Agoti Charles N, Munywoki Patrick K, Phan My V T, Otieno James R, Kamau Everlyn, Bett Anne, Kombe Ivy, Githinji George, Medley Graham F, Cane Patricia A, Kellam Paul, Cotten Matthew, Nokes D James
Epidemiology and Demography Department, Kenya Medical Research Institute (KEMRI) - Wellcome Trust Research Collaborative Programme, Kilifi, Kenya.
School of Health and Human Sciences, Pwani University, Kilifi, Kenya.
Virus Evol. 2017 Mar 11;3(1):vex006. doi: 10.1093/ve/vex006. eCollection 2017 Jan.
Detailed information on the source, spread and evolution of respiratory syncytial virus (RSV) during seasonal community outbreaks remains sparse. Molecular analyses of attachment (G) gene sequences from hospitalized cases suggest that multiple genotypes and variants co-circulate during epidemics and that RSV persistence over successive seasons is characterized by replacement and multiple new introductions of variants. No studies have defined the patterns of introduction, spread and evolution of RSV at the local community and household level. We present a whole genome sequence analysis of 131 RSV group A viruses collected during 6-month household-based RSV infection surveillance in Coastal Kenya, 2010 within an area of 12 km. RSV infections were identified by regular symptom-independent screening of all household members twice weekly. Phylogenetic analysis revealed that the RSV A viruses in nine households were closely related to genotype GA2 and fell within a single branch of the global phylogeny. Genomic analysis allowed the detection of household-specific variation in seven households. For comparison, using only G gene analysis, household-specific variation was found only in one of the nine households. Nucleotide changes were observed both intra-host (viruses identified from same individual in follow-up sampling) and inter-host (viruses identified from different household members) and these coupled with sampling dates enabled a partial reconstruction of the within household transmission chains. The genomic evolutionary rate for the household dataset was estimated as 2.307 × 10 (95% highest posterior density: 0.935-4.165× 10 ) substitutions/site/year. We conclude that (i) at the household level, most RSV infections arise from the introduction of a single virus variant followed by accumulation of household specific variation and (ii) analysis of complete virus genomes is crucial to better understand viral transmission in the community. A key question arising is whether prevention of RSV introduction or spread within the household by vaccinating key transmitting household members would lead to a reduced onward community-wide transmission.
关于呼吸道合胞病毒(RSV)在季节性社区暴发期间的来源、传播和演变的详细信息仍然匮乏。对住院病例的附着(G)基因序列进行的分子分析表明,多种基因型和变异株在流行期间共同传播,并且RSV在连续季节中的持续存在表现为变异株的替代和多次新引入。尚无研究明确RSV在当地社区和家庭层面的引入、传播和演变模式。我们对2010年在肯尼亚沿海地区12公里范围内进行的为期6个月的基于家庭的RSV感染监测期间收集的131株RSV A组病毒进行了全基因组序列分析。通过每周对所有家庭成员进行两次常规的与症状无关的筛查来确定RSV感染。系统发育分析显示,九个家庭中的RSV A病毒与GA2基因型密切相关,并属于全球系统发育的一个单一分支。基因组分析能够检测到七个家庭中的家庭特异性变异。相比之下,仅使用G基因分析时,仅在九个家庭中的一个家庭中发现了家庭特异性变异。在宿主内(后续采样中从同一个体鉴定出的病毒)和宿主间(从不同家庭成员鉴定出的病毒)均观察到核苷酸变化,这些变化与采样日期相结合,使得能够部分重建家庭内传播链。家庭数据集的基因组进化速率估计为2.307×10(95%最高后验密度:0.935 - 4.165×10)替换/位点/年。我们得出结论:(i)在家庭层面,大多数RSV感染源于单一病毒变异株的引入,随后是家庭特异性变异的积累;(ii)对完整病毒基因组的分析对于更好地理解社区中的病毒传播至关重要。由此产生的一个关键问题是,通过为关键的家庭传播成员接种疫苗来预防RSV在家庭内的引入或传播,是否会导致社区范围内后续传播的减少。