Susceptibility of Vibrio cholerae O139 to Antibody-Dependent, Complement-Mediated Bacteriolysis
Open Access
- 1 May 2000
- journal article
- research article
- Published by American Society for Microbiology in Clinical and Diagnostic Laboratory Immunology
- Vol. 7 (3) , 444-450
- https://doi.org/10.1128/cdli.7.3.444-450.2000
Abstract
Volunteer studies with Vibrio cholerae O1 have shown that the best correlate of a vaccine's protective efficacy is its propensity to elicit serum bactericidal responses in its recipients. Attempts to detect such responses following infection with V. cholerae O139, however, have met with varying success. Using a tube-based assay which involves viable counting, we now report that strains of serogroup O139 can appear to be sensitive or resistant to a fixed concentration of complement in the presence of antibody, depending on assay conditions. Susceptibility to lysis is critically dependent on the availability of complement, but with O139 indicator strains this is not simply determined by the concentration of serum added to the reaction mix. The nature of the assay diluent and the concentration of indicator bacteria can also dramatically affect bactericidal end points, whereas such variables have minimal significance with O1 indicator bacteria. Although some laboratories use unencapsulated mutant strains to seek evidence of seroconversion following exposure to V. cholerae O139, this is not necessary, and our findings question the significance of capsule expression as a determinant of complement sensitivity when antibody is present. The medium used for growth of the indicator strain and the particular strain used appeared to be unimportant. Each of seven O139 isolates tested was found to be lysed by antibody and complement in our standard assay system, which allowed the detection of significant serum bactericidal responses in 9 of 11 cases of O139 disease.Keywords
This publication has 14 references indexed in Scilit:
- Intestinal and systemic immune responses in humans after oral immunization with a bivalent B subunit-O1/O139 whole cell cholera vaccineVaccine, 1996
- Genetic rearrangements in the rfb regions of Vibrio cholerae O1 and O139.Proceedings of the National Academy of Sciences, 1995
- Initial Clinical Studies of CVD 112 Vibrio cholerae O139 Live Oral Vaccine: Safety and Efficacy against Experimental ChallengeThe Journal of Infectious Diseases, 1995
- Safety, immunogenicity, and efficacy of live attenuated Vibrio cholerae 0139 vaccine prototypeThe Lancet, 1995
- The Vibrio cholerae O139 serogroup antigen includes an O-antigen capsule and lipopolysaccharide virulence determinants.Proceedings of the National Academy of Sciences, 1994
- Spread of Vibrio cholerae 0139 Bengal in IndiaThe Journal of Infectious Diseases, 1994
- The role of toxin-coregulated pili in the pathogenesis of Vibrio cholerae O1 El TorMicrobial Pathogenesis, 1993
- In vitro production of toxin-coregulated pili by Vibrio cholerae El TorMicrobial Pathogenesis, 1993
- Large epidemic of cholera-like disease in Bangladesh caused by Vibrio cholerae 0139 synonym BengalThe Lancet, 1993
- Surface co-expression of Vibrio cholerae and Salmonella typhi O-antigens on Ty21a clone EX210Microbial Pathogenesis, 1990