Cargando…

The antimicrobial volatile power of the rhizospheric isolate Pseudomonas donghuensis P482

Soil and rhizosphere bacteria produce an array of secondary metabolites including a wide range of volatile organic compounds (VOCs). These compounds play an important role in the long-distance interactions and communication between (micro)organisms. Furthermore, bacterial VOCs are involved in plant...

Descripción completa

Detalles Bibliográficos
Autores principales: Ossowicki, Adam, Jafra, Sylwia, Garbeva, Paolina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5373542/
https://www.ncbi.nlm.nih.gov/pubmed/28358818
http://dx.doi.org/10.1371/journal.pone.0174362
_version_ 1782518783493013504
author Ossowicki, Adam
Jafra, Sylwia
Garbeva, Paolina
author_facet Ossowicki, Adam
Jafra, Sylwia
Garbeva, Paolina
author_sort Ossowicki, Adam
collection PubMed
description Soil and rhizosphere bacteria produce an array of secondary metabolites including a wide range of volatile organic compounds (VOCs). These compounds play an important role in the long-distance interactions and communication between (micro)organisms. Furthermore, bacterial VOCs are involved in plant pathogens inhibition and induction of soil fungistasis and suppressivenes. In the present study, we analysed the volatile blend emitted by the rhizospheric isolate Pseudomonas donghuensis P482 and evaluated the volatile effect on the plant pathogenic fungi and bacteria as well as one oomycete. Moreover, we investigated the role of the GacS/GacA system on VOCs production in P. donghuensis P482. The results obtained demonstrated that VOCs emitted by P. donghuensis P482 have strong antifungal and antioomycete, but not antibacterial activity. The production of certain volatiles such as dimethyl sulfide, S-methyl thioacetate, methyl thiocyanate, dimethyl trisulfide, 1-undecan and HCN is depended on the GacS/GacA two-component regulatory system. Apparently, these compounds play an important role in the pathogens suppression as the gacA mutant entirely lost the ability to inhibit via volatiles the growth of tested plant pathogens.
format Online
Article
Text
id pubmed-5373542
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-53735422017-04-07 The antimicrobial volatile power of the rhizospheric isolate Pseudomonas donghuensis P482 Ossowicki, Adam Jafra, Sylwia Garbeva, Paolina PLoS One Research Article Soil and rhizosphere bacteria produce an array of secondary metabolites including a wide range of volatile organic compounds (VOCs). These compounds play an important role in the long-distance interactions and communication between (micro)organisms. Furthermore, bacterial VOCs are involved in plant pathogens inhibition and induction of soil fungistasis and suppressivenes. In the present study, we analysed the volatile blend emitted by the rhizospheric isolate Pseudomonas donghuensis P482 and evaluated the volatile effect on the plant pathogenic fungi and bacteria as well as one oomycete. Moreover, we investigated the role of the GacS/GacA system on VOCs production in P. donghuensis P482. The results obtained demonstrated that VOCs emitted by P. donghuensis P482 have strong antifungal and antioomycete, but not antibacterial activity. The production of certain volatiles such as dimethyl sulfide, S-methyl thioacetate, methyl thiocyanate, dimethyl trisulfide, 1-undecan and HCN is depended on the GacS/GacA two-component regulatory system. Apparently, these compounds play an important role in the pathogens suppression as the gacA mutant entirely lost the ability to inhibit via volatiles the growth of tested plant pathogens. Public Library of Science 2017-03-30 /pmc/articles/PMC5373542/ /pubmed/28358818 http://dx.doi.org/10.1371/journal.pone.0174362 Text en © 2017 Ossowicki et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ossowicki, Adam
Jafra, Sylwia
Garbeva, Paolina
The antimicrobial volatile power of the rhizospheric isolate Pseudomonas donghuensis P482
title The antimicrobial volatile power of the rhizospheric isolate Pseudomonas donghuensis P482
title_full The antimicrobial volatile power of the rhizospheric isolate Pseudomonas donghuensis P482
title_fullStr The antimicrobial volatile power of the rhizospheric isolate Pseudomonas donghuensis P482
title_full_unstemmed The antimicrobial volatile power of the rhizospheric isolate Pseudomonas donghuensis P482
title_short The antimicrobial volatile power of the rhizospheric isolate Pseudomonas donghuensis P482
title_sort antimicrobial volatile power of the rhizospheric isolate pseudomonas donghuensis p482
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5373542/
https://www.ncbi.nlm.nih.gov/pubmed/28358818
http://dx.doi.org/10.1371/journal.pone.0174362
work_keys_str_mv AT ossowickiadam theantimicrobialvolatilepoweroftherhizosphericisolatepseudomonasdonghuensisp482
AT jafrasylwia theantimicrobialvolatilepoweroftherhizosphericisolatepseudomonasdonghuensisp482
AT garbevapaolina theantimicrobialvolatilepoweroftherhizosphericisolatepseudomonasdonghuensisp482
AT ossowickiadam antimicrobialvolatilepoweroftherhizosphericisolatepseudomonasdonghuensisp482
AT jafrasylwia antimicrobialvolatilepoweroftherhizosphericisolatepseudomonasdonghuensisp482
AT garbevapaolina antimicrobialvolatilepoweroftherhizosphericisolatepseudomonasdonghuensisp482