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

Author:

Thi Hue Kien DuongORCID,Edenborough Kathryn123ORCID,da Silva Goncalves Daniela1,Thuy Vi Tran3,Casagrande Etiene14,Thi Le Duyen Huynh3,Thi Long Vo3,Thi Dui Le3,Thi Tuyet Nhu Vu3,Thi Giang Nguyen3,Thi Xuan Trang Huynh3,Lee Elvina1,Donovan-Banfield I’ah1,Thi Thuy Van Huynh3,Minh Nguyet NguyenORCID,Thanh Phong Nguyen5,Van Vinh Chau Nguyen5,Wills Bridget36,Yacoub Sophie3ORCID,Flores Heather14,Simmons Cameron123

Affiliation:

1. World Mosquito Program, Institute of Vector-Borne Disease, Monash University , Clayton, VIC 3800, Australia

2. Department of Microbiology, Biomedicine Discovery Institute, Monash University , Clayton, VIC 3800, Australia

3. Oxford University Clinical Research Unit, Hospital for Tropical Disease , Ho Chi Minh City, Vietnam

4. School of Biological Sciences, Monash University , Clayton, VIC 3800, Australia

5. Hospital for Tropical Diseases , 190 Ben Ham Tu, District 5, Ho Chi Minh City, Vietnam

6. Nuffield Department of Medicine, University of Oxford , Oxford, UK

Abstract

Abstract 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 wMel 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 wMel-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 wMel-associated selection of virus populations can occur in experimental conditions. Field-based studies are needed to explore whether wMel imparts selective pressure on DENV evolution in locations where wMel is established.

Funder

National Health and Medical Research Council

Publisher

Oxford University Press (OUP)

Subject

Virology,Microbiology

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