Midgut transcriptomic responses to dengue and chikungunya viruses in the vectors Aedes albopictus and Aedes malayensis

被引:2
|
作者
Modahl, Cassandra M. [1 ,4 ]
Chowdhury, Avisha [1 ,5 ]
Low, Dolyce H. W. [2 ]
Manuel, Menchie C. [2 ]
Misse, Dorothee [6 ]
Kini, R. Manjunatha [1 ,3 ]
Mendenhall, Ian H. [2 ]
Pompon, Julien [2 ,6 ]
机构
[1] Natl Univ Singapore, Dept Biol Sci, Singapore, Singapore
[2] Duke NUS Med Sch, Programme Emerging Infect Dis, Singapore, Singapore
[3] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Pharmacol, Singapore, Singapore
[4] Univ Liverpool Liverpool Sch Trop Med, Liverpool, England
[5] Univ Toronto, Univ Hlth Network, Toronto Gen Hosp, Toronto Ctr Liver Dis, Toronto, ON, Canada
[6] Univ Montpellier, MIVEGEC, IRD, CNRS, Montpellier, France
基金
英国医学研究理事会;
关键词
DOMAIN SERINE PROTEASES; IMMUNE-RELATED GENES; CD-HIT; INFECTION; FEVER; SUSCEPTIBILITY; EXPRESSION; WOLBACHIA; ALIGNMENT; OUTBREAK;
D O I
10.1038/s41598-023-38354-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Dengue (DENV) and chikungunya (CHIKV) viruses are among the most preponderant arboviruses. Although primarily transmitted through the bite of Aedes aegypti mosquitoes, Aedes albopictus and Aedes malayensis are competent vectors and have an impact on arbovirus epidemiology. Here, to fill the gap in our understanding of the molecular interactions between secondary vectors and arboviruses, we used transcriptomics to profile the whole-genome responses of A. albopictus to CHIKV and of A. malayensis to CHIKV and DENV at 1 and 4 days post-infection (dpi) in midguts. In A. albopictus, 1793 and 339 genes were significantly regulated by CHIKV at 1 and 4 dpi, respectively. In A. malayensis, 943 and 222 genes upon CHIKV infection, and 74 and 69 genes upon DENV infection were significantly regulated at 1 and 4 dpi, respectively. We reported 81 genes that were consistently differentially regulated in all the CHIKV-infected conditions, identifying a CHIKV-induced signature. We identified expressed immune genes in both mosquito species, using a de novo assembled midgut transcriptome for A. malayensis, and described the immune architectures. We found the JNK pathway activated in all conditions, generalizing its antiviral function to Aedines. Our comprehensive study provides insight into arbovirus transmission by multiple Aedes vectors.
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页数:13
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