Banik Urmila, Adhikary Arun Kumar, Suzuki Eiko, Inada Toshiki, Okabe Nobuhiko
Infectious Disease Surveillance Center, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku-ku, Tokyo 162-8640, Japan.
J Clin Microbiol. 2005 Mar;43(3):1064-8. doi: 10.1128/JCM.43.3.1064-1068.2005.
Eye infections caused by adenovirus (Ad) often result in nosocomial infections and community epidemics with significant rates of morbidity. No antiviral agent effective against Ad is yet available for clinical use. Therefore, early diagnosis is still the mainstay for patient management and the prevention of epidemics. A multiplex PCR assay based on amplification of a combination of the fiber and hexon genes which can identify the six important oculopathogenic serotypes of Ads (Ad serotype 3[Ad3], Ad4, Ad7, Ad8, Ad19, and Ad37) in a single-tube amplification reaction was developed. Ad serotypes could be distinguished by the different amplicon sizes. The assay correctly identified prototype strains as well as isolates in clinical specimens. In comparison with a previously described PCR-restriction fragment polymorphism method, our assay gave unequivocal results for clinical specimens. Our multiplex PCR has the potential to serve as a rapid and cost-effective tool for the typing of important ocular Ads.
由腺病毒(Ad)引起的眼部感染常导致医院感染和社区流行,发病率很高。目前尚无有效的抗腺病毒抗病毒药物可供临床使用。因此,早期诊断仍是患者管理和预防疫情的主要手段。我们开发了一种多重聚合酶链反应(PCR)检测方法,该方法基于对纤维蛋白和六邻体基因组合的扩增,能够在单管扩增反应中识别腺病毒的六种重要眼致病性血清型(Ad血清型3[Ad3]、Ad4、Ad7、Ad8、Ad19和Ad37)。通过不同的扩增子大小可以区分腺病毒血清型。该检测方法能够正确识别临床标本中的原型菌株和分离株。与先前描述的PCR-限制性片段多态性方法相比,我们的检测方法对临床标本给出了明确的结果。我们的多重PCR有潜力成为一种快速且经济高效的重要眼部腺病毒分型工具。