Department of Microbiology, Faculty of Sciences, Lagos State University, Ojo, Lagos State, Nigeria.
Centre for Human Virology and Genomics, Nigerian Institute of Medical Research, Yaba, Lagos State, Nigeria.
BMC Infect Dis. 2023 Aug 18;23(1):538. doi: 10.1186/s12879-023-08526-z.
Arboviral infections are fast becoming a global public health concern as a result of its high fatality rate and sporadic spread. From the outbreak of Zika virus in the Americas, the endemicity of Yellow fever in West Africa and South America, outbreaks of West Nile virus in South Africa to the year-round and national risk of Dengue fever in Mainland China and India. The war against emerging and re-emerging viral infection could probably lead to the next pandemic. To be above the pending possible arboviral pandemic, consistent surveillance of these pathogens is necessary in every society. This study was aimed at conducting a surveillance for Yellow fever virus, Zika virus, Chikungunya virus, Dengue virus and Rift Valley fever virus in four states in Nigeria using molecular techniques. A cross-sectional study involving 1600 blood samples collected from febrile patients in Lagos, Kwara, Ondo and Delta States between 2018 and 2021 was conducted using Real time polymerase chain reaction for detection of the pathogens. Extraction and purification of viral RNA were done using Qiagen Viral RNA Mini Kit. Samples were analyzed using One Step PrimeScript III RT-PCR mix (Takara Bio) alongside optimized primers and probes designed in-house. Positive samples were sequenced on MinION platform (Nanopore technologies). Bioinformatic and phylogenetic analysis were performed with DNASTAR Lasergene 17.3. All the RNA extracted from samples collected from the four states were negative for ZIKV RNA, RVFV RNA, CHIKV RNA and DENV RNA. However, twelve of the samples (2%) tested positive for YFV RNA. Three full genomes of sizes 10,751 bp, 10,500 bp and 10,715 bp were generated and deposited in GenBank with accession numbers: ON323052, ON323053 and ON323054 respectively. Phylogenetic analysis shows clustering within lineage 3 of West African genotype. This result shows an active spread of Yellow fever in Delta State, Nigeria. However, there is no emergence of a new genotype There is a need for an intense surveillance of Yellow fever virus in Nigeria to avert a major outbreak.
虫媒病毒感染由于其高死亡率和零星传播,正迅速成为全球公共卫生关注的焦点。从美洲的寨卡病毒爆发,西非和南美洲的黄热病地方性流行,南非的西尼罗河病毒爆发,到中国大陆和印度全年和全国登革热的风险。与新发和再发病毒感染的斗争可能导致下一次大流行。为了预防即将发生的虫媒病毒大流行,每个社会都有必要对这些病原体进行持续监测。本研究旨在使用分子技术对尼日利亚四个州的黄热病病毒、寨卡病毒、基孔肯雅热病毒、登革热病毒和裂谷热病毒进行监测。这是一项横断面研究,涉及 2018 年至 2021 年间从拉各斯、夸拉、翁多和三角洲州发热患者中采集的 1600 份血液样本,使用实时聚合酶链反应检测病原体。使用 Qiagen Viral RNA Mini Kit 提取和纯化病毒 RNA。使用 One Step PrimeScript III RT-PCR 试剂盒(Takara Bio)和内部设计的优化引物和探针对样本进行分析。阳性样本在 MinION 平台(Nanopore technologies)上进行测序。使用 DNASTAR Lasergene 17.3 进行生物信息学和系统发育分析。从四个州采集的样本中提取的所有 RNA 均为 ZIKV RNA、RVFV RNA、CHIKV RNA 和 DENV RNA 阴性。然而,有 12 份样本(2%)检测到 YFV RNA 阳性。生成并在 GenBank 中分别以注册号 ON323052、ON323053 和 ON323054 提交了三个全长 10,751bp、10,500bp 和 10,715bp 的基因组。系统发育分析显示,聚类位于西非基因型 3 谱系内。这一结果表明,尼日利亚三角洲州的黄热病正在广泛传播。然而,并没有出现新的基因型。尼日利亚需要加强对黄热病病毒的监测,以避免重大疫情的发生。