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BioMed Research International
Volume 2013 (2013), Article ID 743509, 8 pages
A History of the Development of Brucella Vaccines
1Departamento de Microbiología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Prolongación Carpio y Plan de Ayala s/n, Col. Sto. Tomás, 11340 México, DF, Mexico
2Center for Molecular Medicine and Infectious Diseases, Virginia-Maryland Regional College of Veterinary Medicine, Virginia Tech, Blacksburg, VA 24060, USA
Received 11 January 2013; Accepted 9 May 2013
Academic Editor: Adolfo Paz Silva
Copyright © 2013 Eric Daniel Avila-Calderón 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.
Brucellosis is a worldwide zoonosis affecting animal and human health. In the last several decades, much research has been performed to develop safer Brucella vaccines to control the disease mainly in animals. Till now, no effective human vaccine is available. The aim of this paper is to review and discuss the importance of methodologies used to develop Brucella vaccines in pursuing this challenge.
Brucellosis is a zoonosis affecting approximately 500,000 people annually around the world. The disease remains endemic in many regions of the world including Latin America, Middle East, Africa, Asia, and the Mediterranean basin . Brucella can be acquired by humans when they come in direct contact with fluid discharges from an infected animal, but in endemic regions people usually get infected through the consumption of unpasteurized dairy products mainly goat’s milk and fresh soft cheese made out of unpasteurized milk. Isolation of Brucella is the gold standard to confirm infection; however, this is time-consuming and requires skilled technicians. Also, the handling of samples containing bacterial pathogen represents a high risk for laboratory personnel, for example, brucellosis is the most common bacterial laboratory-acquired infection worldwide [1, 2]. Therefore, brucellosis is generally diagnosed based on serological tests, in both animals and humans. However, human brucellosis is often misdiagnosed and underreported basically because the flu-like symptoms are protean and not specific. The treatment of human brucellosis requires the prolonged use of combination of antibiotics . Brucella as facultative intracellular pathogen establishes an intimate relationship with the immune cells of the host. Through the subversion of the immune system, the pathogen is able to maintain a chronic infection that often makes treatment and diagnosis difficult. In the last decades, much research has been conducted in an attempt to develop safer and more effective Brucella vaccines for animals. There is no licensed vaccine for prevention of human brucellosis. A human vaccine would be useful to protect farmers, veterinarians, animal care workers, laboratory personnel, and general population living in endemic brucellosis areas . The aim of this paper is to review and discuss the importance of the development of Brucella vaccines and some of the current methodologies used to pursue this goal.
Research focused on the development of an ideal Brucella vaccine to prevent brucellosis in animals and humans has been sought since the beginning of twentieth century . Live vaccines as well as inactivated ones have been developed; nevertheless, modified live vaccines have been shown to be superior protective immunogens as is the case with most diseases caused by facultative intracellular pathogens.
The attenuated live vaccine B. suis strain 2 was extensively used in several animals species in China. This vaccine did not induce persistent antibodies. B. abortus strain 104-M was developed in China and used as vaccine in humans. This vaccine was reported to be stable in antigenic structure, virulence, and immunogenicity . Immunity derived from the use of live attenuated vaccines tends to be cell mediated and long lasting. Also, as they are administered live, the organism is allowed to replicate within the host allowing in vivo gene expression, thus making them less expensive .
Two live attenuated vaccines strains were selected for their safety, stability, and immunogenicity for human protection. In 1952, B. abortus VA 19 was used in a mass epidemiological campaign in the former USSR, while in China B. abortus 104 M was tested in humans by intradermal, oral, and nasal routes .
Over the years, a wide variety of killed vaccines have been developed for protection against brucellosis. They have had limited acceptance and success. None have approached the protection levels afforded by the live attenuated vaccines. Examples of killed vaccines are B. abortus strain 45/20 and B. melitensis H38 . B. abortus strain 45/20 was used in cattle and sheep, while B. melitensis H38 was tested in mice and cows. In addition to the lack of sufficient protection after challenge, killed vaccines such as strains 45/20 and H38 can induce persistent antibody titers. Killed vaccines for humans were first used in Malta in 1906 by Eyre, who vaccinated 51 soldiers .
Several antigenic fractions extracted from Brucella have been tested as a vaccine candidates, mainly in association with a variety of adjuvants; some of them included cell envelopes , outer membrane proteins [8, 9], insoluble residues of hot sodium dodecyl sulfate (SDS) extracts of cell envelopes (PG) , phenol insoluble fraction (PI) , soluble SDS extracts , Brucella soluble antigens (BASA) , periplasmic proteins and salt extractable proteins , chemically modified Brucella proteins , smooth and rough LPS , recombinant Cu-Zn superoxide dismutase (SOD), and synthetic peptides , among others. From all these fractions, only the phenol insoluble (PI) fraction has been used in humans [10, 17]. PI was an extract from the cell wall of B. melitensis. PI was applied subcutaneously in two doses of 1 mg with 15 hours interval. In humans, this vaccine showed low toxicity, hypersensitivity, and good immune response. The PI vaccine was used massively in 1967 in 800 laboratory workers who were often in contact with the bacteria. It was reported that all of them were protected except one who had immunodeficiency. The protection conferred by PI lasted around 18 to 24 months .
3. Current Vaccines for the Prevention of Animal Brucellosis
Vaccination is probably the most economic measure for control of brucellosis in endemic areas. Many countries have developed control measures for the eradication of the disease in livestock animal. These programs minimized the economic losses due to the abortion, infertility, and weak offspring and decreased milk production . Presently, the vaccination programs are based on control of brucellosis mainly due to B. melitensis and B. abortus [20, 21].
