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反刍动物产志贺毒素大肠杆菌的分离鉴定和致病潜力分析
引用本文:胡夏佩,王惠,孔学维,佟盼盼,田睿,刘茂军,马勋,张海燕,张炜.反刍动物产志贺毒素大肠杆菌的分离鉴定和致病潜力分析[J].微生物学报,2021,61(8):2495-2505.
作者姓名:胡夏佩  王惠  孔学维  佟盼盼  田睿  刘茂军  马勋  张海燕  张炜
作者单位:南京农业大学动物医学院, 江苏 南京 210095;新疆农业大学动物医学院, 新疆 乌鲁木齐 830052;江苏省农业科学研究院, 江苏 南京 210014;新疆石河子大学动物科技学院, 新疆 石河子 832003;芜湖职业技术学院生物工程学院, 安徽 芜湖 241003
基金项目:国家重点研发计划(2018YFC1602500);国家自然科学基金(U1803109);安徽省高校优秀青年人才支持计划(gxyq2019201);芜湖职业技术学院校级科技团队(wzykjtd202002)
摘    要:产志贺毒素大肠杆菌(Shiga toxin-producing Escherichia coli,STEC)是重要的食源性病原,而STEC往往以正常菌群的形式存在于牛羊等反刍动物肠道。目的] 本研究对牛羊粪便样品中的STEC分离和鉴定并对分离株进行致病潜力分析。从江苏、云南和河北等地共分离到羊源STEC菌株11株,牛源STEC菌株1株,另新疆农业大学佟盼盼组馈赠牛源菌株10株。方法] 通过细菌选择培养及特异性基因stx1stx2的检测进行分离鉴定;并通过Vero细胞毒性试验、溶血活性试验和毒力因子的检测分析STEC分离株的致病潜力。结果] 分离到羊源分离株11株,分离率17.5%(11/63);分离得到牛源分离株1株,分离率0.7%(1/134);11株羊源分离株中有5株对Vero细胞具有强的毒性,3株有溶血活性;11株牛源分离株中有5株对Vero细胞具有强的毒性,3株有溶血活性。11株羊源STEC分离株eae基因携带率为63.6%(7/11),而11株牛源STEC分离株eae基因携带率仅为9.0%(1/11)。结论] 结果表明羊源STEC菌株的分离率和致病潜力高于牛源菌株,所以,除牛外,羊作为STEC菌株宿主也应该得到更多的重视。

关 键 词:产志贺毒素大肠杆菌  Vero细胞毒性  毒力基因  致病潜力  溶血活性
收稿时间:2020/10/10 0:00:00
修稿时间:2020/12/18 0:00:00

Isolation, identification and pathogenic potential analysis of Shiga toxin-producing Escherichia from ruminants
Xiapei Hu,Hui Wang,Xuewei Kong,Panpan Tong,Rui Tian,Maojun Liu,Xun M,Haiyan Zhang,Wei Zhang.Isolation, identification and pathogenic potential analysis of Shiga toxin-producing Escherichia from ruminants[J].Acta Microbiologica Sinica,2021,61(8):2495-2505.
Authors:Xiapei Hu  Hui Wang  Xuewei Kong  Panpan Tong  Rui Tian  Maojun Liu  Xun M  Haiyan Zhang  Wei Zhang
Institution:College of Animal Medical, Nanjing Agricultural University, Nanjing 210095, Jiangsu Province, China;College of Animal Medical, Xinjiang Agricultural University, Urumqi 830052, Xinjiang Uygur Autonomous Region, China;Jiangsu Academy of Agricultural Sciences, Nanjing 210014, Jiangsu Province, China;College of Animal Technology, Xinjiang Shihezi University, Shihezi 832003, Xinjiang Uygur Autonomous Region, China;School of Bioengineering, Wuhu Vocational and Technical College, Wuhu 241003, Anhui Province, China
Abstract:Shiga toxin-producing Escherichia coli (STEC) is an important food-borne pathogen, which often exists in the intestines of ruminants, such as cow and sheep, as normal flora.Objective] In this study, we isolated and identified Shiga toxin-producing Escherichia coli isolates from cow and sheep feces samples, and analyzed their pathogenic potentials Totally 11 Shiga toxin-producing Escherichia coli strains from sheeps and 1 isolate from cattle were isolated from Jiangsu, Yunnan, and Hebei, and another 10 isolates of STEC from cattle were donated by Tong Pan Group of Xinjiang Agricultural University. Methods] We conducted the separation and identification through bacterial selective culture and detection of specific genes stx1 and stx2. We analyzed the pathogenic potential of the Shiga toxin-producing Escherichia coli isolates by Vero cytotoxicity test, hemolytic activity test, and toxin factor detection. Results] In this study, the separation and identification result revealed that 11 isolates of sheep origin were isolated with an isolation rate of 17.5% (11/63); 1 isolate from cow origin was isolated with an isolation rate of 0.7% (1/134). The pathogenic potential results showed that, among the 11 sheep-derived isolates, 5 of them had strong toxicity to Vero cells, and 3 had hemolytic activity. Among the 11 cow-derived isolates, 5 had strong toxicity to Vero cells, and 3 had hemolytic activity. The eae gene carrying rate of the 11 sheep-derived Shiga toxin-producing Escherichia coli isolates was 63.6% (7/11), while the eae gene carrying rate of the cow-derived 11 Shiga toxin-producing Escherichia coli isolates was only 9.0% (1/11). Conclusion] The results indicated that the isolation rate and pathogenic potential of the Shiga toxin-producing Escherichia coli strains derived from sheep were higher than the strains of cow origin. Therefore, sheep, as the host of Shiga toxin-producing Escherichia coli strains, should be paid higher attention than cow.
Keywords:Shiga toxin-producing Escherichia coli  Vero cytotoxicity  virulence gene  pathogenicity  hemolytic activity
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