Institute of Health and Biomedical Innovation, and School of Biomedical Sciences, Faculty of Health, Queensland University of Technology, Brisbane, Queensland, Australia.
Department of Medical Laboratory Sciences, Faculty of Health Science, Open University of Sri Lanka, Nugegoda, Colombo, Sri Lanka.
Open Biol. 2021 Jan;11(1):200246. doi: 10.1098/rsob.200246. Epub 2021 Jan 6.
The principal vector of dengue, Zika and chikungunya viruses is the mosquito , with its ability to transmit pathogens influenced by ambient temperature. We use chikungunya virus (CHIKV) to understand how the mosquito transcriptome responds to arbovirus infection at different ambient temperatures. We exposed CHIKV-infected mosquitoes to 18, 28 and 32°C, and found that higher temperature correlated with higher virus levels, particularly at 3 days post infection, but lower temperature resulted in reduced virus levels. RNAseq analysis indicated significantly altered gene expression levels in CHIKV infection. The highest number of significantly differentially expressed genes was observed at 28°C, with a more muted effect at the other temperatures. At the higher temperature, the expression of many classical immune genes, including , was not substantially altered in response to CHIKV. The upregulation of Toll, IMD and JAK-STAT pathways was only observed at 28°C. Functional annotations suggested that genes in immune response and metabolic pathways related to energy supply and DNA replication were involved in temperature-dependent changes. Time post infection also led to substantially different gene expression profiles, and this varied with temperature. In conclusion, temperature significantly modulates mosquito gene expression in response to infection, potentially leading to impairment of immune defences at higher temperatures.
登革热、寨卡和基孔肯雅热病毒的主要载体是蚊子,其传播病原体的能力受环境温度的影响。我们使用基孔肯雅病毒(CHIKV)来了解蚊子转录组如何在不同环境温度下对虫媒病毒感染做出反应。我们将感染 CHIKV 的蚊子暴露在 18、28 和 32°C 下,发现较高的温度与较高的病毒水平相关,尤其是在感染后 3 天,但较低的温度会导致病毒水平降低。RNAseq 分析表明,CHIKV 感染导致基因表达水平发生显著变化。在 28°C 时观察到的显著差异表达基因数量最多,而在其他温度下则效果较为温和。在较高的温度下,许多经典免疫基因的表达,包括 ,并未因 CHIKV 而发生实质性改变。Toll、IMD 和 JAK-STAT 途径的上调仅在 28°C 时观察到。功能注释表明,与免疫反应和与能量供应和 DNA 复制相关的代谢途径相关的基因参与了温度依赖性变化。感染后时间也导致了截然不同的基因表达谱,并且这种情况随温度而变化。总之,温度显著调节蚊子对感染的基因表达,可能导致在较高温度下免疫防御受损。