Bbosa Nicholas, Kiiza Ronald, Ssekagiri Alfred, Namagembe Hamidah Suubi, Nabirye Stella Esther, Kabuuka Danstan, Rwankindo Cleophous, Kisakye Annet, Woldemariam Yonas T, Kusemererwa Sylvia, Ongaria Terry A, Kakande Ayoub, Abaasa Andrew, Kimbugwe Geofrey, Bosa Henry Kyobe, Driwale Alfred, Mwenda Jason M, Worwui Archibald K, Humphreys James, Cohuet Sandra, Elliott Alison M, Ruzagira Eugene, Kaleebu Pontiano, Ssemwanga Deogratius
MRC/UVRI & LSHTM Uganda Research Unit, Entebbe 256, Uganda.
Uganda Virus Research Institute, Entebbe 256, Uganda.
Viruses. 2024 Nov 29;16(12):1860. doi: 10.3390/v16121860.
The emergence of SARS-CoV-2 variants has heightened concerns about vaccine efficacy, posing challenges in controlling the spread of COVID-19. As part of the COVID-19 Vaccine Effectiveness and Variants (COVVAR) study in Uganda, this study aimed to genotype and characterize SARS-CoV-2 variants in patients with COVID-19-like symptoms who tested positive on a real-time PCR. Amplicon deep sequencing was performed on 163 oropharyngeal/nasopharyngeal swabs collected from symptomatic patients. Genome assembly, lineage classification and phylogenetic analysis was performed using the Edge Bioinformatics pipeline version 2.4.0, Pangolin version 4.3.1 and iqtree version 2.3.6 software respectively. Of the 163 deep sequences analyzed between April 2023 and March 2024, the most common were XBB.1 lineages and sublineages (113, 69.3%), followed by JN.1* (12, 7.4%), XBB.2* (11, 6.7%) and FL* (11, 6.7%), EG* (7, 4.3%), others (BQ.1.1, FY.4.1, FY.4.1.2, GY.2.1, HK.27.1) (5, 3.1%) and CM* (4, 2.5%). XBB.1* dominated from April to July 2023; thereafter, other variants, including JN.1* were increasingly detected. There was no statistically significant association between vaccine status and lineage assignment (Fisher's exact test, -value = 0.994). Our findings showed that the Omicron variant, specifically the XBB.1* lineage, was the dominant circulating virus. However, the emergence of the JN.1 variant that exhibits a significant spike protein mutation profile could impact COVID-19 transmission in Uganda.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)变异株的出现加剧了人们对疫苗效力的担忧,给控制新型冠状病毒肺炎(COVID-19)的传播带来了挑战。作为乌干达COVID-19疫苗效力与变异株(COVVAR)研究的一部分,本研究旨在对实时聚合酶链反应检测呈阳性、有COVID-19样症状的患者的SARS-CoV-2变异株进行基因分型和特征分析。对从有症状患者采集的163份口咽/鼻咽拭子进行扩增子深度测序。分别使用Edge生物信息学管道2.4.0版、穿山甲4.3.1版和iqtree 2.3.6版软件进行基因组组装、谱系分类和系统发育分析。在2023年4月至2024年3月期间分析的163条深度序列中,最常见的是XBB.1谱系和亚谱系(113条,占69.3%),其次是JN.1*(12条,占7.4%)、XBB.2*(11条,占6.7%)和FL*(11条,占6.7%)、EG*(7条,占4.3%)、其他(BQ.1.1、FY.4.1、FY.4.1.2、GY.2.1、HK.27.1)(5条,占3.1%)和CM*(4条,占2.5%)。XBB.1在2023年4月至7月占主导地位;此后,包括JN.1在内的其他变异株被越来越多地检测到。疫苗接种状态与谱系分类之间无统计学显著关联(Fisher精确检验,P值 = 0.994)。我们的研究结果表明,奥密克戎变异株,特别是XBB.1*谱系,是主要的流行病毒。然而,具有显著刺突蛋白突变特征的JN.1变异株的出现可能会影响乌干达的COVID-19传播。