisher Site | Google Scholar
V. J. Torres, S. E. VanCompernolle, M. S. Sundrud, D. Unutmaz, and T. L. Cover, “Helicobacter pylori vacuolating cytotoxin inhibits activation-induced proliferation of human T and B lymphocyte subsets,” Journal of Immunology, vol. 179, no. 8, pp. 5433–5440, 2007.View at: Google Scholar
J. Zabaleta, D. J. McGee, A. H. Zea et al., “Helicobacter pylori arginase inhibits T cell proliferation and reduces the expression of the TCR zeta-chain (CD3zeta),” Journal of Immunology, vol. 173, no. 1, pp. 586–593, 2004.View at: Google Scholar
A. P. Gobert, D. J. McGee, M. Akhtar et al., “Helicobacter pylori arginase inhibits nitric oxide production by eukaryotic cells: a strategy for bacterial survival,” Proceedings of the National Academy of Sciences of the United States of America, vol. 98, no. 24, pp. 13844–13849, 2001.View at: Publisher Site | Google Scholar
N. Akopyanz, N. O. Bukanov, T. U. Westblom, S. Kresovich, and D. E. Berg, “DNA diversity among clinical isolates of helicobacter pylori detected by PCR-based RAPD fingerprinting,” Nucleic Acids Research, vol. 20, no. 19, pp. 5137–5142, 1992.View at: Google Scholar
B. Björkholm, M. Sjölund, P. G. Falk, O. G. Berg, L. Engstrand, and D. I. Andersson, “Mutation frequency and biological cost of antibiotic resistance in Helicobacter pylori,” Proceedings of the National Academy of Sciences of the United States of America, vol. 98, no. 25, pp. 14607–14612, 2001.View at: Publisher Site | Google Scholar
B. D. Robertson and T. F. Meyer, “Genetic variation in pathogenic bacteria,” Trends in Genetics, vol. 8, no. 12, pp. 422–427, 1992.View at: Google Scholar
L. Salaün, B. Linz, S. Suerbaum, and N. J. Saunders, “The diversity within an expanded and redefined repertoire of phase-variable genes in Helicobacter pylori,” Microbiology, vol. 150, no. 4, pp. 817–830, 2004.View at: Google Scholar
D. M. Parkin, F. Bray, J. Ferlay, and P. Pisani, “Global cancer statistics, 2002,” CA: A Cancer Journal for Clinicians, vol. 55, no. 2, pp. 74–108, 2002.View at: Google Scholar
World Health Organization, “Disease and injury country estimates,” 2009.View at: Google Scholar
P. Lauren, “The two histological main types of gastric carcinoma: diffuse and so-called intestinal-type carcinoma. An attempt at a histo-clinical classification,” Acta Pathologica et Microbiologica Scandinavica, vol. 64, pp. 31–49, 1965.View at: Google Scholar
P. Correa, “Diet modification and gastric cancer prevention,” Journal of the National Cancer Institute. Monographs, vol. 12, no. 12, pp. 75–78, 1992.View at: Google Scholar
J. H. Kurata and B. M. Haile, “Epidemiology of peptic ulcer disease,” Clinics in Gastroenterology, vol. 13, no. 2, pp. 289–307, 1984.View at: Google Scholar
C. Holcombe, “Helicobacter pylori: the African enigma,” Gut, vol. 33, no. 4, pp. 429–431, 1992.View at: Google Scholar
R. Ally, H. M. Mitchell, and I. Segal, “Differences in the immune response to H. pylori infection in Sowetan subjects may relate to concurrent parasitic infections,” South African Medical Journal, vol. 90, p. 642, 2000.View at: Google Scholar
R. D. Leunk, P. T. Johnson, B. C. David, W. G. Kraft, and D. R. Morgan, “Cytotoxic activity in broth-culture filtrates of Campylobacter pylori,” Journal of Medical Microbiology, vol. 26, no. 2, pp. 93–99, 1988.View at: Google Scholar