Females are the most important targets for the vaccination programs as some vaccines cause severe tissue damage in male and lateral or vertical transmission occurs mainly via fluids associated with abortion or birth of infected calves or through shedding in milk. Vaccination by intramuscular or subcutaneous route is the most frequently used in livestock, but also the intraconjunctival route also has been used with good results .
Currently, only three live attenuated vaccines for the control of B. abortus infection in cattle are recommended: B. abortus 45/20, B. abortus strain 19 (S19), and B. abortus RB51 [5, 11, 22]. B. abortus strain 45/20 was isolated following twenty passages in guinea pigs; this rough strain is used only as heat-killed vaccine to avoid reversion to a virulent strain. Also this vaccine needs to be administrated with an adjuvant in adult cattle; it does not interfere with serological diagnosis and it is safer in pregnant animals but only has been tested in some countries .
Another licensed live smooth attenuated vaccine for control of bovine brucellosis is B. abortus S19. This strain was isolated in the early twentieth century and was naturally attenuated when a virulent culture of B. abortus was left at room temperature for one year . B. abortus S19 has been effective for the control of brucellosis in adult bovines and prevents abortion as well as decreasing the prevalence in herds. However due to the smooth nature of the strain S19 and the strong antibody response against the O-side chain, it does not permit discrimination of infected from vaccinated animals. The competitive ELISA assay and radial immunodiffusion test have been used to permit differentiation between vaccinated or infected animals in field . A low rate of abortion in livestock and significant reduction in milk production has been reported with B. abortus S19 vaccination [19, 22].
The live vaccine B. abortus RB51 is a spontaneous rough mutant obtained by subculturing the virulent strain B. abortus 2308 on medium containing rifampicin and penicillin . Subsequently, it was found to contain an IS711 element disrupting the wboA gene encoding a glycosyl transferase responsible for O-side chain synthesis ; hence it has a rough phenotype. In contrast to strain 45/20, B. abortus RB51 is very stable and it is currently used in many countries instead of B. abortus S19. Rough strain RB51 is less virulent and it does not induce a positive response in typical serological diagnostic test [5, 22, 25]. Vaccination of pregnant cows with strain RB51 can induce low levels of abortion (less than 0.2%); however it is safe at lower doses during pregnancy . Vaccine strain RB51 can infect humans but it is less virulent than strain S19 .
Currently, the live vaccine B. melitensis Rev. 1 is used for the control of brucellosis in small ruminants. This strain was developed by Herzberg and Elberg in mid-1950s and retains the common characteristics of the Brucella species, but it is resistant to 2.5 μg/mL streptomycin and susceptible to 5 IU penicillin G that allows differentiation from field strains . Subcutaneous or conjunctival immunization with B. melitensis Rev. 1 confers adequate immunity in small ruminants. B. melitensis Rev. 1 induces a positive antibody response in serological tests in vaccinated animals. Also B. melitensis Rev. 1 can infect humans. The vaccination is recommended prior to the first gestation between 3 and 7 months of age to avoid abortion in pregnant animals . As B. melitensis can be isolated from cattle, some scientists proposed use of the live attenuated vaccine B. melitensis Rev. 1 to control the disease in cattle .
Compared to the extensive research effort for developing new vaccines against B. melitensis or B. abortus, little research has been conducted to protect swine against B. suis . Oral or intramuscular vaccination with strain RB51, killed B. suis, or purified O-polysaccharide was reported to be efficacious in protecting swine exposed to infected boars . However, other studies have shown very little protection by strain RB51 in immunized swine against wild type challenge .
4. Brucellosis Eradication Programs
The general strategies proposed in 1998 by the WHO including Mediterranean Zoonoses Control Program to eradicate animal brucellosis were the following: (i) prevention of spread between animals and monitoring of brucellosis-free herds and zones, (ii) elimination of infected animals by test and slaughter programs to obtain brucellosis-free herds and regions, and (iii) vaccination to reduce the prevalence .
Due to the lack of a human vaccine against brucellosis, animal vaccination is a critical factor for the control and eradication of brucellosis in animals and humans. However this approach could be complemented with surveillance of livestock and/or elimination of infected animals as well as other critical control measures.
Regulatory programs for brucellosis are influenced by the prevalence of the disease in livestock or humans and economic considerations. The majority of programs for the eradication of animal brucellosis are aimed at reducing the prevalence that include test and removal programs, sanitization, and/or vaccination .
In general, sanitization programs are based on the education of the producers for elimination of contaminated material, decontamination, and other methods to avoid exposure and the dissemination of the disease agent. Test and removal programs are applicable in areas with high prevalence but not for eradication programs, and this should be stricter in surveillance herds of individual livestock . However for developing countries, the elimination of the Brucella-infected animals is not affordable.
In endemic regions where the prevalence of brucellosis was low and vaccination was stopped, outbreaks of human and animal brucellosis were reported .
In 2001, Brazil implemented control measures for eradication of bovine brucellosis, which included vaccination of the cows aged 3–8 months with B. abortus S19, accreditation of brucellosis-free herds, periodic surveillance, requirement of serological testing for movement or entry of livestock fairs, and compulsory slaughter of animals positive for brucellosis and permanent refresher training for accredited veterinarians . It is clear that for the successful eradication and control programs for brucellosis in endemic areas, the government should be involved. They can raise the awareness of the risk of the disease, while also raising specific concern about infecting individual human subjects and the potential risk of horizontal transfer in the field. To circumvent these problems, the national veterinary services needed to maintain a certain level of competence as well as adopt a method to identify and register vaccinated animals.
