ABC-F Proteins Mediate Antibiotic Resistance through Ribosomal Protection

Members of the ABC-F subfamily of ATP-binding cassette proteins mediate resistance to a broad array of clinically important antibiotic classes that target the ribosome of Gram-positive pathogens. The mechanism by which these proteins act has been a subject of long-standing controversy, with two comp...

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Main Authors: Liam K. R. Sharkey, Thomas A. Edwards, Alex J. O’Neill
Format: Article
Language:English
Published: American Society for Microbiology 2016-03-01
Series:mBio
Online Access:http://mbio.asm.org/cgi/content/full/7/2/e01975-15
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spelling doaj-a840a79eeb034b45acd63679031d7a092021-07-02T04:24:23ZengAmerican Society for MicrobiologymBio2150-75112016-03-0172e01975-1510.1128/mBio.01975-15ABC-F Proteins Mediate Antibiotic Resistance through Ribosomal ProtectionLiam K. R. SharkeyThomas A. EdwardsAlex J. O’NeillMembers of the ABC-F subfamily of ATP-binding cassette proteins mediate resistance to a broad array of clinically important antibiotic classes that target the ribosome of Gram-positive pathogens. The mechanism by which these proteins act has been a subject of long-standing controversy, with two competing hypotheses each having gained considerable support: antibiotic efflux versus ribosomal protection. Here, we report on studies employing a combination of bacteriological and biochemical techniques to unravel the mechanism of resistance of these proteins, and provide several lines of evidence that together offer clear support to the ribosomal protection hypothesis. Of particular note, we show that addition of purified ABC-F proteins to an in vitro translation assay prompts dose-dependent rescue of translation, and demonstrate that such proteins are capable of displacing antibiotic from the ribosome in vitro. To our knowledge, these experiments constitute the first direct evidence that ABC-F proteins mediate antibiotic resistance through ribosomal protection.http://mbio.asm.org/cgi/content/full/7/2/e01975-15
collection DOAJ
language English
format Article
sources DOAJ
author Liam K. R. Sharkey
Thomas A. Edwards
Alex J. O’Neill
spellingShingle Liam K. R. Sharkey
Thomas A. Edwards
Alex J. O’Neill
ABC-F Proteins Mediate Antibiotic Resistance through Ribosomal Protection
mBio
author_facet Liam K. R. Sharkey
Thomas A. Edwards
Alex J. O’Neill
author_sort Liam K. R. Sharkey
title ABC-F Proteins Mediate Antibiotic Resistance through Ribosomal Protection
title_short ABC-F Proteins Mediate Antibiotic Resistance through Ribosomal Protection
title_full ABC-F Proteins Mediate Antibiotic Resistance through Ribosomal Protection
title_fullStr ABC-F Proteins Mediate Antibiotic Resistance through Ribosomal Protection
title_full_unstemmed ABC-F Proteins Mediate Antibiotic Resistance through Ribosomal Protection
title_sort abc-f proteins mediate antibiotic resistance through ribosomal protection
publisher American Society for Microbiology
series mBio
issn 2150-7511
publishDate 2016-03-01
description Members of the ABC-F subfamily of ATP-binding cassette proteins mediate resistance to a broad array of clinically important antibiotic classes that target the ribosome of Gram-positive pathogens. The mechanism by which these proteins act has been a subject of long-standing controversy, with two competing hypotheses each having gained considerable support: antibiotic efflux versus ribosomal protection. Here, we report on studies employing a combination of bacteriological and biochemical techniques to unravel the mechanism of resistance of these proteins, and provide several lines of evidence that together offer clear support to the ribosomal protection hypothesis. Of particular note, we show that addition of purified ABC-F proteins to an in vitro translation assay prompts dose-dependent rescue of translation, and demonstrate that such proteins are capable of displacing antibiotic from the ribosome in vitro. To our knowledge, these experiments constitute the first direct evidence that ABC-F proteins mediate antibiotic resistance through ribosomal protection.
url http://mbio.asm.org/cgi/content/full/7/2/e01975-15
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