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BioMed Research International
Volume 2016 (2016), Article ID 9032085, 18 pages
http://dx.doi.org/10.1155/2016/9032085
Review Article

Anaplasma marginale: Diversity, Virulence, and Vaccine Landscape through a Genomics Approach

Unidad de Anaplasmosis, Centro Nacional en Investigación Disciplinaria en Parasitología Veterinaria, INIFAP, Carretera Federal Cuernavaca-Cuautla 8534, 62574 Jiutepec, MOR, Mexico

Received 4 May 2016; Accepted 26 July 2016

Academic Editor: Jozef Anné

Copyright © 2016 Rosa Estela Quiroz-Castañeda et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

In order to understand the genetic diversity of A. marginale, several efforts have been made around the world. This rickettsia affects a significant number of ruminants, causing bovine anaplasmosis, so the interest in its virulence and how it is transmitted have drawn interest not only from a molecular point of view but also, recently, some genomics research have been performed to elucidate genes and proteins with potential as antigens. Unfortunately, so far, we still do not have a recombinant anaplasmosis vaccine. In this review, we present a landscape of the multiple approaches carried out from the genomic perspective to generate valuable information that could be used in a holistic way to finally develop an anaplasmosis vaccine. These approaches include the analysis of the genetic diversity of A. marginale and how this affects control measures for the disease. Anaplasmosis vaccine development is also reviewed from the conventional vaccinomics to genome-base vaccinology approach based on proteomics, metabolomics, and transcriptomics analyses reported. The use of these new omics approaches will undoubtedly reveal new targets of interest in the near future, comprising information of potential antigens and the immunogenic effect of A. marginale proteins.

1. Introduction

Tick-borne diseases are major obstacles and are considered the cause of great economic impact for livestock production [1]. Tick-borne rickettsial diseases are important problems of management in livestock health in Africa, Australia, Asia, and Latin America. Globally, the most important rickettsial disease in cattle is bovine anaplasmosis caused by Anaplasma marginale, an infectious, noncontagious disease characterized by progressive hemolytic anemia, abortions, loss of condition, milk production, and death [2, 3]. Clinical disease in most notable in cattle, but other ruminants including water buffalo, bison, African antelopes, and some species of deer can become infected [4].

In endemic areas, indigenous cattle have developed resistance to ticks and anaplasmosis [1]. Control measures currently available include the use of acaricides, animal treatment, chemoprophylaxis, controlled exposure, and vaccination. Most of these approaches only limit losses caused by ticks and tick-borne diseases [5]. The use of acaricides is becoming more problematic due to the selection of tick resistant populations; furthermore the presence of acaricide residues in meat and milk is public health concerns and ultimately can interfere with the enzootic stability making animals susceptible to both anaplasmosis and bovine babesiosis [6]. Chemoprophylaxis (treatment-exposure) and controlled infection (exposure-treatment) may or may not be effective even if carried under strict veterinary supervision. Immunoprophylaxis is then the method of choice for the prevention of infectious diseases [7, 8].

Control of bovine anaplasmosis is, however, compounded by the large antigenic and genetic diversity found in strains from one region to another, within the same herd and even within the same animal [912].

Current research efforts aim at new alternatives for designing vaccines including the use of sequencing technologies and omics approaches [1317].

High-throughput sequencing technologies currently available are fast and inexpensive enough processes and currently included in almost any bacteria related project [18]. Whole-genome sequences (WGS) data provides information of gene repertoire and sequence variation and is also an approach to associate genotype with phenotype [19]. Genomics analyses of these data represent a significant tool to understand the bacterial diversity, their phylogenetic relationships, and the mechanisms related to their vital functions (transmission, pathogenicity, metabolic processes, etc.).

The first complete genome sequence of Anaplasma marginale (St. Maries strain) was published eleven years earlier with the promise of better immunogens based on more complete knowledge of the genetic makeup of the rickettsia [20]. In addition to A. marginale St Maries genome, the genomes of other rickettsial agents of human and animal importance have been reported and analyzed, including A. marginale American strain Florida, Gypsy Plains, and Dawn strains from Australia, A. marginale subsp. centrale (strain Israel), A. phagocytophilum, Ehrlichia chaffeensis, Rickettsia prowazekii, and R. typhi [2026]. In spite of this wealth of genetic information, development of vaccines that can induce protection against an array of strains of A. marginale is still pending.

In this review, we analyze the available information with regard to molecular diversity and variability that make A. marginale a rickettsia for which vaccine design has turned very difficult. We also present an update of the information of strains reported worldwide and highlight the relevant information for regional vaccine development. In addition, we focus on the A. marginale vaccine approaches through conventional, reverse vaccinology, and omics approaches carried so far. Finally, the immunological effect of A. marginale proteins with potential as immunogens is also reviewed.

2. Diversity of Anaplasma marginale

Characterization of strains from diverse geographical origin of A. marginale includes morphology, protein sequence, antigenicity, and their ability to be transmitted by ticks [4, 27, 28]. The genetic diversity of A. marginale has been classified by using major surface proteins (MSP) such as MSP1a, MSP4, and MSP5, which are encoded by single genes. These genes have been widely used for molecular characterization of A. marginale [4]. msp1a gene which shows wide genetic diversity has been used for identification of A. marginale strains worldwide and is considered a stable genetic marker conserved during acute and persistent rickettsemia in cattle and during multiplication in ticks [27, 29, 30]. msp4 gene, which shows a very low variation index, has also been used as a stable marker for phylogeographic studies [9]. On the contrary, msp5 is extremely conserved between isolates of A. marginale and is not phylogenetically informative but rather used in molecular diagnosis of infection by this rickettsia. msp5 product MSP5 is highly immunogenic and has also been used for serologic diagnostic of the disease [31].

Several geographic strains of A. marginale differing in their biology, genetic characteristics, and transmissibility by ticks have been identified using MSP1a; this protein is composed by a C terminal conserved domain and a N-terminal variable domain composed of one or more peptides of 23 to 31 amino acids very similar among them known as repeats [1416]. MSP1a has evolved under positive selective pressure of the host immune system and molecular weight difference of the peptides in geographic strains is the result of variations in the numbers of tandem repeat units. MSP1a, used as molecular marker, has provided phylogenetic and evolutionary information about A. marginale strains [10].

The genetic diversity of A. marginale based on MSP1a has been reported in several countries all over the world [30, 3237]. A global analysis using 131 strains of A. marginale from North and South America, Europe, Africa, Asia, and Australia provided information about the genetic heterogeneity of the rickettsia [30]. de la Fuente et al. using msp1a [30] found 79 different repeat sequences in 131 strains, thus corroborating the known genetic heterogeneity of A. marginale [38]. Although MSP1a repeat sequences did not group in clusters geographically related or offered phylogenetic relationships, they did provide phylogeographic information, as 78% of the repeat sequences were present in strains from a single geographic region. Some MSP1a repeats clustered and were unique to certain regions such as Italy, Spain, China, Argentina, and South America. Australia was a special case, where a single genotype is found, which suggests that multiple introductions of A. marginale strains from different geographic locations occurred in the rest of the continental countries.

These authors also found that repeats 27 and 13 were present in strains from geographic regions as distant as Latin America and South Africa, but with the common tick vector, Rhipicephalus microplus. In this case, it is impossible to rule the role of other tick species out or mechanical transmission in the evolution of the rickettsia [30].

A molecular analysis using MSP1a revealed the genetic diversity of Mexican strains of A. marginale from different geographic origins. Jimenez-Ocampo et al. [32] reported the presence of repeats, such as F, M, and M in a strain from Ticul, Yucatán, also commonly found in Argentina (F, M, M, and M), Israel (F, M), and Italy (M). Some other Mexican strains including Tizimin, Playa Vicente, and Tlapacoyan share a significant sequence of tandem repeats with Florida strain (A, B, B, B, B, B, and B). Strains from central states of Mexico (Yautepec, Morelos) and states near the Gulf of Mexico (Veracruz, Veracruz) and the West coast (Tepic, Nayarit) have some variants of the repeats α, β, β, and Γ, also found in strains from Argentina and Brazil.

Recently, Castañeda-Ortiz et al. [12] reported 14 new msp1a genotypes detected in infected animals from two cattle herds in Mexico, called EV1–12 and LJ1-LJ2.

The wide genetic diversity observed in Mexican strains of A. marginale reveals the significant role of cattle movement and reinforces the proposal of regional vaccines to control anaplasmosis.

