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Review
. 2013 Dec 11:3:97.
doi: 10.3389/fcimb.2013.00097. eCollection 2013.

Distribution and dynamics of epidemic and pandemic Vibrio parahaemolyticus virulence factors

Affiliations
Review

Distribution and dynamics of epidemic and pandemic Vibrio parahaemolyticus virulence factors

Daniela Ceccarelli et al. Front Cell Infect Microbiol. .

Abstract

Vibrio parahaemolyticus, autochthonous to estuarine, marine, and coastal environments throughout the world, is the causative agent of food-borne gastroenteritis. More than 80 serotypes have been described worldwide, based on antigenic properties of the somatic (O) and capsular (K) antigens. Serovar O3:K6 emerged in India in 1996 and subsequently was isolated worldwide, leading to the conclusion that the first V. parahaemolyticus pandemic had taken place. Most strains of V. parahaemolyticus isolated from the environment or seafood, in contrast to clinical strains, do not produce a thermostable direct hemolysin (TDH) and/or a TDH-related hemolysin (TRH). Type 3 secretion systems (T3SSs), needle-like apparatuses able to deliver bacterial effectors into host cytoplasm, were identified as triggering cytotoxicity and enterotoxicity. Type 6 secretion systems (T6SS) predicted to be involved in intracellular trafficking and vesicular transport appear to play a role in V. parahaemolyticus virulence. Recent advances in V. parahaemolyticus genomics identified several pathogenicity islands (VpaIs) located on either chromosome in both epidemic and pandemic strains and comprising additional colonization factors, such as restriction-modification complexes, chemotaxis proteins, classical bacterial surface virulence factors, and putative colicins. Furthermore, studies indicate strains lacking toxins and genomic regions associated with pathogenicity may also be pathogenic, suggesting other important virulence factors remain to be identified. The unique repertoire of virulence factors identified to date, their occurrence and distribution in both epidemic and pandemic strains worldwide are described, with the aim of highlighting the complexity of V. parahaemolyticus pathogenicity as well as its dynamic genome.

Keywords: O3:K6; PAI; V. parahaemolyticus; epidemic strains; pandemic strains; tdh; trh; virulence markers.

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Figures

Figure 1
Figure 1
Worldwide distribution of V. parahaemolyticus featuring virulence markers. Red, O3:K6 (or serovariants) clinical isolates; blue, O3:K6 (or serovariants) environmental isolates (water, seafood); green, non O3:K6 strains showing pandemic features (tdh, trh, PAI, T3SS, and/or T6SS). References to these data are a small portion of the published studies and should guide as an example. (Myers et al., ; Islam et al., ; Quilici et al., ; Nair et al., ; Ellingsen et al., ; Ottaviani et al., , ; Chao et al., , ; Baker-Austin et al., ; Jones et al., ; Velazquez-Roman et al., ; Powell et al., 2013).

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