Macrolide resistance due to (55).

Barbara A Brown-Elliott, Richard J Wallace, Andrew D S Cameron, Omar M El-Halfawy, David C Alexander, Tayah Farquhar, Joshua M E Adams, Danae M Suchan, Sean D Workman

Journal: Microbiology spectrum 2025;13(3):e0239724

PMID: 39817789

Abstract

UNLABELLED

Antimicrobial resistance (AMR) is a global threat. The identification and characterization of novel resistance genes is integral to AMR surveillance. The (55) gene was originally identified through whole genome sequencing of macrolide-resistant strains of . The gene was annotated as a ribosomal methyltransferase, but its role as a determinant of macrolide resistance was not formally demonstrated. Three (55) alleles have now been documented. The plasmid-borne (55), the transposon-associated (55), and the chromosomal encoded (55) exhibit ≈82% amino acid sequence identity. Here, we confirm that, when expressed from plasmids in a macrolide-susceptible strain of , all three (55) variants confer resistance to azithromycin and clarithromycin.

IMPORTANCE

Macrolide antibiotics are often the only oral treatment option for infections with rapidly growing mycobacteria such as and . We previously identified three variants of a newly predicted macrolide resistance gene, (55), in , including the first case of a plasmid-mediated macrolide resistance in mycobacteria. The present study provides experimental evidence that the three (55) variants confer macrolide resistance and that each variant is unique in the degree to which it reduces susceptibility to clinically relevant macrolides.

Address: Department of Medical Microbiology and Infectious Diseases, Max Rady College of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.; Cadham Provincial Laboratory, Diagnostic Services, Shared Health, Winnipeg, Manitoba, Canada.; Institute for Microbial Systems and Society, Faculty of Science, University of Regina, Regina, Saskatchewan, Canada.; Department of Biology, Faculty of Science, University of Regina, Regina, Saskatchewan, Canada.; Department of Chemistry and Biochemistry, Faculty of Science, University of Regina, Regina, Saskatchewan, Canada.; Mycobacteria/Nocardia Laboratory, The University of Texas at Tyler Health Science Center, UT Tyler School of Medicine, Tyler, Texas, USA.; Department of Chemistry and Biochemistry, Faculty of Science, University of Regina, Regina, Saskatchewan, Canada.; Department of Microbiology and Immunology, Faculty of Pharmacy, Alexandria University, Alexandria, Egypt.
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