Division of Molecular Pathobiology, Research Center for Zoonosis Control, Hokkaido University, Sapporo 001-0020, Japan.
Hokudai Center for Zoonosis Control in Zambia, Research Center for Zoonosis Control, Hokkaido University, Lusaka 10101, Zambia.
Viruses. 2020 Sep 11;12(9):1017. doi: 10.3390/v12091017.
To monitor the arthropod-borne virus transmission in mosquitoes, we have attempted both to detect and isolate viruses from 3304 wild-caught female mosquitoes in the Livingstone (Southern Province) and Mongu (Western Province) regions in Zambia in 2017. A pan-flavivirus RT-PCR assay was performed to identify flavivirus genomes in total RNA extracted from mosquito lysates, followed by virus isolation and full genome sequence analysis using next-generation sequencing and rapid amplification of cDNA ends. We isolated a newly identified Barkedji virus (BJV Zambia) (10,899 nt) and a novel flavivirus, tentatively termed Barkedji-like virus (BJLV) (10,885 nt) from spp. mosquitoes which shared 96% and 75% nucleotide identity with BJV which has been isolated in Israel, respectively. These viruses could replicate in C6/36 cells but not in mammalian and avian cell lines. In parallel, a comparative genomics screening was conducted to study evolutionary traits of the 5'- and 3'-untranslated regions (UTRs) of isolated viruses. Bioinformatic analyses of the secondary structures in the UTRs of both viruses revealed that the 5'-UTRs exhibit canonical stem-loop structures, while the 3'-UTRs contain structural homologs to exoribonuclease-resistant RNAs (xrRNAs), SL-III, dumbbell, and terminal stem-loop (3'SL) structures. The function of predicted xrRNA structures to stop RNA degradation by Xrn1 exoribonuclease was further proved by the in vitro Xrn1 resistance assay.
为了监测蚊媒传播的虫媒病毒,我们尝试从 2017 年赞比亚利文斯顿(南部省)和蒙古(西部省)地区采集的 3304 只野生雌性蚊子中检测和分离病毒。我们使用 pan-flavivirus RT-PCR 检测从蚊子裂解物中提取的总 RNA 中的黄病毒基因组,然后使用下一代测序和快速扩增 cDNA 末端进行病毒分离和全基因组序列分析。我们从 种蚊子中分离出一种新鉴定的 Barkedji 病毒(BJV Zambia)(10899nt)和一种新的黄病毒,暂命名为 Barkedji-like 病毒(BJLV)(10885nt),它们与在以色列分离的 BJV 的核苷酸同一性分别为 96%和 75%。这些病毒可以在 C6/36 细胞中复制,但不能在哺乳动物和禽类细胞系中复制。同时,我们进行了比较基因组学筛选,以研究分离病毒 5'-和 3'-非翻译区(UTR)的进化特征。对两种病毒 UTR 二级结构的生物信息学分析表明,5'-UTR 具有典型的茎环结构,而 3'-UTR 包含结构类似物的外切核酸酶抗性 RNA(xrRNA)、SL-III、哑铃和末端茎环(3'SL)结构。通过体外 Xrn1 抗性测定进一步证明了预测的 xrRNA 结构对 Xrn1 外切核酸酶阻止 RNA 降解的功能。