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Identification and initial characterization of Hfq-associated sRNAs in Histophilus somni strain 2336
Small RNAs (sRNA), in association with the global chaperone regulator Hfq, positively or negatively regulate gene expression in bacteria. For this study, Histophilus somni sRNAs that bind to Hfq were identified and then partially characterized. The Hfq-associated sRNAs in H. somni were isolated and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10204968/ https://www.ncbi.nlm.nih.gov/pubmed/37220152 http://dx.doi.org/10.1371/journal.pone.0286158 |
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author | Subhadra, Bindu Cao, Dianjun Jensen, Roderick Caswell, Clayton Inzana, Thomas J. |
author_facet | Subhadra, Bindu Cao, Dianjun Jensen, Roderick Caswell, Clayton Inzana, Thomas J. |
author_sort | Subhadra, Bindu |
collection | PubMed |
description | Small RNAs (sRNA), in association with the global chaperone regulator Hfq, positively or negatively regulate gene expression in bacteria. For this study, Histophilus somni sRNAs that bind to Hfq were identified and then partially characterized. The Hfq-associated sRNAs in H. somni were isolated and identified by co-immunoprecipitation using anti-Hfq antibody, followed by sRNA sequencing. Sequence analysis of the sRNA samples identified 100 putative sRNAs, out of which 16 were present in pathogenic strain 2336, but not in non-pathogenic strain 129Pt. Bioinformatic analyses suggested that the sRNAs HS9, HS79, and HS97 could bind to many genes putatively involved in virulence/biofilm formation. Furthermore, multi-sequence alignment of the sRNA regions in the genome revealed that HS9 and HS97 could interact with sigma 54, which is a transcription factor linked to important bacterial traits, including motility, virulence, and biofilm formation. Northern blotting was used to determine the approximate size, abundance and any processing events attributed to the sRNAs. Selected sRNA candidates were confirmed to bind Hfq, as determined by electrophoretic mobility shift assays using sRNAs synthesized by in vitro transcription and recombinant Hfq. The exact transcriptional start site of the sRNA candidates was determined by RNA ligase-mediated rapid amplification of cDNA ends, followed by cloning and sequencing. This is the first investigation of H. somni sRNAs that show they may have important regulatory roles in virulence and biofilm formation. |
format | Online Article Text |
id | pubmed-10204968 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-102049682023-05-24 Identification and initial characterization of Hfq-associated sRNAs in Histophilus somni strain 2336 Subhadra, Bindu Cao, Dianjun Jensen, Roderick Caswell, Clayton Inzana, Thomas J. PLoS One Research Article Small RNAs (sRNA), in association with the global chaperone regulator Hfq, positively or negatively regulate gene expression in bacteria. For this study, Histophilus somni sRNAs that bind to Hfq were identified and then partially characterized. The Hfq-associated sRNAs in H. somni were isolated and identified by co-immunoprecipitation using anti-Hfq antibody, followed by sRNA sequencing. Sequence analysis of the sRNA samples identified 100 putative sRNAs, out of which 16 were present in pathogenic strain 2336, but not in non-pathogenic strain 129Pt. Bioinformatic analyses suggested that the sRNAs HS9, HS79, and HS97 could bind to many genes putatively involved in virulence/biofilm formation. Furthermore, multi-sequence alignment of the sRNA regions in the genome revealed that HS9 and HS97 could interact with sigma 54, which is a transcription factor linked to important bacterial traits, including motility, virulence, and biofilm formation. Northern blotting was used to determine the approximate size, abundance and any processing events attributed to the sRNAs. Selected sRNA candidates were confirmed to bind Hfq, as determined by electrophoretic mobility shift assays using sRNAs synthesized by in vitro transcription and recombinant Hfq. The exact transcriptional start site of the sRNA candidates was determined by RNA ligase-mediated rapid amplification of cDNA ends, followed by cloning and sequencing. This is the first investigation of H. somni sRNAs that show they may have important regulatory roles in virulence and biofilm formation. Public Library of Science 2023-05-23 /pmc/articles/PMC10204968/ /pubmed/37220152 http://dx.doi.org/10.1371/journal.pone.0286158 Text en © 2023 Subhadra et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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 Subhadra, Bindu Cao, Dianjun Jensen, Roderick Caswell, Clayton Inzana, Thomas J. Identification and initial characterization of Hfq-associated sRNAs in Histophilus somni strain 2336 |
title | Identification and initial characterization of Hfq-associated sRNAs in Histophilus somni strain 2336 |
title_full | Identification and initial characterization of Hfq-associated sRNAs in Histophilus somni strain 2336 |
title_fullStr | Identification and initial characterization of Hfq-associated sRNAs in Histophilus somni strain 2336 |
title_full_unstemmed | Identification and initial characterization of Hfq-associated sRNAs in Histophilus somni strain 2336 |
title_short | Identification and initial characterization of Hfq-associated sRNAs in Histophilus somni strain 2336 |
title_sort | identification and initial characterization of hfq-associated srnas in histophilus somni strain 2336 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10204968/ https://www.ncbi.nlm.nih.gov/pubmed/37220152 http://dx.doi.org/10.1371/journal.pone.0286158 |
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