Discrete cyclic di-GMP-dependent control of bacterial predation versus axenic growth in Bdellovibrio bacteriovorus

Bdellovibrio bacteriovorus is a Delta-proteobacterium that oscillates between free-living growth and predation on Gram-negative bacteria including important pathogens of man, animals and plants. After entering the prey periplasm, killing the prey and replicating inside the prey bdelloplast, several...

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Main Authors: Hobley, Laura, Fung, Rowena K. Y., Lambert, Carey, Harris, Maximilian A.T.S., Dabh, Jayesh M., King, Simon S., Basford, Sarah M., Uchida, Kaoru, Till, Robert, Ahmad, Rashidah, Aizawa, Shin-Ichi, Gomelsky, Mark, Sockett, R. Elizabeth
Format: Article
Published: Public Library of Science 2012
Online Access:https://eprints.nottingham.ac.uk/2606/
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author Hobley, Laura
Fung, Rowena K. Y.
Lambert, Carey
Harris, Maximilian A.T.S.
Dabh, Jayesh M.
King, Simon S.
Basford, Sarah M.
Uchida, Kaoru
Till, Robert
Ahmad, Rashidah
Aizawa, Shin-Ichi
Gomelsky, Mark
Sockett, R. Elizabeth
author_facet Hobley, Laura
Fung, Rowena K. Y.
Lambert, Carey
Harris, Maximilian A.T.S.
Dabh, Jayesh M.
King, Simon S.
Basford, Sarah M.
Uchida, Kaoru
Till, Robert
Ahmad, Rashidah
Aizawa, Shin-Ichi
Gomelsky, Mark
Sockett, R. Elizabeth
author_sort Hobley, Laura
building Nottingham Research Data Repository
collection Online Access
description Bdellovibrio bacteriovorus is a Delta-proteobacterium that oscillates between free-living growth and predation on Gram-negative bacteria including important pathogens of man, animals and plants. After entering the prey periplasm, killing the prey and replicating inside the prey bdelloplast, several motile B. bacteriovorus progeny cells emerge. The B. bacteriovorus HD100 genome encodes numerous proteins predicted to be involved in signalling via the secondary messenger cyclic di-GMP (c-di-GMP), which is known to affect bacterial lifestyle choices. We investigated the role of c-di-GMP signalling in B. bacteriovorus, focussing on the five GGDEF domain proteins that are predicted to function as diguanylyl cyclases initiating c-di-GMP signalling cascades. Inactivation of individual GGDEF domain genes resulted in remarkably distinct phenotypes. Deletion of dgcB (Bd0742) resulted in a predation impaired, obligately axenic mutant, while deletion of dgcC (Bd1434) resulted in the opposite, obligately predatory mutant. Deletion of dgcA (Bd0367) abolished gliding motility, producing bacteria capable of predatory invasion but unable to leave the exhausted prey. Complementation was achieved with wild type dgc genes, but not with GGAAF versions. Deletion of cdgA (Bd3125) substantially slowed predation; this was restored by wild type complementation. Deletion of dgcD (Bd3766) had no observable phenotype. In vitro assays showed that DgcA, DgcB, and DgcC were diguanylyl cyclases. CdgA lacks enzymatic activity but functions as a c-di-GMP receptor apparently in the DgcB pathway. Activity of DgcD was not detected. Deletion of DgcA strongly decreased the extractable c-di-GMP content of axenic Bdellovibrio cells. We show that c-di-GMP signalling pathways are essential for both the free-living and predatory lifestyles of B. bacteriovorus and that obligately predatory dgcC- can be made lacking a propensity to survive without predation of bacterial pathogens and thus possibly useful in anti-pathogen applications. In contrast to many studies in other bacteria, Bdellovibrio shows specificity and lack of overlap in c-di-GMP signalling pathways.