Phylogeographic analysis of MSP1a has also revealed an association between the first (R1) and last (RL) MSP1a repeat sequences and world ecological regions (ecoregions) specific signatures, which implies a different evolutionary pressure and the MSP1a sequences [39]. The authors found 39 and 28 unique R1 and RL sequences, respectively, of 111 A. marginale strains. The MSP1a R1 is associated with four ecoregions, each of them with unique repeats sequences (i.e., ecoregion 1: 4, 8, 16, 56, 60, 64, 67, γ, π, τ; ecoregion 2: 28, 48, 53, E, F, Σ; ecoregion 3: 1, 3, 5, 6, 27, 33, 34, 39, M, O, Q, U; and ecoregion 4: I, J, K). The RL MSP1a repeat is also associated with four ecoregions (i.e., ecoregion 1: 8, 9, 12, 15, 59, 61, 66; ecoregion 2: 10, 31, 52, π, β; ecoregion 3: 3, 7, 35, 37, 38, 44, E, N, P, Q, U, ρ; and ecoregion 4: none). This was the first evidence that the evolution of A. marginale was linked to ecological traits affecting tick vector performance and how these traits have driven the evolution of vector-borne pathogens.

Recently, Machado et al. [35] reported outbreaks of anaplasmosis in two municipalities of Brazil, Lins and Mambaí. According to the analysis of the tandem repeat structures of MSP1a, nine different strains were found in Lins (τ, 10, 15; α, β, β; α, β, β, β, 13; α, β, β, 192; τ, β, 100; α, β, β, Γ; 193, β, 100; 191, 13, Γ; and 191, 13, 18) and two in Mambaí (α, β, β, Γ and E, F, φ, φ, F, F). The limited genetic diversity of A. marginale observed in the Mambaí region is attributed to an intensive tick control program prior to the anaplasmosis outbreak among the cattle sampled in this location, and authors believe that transmission occurred mainly through bloodsucking flies instead of tick vectors. The authors also described three new repeats of MSP1a (191, 192, and 193) and associated the τ-10-15 and α-β3-Γ strains with the occurrence of clinical anaplasmosis and mortality in calves, heifers, and lactating cows. As reported before, out of the different strains of A. marginale identified worldwide some have been associated with the occurrence of anaplasmosis outbreaks; specifically, the α, β, Γ and τ, 10, 15 strains have been previously described in outbreaks of bovine anaplasmosis in Mexico and Argentina [40, 41].

Likewise, but in Rio de Janeiro in Brazil, Baêta et al. [36] reported two strains of A. marginale, AmRio1 and AmRio2, that were isolated and propagated in IDE8 cells from blood of two cattle. One of the isolates, AmRio1, has a new amino acid sequence of the MSP1a tandem repeat (named 162). The authors also performed a phylogenetic analysis using Argentinian and Brazilian strains. They observed that the population of A. marginale in both countries form two big clusters: α and τ; cluster τ has wider genetic variability than cluster α, suggesting that lineages belonging to these two clusters may be under different sources of selective pressure, specifically host immunity and tick transmission. Then, new combinations of tandem repeats may give these strains adaptive advantages over those pressure factors.

An interesting case was reported by Mutshembele et al. [37]; these authors carried a prevalence analysis and evaluated the diversity and evolution of MSP1a in South African strains of A. marginale. They found that tandem repeats 3, 4, 13, 34, Q, and 37 had a high frequency and have been reported in strains of Israel (3, 4), South America (4, 13), and Europe (Q). Repeats 34 and 37 were abundant only in South Africa with rare exceptions. Through a reconstruction of ancestral amino acid sequence, they found that tandem 4 is the ancestral state of all new repeats reported in South Africa. It should be interesting to test whether the tandem repeat 4 from MSP1a reported in Mexican A. marginale strains evolved from the South African repeat [41]. The authors suggest that the repeated sequences identified in South Africa may constitute a group of recently evolved tandem repeats, which have not been reported elsewhere [27].

In 2014, Ybañez et al. [42] using MSP1a and GroEL as molecular markers reported high genetic diversity of A. marginale in Philippine cattle; this was the first report of A. marginale genotypes in Southeast Asia. They identified 20 novel and unique tandem repeat sequences arranged in 44 new genotypes; repeats showed an identity of 90–96% to those found in Mexico, Brazil, Argentina, South Africa, Venezuela, Japan, Israel, China, United States, and Italy. In some samples, multiple infections of even three and four different genotypes of A. marginale were observed, being dual infections, the most common cases. The superinfection may be the consequence of a common exposure or source of the infection despite geographical boundaries, the cattle trade, or movement among different islands in the country.

Different structure of tandem repeats of MSP1a reported worldwide is shown in Table 1.

Table 1: MSP1a tandem repeats reported worldwide. The wide genetic diversity observed is result, in most cases, of cattle movements, veterinary practices, and vector population dynamics.

Information available on genetic diversity of A. marginale highlights the fact that variation observed is only the result of natural adaptation processes and pressure exerted on the rickettsia A. marginale and cattle movements that occurs in a global trade system. So far, the isolation and identification of strains of A. marginale provide the information necessary in a wide landscape of how this rickettsia is distributed all over the world to have better control and prevention strategies.

In these latter strategies, vaccination is proposed as one of the most effective tools for the prevention of infectious diseases. Along with the continuous sequencing of genomes, the availability of the information has led to a new paradigm in vaccine development using technologies such as functional and structural genomics [44].

Figure 1 shows a schematic overview of conventional vaccinology versus vaccinology in the genomic era. We present two proposals to follow based on pathogen characteristics in order to achieve potential vaccines and compare conventional vaccinology and genome-based vaccinology approaches as tools to vaccine development. We believe that new strategies, especially those focusing on omics techniques, will lead to a better design of vaccines.

Figure 1: General scheme of A. marginale vaccine development using conventional and genome-based vaccinology.

3. Vaccine Approach: Conventional Vaccinology of Anaplasma marginale

Although A. marginale has a global impact on animal health, so far there is no worldwide-accepted vaccine for bovine anaplasmosis.

The first attempt at vaccine was in the early 1900s, with the isolation of A. marginale subsp. centrale, a less virulent strain that induces cross protection to virulent strains [2]. A. centrale has been used as a live blood vaccine, for over 100 years, and is currently used in Australia and several African, South American, and Middle Eastern countries including Israel [45]. Although A. centrale has been used as live vaccine and gives protection against some strains of A. marginale, in countries like Zimbabwe, Paraguay, and Argentina some studies have shown that A. centrale provides little to no protection, which means that this rickettsia does not provides 100% protection, maybe probably to dissimilar endemic strains by country and variation in the challenge dose among studies [4649].

Despite the benefits of this live vaccine, its use represents the risk of cotransmission of other ruminant pathogens (blood-borne pathogens: bovine leukemia virus, unknown or recently emergent pathogens) and hemolytic diseases in calves born to immunized dams, the potential risk of disease induced by the vaccine strains themselves, besides the fact that live vaccines are not licensed for use in many countries, including the United States, Mexico, and European Union [25, 45, 50, 51].

Inactivated vaccines based on the use of the bacteria extracted from bovine erythrocytes are very effective but have disadvantages such as the possible contamination with the erythrocyte membrane antigens and wide antigenic variation between geographic strains [52]; and while they diminish the intensity of clinical signs, they do not prevent infection; thus, animals may remain carriers for the rest of their lives [53].

Rodríguez Camarillo et al. [54] assessed the effect of Yucatan strain, a low virulence A. marginale strain, and inoculated 113 susceptible cattle at increasing doses (104–1010 infected erythrocytes) of Yucatan strain. Only one animal out of 113 (0.9%) required treatment for clinical disease. These results are comparable with those obtained from other attenuated strain vaccines trials. According to de la Fuente et al. [55], live vaccines result in persistent, life-long infections and allow the maintenance of solid and long-lasting immunity against homologous and heterologous strains. Another naturally avirulent strain of A. marginale was reported in Australia by Bock et al. [56], the strain of Dawn. They found that cattle vaccinated with A. marginale Dawn strain were strongly immune to challenge with heterologous A. marginale isolates. Dawn’s virulence was not significantly different between steers vaccinated with Dawn A. marginale and those receiving A. centrale; in fact, Dawn strain offered better protection than A. centrale against virulent heterologous challenge in Australia. These results indicate that this strain could be a useful vaccine alternative in Australia although validation of its safety and protection against African and New World isolates in a large scale should be performed [57].

However, not all the low virulent strains exert a positive effect on cattle. The low pathogenic Brazilian strain UFMG1 has been shown to protect cattle against a high pathogenic Brazilian isolate (UFMG2) [58]; however, this protection was not observed when the geographically distant Israeli A. marginale Gonen strain was used to challenge cattle inoculated with UFMG1 [59]. With these results, it is clear that UFMG1 had a negligible effect on disease prevention caused by the geographically distant heterologous Gonen strain and this response may be constrained by limited antibody responses.

The use of killed vaccines is another alternative in conventional vaccinology; these vaccines have advantages over live vaccines; that is, the risk of contamination with undesirable infections is low and the cost of storage is inexpensive; besides, only minimal postinoculation reactions are caused. Some disadvantages are the constant use of boosters, the cost of purification of A. marginale from erythrocytes, and the lack of cross protection among isolates from geographically distant areas [60].

