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High-throughput sequencing identification and characterization of potentially adhesion-related small RNAs in Streptococcus mutans
PURPOSE: Adherence capacity is one of the principal virulence factors of Streptococcus mutans, and adhesion virulence factors are controlled by small RNAs (sRNAs) at the post-transcriptional level in various bacteria. Here, we aimed to identify and decipher putative adhesion-related sRNAs in clinica...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Microbiology Society
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5994696/ https://www.ncbi.nlm.nih.gov/pubmed/29595415 http://dx.doi.org/10.1099/jmm.0.000718 |
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author | Zhu, Wenhui Liu, Shanshan Liu, Jia Zhou, Yan Lin, Huancai |
author_facet | Zhu, Wenhui Liu, Shanshan Liu, Jia Zhou, Yan Lin, Huancai |
author_sort | Zhu, Wenhui |
collection | PubMed |
description | PURPOSE: Adherence capacity is one of the principal virulence factors of Streptococcus mutans, and adhesion virulence factors are controlled by small RNAs (sRNAs) at the post-transcriptional level in various bacteria. Here, we aimed to identify and decipher putative adhesion-related sRNAs in clinical strains of S. mutans. METHODOLOGY: RNA deep-sequencing was performed to identify potential sRNAs under different adhesion conditions. The expression of sRNAs was analysed by quantitative real-time PCR (qRT-PCR), and bioinformatic methods were used to predict the functional characteristics of sRNAs. RESULTS: A total of 736 differentially expressed candidate sRNAs were predicted, and these included 352 sRNAs located on the antisense to mRNA (AM) and 384 sRNAs in intergenic regions (IGRs). The top 7 differentially expressed sRNAs were successfully validated by qRT-PCR in UA159, and 2 of these were further confirmed in 100 clinical isolates. Moreover, the sequences of two sRNAs were conserved in other Streptococcus species, indicating a conserved role in such closely related species. A good correlation between the expression of sRNAs and the adhesion of 100 clinical strains was observed, which, combined with GO and KEGG, provides a perspective for the comprehension of sRNA function annotation. CONCLUSION: This study revealed a multitude of novel putative adhesion-related sRNAs in S. mutans and contributed to a better understanding of information concerning the transcriptional regulation of adhesion in S. mutans. |
format | Online Article Text |
id | pubmed-5994696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Microbiology Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-59946962018-06-13 High-throughput sequencing identification and characterization of potentially adhesion-related small RNAs in Streptococcus mutans Zhu, Wenhui Liu, Shanshan Liu, Jia Zhou, Yan Lin, Huancai J Med Microbiol Research Article PURPOSE: Adherence capacity is one of the principal virulence factors of Streptococcus mutans, and adhesion virulence factors are controlled by small RNAs (sRNAs) at the post-transcriptional level in various bacteria. Here, we aimed to identify and decipher putative adhesion-related sRNAs in clinical strains of S. mutans. METHODOLOGY: RNA deep-sequencing was performed to identify potential sRNAs under different adhesion conditions. The expression of sRNAs was analysed by quantitative real-time PCR (qRT-PCR), and bioinformatic methods were used to predict the functional characteristics of sRNAs. RESULTS: A total of 736 differentially expressed candidate sRNAs were predicted, and these included 352 sRNAs located on the antisense to mRNA (AM) and 384 sRNAs in intergenic regions (IGRs). The top 7 differentially expressed sRNAs were successfully validated by qRT-PCR in UA159, and 2 of these were further confirmed in 100 clinical isolates. Moreover, the sequences of two sRNAs were conserved in other Streptococcus species, indicating a conserved role in such closely related species. A good correlation between the expression of sRNAs and the adhesion of 100 clinical strains was observed, which, combined with GO and KEGG, provides a perspective for the comprehension of sRNA function annotation. CONCLUSION: This study revealed a multitude of novel putative adhesion-related sRNAs in S. mutans and contributed to a better understanding of information concerning the transcriptional regulation of adhesion in S. mutans. Microbiology Society 2018-05 2018-03-29 /pmc/articles/PMC5994696/ /pubmed/29595415 http://dx.doi.org/10.1099/jmm.0.000718 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Zhu, Wenhui Liu, Shanshan Liu, Jia Zhou, Yan Lin, Huancai High-throughput sequencing identification and characterization of potentially adhesion-related small RNAs in Streptococcus mutans |
title | High-throughput sequencing identification and characterization of potentially adhesion-related small RNAs in Streptococcus mutans |
title_full | High-throughput sequencing identification and characterization of potentially adhesion-related small RNAs in Streptococcus mutans |
title_fullStr | High-throughput sequencing identification and characterization of potentially adhesion-related small RNAs in Streptococcus mutans |
title_full_unstemmed | High-throughput sequencing identification and characterization of potentially adhesion-related small RNAs in Streptococcus mutans |
title_short | High-throughput sequencing identification and characterization of potentially adhesion-related small RNAs in Streptococcus mutans |
title_sort | high-throughput sequencing identification and characterization of potentially adhesion-related small rnas in streptococcus mutans |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5994696/ https://www.ncbi.nlm.nih.gov/pubmed/29595415 http://dx.doi.org/10.1099/jmm.0.000718 |
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