Danieli Conte , Dany Mesa , Damaris Krul , Larissa Bail , Carmen Antônia Sanches Ito , Jussara Kasuko Palmeiro , Libera Maria Dalla-Costa
{"title":"巴西临床和环境来源中携带 blaGES 变体的 IncQ1 质粒的比较基因组学。","authors":"Danieli Conte , Dany Mesa , Damaris Krul , Larissa Bail , Carmen Antônia Sanches Ito , Jussara Kasuko Palmeiro , Libera Maria Dalla-Costa","doi":"10.1016/j.meegid.2024.105644","DOIUrl":null,"url":null,"abstract":"<div><p>IncQ-type plasmids have become important vectors in the dissemination of <em>bla</em><sub>GES</sub> among different bacterial genera and species from different environments around the world, and studies estimating the occurrence of Guiana extended-spectrum (GES)-type β-lactamases are gaining prominence. We analyzed the genetic aspects of two IncQ1 plasmids harboring different <em>bla</em><sub>GES</sub> variants from human and environmental sources. The <em>bla</em><sub>GES</sub> variants were identified using polymerase chain reaction (PCR) in <em>Aeromonas veronii</em> isolated from hospital effluent and <em>Klebsiella variicola</em> isolated from a rectal swab of a patient admitted to the cardiovascular intensive care unit in a different hospital. Antimicrobial-susceptibility testing and transformation experiments were performed for phenotypic analysis. Whole-genome sequencing was performed using Illumina and Oxford Nanopore platforms. The comparative analysis of plasmids was performed using BLASTn, and the IncQ1 plasmids showed a high identity and similar size. <em>A. veronii</em> harbored <em>bla</em><sub>GES-7</sub> in a class 1 integron (In2061), recently described by our group, and <em>K. variicola</em> carried <em>bla</em><sub>GES-5</sub> in the known class 1 integron. Both integrons showed a fused gene cassette that encodes resistance to aminoglycosides and fluoroquinolones, with an IS<em>6100</em> truncating the 3′-conserved segment. The fused genes are transcribed together, although the <em>attC</em> site is disrupted. These gene cassettes can no longer be mobilized. This study revealed a mobilome that may contribute to the dissemination of GES-type β-lactamases in Brazil. Class 1 integrons are hot spots for bacterial evolution, and their insertion into small IncQ-like plasmids displayed successful recombination, allowing the spread of <em>bla</em><sub>GES</sub> variants in various environments. Therefore, they can become prevalent across clinically relevant pathogens.</p></div>","PeriodicalId":54986,"journal":{"name":"Infection Genetics and Evolution","volume":"123 ","pages":"Article 105644"},"PeriodicalIF":2.6000,"publicationDate":"2024-07-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1567134824000959/pdfft?md5=13fd2c4522f11cb05edf810382fbf2d8&pid=1-s2.0-S1567134824000959-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Comparative genomics of IncQ1 plasmids carrying blaGES variants from clinical and environmental sources in Brazil\",\"authors\":\"Danieli Conte , Dany Mesa , Damaris Krul , Larissa Bail , Carmen Antônia Sanches Ito , Jussara Kasuko Palmeiro , Libera Maria Dalla-Costa\",\"doi\":\"10.1016/j.meegid.2024.105644\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>IncQ-type plasmids have become important vectors in the dissemination of <em>bla</em><sub>GES</sub> among different bacterial genera and species from different environments around the world, and studies estimating the occurrence of Guiana extended-spectrum (GES)-type β-lactamases are gaining prominence. We analyzed the genetic aspects of two IncQ1 plasmids harboring different <em>bla</em><sub>GES</sub> variants from human and environmental sources. The <em>bla</em><sub>GES</sub> variants were identified using polymerase chain reaction (PCR) in <em>Aeromonas veronii</em> isolated from hospital effluent and <em>Klebsiella variicola</em> isolated from a rectal swab of a patient admitted to the cardiovascular intensive care unit in a different hospital. Antimicrobial-susceptibility testing and transformation experiments were performed for phenotypic analysis. Whole-genome sequencing was performed using Illumina and Oxford Nanopore platforms. The comparative analysis of plasmids was performed using BLASTn, and the IncQ1 plasmids showed a high identity and similar size. <em>A. veronii</em> harbored <em>bla</em><sub>GES-7</sub> in a class 1 integron (In2061), recently described by our group, and <em>K. variicola</em> carried <em>bla</em><sub>GES-5</sub> in the known class 1 integron. Both integrons showed a fused gene cassette that encodes resistance to aminoglycosides and fluoroquinolones, with an IS<em>6100</em> truncating the 3′-conserved segment. The fused genes are transcribed together, although the <em>attC</em> site is disrupted. These gene cassettes can no longer be mobilized. This study revealed a mobilome that may contribute to the dissemination of GES-type β-lactamases in Brazil. Class 1 integrons are hot spots for bacterial evolution, and their insertion into small IncQ-like plasmids displayed successful recombination, allowing the spread of <em>bla</em><sub>GES</sub> variants in various environments. 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Comparative genomics of IncQ1 plasmids carrying blaGES variants from clinical and environmental sources in Brazil
