Author
Listed:
- Henrik Almblad
(University of Calgary)
- Trevor E. Randall
(University of Calgary)
- Fanny Liu
(University of Calgary)
- Katherine Leblanc
(University of Calgary)
- Ryan A. Groves
(University of Calgary)
- Weerayuth Kittichotirat
(Pilot Plant Development and Training Institute, King Mongkut’s University of Technology Thonburi)
- Geoffrey L. Winsor
(Simon Fraser University)
- Nicolas Fournier
(University of Calgary)
- Emily Au
(University of Calgary)
- Julie Groizeleau
(University of Calgary)
- Jacquelyn D. Rich
(University of Calgary)
- Yuefei Lou
(University of Calgary)
- Elise Granton
(University of Calgary)
- Laura K. Jennings
(University of Washington)
- Larissa A. Singletary
(University of Washington)
- Tara M. L. Winstone
(University of Calgary)
- Nathan M. Good
(University of Washington)
- Roger E. Bumgarner
(University of Washington)
- Michael F. Hynes
(University of Calgary)
- Manu Singh
(University of Manitoba)
- Maria Silvina Stietz
(University of Calgary)
- Fiona S. L. Brinkman
(Simon Fraser University)
- Ayush Kumar
(University of Manitoba)
- Ann Karen Cornelia Brassinga
(University of Manitoba)
- Matthew R. Parsek
(University of Washington)
- Boo Shan Tseng
(University of Nevada Las Vegas)
- Ian A. Lewis
(University of Calgary)
- Bryan G. Yipp
(University of Calgary)
- Justin L. MacCallum
(University of Calgary)
- Joe Jonathan Harrison
(University of Calgary)
Abstract
Many bacteria use the second messenger cyclic diguanylate (c-di-GMP) to control motility, biofilm production and virulence. Here, we identify a thermosensory diguanylate cyclase (TdcA) that modulates temperature-dependent motility, biofilm development and virulence in the opportunistic pathogen Pseudomonas aeruginosa. TdcA synthesizes c-di-GMP with catalytic rates that increase more than a hundred-fold over a ten-degree Celsius change. Analyses using protein chimeras indicate that heat-sensing is mediated by a thermosensitive Per-Arnt-SIM (PAS) domain. TdcA homologs are widespread in sequence databases, and a distantly related, heterologously expressed homolog from the Betaproteobacteria order Gallionellales also displayed thermosensitive diguanylate cyclase activity. We propose, therefore, that thermotransduction is a conserved function of c-di-GMP signaling networks, and that thermosensitive catalysis of a second messenger constitutes a mechanism for thermal sensing in bacteria.
Suggested Citation
Henrik Almblad & Trevor E. Randall & Fanny Liu & Katherine Leblanc & Ryan A. Groves & Weerayuth Kittichotirat & Geoffrey L. Winsor & Nicolas Fournier & Emily Au & Julie Groizeleau & Jacquelyn D. Rich , 2021.
"Bacterial cyclic diguanylate signaling networks sense temperature,"
Nature Communications, Nature, vol. 12(1), pages 1-14, December.
Handle:
RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-22176-2
DOI: 10.1038/s41467-021-22176-2
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