J. C. Atherton, “H. pylori virulence factors,” British Medical Bulletin, vol. 54, no. 1, pp. 105–120, 1998.View at: Google Scholar
C. Weydig, A. Starzinski-Powitz, G. Carra, J. Löwer, and S. Wessler, “CagA-independent disruption of adherence junction complexes involves E-cadherin shedding and implies multiple steps in Helicobacter pylori pathogenicity,” Experimental Cell Research, vol. 313, no. 16, pp. 3459–3471, 2007.View at: Publisher Site | Google Scholar
A. M. Y. Nomura, J. Lee, G. N. Stemmermann, R. Y. Nomura, G. I. Perez-Perez, and M. J. Blaser, “Helicobacter pylori CagA seropositivity and gastric carcinoma risk in a Japanese American population,” Journal of Infectious Diseases, vol. 186, no. 8, pp. 1138–1144, 2002.View at: Publisher Site | Google Scholar
M. J. Blaser, G. I. Perez-Perez, H. Kleanthous et al., “Infection with Helicobacter pylori strains possessing cagA is associated with an increased risk of developing adenocarcinoma of the stomach,” Cancer Research, vol. 55, no. 10, pp. 2111–2115, 1995.View at: Google Scholar
N. Ohnishi, H. Yuasa, S. Tanaka et al., “Transgenic expression of Helicobacter pylori CagA induces gastrointestinal and hematopoietic neoplasms in mouse,” Proceedings of the National Academy of Sciences of the United States of America, vol. 105, no. 3, pp. 1003–1008, 2008.View at: Publisher Site | Google Scholar
S. Brandt, T. Kwok, R. Hartig, W. König, and S. Backert, “NF-kappaB activation and potentiation of proinflammatory responses by the Helicobacter pylori CagA protein,” Proceedings of the National Academy of Sciences of the United States of America, vol. 102, no. 26, pp. 9300–9305, 2005.View at: Publisher Site | Google Scholar
N. Murata-Kamiya, K. Kikuchi, T. Hayashi, H. Higashi, and M. Hatakeyama, “Helicobacter pylori exploits host membrane phosphatidylserine for delivery, localization, and pathophysiological action of the CagA oncoprotein,” Cell Host and Microbe, vol. 7, no. 5, pp. 399–411, 2010.View at: Publisher Site | Google Scholar
M. Stein, R. Rappuoli, and A. Covacci, “Tyrosine phosphorylation of the Helicobacter pylori CagA antigen after cag-driven host cell translocation,” Proceedings of the National Academy of Sciences of the United States of America, vol. 97, no. 3, pp. 1263–1268, 2000.View at: Publisher Site | Google Scholar
E. D. Segal, J. Cha, J. Lo, S. Falkow, and L. S. Tompkins, “Altered states: involvement of phosphorylated CagA in the induction of host cellular growth changes by Helicobacter pylori,” Proceedings of the National Academy of Sciences of the United States of America, vol. 96, no. 25, pp. 14559–14564, 1999.View at: Publisher Site | Google Scholar
N. Murata-Kamiya, Y. Kurashima, Y. Teishikata et al., “Helicobacter pylori CagA interacts with E-cadherin and deregulates the β-catenin signal that promotes intestinal transdifferentiation in gastric epithelial cells,” Oncogene, vol. 26, no. 32, pp. 4617–4626, 2007.View at: Publisher Site | Google Scholar
M. Suzuki, H. Mimuro, T. Suzuki, M. Park, T. Yamamoto, and C. Sasakawa, “Interaction of CagA with Crk plays an important role in Helicobacter pylori-induced loss of gastric epithelial cell adhesion,” Journal of Experimental Medicine, vol. 202, no. 9, pp. 1235–1247, 2005.View at: Publisher Site | Google Scholar
