Cholera is an ancient disease in the midst of a modern resurgence, with cases reported to WHO by 65 member nations in Asia, Africa, the Americas, and Europe in 1997. With the appearance of V. cholerae 0139 Bengal and the recent identification of epidemic-associated 037 strains, there is increasing recognition that modifications in bacterial surface polysaccharides play a key role in the emergence of new, epidemic-associated strains. While the number of constituent sugars appears to be relatively small (less than 25), there are hundreds of O antigen/capsule types recognized among V. cholerae and other Vibrionaceae strains. Initial phylogenetic studies suggest that serotype and/or capsule type are independent of phylogeny. We hypothesize that there is frequent horizontal/sexual transfer and rearrangement of surface polysaccharide biosynthetic gene cassettes in V. cholerae, providing an opportunity for periodic emergence of new, pandemic cholera strains. Making use of our collection of Vibrionaceae (including the Smith Vibrio Reference Laboratory/serotype collection) and ongoing strain acquisition, we propose: 1) To describe and define the genetic relatedness of a 192-strain V. cholerae test collection, utilizing sequence analysis of conserved genetic elements (multilocus sequence typing) including genes used in multilocus enzyme electrophoresis/zymovar analysis. 2) To identify and characterize V. cholerae O antigen and capsular polysaccharides for stains within this collection, as a basis for assessing horizontal transfer of surface polysaccharide genes. This will include a) determination of sugar composition of O-antigen side chain and capsule; and b) identification and correlation of sugars with specific biosynthetic genes/gene combinations. 3) To assess the extent of genetic variability in surface polysaccharides plausibly available to V. cholerae, and, in particular, to V. cholerae strains with pandemic potential. For these latter studies we will a) correlate genetic relatedness (as determined above) with transfer/acceptance of specific polysaccharide genes; b) determine the placement and organization of biosynthesis genes for the sugars of the O side chain and capsule; and c) assess the nucleotide sequence divergence of the most commonly identified polysaccharide biosynthesis genes. Taken together, these studies will substantively expand our understanding of the evolutionary biology of V. cholerae, giving us a much better appreciation of the potential for changes in V. cholerae surface polysaccharides and, in turn, for the emergence of V. cholerae strains which can form the basis for new cholera pandemics.
|Aydanian, Antonina; Tang, Li; Morris, J Glenn et al. (2011) Genetic diversity of O-antigen biosynthesis regions in Vibrio cholerae. Appl Environ Microbiol 77:2247-53
|Chen, Yuansha; Bystricky, Peter; Adeyeye, Jacob et al. (2007) The capsule polysaccharide structure and biogenesis for non-O1 Vibrio cholerae NRT36S: genes are embedded in the LPS region. BMC Microbiol 7:20
|Ali, Afsar; Morris Jr, J Glenn; Johnson, Judith A (2005) Sugars inhibit expression of the rugose phenotype of Vibrio cholerae. J Clin Microbiol 43:1426-9
|Chowdhury, Nandini Roy; Stine, O Colin; Morris, J Glenn et al. (2004) Assessment of evolution of pandemic Vibrio parahaemolyticus by multilocus sequence typing. J Clin Microbiol 42:1280-2
|Morris Jr, J Glenn (2003) Cholera and other types of vibriosis: a story of human pandemics and oysters on the half shell. Clin Infect Dis 37:272-80
|Kotetishvili, Mamuka; Stine, O Colin; Chen, Yuansha et al. (2003) Multilocus sequence typing has better discriminatory ability for typing Vibrio cholerae than does pulsed-field gel electrophoresis and provides a measure of phylogenetic relatedness. J Clin Microbiol 41:2191-6
|Li, Manrong; Shimada, Toshio; Morris Jr, J Glenn et al. (2002) Evidence for the emergence of non-O1 and non-O139 Vibrio cholerae strains with pathogenic potential by exchange of O-antigen biosynthesis regions. Infect Immun 70:2441-53