首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Typing of Pneumocystis carinii strains that infect humans based on nucleotide sequence variations of internal transcribed spacers of rRNA genes.
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Typing of Pneumocystis carinii strains that infect humans based on nucleotide sequence variations of internal transcribed spacers of rRNA genes.

机译:基于rRNA基因内部转录间隔区的核苷酸序列变异对感染人类的​​卡氏肺孢子虫菌株进行分型。

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摘要

Small portions of the 18S and the 26S rRNA genes, the entire 5.8S rRNA gene, and internal transcribed spacers ITS1 and ITS2 (located between the 18S and 5.8S rRNA genes and between the 5.8S and 26S rRNA genes, respectively) of Pneumocystis carinii that infect humans were cloned and sequenced. The nucleotide sequences of the 18S, 5.8S, and 26S rRNA genes determined in the study were approximately 90% homologous to those of P. carinii that infect rats, while the sequences of ITS1 and ITS2 of P. carinii from the two different hosts were only 60% homologous. The 18S, 5.8S, and 26S rRNA gene sequences of P. carinii from 15 patient specimens were determined and were found to be identical to each other, whereas the ITS sequences were found to be variable. With the observed sequence variation, it was possible to classify the ITS1 sequences into two types and the ITS2 sequences into three types. P. carinii strains that had the same type of ITS1 sequence could have a different type of ITS2 sequence. On the basis of the sequence types of the two ITS regions, P. carinii from the 15 patients were classified into four groups. P. carinii from three patient specimens were found to contain two different ITS sequence patterns. More surprisingly, one additional specimen was found to have one ITS sequence typical of P. carinii isolates that infect humans and another typical of P. carinii isolates that infect rats. The studies indicate that it is possible to type P. carinii strains on the basis from one patient, suggesting that coinfection with more than one strain of P. carinii may occur in the same patient.
机译:卡氏肺孢子虫的18S和26S rRNA基因的一小部分,整个5.8S rRNA基因以及内部转录的间隔子ITS1和ITS2(分别位于18S和5.8S rRNA基因之间以及5.8S和26S rRNA基因之间)。克隆感染人类并进行​​测序。在这项研究中确定的18S,5.8S和26S rRNA基因的核苷酸序列与感染大鼠的卡氏假单胞菌大约90%同源,而来自两个不同宿主的卡氏假单胞菌ITS1和ITS2的序列分别是只有60%同源。确定了15个患者标本中卡氏假单胞菌的18S,5.8S和26S rRNA基因序列,发现它们彼此相同,而ITS序列却是可变的。通过观察到的序列变异,可以将ITS1序列分为两种类型,而将ITS2序列分为三种类型。具有相同类型的ITS1序列的卡氏疟原虫菌株可能具有不同类型的ITS2序列。根据两个ITS区的序列类型,将15例患者的卡氏疟原虫分为四组。发现来自三个患者标本的卡氏疟原虫含有两种不同的ITS序列模式。更令人惊讶的是,发现另外一个标本具有一个典型的感染人的卡氏疟原虫分离株和另一个典型的感染大鼠的卡氏疟原虫分离株的ITS序列。研究表明,有可能根据一名患者对卡氏疟原虫进行分型,这表明同一名患者可能发生多于一种卡氏疟原虫的合并感染。

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