Sekee Tumelo Robert, Wiid Siewert Christiaan, Dimaculangan Micah, Masilo Bonolo Betty, Bester Philip Armand, van Jaarsveldt Danelle, Terblanche Gert Ignatius Du Preez, Litabe Matefo Millicent, Makoah Nigel Aminake, Burt Felicity Jane
Division of Virology, Faculty of Health Sciences, University of the Free State, Bloemfontein, South Africa.
Division of Virology, Faculty of Health Sciences, University of the Free State, Bloemfontein, South Africa; Emerging Viral Threats, One Health Surveillance and Vaccines (EViTOH) Division, Infectious Diseases and Oncology Research Institute (IDORI), Faculty of Health Sciences, University of Witwatersrand, Johannesburg, South Africa.
Virology. 2025 Aug 27;612:110668. doi: 10.1016/j.virol.2025.110668.
Surveillance plays an important role in early detection of circulating arboviruses with potential to cause outbreaks of disease. In South Africa (SA) there are several endemic mosquito-borne viruses of medical and veterinary importance associated with outbreaks of disease in humans and domestic animals (livestock and horses) usually occurring after heavy rainfall. In addition, there are historical reports of viruses that were isolated from mosquitoes during vector surveillance studies with demonstration of antibodies in human populations during serosurveys. However, for many of these viruses detected historically there is no recent evidence of their circulation in the country. This study was initiated to screen mosquitoes in central South Africa for evidence of known and less common mosquito-borne viruses. Mosquitoes were collected from selected sites including two urban sites, a rural and a conservation area in central South Africa and were screened for arboviruses from the families Togaviridae, Orthoflaviviridae and Peribunyaviridae. A total of 10 332 mosquitoes were collected between November 2019 and March 2023. Most of the collection was obtained from the two urban sites in Bloemfontein, 8 236/10 332 (79.7 %), 1 075/10 332 (10.4 %) from the conservation site and 1 021/10 332 (9.9 %) from the rural site. Mosquito pool homogenates were screened using nested in-house RT-PCR. The nucleotide sequence of each amplicon of predicted size was determined using Sanger sequencing or Oxford Nanopore sequencing, and the virus identification confirmed using BLASTn analysis. Partial genes for Sindbis virus (SINV) genotype 1 were detected in three mosquito pools, for Middelburg virus (MIDV) in two pools, for Germiston virus (GERV) in one pool, for bunyamwera virus (BUNV) in four pools, for West Nile virus (WNV) lineage 2 in four pools, for Bagaza virus (BAGV) in one pool, and an insect specific virus was detected in one pool. Due to the short length of sequence data obtained, cluster maps were used to determine relationships with previous isolates using sequence data retrieved from GenBank. Cluster maps confirmed that none of the isolates were newly introduced but closely related to isolates previously detected in the country. Sindbis virus genotype 1 and WNV lineage 2 are known to cause outbreaks of human disease after heavy rainfall, favoring an increase in mosquito populations. Middelburg virus has been associated with neurological disease in horses and some recent evidence in humans. Bunyamwera virus has previously been associated with mild febrile disease and GERV with laboratory acquired infections, but the public health significance is not well known and similarly with BAGV. This study confirmed the current circulation of mosquito-borne viruses other than the common viruses and suggest further investigation to determine the medical significance would be important.
监测在早期发现具有引发疾病暴发潜力的传播中的虫媒病毒方面发挥着重要作用。在南非,有几种具有医学和兽医重要性的地方性蚊媒病毒,与人类和家畜(牲畜和马匹)疾病暴发有关,这些暴发通常发生在暴雨之后。此外,在病媒监测研究期间从蚊子中分离出病毒的历史报告显示,在血清学调查中人群体内存在抗体。然而,对于历史上检测到的许多这些病毒,目前没有它们在该国传播的证据。本研究旨在筛查南非中部的蚊子,以寻找已知和不太常见的蚊媒病毒的证据。从选定地点收集蚊子,包括南非中部的两个城市地点、一个农村地区和一个保护区,并对其进行筛查,以寻找披膜病毒科、正黄病毒科和布尼亚病毒科的虫媒病毒。2019年11月至2023年3月期间共收集了10332只蚊子。大部分样本来自布隆方丹的两个城市地点,为8236/10332(79.7%),1075/10332(10.4%)来自保护区,1021/10332(9.9%)来自农村地区。使用巢式内部逆转录聚合酶链反应(RT-PCR)对蚊群匀浆进行筛查。使用桑格测序或牛津纳米孔测序确定预测大小的每个扩增子的核苷酸序列,并使用BLASTn分析确认病毒鉴定。在三个蚊群中检测到辛德毕斯病毒(SINV)基因型1的部分基因,在两个蚊群中检测到米德尔堡病毒(MIDV),在一个蚊群中检测到杰米斯顿病毒(GERV),在四个蚊群中检测到布尼亚姆韦拉病毒(BUNV),在四个蚊群中检测到西尼罗河病毒(WNV)谱系2,在一个蚊群中检测到巴加扎病毒(BAGV),在一个蚊群中检测到一种昆虫特异性病毒。由于获得的序列数据长度较短,使用聚类图根据从GenBank检索到的序列数据确定与先前分离株的关系。聚类图证实,没有一个分离株是新引入的,而是与该国先前检测到的分离株密切相关。已知辛德毕斯病毒基因型1和西尼罗河病毒谱系2在暴雨后会引发人类疾病暴发,这有利于蚊群数量增加。米德尔堡病毒与马的神经疾病有关,最近在人类中也有一些证据。布尼亚姆韦拉病毒以前与轻度发热疾病有关,杰米斯顿病毒与实验室获得性感染有关,但它们的公共卫生意义尚不清楚,巴加扎病毒也是如此。本研究证实了除常见病毒外蚊媒病毒的当前传播情况,并表明进一步调查以确定其医学意义将很重要。