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Next Generation Sequencing Reveals Regulation of Distinct Aedes microRNAs during Chikungunya Virus Development
BACKGROUND: Application of genomics and Next Generation sequencing has led to the identification of new class of cellular functional molecules, namely, small RNAs. Of the several classes of ncRNAs (non-coding RNA), microRNAs have been demonstrated to exert determinative influence on various cellular...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3888459/ https://www.ncbi.nlm.nih.gov/pubmed/24421911 http://dx.doi.org/10.1371/journal.pntd.0002616 |
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author | Shrinet, Jatin Jain, Shanu Jain, Jaspreet Bhatnagar, Raj K. Sunil, Sujatha |
author_facet | Shrinet, Jatin Jain, Shanu Jain, Jaspreet Bhatnagar, Raj K. Sunil, Sujatha |
author_sort | Shrinet, Jatin |
collection | PubMed |
description | BACKGROUND: Application of genomics and Next Generation sequencing has led to the identification of new class of cellular functional molecules, namely, small RNAs. Of the several classes of ncRNAs (non-coding RNA), microRNAs have been demonstrated to exert determinative influence on various cellular processes. It is becoming abundantly clear that host/vector/pathogen encoded microRNAs impact eventual pathogenesis. In this context, the participation of vector based microRNAs in disease transmission and pathogen development is being investigated intensively. A few studies have highlighted the role of vector encoded microRNAs in pathogen infection. We conducted this study to evaluate the role of host miRNAs upon CHIKV (Chikungunya Virus) infection in an important vector, Aedes albopictus. FINDINGS: We identified 88 and 79 known miRNAs in uninfected and CHIKV infected Ae. albopictus Singh's cell line respectively. We further identified nine novel miRNAs in Ae. albopictus. Comparison of the two libraries revealed differential expression of 77 common miRNAs between them. CHIKV infection specifically altered the miRNA profile of a specific set of eight miRNAs. Putative targets of these regulated miRNAs were identified and classified into their pathways. CONCLUSIONS: In our study we have identified and described the profiles of various miRNAs upon CHIKV infection in Ae. albopictus. This investigation provides an insight about cellular modification by miRNAs during CHIKV infection and the results provide leads for identifying potential candidates for vector based antiviral strategies. |
format | Online Article Text |
id | pubmed-3888459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38884592014-01-13 Next Generation Sequencing Reveals Regulation of Distinct Aedes microRNAs during Chikungunya Virus Development Shrinet, Jatin Jain, Shanu Jain, Jaspreet Bhatnagar, Raj K. Sunil, Sujatha PLoS Negl Trop Dis Research Article BACKGROUND: Application of genomics and Next Generation sequencing has led to the identification of new class of cellular functional molecules, namely, small RNAs. Of the several classes of ncRNAs (non-coding RNA), microRNAs have been demonstrated to exert determinative influence on various cellular processes. It is becoming abundantly clear that host/vector/pathogen encoded microRNAs impact eventual pathogenesis. In this context, the participation of vector based microRNAs in disease transmission and pathogen development is being investigated intensively. A few studies have highlighted the role of vector encoded microRNAs in pathogen infection. We conducted this study to evaluate the role of host miRNAs upon CHIKV (Chikungunya Virus) infection in an important vector, Aedes albopictus. FINDINGS: We identified 88 and 79 known miRNAs in uninfected and CHIKV infected Ae. albopictus Singh's cell line respectively. We further identified nine novel miRNAs in Ae. albopictus. Comparison of the two libraries revealed differential expression of 77 common miRNAs between them. CHIKV infection specifically altered the miRNA profile of a specific set of eight miRNAs. Putative targets of these regulated miRNAs were identified and classified into their pathways. CONCLUSIONS: In our study we have identified and described the profiles of various miRNAs upon CHIKV infection in Ae. albopictus. This investigation provides an insight about cellular modification by miRNAs during CHIKV infection and the results provide leads for identifying potential candidates for vector based antiviral strategies. Public Library of Science 2014-01-09 /pmc/articles/PMC3888459/ /pubmed/24421911 http://dx.doi.org/10.1371/journal.pntd.0002616 Text en © 2014 Shrinet et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Shrinet, Jatin Jain, Shanu Jain, Jaspreet Bhatnagar, Raj K. Sunil, Sujatha Next Generation Sequencing Reveals Regulation of Distinct Aedes microRNAs during Chikungunya Virus Development |
title | Next Generation Sequencing Reveals Regulation of Distinct Aedes microRNAs during Chikungunya Virus Development |
title_full | Next Generation Sequencing Reveals Regulation of Distinct Aedes microRNAs during Chikungunya Virus Development |
title_fullStr | Next Generation Sequencing Reveals Regulation of Distinct Aedes microRNAs during Chikungunya Virus Development |
title_full_unstemmed | Next Generation Sequencing Reveals Regulation of Distinct Aedes microRNAs during Chikungunya Virus Development |
title_short | Next Generation Sequencing Reveals Regulation of Distinct Aedes microRNAs during Chikungunya Virus Development |
title_sort | next generation sequencing reveals regulation of distinct aedes micrornas during chikungunya virus development |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3888459/ https://www.ncbi.nlm.nih.gov/pubmed/24421911 http://dx.doi.org/10.1371/journal.pntd.0002616 |
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