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Antagonistic potential of Pseudomonasgraminis 49M against Erwiniaamylovora, the causal agent of fire blight

In a previous study (Mikiciński et al. in Eur J Plant Pathol, doi:10.1007/s10658-015-0837-y, 2015), we described the characterization of novel strain 49M of Pseudomonasgraminis, isolated from the phyllosphere of apple trees in Poland showing a good protective activity against fire blight on differen...

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Autores principales: Mikiciński, Artur, Sobiczewski, Piotr, Puławska, Joanna, Malusa, Eligio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930463/
https://www.ncbi.nlm.nih.gov/pubmed/27002332
http://dx.doi.org/10.1007/s00203-016-1207-7
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author Mikiciński, Artur
Sobiczewski, Piotr
Puławska, Joanna
Malusa, Eligio
author_facet Mikiciński, Artur
Sobiczewski, Piotr
Puławska, Joanna
Malusa, Eligio
author_sort Mikiciński, Artur
collection PubMed
description In a previous study (Mikiciński et al. in Eur J Plant Pathol, doi:10.1007/s10658-015-0837-y, 2015), we described the characterization of novel strain 49M of Pseudomonasgraminis, isolated from the phyllosphere of apple trees in Poland showing a good protective activity against fire blight on different organs of host plants. We now report investigations to clarify the basis for this activity. Strain 49M was found to produce siderophores on a medium containing complex CAS-Fe(3+) and HDTMA, but was not able to produce N-acyl homoserine lactones (AHLs). Moreover, it formed a biofilm on polystyrene and polyvinyl chloride (PVC) surfaces. Strain 49M gave a positive reaction in PCR with primers complementary to gacA, the regulatory gene influencing the production of several secondary metabolites including antibiotics. The genes prnD (encoding pyrrolnitrin), pltC, pltB (pyoluteorin), phlD (2,4-diacetyl-phloroglucinol) and phzC as well as phzD (and their homologs phzF and phzA encoding phenazine), described for antagonistic fluorescent pseudomonads, however, were not detected. Research into the biotic relationship between strain 49M and Erwiniaamylovora strain Ea659 on five microbiological media showed that this strain clearly inhibited the growth of the pathogen on King’s B and nutrient agar with glycerol media, to a very small extent on nutrient agar with sucrose, and not at all on Luria–Bertani agar. On medium 925, strain 49M even stimulated E. amylovora growth. The addition of ferric chloride to King’s B resulted in the loss of its inhibitory ability. Testing the survival of 49M in vitro showed its resistance to drought, greater than that of E. amylovora.
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spelling pubmed-49304632016-07-13 Antagonistic potential of Pseudomonasgraminis 49M against Erwiniaamylovora, the causal agent of fire blight Mikiciński, Artur Sobiczewski, Piotr Puławska, Joanna Malusa, Eligio Arch Microbiol Original Paper In a previous study (Mikiciński et al. in Eur J Plant Pathol, doi:10.1007/s10658-015-0837-y, 2015), we described the characterization of novel strain 49M of Pseudomonasgraminis, isolated from the phyllosphere of apple trees in Poland showing a good protective activity against fire blight on different organs of host plants. We now report investigations to clarify the basis for this activity. Strain 49M was found to produce siderophores on a medium containing complex CAS-Fe(3+) and HDTMA, but was not able to produce N-acyl homoserine lactones (AHLs). Moreover, it formed a biofilm on polystyrene and polyvinyl chloride (PVC) surfaces. Strain 49M gave a positive reaction in PCR with primers complementary to gacA, the regulatory gene influencing the production of several secondary metabolites including antibiotics. The genes prnD (encoding pyrrolnitrin), pltC, pltB (pyoluteorin), phlD (2,4-diacetyl-phloroglucinol) and phzC as well as phzD (and their homologs phzF and phzA encoding phenazine), described for antagonistic fluorescent pseudomonads, however, were not detected. Research into the biotic relationship between strain 49M and Erwiniaamylovora strain Ea659 on five microbiological media showed that this strain clearly inhibited the growth of the pathogen on King’s B and nutrient agar with glycerol media, to a very small extent on nutrient agar with sucrose, and not at all on Luria–Bertani agar. On medium 925, strain 49M even stimulated E. amylovora growth. The addition of ferric chloride to King’s B resulted in the loss of its inhibitory ability. Testing the survival of 49M in vitro showed its resistance to drought, greater than that of E. amylovora. Springer Berlin Heidelberg 2016-03-22 2016 /pmc/articles/PMC4930463/ /pubmed/27002332 http://dx.doi.org/10.1007/s00203-016-1207-7 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Paper
Mikiciński, Artur
Sobiczewski, Piotr
Puławska, Joanna
Malusa, Eligio
Antagonistic potential of Pseudomonasgraminis 49M against Erwiniaamylovora, the causal agent of fire blight
title Antagonistic potential of Pseudomonasgraminis 49M against Erwiniaamylovora, the causal agent of fire blight
title_full Antagonistic potential of Pseudomonasgraminis 49M against Erwiniaamylovora, the causal agent of fire blight
title_fullStr Antagonistic potential of Pseudomonasgraminis 49M against Erwiniaamylovora, the causal agent of fire blight
title_full_unstemmed Antagonistic potential of Pseudomonasgraminis 49M against Erwiniaamylovora, the causal agent of fire blight
title_short Antagonistic potential of Pseudomonasgraminis 49M against Erwiniaamylovora, the causal agent of fire blight
title_sort antagonistic potential of pseudomonasgraminis 49m against erwiniaamylovora, the causal agent of fire blight
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930463/
https://www.ncbi.nlm.nih.gov/pubmed/27002332
http://dx.doi.org/10.1007/s00203-016-1207-7
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