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The Intracellular Citrus Huanglongbing Bacterium, ‘Candidatus Liberibacter asiaticus’ Encodes Two Novel Autotransporters

Proteins secreted by the type V secretion system (T5SS), known as autotransporters, are large extracellular virulence proteins localized to the bacterial poles. In this study, we characterized two novel autotransporter proteins of ‘ Candidatus Liberibacter asiaticus’ (Las), and redesignated them as...

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Detalles Bibliográficos
Autores principales: Hao, Guixia, Boyle, Michael, Zhou, Lijuan, Duan, Yongping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3708911/
https://www.ncbi.nlm.nih.gov/pubmed/23874813
http://dx.doi.org/10.1371/journal.pone.0068921
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author Hao, Guixia
Boyle, Michael
Zhou, Lijuan
Duan, Yongping
author_facet Hao, Guixia
Boyle, Michael
Zhou, Lijuan
Duan, Yongping
author_sort Hao, Guixia
collection PubMed
description Proteins secreted by the type V secretion system (T5SS), known as autotransporters, are large extracellular virulence proteins localized to the bacterial poles. In this study, we characterized two novel autotransporter proteins of ‘ Candidatus Liberibacter asiaticus’ (Las), and redesignated them as LasA(I) and LasA(II) in lieu of the previous names Hyv(I) and Hyv(II). As a phloem-limited, intracellular bacterial pathogen, Las has a significantly reduced genome and causes huanglongbing (HLB), a devastating disease of citrus worldwide. Bioinformatic analyses revealed that LasA(I) and LasA(II) share the structural features of an autotransporter family containing large repeats of a passenger domain and a unique C-terminal translocator domain. When fused to the GFP gene and expressed in E. coli, the LasA(I) C-terminus and the full length LasA(II) were localized to the bacterial poles, similar to other members of autotransporter family. Despite the absence of a typical signal peptide, LasA(I) was found to localize at the cell surface by immuno-dot blot using a monoclonal antibody against the partial LasA(I) protein. Its surface localization was also confirmed by the removal of the LasA(I) antigen using a proteinase K treatment of the intact bacterial cells. When co-inoculated with a P19 gene silencing suppressor and transiently expressed in tobacco leaves, the GFP-LasA(I) translocator targeted to the mitochondria. This is the first report that Las encodes novel autotransporters that target to mitochondria when expressed in the plants. These findings may lead to a better understanding of the pathogenesis of this intracellular bacterium.
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spelling pubmed-37089112013-07-19 The Intracellular Citrus Huanglongbing Bacterium, ‘Candidatus Liberibacter asiaticus’ Encodes Two Novel Autotransporters Hao, Guixia Boyle, Michael Zhou, Lijuan Duan, Yongping PLoS One Research Article Proteins secreted by the type V secretion system (T5SS), known as autotransporters, are large extracellular virulence proteins localized to the bacterial poles. In this study, we characterized two novel autotransporter proteins of ‘ Candidatus Liberibacter asiaticus’ (Las), and redesignated them as LasA(I) and LasA(II) in lieu of the previous names Hyv(I) and Hyv(II). As a phloem-limited, intracellular bacterial pathogen, Las has a significantly reduced genome and causes huanglongbing (HLB), a devastating disease of citrus worldwide. Bioinformatic analyses revealed that LasA(I) and LasA(II) share the structural features of an autotransporter family containing large repeats of a passenger domain and a unique C-terminal translocator domain. When fused to the GFP gene and expressed in E. coli, the LasA(I) C-terminus and the full length LasA(II) were localized to the bacterial poles, similar to other members of autotransporter family. Despite the absence of a typical signal peptide, LasA(I) was found to localize at the cell surface by immuno-dot blot using a monoclonal antibody against the partial LasA(I) protein. Its surface localization was also confirmed by the removal of the LasA(I) antigen using a proteinase K treatment of the intact bacterial cells. When co-inoculated with a P19 gene silencing suppressor and transiently expressed in tobacco leaves, the GFP-LasA(I) translocator targeted to the mitochondria. This is the first report that Las encodes novel autotransporters that target to mitochondria when expressed in the plants. These findings may lead to a better understanding of the pathogenesis of this intracellular bacterium. Public Library of Science 2013-07-11 /pmc/articles/PMC3708911/ /pubmed/23874813 http://dx.doi.org/10.1371/journal.pone.0068921 Text en © 2013 hao et al https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Hao, Guixia
Boyle, Michael
Zhou, Lijuan
Duan, Yongping
The Intracellular Citrus Huanglongbing Bacterium, ‘Candidatus Liberibacter asiaticus’ Encodes Two Novel Autotransporters
title The Intracellular Citrus Huanglongbing Bacterium, ‘Candidatus Liberibacter asiaticus’ Encodes Two Novel Autotransporters
title_full The Intracellular Citrus Huanglongbing Bacterium, ‘Candidatus Liberibacter asiaticus’ Encodes Two Novel Autotransporters
title_fullStr The Intracellular Citrus Huanglongbing Bacterium, ‘Candidatus Liberibacter asiaticus’ Encodes Two Novel Autotransporters
title_full_unstemmed The Intracellular Citrus Huanglongbing Bacterium, ‘Candidatus Liberibacter asiaticus’ Encodes Two Novel Autotransporters
title_short The Intracellular Citrus Huanglongbing Bacterium, ‘Candidatus Liberibacter asiaticus’ Encodes Two Novel Autotransporters
title_sort intracellular citrus huanglongbing bacterium, ‘candidatus liberibacter asiaticus’ encodes two novel autotransporters
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3708911/
https://www.ncbi.nlm.nih.gov/pubmed/23874813
http://dx.doi.org/10.1371/journal.pone.0068921
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