Abstract
Brucellosis research is currently focused on the identification of nonlipopolysaccharide (LPS) antigens which could potentially be useful for the specific serologic diagnosis of brucellosis as well as for vaccinal prophylaxis. On the basis of previous reports, we selected eight Brucella proteins (OMP36, OMP25, OMP19, OMP16, OMP10, p17, p15, and p39) as candidate antigens to be further evaluated. The genes encoding these proteins were cloned, sequenced, and overexpressed in Escherichia coli. The recombinant proteins were purified with a polyhistidine tag and metal chelate affinity chromatography and evaluated in an indirect enzyme-linked immunosorbent assay (iELISA). The specificity of the iELISA was determined with sera from healthy cattle, sheep, and goats and ranged from 95 to 99%, depending on the recombinant antigen and the species tested. Sera from experimentally infected, and from naturally infected, animals were used to evaluate the sensitivity of the iELISA. The antiprotein antibody response was often delayed when compared to the anti-smooth LPS (S-LPS) response and was limited to animals which developed an active brucellosis infection (experimentally infected pregnant animals and sheep and goats from areas where brucellosis is still endemic). Among the recombinant antigens, the three cytoplasmic proteins (p17, p15, and p39) gave the most useful results. More than 80% of the animals positive in S-LPS serology were also positive with one of these cytoplasmic proteins alone or a combination of two of them. None of the recombinant antigens detected experimentally infected nonpregnant cows and sheep or naturally infected cattle. This study is a first step towards the development of a multiprotein diagnostic reagent for brucellosis.
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- Ala'Aldeen D. A., Stevenson P., Griffiths E., Gorringe A. R., Irons L. I., Robinson A., Hyde S., Borriello S. P. Immune responses in humans and animals to meningococcal transferrin-binding proteins: implications for vaccine design. Infect Immun. 1994 Jul;62(7):2984–2990. doi: 10.1128/iai.62.7.2984-2990.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Baldi P. C., Giambartolomei G. H., Goldbaum F. A., Abdón L. F., Velikovsky C. A., Kittelberger R., Fossati C. A. Humoral immune response against lipopolysaccharide and cytoplasmic proteins of Brucella abortus in cattle vaccinated with B. abortus S19 or experimentally infected with Yersinia enterocolitica serotype 0:9. Clin Diagn Lab Immunol. 1996 Jul;3(4):472–476. doi: 10.1128/cdli.3.4.472-476.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Blasco J. M., Marín C., Jiménez de Bagués M., Barberán M., Hernández A., Molina L., Velasco J., Díaz R., Moriyón I. Evaluation of allergic and serological tests for diagnosing Brucella melitensis infection in sheep. J Clin Microbiol. 1994 Aug;32(8):1835–1840. doi: 10.1128/jcm.32.8.1835-1840.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cloeckaert A., Jacques I., Bosseray N., Limet J. N., Bowden R., Dubray G., Plommet M. Protection conferred on mice by monoclonal antibodies directed against outer-membrane-protein antigens of Brucella. J Med Microbiol. 1991 Mar;34(3):175–180. doi: 10.1099/00222615-34-3-175. [DOI] [PubMed] [Google Scholar]
- Cloeckaert A., Kerkhofs P., Limet J. N. Antibody response to Brucella outer membrane proteins in bovine brucellosis: immunoblot analysis and competitive enzyme-linked immunosorbent assay using monoclonal antibodies. J Clin Microbiol. 1992 Dec;30(12):3168–3174. doi: 10.1128/jcm.30.12.3168-3174.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cloeckaert A., Verger J. M., Grayon M., Zygmunt M. S., Grépinet O. Nucleotide sequence and expression of the gene encoding the major 25-kilodalton outer membrane protein of Brucella ovis: Evidence for antigenic shift, compared with other Brucella species, due to a deletion in the gene. Infect Immun. 1996 Jun;64(6):2047–2055. doi: 10.1128/iai.64.6.2047-2055.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cloeckaert A., Zygmunt M. S., de Wergifosse P., Dubray G., Limet J. N. Demonstration of peptidoglycan-associated Brucella outer-membrane proteins by use of monoclonal antibodies. J Gen Microbiol. 1992 Jul;138(7):1543–1550. doi: 10.1099/00221287-138-7-1543. [DOI] [PubMed] [Google Scholar]
