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基于 hexon L1 基因区的系统进化分析和高分辨率熔解曲线分析对禽腺病毒进行分类。

Classification of fowl adenoviruses by use of phylogenetic analysis and high-resolution melting-curve analysis of the hexon L1 gene region.

机构信息

Clinic for Avian, Reptile and Fish Medicine, Department for Farm Animals and Veterinary Public Health, University of Veterinary Medicine, Veterinaerplatz 1, Vienna, Austria.

出版信息

J Virol Methods. 2010 Dec;170(1-2):147-54. doi: 10.1016/j.jviromet.2010.09.019. Epub 2010 Sep 24.

Abstract

A total of 44 fowl adenovirus (FAdV) samples from 6 European countries, Pakistan, India, Kuwait, Mexico, Peru and Ecuador were used in this study and the phylogenetic analyses based on the loop 1 (L1) region of hexon gene were performed. For comparison, available hexon sequences of representatives of different FAdV species were also used. At least 12 genotypes within the five FAdV species (A-E) were revealed and the existence of these genotypes was supported by high bootstrap values. Furthermore, three primer pairs binding to the conserved pedestal regions (HexL1s/HexL1as and HexA/HexB) and pedestal (P1) region and loop 2 (L2) region (HexF1/HexR1) of the FAdV hexon gene were used for high-resolution melting (HRM)-curve analysis and results were compared with those of phylogenetic analyses. HRM-curve analysis based on the HexL1s/HexL1as region grouped all tested field isolates and reference strains into 22 subgroups, consistently with phylogenetic analysis. This method is a rapid and cost-effective alternative to existing serotype identification methods and offers a possibility to classify FAdV isolates more precisely. However, it has limitations such as need for extensive interpretation of results and potential for indeterminate results. Gaining of hexon sequences of further field isolates offers the potential for novel and additional information in analysis of the molecular epidemiology of FAdV.

摘要

本研究共使用了来自 6 个欧洲国家(包括法国、德国、意大利、荷兰、波兰和西班牙)、巴基斯坦、印度、科威特、墨西哥、秘鲁和厄瓜多尔的 44 份禽腺病毒(FAdV)样本,并基于六邻体基因的环 1(L1)区进行了系统进化分析。此外,还使用了不同 FAdV 种代表的可用六邻体序列进行比较。结果揭示了至少 12 种 FAdV 种(A-E)的基因型,这些基因型的存在得到了高支持度bootstrap 值的支持。此外,还使用了三对结合 FAdV 六邻体基因保守基序区(HexL1s/HexL1as 和 HexA/HexB)和基序(P1)区和环 2(L2)区(HexF1/HexR1)的引物对进行高分辨率熔解(HRM)-曲线分析,并将结果与系统进化分析进行比较。基于 HexL1s/HexL1as 区的 HRM-曲线分析将所有测试的田间分离株和参考株分为 22 个亚群,与系统进化分析一致。这种方法是一种快速、具有成本效益的替代现有血清型鉴定方法的方法,为更精确地分类 FAdV 分离株提供了可能性。然而,它存在需要广泛解释结果和可能出现不确定结果的局限性。进一步获得六邻体序列的田间分离株,为分析 FAdV 的分子流行病学提供了新的和额外信息的潜力。

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