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Strain Variation Can Significantly Modulate the miRNA Response to Zika Virus Infection
Zika virus (ZIKV) is a mosquito-transmitted virus that has emerged as a major public health concern due to its association with neurological disorders in humans, including microcephaly in fetuses. ZIKV infection has been shown to alter the miRNA profile in host cells, and these changes can contain e...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10671159/ https://www.ncbi.nlm.nih.gov/pubmed/38003407 http://dx.doi.org/10.3390/ijms242216216 |
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author | Ramphan, Suwipa Chumchanchira, Chanida Sornjai, Wannapa Chailangkarn, Thanathom Jongkaewwattana, Anan Assavalapsakul, Wanchai Smith, Duncan R. |
author_facet | Ramphan, Suwipa Chumchanchira, Chanida Sornjai, Wannapa Chailangkarn, Thanathom Jongkaewwattana, Anan Assavalapsakul, Wanchai Smith, Duncan R. |
author_sort | Ramphan, Suwipa |
collection | PubMed |
description | Zika virus (ZIKV) is a mosquito-transmitted virus that has emerged as a major public health concern due to its association with neurological disorders in humans, including microcephaly in fetuses. ZIKV infection has been shown to alter the miRNA profile in host cells, and these changes can contain elements that are proviral, while others can be antiviral in action. In this study, the expression of 22 miRNAs in human A549 cells infected with two different ZIKV isolates was investigated. All of the investigated miRNAs showed significant changes in expression at at least one time point examined. Markedly, 18 of the miRNAs examined showed statistically significant differences in expression between the two strains examined. Four miRNAs (miR-21, miR-34a, miR-128 and miR-155) were subsequently selected for further investigation. These four miRNAs were shown to modulate antiviral effects against ZIKV, as downregulation of their expression through anti-miRNA oligonucleotides resulted in increased virus production, whereas their overexpression through miRNA mimics reduced virus production. However, statistically significant changes were again seen when comparing the two strains investigated. Lastly, candidate targets of the miRNAs miR-34a and miR-128 were examined at the level of the mRNA and protein. HSP70 was identified as a target of miR-34a, but, again, the effects were strain type-specific. The two ZIKV strains used in this study differ by only nine amino acids, and the results highlight that consideration must be given to strain type variation when examining the roles of miRNAs in ZIKV, and probably other virus infections. |
format | Online Article Text |
id | pubmed-10671159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106711592023-11-11 Strain Variation Can Significantly Modulate the miRNA Response to Zika Virus Infection Ramphan, Suwipa Chumchanchira, Chanida Sornjai, Wannapa Chailangkarn, Thanathom Jongkaewwattana, Anan Assavalapsakul, Wanchai Smith, Duncan R. Int J Mol Sci Article Zika virus (ZIKV) is a mosquito-transmitted virus that has emerged as a major public health concern due to its association with neurological disorders in humans, including microcephaly in fetuses. ZIKV infection has been shown to alter the miRNA profile in host cells, and these changes can contain elements that are proviral, while others can be antiviral in action. In this study, the expression of 22 miRNAs in human A549 cells infected with two different ZIKV isolates was investigated. All of the investigated miRNAs showed significant changes in expression at at least one time point examined. Markedly, 18 of the miRNAs examined showed statistically significant differences in expression between the two strains examined. Four miRNAs (miR-21, miR-34a, miR-128 and miR-155) were subsequently selected for further investigation. These four miRNAs were shown to modulate antiviral effects against ZIKV, as downregulation of their expression through anti-miRNA oligonucleotides resulted in increased virus production, whereas their overexpression through miRNA mimics reduced virus production. However, statistically significant changes were again seen when comparing the two strains investigated. Lastly, candidate targets of the miRNAs miR-34a and miR-128 were examined at the level of the mRNA and protein. HSP70 was identified as a target of miR-34a, but, again, the effects were strain type-specific. The two ZIKV strains used in this study differ by only nine amino acids, and the results highlight that consideration must be given to strain type variation when examining the roles of miRNAs in ZIKV, and probably other virus infections. MDPI 2023-11-11 /pmc/articles/PMC10671159/ /pubmed/38003407 http://dx.doi.org/10.3390/ijms242216216 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ramphan, Suwipa Chumchanchira, Chanida Sornjai, Wannapa Chailangkarn, Thanathom Jongkaewwattana, Anan Assavalapsakul, Wanchai Smith, Duncan R. Strain Variation Can Significantly Modulate the miRNA Response to Zika Virus Infection |
title | Strain Variation Can Significantly Modulate the miRNA Response to Zika Virus Infection |
title_full | Strain Variation Can Significantly Modulate the miRNA Response to Zika Virus Infection |
title_fullStr | Strain Variation Can Significantly Modulate the miRNA Response to Zika Virus Infection |
title_full_unstemmed | Strain Variation Can Significantly Modulate the miRNA Response to Zika Virus Infection |
title_short | Strain Variation Can Significantly Modulate the miRNA Response to Zika Virus Infection |
title_sort | strain variation can significantly modulate the mirna response to zika virus infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10671159/ https://www.ncbi.nlm.nih.gov/pubmed/38003407 http://dx.doi.org/10.3390/ijms242216216 |
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