- Cloeckaert A., de Wergifosse P., Dubray G., Limet J. N. Identification of seven surface-exposed Brucella outer membrane proteins by use of monoclonal antibodies: immunogold labeling for electron microscopy and enzyme-linked immunosorbent assay. Infect Immun. 1990 Dec;58(12):3980–3987. doi: 10.1128/iai.58.12.3980-3987.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Denoel P. A., Vo T. K., Tibor A., Weynants V. E., Trunde J. M., Dubray G., Limet J. N., Letesson J. J. Characterization, occurrence, and molecular cloning of a 39-kilodalton Brucella abortus cytoplasmic protein immunodominant in cattle. Infect Immun. 1997 Feb;65(2):495–502. doi: 10.1128/iai.65.2.495-502.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Denoel P. A., Zygmunt M. S., Weynants V., Tibor A., Lichtfouse B., Briffeuil P., Limet J. N., Letesson J. J. Cloning and sequencing of the bacterioferritin gene of Brucella melitensis 16M strain. FEBS Lett. 1995 Mar 20;361(2-3):238–242. doi: 10.1016/0014-5793(95)00189-g. [DOI] [PubMed] [Google Scholar]
- Ficht T. A., Bearden S. W., Sowa B. A., Adams L. G. DNA sequence and expression of the 36-kilodalton outer membrane protein gene of Brucella abortus. Infect Immun. 1989 Nov;57(11):3281–3291. doi: 10.1128/iai.57.11.3281-3291.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gilot P., De Kesel M., Machtelinckx L., Coene M., Cocito C. Isolation and sequencing of the gene coding for an antigenic 34-kilodalton protein of Mycobacterium paratuberculosis. J Bacteriol. 1993 Aug;175(15):4930–4935. doi: 10.1128/jb.175.15.4930-4935.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goldbaum F. A., Leoni J., Wallach J. C., Fossati C. A. Characterization of an 18-kilodalton Brucella cytoplasmic protein which appears to be a serological marker of active infection of both human and bovine brucellosis. J Clin Microbiol. 1993 Aug;31(8):2141–2145. doi: 10.1128/jcm.31.8.2141-2145.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goldbaum F. A., Rubbi C. P., Wallach J. C., Miguel S. E., Baldi P. C., Fossati C. A. Differentiation between active and inactive human brucellosis by measuring antiprotein humoral immune responses. J Clin Microbiol. 1992 Mar;30(3):604–607. doi: 10.1128/jcm.30.3.604-607.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gorrell M. D., Milliken G. L., Anderson B. J., Pucci A. An enzyme immunoassay for bovine brucellosis using a monoclonal antibody specific for field strains of Brucella abortus. Dev Biol Stand. 1984;56:491–494. [PubMed] [Google Scholar]
- Gottesman S., Gottesman M., Shaw J. E., Pearson M. L. Protein degradation in E. coli: the lon mutation and bacteriophage lambda N and cII protein stability. Cell. 1981 Apr;24(1):225–233. doi: 10.1016/0092-8674(81)90518-3. [DOI] [PubMed] [Google Scholar]
- Gómez-Miguel M. J., Moriyón I., Alonso-Urmeneta B., Riezu-Boj J. I., Díaz R. Serological response to the outer membrane lipoprotein in animal brucellosis. Infect Immun. 1988 Mar;56(3):716–718. doi: 10.1128/iai.56.3.716-718.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hemmen F., Weynants V., Scarcez T., Letesson J. J., Saman E. Cloning and sequence analysis of a newly identified Brucella abortus gene and serological evaluation of the 17-kilodalton antigen that it encodes. Clin Diagn Lab Immunol. 1995 May;2(3):263–267. doi: 10.1128/cdli.2.3.263-267.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kittelberger R., Hilbink F., Hansen M. F., Penrose M., de Lisle G. W., Letesson J. J., Garin-Bastuji B., Searson J., Fossati C. A., Cloeckaert A. Serological crossreactivity between Brucella abortus and Yersinia enterocolitica 0:9 I immunoblot analysis of the antibody response to Brucella protein antigens in bovine brucellosis. Vet Microbiol. 1995 Dec;47(3-4):257–270. doi: 10.1016/0378-1135(95)00122-0. [DOI] [PubMed] [Google Scholar]
- Limet J. N., Cloeckaert A., Bezard G., Van Broeck J., Dubray G. Antibody response to the 89-kDa outer membrane protein of Brucella in bovine brucellosis. J Med Microbiol. 1993 Dec;39(6):403–407. doi: 10.1099/00222615-39-6-403. [DOI] [PubMed] [Google Scholar]