In the Middle East, brucellosis has been reported in almost all domestic animals, particularly cattle, sheep, and goats. However, there is a controversy on the best choice of the strategy for the brucellosis control. In some countries, the test and slaughter policy together with the vaccination of the young females was adopted; in others, particularly with regard to sheep and goats, mass vaccination was utilized. Regardless, vaccination was limited to cattle and small ruminants. In several countries, little is done to control the disease in humans because of lack of financial and technical facilities .
In the case of B. suis, dissemination in swine is primarily the result of B. suis biovar 1 and 3, and some cases of transmission of biovar 2 from wild pig to domestic swine have been reported. Due to the low pathogenicity of biovar 2 in humans, it is not considered to be a significant zoonotic threat and therefore likely not to have an adequate serologic surveillance [35, 36].
Although B. ovis rarely causes abortion in ewes, the infection manifests with testicular lesions and reduced infertility in rams . As epididymal lesions in rams are not pathognomonic for the infection by Brucella, surveillance relies on serodiagnosis and isolation of the bacteria from infected animals [19, 38].
5. Subunit Vaccines against Brucellosis
As we mentioned earlier, the use of the live-attenuated vaccines against brucellosis represents a risk due to its potential ability to revert to virulence, cause abortion in pregnant animals, and be shed in milk, but also live strains could infect people coming into contact with the vaccine for example, farmers, abattoir workers, and veterinarians.
An ideal vaccine for use either in humans or in animals should meet the following criteria: should be effective and avirulent and induce long-lasting protection .
Subunit vaccines, like recombinant proteins, are promising vaccine candidates because they are less biohazardous, well defined, avirulent, noninfectious, and nonviable .
For the development of an effective vaccine against brucellosis, it is necessary to elicit an adequate immunological response (biased towards a Th1) and then choose the best antigen that induces protective immunity. It is well known that for an intracellular pathogen represented by Brucella, the production of IFNγ, TNFα, and IL-12 from the T helper cells (Th1 response), as well as CD8+ and CD4+ T lymphocytes, activated macrophages and dendritic cells are necessary for the control of the infection; whereas Th2 components have a minor role in the control of infection [21, 35, 36]. There appear to be three mechanisms of the adaptive immune response against brucellosis that are important: (1) production of IFN (produced by CD4+, CD8+, and γδ T cells) activates the bactericidal action of the macrophages to hamper the intracellular survival of Brucella; (2) the cytotoxic action of the CD8+ and γδ T cells kills infected macrophages; (3) Th1 antibody IgG2a isotypes opsonize the bacteria to facilitate effective phagocytosis [39, 41]. Subunit vaccines appear to be a promising option to develop safer vaccines because they are not able to regain virulence as opposed to live strains. However subunit vaccines also sometimes fail to elicit the magnitude of the immune response and/or induce protection comparable to live vaccines . Since they tend to be poorly immunogenic stimulators, they require the coadministration of an adjuvant. Therefore the success of the subunit vaccine depends of the use of the substances endowed with immunomodulatory properties that control the selective induction of the appropriate type of antigenic-immune response. Moreover, the success of the subunit vaccine is associated with the route of administration .
5.1. Recombinant Proteins
Selecting the optimal antigens represents the cornerstone in vaccine design. Depending on the desired response, the antigenic proteins should contain appropriate epitopes to B-cell receptors and can be recognized by the T-cell receptor in a complex with MHC molecules .
Several Brucella immunogenic antigens have been found in the outer membrane of this Gram-negative pathogen. Bacterial cell surface antigens are prime candidates as they represent the initial point of contact between the pathogen and its host .
For instance, the recombinant 31 kDa outer membrane protein (Omp31) in aluminum hydroxide or Incomplete Freud Adjuvant (IFA) induced significant levels of protection against B. melitensis challenge in the mouse model . Also the purified recombinant lipoproteins Omp16 and Omp19 induce significant protection against oral or systemic B. abortus challenge when delivered by a parental or oral route without adjuvant, yet by a different immune mechanism. Also plant-made vaccines expressing Omp16 or Omp19 were able to induce significant protective immune response when administrated to mice by the oral route as purified proteins and within the crude leaf material of transgenic tobacco plants [40, 42].
The Omp25 (a peptidoglycan-layer protein) is an important Brucella virulence factor involved in survival; B. melitensis, B. abortus, and B. ovis Omp25 deletion mutants are attenuated in mice . As a recombinant protein, Omp25 from B. abortus S19 induced protection against B. abortus 544 challenge in mice when it was administrated by intradermal or intraperitoneal routes .
In contrast, three peptides from the periplasmic protein Cu-Zn superoxide dismutase from B. abortus were assayed for induction of protection in mice; however only one was able to induce significant protection against B. abortus 2308 .
Also the cytosolic proteins SurA and DnaK were evaluated in mice as purified recombinant proteins. Both proteins induced similar levels of protection against B. abortus (moderate levels compared with the live vaccine control) .
Combining several antigens in a vaccine formulation does not always induce higher levels of protection compared to the use of a single antigen. The immunization with DnaK and SurA did not show a synergistic effect compared with the vaccination of either antigen alone . A similar effect was observed when Omp31 and Brucella lumazine synthase (BSL) were used together versus individually. However, chimeric formulation of Omp31-BSL augmented the protection achieved by either single antigen .
