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The Lethal(2)-Essential-for-Life [L(2)EFL] Gene Family Modulates Dengue Virus Infection in Aedes aegypti

Efforts to determine the mosquito genes that affect dengue virus replication have identified a number of candidates that positively or negatively modify amplification in the invertebrate host. We used deep sequencing to compare the differential transcript abundances in Aedes aegypti 14 days post den...

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Autores principales: Runtuwene, Lucky R., Kawashima, Shuichi, Pijoh, Victor D., Tuda, Josef S. B., Hayashida, Kyoko, Yamagishi, Junya, Sugimoto, Chihiro, Nishiyama, Shoko, Sasaki, Michihito, Orba, Yasuko, Sawa, Hirofumi, Takasaki, Tomohiko, James, Anthony A., Kobayashi, Takashi, Eshita, Yuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593908/
https://www.ncbi.nlm.nih.gov/pubmed/33053895
http://dx.doi.org/10.3390/ijms21207520
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author Runtuwene, Lucky R.
Kawashima, Shuichi
Pijoh, Victor D.
Tuda, Josef S. B.
Hayashida, Kyoko
Yamagishi, Junya
Sugimoto, Chihiro
Nishiyama, Shoko
Sasaki, Michihito
Orba, Yasuko
Sawa, Hirofumi
Takasaki, Tomohiko
James, Anthony A.
Kobayashi, Takashi
Eshita, Yuki
author_facet Runtuwene, Lucky R.
Kawashima, Shuichi
Pijoh, Victor D.
Tuda, Josef S. B.
Hayashida, Kyoko
Yamagishi, Junya
Sugimoto, Chihiro
Nishiyama, Shoko
Sasaki, Michihito
Orba, Yasuko
Sawa, Hirofumi
Takasaki, Tomohiko
James, Anthony A.
Kobayashi, Takashi
Eshita, Yuki
author_sort Runtuwene, Lucky R.
collection PubMed
description Efforts to determine the mosquito genes that affect dengue virus replication have identified a number of candidates that positively or negatively modify amplification in the invertebrate host. We used deep sequencing to compare the differential transcript abundances in Aedes aegypti 14 days post dengue infection to those of uninfected A. aegypti. The gene lethal(2)-essential-for-life [l(2)efl], which encodes a member of the heat shock 20 protein (HSP20) family, was upregulated following dengue virus type 2 (DENV-2) infection in vivo. The transcripts of this gene did not exhibit differential accumulation in mosquitoes exposed to insecticides or pollutants. The induction and overexpression of l(2)efl gene products using poly(I:C) resulted in decreased DENV-2 replication in the cell line. In contrast, the RNAi-mediated suppression of l(2)efl gene products resulted in enhanced DENV-2 replication, but this enhancement occurred only if multiple l(2)efl genes were suppressed. l(2)efl homologs induce the phosphorylation of eukaryotic initiation factor 2α (eIF2α) in the fruit fly Drosophila melanogaster, and we confirmed this finding in the cell line. However, the mechanism by which l(2)efl phosphorylates eIF2α remains unclear. We conclude that l(2)efl encodes a potential anti-dengue protein in the vector mosquito.
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spelling pubmed-75939082020-10-30 The Lethal(2)-Essential-for-Life [L(2)EFL] Gene Family Modulates Dengue Virus Infection in Aedes aegypti Runtuwene, Lucky R. Kawashima, Shuichi Pijoh, Victor D. Tuda, Josef S. B. Hayashida, Kyoko Yamagishi, Junya Sugimoto, Chihiro Nishiyama, Shoko Sasaki, Michihito Orba, Yasuko Sawa, Hirofumi Takasaki, Tomohiko James, Anthony A. Kobayashi, Takashi Eshita, Yuki Int J Mol Sci Article Efforts to determine the mosquito genes that affect dengue virus replication have identified a number of candidates that positively or negatively modify amplification in the invertebrate host. We used deep sequencing to compare the differential transcript abundances in Aedes aegypti 14 days post dengue infection to those of uninfected A. aegypti. The gene lethal(2)-essential-for-life [l(2)efl], which encodes a member of the heat shock 20 protein (HSP20) family, was upregulated following dengue virus type 2 (DENV-2) infection in vivo. The transcripts of this gene did not exhibit differential accumulation in mosquitoes exposed to insecticides or pollutants. The induction and overexpression of l(2)efl gene products using poly(I:C) resulted in decreased DENV-2 replication in the cell line. In contrast, the RNAi-mediated suppression of l(2)efl gene products resulted in enhanced DENV-2 replication, but this enhancement occurred only if multiple l(2)efl genes were suppressed. l(2)efl homologs induce the phosphorylation of eukaryotic initiation factor 2α (eIF2α) in the fruit fly Drosophila melanogaster, and we confirmed this finding in the cell line. However, the mechanism by which l(2)efl phosphorylates eIF2α remains unclear. We conclude that l(2)efl encodes a potential anti-dengue protein in the vector mosquito. MDPI 2020-10-12 /pmc/articles/PMC7593908/ /pubmed/33053895 http://dx.doi.org/10.3390/ijms21207520 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Runtuwene, Lucky R.
Kawashima, Shuichi
Pijoh, Victor D.
Tuda, Josef S. B.
Hayashida, Kyoko
Yamagishi, Junya
Sugimoto, Chihiro
Nishiyama, Shoko
Sasaki, Michihito
Orba, Yasuko
Sawa, Hirofumi
Takasaki, Tomohiko
James, Anthony A.
Kobayashi, Takashi
Eshita, Yuki
The Lethal(2)-Essential-for-Life [L(2)EFL] Gene Family Modulates Dengue Virus Infection in Aedes aegypti
title The Lethal(2)-Essential-for-Life [L(2)EFL] Gene Family Modulates Dengue Virus Infection in Aedes aegypti
title_full The Lethal(2)-Essential-for-Life [L(2)EFL] Gene Family Modulates Dengue Virus Infection in Aedes aegypti
title_fullStr The Lethal(2)-Essential-for-Life [L(2)EFL] Gene Family Modulates Dengue Virus Infection in Aedes aegypti
title_full_unstemmed The Lethal(2)-Essential-for-Life [L(2)EFL] Gene Family Modulates Dengue Virus Infection in Aedes aegypti
title_short The Lethal(2)-Essential-for-Life [L(2)EFL] Gene Family Modulates Dengue Virus Infection in Aedes aegypti
title_sort lethal(2)-essential-for-life [l(2)efl] gene family modulates dengue virus infection in aedes aegypti
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593908/
https://www.ncbi.nlm.nih.gov/pubmed/33053895
http://dx.doi.org/10.3390/ijms21207520
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