Repeated Emergence of Variant TetR Family Regulator, FarR, and Increased Resistance to Antimicrobial Unsaturated Fatty Acid among Clonal Complex 5 Methicillin-Resistant Staphylococcus aureus.
Camryn M BonnIftekhar M RafiqullahJohn A CrawfordYi Meng QianJennifer L GuthrieMarta MatuszewskaD Ashley RobinsonMartin J McGavinPublished in: Antimicrobial agents and chemotherapy (2023)
Resistance-nodulation-division (RND) superfamily efflux pumps promote antibiotic resistance in Gram-negative pathogens, but their role in Gram-positive pathogens, including methicillin-resistant Staphylococcus aureus (MRSA) is undocumented. However, recent in vitro selections for resistance of S. aureus to an antimicrobial fatty acid, linoleic acid, and an antibiotic, rhodomyrtone, identified H121Y and C116R substitution variants, respectively, in a TetR family regulator, FarR, promoting increased expression of the RND pump FarE. Hypothesizing that in vivo selection pressures have also promoted the emergence of FarR variants, we searched available genome data and found that strains with FarR H121Y from human and bovine hosts have emerged sporadically in clonal complexes (CCs) CC1, CC30, CC8, CC22, and CC97, whereas multiple FarR variants have occurred within CC5 hospital-associated (HA)-MRSA. Of these, FarR E160G and FarR E93EE were exclusive to CC5, while FarR C116Y , FarR P165L , and FarR G166D also occurred in nonrelated CCs, primarily from bovine hosts. Within CC5, FarR C116Y and FarR G166D strains were polyphyletic, each exhibiting two emergence events. FarR C116Y and FarR E160G were individually sufficient to confer increased expression of FarE and enhanced resistance to linoleic acid (LA). Isolates with FarR E93EE were most closely related to S. aureus N315 MRSA and exhibited increased resistance independently of FarR E93EE . Accumulation of pseudogenes and additional polymorphisms in FarR E93EE strains contributed to a multiresistance phenotype which included fosfomycin and fusidic acid resistance in addition to increased linoleic acid resistance. These findings underscore the remarkable adaptive capacity of CC5 MRSA, which includes the polyphyletic USA100 lineage of HA-MRSA that is endemic in the Western hemisphere and known for the acquisition of multiple resistance phenotypes.