The need of the appropriate adjuvant is also important for obtaining protection in case of subunit vaccines. When recombinant periplasmic protein P39 was combined with CpG oligonucleotides, the protein induced a Th1 response and protection against B. abortus . Recently recombinant Omp28 from B. melitensis adjuvanted with CpG conferred moderate levels of protection in mice against B. abortus 544 challenge .
5.2. Vectored Vaccines
Antigen delivery systems become necessary when antigens are not efficiently transported to the appropriate sites or presented to the immune system. For example, rapid degradation can result in weak or virtual lack of responses to otherwise immunogenic antigens .
BP26 is a 26 kDa periplasmic protein with an unknown function. Recently, a vectored vaccine has been developed based on protein BP26 or Omp16 and Omp31; that is, E. coli expressing B. melitensis BP26 induced lymphocyte proliferation, IFN-γ production, and protection in mice. On the other hand E. coli (K12) may be an ideal vaccine platform with natural adjuvant properties since it is nonpathogenic and can delivery antigens to antigen-presenting cells promoting cellular immune responses .
Lactococcus lactis expressing Cu-Zn SOD has also been used as a delivery system in mouse model and induced protection against a B. abortus challenge .
Semliki Forest Virus (SFV) was packed with RNA encoding the B. abortus Cu-Zn SOD and was able to induce protection in mice against B. abortus . However, viral delivery systems do not always work, as in the case of the vaccinia virus delivering DNA encoding B. abortus GroEL (a chaperonin) or L7/L12 (ribosomal protein) was unable to induce a protective response against B. abortus challenge .
5.3. DNA Vaccines
DNA vaccines are able to induce both humoral and cellular immune responses. However, it is generally perceived that they induce less potent immune responses than protein vaccines . Nevertheless, this may not be the case for brucellosis; for example, a DNA vaccine expressing Omp31 appears to elicit similar levels of protection as the recombinant protein combined with IFA . Moreover, a BSL-DNA vaccine was more effective than the same recombinant protein against B. abortus challenge .
The use of the DNA vaccines resulted in the induction of a diverse immune response, which led to different levels of protection, which, in many cases, were not as high when compared with the commercial live attenuated Brucella vaccine .
Strategies to enhance the efficacy of DNA vaccines are constantly emerging to maximize immune responses. This is of particular importance in order to aid the transition of these vaccines into larger animal models and also humans .
One advantage of DNA vaccines is that multiple antigens can be expressed. A fusion of the antigens L7/L12 and Omp16 induced higher level of protection in mice than DNA vaccines expressing individual antigens . Another study reported the fusion of L7/L12 and P39 genes (encoding ribosomal and periplasmic proteins, resp.) within a DNA vaccine that improved the protection compared with individual DNA vaccines encoding either alone .
In contrast, the coadministration of multiple plasmids expressing BSCP31 (31 kDa protein), Cu/Zn SOD, or L7/L12 strikingly enhanced the protection against B. abortus challenge compared with live vaccine B. abortus strain S19 .
Another strategy to improve brucellosis DNA vaccines is through the modulation of the immune response by the coexpression of cytokines as adjuvants . When genes encoding IL-2 or IL-18 were fused to SOD and expressed in a single DNA vaccine, improved protection was observed compared to a SOD DNA vaccine alone [61, 62]. In contrast, when IL-15 or IL-12 genes were coadministrated on separate plasmids along with the multigenic vaccine containing the bscp31, sod, and L7/L12 genes, their efficacy was increased against B. abortus challenge compared to that observed with live vaccine S19 [63, 64].
5.4. Outer Membrane Vesicles: New Promising Vaccines against Brucellosis
Over 50 years ago, it was reported that Gram-negative bacteria shed outer membrane vesicles (OMVs) . Production of these vesicles occurs spontaneously and during the normal growth of Gram-negative bacteria in many different environments including soil, biofilms, and enriched culture medium and during the infective process in the case of pathogens. As OMVs are shed from the outer membrane, their general composition has been characterized to contain outer membrane proteins, phosphoslipids, lipopolysaccharide (LPS), and some periplasmic compounds that are entrapped during the bulging of the outer membrane [66–69].
OMVs from the Gram-negative bacteria have been implicated in many processes including the release of virulence factors to the host as well as in the delivery of toxins, modulation of the immune system, trafficking of signaling molecules between bacterial cells, and biofilm formation [67–69]. Taking advantage of the immunomodulatory role of the OMVs from Gram-negative pathogens, the use of the OMVs as acellular vaccines against the OMVs-producing pathogens in vivo and in vitro has been tested [67, 70].
Brucella also release OMVs to the external milieu [71, 72]. Recently, the use of Brucella OMVs as a potential vaccine has been explored. Purified OMVs from both B. melitensis strains 16 M (smooth strain) and VTRM1 (rough lacking O-side chain) by differential centrifugation were used to immunize mice. When Brucella OMVs were administrated by an intramuscular route, OMVs from both strains induced similar levels of protection against virulent B. melitensis challenge compared with the live vaccine B. melitensis Rev. 1. In contrast, rough OMVs induced better levels of IgG2a antibodies than OMVs from smooth and live vaccine strain .
To improve the immune responses and subsequent protection by Brucella OMVs, Pluronic-85 was used as adjuvant. This adjuvant enhances the immune response and the protection against challenge with virulent B. melitensis strain compared to OMVs alone .
