Suitable Mouse Model to Study Dynamics of West Nile Virus Infection in Culex quinquefasciatus Mosquitoes

Author:

Baldon Lívia1ORCID,de Mendonça Silvana1,Santos Ellen2,Marçal Bruno1,de Freitas Amanda Cupertino1ORCID,Rezende Fernanda1,Moreira Rafaela13,Sousa Viviane1,Comini Sara1,Lima Mariana1,Ferreira Flávia2,de Almeida João Paulo2ORCID,Silva Emanuele2,Amadou Siad2,Rocha Marcele1,Leite Thiago2ORCID,Todjro Yaovi2,de Carvalho Camila4,Santos Viviane5,Giovanetti Marta16ORCID,Alcantara Luiz1,Moreira Luciano A.1,Ferreira Alvaro1

Affiliation:

1. Mosquitos Vetores: Endossimbiontes e Interação Patógeno-Vetor, Instituto René Rachou-Fiocruz, Belo Horizonte 30190-002, Brazil

2. Departamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, 6627-Pampulha, Belo Horizonte 31270-901, Brazil

3. Laboratório de Ecologia do Adoecimento & Florestas NUPEB/ICEB, Universidade Federal de Ouro Preto, Ouro Preto 35402-163, Brazil

4. Plataforma de Microscopia e Microanálises de Imagens, Instituto René Rachou-Fiocruz, Belo Horizonte 30190-002, Brazil

5. Plataforma de PCR em Tempo Real, Instituto René Rachou-Fiocruz, Belo Horizonte 30190-002, Brazil

6. Department of Sciences and Technologies for Sustainable Development and One Health, University of Campus Bio-Medico, 00128 Rome, Italy

Abstract

West Nile Virus (WNV) poses a significant global public health threat as a mosquito-borne pathogen. While laboratory mouse models have historically played a crucial role in understanding virus biology, recent research has focused on utilizing immunocompromised models to study arboviruses like dengue and Zika viruses, particularly their interactions with Aedes aegypti mosquitoes. However, there has been a shortage of suitable mouse models for investigating WNV and St. Louis encephalitis virus interactions with their primary vectors, Culex spp. mosquitoes. Here, we establish the AG129 mouse (IFN α/β/γ R−/−) as an effective vertebrate model for examining mosquito–WNV interactions. Following intraperitoneal injection, AG129 mice exhibited transient viremia lasting several days, peaking on the second or third day post-infection, which is sufficient to infect Culex quinquefasciatus mosquitoes during a blood meal. We also observed WNV replication in the midgut and dissemination to other tissues, including the fat body, in infected mosquitoes. Notably, infectious virions were present in the saliva of a viremic AG129 mouse 16 days post-exposure, indicating successful transmission capacity. These findings highlight the utility of AG129 mice for studying vector competence and WNV–mosquito interactions.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

FAPEMIG

CNPq

Brazilian Ministry of Health

National Institutes of Health USA

Publisher

MDPI AG

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