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Phenotypic and genetic barriers to establishment of horizontally transferred genes encoding ribosomal protection proteins

BACKGROUND: Ribosomal protection proteins (RPPs) interact with bacterial ribosomes to prevent inhibition of protein synthesis by tetracycline. RPP genes have evolved from a common ancestor into at least 12 distinct classes and spread by horizontal genetic transfer into a wide range of bacteria. Many...

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Autores principales: Yadav, Kavita, Garoff, Linnéa, Huseby, Douglas L, Hughes, Diarmaid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8120329/
https://www.ncbi.nlm.nih.gov/pubmed/33655294
http://dx.doi.org/10.1093/jac/dkab056
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author Yadav, Kavita
Garoff, Linnéa
Huseby, Douglas L
Hughes, Diarmaid
author_facet Yadav, Kavita
Garoff, Linnéa
Huseby, Douglas L
Hughes, Diarmaid
author_sort Yadav, Kavita
collection PubMed
description BACKGROUND: Ribosomal protection proteins (RPPs) interact with bacterial ribosomes to prevent inhibition of protein synthesis by tetracycline. RPP genes have evolved from a common ancestor into at least 12 distinct classes and spread by horizontal genetic transfer into a wide range of bacteria. Many bacterial genera host RPP genes from multiple classes but tet(M) is the predominant RPP gene found in Escherichia coli. OBJECTIVES: We asked whether phenotypic barriers (low-level resistance, high fitness cost) might constrain the fixation of other RPP genes in E. coli. METHODS: We expressed a diverse set of six different RPP genes in E. coli, including tet(M), and quantified tetracycline susceptibility and growth phenotypes as a function of expression level, and evolvability to overcome identified phenotypic barriers. RESULTS: The genes tet(M) and tet(Q) conferred high-level tetracycline resistance without reducing fitness; tet(O) and tet(W) conferred high-level resistance but significantly reduced growth fitness; tetB(P) conferred low-level resistance and while mutants conferring high-level resistance were selectable these had reduced growth fitness; otr(A) did not confer resistance and resistant mutants could not be selected. Evolution experiments suggested that codon usage patterns in tet(O) and tet(W), and transcriptional silencing associated with nucleotide composition in tetB(P), accounted for the observed phenotypic barriers. CONCLUSIONS: With the exception of tet(Q), the data reveal significant phenotypic and genetic barriers to the fixation of additional RPP genes in E. coli.
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spelling pubmed-81203292021-05-19 Phenotypic and genetic barriers to establishment of horizontally transferred genes encoding ribosomal protection proteins Yadav, Kavita Garoff, Linnéa Huseby, Douglas L Hughes, Diarmaid J Antimicrob Chemother Original Research BACKGROUND: Ribosomal protection proteins (RPPs) interact with bacterial ribosomes to prevent inhibition of protein synthesis by tetracycline. RPP genes have evolved from a common ancestor into at least 12 distinct classes and spread by horizontal genetic transfer into a wide range of bacteria. Many bacterial genera host RPP genes from multiple classes but tet(M) is the predominant RPP gene found in Escherichia coli. OBJECTIVES: We asked whether phenotypic barriers (low-level resistance, high fitness cost) might constrain the fixation of other RPP genes in E. coli. METHODS: We expressed a diverse set of six different RPP genes in E. coli, including tet(M), and quantified tetracycline susceptibility and growth phenotypes as a function of expression level, and evolvability to overcome identified phenotypic barriers. RESULTS: The genes tet(M) and tet(Q) conferred high-level tetracycline resistance without reducing fitness; tet(O) and tet(W) conferred high-level resistance but significantly reduced growth fitness; tetB(P) conferred low-level resistance and while mutants conferring high-level resistance were selectable these had reduced growth fitness; otr(A) did not confer resistance and resistant mutants could not be selected. Evolution experiments suggested that codon usage patterns in tet(O) and tet(W), and transcriptional silencing associated with nucleotide composition in tetB(P), accounted for the observed phenotypic barriers. CONCLUSIONS: With the exception of tet(Q), the data reveal significant phenotypic and genetic barriers to the fixation of additional RPP genes in E. coli. Oxford University Press 2021-02-28 /pmc/articles/PMC8120329/ /pubmed/33655294 http://dx.doi.org/10.1093/jac/dkab056 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Research
Yadav, Kavita
Garoff, Linnéa
Huseby, Douglas L
Hughes, Diarmaid
Phenotypic and genetic barriers to establishment of horizontally transferred genes encoding ribosomal protection proteins
title Phenotypic and genetic barriers to establishment of horizontally transferred genes encoding ribosomal protection proteins
title_full Phenotypic and genetic barriers to establishment of horizontally transferred genes encoding ribosomal protection proteins
title_fullStr Phenotypic and genetic barriers to establishment of horizontally transferred genes encoding ribosomal protection proteins
title_full_unstemmed Phenotypic and genetic barriers to establishment of horizontally transferred genes encoding ribosomal protection proteins
title_short Phenotypic and genetic barriers to establishment of horizontally transferred genes encoding ribosomal protection proteins
title_sort phenotypic and genetic barriers to establishment of horizontally transferred genes encoding ribosomal protection proteins
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8120329/
https://www.ncbi.nlm.nih.gov/pubmed/33655294
http://dx.doi.org/10.1093/jac/dkab056
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