TY - JOUR
T1 - The anti-immune dengue subgenomic flaviviral RNA is present in vesicles in mosquito saliva and is associated with increased infectivity
AU - Yeh, Shih Chia
AU - Strilets, Tania
AU - Tan, Wei Lian
AU - Castillo, David
AU - Medkour, Hacène
AU - Rey-Cadilhac, Félix
AU - Serrato-Pomar, Idalba M.
AU - Rachenne, Florian
AU - Chowdhury, Avisha
AU - Chuo, Vanessa
AU - Azar, Sasha
AU - Kiran Singh, Moirangthem
AU - Hamel, Rodolphe
AU - Missé, Dorothée
AU - Kini, R. Manjunatha
AU - Kenney, Linda J.
AU - Vasilakis, Nikos
AU - Marti-Renom, Marc A.
AU - Nir, Guy
AU - Pompon, Julien
AU - Garcia-Blanco, Mariano
N1 - Publisher Copyright:
© 2023 Yeh et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2023/3
Y1 - 2023/3
N2 - Mosquito transmission of dengue viruses to humans starts with infection of skin resident cells at the biting site. There is great interest in identifying transmission-enhancing factors in mosquito saliva in order to counteract them. Here we report the discovery of high levels of the anti-immune subgenomic flaviviral RNA (sfRNA) in dengue virus 2-infected mosquito saliva. We established that sfRNA is present in saliva using three different methods: northern blot, RT-qPCR and RNA sequencing. We next show that salivary sfRNA is protected in detergent-sensitive compartments, likely extracellular vesicles. In support of this hypothesis, we visualized viral RNAs in vesicles in mosquito saliva and noted a marked enrichment of signal from 3’UTR sequences, which is consistent with the presence of sfRNA. Furthermore, we show that incubation with mosquito saliva containing higher sfRNA levels results in higher virus infectivity in a human hepatoma cell line and human primary dermal fibroblasts. Transfection of 3’UTR RNA prior to DENV2 infection inhibited type I and III interferon induction and signaling, and enhanced viral replication. Therefore, we posit that sfRNA present in salivary extracellular vesicles is delivered to cells at the biting site to inhibit innate immunity and enhance dengue virus transmission.
AB - Mosquito transmission of dengue viruses to humans starts with infection of skin resident cells at the biting site. There is great interest in identifying transmission-enhancing factors in mosquito saliva in order to counteract them. Here we report the discovery of high levels of the anti-immune subgenomic flaviviral RNA (sfRNA) in dengue virus 2-infected mosquito saliva. We established that sfRNA is present in saliva using three different methods: northern blot, RT-qPCR and RNA sequencing. We next show that salivary sfRNA is protected in detergent-sensitive compartments, likely extracellular vesicles. In support of this hypothesis, we visualized viral RNAs in vesicles in mosquito saliva and noted a marked enrichment of signal from 3’UTR sequences, which is consistent with the presence of sfRNA. Furthermore, we show that incubation with mosquito saliva containing higher sfRNA levels results in higher virus infectivity in a human hepatoma cell line and human primary dermal fibroblasts. Transfection of 3’UTR RNA prior to DENV2 infection inhibited type I and III interferon induction and signaling, and enhanced viral replication. Therefore, we posit that sfRNA present in salivary extracellular vesicles is delivered to cells at the biting site to inhibit innate immunity and enhance dengue virus transmission.
UR - http://www.scopus.com/inward/record.url?scp=85151573840&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85151573840&partnerID=8YFLogxK
U2 - 10.1371/JOURNAL.PPAT.1011224
DO - 10.1371/JOURNAL.PPAT.1011224
M3 - Article
C2 - 36996041
AN - SCOPUS:85151573840
SN - 1553-7366
VL - 19
JO - PLoS pathogens
JF - PLoS pathogens
IS - 3
M1 - e1011224
ER -