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1 , V. parahaemolyticus, V. vulnificus, and V. mimicus).
2 , V. parahaemolyticus, V. vulnificus, and V. mimicus.
3 erae and the heat-labile hemolysin of Vibrio mimicus.
4 0 strains), V. metschnikovii (9 strains), V. mimicus (10 strains), V. parahaemolyticus (30 strains),
5 othesis that, in the course of evolution, V. mimicus and V. cholerae diverged from a common ancestor
9 integrated at different sites within the V. mimicus genome whereas V. mimicus strains PT48, 523-80,
18 uences of VPIPhi genes aldA and toxT from V. mimicus strain PT5 and V. cholerae N16961 were identical
19 quences of CTXPhi genes orfU and zot from V. mimicus strain PT5 and V. cholerae strain N16961 were id
21 ites within the V. mimicus genome whereas V. mimicus strains PT48, 523-80, and 9583 each contain tand
22 including some not previously reported in V. mimicus, such as mannose-sensitive hemagglutinin (MSHA),
24 man intestinal pathogenic Vibrio species, V. mimicus, V. fluvialis, and V. parahaemolyticus, display
25 , with probabilities averaging 10%, while V. mimicus was a major problem with the Crystal E/NF, which
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