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中国农学通报 ›› 2009, Vol. 25 ›› Issue (6): 9-12.

所属专题: 畜牧兽医

• 畜牧 动物医学 蚕 蜂 • 上一篇    下一篇

16S rRNA与Vitek-32对临床感染猪肠球菌鉴定结果比较

王亚宾,崔保安,陈丽颖,张红英,程金平,刘磊   

  • 收稿日期:2008-12-01 修回日期:2009-01-23 出版日期:2009-03-20 发布日期:2009-03-20

Comparison of 16S rRNA and VITEK-32 Identification Results for Enterococcus Isolates from Clinical Swine Infections

  • Received:2008-12-01 Revised:2009-01-23 Online:2009-03-20 Published:2009-03-20

摘要: 【研究目的】旨在研究两种常用的细菌分型方法对感染猪的肠球菌鉴定结果进行比较。【方法】对从河南洛阳、济源、许昌、南阳等地送检病猪体内分离到42株革兰阳性球菌分离纯化后,分别用16S rRNA基因序列和Vitek-32全自动细菌鉴定系统对其进行鉴定。【结果】Vitek-32对42株分离菌中的34株鉴定到种的水平,分别是粪肠球菌(E. faecalis) 10株、屎肠球菌(E. faecium) 2株、铅黄肠球菌(E. casseliflavus) 22株;另有8株未成功鉴定。16S rRNA基因序列分析对42株分离菌成功进行了鉴定,分别为粪肠球菌12株,屎肠球菌30株。通过对两种方法鉴定结果比较发现,Vitek-32鉴定的10株粪肠球菌中除1株被16S rRNA鉴定为屎肠球菌外,其余9株均相同;Vitek-32鉴定的2株屎肠球菌与16S rRNA鉴定结果相同;Vitek-32鉴定的22株铅黄肠球菌除了1株被16S rRNA鉴定为粪肠球菌外,其余全部被鉴定为屎肠球菌;8株未被Vitek-32鉴定的肠球菌中,16S rRNA将其鉴定为2株粪肠球菌和6株屎肠球菌。【结论】在感染猪的肠球菌分型鉴定中,Vitek-32对粪肠球菌鉴定结果与16S rRNA比较具有较高的一致性(75%);而对于屎肠球菌的鉴定结果与16S rRNA比较出现了较大的差异(93.3%)。

关键词: 水产科技期刊, 水产科技期刊, 国际化, 发展对策

Abstract: [Objectives] To compare the two bacteria typing methods as used in Enterococcus identification for swine infection. [Methods] Forty-two Gram-positive coccal isolates were acquired from infection cases in Luoyang, Jiyuan, Xuchang and Nanyang of Henan Province, and were analysed by means of 16S rRNA gene sequencing and Vitec-32 automatic identification system respectively. [Results] 34 out of 42 isolates were determined to species level by Vitec-32, among which were 10 isolates of E. faecalis, 2 of E. faecium, 22 of E. casseliflavus, whereas the other 8 failed to be identified. The 16S rRNA gene sequencing showed that all the isolates were Enterococcus species, with 12 of E. faecalis and 30 of E. faecium. In comparison, among the 10 isolates of E. faecalis by Vitec-32, 9 were verified as the same and the other 1 was identified as E. faecium by 16S rRNA gene sequencing. Both methods showed identical results with the two E. faecium isolates. All the 22 Vitec-32-determined E. casseliflavus were re-decided by 16S rRNA gene sequencing as 1 of E. faecalis and 21 of E. faecium species. The 8 unidentified isolates turned out to be E. faecalis(2) and E. faecium(6). [Conclusion] Vitec-32 results showed good consistence(75%) to that of16S rRNA gene sequencing when applied to E. faecalis identification, and significant discrepancy(93.3%) occurred in identifying the E. faecium sp isolates.

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