Department of Microbiology, Faculty of Science, Obafemi Awolowo University, Ile-Ife, Osun State, Nigeria.
Department of Microbiology, Faculty of Science, Ekiti State University, Ado-Ekiti, Ekiti State, Nigeria.
J Med Virol. 2018 Feb;90(2):239-249. doi: 10.1002/jmv.24949. Epub 2017 Sep 26.
Nigeria having approximately 50 000 Rotavirus A (RVA) deaths annually is yet to introduce RVA vaccine into routine national immunization; therefore surveillance of RVA strains circulating before vaccine introduction is essential in evaluating impact of the intervention. Stool samples and sociodemographic data of diarrhoeic children, <5 years were collected between August 2012 and December 2013. While a high prevalence of RVA infection (47.6%; 49/103) was observed by quantitative reverse transcription real time PCR, only 25% (26/103) had high RVA genome concentrations and were antigen positive. G and P types were obtained for 31 and 37 samples respectively. G12P[8] strains were predominant (30.6%; 16/31); Other genotypes found included G9, G3, G2 and P[4], P[6], P[8]. A G12 + G2/P[8] + P[6] mixed infection was detected. The P[8] genotype showed divergence with strains distributed in lineage III and IV. Compared to the vaccines, changes in antigenic sites of VP8* and VP7 were found. The finding of the G2P[6] genotype combination and emergence of G12 strains support observations in most of the recent RVA studies from Africa. P[6] is common in many African countries, in contrast to countries in Europe and the Americas. In conclusion, this study shows the circulation of other RVA genotypes compared to the common RVA genotypes in Nigeria. PCR results should be interpreted with caution to avoid significant bias from samples with low RVA genome concentrations. These findings provide important information on the detection and molecular epidemiology of RVA prior to vaccination and contribute as a baseline for future evaluations after possible vaccine introduction.
尼日利亚每年约有 50000 人死于轮状病毒 A(RVA),尚未将 RVA 疫苗纳入常规国家免疫计划;因此,在疫苗引入之前,对循环 RVA 株的监测对于评估干预措施的影响至关重要。本研究于 2012 年 8 月至 2013 年 12 月期间收集了 5 岁以下腹泻儿童的粪便样本和社会人口统计学数据。虽然定量逆转录实时 PCR 检测到 RVA 感染率很高(47.6%;49/103),但只有 25%(26/103)具有高 RVA 基因组浓度和抗原阳性。分别获得了 31 个和 37 个样本的 G 和 P 型。G12P[8]株占主导地位(30.6%;16/31);其他基因型包括 G9、G3、G2 和 P[4]、P[6]、P[8]。检测到 G12+G2/P[8]+P[6]混合感染。P[8]基因型与分布在谱系 III 和 IV 的菌株有差异。与疫苗相比,VP8*和 VP7 的抗原位点发生了变化。G2P[6]基因型组合和 G12 株的出现支持了最近来自非洲的大多数 RVA 研究的观察结果。P[6]在许多非洲国家很常见,而在欧洲和美洲国家则不然。综上所述,本研究显示,与尼日利亚常见的 RVA 基因型相比,目前循环的 RVA 基因型有所不同。PCR 结果应谨慎解释,以避免低 RVA 基因组浓度样本的显著偏差。这些发现为疫苗接种前 RVA 的检测和分子流行病学提供了重要信息,并为可能引入疫苗后的未来评估提供了基线。