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Characterization of bla(AFM-1)-positive carbapenem-resistant strains isolated in Guangzhou, China

BACKGROUND: Carbapenemase-producing makes a great contribution to carbapenem resistance in Gram-negative bacilli. Bla(AFM-1) gene was first discovered by us in Alcaligenes faecalis AN70 strain isolated in Guangzhou of China and, was submitted to NCBI on 16 November 2018. METHODS: Antimicrobial susce...

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Detalles Bibliográficos
Autores principales: Qin, Yingcheng, Peng, Yuan, Duan, Xiaonv, Song, Zhenli, Huang, Rong, Rui, Yongyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10189940/
https://www.ncbi.nlm.nih.gov/pubmed/37198688
http://dx.doi.org/10.1186/s12941-023-00592-0
Descripción
Sumario:BACKGROUND: Carbapenemase-producing makes a great contribution to carbapenem resistance in Gram-negative bacilli. Bla(AFM-1) gene was first discovered by us in Alcaligenes faecalis AN70 strain isolated in Guangzhou of China and, was submitted to NCBI on 16 November 2018. METHODS: Antimicrobial susceptibility testing was performed by broth microdilution assay using BD Phoenix 100. The phylogenetic tree of AFM and other B1 metallo-β-lactamases was visualized by MEGA7.0. Whole-genome sequencing technology was used to sequence carbapenem-resistant strains including the bla(AFM-1) gene. Cloning and expressing of bla(AFM-1) were designed to verify the function of AFM-1 to hydrolyze carbapenems and common β-lactamase substrates. Carba NP and Etest experiments were conducted to evaluate the activity of carbapenemase. Homology modeling was applied to predict the spatial structure of AFM-1. A conjugation assay was performed to test the ability of horizontal transfer of AFM-1 enzyme. The genetic context of bla(AFM-1) was performed by Blast alignment. RESULTS: Alcaligenes faecalis strain AN70, Comamonas testosteroni strain NFYY023, Bordetella trematum strain E202, and Stenotrophomonas maltophilia strain NCTC10498 were identified as carrying the bla(AFM-1) gene. All of these four strains were carbapenem-resistant strains. Phylogenetic analysis revealed that AFM-1 shares little nucleotide and amino acid identity with other class B carbapenemases (the highest identity (86%) with NDM-1 at the amino acid sequence level). The spatial structure of the AFM-1 enzyme was predicted to be αβ/βα sandwich structure, with two zinc atoms at its active site structure. Cloning and expressing of bla(AFM-1) verified AFM-1 could hydrolyze carbapenems and common β-lactamase substrates. Carba NP test presented that the AFM-1 enzyme possesses carbapenemase activity. The successful transfer of pAN70-1(plasmid of AN70) to E.coli J53 suggested that the bla(AFM-1) gene could be disseminated by the plasmid. The genetic context of bla(AFM) indicated that the downstream of the bla(AFM) gene was always adjacent to trpF and ble(MBL). Comparative genome analysis revealed that bla(AFM) appeared to have been mobilized by an ISCR27-related mediated event. CONCLUSIONS: The bla(AFM-1) gene is derived from chromosome and plasmid, and the bla(AFM-1) gene derived from the pAN70-1 plasmid can transfer carbapenem resistance to susceptible strains through horizontal transfer. Several bla(AFM-1)-positive species have been isolated from feces in Guangzhou, China. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12941-023-00592-0.