V. Ricci, C. Ciacci, R. Zarrilli et al., “Effect of Helicobacter pylori on gastric epithelial cell migration and proliferation in vitro: role of VacA and CagA,” Infection and Immunity, vol. 64, no. 7, pp. 2829–2833, 1996.View at: Google Scholar
S. A. Sharma, M. K. R. Tummuru, M. J. Blaser, and L. D. Kerr, “Activation of IL-8 gene expression by Helicobacter pylori is regulated by transcription factor nuclear factor-kappa B in gastric epithelial cells,” Journal of Immunology, vol. 160, no. 5, pp. 2401–2407, 1998.View at: Google Scholar
A. Bhattacharyya, S. Pathak, S. Datta, S. Chattopadhyay, J. Basu, and M. Kundu, “Mitogen-activated protein kinases and nuclear factor-κB regulate Helicobacter pylori-mediated interleukin-8 release from macrophages,” Biochemical Journal, vol. 368, no. 1, pp. 121–129, 2002.View at: Publisher Site | Google Scholar
M. Naumann, S. Wessler, C. Bartsch et al., “Activation of activator protein 1 and stress response kinases in epithelial cells colonized by Helicobacter pylori encoding the cag pathogenicity island,” Journal of Biological Chemistry, vol. 274, no. 44, pp. 31655–31662, 1999.View at: Publisher Site | Google Scholar
M. L. Hutton, M. Kaparakis-Liaskos, L. Turner, A. Cardona, T. Kwok, and R. L. Ferrero, “Helicobacter pylori exploits cholesterol-rich microdomains for induction of NF-κB-dependent responses and peptidoglycan delivery in epithelial cells,” Infection and Immunity, vol. 78, no. 11, pp. 4523–4531, 2010.View at: Publisher Site | Google Scholar
V. Necchi, P. Sommi, V. Ricci, and E. Solcia, “In vivo accumulation of Helicobacter pylori products, NOD1, ubiquitinated proteins and proteasome in a novel cytoplasmic structure,” PloS One, vol. 5, no. 3, article e9716, 2010.View at: Google Scholar
J. C. Atherton, P. Cao, R. M. Peek, M. K. R. Tummuru, M. J. Blaser, and T. L. Cover, “Mosaicism in vacuolating cytotoxin alleles of helicobacter pylori. Association of specific vacA types with cytotoxin production and peptic ulceration,” Journal of Biological Chemistry, vol. 270, no. 30, pp. 17771–17777, 1995.View at: Publisher Site | Google Scholar
C. Figueiredo, J. C. Machado, P. Pharoah et al., “Helicobacter pylori and interleukin 1 genotyping: an opportunity to identify high-risk individuals for gastric carcinoma,” Journal of the National Cancer Institute, vol. 94, no. 22, pp. 1680–1687, 2002.View at: Google Scholar
L. J. Van Doorn, C. Figueiredo, F. Megraud et al., “Geographic distribution of vacA allelic types of Helicobacter pylori,” Gastroenterology, vol. 116, no. 4, pp. 823–830, 1999.View at: Google Scholar
J. L. Telford, P. Ghiara, M. Dell'Orco et al., “Gene structure of the Helicobacter pylori cytotoxin and evidence of its key role in gastric disease,” Journal of Experimental Medicine, vol. 179, no. 5, pp. 1653–1658, 1994.View at: Google Scholar
T. L. Cover and M. J. Blaser, “Purification and characterization of the vacuolating toxin from Helicobacter pylori,” Journal of Biological Chemistry, vol. 267, no. 15, pp. 10570–10575, 1992.View at: Google Scholar
P. Lupetti, J. E. Heuser, and R. Manetti, “Oligomeric and subunit structure of the Helicobacter pylori vacuolating cytotoxin,” Journal of Cell Biology, vol. 133, no. 4, pp. 801–807, 1996.View at: Google Scholar
J. A. Garner and T. L. Cover, “Binding and internalization of the Helicobacter pylori vacuolating cytotoxin by epithelial cells,” Infection and Immunity, vol. 64, no. 10, pp. 4197–4203, 1996.View at: Google Scholar
