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A new class of protein sensor links spirochete pleomorphism, persistence, and chemotaxis
Pathogenic spirochetes can alter their morphologies and behaviors to infect and survive within their hosts. Previous reports demonstrate that the formation of the so-called “round bodies” and biofilms, and chemotaxis are involved in spirochete pathogenesis. Here, we report a direct link between thes...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10653840/ https://www.ncbi.nlm.nih.gov/pubmed/37607060 http://dx.doi.org/10.1128/mbio.01598-23 |
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author | Muok, A. R. Kurniyati, K. Cassidy, C. K. Olsthoorn, F. A. Ortega, D. R. Mabrouk, A. Sidi Li, C. Briegel, A. |
author_facet | Muok, A. R. Kurniyati, K. Cassidy, C. K. Olsthoorn, F. A. Ortega, D. R. Mabrouk, A. Sidi Li, C. Briegel, A. |
author_sort | Muok, A. R. |
collection | PubMed |
description | Pathogenic spirochetes can alter their morphologies and behaviors to infect and survive within their hosts. Previous reports demonstrate that the formation of the so-called “round bodies” and biofilms, and chemotaxis are involved in spirochete pathogenesis. Here, we report a direct link between these cellular states that involve a new class of protein sensor with hitherto unclear function. Using cryo-electron microscopy, genetics, behavioral assays, and molecular modeling, we demonstrate that spirochetes regulate these behaviors in response to the small molecule S-adenosylmethionine (SAM) via a SAM sensor that is anchored to chemotaxis arrays. Furthermore, we establish an improved model for round body formation that now includes characterizations during log phase growth. IMPORTANCE: A new class of bacterial protein sensors monitors intracellular levels of S-adenosylmethionine to modulate cell morphology, chemotaxis, and biofilm formation. Simultaneous regulation of these behaviors enables bacterial pathogens to survive within their niche. This sensor, exemplified by Treponema denticola CheWS, is anchored to the chemotaxis array and its sensor domain is located below the chemotaxis rings. This position may allow the sensor to directly interact with the chemotaxis histidine kinase CheA. Collectively, these data establish a critical role of CheWS in pathogenesis and further illustrate the impact of studying non-canonical chemotaxis proteins. |
format | Online Article Text |
id | pubmed-10653840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-106538402023-08-21 A new class of protein sensor links spirochete pleomorphism, persistence, and chemotaxis Muok, A. R. Kurniyati, K. Cassidy, C. K. Olsthoorn, F. A. Ortega, D. R. Mabrouk, A. Sidi Li, C. Briegel, A. mBio Research Article Pathogenic spirochetes can alter their morphologies and behaviors to infect and survive within their hosts. Previous reports demonstrate that the formation of the so-called “round bodies” and biofilms, and chemotaxis are involved in spirochete pathogenesis. Here, we report a direct link between these cellular states that involve a new class of protein sensor with hitherto unclear function. Using cryo-electron microscopy, genetics, behavioral assays, and molecular modeling, we demonstrate that spirochetes regulate these behaviors in response to the small molecule S-adenosylmethionine (SAM) via a SAM sensor that is anchored to chemotaxis arrays. Furthermore, we establish an improved model for round body formation that now includes characterizations during log phase growth. IMPORTANCE: A new class of bacterial protein sensors monitors intracellular levels of S-adenosylmethionine to modulate cell morphology, chemotaxis, and biofilm formation. Simultaneous regulation of these behaviors enables bacterial pathogens to survive within their niche. This sensor, exemplified by Treponema denticola CheWS, is anchored to the chemotaxis array and its sensor domain is located below the chemotaxis rings. This position may allow the sensor to directly interact with the chemotaxis histidine kinase CheA. Collectively, these data establish a critical role of CheWS in pathogenesis and further illustrate the impact of studying non-canonical chemotaxis proteins. American Society for Microbiology 2023-08-21 /pmc/articles/PMC10653840/ /pubmed/37607060 http://dx.doi.org/10.1128/mbio.01598-23 Text en Copyright © 2023 Muok et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Muok, A. R. Kurniyati, K. Cassidy, C. K. Olsthoorn, F. A. Ortega, D. R. Mabrouk, A. Sidi Li, C. Briegel, A. A new class of protein sensor links spirochete pleomorphism, persistence, and chemotaxis |
title | A new class of protein sensor links spirochete pleomorphism, persistence, and chemotaxis |
title_full | A new class of protein sensor links spirochete pleomorphism, persistence, and chemotaxis |
title_fullStr | A new class of protein sensor links spirochete pleomorphism, persistence, and chemotaxis |
title_full_unstemmed | A new class of protein sensor links spirochete pleomorphism, persistence, and chemotaxis |
title_short | A new class of protein sensor links spirochete pleomorphism, persistence, and chemotaxis |
title_sort | new class of protein sensor links spirochete pleomorphism, persistence, and chemotaxis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10653840/ https://www.ncbi.nlm.nih.gov/pubmed/37607060 http://dx.doi.org/10.1128/mbio.01598-23 |
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