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http://hdl.handle.net/10553/119381
Title: | Subinhibitory antibiotic concentrations promote the horizontal transfer of plasmid-borne resistance genes from Klebsiellae pneumoniae to Escherichia coli | Authors: | Ding, Manlin Ye, Zi Liu, Lu Wang, Wei Chen, Qiao Zhang, Feiyang Wang, Ying Sjöling, Åsa Martín Rodríguez, Alberto Jonatan Hu, Renjing Chen, Wenbi Zhou, Yingshun |
UNESCO Clasification: | 32 Ciencias médicas 320103 Microbiología clínica |
Keywords: | Antibiotic sub-MIC Plasmid Conjugation frequency T4SS, et al |
Issue Date: | 2022 | Journal: | Frontiers in Microbiology | Abstract: | Horizontal gene transfer plays an important role in the spread of antibiotic resistance, in which plasmid-mediated conjugation transfer is the most important mechanism. While sub-minimal inhibitory concentrations (sub-MIC) of antibiotics could promote conjugation frequency, the mechanism by which sub-MIC levels of antibiotics affect conjugation frequency is not clear. Here, we used Klebsiella pneumoniae SW1780 carrying the multi-drug resistance plasmid pSW1780-KPC as the donor strain, to investigate the effects of sub-MICs of meropenem (MEM), ciprofloxacin (CIP), cefotaxime (CTX), and amikacin (AK) on conjugational transfer of pSW1780-KPC from SW1780 to Escherichia coli J53. Our results showed that the transfer frequencies increased significantly by treating SW1780 strain with sub-MIC levels of MEM, CIP, CTX and AK. Transfer frequencies at sub-MIC conditions in a Galleria mellonella were significantly higher than in vitro. To investigate gene expression and metabolic effects, RT-qPCR and LC–MS-based metabolome sequencing were performed. Transcript levels of T4SS genes virB1, virB2, virB4, virB8, and conjugation-related genes traB, traK, traE, and traL were significantly upregulated by exposure to sub-MICs of MEM, CIP, CTX, and AK. Metabolome sequencing revealed nine differentially regulated metabolites. Our findings are an early warning for a wide assessment of the roles of sub-MIC levels of antibiotics in the spread of antibiotic resistance. | URI: | http://hdl.handle.net/10553/119381 | ISSN: | 1664-302X | DOI: | 10.3389/fmicb.2022.1017092 | Source: | Frontiers in Microbiology [1664-302x], v. 13: 1017092 (Noviembre 2022) |
Appears in Collections: | Artículos |
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