K. Yahiro, T. Niidome, M. Kimura et al., “Activation of Helicobacter pylori VacA toxin by alkaline or acid conditions increases its binding to a 250-kDa receptor protein-tyrosine phosphatase β,” Journal of Biological Chemistry, vol. 274, no. 51, pp. 36693–36699, 1999.View at: Publisher Site | Google Scholar
E. E. Hennig, M. M. Godlewski, E. Butruk, and J. Ostrowski, “Helicobacter pylori VacA cytotoxin interacts with fibronectin and alters HeLa cell adhesion and cytoskeletal organization in vitro,” FEMS Immunology and Medical Microbiology, vol. 44, no. 2, pp. 143–150, 2005.View at: Publisher Site | Google Scholar
T. L. Cover, U. S. Krishna, D. A. Israel, and R. M. Peek, “Induction of gastric epithelial cell apoptosis by Helicobacter pylori vacuolating cytotoxin,” Cancer Research, vol. 63, no. 5, pp. 951–957, 2003.View at: Google Scholar
D. C. Willhite and S. R. Blanke, “Helicobacter pylori vacuolating cytotoxin enters cells, localizes to the mitochondria, and induces mitochondrial membrane permeability changes correlated to toxin channel activity,” Cellular Microbiology, vol. 6, no. 2, pp. 143–154, 2004.View at: Publisher Site | Google Scholar
A. Galmiche, J. Rassow, A. Doye et al., “The N-terminal 34 kDa fragment of Helicobacter pylori vacuolating cytotoxin targets mitochondria and induces cytochrome c release,” EMBO Journal, vol. 19, no. 23, pp. 6361–6370, 2000.View at: Google Scholar
D. C. Willhite, T. L. Cover, and S. R. Blanke, “Cellular vacuolation and mitochondrial cytochrome c release are independent outcomes of Helicobacter pylori vacuolating cytotoxin activity that are each dependent on membrane channel formation,” Journal of Biological Chemistry, vol. 278, no. 48, pp. 48204–48209, 2003.View at: Publisher Site | Google Scholar
A. Oldani, M. Cormont, and V. Hofman, “Helicobacter pylori counteracts the apoptotic action of its VacA toxin by injecting the CagA protein into gastric epithelial cells,” PLoS Pathogens, vol. 5, no. 10, article e1000603, 2009.View at: Google Scholar
N. Tegtmeyer, D. Zabler, D. Schmidt, R. Hartig, S. Brandt, and S. Backert, “Importance of EGF receptor, HER2/Neu and Erk1/2 kinase signalling for host cell elongation and scattering induced by the Helicobacter pylori CagA protein: antagonistic effects of the vacuolating cytotoxin VacA,” Cellular Microbiology, vol. 11, no. 3, pp. 488–505, 2009.View at: Publisher Site | Google Scholar
N. R. Hussein, R. H. Argent, C. K. Marx, S. R. Patel, K. Robinson, and J. C. Atherton, “Helicobacter pylori dupA is polymorphic, and its active form induces proinflammatory cytokine secretion by mononuclear cells,” Journal of Infectious Diseases, vol. 202, no. 2, pp. 261–269, 2010.View at: Publisher Site | Google Scholar
Y. Yamaoka, T. Kodama, O. Gutierrez, J. G. Kim, K. Kashima, and D. Y. Graham, “Relationship between Helicobacter priori iceA, cagA, and vacA status and clinical outcome: studies in four different countries,” Journal of Clinical Microbiology, vol. 37, no. 7, pp. 2274–2279, 1999.View at: Google Scholar
Q. Xu, R. D. Morgan, R. J. Roberts et al., “Functional analysis of iceA1, a CATG-recognizing restriction endonuclease gene in Helicobacter pylori,” Nucleic Acids Research, vol. 30, no. 17, pp. 3839–3847, 2002.View at: Google Scholar
