Cargando…

Functional Genomics Insights Into the Pathogenicity, Habitat Fitness, and Mechanisms Modifying Plant Development of Rhodococcus sp. PBTS1 and PBTS2

Pistachio Bushy Top Syndrome (PBTS) is a recently emerged disease that has strongly impacted the pistachio industry in California, Arizona, and New Mexico. The disease is caused by two bacteria, designated PBTS1 that is related to Rhodococcus corynebacterioides and PBTS2 that belongs to the species...

Descripción completa

Detalles Bibliográficos
Autores principales: Vereecke, Danny, Zhang, Yucheng, Francis, Isolde M., Lambert, Paul Q., Venneman, Jolien, Stamler, Rio A., Kilcrease, James, Randall, Jennifer J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002392/
https://www.ncbi.nlm.nih.gov/pubmed/32082278
http://dx.doi.org/10.3389/fmicb.2020.00014
_version_ 1783494368138625024
author Vereecke, Danny
Zhang, Yucheng
Francis, Isolde M.
Lambert, Paul Q.
Venneman, Jolien
Stamler, Rio A.
Kilcrease, James
Randall, Jennifer J.
author_facet Vereecke, Danny
Zhang, Yucheng
Francis, Isolde M.
Lambert, Paul Q.
Venneman, Jolien
Stamler, Rio A.
Kilcrease, James
Randall, Jennifer J.
author_sort Vereecke, Danny
collection PubMed
description Pistachio Bushy Top Syndrome (PBTS) is a recently emerged disease that has strongly impacted the pistachio industry in California, Arizona, and New Mexico. The disease is caused by two bacteria, designated PBTS1 that is related to Rhodococcus corynebacterioides and PBTS2 that belongs to the species R. fascians. Here, we assessed the pathogenic character of the causative agents and examined their chromosomal sequences to predict the presence of particular functions that might contribute to the observed co-occurrence and their effect on plant hosts. In diverse assays, we confirmed the pathogenicity of the strains on “UCB-1” pistachio rootstock and showed that they can also impact the development of tobacco species, but concurrently inconsistencies in the ability to induce symptoms were revealed. We additionally evidence that fas genes are present only in a subpopulation of pure PBTS1 and PBTS2 cultures after growth on synthetic media, that these genes are easily lost upon cultivation in rich media, and that they are enriched for in an in planta environment. Analysis of the chromosomal sequences indicated that PBTS1 and PBTS2 might have complementary activities that would support niche partitioning. Growth experiments showed that the nutrient utilization pattern of both PBTS bacteria was not identical, thus avoiding co-inhabitant competition. PBTS2 appeared to have the potential to positively affect the habitat fitness of PBTS1 by improving its resistance against increased concentrations of copper and penicillins. Finally, mining the chromosomes of PBTS1 and PBTS2 suggested that the bacteria could produce cytokinins, auxins, and plant growth-stimulating volatiles and that PBTS2 might interfere with ethylene levels, in support of their impact on plant development. Subsequent experimentation supported these in silico predictions. Altogether, our data provide an explanation for the observed pathogenic behavior and unveil part of the strategies used by PBTS1 and PBTS2 to interact with plants.
format Online
Article
Text
id pubmed-7002392
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-70023922020-02-20 Functional Genomics Insights Into the Pathogenicity, Habitat Fitness, and Mechanisms Modifying Plant Development of Rhodococcus sp. PBTS1 and PBTS2 Vereecke, Danny Zhang, Yucheng Francis, Isolde M. Lambert, Paul Q. Venneman, Jolien Stamler, Rio A. Kilcrease, James Randall, Jennifer J. Front Microbiol Microbiology Pistachio Bushy Top Syndrome (PBTS) is a recently emerged disease that has strongly impacted the pistachio industry in California, Arizona, and New Mexico. The disease is caused by two bacteria, designated PBTS1 that is related to Rhodococcus corynebacterioides and PBTS2 that belongs to the species R. fascians. Here, we assessed the pathogenic character of the causative agents and examined their chromosomal sequences to predict the presence of particular functions that might contribute to the observed co-occurrence and their effect on plant hosts. In diverse assays, we confirmed the pathogenicity