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Genome evolution of dengue virus serotype 1 under selection by Wolbachia pipientis in Aedes aegypti mosquitoes.

Duong Thi Hue KienKathryn M EdenboroughDaniela da Silva GoncalvesTran Thuy ViEtiene CasagrandeHuynh Thi Le DuyenVo Thi LongLe Thi DuiVu Thi Tuyet NhuNguyen Thi GiangHuynh Thi Xuan TrangElvina LeeI'ah Donovan-BanfieldHuynh Thi Thuy VanNguyen Minh NguyetNguyen Thanh PhongNguyen Van Vinh ChauBridget WillsSophie YacoubHeather FloresCameron Simmons
Published in: Virus evolution (2023)
The introgression of antiviral strains of Wolbachia into Aedes aegypti mosquito populations is a public health intervention for the control of dengue. Plausibly, dengue virus (DENV) could evolve to bypass the antiviral effects of Wolbachia and undermine this approach. Here, we established a serial-passage system to investigate the evolution of DENV in Ae. aegypti mosquitoes infected with the w Mel strain of Wolbachia . Using this system, we report on virus genetic outcomes after twenty passages of serotype 1 of DENV (DENV-1). An amino acid substitution, E203K, in the DENV-1 envelope protein was more frequently detected in the consensus sequence of virus populations passaged in w Mel-infected Ae. aegypti than wild-type counterparts. Positive selection at residue 203 was reproducible; it occurred in passaged virus populations from independent DENV-1-infected patients and also in a second, independent experimental system. In wild-type mosquitoes and human cells, the 203K variant was rapidly replaced by the progenitor sequence. These findings provide proof of concept that w Mel-associated selection of virus populations can occur in experimental conditions. Field-based studies are needed to explore whether w Mel imparts selective pressure on DENV evolution in locations where w Mel is established.
Keyphrases
  • dengue virus
  • aedes aegypti
  • zika virus
  • wild type
  • amino acid
  • public health
  • randomized controlled trial
  • genome wide
  • genetic diversity
  • dna methylation
  • multidrug resistant
  • disease virus
  • binding protein