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首页> 外文期刊>Journal of Clinical Microbiology >Genetic diversity and identification of human infection by amplification of the chlamydial 60-kilodalton cysteine-rich outer membrane protein gene.
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Genetic diversity and identification of human infection by amplification of the chlamydial 60-kilodalton cysteine-rich outer membrane protein gene.

机译:遗传多样性和人类感染的鉴定,通过扩增富含衣原体的60-千达尔顿半胱氨酸的外膜蛋白基因来实现。

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摘要

The 60-kDa cysteine-rich outer membrane protein genes of Chlamydia psittaci, Chlamydia pneumoniae, and Chlamydia trachomatis have very different 5' ends, but two areas flanking this variable region show absolute sequence conservation. This observation permitted differentiation of the three species of Chlamydia by the polymerase chain reaction (PCR), forming the basis of a diagnostic test for chlamydial infections. The PCR product containing the variable region of the respective 60-kDa CrP genes was also subjected to restriction endonuclease digestion, enabling differentiation of individual type strains of C. psittaci. Differentiation was possible between lymphogranuloma venereum and trachoma isolates of C. trachomatis. The PCR-based diagnostic test was successful with all strains of chlamydiae studied. The PCR primers showed high specificity and did not produce any product with common bacterial pathogens that may share the same sites of infection.
机译:鹦鹉热衣原体,肺炎衣原体和沙眼衣原体的富含60 kDa半胱氨酸的外膜蛋白基因的5'端截然不同,但位于该可变区两侧的两个区域显示出绝对的序列保守性。该观察结果允许通过聚合酶链反应(PCR)区分三种衣原体,为衣原体感染的诊断测试奠定了基础。含有各自的60-kDa CrP基因可变区的PCR产物也经过限制性核酸内切酶消化,能够区分鹦鹉热衣原体的各个类型菌株。性病淋巴肉芽肿和沙眼衣原体分离株之间可能存在区别。所有研究的衣原体菌株均基于PCR的诊断测试成功。 PCR引物显示出高特异性,并且没有产生任何可能带有相同感染部位的常见细菌病原体。

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