Cargando…

Interactions of Salmonella enterica Serovar Typhimurium and Pectobacterium carotovorum within a Tomato Soft Rot

Salmonella spp. are remarkably adaptable pathogens, and this adaptability allows these bacteria to thrive in a variety of environments and hosts. The mechanisms with which these pathogens establish within a niche amid the native microbiota remain poorly understood. Here, we aimed to uncover the mech...

Descripción completa

Detalles Bibliográficos
Autores principales: George, Andrée S., Cox, Clayton E., Desai, Prerak, Porwollik, Steffen, Chu, Weiping, de Moraes, Marcos H., McClelland, Michael, Brandl, Maria T., Teplitski, Max
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5812938/
https://www.ncbi.nlm.nih.gov/pubmed/29247060
http://dx.doi.org/10.1128/AEM.01913-17
_version_ 1783300090558939136
author George, Andrée S.
Cox, Clayton E.
Desai, Prerak
Porwollik, Steffen
Chu, Weiping
de Moraes, Marcos H.
McClelland, Michael
Brandl, Maria T.
Teplitski, Max
author_facet George, Andrée S.
Cox, Clayton E.
Desai, Prerak
Porwollik, Steffen
Chu, Weiping
de Moraes, Marcos H.
McClelland, Michael
Brandl, Maria T.
Teplitski, Max
author_sort George, Andrée S.
collection PubMed
description Salmonella spp. are remarkably adaptable pathogens, and this adaptability allows these bacteria to thrive in a variety of environments and hosts. The mechanisms with which these pathogens establish within a niche amid the native microbiota remain poorly understood. Here, we aimed to uncover the mechanisms that enable Salmonella enterica serovar Typhimurium strain ATCC 14028 to benefit from the degradation of plant tissue by a soft rot plant pathogen, Pectobacterium carotovorum. The hypothesis that in the soft rot, the liberation of starch (not utilized by P. carotovorum) makes this polymer available to Salmonella spp., thus allowing it to colonize soft rots, was tested first and proven null. To identify the functions involved in Salmonella soft rot colonization, we carried out transposon insertion sequencing coupled with the phenotypic characterization of the mutants. The data indicate that Salmonella spp. experience a metabolic shift in response to the changes in the environment brought on by Pectobacterium spp. and likely coordinated by the csrBC small regulatory RNA. While csrBC and flhD appear to be of importance in the soft rot, the global two-component system encoded by barA sirA (which controls csrBC and flhDC under laboratory conditions) does not appear to be necessary for the observed phenotype. Motility and the synthesis of nucleotides and amino acids play critical roles in the growth of Salmonella spp. in the soft rot. IMPORTANCE Outbreaks of produce-associated illness continue to be a food safety concern. Earlier studies demonstrated that the presence of phytopathogens on produce was a significant risk factor associated with increased Salmonella carriage on fruits and vegetables. Here, we genetically characterize some of the requirements for interactions between Salmonella and phytobacteria that allow Salmonella spp. to establish a niche within an alternate host (tomato). Pathways necessary for nucleotide synthesis, amino acid synthesis, and motility are identified as contributors to the persistence of Salmonella spp. in soft rots.
format Online
Article
Text
id pubmed-5812938
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-58129382018-02-21 Interactions of Salmonella enterica Serovar Typhimurium and Pectobacterium carotovorum within a Tomato Soft Rot George, Andrée S. Cox, Clayton E. Desai, Prerak Porwollik, Steffen Chu, Weiping de Moraes, Marcos H. McClelland, Michael Brandl, Maria T. Teplitski, Max Appl Environ Microbiol Environmental Microbiology Salmonella spp. are remarkably adaptable pathogens, and this adaptability allows these bacteria to thrive in a variety of environments and hosts. The mechanisms with which these pathogens establish within a niche amid the native microbiota remain poorly understood. Here, we aimed to uncover the mechanisms that enable Salmonella enterica serovar Typhimurium strain ATCC 14028 to benefit from the degradation of