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The origin and evolution of IncF33 plasmids based on large-scale data sets

To comprehensively understand the formation and evolution of IncF33 plasmids, a global collection of whole-genome sequences of 863 strains positive for IncF33 plasmid replicons was analyzed. The results showed that the IncF33 plasmids were mainly identified in Enterobacterales, of which Escherichia...

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Autores principales: Gao, Guolong, He, Wanyun, Jiao, Yanxiang, Cai, Zhongpeng, Lv, Luchao, Liu, Jian-Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10654068/
https://www.ncbi.nlm.nih.gov/pubmed/37750716
http://dx.doi.org/10.1128/msystems.00508-23
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author Gao, Guolong
He, Wanyun
Jiao, Yanxiang
Cai, Zhongpeng
Lv, Luchao
Liu, Jian-Hua
author_facet Gao, Guolong
He, Wanyun
Jiao, Yanxiang
Cai, Zhongpeng
Lv, Luchao
Liu, Jian-Hua
author_sort Gao, Guolong
collection PubMed
description To comprehensively understand the formation and evolution of IncF33 plasmids, a global collection of whole-genome sequences of 863 strains positive for IncF33 plasmid replicons was analyzed. The results showed that the IncF33 plasmids were mainly identified in Enterobacterales, of which Escherichia coli (86.44%) was the dominant host, followed by Salmonella (8.57%) and Klebsiella pneumoniae (3.48%). Salmonella ST11 and K. pneumoniae ST11 were common and mostly from humans. IncF33 plasmids were found worldwide but prevalent in Chinese farm animals, predominantly carrying antibiotic resistance genes such as bla (CTX-M-55), fosA3, bla (TEM-1B), rmtB, and floR. Comparative genomics analysis of 103 complete IncF33 plasmid sequences showed highly similar backbones except for 16 lacking partial backbone fragments. Variable regions were diverse, containing various antibiotic resistance genes, insertion sequences, or other plasmid fragments. They can be roughly divided into two sublines based on the production of different CTX-M enzymes. Similar IncF33 plasmids from different countries were identified. Some early IncF33 plasmids lacked part of their leader regions, which showed over 99% homology with early F2:A-:B- plasmids, indicating that leader regions of IncF33 likely came from F2:A-:B- plasmids. In addition, IncF33 plasmids cointegrating with other types of plasmids to form new cointegrate plasmids are increasing, making them more efficient in their dissemination and persistence in Enterobacterales, which could pose a significant threat to global public health. IMPORTANCE: Plasmids that capture multiple antibiotic resistance genes are spreading widely, leading to the emergence and prevalence of multidrug-resistant bacteria. IncF33 plasmids are a newly emerged plasmid type highly prevalent in animal-source Enterobacterales in China, and they are important vectors for transmitting several clinically important antibiotic resistance genes. The study revealed that the IncF33 plasmid is mainly prevalent in China animal-derived Escherichia coli and has the potential for cointegration and intercontinental dissemination. Therefore, it is crucial to enhance surveillance and control measures to limit the spread of IncF33 plasmids and their associated antibiotic resistance genes.
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spelling pubmed-106540682023-09-26 The origin and evolution of IncF33 plasmids based on large-scale data sets Gao, Guolong He, Wanyun Jiao, Yanxiang Cai, Zhongpeng Lv, Luchao Liu, Jian-Hua mSystems Research Article To comprehensively understand the formation and evolution of IncF33 plasmids, a global collection of whole-genome sequences of 863 strains positive for IncF33 plasmid replicons was analyzed. The results showed that the IncF33 plasmids were mainly identified in Enterobacterales, of which Escherichia coli (86.44%) was the dominant host, followed by Salmonella (8.57%) and Klebsiella pneumoniae (3.48%). Salmonella ST11 and K. pneumoniae ST11 were common and mostly from humans. IncF33 plasmids were found worldwide but prevalent in Chinese farm animals, predominantly carrying antibiotic resistance genes such as bla (CTX-M-55), fosA3, bla (TEM-1B), rmtB, and floR. Comparative genomics analysis of 103 complete IncF33 plasmid sequences showed highly similar backbones except for 16 lacking partial backbone fragments. Variable regions were diverse, containing various antibiotic resistance genes, insertion sequences, or other plasmid fragments. They can be roughly divided into two sublines based on the production of different CTX-M enzymes. Similar IncF33 plasmids from different countries were identified. Some early IncF33 plasmids lacked part of their leader regions, which showed over 99% homology with early F2:A-:B- plasmids, indicating that leader regions of IncF33 likely came from F2:A-:B- plasmids. In addition, IncF33 plasmids cointegrating with other types of plasmids to form new cointegrate plasmids are increasing, making them more efficient in their dissemination and persistence in Enterobacterales, which could pose a significant threat to global public health. IMPORTANCE: Plasmids that capture multiple antibiotic resistance genes are spreading widely, leading to the emergence and prevalence of multidrug-resistant bacteria. IncF33 plasmids are a newly emerged plasmid type highly prevalent in animal-source Enterobacterales in China, and they are important vectors for transmitting several clinically important antibiotic resistance genes. The study revealed that the IncF33 plasmid is mainly prevalent in China animal-derived Escherichia coli and has the potential for cointegration and intercontinental dissemination. Therefore, it is crucial to enhance surveillance and control measures to limit the spread of IncF33 plasmids and their associated antibiotic resistance genes. American Society for Microbiology 2023-09-26 /pmc/articles/PMC10654068/ /pubmed/37750716 http://dx.doi.org/10.1128/msystems.00508-23 Text en Copyright © 2023 Gao et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Gao, Guolong
He, Wanyun
Jiao, Yanxiang
Cai, Zhongpeng
Lv, Luchao
Liu, Jian-Hua
The origin and evolution of IncF33 plasmids based on large-scale data sets
title The origin and evolution of IncF33 plasmids based on large-scale data sets
title_full The origin and evolution of IncF33 plasmids based on large-scale data sets
title_fullStr The origin and evolution of IncF33 plasmids based on large-scale data sets
title_full_unstemmed The origin and evolution of IncF33 plasmids based on large-scale data sets
title_short The origin and evolution of IncF33 plasmids based on large-scale data sets
title_sort origin and evolution of incf33 plasmids based on large-scale data sets
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10654068/
https://www.ncbi.nlm.nih.gov/pubmed/37750716
http://dx.doi.org/10.1128/msystems.00508-23
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