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spelling nottingham-26062020-05-04T16:32:38Z https://eprints.nottingham.ac.uk/2606/ Discrete cyclic di-GMP-dependent control of bacterial predation versus axenic growth in Bdellovibrio bacteriovorus Hobley, Laura Fung, Rowena K. Y. Lambert, Carey Harris, Maximilian A.T.S. Dabh, Jayesh M. King, Simon S. Basford, Sarah M. Uchida, Kaoru Till, Robert Ahmad, Rashidah Aizawa, Shin-Ichi Gomelsky, Mark Sockett, R. Elizabeth Bdellovibrio bacteriovorus is a Delta-proteobacterium that oscillates between free-living growth and predation on Gram-negative bacteria including important pathogens of man, animals and plants. After entering the prey periplasm, killing the prey and replicating inside the prey bdelloplast, several motile B. bacteriovorus progeny cells emerge. The B. bacteriovorus HD100 genome encodes numerous proteins predicted to be involved in signalling via the secondary messenger cyclic di-GMP (c-di-GMP), which is known to affect bacterial lifestyle choices. We investigated the role of c-di-GMP signalling in B. bacteriovorus, focussing on the five GGDEF domain proteins that are predicted to function as diguanylyl cyclases initiating c-di-GMP signalling cascades. Inactivation of individual GGDEF domain genes resulted in remarkably distinct phenotypes. Deletion of dgcB (Bd0742) resulted in a predation impaired, obligately axenic mutant, while deletion of dgcC (Bd1434) resulted in the opposite, obligately predatory mutant. Deletion of dgcA (Bd0367) abolished gliding motility, producing bacteria capable of predatory invasion but unable to leave the exhausted prey. Complementation was achieved with wild type dgc genes, but not with GGAAF versions. Deletion of cdgA (Bd3125) substantially slowed predation; this was restored by wild type complementation. Deletion of dgcD (Bd3766) had no observable phenotype. In vitro assays showed that DgcA, DgcB, and DgcC were diguanylyl cyclases. CdgA lacks enzymatic activity but functions as a c-di-GMP receptor apparently in the DgcB pathway. Activity of DgcD was not detected. Deletion of DgcA strongly decreased the extractable c-di-GMP content of axenic Bdellovibrio cells. We show that c-di-GMP signalling pathways are essential for both the free-living and predatory lifestyles of B. bacteriovorus and that obligately predatory dgcC- can be made lacking a propensity to survive without predation of bacterial pathogens and thus possibly useful in anti-pathogen applications. In contrast to many studies in other bacteria, Bdellovibrio shows specificity and lack of overlap in c-di-GMP signalling pathways. Public Library of Science 2012-02-02 Article PeerReviewed Hobley, Laura, Fung, Rowena K. Y., Lambert, Carey, Harris, Maximilian A.T.S., Dabh, Jayesh M., King, Simon S., Basford, Sarah M., Uchida, Kaoru, Till, Robert, Ahmad, Rashidah, Aizawa, Shin-Ichi, Gomelsky, Mark and Sockett, R. Elizabeth (2012) Discrete cyclic di-GMP-dependent control of bacterial predation versus axenic growth in Bdellovibrio bacteriovorus. PloS Pathogens, 8 (2). e1002493/1- e1002493/13. ISSN 1553-7374 http://www.plospathogens.org/article/info%3Adoi%2F10.1371%2Fjournal.ppat.1002493 doi:10.1371/journal.ppat.1002493 doi:10.1371/journal.ppat.1002493
spellingShingle Hobley, Laura
Fung, Rowena K. Y.
Lambert, Carey
Harris, Maximilian A.T.S.
Dabh, Jayesh M.
King, Simon S.
Basford, Sarah M.
Uchida, Kaoru
Till, Robert
Ahmad, Rashidah
Aizawa, Shin-Ichi
Gomelsky, Mark
Sockett, R. Elizabeth
Discrete cyclic di-GMP-dependent control of bacterial predation versus axenic growth in Bdellovibrio bacteriovorus
title Discrete cyclic di-GMP-dependent control of bacterial predation versus axenic growth in Bdellovibrio bacteriovorus
title_full Discrete cyclic di-GMP-dependent control of bacterial predation versus axenic growth in Bdellovibrio bacteriovorus
title_fullStr Discrete cyclic di-GMP-dependent control of bacterial predation versus axenic growth in Bdellovibrio bacteriovorus
title_full_unstemmed Discrete cyclic di-GMP-dependent control of bacterial predation versus axenic growth in Bdellovibrio bacteriovorus
title_short Discrete cyclic di-GMP-dependent control of bacterial predation versus axenic growth in Bdellovibrio bacteriovorus
title_sort discrete cyclic di-gmp-dependent control of bacterial predation versus axenic growth in bdellovibrio bacteriovorus
url https://eprints.nottingham.ac.uk/2606/
https://eprints.nottingham.ac.uk/2606/
https://eprints.nottingham.ac.uk/2606/