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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Microbiology
2013
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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. |
format | Online Article Text |
id | pubmed-3638310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | American Society of Microbiology |
record_format | MEDLINE/PubMed |
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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