R. M. Peek, S. A. Thompson, J. P. Donahue et al., “Adherence to gastric epithelial cells induces expression of a Helicobacter pylori gene, iceA, that is associated with clinical outcome,” Proceedings of the Association of American Physicians, vol. 110, no. 6, pp. 531–544, 1998.View at: Google Scholar
Y. Yamaoka, S. Kikuchi, H. M. T. ElZimaity, O. Gutierrez, M. S. Osato, and D. Y. Graham, “Importance of Helicobacter pylori OipA in clinical presentation, gastric inflammation, and mucosal interleukin 8 production,” Gastroenterology, vol. 123, no. 2, pp. 414–424, 2002.View at: Publisher Site | Google Scholar
J. Calam, “Helicobacter pylori modulation of gastric acid,” Yale Journal of Biology and Medicine, vol. 72, no. 2-3, pp. 195–202, 1999.View at: Google Scholar
E. M. El-Omar, M. Carrington, and W. H. Chow, “The role of interleukin-1 polymorphisms in the pathogenesis of gastric cancer.,” Nature, vol. 412, no. 6842, p. 99, 2001.View at: Google Scholar
R. Rad, C. Prinz, B. Neu et al., “Synergistic effect of Helicobacter pylori virulence factors and interleukin-1 polymorphisms for the development of severe histological changes in the gastric mucosa,” Journal of Infectious Diseases, vol. 188, no. 2, pp. 272–281, 2003.View at: Publisher Site | Google Scholar
T. Suzuki, E. Grand, and C. Bowman, “TNF-α and interleukin 1 activate gastrin gene expression via MAPK- and PKC-dependent mechanisms,” American Journal of Physiology Gastrointestinal and Liver Physiology, vol. 281, no. 6, pp. G1405–G1412, 2001.View at: Google Scholar
I. Ohyama, N. Ohmiya, Y. Niwa et al., “The association between tumour necrosis factor-α gene polymorphism and the susceptibility to rugal hyperplastic gastritis and gastric carcinoma,” European Journal of Gastroenterology and Hepatology, vol. 16, no. 7, pp. 693–700, 2004.View at: Publisher Site | Google Scholar
S. S. Yea, Y. I. Yang, W. H. Jang, Y. J. Lee, H. S. Bae, and K. H. Paik, “Association between TNF-α promoter polymorphism and Helicobacter pylori cagA subtype infection,” Journal of Clinical Pathology, vol. 54, no. 9, pp. 703–706, 2001.View at: Google Scholar
M. T. H. Ng, R. Van't Hof, and J. C. Crockett, “Increase in NF-κB binding affinity of the variant C allele of the toll-like receptor 9 -1237T/C polymorphism is associated with Helicobacter pylori-induced gastric disease,” Infection and Immunity, vol. 78, no. 3, pp. 1345–1352, 2010.View at: Publisher Site | Google Scholar
M. Macarthur, G. L. Hold, and E. M. El-Omar, “Inflammation and Cancer II. Role of chronic inflammation and cytokine gene polymorphisms in the pathogenesis of gastrointestinal malignancy,” American Journal of Physiology Gastrointestinal and Liver Physiology, vol. 286, no. 4, pp. G515–G520, 2004.View at: Google Scholar
S. Eidt, M. Stolte, and R. Fischer, “Helicobacter pylori gastritis and primary gastric non-Hodgkin's lymphomas,” Journal of Clinical Pathology, vol. 47, no. 5, pp. 436–439, 1994.View at: Google Scholar
A. De Mascarel, A. Ruskone-Fourmestraux, A. Lavergne-Slove, F. Megraud, P. Dubus, and J. P. Merlio, “Clinical, histological and molecular follow-up of 60 patients with gastric marginal zone lymphoma of mucosa-associated lymphoid tissue,” Virchows Archiv, vol. 446, no. 3, pp. 219–224, 2005.View at: Publisher Site | Google Scholar