4. Genome-Based Vaccinology

The completion of the genome sequence of Haemophilus influenza, in 1995 (the first bacterial genome sequenced), along with the advances in bioinformatics and sequencing technology set the start of a dramatic boom in the sequencing field [61]. By April of 2016, 8,032 completed sequencing projects (completed and published) and 33,496 permanent drafts were reported [62]; this trend highlights the valuable information contained in the microorganisms genomes and the subsequent possibilities to explore. Currently, genomics-based vaccines projects will increase our knowledge and understanding of microbial physiology, epidemiology, pathogenesis, and protein function and further impact the vaccine design and therapeutic development [63].

Today, the research in omics sciences is moving from a hypothesis-driven to a data-driven approach. The availability of omics data is the result of the acquisition of molecular biology results and represents an unprecedented opportunity and also a major challenge [64].

Once the genome of a pathogen is available, several approaches can be taken to identify vaccine/therapeutic targets: reverse vaccinology, pangenomics, comparative genomics, transcriptomics, functional genomics, proteomics, immunomics, structural genomics, and so forth.

Once the A. marginale genome was reported by Brayton et al. [20], the genome-wide screening was the next step. They found two families containing immunodominant proteins: MSP1 and MSP2 superfamilies, both members of the Outer Membrane Proteins (OMPs). These two families comprise more than half of the molecules predicted to be on the surface of A. marginale and it was hypothesized that they would be good candidates to induce protection. Indeed, protection was achieved in immunization experiments using native MSP1; however, this protection was not observed using recombinant proteins. Unfortunately, recombinant vaccines failed either due to lack of all MSP1b variants used in the recombinant vaccine construct or their the inability to covalently dimerize as native MSP1 molecules do [65, 66].

Santos et al. [67] provided a successful demonstration of epitope-based vaccines using a functional motif of MSP1 and STSSxL (specifically, Am1, STSSQL and Am2, SEASTSSQLGA) which induced a balanced humoral and cellular immune response in mice. They found that this immunogen significantly induced higher IgG2 than IgG1 response, followed by an increased expression of proinflammatory cytokines such as IL-10, IL-12, IL-8, and TNF-α involved in the early response and cytokines involved in the postchallenge stage such as IFN-γ and TGF-β. The authors demonstrated that immunization with Am1 peptide induced higher expression levels of IL12, IL8, and TNF-α, molecules involved in differentiation and maintenance of naïve CD4+ T-cells to Th1 cytokines and activation of NK cells to produce IFN-γ and other Th1 cytokines related to innate and adaptive immunity. In contrast, the response postchallenge of Am2 peptide revealed an upregulation of IL-10 and a weak upregulation of IFN-γ. This work is an example of how epitope-base vaccines could be a viable alternative to induce protective immunity against bovine anaplasmosis.

Control of bovine anaplasmosis is made difficult by the genetic variability mechanisms A. marginale uses to evade the immune system of the host [68]. An example of this is the appearance of MSP2 and MSP3 variants, which create a wide repertoire of expression site variants through segmental gene conversion [69, 70]. Nevertheless, immunization with native purified MSP2 containing a wide number of variants did not confer protection to cattle challenged with A. marginale expressing the same variants as in the immunogen [71].

Additionally, MSP2 and MSP3 are variable among strains with strain-specific alleles encoding structurally and antigenically distinct proteins; thus these proteins are poor candidates for vaccine development [72].

While bacterial pathogens express surface exposed protein complexes structurally and functionally involved in the infective process and many are well characterized, the search for vaccine candidates in A. marginale that influence the host immune system still remains [73].

The lack of success using dominant antigens has led vaccine development to focus on subdominant outer membrane proteins (OMP) antigens; however, the challenge still is to select the best candidates for testing in immunization and challenge experiments in order to develop an effective vaccine [13].

Ducken et al. [13] cloned and sequenced genes encoding major subdominant components of the outer membrane from geographically diverse strains. They reported that AM202, Am936, AM854, and AM1096 were recognized by IgG from animals immunized with outer membranes and shown to be protected from challenge; the highest antibody titers and consistent recognition among vaccinates were directed to AM854 and Am936. The animals immunized with recombinant AM854 and AM936 and challenged had similar IgG and IgG2 responses to both proteins. As such, the possible utility of these two proteins as effective vaccine antigens cannot be dismissed.

This approach represents a progress in the search of membrane protein formulations that may have an important role in a protective immune response in immunized animals. Yet, not all proteins are equally capable of inducing protective immunity. AM779 is a highly conserved but minor component of A. marginale and it is a subdominant protein of A. marginale located in the outer membrane that is not associated with protective immunity [74].

While It seemed that protein complexes or the outer membrane extracts could be used as vaccine candidates given to the protection observed, it is difficult and expensive to isolate them, making it impractical for development and implementation in vaccination programs. In contrast, individual proteins, easily cloned and expressed and adapted for use in subunit vaccines have not shown a significant protection [75]. The effect of the protein complexed as immunogens strongly suggests that new vaccines candidates may work better as a complex instead of as free proteins.

Once the surface expressed proteins were characterized, these complexes were used as an immunogen to test the protective immunity induced by whole outer membranes. Noh et al. [76] induced protection against high-level bacteremia and anemia upon A. marginale challenge of cattle and effectively summed up the protection induced by immunization with whole outer membranes.

Noh et al. [75] tested outer membrane-based immunogens to determine whether membrane context affected immunogenicity and the capacity to induce protection. The first immunogen was composed of a complex of outer membrane proteins linked by covalent bonds and known to be protective. The second immunogen was derived directly from the first one, but the proteins were individualized rather than linked. The authors stated that two common features of these effective immunogens were the presence of multiple antigens and the maintenance of spatial relationships among the antigens comprising the immunogen [75]. They also found that the antibody response induced by the linked immunogen was of greater magnitude than that induced by the unlinked-proteins immunogen. These authors believe that the differences in protein content between immunogens may play a significant role in recognition process by B cells activated by helper T-cells. Despite this difference in magnitude, both immunogens induced protective immunity in animals indicating that protective epitopes were present in both antigens and significantly protected animals from challenge.

These findings suggest that future studies to identify protective antigens can consider testing of individual or groups of candidate proteins and arrange only those protective antigens into high molecular weight complexes as a tool to enhance their immunogenicity [75].

5. Immunogenic Effects of A. marginale Proteins

Derived from the sequence of the A. marginale genome, a number of putative surface proteins have been predicted through bioinformatic analysis. These proteins are proposed as potential targets of the immunoprotective response in cattle for the development of a recombinant vaccine. Based on empirical evidence that has shown immunity in cattle, induced by exposure to crosslinked outer membrane fragments and bioinformatics analysis of proteins potentially expressed in the outer membrane with a probable functional role, of which there is no previous information available, Ducken et al. [13] chose six proteins, AM202, AM368, AM854, AM936, AM1041, and AM109, to be compared between distinct geographical strains. Those most highly conserved were recognized in their recombinant form by IgG from animals immunized with outer membranes. In spite of higher recognition titers and IgG and IgG2 production, animals immunized with AM854 or AM936 developed higher bacteremia and anemia after challenge than the adjuvant-only controls [13]. This observation reinforces the notion that surface exposure alone is not sufficient to predict the protective function of a protein and additional elements must be considered.

Protective responses against several bacterial pathogens including A. marginale are based on CD4+ T-cell action. Cattle immunized with whole initial bodies from a Mexican strain of A. marginale were challenged and shown to be tolerant to the infection. In order to identify the molecules involved in protection response, protein recognized by IgG2 produced after immunization protocol were isolated, and MSP1, MSP2, MSP5, and other putative MPs were identified [14]. Proteins not previously reported were recuperated, although whole initial bodies induced immunity in this study, and additional information should be obtained in order to determine each protein role in immunity induction.

In other experiments, a fraction enriched with A. marginale outer membranes was found to induce complete protection against homologous experimental infection, elicit CD4+ T-lymphocyte proliferation, and IgG2 production [76, 77]. Analysis by two-dimensional electrophoresis, mass spectrometry, and genomic mapping of this outer membrane immunogen identified more than 20 proteins. Native proteins VirB9, Virb10, and CTP reacted with immune bovine sera. An in depth bioinformatic analysis on subdominant antigens determined that these antigens were also outer membrane surface proteins [78].

Analyses based on highly conserved sequences, potential functional role, and surface localization led to the use of type IV secretion system proteins and conjugal transfer protein (CTP) as candidates components in vaccine design. The use of native protein preparations, however, is an obstacle in the production of nonviable commercial vaccines. Therefore, recombinant VirB9, VirB10, and CTP were produced in E. coli, and all proteins were able to stimulate T-lymphocyte proliferation and gamma interferon secretion [16]. Furthermore, these recombinant proteins reacted with IgG2 from outer membrane-immunized cattle. It has been well established that IgG2 subclass is associated with Th1 protective immunity in bovine anaplasmosis [14, 77].

