Multidrug Resistance (MDR) and Collateral Sensitivity in Bacteria, with Special Attention to Genetic and Evolutionary Aspects and to the Perspectives of Antimicrobial Peptides—A Review

Antibiotic poly-resistance (multidrug-, extreme-, and pan-drug resistance) is controlled by adaptive evolution. Darwinian and Lamarckian interpretations of resistance evolution are discussed. Arguments for, and against, pessimistic forecasts on a fatal “post-antibiotic era” are evaluated. In commens...

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Main Authors: András Fodor, Birhan Addisie Abate, Péter Deák, László Fodor, Ervin Gyenge, Michael G. Klein, Zsuzsanna Koncz, Josephat Muvevi, László Ötvös, Gyöngyi Székely, Dávid Vozik, László Makrai
Format: Article
Language:English
Published: MDPI AG 2020-06-01
Series:Pathogens
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Online Access:https://www.mdpi.com/2076-0817/9/7/522
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author András Fodor
Birhan Addisie Abate
Péter Deák
László Fodor
Ervin Gyenge
Michael G. Klein
Zsuzsanna Koncz
Josephat Muvevi
László Ötvös
Gyöngyi Székely
Dávid Vozik
László Makrai
author_facet András Fodor
Birhan Addisie Abate
Péter Deák
László Fodor
Ervin Gyenge
Michael G. Klein
Zsuzsanna Koncz
Josephat Muvevi
László Ötvös
Gyöngyi Székely
Dávid Vozik
László Makrai
author_sort András Fodor
collection DOAJ
description Antibiotic poly-resistance (multidrug-, extreme-, and pan-drug resistance) is controlled by adaptive evolution. Darwinian and Lamarckian interpretations of resistance evolution are discussed. Arguments for, and against, pessimistic forecasts on a fatal “post-antibiotic era” are evaluated. In commensal niches, the appearance of a new antibiotic resistance often reduces fitness, but compensatory mutations may counteract this tendency. The appearance of new antibiotic resistance is frequently accompanied by a collateral sensitivity to other resistances. Organisms with an expanding open pan-genome, such as <i>Acinetobacter baumannii, Pseudomonas aeruginosa</i>, and <i>Klebsiella pneumoniae</i>, can withstand an increased number of resistances by exploiting their evolutionary plasticity and disseminating clonally or poly-clonally. Multidrug-resistant pathogen clones can become predominant under antibiotic stress conditions but, under the influence of negative frequency-dependent selection, are prevented from rising to dominance in a population in a commensal niche. Antimicrobial peptides have a great potential to combat multidrug resistance, since antibiotic-resistant bacteria have shown a high frequency of collateral sensitivity to antimicrobial peptides. In addition, the mobility patterns of antibiotic resistance, and antimicrobial peptide resistance, genes are completely different. The integron trade in commensal niches is fortunately limited by the species-specificity of resistance genes. Hence, we theorize that the suggested post-antibiotic era has not yet come, and indeed might never come.
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spelling doaj.art-6e1421dd69f94a678073310d05df321f2023-11-20T05:16:21ZengMDPI AGPathogens2076-08172020-06-019752210.3390/pathogens9070522Multidrug Resistance (MDR) and Collateral Sensitivity in Bacteria, with Special Attention to Genetic and Evolutionary Aspects and to the Perspectives of Antimicrobial Peptides—A ReviewAndrás Fodor0Birhan Addisie Abate1Péter Deák2László Fodor3Ervin Gyenge4Michael G. Klein5Zsuzsanna Koncz6Josephat Muvevi7László Ötvös8Gyöngyi Székely9Dávid Vozik10László Makrai11Department of Genetics, University of Szeged, H-6726 Szeged, HungaryEthiopian Biotechnology Institute, Agricultural Biotechnology Directorate, Addis Ababa 5954, EthiopiaDepartment of Genetics, University of Szeged, H-6726 Szeged, HungaryDepartment of Microbiology and Infectious Diseases, University of Veterinary Medicine, P.O. Box 22, H-1581 Budapest, HungaryHungarian Department of Biology and Ecology, Faculty of Biology and Geology, Babeș-Bolyai University, 5-7 Clinicilor St., 400006 Cluj-Napoca, RomaniaDepartment of Entomology, The Ohio State University, 1680 Madison Ave., Wooster, OH 44691, USAMax-Planck Institut für Pflanzenzüchtungsforschung, Carl-von-Linné-Weg 