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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...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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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. |
format | Online Article Text |
id | pubmed-7593908 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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