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通过聚合酶链反应检测血清中的白色念珠菌DNA。

Detection of Candida albicans DNA in serum by polymerase chain reaction.

作者信息

Chryssanthou E, Andersson B, Petrini B, Löfdahl S, Tollemar J

机构信息

Department of Clinical Microbiology, Karolinska Hospital, Stockholm, Sweden.

出版信息

Scand J Infect Dis. 1994;26(4):479-85. doi: 10.3109/00365549409008623.

Abstract

Polymerase chain reaction (PCR) was applied in order to improve the diagnosis of disseminated candidosis. A nested PCR technique with 2 primer pairs was used to increase the sensitivity. We were able to detect Candida DNA in serum and tissue samples from experimentally infected mice as well as in serum samples from candidemia patients and patients with deep-seated Candida infection. Our PCR could detect as little as 1 pg Candida albicans DNA. The PCR method was more sensitive than culture in both the mouse experiments and the patients with deep candidosis (5/7 were PCR positive and 0/7 blood culture positive), and of similar sensitivity in candidemia patients (11/17 were 15/17 blood culture positive). The relatively short processing time of PCR, when compared with culturing, its sensitivity, as well as the possibility of using serum samples for analysis, all helped improve the diagnostics in deep-seated candidosis and candidemia.

摘要

为提高播散性念珠菌病的诊断水平,应用了聚合酶链反应(PCR)。采用含两对引物的巢式PCR技术提高灵敏度。我们能够在实验感染小鼠的血清和组织样本中以及念珠菌血症患者和深部念珠菌感染患者的血清样本中检测到念珠菌DNA。我们的PCR能够检测低至1 pg的白色念珠菌DNA。在小鼠实验和深部念珠菌病患者中,PCR方法比培养更敏感(5/7为PCR阳性,0/7血培养阳性),在念珠菌血症患者中灵敏度相似(11/17为PCR阳性,15/17血培养阳性)。与培养相比,PCR处理时间相对较短,其灵敏度以及使用血清样本进行分析的可能性,均有助于改善深部念珠菌病和念珠菌血症的诊断。

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