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欧洲2型蝙蝠狂犬病病毒的进化趋势,包括相隔24年的源自人类和蝙蝠的芬兰毒株的基因特征分析

Evolutionary trends of European bat lyssavirus type 2 including genetic characterization of Finnish strains of human and bat origin 24 years apart.

作者信息

Jakava-Viljanen Miia, Nokireki Tiina, Sironen Tarja, Vapalahti Olli, Sihvonen Liisa, Huovilainen Anita

出版信息

Arch Virol. 2015 Jun;160(6):1489-98. doi: 10.1007/s00705-015-2424-0. Epub 2015 Apr 17.

Abstract

Among other Lyssaviruses, Daubenton's and pond-bat-related European bat lyssavirus type 2 (EBLV-2) can cause human rabies. To investigate the diversity and evolutionary trends of EBLV-2, complete genome sequences of two Finnish isolates were analysed. One originated from a human case in 1985, and the other originated from a bat in 2009. The overall nucleotide and deduced amino acid sequence identity of the two Finnish isolates were high, as well as the similarity to fully sequenced EBLV-2 strains originating from the UK and the Netherlands. In phylogenetic analysis, the EBLV-2 strains formed a monophyletic group that was separate from other bat-type lyssaviruses, with significant support. EBLV-2 shared the most recent common ancestry with Bokeloh bat lyssavirus (BBLV) and Khujan virus (KHUV). EBLV-2 showed limited diversity compared to RABV and appears to be well adapted to its host bat species. The slow tempo of viral evolution was evident in the estimations of divergence times for EBLV-2: the current diversity was estimated to have built up during the last 2000 years, and EBLV-2 diverged from KHUV about 8000 years ago. In a phylogenetic tree of partial N gene sequences, the Finnish EBLV-2 strains clustered with strains from Central Europe, supporting the hypothesis that EBLV-2 circulating in Finland might have a Central European origin. The Finnish EBLV-2 strains and a Swiss strain were estimated to have diverged from other EBLV-2 strains during the last 1000 years, and the two Finnish strains appear to have evolved from a common ancestor during the last 200 years.

摘要

在其他狂犬病毒属病毒中,道本病毒及与池栖蝙蝠相关的欧洲蝙蝠狂犬病毒2型(EBLV - 2)可导致人类狂犬病。为研究EBLV - 2的多样性和进化趋势,对两株芬兰分离株的全基因组序列进行了分析。一株源自1985年的一例人类病例,另一株源自2009年的一只蝙蝠。这两株芬兰分离株的总体核苷酸和推导氨基酸序列同一性很高,与源自英国和荷兰的已完成全序列测定的EBLV - 2毒株的相似性也很高。在系统发育分析中,EBLV - 2毒株形成了一个单系群,与其他蝙蝠型狂犬病毒属病毒分开,且有显著的支持度。EBLV - 2与博克洛蝙蝠狂犬病毒(BBLV)和库占病毒(KHUV)拥有最近的共同祖先。与狂犬病病毒(RABV)相比,EBLV - 2显示出有限的多样性,并且似乎已很好地适应了其宿主蝙蝠物种。EBLV - 2分歧时间的估计表明病毒进化速度缓慢:目前的多样性估计是在过去2000年中积累起来的,EBLV - 2约在8000年前与KHUV分化。在部分N基因序列的系统发育树中,芬兰的EBLV - 2毒株与来自中欧的毒株聚类,支持了在芬兰传播的EBLV - 2可能起源于中欧的假说。估计芬兰的EBLV - 2毒株和一株瑞士毒株在过去1000年中与其他EBLV - 2毒株发生了分化,而这两株芬兰毒株似乎在过去200年中从一个共同祖先进化而来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2341/4429142/2b23813ad19c/705_2015_2424_Fig1_HTML.jpg

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