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Production of 3′,3′-cGAMP by a Bdellovibrio bacteriovorus promiscuous GGDEF enzyme, Bd0367, regulates exit from prey by gliding motility

Lowry, Rebecca C.; Hallberg, Zachary F.; Till, Rob; Simons, Tyler J.; Nottingham, Ruth; Want, Fiona; Sockett, R. Elizabeth; Hammond, Ming C.; Lambert, Carey

Production of 3′,3′-cGAMP by a Bdellovibrio bacteriovorus promiscuous GGDEF enzyme, Bd0367, regulates exit from prey by gliding motility Thumbnail


Authors

Rebecca C. Lowry

Zachary F. Hallberg

Rob Till

Tyler J. Simons

Ruth Nottingham

Fiona Want

Ming C. Hammond



Contributors

Sean Crosson
Editor

Abstract

Bacterial second messengers are important for regulating diverse bacterial lifestyles. Cyclic di-GMP (c-di-GMP) is produced by diguanylate cyclase enzymes, named GGDEF proteins, which are widespread across bacteria. Recently, hybrid promiscuous (Hypr) GGDEF proteins have been described in some bacteria, which produce both c-di-GMP and a more recently identified bacterial second messenger, 3′,3′-cyclic-GMP-AMP (cGAMP). One of these proteins was found in the predatory Bdellovibrio bacteriovorus, Bd0367. The bd0367 GGDEF gene deletion strain was found to enter prey cells, but was incapable of leaving exhausted prey remnants via gliding motility on a solid surface once predator cell division was complete. However, it was unclear which signal regulated this process. We show that cGAMP signalling is active within B. bacteriovorus and that, in addition to producing c-di-GMP and some c-di-AMP, Bd0367 is a primary producer of cGAMP in vivo. Site-directed mutagenesis of serine 214 to an aspartate rendered Bd0367 into primarily a c-di-GMP synthase. B. bacteriovorus strain bd0367S214D phenocopies the bd0367 deletion strain by being unable to glide on a solid surface, leading to an inability of new progeny to exit from prey cells post-replication. Thus, this process is regulated by cGAMP. Deletion of bd0367 was also found to be incompatible with wild-type flagellar biogenesis, as a result of an acquired mutation in flagellin chaperone gene homologue fliS, implicating c-di-GMP in regulation of swimming motility. Thus the single Bd0367 enzyme produces two secondary messengers by action of the same GGDEF domain, the first reported example of a synthase that regulates multiple second messengers in vivo. Unlike roles of these signalling molecules in other bacteria, these signal to two separate motility systems, gliding and flagellar, which are essential for completion of the bacterial predation cycle and prey exit by B. bacteriovorus.

Citation

Lowry, R. C., Hallberg, Z. F., Till, R., Simons, T. J., Nottingham, R., Want, F., …Lambert, C. (2022). Production of 3′,3′-cGAMP by a Bdellovibrio bacteriovorus promiscuous GGDEF enzyme, Bd0367, regulates exit from prey by gliding motility. PLoS Genetics, 18(5), Article e1010164. https://doi.org/10.1371/journal.pgen.1010164

Journal Article Type Article
Acceptance Date Mar 24, 2022
Online Publication Date May 27, 2022
Publication Date May 27, 2022
Deposit Date Jul 21, 2022
Publicly Available Date Jul 22, 2022
Journal PLoS Genetics
Print ISSN 1553-7390
Electronic ISSN 1553-7404
Publisher Public Library of Science (PLoS)
Peer Reviewed Peer Reviewed
Volume 18
Issue 5
Article Number e1010164
DOI https://doi.org/10.1371/journal.pgen.1010164
Keywords Cancer Research; Genetics (clinical); Genetics; Molecular Biology; Ecology, Evolution, Behavior and Systematics
Public URL https://nottingham-repository.worktribe.com/output/8309948
Publisher URL https://journals.plos.org/plosgenetics/article?id=10.1371/journal.pgen.1010164

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