Your browser doesn't support javascript.
loading
Comparative genomics of IncQ1 plasmids carrying blaGES variants from clinical and environmental sources in Brazil.
Conte, Danieli; Mesa, Dany; Krul, Damaris; Bail, Larissa; Ito, Carmen Antônia Sanches; Palmeiro, Jussara Kasuko; Dalla-Costa, Libera Maria.
Affiliation
  • Conte D; Faculdades Pequeno Príncipe, Curitiba, Paraná, Brazil; Instituto de Pesquisa Pelé Pequeno Príncipe, Curitiba, Paraná, Brazil. Electronic address: conte.danieli@gmail.com.
  • Mesa D; Faculdades Pequeno Príncipe, Curitiba, Paraná, Brazil; Instituto de Pesquisa Pelé Pequeno Príncipe, Curitiba, Paraná, Brazil.
  • Krul D; Faculdades Pequeno Príncipe, Curitiba, Paraná, Brazil; Instituto de Pesquisa Pelé Pequeno Príncipe, Curitiba, Paraná, Brazil.
  • Bail L; Universidade Estadual de Ponta Grossa, Ponta Grossa, Paraná, Brazil.
  • Ito CAS; Universidade Estadual de Ponta Grossa, Ponta Grossa, Paraná, Brazil.
  • Palmeiro JK; Departamento de Análises Clínicas, Universidade Federal de Santa Catarina, Florianópolis, Santa Catarina, Brazil; Laboratório de Microbiologia Molecular Aplicada, Universidade Federal de Santa Catarina, Florianópolis, Santa Catarina, Brazil.
  • Dalla-Costa LM; Faculdades Pequeno Príncipe, Curitiba, Paraná, Brazil; Instituto de Pesquisa Pelé Pequeno Príncipe, Curitiba, Paraná, Brazil.
Infect Genet Evol ; 123: 105644, 2024 Sep.
Article in En | MEDLINE | ID: mdl-39038632
ABSTRACT
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 ß-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 ß-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.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Plasmids / Beta-Lactamases Limits: Humans Country/Region as subject: America do sul / Brasil Language: En Journal: Infect Genet Evol / Infect. gent. evol / Infection, genetics and evolution Journal subject: BIOLOGIA / DOENCAS TRANSMISSIVEIS / GENETICA Year: 2024 Document type: Article Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Plasmids / Beta-Lactamases Limits: Humans Country/Region as subject: America do sul / Brasil Language: En Journal: Infect Genet Evol / Infect. gent. evol / Infection, genetics and evolution Journal subject: BIOLOGIA / DOENCAS TRANSMISSIVEIS / GENETICA Year: 2024 Document type: Article Country of publication: Netherlands