On the other hand, adaptive immune responses involving specific MHC molecules and their interaction with T-cell receptors are an early step for processing and elimination of pathogens. Two MHC class II proteins are expressed in cattle, DR, and DQ, and antigenic peptides are classically presented by monomorphic DRA with polymorphic DRB molecules to T-cells [79, 80]. Therefore, the characterization of relevant alleles during A. marginale antigen presentation is significant for response modulation and vaccine design. In this way, VirB9-1, VirB9-2, and VirB10 overlapping peptides were assayed on peripheral blood mononuclear cells from varying and heterozygous MHC class II bovines [81], and the authors reported several combinations of MHC alleles recognized by the peptides, mainly alleles prevalent in Holstein cattle. However, these results are most likely influenced by the population under study. Despite the above-reported results, additional assays need to be carried before practical use of VirB9 and VirB10 proteins can be achieved.

Type IV secretion system members such as VirB11 and VirD4 are not predicted as surface proteins; nevertheless they could play a relevant function and may be part of a heterogeneous vaccine [16].

While many investigations have focused on major surface proteins as immunogenic molecules, other predicted proteins have also shown potential at inducing specific immune responses. A. marginale characteristic wide diversity, high variability, immune evasion mechanisms, and unknown interactions with the host, however, have made it very difficult to design efficient immunoprophylactics to prevent the disease.

Furthermore, in order to avoid immune response variations in testing potential immunogens, experimental designs should include larger numbers of animals. These type of experiments are very costly and the criteria for selecting potential antigen should be carefully revised.

The identification of successful targets of the protective immune response against A. marginale is a great challenge, functional elements remain unknown despite the publication of A. marginale genome sequences, and further efforts are required in order to complement bioinformatics analysis if an effective vaccine is to be achieved. As efforts to design a vaccine that will induce solid and long-lasting immunity against a wide array of diverse A. marginale, new approaches have been tested, including synthetic and truncated peptides, overlapping peptides, and more recently, while not in the field of anaplasmosis, the use of multiple antigenic peptides (MAPs). MAPs are peptides that are branched artificially, in which Lys residues are used as the scaffolding core to support the formation ≤8 branches with varying or the same peptide sequences [82]. MAPs, if used as immunogens, present many advantages over conventional vaccines; they can include one or more relevant epitopes of a single or multiple organisms providing protection against one or more antigens. MAPs are highly immunogenic thus inducing antibody responses capable of neutralizing receptors or invasion associated proteins in virus like dengue [83], bacteria like anthrax [84], or even tumors [85]. The plethora of information generated with regard to A. marginale outer membrane proteins so far tested in the laboratory and even those already used for animal inoculation [81, 86, 87], and other proteins yet to be tested, could be used for designing MAPs which can easily be assayed in the laboratory for immunogenicity against sera (IgG2) or even lymphocytes of from animals experimentally or naturally immunized.

6. New Omics Perspectives

More recently, genomic and proteomic approaches have facilitated the identification of minor components of the bacterial outer membrane that could be used as vaccines, so far the most effective mean to control infections in humans and animals [74, 78, 88]. Thus, omics approaches represent an alternative that may give information about A. marginale so far unknown.

New methodologies such as metabolomics profiling are, for example, a helpful tool to identify those metabolites involved in the induction of immune protection after vaccination which may have a potential use as a candidate vaccine and provide novel perspectives to vaccine design. Gray et al. [89] identified metabolites in the plasma of calves vaccinated with an intranasally delivered respiratory vaccine. Furthermore, metabolites may play important roles as ultimate end stage products or mediators of biological processes, so the analysis of the metabolites present in bovine plasma is the result of the mucosal immune response of the host.

While new information is continuously generated to identify possible vaccine candidates against bovine anaplasmosis, today there are no commercial vaccines in the world, and the efforts must continue to gain a better understanding of A. marginale and its relationship with their hosts (mammalian and tick) in order to have a vaccination program in the near future.

Development of new vaccines and therapeutics has been driven mainly by the understanding of the pathogenesis of infectious agents; however, the development of vaccines of many pathogens, including A. marginale, remains elusive [90]. Today, it is clear that the antigens used do not necessarily have to be virulence factors and other proteins have been identified by “omics” techniques. For instance, transcriptomics and proteomics analyses enable the identification of array of antigens expressed by a pathogen under specified conditions, by examining mRNA and proteins, respectively. When this analysis is made on the subset of proteins located in the surface of the pathogen, we refer to this as surface proteome; also, we can analyzed genes that are functionally important for infection by functional genomics [91].

The surface proteome represents information particularly important in order to understand the induction of protective immunity in the mammalian host and the transition from the mammalian host to the tick vector. A proteomics analysis using liquid chromatography and tandem mass spectroscopy (LC-MS/MS) revealed the idea that the surface complexes of A. marginale isolated from erythrocytes of the mammalian host were composed of multiple membrane proteins, most of which belong to protein family pfam 01617, which is conserved among members of the closely related genera Anaplasma and Ehrlichia [76]. On the contrary, the surface proteome of A. marginale isolated from tick cells was less complex and contained a novel protein, AM778, not identified in the surface proteome obtained from erythrocytes of the mammalian host [76].

Studies in A. marginale isolated from erythrocytes showed a number of proteins identified including Omp1, Omp7–9, Omp11, Msp1a, Msp2–4, OpAG2, Am1011, Am780, Am779, Am854, VirB10, while in A. marginale isolated from tick cells some of the proteins were Msp2–4 and Am778 [76]. These results support the contention that different proteins are expressed in A. marginale surface when it is in the mammalian host or in the tick, which open possibilities to new targets.

Today, almost any cellular condition can be analyzed, and new fields of study have arisen. Through immunomics, we can elucidate the set of antigens that interact with the host immune system and the mechanisms involved in these interactions; structural vaccinology reveals the structural epitopes of immunogenic antigens and vaccinomics explains the way in which the host’s immune system responds to vaccines [91, 92].

Vaccinomics is based on the use of the genome-scale or “omics” technologies and bioinformatics for the development of next generation vaccines and refers to the “integration of immunogenetics and immunogenomics with systems biology and immune profiling” [9395]. Vaccinomics is a holistic field that can take advantage of the information derived from the immune responses network theory and applies this information to the practical aspects of conceiving, designing, and delivering new vaccine candidates, which in turn is based on a better understanding of the key drivers of the immune system response to antigens at systems level in the host as well as advances in the understanding of genetic and nongenetic drivers of the immune response [96].

The main goals of vaccinomics or systems vaccinology [97] are, on one hand, the development of new vaccines through understanding the global architecture of the host immune response and the changes that occur following vaccination and, on the other hand, defining the signatures of protection required to elicit a protective immune response [94].

de la Fuente and Merino [98] have proposed the use of vaccinomics methodology as an alternative for developing new tick vaccines. First, they proposed the characterization of tick-host-pathogen interactions through genomics, transcriptomics, proteomics, metabolomics, and immunogenomics in order to perform data integration and a further analysis. Then, the development of algorithms that allow the identification of protective antigens in this plethora of information is critical for the formulation of candidate vaccines and its validation.

This strategy could be time-consuming and expensive and requires bioinformatics skills and trained personnel; however, the possibilities for the identification of candidate protective antigens and fulfilling the whole process of characterization and validation are a risk worth taking.

Vaccinology in the genome era has a wide repertoire of alternatives to analyze genomes. Out of these alternatives, pangenomic analysis compares the genomes of multiple isolates of a pathogen and those of close pathogenic and nonpathogenic relatives and bacteria of special interest. This analysis is not restricted to genome size, gene content, and gene conservation or variability among different strains, but it is also for the implications for effective vaccine and drug-discovery programs [91]. The pangenome concept is defined as the entire genomic repertoire of a given species or phylogenetic clade when multiple species are defined by systematics. The information provided by pangenomic analyses is divided into three groups: the core genes (shared by all genomes), the dispensable genes, and the strains (or isolate) specific genes [99101].

Through pangenomic analyses, Dark et al. [72] found that A. marginale has a closed-core genome with few highly plastic regions including msp2 and msp3 genes and the aaap locus that appears to be expanding and contracting within and between strains. Although A. marginale genome sequence is highly conserved in gene content, it is also highly recombinogenic, which leads to plasticity. An example of this is msp2 gene, which encodes a highly antigenic protein that varies over time during infection by gene conversion of functional pseudogenes into a single expression site to create new antigenic variants capable of evading host immune response. Comparison of St. Maries genome with Florida strain genome showed that Florida’s genome contains one additional msp2 functional pseudogene and, out of the eight Florida msp2 functional pseudogenes, four are identical to St. Maries’. In contrast, only two of the seven msp3 functional pseudogenes are shared between Florida and St. Maries. Finally, no new genes were detected in the pyrosequenced contigs of any of the strains. Dark et al. [72] also compared five A. marginale strains (Florida, St. Maries, Puerto Rico, Mississippi, and Virginia) that have differing abilities to be transmitted by Dermacentor andersoni ticks, with each phenotype represented by at least two geographically distinct isolations. The authors found that the number of single nucleotide polymorphism (SNP) between Puerto Rico, Virginia, and Mississippi strains is minimal (2,729, 3,868, and 6773, resp.); on the contrary, there were 9,609 SNPs between Florida and St. Maries strains, comprising 0.80% of the larger Florida genome. This indicates that the interstrain SNP diversity neither appears to be influenced by the environmental niche an organism occupies, nor is it generally consistent throughout a specific family or genera.

