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Partial Disruption of Translational and Posttranslational Machinery Reshapes Growth Rates of Bartonella birtlesii

Specialization of bacteria in a new niche is associated with genome repertoire changes, and speciation in bacterial specialists is associated with genome reduction. Here, we tested a signature-tagged mutant library of 3,456 Bartonella birtlesii clones to detect mutants that could grow rapidly in vit...

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Autores principales: Rolain, Jean Marc, Vayssier-Taussat, Muriel, Saisongkorh, Watcharee, Merhej, Vicky, Gimenez, Gregory, Robert, Catherine, Le Rhun, Danielle, Dehio, Christoph, Raoult, Didier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Microbiology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3638310/
https://www.ncbi.nlm.nih.gov/pubmed/23611908
http://dx.doi.org/10.1128/mBio.00115-13
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author Rolain, Jean Marc
Vayssier-Taussat, Muriel
Saisongkorh, Watcharee
Merhej, Vicky
Gimenez, Gregory
Robert, Catherine
Le Rhun, Danielle
Dehio, Christoph
Raoult, Didier
author_facet Rolain, Jean Marc
Vayssier-Taussat, Muriel
Saisongkorh, Watcharee
Merhej, Vicky
Gimenez, Gregory
Robert, Catherine
Le Rhun, Danielle
Dehio, Christoph
Raoult, Didier
author_sort Rolain, Jean Marc
collection PubMed
description Specialization of bacteria in a new niche is associated with genome repertoire changes, and speciation in bacterial specialists is associated with genome reduction. Here, we tested a signature-tagged mutant library of 3,456 Bartonella birtlesii clones to detect mutants that could grow rapidly in vitro. Overall, we found 124 mutants that grew faster than the parental wild-type strain in vitro. We sequenced the genomes of the four mutants with the most rapid growth (formed visible colonies in only 1 to 2 days compared with 5 days for the wild type) and compared them to the parental isolate genome. We found that the number of disrupted genes associated with translation in the 124 rapid-growth clones was significantly higher than the number of genes involved in translation in the full genome (P < 10(−6)). Analysis of transposon integration in the genome of the four most rapidly growing clones revealed that one clone lacked one of the two wild-type RNA ribosomal operons. Finally, one of the four clones did not induce bacteremia in our mouse model, whereas infection with the other three resulted in a significantly lower bacterial count in blood than that with the wild-type strain.
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spelling pubmed-36383102013-04-29 Partial Disruption of Translational and Posttranslational Machinery Reshapes Growth Rates of Bartonella birtlesii Rolain, Jean Marc Vayssier-Taussat, Muriel Saisongkorh, Watcharee Merhej, Vicky Gimenez, Gregory Robert, Catherine Le Rhun, Danielle Dehio, Christoph Raoult, Didier mBio Research Article Specialization of bacteria in a new niche is associated with genome repertoire changes, and speciation in bacterial specialists is associated with genome reduction. Here, we tested a signature-tagged mutant library of 3,456 Bartonella birtlesii clones to detect mutants that could grow rapidly in vitro. Overall, we found 124 mutants that grew faster than the parental wild-type strain in vitro. We sequenced the genomes of the four mutants with the most rapid growth (formed visible colonies in only 1 to 2 days compared with 5 days for the wild type) and compared them to the parental isolate genome. We found that the number of disrupted genes associated with translation in the 124 rapid-growth clones was significantly higher than the number of genes involved in translation in the full genome (P < 10(−6)). Analysis of transposon integration in the genome of the four most rapidly growing clones revealed that one clone lacked one of the two wild-type RNA ribosomal operons. Finally, one of the four clones did not induce bacteremia in our mouse model, whereas infection with the other three resulted in a significantly lower bacterial count in blood than that with the wild-type strain. American Society of Microbiology 2013-04-23 /pmc/articles/PMC3638310/ /pubmed/23611908 http://dx.doi.org/10.1128/mBio.00115-13 Text en Copyright © 2013 Rolain et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Rolain, Jean Marc
Vayssier-Taussat, Muriel
Saisongkorh, Watcharee
Merhej, Vicky
Gimenez, Gregory
Robert, Catherine
Le Rhun, Danielle
Dehio, Christoph
Raoult, Didier
Partial Disruption of Translational and Posttranslational Machinery Reshapes Growth Rates of Bartonella birtlesii
title Partial Disruption of Translational and Posttranslational Machinery Reshapes Growth Rates of Bartonella birtlesii
title_full Partial Disruption of Translational and Posttranslational Machinery Reshapes Growth Rates of Bartonella birtlesii
title_fullStr Partial Disruption of Translational and Posttranslational Machinery Reshapes Growth Rates of Bartonella birtlesii
title_full_unstemmed Partial Disruption of Translational and Posttranslational Machinery Reshapes Growth Rates of Bartonella birtlesii
title_short Partial Disruption of Translational and Posttranslational Machinery Reshapes Growth Rates of Bartonella birtlesii
title_sort partial disruption of translational and posttranslational machinery reshapes growth rates of bartonella birtlesii
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3638310/
https://www.ncbi.nlm.nih.gov/pubmed/23611908
http://dx.doi.org/10.1128/mBio.00115-13
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