Compared to other subunit vaccines, OMVs may possess considerable advantages. OMVs are multicomplex antigens due to their numerous bacterial components and are composed of bacterial phospholipids that can act as natural bacterial adjuvants. Recently, it has been demonstrated that OMVs can interact with the eukaryotic host cell and enter by endocytic pathways; OMVs from Brucella are not the exception . Therefore not only can membrane receptor dependent-pathways be induced, but also cytoplasmic receptors such as NOD (nucleotide binding and oligomerization receptor) or others could help trigger an immune response.
Compared to recombinant proteins, DNA vaccine, or vectored vaccines, OMVs could be less expensive in terms of production and purification. OMVs are purified from the Brucella culture medium by differential centrifugation and washing .
Because the genome sequences of many Brucella species are available, this makes it possible to genetically modify the content of OMVs using recombinant DNA technology, for example, overexpression of protective antigens that are expressed in vivo. In this way, it should be possible to enhance the efficacy of Brucella OMVs as has been reported by others [67, 68]. However, further research is essential to fully evaluate the benefits and risks of these types of acellular vaccines for the prevention of brucellosis in animals and especially humans.
This work was funded by CONACYT CB-2011-01 no. 169259, SIP-IPN 20110891, SIP-IPN 20134610, and ICYTDF-IPN (Project of Investigation under the consolitadation of professors from Instituto Politecnico Nacional, with the level of National Research Candidates ICYTDF-IPN). Eric Daniel Avila-Calderón was supported by CONACYT and PIFI-IPN scholarships. Araceli Contreras-Rodríguez and Ahidé Lopez-Merino were supported by fellowships from COFAA, SIP-EDI, and SNI-CONACYT.
- G. Pappas, P. Papadimitriou, N. Akritidis, L. Christou, and E. V. Tsianos, “The new global map of human brucellosis,” Lancet Infectious Diseases, vol. 6, no. 2, pp. 91–99, 2006.
- J. E. Luna-Martínez and C. Mejía-Terán, “Brucellosis in Mexico: current status and trend,” Veterinary Microbiology, vol. 90, no. 1–4, pp. 19–30, 2002.
- J. Ariza, M. Bosilkovski, A. Cascio et al., “Perspectives for the treatment of brucellosis in the 21st century: the Ioannina recommendations,” PLoS Medicine, vol. 4, no. 12, article e317, 2007.
- P. Nicoletti, “Vaccination,” in Animal Brucellosis, K. Nielsen and J. R. Duncan, Eds., pp. 284–299, CRC Press, Boca Raton, Fla, USA, 1990.
- G. G. Schurig, N. Sriranganathan, and M. J. Corbel, “Brucellosis vaccines: past, present and future,” Veterinary Microbiology, vol. 90, no. 1–4, pp. 479–496, 2002.
- J. Roux, “Brucella vaccines in humans,” in Brucellosis, M. M. Madkour, Ed., pp. 244–249, Butterworths, London, UK, 1989.
- M. Plommet, G. Renoux, A. Philppon, C. Lorentz, and J. Gestin, “Brucellose experimentale. I. Comparison de l’efficacite des vaccines B19 and H38 vaccine,” Annales de Recherches Veterinaires (Paris), vol. 1, pp. 189–201, 1970.
- J. A. Montaraz and A. J. Winter, “Comparison of living and nonliving vaccines for Brucella abortus in BALB/c mice,” Infection and Immunity, vol. 53, no. 2, pp. 245–251, 1986.
- A. J. Winter and G. E. Rowe, “Comparative immune responses to native cell envelope antigens and the hot sodium dodecyl sulfate insoluble fraction (PG) of Brucella abortus in cattle and mice,” Veterinary Immunology and Immunopathology, vol. 18, no. 2, pp. 149–163, 1988.
- J. Roux and A. Serre, “Prophylaxie individuelle et vaccination contre les brucelloses humaines par une fraction antigénique de Brucella melitensis (complexe proteines-glycoproteines-glycosaminopeptides),” Revue d'épidémiologie, Médecine Sociale et Santé Publique, vol. 19, pp. 503–516, 1971.
- M. Sterne, G. Trim, and E. S. Broughton, “Immunisation of laboratory animals and cattle with non-agglutinogenic extracts of Brucella abortus strain 45-20,” Journal of Medical Microbiology, vol. 4, no. 2, pp. 185–194, 1971.
- G. K. Dzata, A. W. Confer, and J. H. Wyckoff, “The effects of adjuvants on immune responses in cattle injected with a Brucella abortus soluble antigen,” Veterinary Microbiology, vol. 29, no. 1, pp. 27–48, 1991.
- G. W. Pugh and L. B. Tabatabai, “Variation in Brucella abortus 2308 infection in BALB/c mice induced by prior vaccination with salt-extractable periplasmic proteins from Brucella abortus 19,” Infection and Immunity, vol. 64, no. 2, pp. 548–556, 1996.
- M. G. Stevens, L. B. Tabatabai, S. C. Olsen, and N. F. Cheville, “Immune responses to superoxide dismutase and synthetic peptides of superoxide dismutase in cattle vaccinated with Brucella abortus strain 19 or RB51,” Veterinary Microbiology, vol. 41, no. 4, pp. 383–389, 1994.
- L. B. Tabatabai, G. W. Pugh Jr., M. G. Stevens, M. Phillips, and T. J. McDonald, “Monophosphoryl lipid A-induced immune enhancement of Brucella abortus salt-extractable protein and lipopolysaccharide vaccines in BALB/c mice,” American Journal of Veterinary Research, vol. 53, no. 10, pp. 1900–1907, 1992.
