Title of article
Detection and molecular characterization of Vibrio parahaemolyticus isolated from seafood harvested along the southwest coast of India Original Research Article
Author/Authors
Pendru Raghunath، نويسنده , , Sadananda Acharya، نويسنده , , Amarbahadur Bhanumathi، نويسنده , , Iddya Karunasagar، نويسنده , , Indrani Karunasagar، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2008
Pages
7
From page
824
To page
830
Abstract
The levels of total and tdh+ Vibrio parahaemolyticus were estimated in 83 seafood samples from southwest coast of India by colony hybridization. Conventional enrichment and isolation technique was also used to study the prevalence. Polymerase chain reaction (PCR) was performed on bacterial cell lyates for detection of total and pathogenic V. parahaemolyticus by amplification of specific genes. Of 83 samples tested, V. parahaemolyticus could be detected in 74 (89.2%) samples and tdh+ V. parahaemolyticus in 5 (6.0%) samples by colony hybridization. V. parahaemolyticus was detected in 68 (81.9%) of 83 samples after 18 h of enrichment by PCR, and isolated from 63 (75.9%) of 83 samples by conventional isolation. The virulence genes tdh and trh could be detected in 8.4% and 25.3%, respectively, in the sample enrichment broths by PCR. Use of colony hybridization following enrichment to achieve sensitive detection of tdh+ V. parahaemolyticus in seafood was evaluated using another set of 58 seafood samples. Thirty pathogenic V. parahaemolyticus strains isolated during the study were screened by PCR for genetic markers to be specific for the detection of the pandemic clone. Results of this study suggest that the GS-PCR may serve as a reliable genetic marker for the pandemic clone of V. parahaemolyticus.
Keywords
Genetic markers , Vibrio parahaemolyticus , Colony hybridization , PCR
Journal title
Food Microbiology
Serial Year
2008
Journal title
Food Microbiology
Record number
1189707
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