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Comment
. 2016 Jun 27;3(7):293-295.
doi: 10.15698/mic2016.07.513.

Inhibition of Zika virus by Wolbachia in Aedes aegypti

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Comment

Inhibition of Zika virus by Wolbachia in Aedes aegypti

Eric Pearce Caragata et al. Microb Cell. .

Abstract

Through association with cases of microcephaly in 2015, Zika virus (ZIKV) has transitioned from a relatively unknown mosquito-transmitted pathogen to a global health emergency, emphasizing the need to improve existing mosquito control programs to prevent future disease outbreaks. The response to Zika must involve a paradigm shift from traditional to novel methods of mosquito control, and according to the World Health Organization should incorporate the release of mosquitoes infected with the bacterial endosymbiont Wolbachiapipientis. In our recent paper [Dutra, HLC et al., Cell Host & Microbe 2016] we investigated the potential of Wolbachia infections in Aedes aegypti to restrict infection and transmission of Zika virus recently isolated in Brazil. Wolbachia is now well known for its ability to block or reduce infection with a variety of pathogens in different mosquito species including the dengue (DENV), yellow fever, and chikungunya viruses, and malaria-causing Plasmodium, and consequently has great potential to control mosquito-transmitted diseases across the globe. Our results demonstrated that the wMel Wolbachia strain in Brazilian Ae. aegypti is a strong inhibitor of ZIKV infection, and furthermore appears to prevent transmission of infectious viral particles in mosquito saliva, which highlights the bacterium's suitability for more widespread use in Zika control.

Keywords: Aedes aegypti; Wolbachia; Zika virus; mosquito-transmitted disease.

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Conflict of interest statement

Conflict of interest: The authors declare that no competing interests exist.

Figures

Figure 1
Figure 1. FIGURE 1: Schematic depicting the prevalence of Zika virus infection in Wolbachia-uninfected (A, Wolb -) and Wolbachia-infected (B, Wolb +) Aedes aegypti.
Data for the BRPE ZIKV isolate were obtained through RT-qPCR analysis. Percentage values represent abdominal infection rates (AI), and disseminated infection rates (DI) at 7 and 14 days post-infection (dpi), or rate of subsequent infection after saliva was injected into naïve Wolbachia-uninfected mosquitoes at 14 dpi (S).

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Grants and funding

This work was supported by FAPEMIG, CNPq, CAPES, the Brazilian Ministry of Health (DECIT/SVS), and a grant to Monash University from the Foundation for the National Institutes of Health through the Vector-Based Transmission of Control: Discovery Research (VCTR) program of the Grand Challenges in Global Health Initiatives of the Bill and Melinda Gates Foundation.

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