- L. B. Tabatabai and G. W. Pugh Jr., “Modulation of immune responses in Balb/c mice vaccinated with Brucella abortus Cu-Zn superoxide dismutase synthetic peptide vaccine,” Vaccine, vol. 12, no. 10, pp. 919–924, 1994.
- P. Desmettre, L. Jouber, L. Valette, and J. Roux, “Vaccin de la brucellose humaine obtenu a partir de la fraction phenolo-insoluble de Brucella abortus souche B19. Production, contrôle, standardisation,” Developments in Biological Standardization, vol. 56, pp. 579–586, 1984.
- J. Roux, “Epidemiology and prevention of brucellosis,” Bulletin of the World Health Organization, vol. 57, no. 2, pp. 179–194, 1979.
- S. C. Olsen and W. S. Stoffregen, “Essential role of vaccines in brucellosis control and eradication programs for livestock,” Expert Review of Vaccines, vol. 4, no. 6, pp. 915–928, 2005.
- S. Marzetti, C. Carranza, M. Roncallo, G. I. Escobar, and N. E. Lucero, “Recent trends in humanBrucellacanisinfection,” Comparative Immunology, Microbiology and Infectious Disease, vol. 36, no. 1, pp. 55–61, 2013.
- S. C. Oliveira, G. H. Giambartolomei, and J. Cassataro, “Confronting the barriers to develop novel vaccines against brucellosis,” Expert Review of Vaccines, vol. 10, no. 9, pp. 1291–1305, 2011.
- I. Moriyón, M. J. Grilló, D. Monreal, et al., “Rough vaccines in animal brucellosis: structural and genetic basis and present status,” , Veterinary Research, vol. 35, no. 1, pp. 1–38, 2004.
- E. L. Thomas, C. D. Bracewell, and M. J. Corbel, “Characterisation of Brucella abortus strain 19 cultures isolated from vaccinated cattle,” Veterinary Record, vol. 108, no. 5, pp. 90–93, 1981.
- L. G. Adams, “Development of live Brucella vaccines,” in Advances of Brucellosis Research, L. G. Adams, Ed., pp. 250–256, 1990.
- G. G. Schurig, R. M. Roop, T. Bagchi, S. Boyle, D. Buhrman, and N. Sriranganathan, “Biological properties of RB51; a stable rough strain of Brucella abortus,” Veterinary Microbiology, vol. 28, no. 2, pp. 171–188, 1991.
- R. Vemulapalli, J. R. McQuiston, G. G. Schurig, N. Sriranganathan, S. M. Halling, and S. M. Boyle, “Identification of an IS711 element interrupting the wboA gene of Brucella abortus vaccine strain RB51 and a PCR assay to distinguish strain RB51 from other Brucella species and strains,” Clinical and Diagnostic Laboratory Immunology, vol. 6, no. 5, pp. 760–764, 1999.
- F. A. Uzal, L. Samartino, G. Schurig et al., “Effect of vaccination with Brucella abortus strain RB51 on heifers and pregnant cattle,” Veterinary Research Communications, vol. 24, no. 3, pp. 143–151, 2000.
- D. A. Ashford, J. Di Pietra, J. Lingappa et al., “Adverse events in humans associated with accidental exposure to the livestock brucellosis vaccine RB51,” Vaccine, vol. 22, no. 25-26, pp. 3435–3439, 2004.
- G. G. Alton and S. S. Elberg, “Rev 1 Brucella melitensis vaccine,” Veterinary Bulletin, vol. 37, pp. 793–800, 1967.
- M. Banai, “Control of small ruminant brucellosis by use of Brucella melitensis Rev.1 vaccine: laboratory aspects and field observations,” Veterinary Microbiology, vol. 90, no. 1–4, pp. 497–519, 2002.
- V. R. Lord, J. W. Cherwonogrodzky, G. G. Schurig, R. D. Lord, M. J. Marcano, and G. E. Meléndez, “Venezuelan field trials of vaccines against brucellosis in swine,” American Journal of Veterinary Research, vol. 59, no. 5, pp. 546–551, 1998.
- WHO/MZCP, Human and Animal Brucellosis, WHO, Damascus, Syria, 1998.
- A. Minas, M. Minas, A. Stournara, and S. Tselepidis, “The “effects” of Rev-1 vaccination of sheep and goats on human brucellosis in Greece,” Preventive Veterinary Medicine, vol. 64, no. 1, pp. 41–47, 2004.
- M. Refai, “Incidence and control of brucellosis in the Near East region,” Veterinary Microbiology, vol. 90, no. 1–4, pp. 81–110, 2002.
- H. N. Becker, R. C. Belden, T. Breault, et al., “Brucellosis in feral swine in Florida,” Journal of the American Veterinary Medical Association, vol. 173, no. 9, pp. 1181–1182, 1978.
- J. Godfroid and A. Käsbohrer, “Brucellosis in the European Union and Norway at the turn of the twenty-first century,” Veterinary Microbiology, vol. 90, no. 1–4, pp. 135–145, 2002.
- R. da Costa Martins, J. M. Irache, and C. Gamazo, “Acellular vaccines for ovine brucellosis: a safer alternative against a worldwide disease,” Expert Review of Vaccines, vol. 11, no. 1, pp. 87–95, 2012.