W. Fischbach, M. E. Goebeler-Kolve, B. Dragosics, A. Greiner, and M. Stolte, “Long term outcome of patients with gastric marginal zone B cell lymphoma of mucosa associated lymphoid tissue (MALT) following exclusive Helicobacter pylori eradication therapy: experience from a large prospective series,” Gut, vol. 53, no. 1, pp. 34–37, 2004.View at: Publisher Site | Google Scholar
H. Liu, H. Ye, and A. RuskoneFourmestraux, “T(11;18) is a marker for all stage gastric MALT lymphomas that will not respond to H. pylori eradication,” Gastroenterology, vol. 122, no. 5, pp. 1286–1294, 2002.View at: Google Scholar
H. Inagaki, T. Nakamura, C. Li et al., “Gastric MALT lymphomas are divided into three groups based on responsiveness to Helicobacter pylori eradication and detection of API2-MALT1 fusion,” American Journal of Surgical Pathology, vol. 28, no. 12, pp. 1560–1567, 2004.View at: Publisher Site | Google Scholar
P. Malfertheiner, F. Megraud, C. O'Morain et al., “Current concepts in the management of Helicobacter pylori infection: the Maastricht III Consensus Report,” Gut, vol. 56, no. 6, pp. 772–781, 2007.View at: Google Scholar
A. Gasbarrini, F. Franceschi, R. Tartaglione, R. Landolfi, P. Pola, and G. Gasbarrini, “Regression of autoimmune thrombocytopenia after eradication of Helicobacter pylori,” Lancet, vol. 352, no. 9131, p. 878, 1998.View at: Google Scholar
A. Asahi, M. Kuwana, H. Suzuki, T. Hibi, Y. Kawakami, and Y. Ikeda, “Effects of a Helicobacter pylori eradication regimen on anti-platelet autoantibody response in infected and uninfected patients with idiopathic thrombocytopenic purpura,” Haematologica, vol. 91, no. 10, pp. 1436–1437, 2006.View at: Google Scholar
M. Kist, “Helicobacter pylori: primary antimicrobial resistance and first-line treatment strategies,” Eurosurveillance, vol. 12, no. 7, pp. E1–2, 2007.View at: Google Scholar
N. Wueppenhorst, H. P. Stueger, M. Kist, and E. Glocker, “Identification and molecular characterization of triple- and quadruple-resistant Helicobacter pylori clinical isolates in Germany,” Journal of Antimicrobial Chemotherapy, vol. 63, no. 4, pp. 648–653, 2009.View at: Publisher Site | Google Scholar
T. Aebischer, D. Bumann, H. J. Epple et al., “Correlation of T cell response and bacterial clearance in human volunteers challenged with Helicobacter pylori revealed by randomised controlled vaccination with Ty21a-based Salmonella vaccines,” Gut, vol. 57, no. 8, pp. 1065–1072, 2008.View at: Publisher Site | Google Scholar
Y. Du, A. Agnew, X.-P. Ye, P. A. Robinson, D. Forman, and J. E. Crabtree, “Helicobacter pylori and Schistosoma japonicum co-infection in a Chinese population: helminth infection alters humoral responses to H. pylori and serum pepsinogen I/II ratio,” Microbes and Infection, vol. 8, no. 1, pp. 52–60, 2006.View at: Publisher Site | Google Scholar
P. D. Midolo, J. R. Lambert, R. Hull, F. Luo, and M. L. Grayson, “In vitro inhibition of Helicobacter pylori NCTC 11637 by organic acids and lactic acid bacteria,” Journal of Applied Bacteriology, vol. 79, no. 4, pp. 475–479, 1995.View at: Google Scholar
I. Sakamoto, M. Igarashi, K. Kimura, A. Takagi, T. Miwa, and Y. Koga, “Suppressive effect of Lactobacillus gasseri OLL 2716 (LG21) on Helicobacter pylori infection in humans,” Journal of Antimicrobial Chemotherapy, vol. 47, no. 5, pp. 709–710, 2001.View at: Google Scholar