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Restriction of Zika virus infection and transmission in Aedes aegypti mediated by an insect-specific flavivirus

Previous studies demonstrated an insect-specific flavivirus, Nhumirim virus (NHUV), can suppress growth of West Nile virus (WNV) and decrease transmission rates in NHUV/WNV co-inoculated Culex quinquefasciatus. To assess whether NHUV might interfere with transmission of other medically important fla...

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Autores principales: Romo, Hannah, Kenney, Joan L., Blitvich, Bradley J., Brault, Aaron C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6235874/
https://www.ncbi.nlm.nih.gov/pubmed/30429457
http://dx.doi.org/10.1038/s41426-018-0180-4
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author Romo, Hannah
Kenney, Joan L.
Blitvich, Bradley J.
Brault, Aaron C.
author_facet Romo, Hannah
Kenney, Joan L.
Blitvich, Bradley J.
Brault, Aaron C.
author_sort Romo, Hannah
collection PubMed
description Previous studies demonstrated an insect-specific flavivirus, Nhumirim virus (NHUV), can suppress growth of West Nile virus (WNV) and decrease transmission rates in NHUV/WNV co-inoculated Culex quinquefasciatus. To assess whether NHUV might interfere with transmission of other medically important flaviviruses, the ability of NHUV to suppress viral growth of Zika virus (ZIKV) and dengue-2 virus (DENV-2) was assessed in Aedes albopictus cells. Significant reductions in ZIKV (100,000-fold) and DENV-2 (10,000-fold) were observed in either cells concurrently inoculated with NHUV or pre-inoculated with NHUV. In contrast, only a transient 10-fold titer reduction was observed with an alphavirus, chikungunya virus. Additionally, restricted in vitro mosquito growth of ZIKV was associated with lowered levels of intracellular ZIKV RNA in NHUV co-inoculated cultures. To assess whether NHUV could modulate vector competence for ZIKV, NHUV-inoculated Aedes aegypti were orally exposed to ZIKV. NHUV-inoculated mosquitoes demonstrated significantly lower ZIKV infection rates (18%) compared to NHUV unexposed mosquitoes (51%) (p < 0.002). Similarly, lower ZIKV transmission rates were observed for NHUV/ZIKV dually intrathoracically inoculated mosquitoes (41%) compared to ZIKV only inoculated mosquitoes (78%) (p < 0.0001), suggesting that NHUV can interfere with both midgut infection and salivary gland infection of ZIKV in Ae. aegypti. These results indicate NHUV could be utilized to model superinfection exclusion mechanism(s) and to study the potential for the mosquito virome to impact transmission of medically important flaviviruses.
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spelling pubmed-62358742018-11-19 Restriction of Zika virus infection and transmission in Aedes aegypti mediated by an insect-specific flavivirus Romo, Hannah Kenney, Joan L. Blitvich, Bradley J. Brault, Aaron C. Emerg Microbes Infect Article Previous studies demonstrated an insect-specific flavivirus, Nhumirim virus (NHUV), can suppress growth of West Nile virus (WNV) and decrease transmission rates in NHUV/WNV co-inoculated Culex quinquefasciatus. To assess whether NHUV might interfere with transmission of other medically important flaviviruses, the ability of NHUV to suppress viral growth of Zika virus (ZIKV) and dengue-2 virus (DENV-2) was assessed in Aedes albopictus cells. Significant reductions in ZIKV (100,000-fold) and DENV-2 (10,000-fold) were observed in either cells concurrently inoculated with NHUV or pre-inoculated with NHUV. In contrast, only a transient 10-fold titer reduction was observed with an alphavirus, chikungunya virus. Additionally, restricted in vitro mosquito growth of ZIKV was associated with lowered levels of intracellular ZIKV RNA in NHUV co-inoculated cultures. To assess whether NHUV could modulate vector competence for ZIKV, NHUV-inoculated Aedes aegypti were orally exposed to ZIKV. NHUV-inoculated mosquitoes demonstrated significantly lower ZIKV infection rates (18%) compared to NHUV unexposed mosquitoes (51%) (p < 0.002). Similarly, lower ZIKV transmission rates were observed for NHUV/ZIKV dually intrathoracically inoculated mosquitoes (41%) compared to ZIKV only inoculated mosquitoes (78%) (p < 0.0001), suggesting that NHUV can interfere with both midgut infection and salivary gland infection of ZIKV in Ae. aegypti. These results indicate NHUV could be utilized to model superinfection exclusion mechanism(s) and to study the potential for the mosquito virome to impact transmission of medically important flaviviruses. Nature Publishing Group UK 2018-11-15 /pmc/articles/PMC6235874/ /pubmed/30429457 http://dx.doi.org/10.1038/s41426-018-0180-4 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Romo, Hannah
Kenney, Joan L.
Blitvich, Bradley J.
Brault, Aaron C.
Restriction of Zika virus infection and transmission in Aedes aegypti mediated by an insect-specific flavivirus
title Restriction of Zika virus infection and transmission in Aedes aegypti mediated by an insect-specific flavivirus
title_full Restriction of Zika virus infection and transmission in Aedes aegypti mediated by an insect-specific flavivirus
title_fullStr Restriction of Zika virus infection and transmission in Aedes aegypti mediated by an insect-specific flavivirus
title_full_unstemmed Restriction of Zika virus infection and transmission in Aedes aegypti mediated by an insect-specific flavivirus
title_short Restriction of Zika virus infection and transmission in Aedes aegypti mediated by an insect-specific flavivirus
title_sort restriction of zika virus infection and transmission in aedes aegypti mediated by an insect-specific flavivirus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6235874/
https://www.ncbi.nlm.nih.gov/pubmed/30429457
http://dx.doi.org/10.1038/s41426-018-0180-4
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