IncQ-type plasmids have become important vectors in the dissemination of blaGES among different bacterial genera and species from different environments around the world, and studies estimating the occurrence of Guiana extended-spectrum (GES)-type β-lactamases are gaining prominence. We analyzed the genetic aspects of two IncQ1 plasmids harboring different blaGES variants from human and environmental sources. The blaGES variants were identified using polymerase chain reaction (PCR) in Aeromonas veronii isolated from hospital effluent and Klebsiella variicola isolated from a rectal swab of a patient admitted to the cardiovascular intensive care unit in a different hospital. Antimicrobial-susceptibility testing and transformation experiments were performed for phenotypic analysis. Whole-genome sequencing was performed using Illumina and Oxford Nanopore platforms. The comparative analysis of plasmids was performed using BLASTn, and the IncQ1 plasmids showed a high identity and similar size. A. veronii harbored blaGES-7 in a class 1 integron (In2061), recently described by our group, and K. variicola carried blaGES-5 in the known class 1 integron. Both integrons showed a fused gene cassette that encodes resistance to aminoglycosides and fluoroquinolones, with an IS6100 truncating the 3′-conserved segment. The fused genes are transcribed together, although the attC site is disrupted. These gene cassettes can no longer be mobilized. This study revealed a mobilome that may contribute to the dissemination of GES-type β-lactamases in Brazil. Class 1 integrons are hot spots for bacterial evolution, and their insertion into small IncQ-like plasmids displayed successful recombination, allowing the spread of blaGES variants in various environments. Therefore, they can become prevalent across clinically relevant pathogens.
期刊介绍:
(aka Journal of Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases -- MEEGID)
Infectious diseases constitute one of the main challenges to medical science in the coming century. The impressive development of molecular megatechnologies and of bioinformatics have greatly increased our knowledge of the evolution, transmission and pathogenicity of infectious diseases. Research has shown that host susceptibility to many infectious diseases has a genetic basis. Furthermore, much is now known on the molecular epidemiology, evolution and virulence of pathogenic agents, as well as their resistance to drugs, vaccines, and antibiotics. Equally, research on the genetics of disease vectors has greatly improved our understanding of their systematics, has increased our capacity to identify target populations for control or intervention, and has provided detailed information on the mechanisms of insecticide resistance.
However, the genetics and evolutionary biology of hosts, pathogens and vectors have tended to develop as three separate fields of research. This artificial compartmentalisation is of concern due to our growing appreciation of the strong co-evolutionary interactions among hosts, pathogens and vectors.
Infection, Genetics and Evolution and its companion congress [MEEGID](http://www.meegidconference.com/) (for Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases) are the main forum acting for the cross-fertilization between evolutionary science and biomedical research on infectious diseases.
Infection, Genetics and Evolution is the only journal that welcomes articles dealing with the genetics and evolutionary biology of hosts, pathogens and vectors, and coevolution processes among them in relation to infection and disease manifestation. All infectious models enter the scope of the journal, including pathogens of humans, animals and plants, either parasites, fungi, bacteria, viruses or prions. The journal welcomes articles dealing with genetics, population genetics, genomics, postgenomics, gene expression, evolutionary biology, population dynamics, mathematical modeling and bioinformatics. We also provide many author benefits, such as free PDFs, a liberal copyright policy, special discounts on Elsevier publications and much more. Please click here for more information on our author services .