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A hemagglutination-inhibition technique for typing adenoviruses.一种用于腺病毒分型的血凝抑制技术。
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ADENOVIRUS INFECTION AS AN AETIOLOGICAL FACTOR IN INTUSSUSCEPTION OF INFANTS AND YOUNG CHILDREN.腺病毒感染作为婴幼儿肠套叠的一个病因学因素
J Pathol Bacteriol. 1964 Jul;88:263-74.
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Viruses in lymph nodes of children with mesenteric adenitis and intussusception.患有肠系膜淋巴结炎和肠套叠的儿童淋巴结中的病毒
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Genetic characterisation of adenovirus type 8 isolated in Hiroshima city over a 15 year period.广岛市15年间分离出的8型腺病毒的基因特征分析
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Evidence for a repeating cross-beta sheet structure in the adenovirus fibre.腺病毒纤维中重复交叉β-折叠结构的证据。
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PCR and restriction endonuclease analysis for rapid identification of human adenovirus subgenera.用于快速鉴定人腺病毒亚属的聚合酶链反应和限制性内切酶分析
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Adenoviruses from human immunodeficiency virus-infected individuals, including two strains that represent new candidate serotypes Ad50 and Ad51 of species B1 and D, respectively.来自人类免疫缺陷病毒感染个体的腺病毒,包括分别代表B1和D种新候选血清型Ad50和Ad51的两种毒株。
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Serotyping of adenoviruses on conjunctival scrapings by PCR and sequence analysis.通过聚合酶链反应(PCR)和序列分析对结膜刮片上的腺病毒进行血清型鉴定。
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Rapid diagnosis of adenoviral conjunctivitis on conjunctival swabs by 10-minute immunochromatography.通过10分钟免疫层析法对结膜拭子上的腺病毒性结膜炎进行快速诊断。
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基于纤维蛋白的多重PCR技术鉴定C亚属腺病毒

Identification of subgenus C adenoviruses by fiber-based multiplex PCR.

作者信息

Adhikary Arun Kumar, Inada Toshiki, Banik Urmila, Numaga Jiro, Okabe Nobuhiko

机构信息

Infectious Disease Surveillance Center, National Institute of Infectious Diseases, Shinjuku-ku, Tokyo 162-8640, Japan.

出版信息

J Clin Microbiol. 2004 Feb;42(2):670-3. doi: 10.1128/JCM.42.2.670-673.2004.

DOI:10.1128/JCM.42.2.670-673.2004
PMID:14766835
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC344504/
Abstract

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.

摘要

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。