- J. Arsenault, C. Girard, P. Dubreuil, and D. Bélanger, “Lack of evidence of Brucella ovis infection in rams in Quebec,” The Canadian Veterinary Journal, vol. 45, no. 4, pp. 312–313, 2004.
- S. D. Perkins, S. J. Smither, and H. S. Atkins, “Towards a Brucella vaccine for humans,” FEMS Microbiology Reviews, vol. 34, no. 3, pp. 379–394, 2010.
- K. A. Pasquevich, A. E. Ibañez, L. M. Coria et al., “An oral vaccine based on U-Omp19 induces protection against B. abortus mucosal challenge by inducing an adaptive IL-17 immune response in mice,” PLoS ONE, vol. 6, no. 1, article e16203, 2011.
- E. Fugier, G. Pappas, and J. P. Gorvel, “Virulence factors in brucellosis: implications for aetiopathogenesis and treatment,” Expert Reviews in Molecular Medicine, vol. 9, no. 35, pp. 1–10, 2007.
- K. A. Pasquevich, C. G. Samartino, L. M. Coria et al., “The protein moiety of Brucella abortus outer membrane protein 16 is a new bacterial pathogen-associated molecular pattern that activates dendritic cells in vivo, induces a Th1 immune response, and is a promising self-adjuvanting vaccine against systemic and oral acquired brucellosis,” Journal of Immunology, vol. 184, no. 9, pp. 5200–5212, 2010.
- C. Ruecker and C. A. Guzmán, “Vaccines: from empirical development to rational desing,” PLOS Pathogens, vol. 8, no. 11, Article ID e1003001, 2012.
- V. G. Delvecchio, T. Alefantis, R. A. Ugalde et al., “Identification of protein candidates for developing bacterial ghost vaccines against Brucella,” Methods of Biochemical Analysis, vol. 49, pp. 363–377, 2006.
- J. Cassataro, S. M. Estein, K. A. Pasquevich et al., “Vaccination with the recombinant Brucella outer membrane protein 31 or a derived 27-amino-acid synthetic peptide elicits a CD4+ T helper 1 response that protects against Brucella melitensis infection,” Infection and Immunity, vol. 73, no. 12, pp. 8079–8088, 2005.
- M. D. Edmonds, A. Cloeckaert, and P. H. Elzer, “Brucella species lacking the major outer membrane protein Omp25 are attenuated in mice and protect against Brucella melitensis and Brucella ovis,” Veterinary Microbiology, vol. 88, no. 3, pp. 205–221, 2002.
- D. Goel and R. Bhatnagar, “Intradermal immunization with outer membrane protein 25 protects Balb/c mice from virulent B. abortus 544,” Molecular Immunology, vol. 51, no. 2, pp. 159–168, 2012.
- M. V. Delpino, S. M. Estein, C. A. Fossati, P. C. Baldi, and J. Cassataro, “Vaccination with Brucella recombinant DnaK and SurA proteins induces protection against Brucella abortus infection in BALB/c mice,” Vaccine, vol. 25, no. 37-38, pp. 6721–6729, 2007.
- J. Cassataro, K. A. Pasquevich, S. M. Estein et al., “A recombinant subunit vaccine based on the insertion of 27 amino acids from Omp31 to the N-terminus of BLS induced a similar degree of protection against B. ovis than Rev.1 vaccination,” Vaccine, vol. 25, no. 22, pp. 4437–4446, 2007.
- A. Al-Mariri, A. Tibor, P. Mertens et al., “Protection of BALB/c mice against Brucella abortus 544 challenge by vaccination with bacterioferritin or P39 recombinant proteins with CpG oligodeoxynucleotides as adjuvant,” Infection and Immunity, vol. 69, no. 8, pp. 4816–4822, 2001.
- P. Kaushik, D. K. Singh, S. V. Kumar et al., “Protection of mice against Brucella abortus 544 challenge by vaccination with recombinant OMP28 adjuvanted with CpG oligonucleotides,” Veterinary Research Communications, vol. 34, no. 2, pp. 119–132, 2010.
- V. K. Gupta, G. Radhakrishnan, J. Harms, and G. Splitter, “Invasive Escherichia coli vaccines expressing Brucella melitensis outer membrane proteins 31 or 16 or periplasmic protein BP26 confer protection in mice challenged with B. melitensis,” Vaccine, vol. 30, no. 27, pp. 4017–4022, 2012.
- D. Sáez, P. Fernández, A. Rivera, E. Andrews, and A. Oñate, “Oral immunization of mice with recombinant Lactococcus lactis expressing Cu, Zn superoxide dismutase of Brucella abortus triggers protective immunity,” Vaccine, vol. 30, no. 7, pp. 1283–1290, 2012.
- A. A. Oñate, G. Donoso, G. Moraga-Cid, H. Folch, S. Céspedes, and E. Andrews, “An RNA vaccine based on recombinant Semliki Forest virus particles expressing the Cu,Zn superoxide dismutase protein of Brucella abortus induces protective immunity in BALB/c mice,” Infection and Immunity, vol. 73, no. 6, pp. 3294–3300, 2005.
- S. Baloglu, S. M. Boyle, R. Vemulapalli, N. Sriranganathan, G. G. Schurig, and T. E. Toth, “Immune responses of mice to vaccinia virus recombinants expressing either Listeria monocytogenes partial listeriolysin or Brucella abortus ribosomal L7/L12 protein,” Veterinary Microbiology, vol. 109, no. 1-2, pp. 11–17, 2005.
