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首页> 外文期刊>Indian journal of comparative microbiology, immunology and infectious dieases >MOLECULAR DIFFERENTIATION OF BRUCELLA ISOLATES BY REPETITIVE SEQUENCE-BASED PCR
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MOLECULAR DIFFERENTIATION OF BRUCELLA ISOLATES BY REPETITIVE SEQUENCE-BASED PCR

机译:通过基于重复序列的PCR对布鲁氏菌分离株进行分子分化

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Brucellosis is a worldwide zoonotic disease of major public health, animal welfare and economic significance. Strain differentiation is very much important for the control and eradication of Brucella. The objective of this study was to perform Entero-bacterial Repetitive Intergenic Consensus (ERIC) sequence-based and Repetitive sequence-based polymerase chain reaction (REP-PCR) for molecular differentiation of field isolates of Brucella. Fingerprinting with ERIC and REP-PCR generated distinct amplifIcation bands ranging from 10-11 and 1-9 bands, respectively. Five profiles (El to E5) were observed for ERIC-PCR with profile E1 as most common having 66 isolates. Out of 32 profiles (R1-R32) observed for REP-PCR, R5 with 7 bands was most common and present in 16 isolates. REP-PCR, in the present study could discriminate isolates at genus and species level.
机译:布鲁氏菌病是一种世界性的人畜共患疾病,具有重大的公共卫生、动物福利和经济意义。菌株分化对于布鲁氏菌的控制和根除非常重要。本研究旨在对布鲁氏菌田间分离株进行基于肠道细菌重复基因间共识(ERIC)序列和基于重复序列的聚合酶链反应(REP-PCR)的分子分化。使用ERIC和REP-PCR进行指纹图谱分析,分别产生了10-11条和1-9条带的不同扩增条带。在ERIC-PCR中观察到5个图谱(El至E5),其中E1图谱最常见,有66个分离株。在 REP-PCR 观察到的 32 个谱图 (R1-R32) 中,具有 7 条带的 R5 最常见,存在于 16 个分离株中。在本研究中,REP-PCR可以在属和种水平上区分分离株。

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