2014
DOI: 10.1007/s13213-014-0884-1
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Predictive model of Vibrio parahaemolyticus O3:K6 growth on cooked Litopenaeus vannamei

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Cited by 13 publications
(16 citation statements)
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“…Although the curve‐fitting approach used by Tang et al. () reported a zero growth rate of V. parahaemolyticus in shrimp at a temperature of 1 °C, previous studies demonstrated that the bacteria may die at temperatures lower than 7 °C in shrimp (Ma et al., ), and at least become inactivated at temperatures lower than 12 °C in raw oyster (Huang et al., ). The minimum temperature for growth and survival of this organism probably depends on the strain and food matrices (Huang et al., ).…”
Section: Resultsmentioning
confidence: 99%
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“…Although the curve‐fitting approach used by Tang et al. () reported a zero growth rate of V. parahaemolyticus in shrimp at a temperature of 1 °C, previous studies demonstrated that the bacteria may die at temperatures lower than 7 °C in shrimp (Ma et al., ), and at least become inactivated at temperatures lower than 12 °C in raw oyster (Huang et al., ). The minimum temperature for growth and survival of this organism probably depends on the strain and food matrices (Huang et al., ).…”
Section: Resultsmentioning
confidence: 99%
“…Theoretically, a zero-growth rate of V. parahaemolyticus in shrimp was observed at a temperature of 1°C reported by Tang, Zhao, Sun, Xie, and Malakar (2015). However, several studies have shown that V. parahaemolyticus should die at temperatures lower than 7°C in shrimp (Ma et al, 2016) and become inactivated at the temperature lower than 12°C in raw oyster (Huang et al, 2018).…”
Section: Exposure Assessment Modelingmentioning
confidence: 95%
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“…Traditionally, conventional plate counting methods have been used to collect data to construct predictive models (26,31). For instance, TCBS agar is widely used to enumerate V. parahaemolyticus colonies and to monitor their growth and survival without enrichment (7).…”
Section: Discussionmentioning
confidence: 99%
“…Traditional plate counting methods (using, e.g., thiosulfate-citrate-bile salts-sucrose [TCBS] or TCBS agar) can detect the total V. parahaemolyticus population but cannot differentiate pathogenic V. parahaemolyticus from nonpathogenic V. parahaemolyticus. Real-time PCR has the advantage of being able to quantify the total V. parahaemolyticus population targeting the tlh gene and to differentiate and quantify the pathogenic V. parahaemolyticus population with the tdh or trh gene (25,26).…”
mentioning
confidence: 99%