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PMID: 7251134 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Ability of an avirulent mutant of Vibrio cholerae to colonize in the infant mouse upper bowel.

Infection and immunity ·Vol. 32 ·No. 2 ·1981-05-00 ·Pages 474-9

Sigel SP, Finkelstein RA, Parker CD

Abstract

Vibrio cholerae strain 3083 (biotype El Tor, serotype Ogawa) and Texas Star-SR (SR), a mutant derived from 3083 that produces the B (binding) but not the A (toxic) subunit of choleragen, were compared in their abilities to: (i) associate with the infant mouse upper bowel; (ii) survive and multiple there; and (iii) induce diarrhea. Vibrios labeled with 35SO4 were used to determine association with the upper bowel and ability to multiply. The parental strain associated significantly better than SR, although viable mutant cells were found in the infant mouse intestine 16 to 18 h after challenge. Addition of exogenous toxin enhanced the rate at which labeled SR (but not 3083) was cleared, further suggesting that SR associates less well with the upper bowel. Both SR and 3083 multiplied in the upper bowel but, due perhaps to slight net killing during the first 3 h and its more rapid rate of clearance, SR achieved a population size only 10% that of 3083 by 8 h postchallenge. Strain 3083 elicited diarrhea in infant mice but SR did not, even after 10 successive passages through the infant mouse intestine. Strain SR was slightly temperature sensitive at 37 and 40 degrees C. Its potential use as a live vaccine is discussed.

MeSH Terms
Animals Cholera Toxin/pharmacology Diarrhea/etiology Intestine, Large/microbiology Kinetics Mice Mutation Temperature Vibrio cholerae/growth & development,pathogenicity
Chemicals
Cholera Toxin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Sigel S P
Finkelstein R A
Parker C D
References (12)
12 references, click to expand
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Article Info
Journal
Infection and immunity
Abbr.
Infect Immun
ISSN
0019-9567
Published
1981-05-00
Pages
474-9
Language
English
Region
United States
NLM ID
0246127
PMCID
PMC351469
Subset
IM
Grants
NIAID NIH HHS · AI-08877 · United States
NIAID NIH HHS · AI-12819 · United States
NIAID NIH HHS · AI-17312 · United States
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