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Year Round Patchiness of Vibrio Vulnificus Within a Temperate Texas Bay

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Date 2012 Jan 4
PMID 22212214
Citations 3
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Abstract

Aims: To investigate with high geographical resolution the small-scale spatial and temporal distribution of the pathogen Vibrio vulnificus throughout the water column in a temperate Texas bay where numerous V. vulnificus infections had been reported by the regional media the previous summer.

Methods And Results: Surface and bottom water samples were collected from 19 sites between April 2005 and October 2006 from Matagorda Bay, TX. Physicochemical parameters were measured and V. vulnificus were analysed using quantitative polymerase chain reaction (Q-PCR) as a means of overcoming constraints of traditional culturing techniques. V. vulnificus was detected through out the year, although its temporal and spatial distribution was patchy. V. vulnificus abundances at individual sites ranged from <10 to >1·1×10(3)cellsml(-1) . No statistically reliable predictive model related to the physicochemical parameters could be developed for this pathogen.

Conclusions: This study demonstrates that year round detection of V. vulnificus while likely in the viable but nonculturable (VBNC) state during the winter months and emphasizes why physicochemical factors are insufficient metrics for robust regression modelling of this pathogen.

Significance And Impact Of The Study: This study provides an effective new tool, Q-PCR, to study environmental distribution of V. vulnificus and that in the light of the patchy distribution observed, new reliable approaches and a mechanistic understanding of pathogen ecology need to be considered to effectively model the aquatic distribution of V. vulnificus.

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References
1.
Hsieh J, Fries J, Noble R . Dynamics and predictive modelling of Vibrio spp. in the Neuse River Estuary, North Carolina, USA. Environ Microbiol. 2008; 10(1):57-64. DOI: 10.1111/j.1462-2920.2007.01429.x. View

2.
Motes M, DePAOLA A, Cook D, Veazey J, Hunsucker J, Garthright W . Influence of water temperature and salinity on Vibrio vulnificus in Northern Gulf and Atlantic Coast oysters (Crassostrea virginica). Appl Environ Microbiol. 1998; 64(4):1459-65. PMC: 106170. DOI: 10.1128/AEM.64.4.1459-1465.1998. View

3.
Abd H, Saeed A, Weintraub A, Nair G, Sandstrom G . Vibrio cholerae O1 strains are facultative intracellular bacteria, able to survive and multiply symbiotically inside the aquatic free-living amoeba Acanthamoeba castellanii. FEMS Microbiol Ecol. 2007; 60(1):33-9. DOI: 10.1111/j.1574-6941.2006.00254.x. View

4.
Sandstrom G, Saeed A, Abd H . Acanthamoeba polyphaga is a possible host for Vibrio cholerae in aquatic environments. Exp Parasitol. 2009; 126(1):65-8. DOI: 10.1016/j.exppara.2009.09.021. View

5.
Ackerman D, Weisberg S . Relationship between rainfall and beach bacterial concentrations on Santa Monica bay beaches. J Water Health. 2004; 1(2):85-9. View