plant tissue by a soft rot plant pathogen, Pectobacterium carotovorum. The hypothesis that in the soft rot, the liberation of starch (not utilized by P. carotovorum) makes this polymer available to Salmonella spp., thus allowing it to colonize soft rots, was tested first and proven null. To identify the functions involved in Salmonella soft rot colonization, we carried out transposon insertion sequencing coupled with the phenotypic characterization of the mutants. The data indicate that Salmonella spp. experience a metabolic shift in response to the changes in the environment brought on by Pectobacterium spp. and likely coordinated by the csrBC small regulatory RNA. While csrBC and flhD appear to be of importance in the soft rot, the global two-component system encoded by barA sirA (which controls csrBC and flhDC under laboratory conditions) does not appear to be necessary for the observed phenotype. Motility and the synthesis of nucleotides and amino acids play critical roles in the growth of Salmonella spp. in the soft rot. IMPORTANCE Outbreaks of produce-associated illness continue to be a food safety concern. Earlier studies demonstrated that the presence of phytopathogens on produce was a significant risk factor associated with increased Salmonella carriage on fruits and vegetables. Here, we genetically characterize some of the requirements for interactions between Salmonella and phytobacteria that allow Salmonella spp. to establish a niche within an alternate host (tomato). Pathways necessary for nucleotide synthesis, amino acid synthesis, and motility are identified as contributors to the persistence of Salmonella spp. in soft rots. American Society for Microbiology 2018-02-14 /pmc/articles/PMC5812938/ /pubmed/29247060 http://dx.doi.org/10.1128/AEM.01913-17 Text en Copyright © 2018 George et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Environmental Microbiology
George, Andrée S.
Cox, Clayton E.
Desai, Prerak
Porwollik, Steffen
Chu, Weiping
de Moraes, Marcos H.
McClelland, Michael
Brandl, Maria T.
Teplitski, Max
Interactions of Salmonella enterica Serovar Typhimurium and Pectobacterium carotovorum within a Tomato Soft Rot
title Interactions of Salmonella enterica Serovar Typhimurium and Pectobacterium carotovorum within a Tomato Soft Rot
title_full Interactions of Salmonella enterica Serovar Typhimurium and Pectobacterium carotovorum within a Tomato Soft Rot
title_fullStr Interactions of Salmonella enterica Serovar Typhimurium and Pectobacterium carotovorum within a Tomato Soft Rot
title_full_unstemmed Interactions of Salmonella enterica Serovar Typhimurium and Pectobacterium carotovorum within a Tomato Soft Rot
title_short Interactions of Salmonella enterica Serovar Typhimurium and Pectobacterium carotovorum within a Tomato Soft Rot
title_sort interactions of salmonella enterica serovar typhimurium and pectobacterium carotovorum within a tomato soft rot
topic Environmental Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5812938/
https://www.ncbi.nlm.nih.gov/pubmed/29247060
http://dx.doi.org/10.1128/AEM.01913-17
work_keys_str_mv AT georgeandrees interactionsofsalmonellaentericaserovartyphimuriumandpectobacteriumcarotovorumwithinatomatosoftrot
AT coxclaytone interactionsofsalmonellaentericaserovartyphimuriumandpectobacteriumcarotovorumwithinatomatosoftrot
AT desaiprerak interactionsofsalmonellaentericaserovartyphimuriumandpectobacteriumcarotovorumwithinatomatosoftrot
AT porwolliksteffen interactionsofsalmonellaentericaserovartyphimuriumandpectobacteriumcarotovorumwithinatomatosoftrot
AT chuweiping interactionsofsalmonellaentericaserovartyphimuriumandpectobacteriumcarotovorumwithinatomatosoftrot
AT demoraesmarcosh interactionsofsalmonellaentericaserovartyphimuriumandpectobacteriumcarotovorumwithinatomatosoftrot
AT mcclellandmichael interactionsofsalmonellaentericaserovartyphimuriumandpectobacteriumcarotovorumwithinatomatosoftrot
AT brandlmariat interactionsofsalmonellaentericaserovartyphimuriumandpectobacteriumcarotovorumwithinatomatosoftrot
AT teplitskimax interactionsofsalmonellaentericaserovartyphimuriumandpectobacteriumcarotovorumwithinatomatosoftrot