Centre National de Référence du virus de l'hépatite E, Laboratoire de Virologie, Hôpital Purpan, CHU de Toulouse, Toulouse, France.
Plateforme Génomique, Centre INRA Occitanie-Toulouse, Castanet-Tolosan, France.
Rev Med Virol. 2018 Sep;28(5):e1987. doi: 10.1002/rmv.1987. Epub 2018 Jun 25.
Hepatitis E virus genotype 3 (HEV-3) can lead to chronic infection in immunocompromised patients, and ribavirin is the treatment of choice. Recently, mutations in the polymerase gene have been associated with ribavirin failure but their frequency before treatment according to HEV-3 subtypes has not been studied on a large data set. We used single-molecule real-time sequencing technology to sequence 115 new complete genomes of HEV-3 infecting French patients. We analyzed phylogenetic relationships, the length of the polyproline region, and mutations in the HEV polymerase gene. Eighty-five (74%) were in the clade HEV-3efg, 28 (24%) in HEV-3chi clade, and 2 (2%) in HEV-3ra clade. Using automated partitioning of maximum likelihood phylogenetic trees, complete genomes were classified into subtypes. Polyproline region length differs within HEV-3 clades (from 189 to 315 nt). Investigating mutations in the polymerase gene, distinct polymorphisms between HEV-3 subtypes were found (G1634R in 95% of HEV-3e, G1634K in 56% of HEV-3ra, and V1479I in all HEV-3efg, clade HEV-3ra, and HEV-3k strains). Subtype-specific polymorphisms in the HEV-3 polymerase have been identified. Our study provides new complete genome sequences of HEV-3 that could be useful for comparing strains circulating in humans and the animal reservoir.
戊型肝炎病毒基因型 3(HEV-3)可导致免疫功能低下患者发生慢性感染,利巴韦林是其治疗的首选药物。最近,聚合酶基因的突变与利巴韦林治疗失败相关,但尚未在大样本数据集中根据 HEV-3 亚型研究治疗前这些突变的发生频率。我们使用单分子实时测序技术对 115 例新的法国感染 HEV-3 的患者的完整基因组进行了测序。我们分析了系统发育关系、多聚脯氨酸区的长度以及 HEV 聚合酶基因的突变。85 例(74%)属于 HEV-3efg 分支,28 例(24%)属于 HEV-3chi 分支,2 例(2%)属于 HEV-3ra 分支。使用最大似然系统发育树的自动分区,对完整基因组进行了亚型分类。HEV-3 分支内的多聚脯氨酸区长度不同(189-315 nt)。对聚合酶基因的突变进行研究,发现了 HEV-3 亚型之间存在独特的多态性(HEV-3e 中 95%存在 G1634R,HEV-3ra 中 56%存在 G1634K,所有 HEV-3efg、HEV-3ra 和 HEV-3k 株均存在 V1479I)。已鉴定出 HEV-3 聚合酶的亚型特异性多态性。本研究提供了 HEV-3 的新的完整基因组序列,可用于比较在人和动物宿主中循环的菌株。