Cargando…

Type 3 Fimbriae Encoded on Plasmids Are Expressed from a Unique Promoter without Affecting Host Motility, Facilitating an Exceptional Phenotype That Enhances Conjugal Plasmid Transfer

Horizontal gene transfer (HGT), the transmission of genetic material to a recipient that is not the progeny of the donor, is fundamental in bacterial evolution. HGT is often mediated by mobile genetic elements such as conjugative plasmids, which may be in conflict with the chromosomal elements of th...

Descripción completa

Detalles Bibliográficos
Autores principales: Madsen, Jonas Stenløkke, Riber, Leise, Kot, Witold, Basfeld, Alrun, Burmølle, Mette, Hansen, Lars Hestbjerg, Sørensen, Søren Johannes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5023117/
https://www.ncbi.nlm.nih.gov/pubmed/27627107
http://dx.doi.org/10.1371/journal.pone.0162390
_version_ 1782453621595570176
author Madsen, Jonas Stenløkke
Riber, Leise
Kot, Witold
Basfeld, Alrun
Burmølle, Mette
Hansen, Lars Hestbjerg
Sørensen, Søren Johannes
author_facet Madsen, Jonas Stenløkke
Riber, Leise
Kot, Witold
Basfeld, Alrun
Burmølle, Mette
Hansen, Lars Hestbjerg
Sørensen, Søren Johannes
author_sort Madsen, Jonas Stenløkke
collection PubMed
description Horizontal gene transfer (HGT), the transmission of genetic material to a recipient that is not the progeny of the donor, is fundamental in bacterial evolution. HGT is often mediated by mobile genetic elements such as conjugative plasmids, which may be in conflict with the chromosomal elements of the genome because they are independent replicons that may petition their own evolutionary strategy. Here we study differences between type 3 fimbriae encoded on wild type plasmids and in chromosomes. Using known and newly characterized plasmids we show that the expression of type 3 fimbriae encoded on plasmids is systematically different, as MrkH, a c-di-GMP dependent transcriptional activator is not needed for strong expression of the fimbriae. MrkH is required for expression of type 3 fimbriae of the Klebsiella pneumoniae chromosome, wherefrom the fimbriae operon (mrkABCDF) of plasmids is believed to have originated. We find that mrkABCDFs of plasmids are highly expressed via a unique promoter that differs from the original Klebsiella promoter resulting in fundamental behavioral consequences. Plasmid associated mrkABCDFs did not influence the swimming behavior of the host, that hereby acquired an exceptional phenotype being able to both actively swim (planktonic behavior) and express biofilm associated fimbriae (sessile behavior). We show that this exceptional phenotype enhances the conjugal transfer of the plasmid.
format Online
Article
Text
id pubmed-5023117
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-50231172016-09-27 Type 3 Fimbriae Encoded on Plasmids Are Expressed from a Unique Promoter without Affecting Host Motility, Facilitating an Exceptional Phenotype That Enhances Conjugal Plasmid Transfer Madsen, Jonas Stenløkke Riber, Leise Kot, Witold Basfeld, Alrun Burmølle, Mette Hansen, Lars Hestbjerg Sørensen, Søren Johannes PLoS One Research Article Horizontal gene transfer (HGT), the transmission of genetic material to a recipient that is not the progeny of the donor, is fundamental in bacterial evolution. HGT is often mediated by mobile genetic elements such as conjugative plasmids, which may be in conflict with the chromosomal elements of the genome because they are independent replicons that may petition their own evolutionary strategy. Here we study differences between type 3 fimbriae encoded on wild type plasmids and in chromosomes. Using known and newly characterized plasmids we show that the expression of type 3 fimbriae encoded on plasmids is systematically different, as MrkH, a c-di-GMP dependent transcriptional activator is not needed for