Drosha, DGCR8, and Dicer mRNAs are down-regulated in human cells infected with dengue virus 4, and play a role in viral pathogenesis

Detalhes bibliográficos
Autor(a) principal: Casseb, Samir Mansour Moraes
Data de Publicação: 2016
Outros Autores: Simith, Darlene de Brito, Melo, Karla Fabiane Lopes de, Mendonça, M. H, Santos, A. C. M, Carvalho, Valéria Lima, Cruz, Ana Cecília Ribeiro, Vasconcelos, Pedro Fernando da Costa
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Digital do Instituto Evandro Chagas (Patuá)
Texto Completo: https://patua.iec.gov.br/handle/iec/2097
Resumo: Dengue virus (DENV) and its four serotypes (DENV1- 4) belong to the Flavivirus genus of the Flaviviridae family. DENV infection is a life-threatening disease, which results in up to 20,000 deaths each year. Viruses have been shown to encode trans-regulatory small RNAs, or microRNAs (miRNAs), which bind to messenger RNA and negatively regulate host or viral gene expression. During DENV infections, miRNAs interact with proteins in the RNAi pathway, and are processed by ribonucleases such as Dicer and Drosha. This study aims to investigate Drosha, DGCR8, and Dicer expression levels in human A-549 cells following DENV4 infection. DENV4 infected A-549 cells were collected daily for 5 days, and RNA was extracted to quantify viral load. Gene expression of Drosha, Dicer, and DGCR8 was determined using quantitative PCR (RT-qPCR). We found that DENV4 infection exhibited the highest viral load 3 days post-infection. Dicer, Drosha, and DGCR8 showed reduced expression following S.M.M. Casseb et al. 2 Genetics and Molecular Research 15 (2): gmr.15027891 ©FUNPEC-RP www.funpecrp.com.br DENV4 infection as compared with negative controls. In addition, we hypothesize that reduced expression of DGCR8 may not only be related to miRNA biogenesis, but also other small RNAs. This study may change our understanding regarding the relationship between host cells and the dengue virus.
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spelling Casseb, Samir Mansour MoraesSimith, Darlene de BritoMelo, Karla Fabiane Lopes deMendonça, M. HSantos, A. C. MCarvalho, Valéria LimaCruz, Ana Cecília RibeiroVasconcelos, Pedro Fernando da Costa2016-06-09T12:01:10Z2016-06-09T12:01:10Z2016CASSEB, Samir Mansour Moraes et al. Drosha, DGCR8, and Dicer mRNAs are down-regulated in human cells infected with dengue virus 4, and play a role in viral pathogenesis. Genetics and Molecular Research, v. 15, n. 2, p. 1-8, May 2016.1676-5680https://patua.iec.gov.br/handle/iec/209710.4238/GMR.15027891Dengue virus (DENV) and its four serotypes (DENV1- 4) belong to the Flavivirus genus of the Flaviviridae family. DENV infection is a life-threatening disease, which results in up to 20,000 deaths each year. Viruses have been shown to encode trans-regulatory small RNAs, or microRNAs (miRNAs), which bind to messenger RNA and negatively regulate host or viral gene expression. During DENV infections, miRNAs interact with proteins in the RNAi pathway, and are processed by ribonucleases such as Dicer and Drosha. This study aims to investigate Drosha, DGCR8, and Dicer expression levels in human A-549 cells following DENV4 infection. DENV4 infected A-549 cells were collected daily for 5 days, and RNA was extracted to quantify viral load. Gene expression of Drosha, Dicer, and DGCR8 was determined using quantitative PCR (RT-qPCR). We found that DENV4 infection exhibited the highest viral load 3 days post-infection. Dicer, Drosha, and DGCR8 showed reduced expression following S.M.M. Casseb et al. 2 Genetics and Molecular Research 15 (2): gmr.15027891 ©FUNPEC-RP www.funpecrp.com.br DENV4 infection as compared with negative controls. In addition, we hypothesize that reduced expression of DGCR8 may not only be related to miRNA biogenesis, but also other small RNAs. This study may change our understanding regarding the relationship between host cells and the dengue virus.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Ananindeua, PA, Brasil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Ananindeua, PA, Brasil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Ananindeua, PA, Brasil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Ananindeua, PA, Brasil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Ananindeua, PA, Brasil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Ananindeua, PA, Brasil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Ananindeua, PA, Brasil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. 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dc.title.pt_BR.fl_str_mv Drosha, DGCR8, and Dicer mRNAs are down-regulated in human cells infected with dengue virus 4, and play a role in viral pathogenesis
