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聚合酶链反应在检测与热带海产品及沿海环境相关的副溶血性弧菌中的应用。

Application of polymerase chain reaction for detection of Vibrio parahaemolyticus associated with tropical seafoods and coastal environment.

作者信息

Dileep V, Kumar H S, Kumar Y, Nishibuchi M, Karunasagar Indrani, Karunasagar Iddya

机构信息

Department of Fishery Microbiology, University of Agricultural Sciences, College of Fisheries, Mangalore-575002, India.

出版信息

Lett Appl Microbiol. 2003;36(6):423-7. doi: 10.1046/j.1472-765x.2003.01333.x.

Abstract

AIMS

To study the incidence of Vibrio parahaemolyticus in seafoods, water and sediment by molecular techniques vs conventional microbiological methods.

METHODS AND RESULTS

Of 86 samples analysed, 28 recorded positive for V. parahaemolyticus by conventional microbiological method, while 53 were positive by the toxR-targeted PCR, performed directly on enrichment broth lysates. While one sample of molluscan shellfish was positive for tdh gene, trh gene was detected in three enrichment broths of molluscan shellfish.

CONCLUSIONS

Direct application of PCR to enrichment broths will be useful for the rapid and sensitive detection of potentially pathogenic strains of V. parahemolyticus in seafoods.

SIGNIFICANCE AND IMPACT OF THE STUDY

Vibrio parahaemolyticus is an important human pathogen responsible for food-borne gastroenteritis world-wide. As, both pathogenic and non-pathogenic strains of V. parahaemolyticus exist in the seafood, application of PCR specific for the virulence genes (tdh & trh) will help in detection of pathogenic strains of V. parahaemolyticus and consequently reduce the risk of food-borne illness.

摘要

目的

通过分子技术与传统微生物学方法研究海产品、水和沉积物中副溶血性弧菌的发生率。

方法与结果

在分析的86个样本中,28个通过传统微生物学方法检测副溶血性弧菌呈阳性,而直接对富集肉汤裂解物进行的靶向toxR的聚合酶链反应(PCR)显示53个呈阳性。虽然一份软体贝类样本tdh基因呈阳性,但在三份软体贝类富集肉汤中检测到trh基因。

结论

将PCR直接应用于富集肉汤,有助于快速、灵敏地检测海产品中潜在致病的副溶血性弧菌菌株。

研究的意义和影响

副溶血性弧菌是一种重要的人类病原体,在全球范围内引发食源性肠胃炎。由于海产品中同时存在致病和非致病的副溶血性弧菌菌株,针对毒力基因(tdh和trh)的PCR应用将有助于检测副溶血性弧菌的致病菌株,从而降低食源性疾病的风险。

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