strong expression of the fimbriae. MrkH is required for expression of type 3 fimbriae of the Klebsiella pneumoniae chromosome, wherefrom the fimbriae operon (mrkABCDF) of plasmids is believed to have originated. We find that mrkABCDFs of plasmids are highly expressed via a unique promoter that differs from the original Klebsiella promoter resulting in fundamental behavioral consequences. Plasmid associated mrkABCDFs did not influence the swimming behavior of the host, that hereby acquired an exceptional phenotype being able to both actively swim (planktonic behavior) and express biofilm associated fimbriae (sessile behavior). We show that this exceptional phenotype enhances the conjugal transfer of the plasmid. Public Library of Science 2016-09-14 /pmc/articles/PMC5023117/ /pubmed/27627107 http://dx.doi.org/10.1371/journal.pone.0162390 Text en © 2016 Madsen 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Madsen, Jonas Stenløkke
Riber, Leise
Kot, Witold
Basfeld, Alrun
Burmølle, Mette
Hansen, Lars Hestbjerg
Sørensen, Søren Johannes
Type 3 Fimbriae Encoded on Plasmids Are Expressed from a Unique Promoter without Affecting Host Motility, Facilitating an Exceptional Phenotype That Enhances Conjugal Plasmid Transfer
title Type 3 Fimbriae Encoded on Plasmids Are Expressed from a Unique Promoter without Affecting Host Motility, Facilitating an Exceptional Phenotype That Enhances Conjugal Plasmid Transfer
title_full Type 3 Fimbriae Encoded on Plasmids Are Expressed from a Unique Promoter without Affecting Host Motility, Facilitating an Exceptional Phenotype That Enhances Conjugal Plasmid Transfer
title_fullStr Type 3 Fimbriae Encoded on Plasmids Are Expressed from a Unique Promoter without Affecting Host Motility, Facilitating an Exceptional Phenotype That Enhances Conjugal Plasmid Transfer
title_full_unstemmed Type 3 Fimbriae Encoded on Plasmids Are Expressed from a Unique Promoter without Affecting Host Motility, Facilitating an Exceptional Phenotype That Enhances Conjugal Plasmid Transfer
title_short Type 3 Fimbriae Encoded on Plasmids Are Expressed from a Unique Promoter without Affecting Host Motility, Facilitating an Exceptional Phenotype That Enhances Conjugal Plasmid Transfer
title_sort type 3 fimbriae encoded on plasmids are expressed from a unique promoter without affecting host motility, facilitating an exceptional phenotype that enhances conjugal plasmid transfer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5023117/
https://www.ncbi.nlm.nih.gov/pubmed/27627107
http://dx.doi.org/10.1371/journal.pone.0162390
work_keys_str_mv AT madsenjonasstenløkke type3fimbriaeencodedonplasmidsareexpressedfromauniquepromoterwithoutaffectinghostmotilityfacilitatinganexceptionalphenotypethatenhancesconjugalplasmidtransfer
AT riberleise type3fimbriaeencodedonplasmidsareexpressedfromauniquepromoterwithoutaffectinghostmotilityfacilitatinganexceptionalphenotypethatenhancesconjugalplasmidtransfer
AT kotwitold type3fimbriaeencodedonplasmidsareexpressedfromauniquepromoterwithoutaffectinghostmotilityfacilitatinganexceptionalphenotypethatenhancesconjugalplasmidtransfer
AT basfeldalrun type3fimbriaeencodedonplasmidsareexpressedfromauniquepromoterwithoutaffectinghostmotilityfacilitatinganexceptionalphenotypethatenhancesconjugalplasmidtransfer
AT burmøllemette type3fimbriaeencodedonplasmidsareexpressedfromauniquepromoterwithoutaffectinghostmotilityfacilitatinganexceptionalphenotypethatenhancesconjugalplasmidtransfer
AT hansenlarshestbjerg type3fimbriaeencodedonplasmidsareexpressedfromauniquepromoterwithoutaffectinghostmotilityfacilitatinganexceptionalphenotypethatenhancesconjugalplasmidtransfer
AT sørensensørenjohannes type3fimbriaeencodedonplasmidsareexpressedfromauniquepromoterwithoutaffectinghostmotilityfacilitatinganexceptionalphenotypethatenhancesconjugalplasmidtransfer