Analysis of multiple genomes provides a plethora of information that could help to better understand the organisms’ environment and how adaptation exerts an important role in bacteria and its genome. We must emphasize the fact that as long as there exist A. marginale with different virulence phenotypes, pangenomic analyses are indispensable.

7. Conclusions

To this day, there are no commercial alternatives for the immunoprophylactic control of bovine anaplasmosis. Conventional vaccinology approaches have resulted in effective live attenuated or avirulent vaccines, which may also transmit other blood-borne pathogens or due to the inclusion of A. centrale may not be used in countries where the organism is absent.

Many molecular and bioinformatics-based studies have defined a number of surface membrane proteins and components of the type IV secretion system as potential antigens.

While the complete genome sequences of several A. marginale strains have been published, most of these sequences come from strains from the United States. Additional genomic information from strains from other countries is needed if a wide spectrum vaccine is to be designed and used over large regions of the world.

Many more genomic and other omics studier will be required in order to unravel the most relevant antigens to be used eventually, in a reliable vaccine for the control of anaplasmosis in large regions of the world.

Competing Interests

The authors declare that there are no competing interests regarding the publication of this paper.

Authors’ Contributions

Rosa Estela Quiroz-Castañeda and Sergio Rodríguez-Camarillo proposed the theoretical frame, and Rosa Estela Quiroz-Castañeda, Itzel Amaro-Estrada, and Sergio Rodríguez-Camarillo wrote the paper.

Acknowledgments

This work was supported by Instituto Nacional de Investigaciones Forestales, Agrícolas y Pecuarias (INIFAP) Project no. SIGI 1320382022 and Consejo Nacional de Ciencia y Tecnología (CONACyT) Projects SEP-CONACYT no. 168167 and PN-CONACYT no. 248855.