10, D-50829 Köln, GermanyNational Cereals and Produce Board, Mombasa 80100, KenyaOLPE, LLC, Audubon, PA 19403-1965, USAHungarian Department of Biology and Ecology, Faculty of Biology and Geology, Babeș-Bolyai University, 5-7 Clinicilor St., 400006 Cluj-Napoca, RomaniaResearch Institute on Bioengineering, Membrane Technology and Energetics, Faculty of Engineering, University of Veszprem, H-8200 Veszprém, HungaryDepartment of Microbiology and Infectious Diseases, University of Veterinary Medicine, P.O. Box 22, H-1581 Budapest, HungaryAntibiotic poly-resistance (multidrug-, extreme-, and pan-drug resistance) is controlled by adaptive evolution. Darwinian and Lamarckian interpretations of resistance evolution are discussed. Arguments for, and against, pessimistic forecasts on a fatal “post-antibiotic era” are evaluated. In commensal niches, the appearance of a new antibiotic resistance often reduces fitness, but compensatory mutations may counteract this tendency. The appearance of new antibiotic resistance is frequently accompanied by a collateral sensitivity to other resistances. Organisms with an expanding open pan-genome, such as <i>Acinetobacter baumannii, Pseudomonas aeruginosa</i>, and <i>Klebsiella pneumoniae</i>, can withstand an increased number of resistances by exploiting their evolutionary plasticity and disseminating clonally or poly-clonally. Multidrug-resistant pathogen clones can become predominant under antibiotic stress conditions but, under the influence of negative frequency-dependent selection, are prevented from rising to dominance in a population in a commensal niche. Antimicrobial peptides have a great potential to combat multidrug resistance, since antibiotic-resistant bacteria have shown a high frequency of collateral sensitivity to antimicrobial peptides. In addition, the mobility patterns of antibiotic resistance, and antimicrobial peptide resistance, genes are completely different. The integron trade in commensal niches is fortunately limited by the species-specificity of resistance genes. Hence, we theorize that the suggested post-antibiotic era has not yet come, and indeed might never come.https://www.mdpi.com/2076-0817/9/7/522MDRintrinsic/acquired resistancecollateral sensitivitynegative frequency-dependent selectionexperimental evolutionpangenome
spellingShingle András Fodor
Birhan Addisie Abate
Péter Deák
László Fodor
Ervin Gyenge
Michael G. Klein
Zsuzsanna Koncz
Josephat Muvevi
László Ötvös
Gyöngyi Székely
Dávid Vozik
László Makrai
Multidrug Resistance (MDR) and Collateral Sensitivity in Bacteria, with Special Attention to Genetic and Evolutionary Aspects and to the Perspectives of Antimicrobial Peptides—A Review
Pathogens
MDR
intrinsic/acquired resistance
collateral sensitivity
negative frequency-dependent selection
experimental evolution
pangenome
title Multidrug Resistance (MDR) and Collateral Sensitivity in Bacteria, with Special Attention to Genetic and Evolutionary Aspects and to the Perspectives of Antimicrobial Peptides—A Review
title_full Multidrug Resistance (MDR) and Collateral Sensitivity in Bacteria, with Special Attention to Genetic and Evolutionary Aspects and to the Perspectives of Antimicrobial Peptides—A Review
title_fullStr Multidrug Resistance (MDR) and Collateral Sensitivity in Bacteria, with Special Attention to Genetic and Evolutionary Aspects and to the Perspectives of Antimicrobial Peptides—A Review
title_full_unstemmed Multidrug Resistance (MDR) and Collateral Sensitivity in Bacteria, with Special Attention to Genetic and Evolutionary Aspects and to the Perspectives of Antimicrobial Peptides—A Review
title_short Multidrug Resistance (MDR) and Collateral Sensitivity in Bacteria, with Special Attention to Genetic and Evolutionary Aspects and to the Perspectives of Antimicrobial Peptides—A Review
title_sort multidrug resistance mdr and collateral sensitivity in bacteria with special attention to genetic and evolutionary aspects and to the perspectives of antimicrobial peptides a review
topic MDR
intrinsic/acquired resistance
collateral sensitivity
negative frequency-dependent selection
experimental evolution
pangenome
url https://www.mdpi.com/2076-0817/9/7/522
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