a Veterinary Department, Faculty of Sciences , Namur Research Institute for Life Sciences (NARILIS), University of Namur (UNamur) Namur , Belgium.
b Department of Morphology and Pathology, FARAH Research Center, Faculty of Veterinary Medicine , University of Liège Liège , Belgium.
Emerg Microbes Infect. 2019;8(1):381-395. doi: 10.1080/22221751.2019.1586410.
Orthobunyaviruses are arboviruses (Arthropod Borne Virus) and possess multipartite genomes made up of three negative RNAs corresponding to the small (S), medium (M) and large (L) segments. Reassortment and recombination are evolutionary driving forces of such segmented viruses and lead to the emergence of new strains and species. Retrospective studies based on phylogenetical analysis are able to evaluate these mechanisms at the end of the selection process but fail to address the dynamics of emergence. This issue was addressed using two Orthobunyaviruses infecting ruminants and belonging to the Simbu serogroup: the Sathuperi virus (SATV) and the Shamonda virus (SHAV). Both viruses were associated with abortion, stillbirth and congenital malformations occurring after transplacental transmission and were suspected to spread together in different ruminant and insect populations. This study showed that different viruses related to SHAV and SATV are spreading simultaneously in ruminants and equids of the Sub-Saharan region. Their reassortment and recombination potential was evaluated in mammalian and in insect contexts. A method was set up to determine the genomic background of any clonal progeny viruses isolated after in vitro coinfections assays. All the reassortment combinations were generated in both contexts while no recombinant virus was isolated. Progeny virus populations revealed a high level of reassortment in mammalian cells and a much lower level in insect cells. In vitro selection pressure that mimicked the host switching (insect-mammal) revealed that the best adapted reassortant virus was connected with an advantageous replicative fitness and with the presence of a specific segment.
正粘病毒是虫媒病毒(节肢动物传播的病毒),具有由三个负 RNA 组成的分段基因组,分别对应小(S)、中(M)和大(L)片段。重配和重组是此类分段病毒的进化驱动力,导致新毒株和新种的出现。基于系统发育分析的回顾性研究能够在选择过程结束时评估这些机制,但无法解决出现的动态问题。本研究使用两种感染反刍动物并属于 Simbu 血清群的正粘病毒:Sathuperi 病毒(SATV)和 Shamonda 病毒(SHAV)来解决这个问题。这两种病毒都与经胎盘传播后的流产、死产和先天性畸形有关,并且怀疑它们在不同的反刍动物和昆虫种群中共同传播。本研究表明,与 SHAV 和 SATV 相关的不同病毒正在撒哈拉以南地区的反刍动物和马属动物中同时传播。评估了它们在哺乳动物和昆虫环境中的重配和重组潜力。建立了一种方法来确定在体外共感染试验后分离的任何克隆后代病毒的基因组背景。在两种情况下都产生了所有的重配组合,而没有分离到重组病毒。子代病毒群体在哺乳动物细胞中表现出高水平的重配,而在昆虫细胞中则水平较低。体外选择压力模拟了宿主转换(昆虫-哺乳动物),表明最佳适应的重组病毒与有利的复制适应性和特定片段的存在有关。