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Chikungunya virus transmission between Aedes albopictus and laboratory mice

BACKGROUND: Chikungunya virus (CHIKV) is a mosquito-borne alphavirus associated with epidemics of acute and chronic arthritic disease in humans. Aedes albopictus has emerged as an important new natural vector for CHIKV transmission; however, mouse models for studying transmission have not been devel...

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Detalles Bibliográficos
Autores principales: Hugo, Leon E., Prow, Natalie A., Tang, Bing, Devine, Greg, Suhrbier, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069946/
https://www.ncbi.nlm.nih.gov/pubmed/27760560
http://dx.doi.org/10.1186/s13071-016-1838-1
Descripción
Sumario:BACKGROUND: Chikungunya virus (CHIKV) is a mosquito-borne alphavirus associated with epidemics of acute and chronic arthritic disease in humans. Aedes albopictus has emerged as an important new natural vector for CHIKV transmission; however, mouse models for studying transmission have not been developed. METHODS: Aedes albopictus mosquitoes were infected with CHIKV via membrane feeding and by using infected adult wild-type C57BL/6 mice. Paraffin sections of infected mosquitoes were analysed by immunofluorescent antibody staining using an anti-CHIKV antibody. CHIKV-infected mosquitoes were used to infect adult C57BL/6 and interferon response factor 3 and 7 deficient (IRF3/7(-/-)) mice. RESULTS: Feeding mosquitoes on blood meals with CHIKV titres > 5 log(10)CCID(50)/ml, either by membrane feeding or feeding on infected mice, resulted in  ≥ 50 % of mosquitoes becoming infected. However, CHIKV titres in blood meals  ≥ 7 log(10)CCID(50)/ml were required before salivary glands showed significant levels of immunofluorescent staining with an anti-CHIKV antibody. Mosquitoes fed on blood meals of 7.5 (but not 5.9) log(10)CCID(50)/ml were able efficiently to transmit virus to adult C57BL/6 and IRF3/7(-/-) mice, with the latter mice showing overt signs of arthritis post-infection. CONCLUSIONS: The results provide a simple in vivo model for studying transmission of CHIKV from mosquitoes to mammals and also argue against a resistance barrier to CHIKV infection in adult mice. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-016-1838-1) contains supplementary material, which is available to authorized users.