2008
DOI: 10.1016/j.fm.2008.04.002
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Detection and molecular characterization of Vibrio parahaemolyticus isolated from seafood harvested along the southwest coast of India

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Cited by 53 publications
(30 citation statements)
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“…Strains that possess tdh, trh, and TTSS2-encoding genes are generally pathogenic and responsible for the vast majority of clinical cases. While such strains account for only 1 to 2% of isolates sampled from water and different marine species (4-6), they are known to have a widespread global distribution, having been reported from cases of infection in Japan, India, Thailand, Malaysia, China, Indonesia, the United Kingdom, Italy, and the East and Gulf Coasts of the United States (7)(8)(9)(10)(11)(12)(13)(14)(15)(16)(17)(18)(19).…”
mentioning
confidence: 99%
“…Strains that possess tdh, trh, and TTSS2-encoding genes are generally pathogenic and responsible for the vast majority of clinical cases. While such strains account for only 1 to 2% of isolates sampled from water and different marine species (4-6), they are known to have a widespread global distribution, having been reported from cases of infection in Japan, India, Thailand, Malaysia, China, Indonesia, the United Kingdom, Italy, and the East and Gulf Coasts of the United States (7)(8)(9)(10)(11)(12)(13)(14)(15)(16)(17)(18)(19).…”
mentioning
confidence: 99%
“…However, for samples with very low V. parahaemolyticus densities, MPN is more sensitive (3 MPN/g) compared to direct plating and the colony hybridisation method (10 cfu/g). Spread plating on T 1 N 3 after APW enrichment followed by colony hybridisation is superior to the conventional streak plate method for the recovery of pathogenic V. parahaemolyticus compared to the traditional streak plate method [8,9]. Digoxygenin labelled probes are simple to prepare in-house from polymerase chain reaction (PCR) amplified fragments and have more reporter groups per probe molecule.…”
Section: Probe Hybridisation Methodsmentioning
confidence: 99%
“…Detection limit of more than 10 4 cfu/g when applied to lysates prepared directly from fish homogenates could be improved (Ͻ10 cfu/mL) by performing PCR after an 8 hour enrichment in alkaline peptone water [20]. PCR performed on lysates obtained from seafood homogenates without enrichment using primers amplifying toxR gene, yielded a higher number of positives compared to conventional isolation and PCR was more sensitive than colony hybridisation for detection of tdh+ and trh+ organisms [9]. Positivity increased with duration of enrichment, up to 18 hours.…”
Section: Detection Of Bacterial Pathogensmentioning
confidence: 99%
“…In the Gulf coast in US, the percentage has been generally less than 1 %, but in the Pacific northwest up to 3.2 % strains could be TDH positive (FAO/WHO 2011). 6-10 % of oysters from India were positive for V. parahaemolyticus carrying the tdh gene (Deepanjali et al 2005, Raghunath et al 2008). Some TDH negative strains from clinical cases were found to produce a TDH-related hemolysin, TRH (Honda et al 1988).…”
Section: Vibrio Speciesmentioning
confidence: 99%