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首页> 外文期刊>Journal of Clinical Microbiology >PCR and Restriction Endonuclease Analysis for Rapid Identification of Human Adenovirus Subgenera
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PCR and Restriction Endonuclease Analysis for Rapid Identification of Human Adenovirus Subgenera

机译:PCR和限制性内切核酸酶分析可快速鉴定人腺病毒亚属

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摘要

Subgenus identification of adenoviruses is of clinical importance and is as informative as identification by serotype in most clinical situations. A PCR-based identification of adenovirus subgenera A, B, C, D, E, and F and sometimes serotypes is described. The PCR uses nonnested primer pair ADRJC1-ADRJC2, which targets a highly conserved region of the adenovirus hexon gene, has a sensitivity of 10 to 40 copies of adenovirus type 2 (Ad2) DNA, and generates 140-bp PCR products from adenovirus serotypes representative of all the subgroups. The PCR products of all subgroups can be differentiated on the basis of the restriction fragment patterns produced by a total of five restriction endonucleases. In addition, serotypes Ad40 and Ad41 (subgroup F) and important serotypes of subgroup D (Ad8, Ad10, Ad19, and Ad37) can easily be differentiated, but serotypes within subgroups B and C cannot. The method was assessed by blind subgenus identification of 56 miscellaneous clinical isolates of adenoviruses. The identities of these isolates at the subgenus level by the PCR correlated 91% (51 of 56) with the results of serotyping by the neutralization test, and 9% (5 of 56) of clinical isolates produced discordant results.
机译:腺病毒的亚属鉴定在临床上具有重要意义,并且在大多数临床情况下与通过血清型鉴定同样有用。描述了基于PCR的腺病毒A,B,C,D,E和F亚型,有时还包括血清型的鉴定。 PCR使用非嵌套引物对ADRJC1-ADRJC2,其靶向腺病毒六邻体基因的高度保守区域,具有10至40拷贝的2型腺病毒(Ad2)DNA敏感性,并从代表腺病毒血清型的样本中产生140 bp的PCR产物所有子组中。可以基于总共五个限制性核酸内切酶产生的限制性片段模式来区分所有亚组的PCR产物。此外,可以轻松地区分Ad40和Ad41血清型(F亚组)和D组重要的血清型(Ad8,Ad10,Ad19和Ad37),但不能区分B和C组内的血清型。该方法是通过对56种腺病毒的临床分离株进行亚盲鉴定来评估的。通过PCR在亚属水平上对这些分离株的鉴定与中和试验的血清分型结果有91%(56个中的51个)相关,而临床分离株中有9%(56个中的5个)产生了不一致的结果。

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