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马疱疹病毒2型(EHV-2)感染的分布及相关性

Distribution and relevance of equine herpesvirus type 2 (EHV-2) infections.

作者信息

Borchers K, Wolfinger U, Goltz M, Broll H, Ludwig H

机构信息

Institut für Virologie, FU Berlin, Federal Republic of Germany.

出版信息

Arch Virol. 1997;142(5):917-28. doi: 10.1007/s007050050128.

Abstract

Equine herpesvirus type 2 (EHV-2) is a slow-growing, cytopathogenic gammaherpesvirus, which is suggested to be ubiquitous in the equine population. However, its precise role as a pathogen and its tissue tropism remains uncertain. To estimate the prevalence of EHV-2 in Germany and to investigate the possible pathogenicity of the virus, peripheral blood leucocytes (PBL) from 172 horses were examined for EHV-2 DNA by a sensitive and specific nested PCR based on the EcoRI-N genomic fragment and by classical cocultivation. PBL samples from 51% of the horses were positive by PCR and virus was isolated from 31% of the horses by cocultivation. However, almost all animals were seropositive for EHV-2. This may indicate that PBL do not harbour EHV-2 indefinitely after infection. Furthermore, a correlation between clinical signs and EHV-2 as a causative agent could not be determined. Nevertheless, the prevalence of virus was high among horses with upper respiratory tract disease, abortion and severe ataxia. The products of the second round of the PCR reactions showed size polymorphism. Sequencing of the products revealed that these size differences were due to repetition of the motif (AGACAGGGGCCATGCTGGC) between 9-16 times depending on the isolate, suggesting that the nested PCR might be a useful tool for the differentiation of EHV-2 isolates.

摘要

马疱疹病毒2型(EHV-2)是一种生长缓慢、具有细胞致病性的γ疱疹病毒,据推测在马群中普遍存在。然而,其作为病原体的确切作用及其组织嗜性仍不确定。为了估计EHV-2在德国的流行情况并研究该病毒可能的致病性,采用基于EcoRI-N基因组片段的灵敏且特异的巢式PCR以及经典的共培养方法,对172匹马的外周血白细胞(PBL)进行EHV-2 DNA检测。51%的马的PBL样本通过PCR呈阳性,31%的马通过共培养分离出病毒。然而,几乎所有动物的EHV-2血清学检测均为阳性。这可能表明感染后PBL不会无限期携带EHV-2。此外,无法确定临床症状与作为病原体的EHV-2之间的相关性。尽管如此,在上呼吸道疾病、流产和严重共济失调的马匹中病毒流行率较高。第二轮PCR反应产物显示出大小多态性。对产物进行测序表明,这些大小差异是由于基序(AGACAGGGGCCATGCTGGC)根据分离株不同重复9至16次所致,这表明巢式PCR可能是区分EHV-2分离株的有用工具。

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