Lobigs M, Marshall I D, Weir R C, Dalgarno L
Aust J Exp Biol Med Sci. 1986 Dec;64 ( Pt 6):571-85. doi: 10.1038/icb.1986.61.
The genetic relatedness of ten Murray Valley encephalitis virus (MVE) isolates from Australia has been examined by comparing HaeIII and TaqI restriction digest profiles of cDNA to virion RNA. The isolates were from the Murray Valley region of south-eastern Australia and from the Ord River region of Western Australia and spanned a period of 23 years (1951-1974). The isolates generated closely similar restriction digest profiles. The extent of similarity suggested that the level of nucleotide sequence divergence between any pair of Australian MVE isolates is probably around 1%. The genetic homogeneity of the MVE isolates contrasts with results obtained for Ross River virus, an alphavirus, using an identical methodological approach; we propose that this difference results from the important role of birds in the life cycle of MVE. Four MVE isolates from three fatal human cases showed small genetic differences one from the other. These isolates did not have a common restriction digest profile which distinguished them from strains obtained from other sources (e.g., from mosquitoes or a heron). The data do not support the view that clinical cases of MVE infection in humans are due to a particular strain of virus although this has not been rigorously excluded. The two available MVE isolates from Papua New Guinea (PNG) were from the Sepik and Port Moresby regions. They generated HaeIII and TaqI restriction digest profiles which were different both from each other and from those of the Australian type. Genetic divergence between the two PNG isolates was estimated to be approximately 6%; divergence between either of the PNG isolates and the Australian type was greater than 6%. Our data suggest that the evolution of MVE in Australia and PNG has proceeded independently and that circulating Australian MVE strains are not systematically re-seeded from regions of endemicity in PNG. Studies on the relatedness of MVE and two close antigenic relatives, Japanese encephalitis virus (JE) and Alfuy virus (ALF), showed that the genetic relatedness between any MVE isolate and JE or ALF is less than that between the most divergent of the MVE isolates, including those from Papua New Guinea.
通过比较病毒粒子RNA的cDNA的HaeIII和TaqI限制性酶切图谱,对来自澳大利亚的10株墨累谷脑炎病毒(MVE)分离株的遗传相关性进行了研究。这些分离株来自澳大利亚东南部的墨累谷地区和西澳大利亚的奥德河地区,跨越了23年(1951 - 1974年)。这些分离株产生了极为相似的限制性酶切图谱。相似程度表明,任何一对澳大利亚MVE分离株之间的核苷酸序列差异水平可能约为1%。MVE分离株的遗传同质性与使用相同方法对甲病毒罗斯河病毒所获得的结果形成对比;我们认为这种差异是由于鸟类在MVE生命周期中的重要作用所致。来自3例致命人类病例的4株MVE分离株彼此之间显示出微小的遗传差异。这些分离株没有共同的限制性酶切图谱,使其与从其他来源(例如蚊子或一只苍鹭)获得的毒株区分开来。尽管尚未严格排除,但这些数据并不支持人类MVE感染临床病例是由特定病毒株引起的观点。来自巴布亚新几内亚(PNG)的两株可用MVE分离株分别来自塞皮克地区和莫尔斯比港地区。它们产生的HaeIII和TaqI限制性酶切图谱彼此不同,也与澳大利亚类型的不同。两株PNG分离株之间的遗传差异估计约为6%;任何一株PNG分离株与澳大利亚类型之间的差异均大于6%。我们的数据表明,MVE在澳大利亚和PNG的进化是独立进行的,并且在澳大利亚传播的MVE毒株并非系统地从PNG的地方性流行区域重新接种而来。对MVE与两个密切抗原相关病毒——日本脑炎病毒(JE)和阿尔富伊病毒(ALF)的相关性研究表明,任何MVE分离株与JE或ALF之间的遗传相关性都小于MVE分离株中差异最大的分离株之间的相关性,包括来自巴布亚新几内亚的分离株。