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通过巢式聚合酶链反应检测人粪便中的微小隐孢子虫DNA。

Detection of Cryptosporidium parvum DNA in human feces by nested PCR.

作者信息

Balatbat A B, Jordan G W, Tang Y J, Silva J

机构信息

Division of Infectious Diseases, University of California, Davis Medical Center, Sacramento 95817, USA.

出版信息

J Clin Microbiol. 1996 Jul;34(7):1769-72. doi: 10.1128/JCM.34.7.1769-1772.1996.

Abstract

Cryptosporidium parvum is a coccidian protozoan that causes diarrhea in humans, often chronic and severe in patients with AIDS. Conventionally, diagnosis is made by concentration of stools followed by acid-fast staining (AF) or immunofluorescent staining. The threshold of detection in human stool specimens by these methods may require the presence of 50,000 (immunofluorescent staining) to 500,000 (AF) oocysts per g of stool. In this study, a nested PCR assay was developed to detect C. parvum DNA directly from stool specimens. After extraction of DNA from formalinized stool, a 400-bp fragment of C. parvum DNA was amplified with two 26-mer outer primers. The amplicon from this reaction was amplified with a second primer pair. With these nested primers, a 194-bp DNA fragment was amplified and confirmed as C. parvum DNA by internal probing with an enzyme-linked chemiluminescence system. This PCR-based test allowed the detection of 500 oocysts per g of stool or 100 ng of C. parvum DNA. Studies indicate that the primers utilized are specific for the DNA of C. parvum. DNA sequences were also detected in stool specimens from 4 of 28 patients previously reported negative by AF. In summary, a rapid, sensitive, and specific assay for the detection of C. parvum directly from stool specimens has been developed. This test has the potential for detecting asymptomatic infection, monitoring the response to therapy, and detecting the organism in environmental sources.

摘要

微小隐孢子虫是一种球虫类原生动物,可导致人类腹泻,对于艾滋病患者,腹泻往往呈慢性且严重。传统上,诊断方法是先对粪便进行浓缩,然后进行抗酸染色(AF)或免疫荧光染色。通过这些方法检测人类粪便标本时,检测阈值可能要求每克粪便中存在50,000个(免疫荧光染色)至500,000个(抗酸染色)卵囊。在本研究中,开发了一种巢式PCR检测法,可直接从粪便标本中检测微小隐孢子虫DNA。从经福尔马林固定的粪便中提取DNA后,用两个26个碱基的外部引物扩增微小隐孢子虫DNA的一个400碱基对片段。该反应的扩增产物用第二对引物进行扩增。使用这些巢式引物,扩增出一个194碱基对的DNA片段,并通过酶联化学发光系统进行内部探针检测,确认为微小隐孢子虫DNA。这种基于PCR的检测方法能够检测出每克粪便中500个卵囊或100纳克微小隐孢子虫DNA。研究表明,所使用的引物对微小隐孢子虫的DNA具有特异性。在之前28例经抗酸染色报告为阴性的患者的粪便标本中,也检测到了DNA序列。总之,已开发出一种直接从粪便标本中检测微小隐孢子虫的快速、灵敏且特异的检测方法。该检测方法有潜力检测无症状感染、监测治疗反应以及检测环境源中的该生物体。

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