Adhikary Arun Kumar, Inada Toshiki, Banik Urmila, Numaga Jiro, Okabe Nobuhiko
Infectious Disease Surveillance Center, National Institute of Infectious Diseases, Shinjuku-ku, Tokyo 162-8640, Japan.
J Clin Microbiol. 2004 Feb;42(2):670-3. doi: 10.1128/JCM.42.2.670-673.2004.
Subgenus C human adenoviruses, which include serotypes 1, 2, 5, and 6, are often associated with respiratory illness, ocular infections, gastroenteritis, and systemic infection among immunocompromised patients. To address the problems associated with the conventional typing methods, we developed a fiber-based multiplex PCR assay for simple and specific identification of adenovirus type 1, 2, 5, and 6 field isolates. To design type-specific primers, adenovirus type 1 and 6 fiber genes were sequenced. The assay correctly identified prototype strains of adenovirus serotypes 1, 2, 5, 6, as well as 21 previously typed adenovirus field isolates. Mixing two different prototype DNAs produced two amplicons of different lengths, thus clearly distinguishing the prototypes. The results correlated 100% with serological tests and 95% with the previously described PCR-restriction fragment length polymorphism method. The detection of dual infection is an added benefit of the assay. No nonspecific amplification was detected with other adenovirus serotypes or with nonadenoviral DNA. Our fiber-based multiplex PCR assay will provide a convenient tool for type-specific identification of subgenus C adenovirus isolates in various clinical situations and in epidemiological investigations and is a better alternative than the hexon-based assay.
C亚属人腺病毒,包括血清型1、2、5和6,常与免疫功能低下患者的呼吸道疾病、眼部感染、肠胃炎及全身感染有关。为解决传统分型方法存在的问题,我们开发了一种基于纤维蛋白的多重PCR检测方法,用于简单、特异性地鉴定腺病毒1型、2型、5型和6型的野外分离株。为设计型特异性引物,对腺病毒1型和6型的纤维蛋白基因进行了测序。该检测方法能正确鉴定腺病毒血清型1、2、5、6的原型菌株,以及21株先前已分型的腺病毒野外分离株。将两种不同的原型DNA混合可产生两个不同长度的扩增子,从而清晰地区分这些原型。结果与血清学检测的相关性为100%,与先前描述的PCR-限制性片段长度多态性方法的相关性为95%。该检测方法的另一个优点是能够检测双重感染。用其他腺病毒血清型或非腺病毒DNA未检测到非特异性扩增。我们基于纤维蛋白的多重PCR检测方法将为在各种临床情况和流行病学调查中对C亚属腺病毒分离株进行型特异性鉴定提供一种便捷工具,并且是比基于六邻体的检测方法更好的选择。