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首页> 外文期刊>Antonie van Leeuwenhoek >Genotyping of Indian Yersinia pestis strains by MLVA and repetitive DNA sequence based PCRs
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Genotyping of Indian Yersinia pestis strains by MLVA and repetitive DNA sequence based PCRs

机译:MLVA和基于重复DNA序列的PCR对印度耶尔森氏鼠疫杆菌菌株进行基因分型

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摘要

India experienced two plague outbreaks in Gujarat and Maharastra during 1994 and then in the Shimla district of Himachal Pradesh during 2002. Yersinia pestis strains recovered from rodents and pneumonic patients during the 1994 outbreaks, pneumonic patients from the 2002 Shimla outbreak and rodents trapped on the Deccan Plateau during a surveillance activity carried out in 1998 were characterized by MLVA, ERIC-PCR and ERIC-BOX-PCR. MLVA genotyping of Indian Y. pestis strains revealed strains of 2 Orientalis, 1 Mediaevalis and 1 Antiqua genotypes distributed in three distinct branches corresponding to their biovar. The Orientalis genotype strains recovered from the 1994 outbreaks and 1998 surveillance activity clustered in one branch while the Antiqua biovar strains from the Shimla outbreak and the Mediaevalis strain recovered from a rodent trapped on the Deccan Plateau region during surveillance formed the other branches. The Orientalis Y. pestis strains recovered from rodents and patients from the 1994 plague outbreaks exhibited similar MLVA, ERIC-PCR and ERIC-BOX-PCR profiles and these were closely related to the Orientalis strains recovered from the rodents trapped on the Deccan Plateau. These data provide evidence for the possible linkage between the Y. pestis strains resident in the endemic region and those that were associated with the 1994 plague outbreaks. Mediaevalis and Antiqua biovars also were recovered from the environmental reservoir on the Deccan Plateau and from the pneumonic patients of 2002 plague outbreak. Therefore, as in Central Asian and African regions, Antiqua and Mediaevalis biovars seem to be well established in the Indian subcontinent as well. ERIC-PCR DNA fingerprinting delineated genotypes similar to those defined by MLVA. Thus ERIC-PCR appears to have the potential to be used as a molecular marker in the molecular epidemiological investigations of plague. Keywords ERIC-PCR - ERIC-BOX PCR - MLVA - Y. pestis
机译:印度于1994年在古吉拉特邦和马哈拉施特拉邦爆发了两次鼠疫,然后在2002年在喜马al尔邦的西姆拉地区爆发了鼠疫。1994年暴发期间,鼠疫和肺炎患者中检出了鼠疫耶尔森菌,2002年西姆拉爆发时,肺炎患者以及在德干河被困的啮齿类动物中均检出了鼠疫耶尔森菌。 1998年进行的监视活动期间的高原以MLVA,ERIC-PCR和ERIC-BOX-PCR为特征。印度鼠疫耶尔森氏菌菌株的MLVA基因分型显示,在对应于它们的生物变体的三个不同的分支中分布了2个Orientalis,1个中膜和1个Antiqua基因型。从1994年暴发和1998年监视活动中恢复的Orientalis基因型菌株聚集在一个分支中,而从Shimla暴发中获得的Antiqua biovar菌株和在监视期间被困在Deccan高原地区的啮齿动物中恢复的Mediaevalis菌株形成了其他分支。从啮齿类动物和1994年鼠疫暴发患者中回收的Orientalis Y. pestis菌株表现出相似的MLVA,ERIC-PCR和ERIC-BOX-PCR谱,并且与从Deccan高原上捕获的啮齿动物中回收的Orientalis菌株密切相关。这些数据提供了证据,证明流行区的鼠疫耶尔森氏菌菌株与1994年鼠疫暴发有关的菌株之间可能存在联系。 Mediadecalis和Antiqua生物变种还从Deccan高原的环境水库和2002年鼠疫暴发的肺炎患者中回收。因此,与中亚和非洲地区一样,Antiqua和Mediaevalis生物变种似乎在印度次大陆也很成熟。 ERIC-PCR DNA指纹图谱描述了与MLVA定义的基因型相似的基因型。因此,ERIC-PCR似乎有潜力在鼠疫的分子流行病学研究中用作分子标记。关键词ERIC-PCR-ERIC-BOX PCR-MLVA-鼠疫杆菌

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