Cargando…

Role of pleiotropy during adaptation of TEM-1 β-lactamase to two novel antibiotics

Pleiotropy is a key feature of the genotype–phenotype map, and its form and extent have many evolutionary implications, including for the dynamics of adaptation and the evolution of specialization. Similarly, pleiotropic effects of antibiotic resistance mutations may affect the evolution of antibiot...

Descripción completa

Detalles Bibliográficos
Autores principales: Schenk, Martijn F, Witte, Sariette, Salverda, Merijn L M, Koopmanschap, Bertha, Krug, Joachim, de Visser, J Arjan G M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4380919/
https://www.ncbi.nlm.nih.gov/pubmed/25861383
http://dx.doi.org/10.1111/eva.12200
_version_ 1782364366091321344
author Schenk, Martijn F
Witte, Sariette
Salverda, Merijn L M
Koopmanschap, Bertha
Krug, Joachim
de Visser, J Arjan G M
author_facet Schenk, Martijn F
Witte, Sariette
Salverda, Merijn L M
Koopmanschap, Bertha
Krug, Joachim
de Visser, J Arjan G M
author_sort Schenk, Martijn F
collection PubMed
description Pleiotropy is a key feature of the genotype–phenotype map, and its form and extent have many evolutionary implications, including for the dynamics of adaptation and the evolution of specialization. Similarly, pleiotropic effects of antibiotic resistance mutations may affect the evolution of antibiotic resistance in the simultaneous or fluctuating presence of different antibiotics. Here, we study the role of pleiotropy during the in vitro adaptation of the enzyme TEM-1 β-lactamase to two novel antibiotics, cefotaxime (CTX) and ceftazidime (CAZ). We subject replicate lines for four rounds of evolution to selection with CTX and CAZ alone, and in their combined and fluctuating presence. Evolved alleles show positive correlated responses when selecting with single antibiotics. Nevertheless, pleiotropic constraints are apparent from the effects of single mutations and from selected alleles showing smaller correlated than direct responses and smaller responses after simultaneous and fluctuating selection with both than with single antibiotics. We speculate that these constraints result from structural changes in the oxyanion pocket surrounding the active site, where accommodation of CTX and the larger CAZ is balanced against their positioning with respect to the active site. Our findings suggest limited benefits from the combined or fluctuating application of these related cephalosporins for containing antibiotic resistance.
format Online
Article
Text
id pubmed-4380919
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Blackwell Publishing Ltd
record_format MEDLINE/PubMed
spelling pubmed-43809192015-04-08 Role of pleiotropy during adaptation of TEM-1 β-lactamase to two novel antibiotics Schenk, Martijn F Witte, Sariette Salverda, Merijn L M Koopmanschap, Bertha Krug, Joachim de Visser, J Arjan G M Evol Appl Original Articles Pleiotropy is a key feature of the genotype–phenotype map, and its form and extent have many evolutionary implications, including for the dynamics of adaptation and the evolution of specialization. Similarly, pleiotropic effects of antibiotic resistance mutations may affect the evolution of antibiotic resistance in the simultaneous or fluctuating presence of different antibiotics. Here, we study the role of pleiotropy during the in vitro adaptation of the enzyme TEM-1 β-lactamase to two novel antibiotics, cefotaxime (CTX) and ceftazidime (CAZ). We subject replicate lines for four rounds of evolution to selection with CTX and CAZ alone, and in their combined and fluctuating presence. Evolved alleles show positive correlated responses when selecting with single antibiotics. Nevertheless, pleiotropic constraints are apparent from the effects of single mutations and from selected alleles showing smaller correlated than direct responses and smaller responses after simultaneous and fluctuating selection with both than with single antibiotics. We speculate that these constraints result from structural changes in the oxyanion pocket surrounding the active site, where accommodation of CTX and the larger CAZ is balanced against their positioning with respect to the active site. Our findings suggest limited benefits from the combined or fluctuating application of these related cephalosporins for containing antibiotic resistance. Blackwell Publishing Ltd 2015-03 2014-09-18 /pmc/articles/PMC4380919/ /pubmed/25861383 http://dx.doi.org/10.1111/eva.12200 Text en © 2015 John Wiley & Sons Ltd http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Schenk, Martijn F
Witte, Sariette
Salverda, Merijn L M
Koopmanschap, Bertha
Krug, Joachim
de Visser, J Arjan G M
Role of pleiotropy during adaptation of TEM-1 β-lactamase to two novel antibiotics
title Role of pleiotropy during adaptation of TEM-1 β-lactamase to two novel antibiotics
title_full Role of pleiotropy during adaptation of TEM-1 β-lactamase to two novel antibiotics
title_fullStr Role of pleiotropy during adaptation of TEM-1 β-lactamase to two novel antibiotics
title_full_unstemmed Role of pleiotropy during adaptation of TEM-1 β-lactamase to two novel antibiotics
title_short Role of pleiotropy during adaptation of TEM-1 β-lactamase to two novel antibiotics
title_sort role of pleiotropy during adaptation of tem-1 β-lactamase to two novel antibiotics
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4380919/
https://www.ncbi.nlm.nih.gov/pubmed/25861383
http://dx.doi.org/10.1111/eva.12200
work_keys_str_mv AT schenkmartijnf roleofpleiotropyduringadaptationoftem1blactamasetotwonovelantibiotics
AT wittesariette roleofpleiotropyduringadaptationoftem1blactamasetotwonovelantibiotics
AT salverdamerijnlm roleofpleiotropyduringadaptationoftem1blactamasetotwonovelantibiotics
AT koopmanschapbertha roleofpleiotropyduringadaptationoftem1blactamasetotwonovelantibiotics
AT krugjoachim roleofpleiotropyduringadaptationoftem1blactamasetotwonovelantibiotics
AT devisserjarjangm roleofpleiotropyduringadaptationoftem1blactamasetotwonovelantibiotics