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通过针对virF和ail基因的双重PCR和斑点杂交检测冷藏和冷冻乳制品中致病性小肠结肠炎耶尔森菌及其流行情况。

Detection and prevalence of pathogenic Yersinia enterocolitica in refrigerated and frozen dairy products by duplex PCR and dot hybridization targeting the virF and ail genes.

作者信息

Ye Y W, Ling N, Han Y J, Wu Q P

机构信息

School of Biotechnology and Food Engineering, Hefei University of Technology, Hefei, 230009, China.

School of Biotechnology and Food Engineering, Hefei University of Technology, Hefei, 230009, China.

出版信息

J Dairy Sci. 2014 Nov;97(11):6785-91. doi: 10.3168/jds.2014-8382. Epub 2014 Sep 11.

Abstract

Pathogenic Yersinia enterocolitica is involved in yersiniosis through expression of chromosome-borne or plasmid-borne virulence factors. Yersinia enterocolitica is a cold-tolerant pathogen frequently isolated from refrigerated or frozen foods. However, little attention has been focused on the prevalence of pathogenic Y. enterocolitica in refrigerated or frozen dairy samples in China. In this study, we developed a new duplex PCR targeting the plasmid-borne virF gene and chromosome-borne ail gene for detection of pathogenic Y. enterocolitica isolates. We established a detection limit for the duplex PCR of 6.5 × 10(2)cfu/mL in artificially contaminated dairy samples. In addition, the duplex PCR could detect directly 4.5 to 5.7 cfu of Y. enterocolitica in 5 mL of brain heart infusion broth after 6 h of enrichment at 28 °C. A newly developed dot hybridization assay further confirmed specificity of the duplex PCR for detection of virulent Y. enterocolitica. Furthermore, 13 Y. enterocolitica and 5 pathogenic strains, from 88 commercial frozen or refrigerated dairy products, were detected successfully by the China National Standard method (GB/T4789.8-2008) and the duplex PCR, respectively. Finally, biotypes and serotypes of pathogenic Y. enterocolitica strains were further characterized. The duplex PCR developed here is reliable for large-scale screening, routine monitoring, and risk assessment of pathogenic Y. enterocolitica in refrigerated or frozen dairy products.

摘要

致病性小肠结肠炎耶尔森菌通过表达染色体携带或质粒携带的毒力因子引发耶尔森菌病。小肠结肠炎耶尔森菌是一种耐冷病原体,常从冷藏或冷冻食品中分离得到。然而,在中国,很少有人关注冷藏或冷冻乳制品中致病性小肠结肠炎耶尔森菌的流行情况。在本研究中,我们开发了一种新的双重PCR方法,靶向质粒携带的virF基因和染色体携带的ail基因,用于检测致病性小肠结肠炎耶尔森菌分离株。我们确定了双重PCR在人工污染乳制品样本中的检测限为6.5×10²cfu/mL。此外,在28℃富集6小时后,双重PCR能够直接检测5 mL脑心浸液肉汤中4.5至5.7 cfu的小肠结肠炎耶尔森菌。新开发的斑点杂交试验进一步证实了双重PCR检测有毒力小肠结肠炎耶尔森菌的特异性。此外,分别采用中国国家标准方法(GB/T4789.8-2008)和双重PCR成功检测了88种市售冷冻或冷藏乳制品中的13株小肠结肠炎耶尔森菌和5株致病菌株。最后,对致病性小肠结肠炎耶尔森菌菌株的生物型和血清型进行了进一步鉴定。本文开发的双重PCR对于冷藏或冷冻乳制品中致病性小肠结肠炎耶尔森菌的大规模筛查、常规监测和风险评估是可靠的。

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