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通过聚合酶链反应(PCR)检测实验性感染小鼠和疑似念珠菌血症患者血样中的念珠菌属。

Detection of Candida species by polymerase chain reaction (PCR) in blood samples of experimentally infected mice and patients with suspected candidemia.

作者信息

Khan Z U, Mustafa A S

机构信息

Department of Microbiology, Faculty of Medicine Kuwait University.

出版信息

Microbiol Res. 2001;156(1):95-102. doi: 10.1078/0944-5013-00072.

Abstract

In this study, we have established and evaluated a genus-specific polymerase chain reaction (PCR) and species-specific nested PCRs for the detection of Candida species in blood samples of neutropenic mice and patients suspected of candidemia. DNA segments of the gene encoding cytochrome P450 L1A1 were targeted for amplification by using genus and species-specific primers. As compared to the genus-specific PCR, the species-specific nested PCRs improved the sensitivity by 10 times with the detection limit < 10 yeast cells. Of the 18 blood samples tested daily over a period of 8 days following Candida albicans infection in neutropenic mice, four samples were positive by genus-specific PCR and 11 were positive by species-specific nested PCR. The PCR results were correlated with culture findings obtained on blood samples. Two of the three blood culture-positive samples were positive by genus-specific PCR and all the three with species-specific nested PCR. Among 15 mice, which were negative by blood culture but had C. albicans isolated from visceral organs, 2 and 8 mice yielded positive results by genus-specific PCR and species-specific nested PCR, respectively. Consistent with the results of the animal study, species-specific nested PCR yielded much higher positivity as compared to culture (52.2% versus 21.2%) in patients suspected for candidemia. Moreover, 8 specimens which were negative for Candida by genus-specific PCR became positive by species-specific nested PCR. No correlation was apparent between PCR positivity and Candida antigen titers. The results suggest that nested PCR is a sensitive technique for the detection of Candida species from blood samples, and thus it may have application in the diagnosis of suspected cases of candidemia and candidiasis.

摘要

在本研究中,我们建立并评估了一种属特异性聚合酶链反应(PCR)和种特异性巢式PCR,用于检测中性粒细胞减少小鼠及疑似念珠菌血症患者血样中的念珠菌属菌种。利用属特异性引物和种特异性引物,对编码细胞色素P450 L1A1的基因DNA片段进行扩增。与属特异性PCR相比,种特异性巢式PCR的灵敏度提高了10倍,检测限<10个酵母细胞。在中性粒细胞减少小鼠白色念珠菌感染后的8天内,每天检测18份血样,属特异性PCR检测出4份阳性,种特异性巢式PCR检测出11份阳性。PCR结果与血样培养结果相关。血培养阳性的3份样本中,2份经属特异性PCR检测为阳性,3份经种特异性巢式PCR检测均为阳性。在15只血培养阴性但从内脏器官分离出白色念珠菌的小鼠中,分别有2只和8只小鼠经属特异性PCR和种特异性巢式PCR检测呈阳性。与动物研究结果一致,在疑似念珠菌血症患者中,种特异性巢式PCR的阳性率远高于培养法(52.2%对21.2%)。此外,8份经属特异性PCR检测念珠菌为阴性的标本经种特异性巢式PCR检测呈阳性。PCR阳性与念珠菌抗原滴度之间无明显相关性。结果表明,巢式PCR是一种从血样中检测念珠菌属菌种的灵敏技术,因此可能在疑似念珠菌血症和念珠菌病病例的诊断中具有应用价值。

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