Publications by authors named "A Robert-Pillot"

Vibrio sp., ubiquitous in the aquatic ecosystem, are bacteria of interest because of their involvement in human health, causing gastroenteritis after ingestion of seafood, as well as their role in vibriosis leading to severe losses in aquaculture production. Their ability to enter a viable but non-culturable (VBNC) state under stressful environmental conditions may lead to underestimation of the Vibrio population by traditional microbiological enumeration methods.

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Unlabelled: Vibrios are natural inhabitants of estuarine ecosystems and some species may pose public health problem as agents of sporadic or collective food-borne infections associated with the consumption of fish or shellfish. Samples of raw shrimp (n = 299), fished in coastal areas of the city of Agadir, Morocco, and collected from its fish marketplace, were examined for the presence of pathogenic vibrios. Microbiological analysis was carried out according to a protocol using thiosulphate citrate bile sucrose (TCBS) agar and CHROMagar Vibrio (CV) as selective media.

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Article Synopsis
  • Vibrio spp. pose a significant health threat globally, particularly through gastrointestinal infections and septicemia linked to raw or undercooked seafood, with V. parahaemolyticus, V. cholerae, and V. vulnificus being the main culprits.
  • A study tested 167 seafood samples in France, finding 34.7% positive for Vibrio, with V. parahaemolyticus most prevalent at 31.1%, followed by V. vulnificus at 12.6%, and a rare occurrence of V. cholerae at 0.6%.
  • The presence of virulence genes in 25% of V. parahaemolyticus-positive samples underlines the risk
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The most-probable-number (MPN) method is often time-consuming for the isolation, detection, and quantification of Vibrio parahaemolyticus from natural sources. MPN counting of V. parahaemolyticus bacteria usually involves the isolation of typical V.

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Vibrio parahaemolyticus is found in aquatic environments and is the leading cause of gastroenteritis due to seafood consumption worldwide. We evaluated a quantitative real-time PCR (Q-PCR) assay with hydrolysis probes, to determine whether this method could be used for the efficient counting of total, tdh and trh-positive V. parahaemolyticus in shrimps.

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