title Drosha, DGCR8, and Dicer mRNAs are down-regulated in human cells infected with dengue virus 4, and play a role in viral pathogenesis
spellingShingle Drosha, DGCR8, and Dicer mRNAs are down-regulated in human cells infected with dengue virus 4, and play a role in viral pathogenesis
Casseb, Samir Mansour Moraes
Dengue
Vírus da Dengue / genética
RNA Viral / genética
MicroRNAs / metabolismo
Replicação Viral
Proteínas de Ligação a RNA
Arbovirus
DGCR8
Reação em Cadeia da Polimerase Via Transcriptase Reversa / métodos
title_short Drosha, DGCR8, and Dicer mRNAs are down-regulated in human cells infected with dengue virus 4, and play a role in viral pathogenesis
title_full Drosha, DGCR8, and Dicer mRNAs are down-regulated in human cells infected with dengue virus 4, and play a role in viral pathogenesis
title_fullStr Drosha, DGCR8, and Dicer mRNAs are down-regulated in human cells infected with dengue virus 4, and play a role in viral pathogenesis
title_full_unstemmed Drosha, DGCR8, and Dicer mRNAs are down-regulated in human cells infected with dengue virus 4, and play a role in viral pathogenesis
title_sort Drosha, DGCR8, and Dicer mRNAs are down-regulated in human cells infected with dengue virus 4, and play a role in viral pathogenesis
author Casseb, Samir Mansour Moraes
author_facet Casseb, Samir Mansour Moraes
Simith, Darlene de Brito
Melo, Karla Fabiane Lopes de
Mendonça, M. H
Santos, A. C. M
Carvalho, Valéria Lima
Cruz, Ana Cecília Ribeiro
Vasconcelos, Pedro Fernando da Costa
author_role author
author2 Simith, Darlene de Brito
Melo, Karla Fabiane Lopes de
Mendonça, M. H
Santos, A. C. M
Carvalho, Valéria Lima
Cruz, Ana Cecília Ribeiro
Vasconcelos, Pedro Fernando da Costa
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Casseb, Samir Mansour Moraes
Simith, Darlene de Brito
Melo, Karla Fabiane Lopes de
Mendonça, M. H
Santos, A. C. M
Carvalho, Valéria Lima
Cruz, Ana Cecília Ribeiro
Vasconcelos, Pedro Fernando da Costa
dc.subject.decsPrimary.pt_BR.fl_str_mv Dengue
Vírus da Dengue / genética
RNA Viral / genética
MicroRNAs / metabolismo
Replicação Viral
Proteínas de Ligação a RNA
Arbovirus
DGCR8
Reação em Cadeia da Polimerase Via Transcriptase Reversa / métodos
topic Dengue
Vírus da Dengue / genética
RNA Viral / genética
MicroRNAs / metabolismo
Replicação Viral
Proteínas de Ligação a RNA
Arbovirus
DGCR8
Reação em Cadeia da Polimerase Via Transcriptase Reversa / métodos
description Dengue virus (DENV) and its four serotypes (DENV1- 4) belong to the Flavivirus genus of the Flaviviridae family. DENV infection is a life-threatening disease, which results in up to 20,000 deaths each year. Viruses have been shown to encode trans-regulatory small RNAs, or microRNAs (miRNAs), which bind to messenger RNA and negatively regulate host or viral gene expression. During DENV infections, miRNAs interact with proteins in the RNAi pathway, and are processed by ribonucleases such as Dicer and Drosha. This study aims to investigate Drosha, DGCR8, and Dicer expression levels in human A-549 cells following DENV4 infection. DENV4 infected A-549 cells were collected daily for 5 days, and RNA was extracted to quantify viral load. Gene expression of Drosha, Dicer, and DGCR8 was determined using quantitative PCR (RT-qPCR). We found that DENV4 infection exhibited the highest viral load 3 days post-infection. Dicer, Drosha, and DGCR8 showed reduced expression following S.M.M. Casseb et al. 2 Genetics and Molecular Research 15 (2): gmr.15027891 ©FUNPEC-RP www.funpecrp.com.br DENV4 infection as compared with negative controls. In addition, we hypothesize that reduced expression of DGCR8 may not only be related to miRNA biogenesis, but also other small RNAs. This study may change our understanding regarding the relationship between host cells and the dengue virus.
publishDate 2016
dc.date.accessioned.fl_str_mv 2016-06-09T12:01:10Z
dc.date.available.fl_str_mv 2016-06-09T12:01:10Z
dc.date.issued.fl_str_mv 2016
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.citation.fl_str_mv CASSEB, Samir Mansour Moraes et al. Drosha, DGCR8, and Dicer mRNAs are down-regulated in human cells infected with dengue virus 4, and play a role in viral pathogenesis. Genetics and Molecular Research, v. 15, n. 2, p. 1-8, May 2016.
dc.identifier.uri.fl_str_mv https://patua.iec.gov.br/handle/iec/2097
dc.identifier.issn.-.fl_str_mv 1676-5680
dc.identifier.doi.-.fl_str_mv 10.4238/GMR.15027891
identifier_str_mv CASSEB, Samir Mansour Moraes et al. Drosha, DGCR8, and Dicer mRNAs are down-regulated in human cells infected with dengue virus 4, and play a role in viral pathogenesis. Genetics and Molecular Research, v. 15, n. 2, p. 1-8, May 2016.
1676-5680
10.4238/GMR.15027891
url https://patua.iec.gov.br/handle/iec/2097
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