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Large-Scale Analysis of Fitness Cost of tet(X4)-Positive Plasmids in Escherichia coli

Tigecycline is one of important antimicrobial agents for the treatment of infections caused by multidrug-resistant (MDR) Gram-negative bacteria. However, the emergence and prevalence of plasmid-mediated tigecycline resistance gene tet(X4) are threatening human and animal health. Fitness cost elicite...

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Autores principales: Tang, Feifei, Cai, Wenhui, Jiang, Lijie, Wang, Zhiqiang, Liu, Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9203853/
https://www.ncbi.nlm.nih.gov/pubmed/35719358
http://dx.doi.org/10.3389/fcimb.2022.798802
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author Tang, Feifei
Cai, Wenhui
Jiang, Lijie
Wang, Zhiqiang
Liu, Yuan
author_facet Tang, Feifei
Cai, Wenhui
Jiang, Lijie
Wang, Zhiqiang
Liu, Yuan
author_sort Tang, Feifei
collection PubMed
description Tigecycline is one of important antimicrobial agents for the treatment of infections caused by multidrug-resistant (MDR) Gram-negative bacteria. However, the emergence and prevalence of plasmid-mediated tigecycline resistance gene tet(X4) are threatening human and animal health. Fitness cost elicited by resistance plasmids is a key factor affecting the maintenance and transmission of antibiotic resistance genes (ARGs) in the host. A comparative analysis of the fitness cost of different types of tet(X4)-positive plasmids is helpful to understand and predict the prevalence of dominant plasmids. In this study, we performed a large-scale analysis of fitness cost of tet(X4)-positive plasmids origin from clinical isolates. These plasmids were successfully electroporated into a reference strain Escherichia coli TOP10, and a series of transformants carrying the tet(X) gene were obtained. The effects of tet(X4)-positive plasmids on the growth rate, plasmid stability, relative fitness, biofilm formation, and virulence in a Galleria mellonella model were evaluated. Consequently, we found that these plasmids resulted in varying degrees of fitness cost on TOP10, including delayed bacterial growth and attenuated virulence. Out of these plasmids, tet(X4)-harboring IncFII plasmids showed the lowest fitness cost on the host. Furthermore, by means of experimental evolution in the presence of commonly used drugs in clinic, the fitness cost of tet(X4)-positive plasmids was substantially alleviated, accompanied by increased plasmid stability. Collectively, our data reveal the differential fitness cost caused by different types of tet(X4)-positive plasmids and suggest that the wide use of tetracycline antibiotics may promote the evolution of plasmids.
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spelling pubmed-92038532022-06-18 Large-Scale Analysis of Fitness Cost of tet(X4)-Positive Plasmids in Escherichia coli Tang, Feifei Cai, Wenhui Jiang, Lijie Wang, Zhiqiang Liu, Yuan Front Cell Infect Microbiol Cellular and Infection Microbiology Tigecycline is one of important antimicrobial agents for the treatment of infections caused by multidrug-resistant (MDR) Gram-negative bacteria. However, the emergence and prevalence of plasmid-mediated tigecycline resistance gene tet(X4) are threatening human and animal health. Fitness cost elicited by resistance plasmids is a key factor affecting the maintenance and transmission of antibiotic resistance genes (ARGs) in the host. A comparative analysis of the fitness cost of different types of tet(X4)-positive plasmids is helpful to understand and predict the prevalence of dominant plasmids. In this study, we performed a large-scale analysis of fitness cost of tet(X4)-positive plasmids origin from clinical isolates. These plasmids were successfully electroporated into a reference strain Escherichia coli TOP10, and a series of transformants carrying the tet(X) gene were obtained. The effects of tet(X4)-positive plasmids on the growth rate, plasmid stability, relative fitness, biofilm formation, and virulence in a Galleria mellonella model were evaluated. Consequently, we found that these plasmids resulted in varying degrees of fitness cost on TOP10, including delayed bacterial growth and attenuated virulence. Out of these plasmids, tet(X4)-harboring IncFII plasmids showed the lowest fitness cost on the host. Furthermore, by means of experimental evolution in the presence of commonly used drugs in clinic, the fitness cost of tet(X4)-positive plasmids was substantially alleviated, accompanied by increased plasmid stability. Collectively, our data reveal the differential fitness cost caused by different types of tet(X4)-positive plasmids and suggest that the wide use of tetracycline antibiotics may promote the evolution of plasmids. Frontiers Media S.A. 2022-06-03 /pmc/articles/PMC9203853/ /pubmed/35719358 http://dx.doi.org/10.3389/fcimb.2022.798802 Text en Copyright © 2022 Tang, Cai, Jiang, Wang and Liu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Tang, Feifei
Cai, Wenhui
Jiang, Lijie
Wang, Zhiqiang
Liu, Yuan
Large-Scale Analysis of Fitness Cost of tet(X4)-Positive Plasmids in Escherichia coli
title Large-Scale Analysis of Fitness Cost of tet(X4)-Positive Plasmids in Escherichia coli
title_full Large-Scale Analysis of Fitness Cost of tet(X4)-Positive Plasmids in Escherichia coli
title_fullStr Large-Scale Analysis of Fitness Cost of tet(X4)-Positive Plasmids in Escherichia coli
title_full_unstemmed Large-Scale Analysis of Fitness Cost of tet(X4)-Positive Plasmids in Escherichia coli
title_short Large-Scale Analysis of Fitness Cost of tet(X4)-Positive Plasmids in Escherichia coli
title_sort large-scale analysis of fitness cost of tet(x4)-positive plasmids in escherichia coli
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9203853/
https://www.ncbi.nlm.nih.gov/pubmed/35719358
http://dx.doi.org/10.3389/fcimb.2022.798802
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