Transcriptome analysis of Aedes aegypti midgut and salivary gland post-Zika virus infection

IF 1.7 Q3 PARASITOLOGY
Chunling Zhu , Yuting Jiang , Qianghui Zhang , Jian Gao , Chaojie Li , Chunxiao Li , Yande Dong , Dan Xing , Hengduan Zhang , Teng Zhao , Xiaoxia Guo , Tongyan Zhao
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Abstract

This study aimed to investigate the transcriptomic changes in the midgut and salivary glands of Aedes aegypti mosquitoes infected with Zika virus (ZIKV), in order to explore the molecular mechanisms underlying the interaction between the virus and the mosquito vector. Aedes aegypti from Jiegao (JG) and Mengding (MD) in China were experimentally infected with ZIKV, and the midgut and salivary gland tissues were collected at 2-, 4- and 6 days post-infection (dpi). High-throughput sequencing was performed to analyze the transcriptomic changes between ZIKV-infected and non-infected Ae. aegypti midgut and salivary gland tissues. Bioinformatics tools were employed for further analysis of the transcriptomic data. The expression levels of 8 significantly differentially expressed genes (DEGs) were validated using RT-qPCR. A conjoint analysis of small RNA-seq and mRNA-seq was performed to screen interactional miRNA-mRNA pairs during ZIKV infection. Using the Search Tool for the Retrieval of Interacting Genes, we constructed a protein-protein interaction network of genes and subsequently identified hub genes. The most significant transcriptional changes in Ae. aegypti occurred at 2 dpi. On 2, 4 and 6 dpi, 11 genes showed significant changes in both the midgut and salivary glands of the same mosquito strain, while 25 genes exhibited significant changes in the same tissue between the JG and MD strains. The expression tendencies of 8 DEGs obtained by RNA-Seq were similar to those detected by RT-qPCR. Furthermore, we individually identified 10 hub genes in the midgut and salivary glands. Based on previous miRNA research, we discovered the involvement of 9 miRNAs in the regulation of these hub genes. Our findings demonstrate that Ae. aegypti exhibit distinct transcriptomic changes in response to ZIKV infection. The identification of the hub genes and their regulatory miRNAs provides valuable insights into the molecular mechanisms underlying ZIKV infection in mosquitoes. This study contributes to a better understanding of the pathogen-vector interactions and may aid in the development of targeted strategies for ZIKV control.

Abstract Image

寨卡病毒感染后埃及伊蚊中肠和唾液腺转录组分析
本研究旨在研究寨卡病毒(Zika virus, ZIKV)感染后埃及伊蚊(Aedes aegypti mosquito)中肠和唾液腺的转录组学变化,探讨寨卡病毒与媒介蚊子相互作用的分子机制。本研究对中国结高市和蒙定市的埃及伊蚊进行寨卡病毒实验感染,分别于感染后2、4、6 d采集其中肠和唾液腺组织。采用高通量测序方法分析感染和未感染伊蚊的转录组变化。埃及伊蚊中肠和唾液腺组织。利用生物信息学工具对转录组数据进行进一步分析。采用RT-qPCR验证8个显著差异表达基因(DEGs)的表达水平。采用小RNA-seq和mRNA-seq联合分析筛选寨卡病毒感染过程中相互作用的miRNA-mRNA对。利用互作基因检索工具,我们构建了一个蛋白质-蛋白质互作基因网络,并随后确定了枢纽基因。伊蚊的转录变化最为显著。埃及伊蚊出现在2 dpi。在2、4和6 dpi时,11个基因在同一蚊株的中肠和唾液腺中均表现出显著变化,25个基因在JG和MD菌株的同一组织中表现出显著变化。RNA-Seq检测得到的8个deg的表达趋势与RT-qPCR检测结果相似。此外,我们在中肠和唾液腺中分别鉴定了10个枢纽基因。基于之前的miRNA研究,我们发现有9种miRNA参与了这些中枢基因的调控。我们的研究结果表明,Ae。埃及伊蚊对寨卡病毒感染表现出明显的转录组变化。枢纽基因及其调控mirna的鉴定为了解蚊子感染寨卡病毒的分子机制提供了有价值的见解。这项研究有助于更好地了解病原体与媒介的相互作用,并可能有助于制定有针对性的寨卡病毒控制策略。
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CiteScore
3.60
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