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Regulation of pneumococcal epigenetic and colony phases by multiple two-component regulatory systems
Streptococcus pneumoniae is well known for phase variation between opaque (O) and transparent (T) colonies within clonal populations. While the O variant is specialized in invasive infection (with a thicker capsule and higher resistance to host clearance), the T counterpart possesses a relatively th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105139/ https://www.ncbi.nlm.nih.gov/pubmed/32187228 http://dx.doi.org/10.1371/journal.ppat.1008417 |
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author | Wang, Juanjuan Li, Jing-Wen Li, Jing Huang, Yijia Wang, Shaomeng Zhang, Jing-Ren |
author_facet | Wang, Juanjuan Li, Jing-Wen Li, Jing Huang, Yijia Wang, Shaomeng Zhang, Jing-Ren |
author_sort | Wang, Juanjuan |
collection | PubMed |
description | Streptococcus pneumoniae is well known for phase variation between opaque (O) and transparent (T) colonies within clonal populations. While the O variant is specialized in invasive infection (with a thicker capsule and higher resistance to host clearance), the T counterpart possesses a relatively thinner capsule and thereby higher airway adherence and colonization. Our previous study found that phase variation is caused by reversible switches of the “opaque ON-or-OFF” methylomes or methylation patterns of pneumococcal genome, which is dominantly driven by the PsrA-catalyzed inversions of the DNA methyltransferase hsdS genes. This study revealed that switch frequency between the O and T variants is regulated by five transcriptional response regulators (rr) of the two-component systems (TCSs). The mutants of rr06, rr08, rr09, rr11 and rr14 produced significantly fewer O and more T colonies. Further mutagenesis revealed that RR06, RR08, RR09 and RR11 enrich the O variant by modulating the directions of the PsrA-catalyzed inversion reactions. In contrast, the impact of RR14 (RitR) on phase variation is independent of PsrA. Consistently, SMRT sequencing uncovered significantly diminished “opaque ON” methylome in the mutants of rr06, rr08, rr09 and rr11 but not that of rr14. Lastly, the phosphorylated form of RR11 was shown to activate the transcription of comW and two sugar utilization systems that are necessary for maintenance of the “opaque ON” genotype and phenotype. This work has thus uncovered multiple novel mechanisms that balance pneumococcal epigenetic status and physiology. |
format | Online Article Text |
id | pubmed-7105139 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-71051392020-04-03 Regulation of pneumococcal epigenetic and colony phases by multiple two-component regulatory systems Wang, Juanjuan Li, Jing-Wen Li, Jing Huang, Yijia Wang, Shaomeng Zhang, Jing-Ren PLoS Pathog Research Article Streptococcus pneumoniae is well known for phase variation between opaque (O) and transparent (T) colonies within clonal populations. While the O variant is specialized in invasive infection (with a thicker capsule and higher resistance to host clearance), the T counterpart possesses a relatively thinner capsule and thereby higher airway adherence and colonization. Our previous study found that phase variation is caused by reversible switches of the “opaque ON-or-OFF” methylomes or methylation patterns of pneumococcal genome, which is dominantly driven by the PsrA-catalyzed inversions of the DNA methyltransferase hsdS genes. This study revealed that switch frequency between the O and T variants is regulated by five transcriptional response regulators (rr) of the two-component systems (TCSs). The mutants of rr06, rr08, rr09, rr11 and rr14 produced significantly fewer O and more T colonies. Further mutagenesis revealed that RR06, RR08, RR09 and RR11 enrich the O variant by modulating the directions of the PsrA-catalyzed inversion reactions. In contrast, the impact of RR14 (RitR) on phase variation is independent of PsrA. Consistently, SMRT sequencing uncovered significantly diminished “opaque ON” methylome in the mutants of rr06, rr08, rr09 and rr11 but not that of rr14. Lastly, the phosphorylated form of RR11 was shown to activate the transcription of comW and two sugar utilization systems that are necessary for maintenance of the “opaque ON” genotype and phenotype. This work has thus uncovered multiple novel mechanisms that balance pneumococcal epigenetic status and physiology. Public Library of Science 2020-03-18 /pmc/articles/PMC7105139/ /pubmed/32187228 http://dx.doi.org/10.1371/journal.ppat.1008417 Text en © 2020 Wang 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 (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 Wang, Juanjuan Li, Jing-Wen Li, Jing Huang, Yijia Wang, Shaomeng Zhang, Jing-Ren Regulation of pneumococcal epigenetic and colony phases by multiple two-component regulatory systems |
title | Regulation of pneumococcal epigenetic and colony phases by multiple two-component regulatory systems |
title_full | Regulation of pneumococcal epigenetic and colony phases by multiple two-component regulatory systems |
title_fullStr | Regulation of pneumococcal epigenetic and colony phases by multiple two-component regulatory systems |
title_full_unstemmed | Regulation of pneumococcal epigenetic and colony phases by multiple two-component regulatory systems |
title_short | Regulation of pneumococcal epigenetic and colony phases by multiple two-component regulatory systems |
title_sort | regulation of pneumococcal epigenetic and colony phases by multiple two-component regulatory systems |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105139/ https://www.ncbi.nlm.nih.gov/pubmed/32187228 http://dx.doi.org/10.1371/journal.ppat.1008417 |
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