Cargando…

The Type VI Secretion Systems in Plant-Beneficial Bacteria Modulate Prokaryotic and Eukaryotic Interactions in the Rhizosphere

Rhizosphere colonizing plant growth promoting bacteria (PGPB) increase their competitiveness by producing diffusible toxic secondary metabolites, which inhibit competitors and deter predators. Many PGPB also have one or more Type VI Secretion System (T6SS), for the delivery of weapons directly into...

Descripción completa

Detalles Bibliográficos
Autores principales: Boak, Emily N., Kirolos, Sara, Pan, Huiqiao, Pierson, Leland S., Pierson, Elizabeth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9022076/
https://www.ncbi.nlm.nih.gov/pubmed/35464916
http://dx.doi.org/10.3389/fmicb.2022.843092
_version_ 1784690001827594240
author Boak, Emily N.
Kirolos, Sara
Pan, Huiqiao
Pierson, Leland S.
Pierson, Elizabeth A.
author_facet Boak, Emily N.
Kirolos, Sara
Pan, Huiqiao
Pierson, Leland S.
Pierson, Elizabeth A.
author_sort Boak, Emily N.
collection PubMed
description Rhizosphere colonizing plant growth promoting bacteria (PGPB) increase their competitiveness by producing diffusible toxic secondary metabolites, which inhibit competitors and deter predators. Many PGPB also have one or more Type VI Secretion System (T6SS), for the delivery of weapons directly into prokaryotic and eukaryotic cells. Studied predominantly in human and plant pathogens as a virulence mechanism for the delivery of effector proteins, the function of T6SS for PGPB in the rhizosphere niche is poorly understood. We utilized a collection of Pseudomonas chlororaphis 30–84 mutants deficient in one or both of its two T6SS and/or secondary metabolite production to examine the relative importance of each T6SS in rhizosphere competence, bacterial competition, and protection from bacterivores. A mutant deficient in both T6SS was less persistent than wild type in the rhizosphere. Both T6SS contributed to competitiveness against other PGPB or plant pathogenic strains not affected by secondary metabolite production, but only T6SS-2 was effective against strains lacking their own T6SS. Having at least one T6SS was also essential for protection from predation by several eukaryotic bacterivores. In contrast to diffusible weapons that may not be produced at low cell density, T6SS afford rhizobacteria an additional, more immediate line of defense against competitors and predators.
format Online
Article
Text
id pubmed-9022076
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-90220762022-04-22 The Type VI Secretion Systems in Plant-Beneficial Bacteria Modulate Prokaryotic and Eukaryotic Interactions in the Rhizosphere Boak, Emily N. Kirolos, Sara Pan, Huiqiao Pierson, Leland S. Pierson, Elizabeth A. Front Microbiol Microbiology Rhizosphere colonizing plant growth promoting bacteria (PGPB) increase their competitiveness by producing diffusible toxic secondary metabolites, which inhibit competitors and deter predators. Many PGPB also have one or more Type VI Secretion System (T6SS), for the delivery of weapons directly into prokaryotic and eukaryotic cells. Studied predominantly in human and plant pathogens as a virulence mechanism for the delivery of effector proteins, the function of T6SS for PGPB in the rhizosphere niche is poorly understood. We utilized a collection of Pseudomonas chlororaphis 30–84 mutants deficient in one or both of its two T6SS and/or secondary metabolite production to examine the relative importance of each T6SS in rhizosphere competence, bacterial competition, and protection from bacterivores. A mutant deficient in both T6SS was less persistent than wild type in the rhizosphere. Both T6SS contributed to competitiveness against other PGPB or plant pathogenic strains not affected by secondary metabolite production, but only T6SS-2 was effective against strains lacking their own T6SS. Having at least one T6SS was also essential for protection from predation by several eukaryotic bacterivores. In contrast to diffusible weapons that may not be produced at low cell density, T6SS afford rhizobacteria an additional, more immediate line of defense against competitors and predators. Frontiers Media S.A. 2022-04-07 /pmc/articles/PMC9022076/ /pubmed/35464916 http://dx.doi.org/10.3389/fmicb.2022.843092 Text en Copyright © 2022 Boak, Kirolos, Pan, Pierson and Pierson. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Boak, Emily N.
Kirolos, Sara
Pan, Huiqiao
Pierson, Leland S.
Pierson, Elizabeth A.
The Type VI Secretion Systems in Plant-Beneficial Bacteria Modulate Prokaryotic and Eukaryotic Interactions in the Rhizosphere
title The Type VI Secretion Systems in Plant-Beneficial Bacteria Modulate Prokaryotic and Eukaryotic Interactions in the Rhizosphere
title_full The Type VI Secretion Systems in Plant-Beneficial Bacteria Modulate Prokaryotic and Eukaryotic Interactions in the Rhizosphere
title_fullStr The Type VI Secretion Systems in Plant-Beneficial Bacteria Modulate Prokaryotic and Eukaryotic Interactions in the Rhizosphere
title_full_unstemmed The Type VI Secretion Systems in Plant-Beneficial Bacteria Modulate Prokaryotic and Eukaryotic Interactions in the Rhizosphere
title_short The Type VI Secretion Systems in Plant-Beneficial Bacteria Modulate Prokaryotic and Eukaryotic Interactions in the Rhizosphere
title_sort type vi secretion systems in plant-beneficial bacteria modulate prokaryotic and eukaryotic interactions in the rhizosphere
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9022076/
https://www.ncbi.nlm.nih.gov/pubmed/35464916
http://dx.doi.org/10.3389/fmicb.2022.843092
work_keys_str_mv AT boakemilyn thetypevisecretionsystemsinplantbeneficialbacteriamodulateprokaryoticandeukaryoticinteractionsintherhizosphere
AT kirolossara thetypevisecretionsystemsinplantbeneficialbacteriamodulateprokaryoticandeukaryoticinteractionsintherhizosphere
AT panhuiqiao thetypevisecretionsystemsinplantbeneficialbacteriamodulateprokaryoticandeukaryoticinteractionsintherhizosphere
AT piersonlelands thetypevisecretionsystemsinplantbeneficialbacteriamodulateprokaryoticandeukaryoticinteractionsintherhizosphere
AT piersonelizabetha thetypevisecretionsystemsinplantbeneficialbacteriamodulateprokaryoticandeukaryoticinteractionsintherhizosphere
AT boakemilyn typevisecretionsystemsinplantbeneficialbacteriamodulateprokaryoticandeukaryoticinteractionsintherhizosphere
AT kirolossara typevisecretionsystemsinplantbeneficialbacteriamodulateprokaryoticandeukaryoticinteractionsintherhizosphere
AT panhuiqiao typevisecretionsystemsinplantbeneficialbacteriamodulateprokaryoticandeukaryoticinteractionsintherhizosphere
AT piersonlelands typevisecretionsystemsinplantbeneficialbacteriamodulateprokaryoticandeukaryoticinteractionsintherhizosphere
AT piersonelizabetha typevisecretionsystemsinplantbeneficialbacteriamodulateprokaryoticandeukaryoticinteractionsintherhizosphere