- J. Cassataro, C. A. Velikovsky, S. de La Barrera et al., “A DNA vaccine coding for the Brucella outer membrane protein 31 confers protection against B. melitensis and B. ovis infection by eliciting a specific cytotoxic response,” Infection and Immunity, vol. 73, no. 10, pp. 6537–6546, 2005.
- C. A. Velikovsky, J. Cassataro, G. H. Giambartolomei et al., “A DNA vaccine encoding lumazine synthase from Brucella abortus induces protective immunity in BALB/c mice,” Infection and Immunity, vol. 70, no. 5, pp. 2507–2511, 2002.
- D. Luo, B. Ni, P. Li et al., “Protective immunity elicited by a divalent DNA vaccine encoding both the L7/L12 and Omp16 genes of Brucella abortus in BALB/c mice,” Infection and Immunity, vol. 74, no. 5, pp. 2734–2741, 2006.
- D. Y. Luo, P. Li, L. Xing et al., “DNA vaccine encoding L7/L12-P39 of Brucella abortus induces protective immunity in BALB/c mice,” Chinese Medical Journal, vol. 119, no. 4, pp. 331–334, 2006.
- D. H. Yu, M. Li, X. D. Hu, and H. Cai, “A combined DNA vaccine enhances protective immunity against Mycobacterium tuberculosis and Brucella abortus in the presence of an IL-12 expression vector,” Vaccine, vol. 25, no. 37-38, pp. 6744–6754, 2007.
- A. González-Smith, R. Vemulapalli, E. Andrews, and A. Oñate, “Evaluation of Brucella abortus DNA vaccine by expression of Cu-Zn superoxide dismutase antigen fused to IL-2,” Immunobiology, vol. 211, no. 1-2, pp. 65–74, 2006.
- H. Singha, A. I. Mallick, C. Jana et al., “Escheriosomes entrapped DNA vaccine co-expressing Cu-Zn superoxide dismutase and IL-18 confers protection against Brucella abortus,” Microbes and Infection, vol. 10, no. 10-11, pp. 1089–1096, 2008.
- X. D. Hu, S. T. Chen, J. Y. Li, D. H. Yu, Yi-zhang, and H. Cai, “An IL-15 adjuvant enhances the efficacy of a combined DNA vaccine against Brucella by increasing the CD8+ cytotoxic T cell response,” Vaccine, vol. 28, no. 12, pp. 2408–2415, 2010.
- D. H. Yu, X. D. Hu, and H. Cai, “A combined DNA vaccine encoding BCSP31, SOD, and L7/L12 confers high protection against Brucella abortus 2308 by inducing specific CTL responses,” DNA and Cell Biology, vol. 26, no. 6, pp. 435–443, 2007.
- A. Amano, H. Takeuchi, and N. Furuta, “Outer membrane vesicles function as offensive weapons in host-parasite interactions,” Microbes and Infection, vol. 12, no. 11, pp. 791–798, 2010.
- T. J. Beveridge, “Structures of gram-negative cell walls and their derived membrane vesicles,” Journal of Bacteriology, vol. 181, no. 16, pp. 4725–4733, 1999.
- T. N. Ellis and M. J. Kuehn, “Virulence and immunomodulatory roles of bacterial outer membrane vesicles,” Microbiology and Molecular Biology Reviews, vol. 74, no. 1, pp. 81–94, 2010.
- M. J. Kuehn and N. C. Kesty, “Bacterial outer membrane vesicles and the host-pathogen interaction,” Genes and Development, vol. 19, no. 22, pp. 2645–2655, 2005.
- L. M. Mashburn-Warren and M. Whiteley, “Special delivery: vesicle trafficking in prokaryotes,” Molecular Microbiology, vol. 61, no. 4, pp. 839–846, 2006.
- C. M. Unal, V. Schaar, and K. Riesbeck, “Bacterial outer membrane vesicles in disease and preventive medicine,” Seminars in Immunopathology, vol. 33, no. 5, pp. 395–408, 2011.
- R. A. Boigegrain, I. Salhi, M. T. Alvarez-Martinez et al., “Release of periplasmic proteins of Brucella suis upon acidic shock involves the outer membrane protein Omp25,” Infection and Immunity, vol. 72, no. 10, pp. 5693–5703, 2004.
- C. Gamazo, A. J. Winter, I. Moriyon, J. I. Riezu-Boj, J. M. Blasco, and R. Diaz, “Comparative analyses of proteins extracted by hot saline or released spontaneously into outer membrane blebs from field strains of Brucella ovis and Brucella melitensis,” Infection and Immunity, vol. 57, no. 5, pp. 1419–1426, 1989.
- E. D. Avila-Calderón, A. Lopez-Merino, N. Jain, et al., “Characterization of outer membrane vesicles from Brucella melitensis and protection induced in mice,” Clinical and Developmental Immunology, vol. 2012, Article ID 352493, 2012.
- N. Jain-Gupta, A. Contreras-Rodriguez, R. Vemulapalli, et al., “Pluronic P85 enhances the efficacy of outer membrane vesicles as a subunit vaccine against Brucella melitensis challenge in mice,” FEMS Immunology and Medical Microbiology, vol. 66, no. 3, pp. 436–444, 2012.
- C. N. Pollak, M. V. Delpino, C. A. Fossati, and P. C. Baldi, “Outer membrane vesicles from Brucella abortus promote bacterial internalization by human monocytes and modulate their innate immune response,” PLoS One, vol. 7, no. 11, Article ID e50214, 2012.