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首页> 外文期刊>Journal of Clinical Microbiology >Discrimination of Campylobacter jejuni isolates by fla gene sequencing.
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Discrimination of Campylobacter jejuni isolates by fla gene sequencing.

机译:通过fla基因测序区分空肠弯曲菌。

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Comparison of the entire coding sequence of flaA (1,764 nucleotides) from 15 isolates of Campylobacter jejuni showed two regions of high variability, one region approximately from base positions 700 to 1,450 and a short variable region (SVR) from base positions 450 to 600. Parsimony analysis of the SVR sequences yielded a dendrogram similar to that which was derived by analysis of the entire gene. PCR was used to generate templates, and the SVR was sequenced with primers constructed to hybridize to conserved flanking sequences. The SVRs of 22 isolates of C. jejuni from four outbreaks that have been well characterized and a larger panel of isolates from three additional outbreaks were sequenced. Analysis of the nucleotide sequences produced results that grouped the isolates very similarly to other subtyping techniques. Sequence data were also generated for isolates from three additional outbreaks. Categorizing the isolates by fla SVR DNA sequence placed them in epidemiologically relevant groups. Sequence analysis of the C. jejuni flaA SVR may be a useful tool for epidemiologic investigations and could complement or replace serotyping and other subtyping methods.
机译:比较来自空肠弯曲菌的15个分离株的flaA的整个编码序列(1,764个核苷酸),显示了两个高度可变的区域,一个区域大约在碱基位置700至1,450之间,一个短可变区域(SVR)在碱基位置450至600之间。对SVR序列的分析得出的树状图与通过对整个基因的分析得出的树状图相似。用PCR产生模板,并用与保守的侧翼序列杂交的引物对SVR进行测序。来自四个已爆发的空肠弯曲杆菌的22个分离株的SVR已被很好地表征,并对来自三个其他爆发的更大的分离株进行了测序。核苷酸序列的分析产生的结果与其他亚型分析技术非常相似地将分离物分组。还为来自另外三个疫情的分离株生成了序列数据。通过fla SVR DNA序列对分离株进行分类,将其置于流行病学相关组中。空肠弯曲杆菌flaA SVR的序列分析可能是流行病学研究的有用工具,可以补充或替代血清分型和其他亚型方法。

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