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Conjugative RP4 Plasmid-Mediated Transfer of Antibiotic Resistance Genes to Commensal and Multidrug-Resistant Enteric Bacteria In Vitro.
Sher, Azam A; VanAllen, Mia E; Ahmed, Husnain; Whitehead-Tillery, Charles; Rafique, Sonia; Bell, Julia A; Zhang, Lixin; Mansfield, Linda S.
Afiliação
  • Sher AA; Comparative Enteric Diseases Laboratory, East Lansing, MI 48824, USA.
  • VanAllen ME; Comparative Medicine and Integrative Biology Graduate Program, College of Veterinary Medicine, Michigan State University, East Lansing, MI 48824, USA.
  • Ahmed H; BEACON Center for the Study of Evolution in Action, Michigan State University, East Lansing, MI 48824, USA.
  • Whitehead-Tillery C; Comparative Enteric Diseases Laboratory, East Lansing, MI 48824, USA.
  • Rafique S; BEACON Center for the Study of Evolution in Action, Michigan State University, East Lansing, MI 48824, USA.
  • Bell JA; Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI 48824, USA.
  • Zhang L; Comparative Enteric Diseases Laboratory, East Lansing, MI 48824, USA.
  • Mansfield LS; Comparative Medicine and Integrative Biology Graduate Program, College of Veterinary Medicine, Michigan State University, East Lansing, MI 48824, USA.
Microorganisms ; 11(1)2023 Jan 12.
Article em En | MEDLINE | ID: mdl-36677486
Many antibiotic-resistant bacteria carry resistance genes on conjugative plasmids that are transferable to commensals and pathogens. We determined the ability of multiple enteric bacteria to acquire and retransfer a broad-host-range plasmid RP4. We used human-derived commensal Escherichia coli LM715-1 carrying a chromosomal red fluorescent protein gene and green fluorescent protein (GFP)-labeled broad-host-range RP4 plasmid with ampR, tetR, and kanR in in vitro matings to rifampicin-resistant recipients, including Escherichia coli MG1655, Dec5α, Vibrio cholerae, Pseudomonas putida, Pseudomonas aeruginosa, Klebsiella pneumoniae, Citrobacter rodentium, and Salmonella Typhimurium. Transconjugants were quantified on selective media and confirmed using fluorescence microscopy and PCR for the GFP gene. The plasmid was transferred from E. coli LM715-1 to all tested recipients except P. aeruginosa. Transfer frequencies differed between specific donor-recipient pairings (10-2 to 10-8). Secondary retransfer of plasmid from transconjugants to E. coli LM715-1 occurred at frequencies from 10-2 to 10-7. A serial passage plasmid persistence assay showed plasmid loss over time in the absence of antibiotics, indicating that the plasmid imposed a fitness cost to its host, although some plasmid-bearing cells persisted for at least ten transfers. Thus, the RP4 plasmid can transfer to multiple clinically relevant bacterial species without antibiotic selection pressure.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article