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TonB Energy Transduction Systems of Riemerella anatipestifer Are Required for Iron and Hemin Utilization

Riemerella anatipestifer (R. anatipestifer) is one of the most important pathogens in ducks. The bacteria causes acute or chronic septicemia characterized by fibrinous pericarditis and meningitis. The R. anatipestifer genome encodes multiple iron/hemin-uptake systems that facilitate adaptation to ir...

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Autores principales: Liao, HeBin, Cheng, XingJun, Zhu, DeKang, Wang, MingShu, Jia, RenYong, Chen, Shun, Chen, XiaoYue, Biville, Francis, Liu, MaFeng, Cheng, AnChun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4446302/
https://www.ncbi.nlm.nih.gov/pubmed/26017672
http://dx.doi.org/10.1371/journal.pone.0127506
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author Liao, HeBin
Cheng, XingJun
Zhu, DeKang
Wang, MingShu
Jia, RenYong
Chen, Shun
Chen, XiaoYue
Biville, Francis
Liu, MaFeng
Cheng, AnChun
author_facet Liao, HeBin
Cheng, XingJun
Zhu, DeKang
Wang, MingShu
Jia, RenYong
Chen, Shun
Chen, XiaoYue
Biville, Francis
Liu, MaFeng
Cheng, AnChun
author_sort Liao, HeBin
collection PubMed
description Riemerella anatipestifer (R. anatipestifer) is one of the most important pathogens in ducks. The bacteria causes acute or chronic septicemia characterized by fibrinous pericarditis and meningitis. The R. anatipestifer genome encodes multiple iron/hemin-uptake systems that facilitate adaptation to iron-limited host environments. These systems include several TonB-dependent transporters and three TonB proteins responsible for energy transduction. These three tonB genes are present in all the R. anatipestifer genomes sequenced so far. Two of these genes are contained within the exbB-exbD-tonB1 and exbB-exbD-exbD-tonB2 operons. The third, tonB3, forms a monocistronic transcription unit. The inability to recover derivatives deleted for this gene suggests its product is essential for R. anatipestifer growth. Here, we show that deletion of tonB1 had no effect on hemin uptake of R. anatipestifer, though disruption of tonB2 strongly decreases hemin uptake, and disruption of both tonB1 and tonB2 abolishes the transport of exogenously added hemin. The ability of R. anatipestifer to grow on iron-depleted medium is decreased by tonB2 but not tonB1 disruption. When expressed in an E. coli model strain, the TonB1 complex, TonB2 complex, and TonB3 protein from R. anatipestifer cannot energize heterologous hemin transporters. Further, only the TonB1 complex can energize a R. anatipestifer hemin transporter when co-expressed in an E. coli model strain.
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spelling pubmed-44463022015-06-09 TonB Energy Transduction Systems of Riemerella anatipestifer Are Required for Iron and Hemin Utilization Liao, HeBin Cheng, XingJun Zhu, DeKang Wang, MingShu Jia, RenYong Chen, Shun Chen, XiaoYue Biville, Francis Liu, MaFeng Cheng, AnChun PLoS One Research Article Riemerella anatipestifer (R. anatipestifer) is one of the most important pathogens in ducks. The bacteria causes acute or chronic septicemia characterized by fibrinous pericarditis and meningitis. The R. anatipestifer genome encodes multiple iron/hemin-uptake systems that facilitate adaptation to iron-limited host environments. These systems include several TonB-dependent transporters and three TonB proteins responsible for energy transduction. These three tonB genes are present in all the R. anatipestifer genomes sequenced so far. Two of these genes are contained within the exbB-exbD-tonB1 and exbB-exbD-exbD-tonB2 operons. The third, tonB3, forms a monocistronic transcription unit. The inability to recover derivatives deleted for this gene suggests its product is essential for R. anatipestifer growth. Here, we show that deletion of tonB1 had no effect on hemin uptake of R. anatipestifer, though disruption of tonB2 strongly decreases hemin uptake, and disruption of both tonB1 and tonB2 abolishes the transport of exogenously added hemin. The ability of R. anatipestifer to grow on iron-depleted medium is decreased by tonB2 but not tonB1 disruption. When expressed in an E. coli model strain, the TonB1 complex, TonB2 complex, and TonB3 protein from R. anatipestifer cannot energize heterologous hemin transporters. Further, only the TonB1 complex can energize a R. anatipestifer hemin transporter when co-expressed in an E. coli model strain. Public Library of Science 2015-05-27 /pmc/articles/PMC4446302/ /pubmed/26017672 http://dx.doi.org/10.1371/journal.pone.0127506 Text en © 2015 Liao 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Liao, HeBin
Cheng, XingJun
Zhu, DeKang
Wang, MingShu
Jia, RenYong
Chen, Shun
Chen, XiaoYue
Biville, Francis
Liu, MaFeng
Cheng, AnChun
TonB Energy Transduction Systems of Riemerella anatipestifer Are Required for Iron and Hemin Utilization
title TonB Energy Transduction Systems of Riemerella anatipestifer Are Required for Iron and Hemin Utilization
title_full TonB Energy Transduction Systems of Riemerella anatipestifer Are Required for Iron and Hemin Utilization
title_fullStr TonB Energy Transduction Systems of Riemerella anatipestifer Are Required for Iron and Hemin Utilization
title_full_unstemmed TonB Energy Transduction Systems of Riemerella anatipestifer Are Required for Iron and Hemin Utilization
title_short TonB Energy Transduction Systems of Riemerella anatipestifer Are Required for Iron and Hemin Utilization
title_sort tonb energy transduction systems of riemerella anatipestifer are required for iron and hemin utilization
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4446302/
https://www.ncbi.nlm.nih.gov/pubmed/26017672
http://dx.doi.org/10.1371/journal.pone.0127506
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