Department of Biochemistry, Kenyatta University, Nairobi, Kenya.
Center for Virus Research, Kenya Medical Research Institute (KEMRI), Nairobi, Kenya.
Influenza Other Respir Viruses. 2022 May;16(3):501-510. doi: 10.1111/irv.12948. Epub 2021 Dec 27.
Human respiratory syncytial virus (HRSV) is a major cause of severe viral acute respiratory illness and contributes significantly to severe pneumonia cases in Africa. Little is known about its spatial-temporal distribution as defined by its genetic diversity.
A retrospective study conducted utilizing archived nasopharyngeal specimens from patients attending outpatient clinics in hospitals located in five demographically and climatically distinct regions of Kenya; Coast, Western, Highlands, Eastern and Nairobi. The viral total RNA was extracted and tested using multiplex real time RT-PCR (reverse transcriptase polymerase chain reaction). A segment of the G-gene was amplified using one-step RT-PCR and sequenced by Sanger di-deoxy method. Bayesian analysis of phylogeny was utilized and subsequently median joining methods for haplotype network reconstruction.
Three genotypes of HRSVA were detected; GA5 (14.0%), GA2 (33.1%), and NA1 (52.9%). HRSVA prevalence varied by location from 33% to 13.2% in the Highlands and the Eastern regions respectively. The mean nucleotide diversity (Pi[π]) varied by genotype: highest of 0.018 for GA5 and lowest of 0.005 for NA1. A total of 58 haplotypes were identified (GA5 10; GA2 20; NA1 28). These haplotypes were introduced into the population locally by single haplotypes and additional subsidiary seeds amongst the GA2 and the NA1 haplotypes.
HRSVA was found across all the regions throughout the study period and comprised three genotypes; GA5, GA2, and NA1 genotypes. The genotypes were disproportionately distributed across the regions with GA5 gradually increasing toward the Western zones and decreasing toward the Eastern zones of the country.
人类呼吸道合胞病毒(HRSV)是导致严重病毒性急性呼吸道疾病的主要原因,也是非洲严重肺炎病例的主要原因。目前,人们对其遗传多样性所定义的时空分布知之甚少。
本研究采用回顾性研究方法,利用肯尼亚五个地理位置和气候截然不同的地区(沿海、西部、高地、东部和内罗毕)医院门诊患者的存档鼻咽标本进行研究。采用多重实时 RT-PCR(逆转录酶聚合酶链反应)提取和检测病毒总 RNA。采用一步 RT-PCR 扩增 G 基因,并通过 Sanger 双脱氧法测序。利用贝叶斯分析方法进行系统发育分析,随后采用中位数连接法进行单倍型网络重建。
检测到三种 HRSVA 基因型;GA5(14.0%)、GA2(33.1%)和 NA1(52.9%)。HRSVA 流行率因地理位置而异,高地区域和东部区域分别为 33%和 13.2%。不同基因型的平均核苷酸多样性(Pi[π])也不同:GA5 最高为 0.018,NA1 最低为 0.005。共鉴定出 58 种单倍型(GA5 10 种;GA2 20 种;NA1 28 种)。这些单倍型是由单倍型和 GA2 及 NA1 单倍型中的额外辅助种子在当地引入人群的。
本研究在整个研究期间在所有地区均发现了 HRSVA,包括三种基因型:GA5、GA2 和 NA1 基因型。基因型在各地区的分布不均,GA5 逐渐向西部区域增加,向东部区域减少。