马尔尼菲青霉菌
聚合酶链反应
生物
DNA
微生物学
分子生物学
青霉属
病毒学
基因
人类免疫缺陷病毒(HIV)
遗传学
共感染
作者
Chularut Prariyachatigul,Angkana Chaiprasert,K. Geenkajorn,R. Kappe,Charoen Chuchottaworn,S. Termsetjaroen,S. Srimuang
出处
期刊:Mycoses
[Wiley]
日期:2003-11-28
卷期号:46 (11-12): 447-454
被引量:18
标识
DOI:10.1046/j.0933-7407.2003.00939.x
摘要
Summary A one‐tube seminested polymerase chain reaction (PCR) assay was developed to detect and identify Penicillium marneffei DNA coding for 18S rRNA both from purified DNA and from clinical samples. DNA from 120 strains of organisms and 19 blood samples from AIDS patients was amplified with F3, CPL1 and PM primers. Under optimized conditions, these primers detected 100% specifically amplified products of 251 and 331 bp from all P. marneffei DNA preparations (47 strains) and from two blood samples of AIDS patients suspected to suffer from penicilliosis marneffei. The assay was sensitive to detect as little as 10 pg purified DNA, which is equivalent to 250 cells. This PCR assay might be useful as an alternative test, if a rapid diagnosis of penicilliosis marneffei is needed.
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