Introduction:
Cholera is a major health issue, affecting millions of lives annually. In light of the recurrent outbreaks of cholera, there is a pressing need for the development of vaccines that allow rapid mass vaccination.
Objectives:
In this study, genetically modified vaccine candidates, VCUSM21P and VCUSM22P, were designed. VCUSM2lP is a prototrophic vaccine which encodes non-toxic cholera toxin A (ctxA) subunit immunogen and has accessory cholera enterotoxin (ace), zonula occludens toxin (zot), and repeats-in-toxin CIA (rtxC/A) mutations. On the other hand, VCUSM22P is ace, zot, ctxA, rtxCIA, and hemagglutinin/protease (hap) mutant. Both mutants were found not to disassemble the actin of HEp2 cells.
Methods:
Mouse colonisation assay was used to determine VCUSM21P and VCUSM22P colonization ability in-vivo. Rabbit ileal loop assay was performed to evaluate the reactogenicity caused by them. The immune responses provoked by the 2 vaccine candidates and their protective function against cholera were evaluated in a rabbit model. The mutants were found to be good colonizer of the mouse intestine. In the ileal loop assay using non-immunised rabbits, fluid accumulation was found in loops injected with 1 × l06 and 1 × l08 colony forming unit (CFU) of wild Type (WT) V. cholerae. Unlike the WT V. cholerae challenge, 1 × l06 and 1 × CFU of the mutants did not cause any reactogenicity in-non immunised rabbits. Immunisation using 1 × l010 CFU of the mutants induced both IgA and IgG antibodies production against cholera toxin (CT) and 139 lipopolysaccharides (LPS), as well as elevated vibriocidal antibody.
Result:
The reactogenicity caused by the WT V. cholerae in rabbits immunised with 1 × 1010 CFU of the mutants was found to be reduced as evidenced by the absence of fluid in loops administered with 1 × l02 - 1 × l07 CFU of WT V. cholerae. In the Removable Intestinal Tie Adult Rabbit Diarrhoea (RIT ARD) experiment, the non-immunised rabbits were found unprotected against a lethal challenge with 1 × 109 CFU WT V. cholerae. However, 100% of rabbits immunised with the mutants survived the WT V. cholerae challenge.
Conclusion:
Immunohistochemical, histopathological, and ultrastructural examination of non-immunised rabbit’s ileum challenged with WT V. cholerae revealed severe ileal damages. But less severe damages were noted following the WT V. cholerae challenge in the ileum of rabbits immunized with VCUSM21P and VCUSM22P. The multigene mutants could be used for vaccination against potentially fatal V. cholerae 0139.
Footnotes
Supervisors:
Prof Dr Lalitha P
Co-supervisor:
Dr Shyamoli Mustafa
