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An Optimized Multilocus Variable-Number Tandem Repeat Analysis Typing Scheme for Listeria monocytogenes from Three Western Provinces in China

机译:中国西部三省单核细胞增生李斯特菌的多基因座可变数串联重复分析优化方案

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Listeria monocytogenes is a foodborne pathogen worldwide. Multilocus variable-number tandem repeat analysis (MLVA) has been used for listeriosis surveillance and outbreak investigations. MLVA typing schemes have been proposed, but their usefulness for typing isolates from the People's Republic of China has not been assessed. To this aim, all L. monocytogenes strains (79) isolated from 1,445 raw meat and abattoir environmental samples of three western provinces in China were characterized with PCR serogrouping, multilocus sequence typing, and MLVA. The isolates were typed into the four PCR serogroups IIb (38.0%), IIc (26.6%), IIa (24.0%), and IVb (11.4%), with a Simpson's index (SI) of 0.7235. With multilocus sequence typing, they were typed into 18 sequence types (STs), including two new STs, ST1029 and ST1011, with an SI of 0.8880. With the 14 MLVA loci from the previous five schemes, the isolates were typed into 39 MLVA genotypes, with an SI of 0.9656. The typing data indicated that MLVA had the highest typing capability among the three methods. A subsequent optimization analysis identified an optimal combination of eight loci (LMV2, LMV9, LMV1, Lm10, Lm11, Lm15, Lm23, and LMTR6) producing the same SI as that of the 14 loci. The present optimized combination shared only six loci with the optimal nine-loci combination proposed in Australia, verifying for the first time that the optimal combinations varied with the isolates' sets. The current optimal typing scheme was ideal for L. monocytogenes isolates from western China.
机译:单核细胞增生李斯特菌是全世界的食源性病原体。多基因座可变数目串联重复分析(MLVA)已用于李斯特菌病监测和暴发调查。已经提出了MLVA分型方案,但是尚未评估其对来自中国的分离株分型的有用性。为此,从中国三个西部省份的1,445个生肉和屠宰场环境样品中分离出的所有单核细胞增生李斯特菌菌株(79)均进行了PCR血清分组,多基因座序列分型和MLVA鉴定。将分离株分为四个PCR血清组IIb(38.0%),IIc(26.6%),IIa(24.0%)和IVb(11.4%),辛普森指数(SI)为0.7235。通过多基因座序列分型,将它们分为18种序列类型(ST),包括两个新的ST,即ST1029和ST1011,其SI为0.8880。使用前五个方案的14个MLVA基因座,将分离株分为39个MLVA基因型,SI为0.9656。打字数据表明,MLVA在三种方法中具有最高的打字能力。随后的优化分析确定了八个基因座(LMV2,LMV9,LMV1,Lm10,Lm11,Lm15,Lm23和LMTR6)的最佳组合,产生了与14个基因座相同的SI。本优化组合仅与澳大利亚提出的最佳9位定位组合共享了6个基因座,这首次验证了最佳组合随分离株的不同而变化。当前的最佳分型方案对于来自中国西部的单核细胞增生李斯特菌菌株是理想的。

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