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两种非A/非B型禽肺炎病毒(APV)的F、L和G蛋白基因的核苷酸序列揭示了一个新的APV亚群。

Nucleotide sequences of the F, L and G protein genes of two non-A/non-B avian pneumoviruses (APV) reveal a novel APV subgroup.

作者信息

Bäyon-Auboyer Marie-Hélène, Arnauld Claire, Toquin Didier, Eterradossi Nicolas

机构信息

Unité de Virologie, Immunologie et Parasitologie Aviaires et Cunicoles1 and Laboratoire de Biologie Moléculaire2, Agence Française de Sécurité Sanitaire des Aliments (AFSSA), BP 53, 22440 Ploufragan, France.

出版信息

J Gen Virol. 2000 Nov;81(Pt 11):2723-2733. doi: 10.1099/0022-1317-81-11-2723.

Abstract

Sequence analysis was performed of all or part of the genes encoding the fusion (F), polymerase (L) and attachment (G) proteins of two French non-A/non-B avian pneumovirus (APV) isolates (Fr/85/1 and Fr/85/2). The two isolates shared at least 99.7% nt and 99.0% aa sequence identity. Comparison with the F genes from subgroup A, subgroup B or Colorado APVs revealed nt and aa identities of 70.0-80. 5% and 77.6-97.2%, respectively, with the L gene sharing 76.1% nt and 85.3% aa identity with that of a subgroup A isolate. The Fr/85/1 and Fr/85/2 G genes comprised 1185 nt, encoding a protein of 389 aa. Common features with subgroup A and subgroup B G proteins included an amino-terminal membrane anchor, a high serine and threonine content, conservation of cysteine residues and a single extracellular region of highly conserved sequence proposed to be the functional domain involved in virus attachment to cellular receptors. However, the Fr/85/1 and Fr/85/2 G sequences shared at best 56.6% nt and 31.2% aa identity with subgroup A and B APVs, whereas these isolates share 38% aa identity. Phylogenetic analysis of the F, G and L genes of pneumoviruses suggested that isolates Fr/85/1 and Fr/85/2 belong to a previously unrecognized APV subgroup, tentatively named D. G-based oligonucleotide primers were defined for the specific molecular identification of subgroup D. These are the first G protein sequences of non-A/non-B APVs to be determined.

摘要

对两株法国非A/非B型禽肺炎病毒(APV)分离株(Fr/85/1和Fr/85/2)编码融合(F)蛋白、聚合酶(L)蛋白和附着(G)蛋白的全部或部分基因进行了序列分析。这两株分离株的核苷酸(nt)序列同一性至少为99.7%,氨基酸(aa)序列同一性至少为99.0%。与A亚组、B亚组或科罗拉多APV的F基因比较显示,nt序列同一性为70.0 - 80.5%,aa序列同一性为77.6 - 97.2%;L基因与一株A亚组分离株的nt序列同一性为76.1%,aa序列同一性为85.3%。Fr/85/1和Fr/85/2的G基因由1185个nt组成,编码一个含389个aa的蛋白。与A亚组和B亚组G蛋白的共同特征包括一个氨基末端膜锚定区、高丝氨酸和苏氨酸含量、半胱氨酸残基的保守性以及一个高度保守序列的单一细胞外区域,该区域被认为是病毒附着细胞受体的功能域。然而,Fr/85/1和Fr/85/2与A亚组和B亚组APV的G序列,nt序列同一性最高为56.6%,aa序列同一性最高为31.2%,而这些分离株之间的aa序列同一性为38%。肺炎病毒F、G和L基因的系统发育分析表明,分离株Fr/85/1和Fr/85/2属于一个先前未被识别的APV亚组,暂命名为D亚组。定义了基于G基因的寡核苷酸引物用于D亚组的特异性分子鉴定。这些是首次测定的非A/非B型APV的G蛋白序列。

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