- Lindler L. E., Hadfield T. L., Tall B. D., Snellings N. J., Rubin F. A., Van De Verg L. L., Hoover D., Warren R. L. Cloning of a Brucella melitensis group 3 antigen gene encoding Omp28, a protein recognized by the humoral immune response during human brucellosis. Infect Immun. 1996 Jul;64(7):2490–2499. doi: 10.1128/iai.64.7.2490-2499.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rossetti O. L., Arese A. I., Boschiroli M. L., Cravero S. L. Cloning of Brucella abortus gene and characterization of expressed 26-kilodalton periplasmic protein: potential use for diagnosis. J Clin Microbiol. 1996 Jan;34(1):165–169. doi: 10.1128/jcm.34.1.165-169.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tabatabai L. B., Hennager S. G. Cattle serologically positive for Brucella abortus have antibodies to B. abortus Cu-Zn superoxide dismutase. Clin Diagn Lab Immunol. 1994 Sep;1(5):506–510. doi: 10.1128/cdli.1.5.506-510.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tibor A., Saman E., de Wergifosse P., Cloeckaert A., Limet J. N., Letesson J. J. Molecular characterization, occurrence, and immunogenicity in infected sheep and cattle of two minor outer membrane proteins of Brucella abortus. Infect Immun. 1996 Jan;64(1):100–107. doi: 10.1128/iai.64.1.100-107.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tibor A., Weynants V., Denoel P., Lichtfouse B., De Bolle X., Saman E., Limet J. N., Letesson J. J. Molecular cloning, nucleotide sequence, and occurrence of a 16.5-kilodalton outer membrane protein of Brucella abortus with similarity to pal lipoproteins. Infect Immun. 1994 Sep;62(9):3633–3639. doi: 10.1128/iai.62.9.3633-3639.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weynants V., Gilson D., Cloeckaert A., Denoel P. A., Tibor A., Thiange P., Limet J. N., Letesson J. J. Characterization of a monoclonal antibody specific for Brucella smooth lipopolysaccharide and development of a competitive enzyme-linked immunosorbent assay to improve the serological diagnosis of brucellosis. Clin Diagn Lab Immunol. 1996 May;3(3):309–314. doi: 10.1128/cdli.3.3.309-314.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weynants V., Tibor A., Denoel P. A., Saegerman C., Godfroid J., Thiange P., Letesson J. J. Infection of cattle with Yersinia enterocolitica O:9 a cause of the false positive serological reactions in bovine brucellosis diagnostic tests. Vet Microbiol. 1996 Jan;48(1-2):101–112. doi: 10.1016/0378-1135(95)00153-0. [DOI] [PubMed] [Google Scholar]
- Zygmunt M. S., Cloeckaert A., Dubray G. Brucella melitensis cell envelope protein and lipopolysaccharide epitopes involved in humoral immune responses of naturally and experimentally infected sheep. J Clin Microbiol. 1994 Oct;32(10):2514–2522. doi: 10.1128/jcm.32.10.2514-2522.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zygmunt M. S., Gilbert F. B., Dubray G. Purification, characterization, and seroactivity of a 20-kilodalton Brucella protein antigen. J Clin Microbiol. 1992 Oct;30(10):2662–2667. doi: 10.1128/jcm.30.10.2662-2667.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zygmunt M. S., Martin J. C., Dubray G. Analysis of immune response: comparison of immunoblots after isoelectric focusing and sodium dodecyl sulfate-polyacrylamide gel electrophoresis using cytoplasmic protein extract from Brucella. FEMS Microbiol Lett. 1990 Aug;58(3):263–268. doi: 10.1111/j.1574-6968.1990.tb13986.x. [DOI] [PubMed] [Google Scholar]
- de Wergifosse P., Lintermans P., Limet J. N., Cloeckaert A. Cloning and nucleotide sequence of the gene coding for the major 25-kilodalton outer membrane protein of Brucella abortus. J Bacteriol. 1995 Apr;177(7):1911–1914. doi: 10.1128/jb.177.7.1911-1914.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- van Gelder P., Bosman F., de Meuter F., van Heuverswyn H., Hérion P. Serodiagnosis of toxoplasmosis by using a recombinant form of the 54-kilodalton rhoptry antigen expressed in Escherichia coli. J Clin Microbiol. 1993 Jan;31(1):9–15. doi: 10.1128/jcm.31.1.9-15.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]