Identification of insect-specific viruses in mosquitoes collected from wildlife and rural areas in north-eastern parts of South Africa using a metagenomic RNA sequencing approach.

IF 5.9 Q2 INFECTIOUS DISEASES
Sascha Kacnik, Caitlin MacIntyre, Milehna Guarido, Marietjie Venter
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Abstract

BACKGROUND: Next generation sequencing (NGS) has expanded virus detection capabilities beyond the limitations of sequence-specific methods. While mosquito collections in South Africa (SA) have been investigated for the major arbovirus genera (Alpha-, Orthobunya-, and Orthoflavivirus), research on insect-specific viruses (ISVs) is limited. METHODS: Here we used an RNA-sequencing viral-metagenomics approach to investigate arboviruses and ISVs in mosquitoes collected in SA. Ten archived mosquito pools, representing up to 50 mosquitoes per pool, previously tested for the major arbovirus genera were investigated for the presence of additional viruses using NGS. These pools included known arbovirus mosquito vectors from the Aedes, Anopheles, Culex, and Mansonia genera, collected from wildlife areas in the Kruger National Park (Mpumalanga/Limpopo) and rural areas of Jozini (KwaZulu-Natal). Extracted RNA was DNA-depleted, subjected to Sequence Independent Single Primer Amplification (SISPA), and sequenced on the Illumina MiSeq platform. RESULTS: Although no mammalian arboviruses were detected, bioinformatic analysis detected several ISVs in pools of Aedes aegypti, Ae.ochraceus, and Anopheles squamosus mosquitoes. These ISVs included the cell fusing agent-, Tesano aedes-, Fako-, formosus-, verdadero-, Aedes partiti-like virus 1 and the Kwale mosquito virus and several novel ISVs within the Iflavivirus genus as well as some unclassified viruses. CONCLUSION: This study confirms the value of sequence independent metagenomics approaches to detect novel viruses in mosquito pools. Such studies provide insight into viral diversity and mosquito-virus interactions, supporting the future evaluation of ISVs as biological control agents. This in turn can contribute to protecting the health of animals and humans within a One Health approach.

利用宏基因组RNA测序方法鉴定从南非东北部野生动物和农村地区采集的蚊子体内的昆虫特异性病毒
背景:下一代测序(NGS)扩展了病毒检测能力,超越了序列特异性方法的限制。虽然南非收集的蚊子已调查了主要虫媒病毒属(α -、正虫亚病毒和正黄病毒),但对昆虫特异性病毒(isv)的研究有限。方法:采用rna测序-病毒宏基因组学方法,对在南非采集的蚊虫进行虫媒病毒和isv的研究。使用NGS对以前检测过主要虫媒病毒属的10个存档蚊子池(每个池最多50只蚊子)进行了调查,以确定是否存在其他病毒。这些池包括从克鲁格国家公园(姆普马兰加/林波波省)野生动物区和Jozini(夸祖鲁-纳塔尔省)农村地区收集的已知的伊蚊、按蚊、库蚊和曼蚊属的虫媒病毒载体。提取的RNA去dna,进行序列独立单引物扩增(SISPA),并在Illumina MiSeq平台上测序。结果:虽然未检出哺乳动物虫媒病毒,但通过生物信息学分析在埃及伊蚊、伊蚊、白纹伊蚊等蚊库中检出多种独立病毒。和鳞状按蚊。这些独立病毒包括细胞融合剂-、Tesano伊蚊-、Fako-、formosus-、verdadero-、部分伊蚊样病毒1和Kwale蚊子病毒,以及伊黄病毒属的几种新型独立病毒和一些未分类的病毒。结论:本研究证实了序列独立的宏基因组学方法在蚊池中检测新型病毒的价值。这些研究提供了对病毒多样性和蚊子-病毒相互作用的深入了解,支持了isv作为生物防治剂的未来评价。这反过来又有助于在“同一个健康”方针下保护动物和人类的健康。
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