Matthijnssens Jelle, Rahman Mustafizur, Van Ranst Marc
Laboratory of Clinical and Epidemiological Virology, Department of Microbiology and Immunology, Rega Institute for Medical Research, University of Leuven, Leuven, Belgium.
Laboratory of Virology, ICDDR,B: Centre for Health and Population Research, Dhaka, Bangladesh.
J Gen Virol. 2008 Oct;89(Pt 10):2630-2635. doi: 10.1099/vir.0.2008/003780-0.
In 2003, we described the first human G6P[6] rotavirus strain (B1711). To investigate further the molecular origin of this strain and to determine the possible reassortments leading to this new gene constellation, the complete genome of strain B1711 was sequenced. SimPlot analyses were conducted to compare strain B1711 with other known rotavirus gene segments, and phylogenetic dendrograms were constructed to analyse the origin of the eleven genome segments of strain B1711. Our analysis indicated that strain B1711 acquired its VP1-, VP2-, VP4-, VP6- and NSP1-5-encoding gene segments from human DS-1-like P[6] rotavirus strains, and its VP3 and VP7 gene segments from a bovine rotavirus strain through reassortment. The introduction of animal-human reassortant strains, which might arise in either of the hosts, into the human rotavirus population is an important mechanism for the generation of rotavirus diversity, and might be a challenge for the current rotavirus vaccines and vaccines under development.
2003年,我们描述了第一株人G6P[6]轮状病毒毒株(B1711)。为了进一步研究该毒株的分子起源,并确定导致这种新基因组合的可能重配情况,我们对B1711毒株的全基因组进行了测序。进行了SimPlot分析,以将B1711毒株与其他已知的轮状病毒基因片段进行比较,并构建了系统发育树状图,以分析B1711毒株11个基因组片段的起源。我们的分析表明,B1711毒株通过重配从人DS-1样P[6]轮状病毒毒株获得了其编码VP1、VP2、VP4、VP6和NSP1-5的基因片段,其VP3和VP7基因片段则来自一株牛轮状病毒毒株。动物-人重配毒株可能在任何一种宿主中出现,并引入人轮状病毒群体,这是轮状病毒多样性产生的一个重要机制,可能对当前的轮状病毒疫苗和正在研发的疫苗构成挑战。