IEM101, a naturally attenuated Vibrio cholerae strain as carrier for genetically detoxified derivatives of cholera toxin

Citation
Mr. Fontana et al., IEM101, a naturally attenuated Vibrio cholerae strain as carrier for genetically detoxified derivatives of cholera toxin, VACCINE, 19(1), 2000, pp. 75-85
Citations number
49
Categorie Soggetti
Veterinary Medicine/Animal Health",Immunology
Journal title
VACCINE
ISSN journal
0264410X → ACNP
Volume
19
Issue
1
Year of publication
2000
Pages
75 - 85
Database
ISI
SICI code
0264-410X(20000815)19:1<75:IANAVC>2.0.ZU;2-J
Abstract
Two mutants of cholera toxin (CTS106 containing a Pro106 --> Ser substituti on and CTK63 containing a Ser63 --> Lys substitution) with greatly reduced or no toxicity respectively, were expressed in the naturally attenuated IEM 101 Vibrio cholerae strain (El Tor, Ogawa) which does not express cholera t oxin (CT). Expression was driven by the natural promoter of CT, or by a pro motor known to induce strong in vivo expression such as nirB. In the rabbit ileal loop assay, where 10(4) wild type bacteria were sufficient to induce fluid accumulation, 10(9) IEM101 expressing CTS106 bacteria were needed to induce some fluid accumulation, while IEM101 expressing CTK63 was inactive , even when 10(10) cells were used. When used to immunize mice intranasally , all bacteria induced vibriocidal antibodies; however, anti-CT antibodies were not induced by bacteria expressing low levels of CTK63 under the contr ol of the ct promoter. Anti-CT antibodies were successfully induced by bact eria expressing high levels of CTK63 under the control of the nirB promoter , or by bacteria expressing low levels of CTS106. These data show that anti bodies against cholera toxin can be induced in vivo by high level expressio n of a non toxic mutant, or by using a mutant with residual ADP-ribosyltran sferase activity. In conclusion, we have shown that IEM101. a naturally attenuated known stra in known to be safe and immunogenic in humans, can be engineered to express immunogenic levels of CTK63, and may represent a good candidate for vaccin ation against cholera, (C) 2000 Elsevier Science Ltd. All rights reserved.