Pervasive sign epistasis between conjugative plasmids and drug-resistance chromosomal mutations.

Multidrug-resistant bacteria arise mostly by the accumulation of plasmids and chromosomal mutations. Typically, these resistant determinants are costly to the bacterial cell. Yet, recently, it has been found that, in Escherichia coli bacterial cells, a mutation conferring resistance to an antibiotic...

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Main Authors: Rui F Silva, Sílvia C M Mendonça, Luís M Carvalho, Ana M Reis, Isabel Gordo, Sandra Trindade, Francisco Dionisio
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-07-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC3145620?pdf=render
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spelling doaj-43f8d7d3a1ae4a718375a6defe0a48072020-11-24T21:55:20ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042011-07-0177e100218110.1371/journal.pgen.1002181Pervasive sign epistasis between conjugative plasmids and drug-resistance chromosomal mutations.Rui F SilvaSílvia C M MendonçaLuís M CarvalhoAna M ReisIsabel GordoSandra TrindadeFrancisco DionisioMultidrug-resistant bacteria arise mostly by the accumulation of plasmids and chromosomal mutations. Typically, these resistant determinants are costly to the bacterial cell. Yet, recently, it has been found that, in Escherichia coli bacterial cells, a mutation conferring resistance to an antibiotic can be advantageous to the bacterial cell if another antibiotic-resistance mutation is already present, a phenomenon called sign epistasis. Here we study the interaction between antibiotic-resistance chromosomal mutations and conjugative (i.e., self-transmissible) plasmids and find many cases of sign epistasis (40%)--including one of reciprocal sign epistasis where the strain carrying both resistance determinants is fitter than the two strains carrying only one of the determinants. This implies that the acquisition of an additional resistance plasmid or of a resistance mutation often increases the fitness of a bacterial strain already resistant to antibiotics. We further show that there is an overall antagonistic interaction between mutations and plasmids (52%). These results further complicate expectations of resistance reversal by interdiction of antibiotic use.http://europepmc.org/articles/PMC3145620?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Rui F Silva
Sílvia C M Mendonça
Luís M Carvalho
Ana M Reis
Isabel Gordo
Sandra Trindade
Francisco Dionisio
spellingShingle Rui F Silva
Sílvia C M Mendonça
Luís M Carvalho
Ana M Reis
Isabel Gordo
Sandra Trindade
Francisco Dionisio
Pervasive sign epistasis between conjugative plasmids and drug-resistance chromosomal mutations.
PLoS Genetics
author_facet Rui F Silva
Sílvia C M Mendonça
Luís M Carvalho
Ana M Reis
Isabel Gordo
Sandra Trindade
Francisco Dionisio
author_sort Rui F Silva
title Pervasive sign epistasis between conjugative plasmids and drug-resistance chromosomal mutations.
title_short Pervasive sign epistasis between conjugative plasmids and drug-resistance chromosomal mutations.
title_full Pervasive sign epistasis between conjugative plasmids and drug-resistance chromosomal mutations.
title_fullStr Pervasive sign epistasis between conjugative plasmids and drug-resistance chromosomal mutations.
title_full_unstemmed Pervasive sign epistasis between conjugative plasmids and drug-resistance chromosomal mutations.
title_sort pervasive sign epistasis between conjugative plasmids and drug-resistance chromosomal mutations.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2011-07-01
description Multidrug-resistant bacteria arise mostly by the accumulation of plasmids and chromosomal mutations. Typically, these resistant determinants are costly to the bacterial cell. Yet, recently, it has been found that, in Escherichia coli bacterial cells, a mutation conferring resistance to an antibiotic can be advantageous to the bacterial cell if another antibiotic-resistance mutation is already present, a phenomenon called sign epistasis. Here we study the interaction between antibiotic-resistance chromosomal mutations and conjugative (i.e., self-transmissible) plasmids and find many cases of sign epistasis (40%)--including one of reciprocal sign epistasis where the strain carrying both resistance determinants is fitter than the two strains carrying only one of the determinants. This implies that the acquisition of an additional resistance plasmid or of a resistance mutation often increases the fitness of a bacterial strain already resistant to antibiotics. We further show that there is an overall antagonistic interaction between mutations and plasmids (52%). These results further complicate expectations of resistance reversal by interdiction of antibiotic use.
url http://europepmc.org/articles/PMC3145620?pdf=render
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