Molecular Analysis of Human Respiratory Syncytial Virus Group B Strains Isolated in Kenya Before and During the Emergence of Pandemic Influenza A/H1N1

被引:1
作者
Wangui, Julia [1 ,2 ]
Gachara, George [3 ]
Mobegi, Victor [4 ]
Agoti, Charles [5 ]
Otieno, James [6 ]
Opanda, Silvanos [1 ]
Opot, Benjamin [1 ]
Ngeranwa, Joseph N. [2 ]
Njeru, Regina [7 ]
Bulimo, Wallace [1 ]
机构
[1] Kenya Med Res Inst KEMRI, Ctr Virus Res, Nairobi, Kenya
[2] Kenyatta Univ, Dept Biochem, Nairobi, Kenya
[3] Kenyatta Univ, Dept Med Lab Sci, Nairobi, Kenya
[4] Univ Nairobi, Dept Biochem, Nairobi, Kenya
[5] Kenya Med Res Inst KEMRI, Dept Epidemiol & Demog, Wellcome Trust Program, Nairobi, Kenya
[6] Theiagen Genom, Highlands Ranch, CO USA
[7] Int Livestock Res Inst, Nairobi, Kenya
关键词
COVID-19; pandemic; evolution; genetic variability; HRSV-B genotypes; pandemic influenza; recombination; SARS-CoV-2; spatial-temporal trends; G-PROTEIN; GENETIC-VARIABILITY; EVOLUTION; GENOTYPES; RECOMBINATION; DUPLICATION; CIRCULATION; INFECTION; INFERENCE; CHILDREN;
D O I
10.1111/irv.70082
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
BackgroundWe conducted a retrospective study to explore molecular insights into human respiratory syncytial virus (HRSV) group B strains among patients attending outpatient clinics at government medical facilities both prior and during the onset of Influenza A/H1N1/2009 pandemic outbreak.MethodsWe screened 2300 nasopharyngeal swabs using multiplex real time reverse transcriptase polymerase chain reaction. We amplified a segment of the first and second hypervariable regions, as well as the conserved portion of the third domain of the G-gene using HRSV-B specific primers, sequenced by Sanger di-deoxy chain termination method and thereafter analyzed the sequences.ResultsWe characterized the circulating strains into three known genotypes: SAB4 (1.4%), BA7 (1.4%), and multiple variants of BA9 (97.2%). The majority of BA9 viruses were uniquely Kenyan with only 4% aligning with BA9 lineages found elsewhere. The mean evolutionary rate of the HRSV-B was estimated to be 3.08 x 10-3 substitutions per site per year.ConclusionOur findings indicate that the circulating HRSV-B viruses in Kenya underwent a slower evolution during the period of 2007-2010. Additionally, our findings reveal the existence of a unique lineage as well as new variants that have not been reported elsewhere to date.
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