Vibrio vulnificus rtxA1 gene recombination generates toxin variants with altered potency during intestinal infection

Jayme S. Kwak, Hee Gon Jeong, Karla J. F. Satchell

Research output: Contribution to journalArticle

63 Scopus citations

Abstract

Vibrio vulnificus is a food-borne bacterial pathogen associated with 1% of all food-related deaths, predominantly because of consumption of contaminated seafood. The ability of V. vulnificus to cause disease is linked to the production of a large cytotoxin called the "multifunctional-autoprocessing RTX" (MARTXVv) toxin, a factor shown here to be an important virulence factor by the intragastric route of infection in mice. In this study, we examined genetic variation of the rtxA1 gene that encodes MARTXVv in 40 V. vulnificus Biotype 1 strains and found four distinct variants of rtxA1 that encode toxins with different arrangements of effector domains. We provide evidence that these variants arose by recombination either with rtxA genes carried on plasmids or with the rtxA gene of Vibrio anguillarum. Contrary to expected results, the most common rtxA1 gene variant in clinical-type V. vulnificus encodes a toxin with reduced potency and is distinct from the toxin produced by strains isolated from market oysters. These results indicate that an important virulence factor of V. vulnificus is undergoing significant genetic rearrangement and may be subject to selection for reduced virulence in the environment. This finding would imply further that in the future on-going genetic variation of the MARTXVv toxins could result in the emergence of novel strains with altered virulence in humans.

Original languageEnglish (US)
Pages (from-to)1645-1650
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume108
Issue number4
DOIs
StatePublished - Jan 25 2011

Keywords

  • Oyster
  • Phylogeny
  • RTX

ASJC Scopus subject areas

  • General

Fingerprint Dive into the research topics of 'Vibrio vulnificus rtxA1 gene recombination generates toxin variants with altered potency during intestinal infection'. Together they form a unique fingerprint.

  • Cite this