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Evaluation of Brucella Abortus Phosphoglucomutase (pgm) Mutant As a New Live Rough-phenotype Vaccine

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Journal Infect Immun
Date 2003 Oct 24
PMID 14573645
Citations 36
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Abstract

Brucella abortus S19 is the vaccine most frequently used against bovine brucellosis. Although it induces good protection levels, it cannot be administered to pregnant cattle, revaccination is not advised due to interference in the discrimination between infected and vaccinated animals during immune-screening procedures, and the vaccine is virulent for humans. Due to these reasons, there is a continuous search for new bovine vaccine candidates that may confer protection levels comparable to those conferred by S19 but without its disadvantages. A previous study characterized the phenotype associated with the phosphoglucomutase (pgm) gene disruption in Brucella abortus S2308, as well as the possible role for the smooth lipopolysaccharide (LPS) in virulence and intracellular multiplication in HeLa cells (J. E. Ugalde, C. Czibener, M. F. Feldman, and R. A. Ugalde, Infect. Immun. 68:5716-5723, 2000). In this report, we analyze the protection, proliferative response, and cytokine production induced in BALB/c mice by a deltapgm deletion strain. We show that this strain synthesizes O antigen with a size of approximately 45 kDa but is rough. This is due to the fact that the deltapgm strain is unable to assemble the O side chain in the complete LPS. Vaccination with the deltapgm strain induced protection levels comparable to those induced by S19 and generated a proliferative splenocyte response and a cytokine profile typical of a Th1 response. On the other hand, we were unable to detect a specific anti-O-antigen antibody response by using the fluorescence polarization assay. In view of these results, the possibility that the deltapgm mutant could be used as a vaccination strain is discussed.

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References
1.
Vemulapalli R, He Y, Buccolo L, Boyle S, Sriranganathan N, Schurig G . Complementation of Brucella abortus RB51 with a functional wboA gene results in O-antigen synthesis and enhanced vaccine efficacy but no change in rough phenotype and attenuation. Infect Immun. 2000; 68(7):3927-32. PMC: 101669. DOI: 10.1128/IAI.68.7.3927-3932.2000. View

2.
Forestier C, Moreno E, Pizarro-Cerda J, Gorvel J . Lysosomal accumulation and recycling of lipopolysaccharide to the cell surface of murine macrophages, an in vitro and in vivo study. J Immunol. 1999; 162(11):6784-91. View

3.
Ugalde J, Czibener C, Feldman M, Ugalde R . Identification and characterization of the Brucella abortus phosphoglucomutase gene: role of lipopolysaccharide in virulence and intracellular multiplication. Infect Immun. 2000; 68(10):5716-23. PMC: 101528. DOI: 10.1128/IAI.68.10.5716-5723.2000. View

4.
Briones G, Inon de Iannino N, Roset M, Vigliocco A, Paulo P, Ugalde R . Brucella abortus cyclic beta-1,2-glucan mutants have reduced virulence in mice and are defective in intracellular replication in HeLa cells. Infect Immun. 2001; 69(7):4528-35. PMC: 98529. DOI: 10.1128/IAI.69.7.4528-4535.2001. View

5.
Delvecchio V, Kapatral V, Redkar R, Patra G, Mujer C, Los T . The genome sequence of the facultative intracellular pathogen Brucella melitensis. Proc Natl Acad Sci U S A. 2002; 99(1):443-8. PMC: 117579. DOI: 10.1073/pnas.221575398. View