Discovery and characterization of genes conferring natural resistance to the antituberculosis antibiotic capreomycin

Metagenomic-based studies have predicted an extraordinary number of potential antibiotic-resistance genes (ARGs). These ARGs are hidden in various environmental bacteria and may become a latent crisis for antibiotic therapy via horizontal gene transfer. In this study, we focus on a resistance gene c...

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Veröffentlicht in:Communications biology 2023-12, Vol.6 (1), p.1282-1282, Article 1282
Hauptverfasser: Toh, Shu-Ing, Elaine Keisha, Johan, Wang, Yung-Lin, Pan, Yi-Chi, Jhu, Yu-Heng, Hsiao, Po-Yun, Liao, Wen-Ting, Chen, Po-Yuan, Ko, Tai-Ming, Chang, Chin-Yuan
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Sprache:eng
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Zusammenfassung:Metagenomic-based studies have predicted an extraordinary number of potential antibiotic-resistance genes (ARGs). These ARGs are hidden in various environmental bacteria and may become a latent crisis for antibiotic therapy via horizontal gene transfer. In this study, we focus on a resistance gene cph , which encodes a phosphotransferase (Cph) that confers resistance to the antituberculosis drug capreomycin (CMN). Sequence Similarity Network (SSN) analysis classified 353 Cph homologues into five major clusters, where the proteins in cluster I were found in a broad range of actinobacteria. We examine the function and antibiotics targeted by three putative resistance proteins in cluster I via biochemical and protein structural analysis. Our findings reveal that these three proteins in cluster I confer resistance to CMN, highlighting an important aspect of CMN resistance within this gene family. This study contributes towards understanding the sequence-structure-function relationships of the phosphorylation resistance genes that confer resistance to CMN. Environmental bacteria contain antibiotic-resistance genes, which worsens the antibiotic resistance crisis. This study helps understanding the sequence-structure-function relationships of the phosphotransferases that confer capreomycin resistance.
ISSN:2399-3642
2399-3642
DOI:10.1038/s42003-023-05681-6