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Autophagy in Zika Virus Infection: A Possible Therapeutic Target to Counteract Viral Replication
Zika virus (ZIKV) still constitutes a public health concern, however, no vaccines or therapies are currently approved for treatment. A fundamental process involved in ZIKV infection is autophagy, a cellular catabolic pathway delivering cytoplasmic cargo to the lysosome for degradation—considered as...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429311/ https://www.ncbi.nlm.nih.gov/pubmed/30823365 http://dx.doi.org/10.3390/ijms20051048 |
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author | Gratton, Rossella Agrelli, Almerinda Tricarico, Paola Maura Brandão, Lucas Crovella, Sergio |
author_facet | Gratton, Rossella Agrelli, Almerinda Tricarico, Paola Maura Brandão, Lucas Crovella, Sergio |
author_sort | Gratton, Rossella |
collection | PubMed |
description | Zika virus (ZIKV) still constitutes a public health concern, however, no vaccines or therapies are currently approved for treatment. A fundamental process involved in ZIKV infection is autophagy, a cellular catabolic pathway delivering cytoplasmic cargo to the lysosome for degradation—considered as a primordial form of innate immunity against invading microorganisms. ZIKV is thought to inhibit the Akt-mTOR signaling pathway, which causes aberrant activation of autophagy promoting viral replication and propagation. It is therefore appealing to study the role of autophagic molecular effectors during viral infection to identify potential targets for anti-ZIKV therapeutic intervention. |
format | Online Article Text |
id | pubmed-6429311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64293112019-04-10 Autophagy in Zika Virus Infection: A Possible Therapeutic Target to Counteract Viral Replication Gratton, Rossella Agrelli, Almerinda Tricarico, Paola Maura Brandão, Lucas Crovella, Sergio Int J Mol Sci Review Zika virus (ZIKV) still constitutes a public health concern, however, no vaccines or therapies are currently approved for treatment. A fundamental process involved in ZIKV infection is autophagy, a cellular catabolic pathway delivering cytoplasmic cargo to the lysosome for degradation—considered as a primordial form of innate immunity against invading microorganisms. ZIKV is thought to inhibit the Akt-mTOR signaling pathway, which causes aberrant activation of autophagy promoting viral replication and propagation. It is therefore appealing to study the role of autophagic molecular effectors during viral infection to identify potential targets for anti-ZIKV therapeutic intervention. MDPI 2019-02-28 /pmc/articles/PMC6429311/ /pubmed/30823365 http://dx.doi.org/10.3390/ijms20051048 Text en © 2019 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 | Review Gratton, Rossella Agrelli, Almerinda Tricarico, Paola Maura Brandão, Lucas Crovella, Sergio Autophagy in Zika Virus Infection: A Possible Therapeutic Target to Counteract Viral Replication |
title | Autophagy in Zika Virus Infection: A Possible Therapeutic Target to Counteract Viral Replication |
title_full | Autophagy in Zika Virus Infection: A Possible Therapeutic Target to Counteract Viral Replication |
title_fullStr | Autophagy in Zika Virus Infection: A Possible Therapeutic Target to Counteract Viral Replication |
title_full_unstemmed | Autophagy in Zika Virus Infection: A Possible Therapeutic Target to Counteract Viral Replication |
title_short | Autophagy in Zika Virus Infection: A Possible Therapeutic Target to Counteract Viral Replication |
title_sort | autophagy in zika virus infection: a possible therapeutic target to counteract viral replication |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429311/ https://www.ncbi.nlm.nih.gov/pubmed/30823365 http://dx.doi.org/10.3390/ijms20051048 |
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