of the strains on “UCB-1” pistachio rootstock and showed that they can also impact the development of tobacco species, but concurrently inconsistencies in the ability to induce symptoms were revealed. We additionally evidence that fas genes are present only in a subpopulation of pure PBTS1 and PBTS2 cultures after growth on synthetic media, that these genes are easily lost upon cultivation in rich media, and that they are enriched for in an in planta environment. Analysis of the chromosomal sequences indicated that PBTS1 and PBTS2 might have complementary activities that would support niche partitioning. Growth experiments showed that the nutrient utilization pattern of both PBTS bacteria was not identical, thus avoiding co-inhabitant competition. PBTS2 appeared to have the potential to positively affect the habitat fitness of PBTS1 by improving its resistance against increased concentrations of copper and penicillins. Finally, mining the chromosomes of PBTS1 and PBTS2 suggested that the bacteria could produce cytokinins, auxins, and plant growth-stimulating volatiles and that PBTS2 might interfere with ethylene levels, in support of their impact on plant development. Subsequent experimentation supported these in silico predictions. Altogether, our data provide an explanation for the observed pathogenic behavior and unveil part of the strategies used by PBTS1 and PBTS2 to interact with plants. Frontiers Media S.A. 2020-01-30 /pmc/articles/PMC7002392/ /pubmed/32082278 http://dx.doi.org/10.3389/fmicb.2020.00014 Text en Copyright © 2020 Vereecke, Zhang, Francis, Lambert, Venneman, Stamler, Kilcrease and Randall. http://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
Vereecke, Danny
Zhang, Yucheng
Francis, Isolde M.
Lambert, Paul Q.
Venneman, Jolien
Stamler, Rio A.
Kilcrease, James
Randall, Jennifer J.
Functional Genomics Insights Into the Pathogenicity, Habitat Fitness, and Mechanisms Modifying Plant Development of Rhodococcus sp. PBTS1 and PBTS2
title Functional Genomics Insights Into the Pathogenicity, Habitat Fitness, and Mechanisms Modifying Plant Development of Rhodococcus sp. PBTS1 and PBTS2
title_full Functional Genomics Insights Into the Pathogenicity, Habitat Fitness, and Mechanisms Modifying Plant Development of Rhodococcus sp. PBTS1 and PBTS2
title_fullStr Functional Genomics Insights Into the Pathogenicity, Habitat Fitness, and Mechanisms Modifying Plant Development of Rhodococcus sp. PBTS1 and PBTS2
title_full_unstemmed Functional Genomics Insights Into the Pathogenicity, Habitat Fitness, and Mechanisms Modifying Plant Development of Rhodococcus sp. PBTS1 and PBTS2
title_short Functional Genomics Insights Into the Pathogenicity, Habitat Fitness, and Mechanisms Modifying Plant Development of Rhodococcus sp. PBTS1 and PBTS2
title_sort functional genomics insights into the pathogenicity, habitat fitness, and mechanisms modifying plant development of rhodococcus sp. pbts1 and pbts2
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002392/
https://www.ncbi.nlm.nih.gov/pubmed/32082278
http://dx.doi.org/10.3389/fmicb.2020.00014
work_keys_str_mv AT vereeckedanny functionalgenomicsinsightsintothepathogenicityhabitatfitnessandmechanismsmodifyingplantdevelopmentofrhodococcussppbts1andpbts2
AT zhangyucheng functionalgenomicsinsightsintothepathogenicityhabitatfitnessandmechanismsmodifyingplantdevelopmentofrhodococcussppbts1andpbts2
AT francisisoldem functionalgenomicsinsightsintothepathogenicityhabitatfitnessandmechanismsmodifyingplantdevelopmentofrhodococcussppbts1andpbts2
AT lambertpaulq functionalgenomicsinsightsintothepathogenicityhabitatfitnessandmechanismsmodifyingplantdevelopmentofrhodococcussppbts1andpbts2
AT vennemanjolien functionalgenomicsinsightsintothepathogenicityhabitatfitnessandmechanismsmodifyingplantdevelopmentofrhodococcussppbts1andpbts2
AT stamlerrioa functionalgenomicsinsightsintothepathogenicityhabitatfitnessandmechanismsmodifyingplantdevelopmentofrhodococcussppbts1andpbts2
AT kilcreasejames functionalgenomicsinsightsintothepathogenicityhabitatfitnessandmechanismsmodifyingplantdevelopmentofrhodococcussppbts1andpbts2
AT randalljenniferj functionalgenomicsinsightsintothepathogenicityhabitatfitnessandmechanismsmodifyingplantdevelopmentofrhodococcussppbts1andpbts2