References

  1. F. Jongejan and G. Uilenberg, “The global importance of ticks,” Parasitology, vol. 129, pp. S3–S14, 2004. View at Publisher · View at Google Scholar · View at Scopus
  2. A. Theiler, “Further investigation into anaplasmosis of South African cattle,” in First Report of the Director of Veterinary Research, A. Theiler, Ed., pp. 7–47, Department of Agriculture of the Union of South Africa, 1911. View at Google Scholar
  3. M. Ristic, “Anaplasmosis,” in Diseases of Cattle in the Tropics. Economic and Zoonotic Relevance, M. Ristic and I. McIntyre, Eds., pp. 327–344, Martinus Nijhoff, The Hague, The Netherlands, 1981. View at Google Scholar
  4. P. Aubry and D. W. Geale, “A review of Bovine anaplasmosis,” Transboundary and Emerging Diseases, vol. 58, no. 1, pp. 1–30, 2011. View at Publisher · View at Google Scholar · View at Scopus
  5. K. M. Kocan, J. de la Fuente, and E. F. Blouin, “Advances toward understanding the molecular biology of the Anaplasma-tick interface,” Frontiers in Bioscience, vol. 13, no. 18, pp. 7032–7045, 2008. View at Publisher · View at Google Scholar · View at Scopus
  6. F. Thullner, P. Willadsen, and D. Kemp, “Acaricide rotation strategy for managing resistance in the tick Rhipicephalus (Boophilus) microplus (Acarina: Ixodidae): laboratory experiment with a field strain from Costa Rica,” Journal of Medical Entomology, vol. 44, no. 5, pp. 817–821, 2007. View at Publisher · View at Google Scholar · View at Scopus
  7. O. Vizcaino, D. E. Corrier, M. K. Terry et al., “Comparison of three methods of immunization against bovine anaplasmosis: evaluation of protection afforded against field challenge exposure,” American Journal of Veterinary Research, vol. 41, no. 7, pp. 1066–1068, 1980. View at Google Scholar · View at Scopus
  8. K. L. Kuttler, J. L. Zaugg, and L. W. Johnson, “Serologic and clinical responses of premunized, vaccinated, and previously infected cattle to challenge exposure by two different Anaplasma marginale isolates,” American Journal of Veterinary Research, vol. 45, no. 11, pp. 2223–2226, 1984. View at Google Scholar · View at Scopus
  9. J. de la Fuente, R. A. Van Den Bussche, and K. M. Kocan, “Molecular phylogeny and biogeography of North American isolates of Anaplasma marginale (Rickettsiaceae: Ehrlichieae),” Veterinary Parasitology, vol. 97, no. 1, pp. 65–76, 2001. View at Publisher · View at Google Scholar · View at Scopus
  10. G. H. Palmer, D. P. Knowles Jr., J.-L. Rodriguez et al., “Stochastic transmission of multiple genotypically distinct Anaplasma marginale strains in a herd with high prevalence of Anaplasma infection,” Journal of Clinical Microbiology, vol. 42, no. 11, pp. 5381–5384, 2004. View at Publisher · View at Google Scholar · View at Scopus
  11. L. E. O. Vega, S. D. Rodríguez, G. J. C. Alarcón et al., “Anaplasma marginale field challenge: protection by an inactivated immunogen that shares partial sequence of msp1α variable region with the challenge strain,” Vaccine, vol. 25, no. 3, pp. 519–525, 2007. View at Publisher · View at Google Scholar · View at Scopus
  12. E. J. Castañeda-Ortiz, M. W. Ueti, M. Camacho-Nuez et al., “Association of anaplasma marginale strain superinfection with infection prevalence within tropical regions,” PLoS ONE, vol. 10, no. 3, Article ID e0120748, 2015. View at Publisher · View at Google Scholar
  13. D. R. Ducken, W. C. Brown, D. C. Alperin et al., “Subdominant outer membrane antigens in anaplasma marginale: conservation, antigenicity, and protective capacity using recombinant protein,” PLoS ONE, vol. 10, no. 6, Article ID e0129309, 2015. View at Publisher · View at Google Scholar · View at Scopus
  14. R. Barigye, M. Á. García-ortiz, E. Enrique, R. Ramírez, and D. Sergio, “Identificación de antígenos IgG2 específicos en tres cepas mexicanas de Anaplasma marginale Identification of IgG2 specific antigens in three Mexican Anaplasma marginale strains,” Tecnica Pecuaria en Mexico, vol. 42, no. 1, pp. 219–236, 2004. View at Google Scholar
  15. G. Riding, M. Hope, D. Waltisbuhl, and P. Willadsen, “Identification of novel protective antigens from Anaplasma marginale,” Vaccine, vol. 21, no. 17-18, pp. 1874–1883, 2003. View at Publisher · View at Google Scholar · View at Scopus
  16. J. E. Lopez, G. H. Palmer, K. A. Brayton, M. J. Dark, S. E. Leach, and W. C. Brown, “Immunogenicity of Anaplasma marginale type IV secretion system proteins in a protective outer membrane vaccine,” Infection and Immunity, vol. 75, no. 5, pp. 2333–2342, 2007. View at Publisher · View at Google Scholar · View at Scopus
  17. P. A. Nuñez, R. Moretta, P. Ruybal, S. Wilkowsky, and M. D. Farber, “Immunogenicity of hypothetical highly conserved proteins as novel antigens in Anaplasma marginale,” Current Microbiology, vol. 68, no. 3, pp. 269–277, 2014. View at Publisher · View at Google Scholar · View at Scopus
  18. D. J. Edwards and K. E. Holt, “Beginner’s guide to comparative bacterial genome analysis using next-generation sequence data,” Microbial Informatics and Experimentation, vol. 3, no. 1, p. 2, 2013. View at Publisher · View at Google Scholar
  19. S. D. Bentley and J. Parkhill, “Genomic perspectives on the evolution and spread of bacterial pathogens,” Proceedings of the Royal Society of London B: Biological Sciences, vol. 282, no. 1821, 2015. View at Publisher · View at Google Scholar · View at Scopus
  20. K. A. Brayton, L. S. Kappmeyer, D. R. Herndon et al., “Complete genome sequencing of Anaplasma marginalereveals that the surface is skewed to two superfamilies of outer membrane proteins,” Proceedings of the National Academy of Sciences of the United States of America, vol. 102, no. 3, pp. 844–849, 2005. View at Publisher · View at Google Scholar · View at Scopus
  21. S. G. E. Andersson, A. Zomorodipour, J. O. Andersson et al., “The genome sequence of Rickettsia prowazekii and the origin of mitochondria,” Nature, vol. 396, no. 6707, pp. 133–140, 1998. View at Publisher · View at Google Scholar · View at Scopus
  22. M. P. McLeod, X. Qin, S. E. Karpathy et al., “Complete genome sequence of Rickettsia typhi and comparison with sequences of other rickettsiae,” Journal of Bacteriology, vol. 186, no. 17, pp. 5842–5855, 2004. View at Publisher · View at Google Scholar · View at Scopus
  23. J. C. Dunning Hotopp, M. Lin, R. Madupu et al., “Comparative genomics of emerging human ehrlichiosis agents,” PLoS Genetics, vol. 2, no. 2, article e21, 2006. View at Publisher · View at Google Scholar · View at Scopus
  24. S. Pierlé, I. Rosshandler, A. Kerudin et al., “Genetic diversity of tick-borne rickettsial pathogens; insights gained from distant strains,” Pathogens, vol. 3, no. 1, pp. 57–72, 2014. View at Publisher · View at Google Scholar
  25. M. J. Dark, B. Al-Khedery, and A. F. Barbet, “Multistrain genome analysis identifies candidate vaccine antigens of Anaplasma marginale,” Vaccine, vol. 29, no. 31, pp. 4923–4932, 2011. View at Publisher · View at Google Scholar · View at Scopus
  26. D. R. Herndon, G. H. Palmer, V. Shkap, D. P. Knowles Jr., and K. A. Brayton, “Complete genome sequence of Anaplasma marginale subsp. centrale,” Journal of Bacteriology, vol. 192, no. 1, pp. 379–380, 2010. View at Publisher · View at Google Scholar · View at Scopus
  27. A. Cabezas-Cruz, L. M. Passos, K. Lis et al., “Functional and immunological relevance of Anaplasma marginale major surface protein 1a sequence and structural analysis,” PLoS ONE, vol. 8, no. 6, Article ID e65243, 2013. View at Publisher · View at Google Scholar
  28. K. M. Kocan, J. De la Fuente, A. A. Guglielmone, and R. D. Meléndez, “Antigens and alternatives for control of Anaplasma marginale infection in cattle,” Clinical Microbiology Reviews, vol. 16, no. 4, pp. 698–712, 2003. View at Publisher · View at Google Scholar · View at Scopus
  29. G. H. Palmer, F. R. Rurangirwa, and T. F. McElwain, “Strain composition of the ehrlichia Anaplasma marginale within persistently infected cattle, a mammalian reservoir for tick transmission,” Journal of Clinical Microbiology, vol. 39, no. 2, pp. 631–635, 2001. View at Publisher · View at Google Scholar · View at Scopus
  30. J. de la Fuente, P. Ruybal, M. S. Mtshali et al., “Analysis of world strains of Anaplasma marginale using major surface protein 1a repeat sequences,” Veterinary Microbiology, vol. 119, no. 2–4, pp. 382–390, 2007. View at Publisher · View at Google Scholar · View at Scopus
  31. S. Torioni De Echaide, D. P. Knowles, T. C. McGuire, G. H. Palmer, C. E. Suarez, and T. F. McElwain, “Detection of cattle naturally infected with Anaplasma marginale in a region of endemicity by nested PCR and a competitive enzyme-linked immunosorbent assay using recombinant major surface protein 5,” Journal of Clinical Microbiology, vol. 36, no. 3, pp. 777–782, 1998. View at Google Scholar · View at Scopus
  32. R. Jimenez-Ocampo, C. A. Vega Y Murguía, N. O. Ortega et al., “Diversidad genética de la región variable de los genes Msp1a y Msp4 en cepas de anaplasma marginale de México,” Revista Mexicana de Ciencias Pecuarias, vol. 3, no. 3, pp. 373–387, 2012. View at Google Scholar
  33. A. E. L. Pohl, A. Cabezas-Cruz, M. F. B. Ribeiro et al., “Detection of genetic diversity of Anaplasma marginale isolates in Minas Gerais, Brazil,” Revista Brasileira de Parasitologia Veterinária, vol. 22, no. 1, pp. 129–135, 2013. View at Publisher · View at Google Scholar · View at Scopus
  34. B. Corona, C. Minet, E. Albina, A. Vega, and S. Martínez, “Sequence of msp1alpha gene of Anaplasma marginale Havana isolate and expression in eukaryotic cells,” Spanish Journal of Agricultural Research, vol. 3, no. 3, pp. 275–280, 2005. View at Publisher · View at Google Scholar
