Lu J J, Bartlett M S, Shaw M M, Queener S F, Smith J W, Ortiz-Rivera M, Leibowitz M J, Lee C H
Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis 46202.
J Clin Microbiol. 1994 Dec;32(12):2904-12. doi: 10.1128/jcm.32.12.2904-2912.1994.
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.
对感染人类的卡氏肺孢子虫的18S和26S rRNA基因的小片段、整个5.8S rRNA基因以及内部转录间隔区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)进行了克隆和测序。本研究中测定的18S、5.8S和26S rRNA基因的核苷酸序列与感染大鼠的卡氏肺孢子虫的序列约90%同源,而来自两种不同宿主的卡氏肺孢子虫的ITS1和ITS2序列仅60%同源。测定了来自15例患者标本的卡氏肺孢子虫的18S、5.8S和26S rRNA基因序列,发现它们彼此相同,而ITS序列是可变的。根据观察到的序列变异,有可能将ITS1序列分为两种类型,ITS2序列分为三种类型。具有相同类型ITS1序列的卡氏肺孢子虫菌株可能具有不同类型的ITS2序列。根据两个ITS区域的序列类型,将15例患者的卡氏肺孢子虫分为四组。发现来自三个患者标本的卡氏肺孢子虫含有两种不同的ITS序列模式。更令人惊讶的是,还发现一个标本具有一种感染人类的卡氏肺孢子虫分离株典型的ITS序列和另一种感染大鼠的卡氏肺孢子虫分离株典型的ITS序列。这些研究表明,有可能根据来自一名患者的样本对卡氏肺孢子虫菌株进行分型,这表明同一患者可能发生不止一种卡氏肺孢子虫菌株的合并感染。