Cited by 4Bacterial Genetics and BiotechnologyBiochemical and Structural CharacterizationEscherichia coli research studies

A new class of protein sensor links spirochete pleomorphism, persistence, and chemotaxis

Open access
Muok, A. R., Kurniyati, K., Cassidy, C. K., Olsthoorn, F. A., Ortega, D. R., Mabrouk, A. Sidi, Li, C., Briegel, A.·2023·mBio

Published version of a preprint

Abstract

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.

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Authors
Muok, A. R., Kurniyati, K., Cassidy, C. K., Olsthoorn, F. A., Ortega, D. R., Mabrouk, A. S., Li, C., & Briegel, A.
Affiliations
  • Leiden University (NL)
  • Virginia Commonwealth University (US)
  • Diamond Light Source (GB)
Corresponding author
  • Li, C.
  • Briegel, A.
Venue
mBio
Published
2023-10-31
Volume
14
Issue
5
Pages
e0159823-e0159823
ISSN
2150-7511 (ISSN-L)
OpenAlex
W4386027311
Cited by
4
References
5
Citations by year
2026: 1 · 2025: 2 · 2024: 1
FWCI
0.66
Type
journal article
Language
en
Open access
Locations
  • mBio (publishedVersion, cc-by)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Leiden Repository (Leiden University) (submittedVersion, cc-by)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • Nederlandse Organisatie voor Wetenschappelijk Onderzoek (184.034.014, VI.Veni.202.079)
  • HHS | National Institutes of Health (R01AI078958, R01DE023080)
  • EC | European Research Council (101021133)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Biochemical and Structural Characterization
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Endocrinology › Escherichia coli research studies
Keywords
spirochetes, pleomorphism, biofilm formation, chemotaxis, S-adenosylmethionine, CheW, CheA histidine kinase, Treponema denticola, bacterial persistence, pathogenesis
MeSH terms
Histidine Kinase, Methyl-Accepting Chemotaxis Proteins, Bacteria, Bacterial Proteins, Chemotaxis, Spirochaetales, Escherichia coli Proteins

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