Cargando…
Coupled induction of prophage and virulence factors during tick transmission of the Lyme disease spirochete
The alternative sigma factor RpoS plays a central role in the critical host-adaptive response of the Lyme disease spirochete, Borrelia burgdorferi. We previously identified bbd18 as a negative regulator of RpoS but could not inactivate bbd18 in wild-type spirochetes. In the current study we employed...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9839762/ https://www.ncbi.nlm.nih.gov/pubmed/36639656 http://dx.doi.org/10.1038/s41467-023-35897-3 |
_version_ | 1784869514772480000 |
---|---|
author | Wachter, Jenny Cheff, Britney Hillman, Chad Carracoi, Valentina Dorward, David W. Martens, Craig Barbian, Kent Nardone, Glenn Renee Olano, L. Kinnersley, Margie Secor, Patrick R. Rosa, Patricia A. |
author_facet | Wachter, Jenny Cheff, Britney Hillman, Chad Carracoi, Valentina Dorward, David W. Martens, Craig Barbian, Kent Nardone, Glenn Renee Olano, L. Kinnersley, Margie Secor, Patrick R. Rosa, Patricia A. |
author_sort | Wachter, Jenny |
collection | PubMed |
description | The alternative sigma factor RpoS plays a central role in the critical host-adaptive response of the Lyme disease spirochete, Borrelia burgdorferi. We previously identified bbd18 as a negative regulator of RpoS but could not inactivate bbd18 in wild-type spirochetes. In the current study we employed an inducible bbd18 gene to demonstrate the essential nature of BBD18 for viability of wild-type spirochetes in vitro and at a unique point in vivo. Transcriptomic analyses of BBD18-depleted cells demonstrated global induction of RpoS-dependent genes prior to lysis, with the absolute requirement for BBD18, both in vitro and in vivo, circumvented by deletion of rpoS. The increased expression of plasmid prophage genes and the presence of phage particles in the supernatants of lysing cultures indicate that RpoS regulates phage lysis-lysogeny decisions. Through this work we identify a mechanistic link between endogenous prophages and the RpoS-dependent adaptive response of the Lyme disease spirochete. |
format | Online Article Text |
id | pubmed-9839762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98397622023-01-15 Coupled induction of prophage and virulence factors during tick transmission of the Lyme disease spirochete Wachter, Jenny Cheff, Britney Hillman, Chad Carracoi, Valentina Dorward, David W. Martens, Craig Barbian, Kent Nardone, Glenn Renee Olano, L. Kinnersley, Margie Secor, Patrick R. Rosa, Patricia A. Nat Commun Article The alternative sigma factor RpoS plays a central role in the critical host-adaptive response of the Lyme disease spirochete, Borrelia burgdorferi. We previously identified bbd18 as a negative regulator of RpoS but could not inactivate bbd18 in wild-type spirochetes. In the current study we employed an inducible bbd18 gene to demonstrate the essential nature of BBD18 for viability of wild-type spirochetes in vitro and at a unique point in vivo. Transcriptomic analyses of BBD18-depleted cells demonstrated global induction of RpoS-dependent genes prior to lysis, with the absolute requirement for BBD18, both in vitro and in vivo, circumvented by deletion of rpoS. The increased expression of plasmid prophage genes and the presence of phage particles in the supernatants of lysing cultures indicate that RpoS regulates phage lysis-lysogeny decisions. Through this work we identify a mechanistic link between endogenous prophages and the RpoS-dependent adaptive response of the Lyme disease spirochete. Nature Publishing Group UK 2023-01-13 /pmc/articles/PMC9839762/ /pubmed/36639656 http://dx.doi.org/10.1038/s41467-023-35897-3 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wachter, Jenny Cheff, Britney Hillman, Chad Carracoi, Valentina Dorward, David W. Martens, Craig Barbian, Kent Nardone, Glenn Renee Olano, L. Kinnersley, Margie Secor, Patrick R. Rosa, Patricia A. Coupled induction of prophage and virulence factors during tick transmission of the Lyme disease spirochete |
title | Coupled induction of prophage and virulence factors during tick transmission of the Lyme disease spirochete |
title_full | Coupled induction of prophage and virulence factors during tick transmission of the Lyme disease spirochete |
title_fullStr | Coupled induction of prophage and virulence factors during tick transmission of the Lyme disease spirochete |
title_full_unstemmed | Coupled induction of prophage and virulence factors during tick transmission of the Lyme disease spirochete |
title_short | Coupled induction of prophage and virulence factors during tick transmission of the Lyme disease spirochete |
title_sort | coupled induction of prophage and virulence factors during tick transmission of the lyme disease spirochete |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9839762/ https://www.ncbi.nlm.nih.gov/pubmed/36639656 http://dx.doi.org/10.1038/s41467-023-35897-3 |
work_keys_str_mv | AT wachterjenny coupledinductionofprophageandvirulencefactorsduringticktransmissionofthelymediseasespirochete AT cheffbritney coupledinductionofprophageandvirulencefactorsduringticktransmissionofthelymediseasespirochete AT hillmanchad coupledinductionofprophageandvirulencefactorsduringticktransmissionofthelymediseasespirochete AT carracoivalentina coupledinductionofprophageandvirulencefactorsduringticktransmissionofthelymediseasespirochete AT dorwarddavidw coupledinductionofprophageandvirulencefactorsduringticktransmissionofthelymediseasespirochete AT martenscraig coupledinductionofprophageandvirulencefactorsduringticktransmissionofthelymediseasespirochete AT barbiankent coupledinductionofprophageandvirulencefactorsduringticktransmissionofthelymediseasespirochete AT nardoneglenn coupledinductionofprophageandvirulencefactorsduringticktransmissionofthelymediseasespirochete AT reneeolanol coupledinductionofprophageandvirulencefactorsduringticktransmissionofthelymediseasespirochete AT kinnersleymargie coupledinductionofprophageandvirulencefactorsduringticktransmissionofthelymediseasespirochete AT secorpatrickr coupledinductionofprophageandvirulencefactorsduringticktransmissionofthelymediseasespirochete AT rosapatriciaa coupledinductionofprophageandvirulencefactorsduringticktransmissionofthelymediseasespirochete |