  35. R. Z. Machado, J. B. da Silva, M. R. André, L. R. Gonçalves, C. A. Matos, and D. Obregón, “Outbreak of anaplasmosis associated with the presence of different Anaplasma marginale strains in dairy cattle in the states of São Paulo and Goiás, Brazil,” Revista Brasileira de Parasitologia Veterinaria, vol. 24, no. 4, pp. 438–446, 2015. View at Publisher · View at Google Scholar · View at Scopus
  36. B. A. Baêta, C. C. D. U. Ribeiro, R. C. Teixeira et al., “Characterization of two strains of Anaplasma marginale isolated from cattle in Rio de Janeiro, Brazil, after propagation in tick cell culture,” Ticks and Tick-Borne Diseases, vol. 6, no. 2, pp. 141–145, 2015. View at Publisher · View at Google Scholar · View at Scopus
  37. A. M. Mutshembele, A. Cabezas-Cruz, M. S. Mtshali, O. M. M. Thekisoe, R. C. Galindo, and J. de la Fuente, “Epidemiology and evolution of the genetic variability of Anaplasma marginale in South Africa,” Ticks and Tick-Borne Diseases, vol. 5, no. 6, pp. 624–631, 2014. View at Publisher · View at Google Scholar · View at Scopus
  38. J. de la Fuente, A. Lew, H. Lutz et al., “Genetic diversity of Anaplasma species major surface proteins and implications for anaplasmosis serodiagnosis and vaccine development,” Animal Health Research Reviews, vol. 6, no. 1, pp. 75–89, 2005. View at Publisher · View at Google Scholar · View at Scopus
  39. A. Estrada-Peña, V. Naranjo, K. Acevedo-Whitehouse, A. J. Mangold, K. M. Kocan, and J. de la Fuente, “Phylogeographic analysis reveals association of tick-borne pathogen, Anaplasma marginale, MSP1a sequences with ecological traits affecting tick vector performance,” BMC Biology, vol. 7, no. 1, article 57, pp. 1–13, 2009. View at Publisher · View at Google Scholar · View at Scopus
  40. P. Ruybal, R. Moretta, A. Perez et al., “Genetic diversity of Anaplasma marginale in Argentina,” Veterinary Parasitology, vol. 162, no. 1-2, pp. 176–180, 2009. View at Publisher · View at Google Scholar · View at Scopus
  41. C. Almazán, C. Medrano, M. Ortiz, and J. de la Fuente, “Genetic diversity of Anaplasma marginale strains from an outbreak of bovine anaplasmosis in an endemic area.,” Veterinary Parasitology, vol. 158, no. 1-2, pp. 103–109, 2008. View at Publisher · View at Google Scholar
  42. A. P. Ybañez, R. H. D. Ybañez, F. G. Claveria et al., “High genetic diversity of Anaplasma marginale detected from Philippine cattle,” Journal of Veterinary Medical Science, vol. 76, no. 7, pp. 1009–1014, 2014. View at Publisher · View at Google Scholar · View at Scopus
  43. M. C. Vidotto, O. Vidotto, G. M. Andrade, G. Palmer, T. McElwain, and D. P. Knowles, “Seroprevalence of Anaplasma marginale in cattle in Parana State, Brazil, by MSP-5 competitive ELISA,” Annals of the New York Academy of Sciences, vol. 849, no. 1, pp. 424–426, 1998. View at Publisher · View at Google Scholar · View at Scopus
  44. S. Bambini and R. Rappuoli, “The use of genomics in microbial vaccine development,” Drug Discovery Today, vol. 14, no. 5-6, pp. 252–260, 2009. View at Publisher · View at Google Scholar · View at Scopus
  45. L. Bell-Sakyi, A. M. Palomar, E. L. Bradford, and V. Shkap, “Propagation of the Israeli vaccine strain of Anaplasma centrale in tick cell lines,” Veterinary Microbiology, vol. 179, no. 3-4, pp. 270–276, 2015. View at Publisher · View at Google Scholar · View at Scopus
  46. G. K. Hammac, P.-S. Ku, M. F. Galletti et al., “Protective immunity induced by immunization with a live, cultured Anaplasma marginale strain,” Vaccine, vol. 31, no. 35, pp. 3617–3622, 2013. View at Publisher · View at Google Scholar · View at Scopus
  47. J. A. Turton, T. C. Katsande, M. B. Matingo, W. K. Jorgensen, U. Ushewokunze-Obatolu, and R. J. Dalgliesh, “Observations on the use of Anaplasma centrale for immunization of cattle against anaplasmosis in Zimbabwe,” Onderstepoort Journal of Veterinary Research, vol. 65, no. 2, pp. 81–86, 1998. View at Google Scholar · View at Scopus
  48. C. M. Brizuela, C. A. Ortellado, E. Sanabria, O. Torres, and D. Ortigosa, “The safety and efficacy of Australian tick-borne disease vaccine strains in cattle in Paraguay,” Veterinary Parasitology, vol. 76, no. 1-2, pp. 27–41, 1998. View at Publisher · View at Google Scholar · View at Scopus
  49. A. A. Abdala, E. Pipano, D. H. Aguirre et al., “Frozen and fresh Anaplasma centrale vaccines in the protection of cattle against Anaplasma marginale infection,” Revue d'Élevage et de Médecine Vétérinaire des Pays Tropicaux, vol. 43, no. 2, pp. 155–158, 1990. View at Google Scholar · View at Scopus
  50. K. A. Brayton, G. H. Palmer, and W. C. Brown, “Genomic and proteomic approaches to vaccine candidate identification for Anaplasma marginale,” Expert Review of Vaccines, vol. 5, no. 1, pp. 95–101, 2006. View at Publisher · View at Google Scholar · View at Scopus
  51. R. J. Rogers, C. K. Dimmock, A. J. de Vos, and B. J. Rodwell, “Bovine leucosis virus contamination of a vaccine produced in vivo against bovine babesiosis and anaplasmosis,” Australian Veterinary Journal, vol. 65, no. 9, pp. 285–287, 1988. View at Publisher · View at Google Scholar · View at Scopus
  52. V. Ocampo Espinoza, J. E. S. Vázquez, M. D. Aguilar, M. Á. G. Ortiz, G. J. C. Alarcón, and S. D. Rodríguez, “Anaplasma marginale: lack of cross-protection between strains that share MSP1a variable region and MSP4,” Veterinary Microbiology, vol. 114, no. 1-2, pp. 34–40, 2006. View at Publisher · View at Google Scholar · View at Scopus
  53. J. F. Coetzee, M. D. Apley, and K. M. Kocan, “Comparison of the efficacy of enrofloxacin, imidocarb, and oxytetracycline for clearance of persistent Anaplasma marginale infections in cattle,” Veterinary Therapeutics, vol. 7, no. 4, pp. 347–360, 2006. View at Google Scholar · View at Scopus
  54. S. D. Rodríguez Camarillo, M. Á. G. Ortiz, E. E. R. Ramírez et al., “Anaplasma marginale Yucatan (Mexico) strain: assessment of low virulence and potential use as a live vaccine,” Annals of the New York Academy of Sciences, vol. 1149, pp. 98–102, 2008. View at Publisher · View at Google Scholar · View at Scopus
  55. J. de la Fuente, J. C. Garcia-Garcia, E. F. Blouin, S. D. Rodríguez, M. A. García, and K. M. Kocan, “Evolution and function of tandem repeats in the major surface protein 1a of the ehrlichial pathogen Anaplasma marginale,” Animal Health Research Reviews, vol. 2, no. 2, pp. 163–174, 2001. View at Google Scholar · View at Scopus
  56. R. E. Bock, A. J. DeVos, T. G. Kingston, and P. D. Carter, “Assessment of a low virulence Australian isolate of Anaplasma marginale for pathogenicity, immunogenicity and transmissibility by Boophilus microplus,” Veterinary Parasitology, vol. 118, no. 1-2, pp. 121–131, 2003. View at Publisher · View at Google Scholar · View at Scopus
  57. P. Carter, R. E. Bock, and A. J. DeVos, “Benefits of improved vaccine for anaplasmosis in Australia,” in Proceedings of the 11th International Symposium on Veterinary Epidemiology and Economics, 2006.
  58. C. V. Bastos, L. M. F. Passos, E. J. Facury-Filho, E. M. Rabelo, J. D. L. Fuente, and M. F. B. Ribeiro, “Protection in the absence of exclusion between two Brazilian isolates of Anaplasma marginale in experimentally infected calves,” Veterinary Journal, vol. 186, no. 3, pp. 374–378, 2010. View at Publisher · View at Google Scholar · View at Scopus
  59. R. Kenneil, V. Shkap, B. Leibovich et al., “Cross-protection between geographically distinct Anaplasma marginale isolates appears to be constrained by limited antibody responses,” Transboundary and Emerging Diseases, vol. 60, no. 2, pp. 97–104, 2013. View at Publisher · View at Google Scholar · View at Scopus
  60. K. M. Kocan, J. de la Fuente, E. F. Blouin, J. F. Coetzee, and S. A. Ewing, “The natural history of Anaplasma marginale,” Veterinary Parasitology, vol. 167, no. 2–4, pp. 95–107, 2010. View at Publisher · View at Google Scholar · View at Scopus
  61. R. D. Fleischmann, M. D. Adams, O. White et al., “Whole-genome random sequencing and assembly of Haemophilus influenzae Rd,” Science, vol. 269, no. 5223, pp. 496–512, 1995. View at Publisher · View at Google Scholar · View at Scopus
  62. T. B. K. Reddy, A. D. Thomas, D. Stamatis et al., “The Genomes OnLine Database (GOLD) v.5: a metadata management system based on a four level (meta)genome project classification,” Nucleic Acids Research, vol. 43, no. 1, pp. D1099–D1106, 2015. View at Publisher · View at Google Scholar · View at Scopus
  63. K. L. Seib, G. Dougan, and R. Rappuoli, “The key role of genomics in modern vaccine and drug design for emerging infectious diseases,” PLoS Genetics, vol. 5, no. 10, Article ID e1000612, 2009. View at Publisher · View at Google Scholar · View at Scopus
  64. I. Merelli, H. Pérez-Sánchez, S. Gesing, and D. D'Agostino, “Managing, analysing, and integrating big data in medical bioinformatics: open problems and future perspectives,” BioMed Research International, vol. 2014, Article ID 134023, 13 pages, 2014. View at Publisher · View at Google Scholar · View at Scopus
  65. G. H. Palmer, A. F. Barbet, G. H. Cantor, and T. C. McGuire, “Immunization of cattle with the MSP-1 surface protein complex induces protection against a structurally variant Anaplasma marginale isolate,” Infection and Immunity, vol. 57, no. 11, pp. 3666–3669, 1989. View at Google Scholar · View at Scopus
  66. G. H. Palmer, A. F. Barbet, W. C. Davis, and T. C. McGuire, “Immunization with an isolate-common surface protein protects cattle against anaplasmosis,” Science, vol. 231, no. 4743, pp. 1299–1302, 1986. View at Publisher · View at Google Scholar · View at Scopus
  67. P. S. Santos, A. A. S. Sena, R. Nascimento et al., “Epitope-based vaccines with the anaplasma marginale MSP1a functional motif induce a balanced humoral and cellular immune response in mice,” PLoS ONE, vol. 8, no. 4, article e60311, 2013. View at Publisher · View at Google Scholar · View at Scopus
