Circulation of Rotavirus Genotypes and their Distribution among Vaccinated and Non-vaccinated Children in Abuja, Nigeria

B. Balarabe-Musa
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Abstract

Introduction: Nigeria had planned to introduce the rotavirus vaccine in the National Immunisation Programme in 2014 but this has yet to be done. Nigeria has the continent’s highest mortality due to diarrhoeal diseases with little information on specific prevalent genotypes. The main objectives of the study were to identify the predominant rotavirus genotypes and to examine the effects of existing local vaccination programmes on prevailing rotavirus genotypes and on preventing rotavirus diarrhoea. Methodology: A one-year prospective descriptive study of children under 5 with acute diarrhoea was conducted from September 2012 to August 2013. Children with acute diarrhoea attending three government hospitals and one private hospital were recruited. Children without diarrhoea were also recruited as a control group. Rotavirus ELISA and RNA extraction were done with commercially available kits and positive samples were subjected to RT-PCR and electrophoresis to determine VP7 (G) and VP4 (P) genotypes. Results: Stool samples were collected from 1240 (93.3%) participants, of whom 957 (77.0%) were ambulatory, 123 (9.9%) hospitalised and 160 (12.8%) controls without diarrhoea. Rotavirus-ELISA was positive among 123 (11.4%) children with diarrhoea. The predominant VP7 genotypes were G2 (n=33, 26.4%) followed by G9 (n=24, 19.2). The main VP4 (P) genotypes included P [4] (n=45, 36.0%) followed by P [6] (n=40, 32.0%). The predominant genotype combinations found were G2 P [4] (n=21, 16.8%), G3 P [6] and G1 P [6] (each n=16, 12.8%), and G12 P [8] (n=15, 12.0%). Very few mixed infections were found in only one government hospital 4 (6.4%). Among 94 unvaccinated children with rotavirus isolates that were genotyped, G2 P [4] (n=19, 20.2%) and G1 P [6] (n=16, 17.0%) were predominant. Among 12 vaccinated children, 2 isolates each (16.6%) were found of G3 P [6], G9 P [4], G12 P [8] and G2 P [NT] with no G1 isolates. Conclusion: The emergence of new genotypes such as G 12 P [8] found in this study emphasizes the need for continued prospective monitoring of rotavirus at the molecular level to detect new threats to vaccine programmes in future.
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尼日利亚阿布贾轮状病毒基因型的传播及其在接种疫苗和未接种疫苗儿童中的分布
导言:尼日利亚曾计划在2014年将轮状病毒疫苗纳入国家免疫规划,但这一计划尚未完成。尼日利亚是非洲大陆腹泻病死亡率最高的国家,而关于具体流行基因型的信息很少。该研究的主要目的是确定主要的轮状病毒基因型,并检查现有的地方疫苗接种规划对流行的轮状病毒基因型和预防轮状病毒腹泻的影响。方法:2012年9月至2013年8月对5岁以下急性腹泻患儿进行为期一年的前瞻性描述性研究。在三所政府医院和一所私立医院招募患有急性腹泻的儿童。没有腹泻的儿童也被招募为对照组。采用市售试剂盒对轮状病毒进行酶联免疫吸附试验和RNA提取,阳性样本进行RT-PCR和电泳检测VP7 (G)和VP4 (P)基因型。结果:收集了1240名(93.3%)参与者的粪便样本,其中957名(77.0%)是流动的,123名(9.9%)是住院的,160名(12.8%)是没有腹泻的对照组。123例(11.4%)腹泻患儿轮状病毒elisa阳性。VP7的优势基因型为G2 (n=33, 26.4%),其次为G9 (n=24, 19.2%)。VP4 (P)主要基因型为P [4] (n=45, 36.0%),其次为P [6] (n=40, 32.0%)。主要基因型组合为G2 P [4] (n=21, 16.8%)、G3 P[6]和G1 P[6](各n=16, 12.8%)和G12 P [8] (n=15, 12.0%)。只有一家政府医院4(6.4%)发现了极少数混合感染。在94例未接种疫苗的轮状病毒分离株中,G2 P [4] (n=19, 20.2%)和G1 P [6] (n=16, 17.0%)占主导地位。12例接种儿童中,G3 P[6]、G9 P[4]、G12 P[8]、G2 P [NT]各2株(16.6%),无G1分离株。结论:本研究中发现的g12p[8]等新基因型的出现,强调需要在分子水平上继续对轮状病毒进行前瞻性监测,以发现未来疫苗规划的新威胁。
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