Department of Medical Microbiology and Parasitology, Ladoke Akintola University of Technology, Osogbo 230222, Nigeria.
Science Laboratory Technology Department, Federal Polytechnic, Ede 232101, Nigeria.
Viruses. 2019 Nov 7;11(11):1037. doi: 10.3390/v11111037.
Human enteroviruses and human parechoviruses are associated with a broad range of diseases and even severe and fatal conditions. For human cosaviruses, the etiological role is yet unknown. Little is known about the circulation of non-polio enteroviruses, human parechoviruses, and human cosaviruses in Nigeria. A total of 113 stool samples were collected from healthy individuals in Osun State between February 2016 and May 2017. RT-PCR assays targeting the 5' non-coding region (5' -NCR) were used to screen for human enteroviruses, human parechoviruses, and human cosaviruses. For human enteroviruses, species-specific RT-PCR assays targeting the VP1 regions were used for molecular typing. Inoculation was carried out on RD-A, CaCo-2, HEp-2C, and L20B cell lines to compare molecular and virological assays. Ten samples tested positive for enterovirus RNA with 11 strains detected, including CV-A13 ( = 3), E-18 ( = 2), CV-A20 ( = 1), CV-A24 ( = 1), EV-C99 ( = 1), and EV-C116 ( = 2). Three samples tested positive for human parechovirus RNA, and full genome sequencing on two samples allowed assignment to a new Parechovirus A type (HPeV-19). Thirty-three samples tested positive for cosavirus with assignment to species Cosavirus D and Cosavirus A based on the 5'-NCR region. Screening of stool samples collected from healthy individuals in Nigeria in 2016 and 2017 revealed a high diversity of circulating human enteroviruses, human parechoviruses, and human cosaviruses. Molecular assays for genotyping showed substantial benefits compared with those of cell-culture assays.
人肠道病毒和人肠道病毒属副病毒与广泛的疾病甚至严重和致命的疾病有关。至于人肠道冠状病毒,其病因作用尚不清楚。关于尼日利亚非脊髓灰质炎肠道病毒、人肠道病毒属副病毒和人肠道冠状病毒的传播情况知之甚少。2016 年 2 月至 2017 年 5 月期间,从奥孙州的健康个体中采集了 113 份粪便样本。使用针对 5'非编码区(5'-NCR)的 RT-PCR 检测方法筛查人肠道病毒、人肠道病毒属副病毒和人肠道冠状病毒。针对 VP1 区的种特异性 RT-PCR 检测方法用于分子分型。在 RD-A、CaCo-2、HEp-2C 和 L20B 细胞系上进行接种,以比较分子和病毒学检测方法。10 个样本的肠道病毒 RNA 检测呈阳性,共检测到 11 株病毒,包括 CV-A13(=3)、E-18(=2)、CV-A20(=1)、CV-A24(=1)、EV-C99(=1)和 EV-C116(=2)。3 个样本的人肠道病毒属副病毒 RNA 检测呈阳性,对 2 个样本进行全基因组测序,将其分配到一种新的肠道病毒属副病毒 A 型(HPeV-19)。33 个样本的肠道冠状病毒检测呈阳性,根据 5'-NCR 区将其分配到肠道冠状病毒 D 种和肠道冠状病毒 A 种。2016 年和 2017 年对尼日利亚健康个体粪便样本的筛查显示,循环的人肠道病毒、人肠道病毒属副病毒和人肠道冠状病毒具有高度多样性。与细胞培养检测方法相比,基因分型的分子检测方法具有明显优势。