  68. M. J. Dark, A. M. Lundgren, and A. F. Barbet, “Determining the repertoire of immunodominant proteins via whole-genome amplification of intracellular pathogens,” PLoS ONE, vol. 7, no. 4, Article ID e36456, 2012. View at Publisher · View at Google Scholar · View at Scopus
  69. A. F. Barbet, J. Yi, A. Lundgren, B. R. McEwen, E. F. Blouin, and K. M. Kocan, “Antigenic variation of Anaplasma marginale: major surface protein 2 diversity during cyclic transmission between ticks and cattle,” Infection and Immunity, vol. 69, no. 5, pp. 3057–3066, 2001. View at Publisher · View at Google Scholar · View at Scopus
  70. P. F. M. Meeus, K. A. Brayton, G. H. Palmer, and A. F. Barbet, “Conservation of a gene conversion mechanism in two distantly related paralogues of Anaplasma marginale,” Molecular Microbiology, vol. 47, no. 3, pp. 633–643, 2003. View at Publisher · View at Google Scholar · View at Scopus
  71. J. R. Abbott, G. H. Palmer, K. A. Kegerreis et al., “Rapid and long-term disappearance of CD4+ T lymphocyte responses specific for Anaplasma marginale major surface protein-2 (MSP2) in MSP2 vaccinates following challenge with live A. marginale,” Journal of Immunology, vol. 174, no. 11, pp. 6702–6715, 2005. View at Publisher · View at Google Scholar · View at Scopus
  72. M. J. Dark, D. R. Herndon, L. S. Kappmeyer et al., “Conservation in the face of diversity: multistrain analysis of an intracellular bacterium,” BMC Genomics, vol. 10, article 16, 2009. View at Publisher · View at Google Scholar · View at Scopus
  73. T. J. Silhavy, D. Kahne, and S. Walker, “The bacterial cell envelope,” Cold Spring Harbor Perspectives in Biology, vol. 2, no. 5, article a000414, 2010. View at Publisher · View at Google Scholar · View at Scopus
  74. S. M. Albarrak, W. C. Brown, S. M. Noh et al., “Subdominant antigens in bacterial vaccines: AM779 is subdominant in the Anaplasma marginale outer membrane vaccine but does not associate with protective immunity,” PLoS ONE, vol. 7, no. 9, Article ID e46372, pp. 1–7, 2012. View at Publisher · View at Google Scholar · View at Scopus
  75. S. M. Noh, J. E. Turse, W. C. Brown, J. Norimine, and G. H. Palmerb, “Linkage between Anaplasma marginale outer membrane proteins enhances immunogenicity but is not required for protection from challenge,” Clinical and Vaccine Immunology, vol. 20, no. 5, pp. 651–656, 2013. View at Publisher · View at Google Scholar · View at Scopus
  76. S. M. Noh, K. A. Brayton, W. C. Brown et al., “Composition of the surface proteome of Anaplasma marginale and its role in protective immunity induced by outer membrane immunization,” Infection and Immunity, vol. 76, no. 5, pp. 2219–2226, 2008. View at Publisher · View at Google Scholar · View at Scopus
  77. W. C. Brown, V. Shkap, D. Zhu et al., “CD4+ T-lymphocyte and immunoglobulin G2 responses in calves immunized with Anaplasma marginale outer membranes and protected against homologous challenge,” Infection and Immunity, vol. 66, no. 11, pp. 5406–5413, 1998. View at Google Scholar · View at Scopus
  78. J. E. Lopez, W. F. Siems, G. H. Palmer et al., “Identification of novel antigenic proteins in a complex Anaplasma marginale outer membrane immunogen by mass spectrometry and genomic mapping,” Infection and Immunity, vol. 73, no. 12, pp. 8109–8118, 2005. View at Publisher · View at Google Scholar · View at Scopus
  79. E. J. Glass, R. A. Oliver, and G. C. Russell, “Duplicated DQ haplotypes increase the complexity of restriction element usage in cattle,” Journal of Immunology, vol. 165, no. 1, pp. 134–138, 2000. View at Publisher · View at Google Scholar · View at Scopus
  80. J. Norimine and W. C. Brown, “Intrahaplotype and interhaplotype pairing of bovine leukocyte antigen DQA and DQB molecules generate functional DQ molecules important for priming CD4+ T-lymphocyte responses,” Immunogenetics, vol. 57, no. 10, pp. 750–762, 2005. View at Publisher · View at Google Scholar · View at Scopus
  81. K. Morse, J. Norimine, J. C. Hope, and W. C. Brown, “Breadth of the CD4 + T cell response to Anaplasma marginale VirB9-1, VirB9-2 and VirB10 and MHC class II DR and DQ restriction elements,” Immunogenetics, vol. 64, no. 7, pp. 507–523, 2012. View at Publisher · View at Google Scholar · View at Scopus
  82. W. Kowalczyk, M. Monsó, B. G. de la Torre, and D. Andreu, “Synthesis of multiple antigenic peptides (MAPs)-strategies and limitations,” Journal of Peptide Science, vol. 17, no. 4, pp. 247–251, 2011. View at Publisher · View at Google Scholar · View at Scopus
  83. G. Amexis and N. S. Young, “Multiple antigenic peptides as vaccine platform for the induction of humoral responses against dengue-2 virus,” Viral Immunology, vol. 20, no. 4, pp. 657–663, 2007. View at Publisher · View at Google Scholar · View at Scopus
  84. J. Oscherwitz, F. Yu, J. L. Jacobs, and K. B. Ceasea, “Recombinant vaccine displaying the loop-neutralizing determinant from protective antigen completely protects rabbits from experimental inhalation anthrax,” Clinical and Vaccine Immunology, vol. 20, no. 3, pp. 341–349, 2013. View at Publisher · View at Google Scholar · View at Scopus
  85. B.-L. Niu, H.-M. Du, H.-P. Shen et al., “Myeloid dendritic cells loaded with dendritic tandem multiple antigenic telomerase reverse transcriptase (hTERT) epitope peptides: a potentially promising tumor vaccine,” Vaccine, vol. 30, no. 23, pp. 3395–3404, 2012. View at Publisher · View at Google Scholar · View at Scopus
  86. E. L. Sutten, J. Norimine, P. A. Beare et al., “Anaplasma marginale type IV secretion system proteins VirB2, VirB7, VirB11, and VirD4 are immunogenic components of a protective bacterial membrane vaccine,” Infection and Immunity, vol. 78, no. 3, pp. 1314–1325, 2010. View at Publisher · View at Google Scholar · View at Scopus
  87. S. Lockwood, D. E. Voth, K. A. Brayton et al., “Identification of Anaplasma marginale type IV secretion system effector proteins,” PLoS ONE, vol. 6, no. 11, article e27724, 2011. View at Publisher · View at Google Scholar · View at Scopus
  88. G. H. Palmer, W. C. Brown, S. M. Noh, and K. A. Brayton, “Genome-wide screening and identification of antigens for rickettsial vaccine development,” FEMS Immunology and Medical Microbiology, vol. 64, no. 1, pp. 115–119, 2012. View at Publisher · View at Google Scholar · View at Scopus
  89. D. W. Gray, M. D. Welsh, S. Doherty et al., “Identification of systemic immune response markers through metabolomic profiling of plasma from calves given an intra-nasally delivered respiratory vaccine,” Veterinary Research, vol. 46, no. 1, article 7, pp. 1–16, 2015. View at Publisher · View at Google Scholar · View at Scopus
  90. I. Delany, R. Rappuoli, and K. L. Seib, “Vaccines, reverse vaccinology, and bacterial pathogenesis,” Cold Spring Harbor Perspectives in Biology, vol. 3, no. 5, article a012476, 2013. View at Publisher · View at Google Scholar · View at Scopus
  91. C. D. Rinaudo, J. L. Telford, R. Rappuoli, and K. L. Seib, “Vaccinology in the genome era,” The Journal of Clinical Investigation, vol. 119, no. 9, pp. 2515–2525, 2009. View at Publisher · View at Google Scholar · View at Scopus
  92. G. A. Poland, I. G. Ovsyannikova, R. B. Kennedy, I. H. Haralambieva, and R. M. Jacobson, “Vaccinomics and a new paradigm for the development of preventive vaccines against viral infections,” OMICS: A Journal of Integrative Biology, vol. 15, no. 9, pp. 625–636, 2011. View at Publisher · View at Google Scholar · View at Scopus
  93. G. A. Poland, R. B. Kennedy, and I. G. Ovsyannikova, “Vaccinomics and personalized vaccinology: is science leading us toward a new path of directed vaccine development and discovery?” PLoS Pathogens, vol. 7, no. 12, Article ID e1002344, pp. 1–6, 2011. View at Publisher · View at Google Scholar · View at Scopus
  94. A. Bernstein, B. Pulendran, and R. Rappuoli, “Systems vaccinomics: the road ahead for vaccinology,” OMICS: A Journal of Integrative Biology, vol. 15, no. 9, pp. 529–531, 2011. View at Publisher · View at Google Scholar · View at Scopus
  95. R. B. Kennedy and G. A. Poland, “The top five ‘game changers’ in vaccinology: toward rational and directed vaccine development,” OMICS: A Journal of Integrative Biology, vol. 15, no. 9, pp. 533–537, 2011. View at Publisher · View at Google Scholar
  96. G. A. Poland, R. B. Kennedy, B. A. McKinney et al., “Vaccinomics, adversomics, and the immune response network theory: individualized vaccinology in the 21st century,” Seminars in Immunology, vol. 25, no. 2, pp. 89–103, 2013. View at Publisher · View at Google Scholar · View at Scopus
  97. B. Pulendran, S. Li, and H. I. Nakaya, “Systems vaccinology,” Immunity, vol. 33, no. 4, pp. 516–529, 2010. View at Publisher · View at Google Scholar · View at Scopus
  98. J. de la Fuente and O. Merino, “Vaccinomics, the new road to tick vaccines,” Vaccine, vol. 31, no. 50, pp. 5923–5929, 2013. View at Publisher · View at Google Scholar · View at Scopus
  99. J. Xiao, Z. Zhang, J. Wu, and J. Yu, “A brief review of software tools for pangenomics,” Genomics, Proteomics and Bioinformatics, vol. 13, no. 1, pp. 73–76, 2015. View at Publisher · View at Google Scholar · View at Scopus
  100. G. Vernikos, D. Medini, D. R. Riley, and H. Tettelin, “Ten years of pan-genome analyses,” Current Opinion in Microbiology, vol. 23, pp. 148–154, 2015. View at Publisher · View at Google Scholar · View at Scopus
  101. H. Tettelin, V. Masignani, M. J. Cieslewicz et al., “Genome analysis of multiple pathogenic isolates of Streptococcus agalactiae: implications for the microbial ‘pan-genome’,” Proceedings of the National Academy of Sciences of the United States of America, vol. 102, no. 39, pp. 13950–13955, 2005. View at Publisher · View at Google Scholar · View at Scopus