PMID- 37732790 OWN - NLM STAT- Publisher LR - 20231020 IS - 2165-0497 (Electronic) IS - 2165-0497 (Linking) VI - 11 IP - 5 DP - 2023 Sep 21 TI - Lugdunin production and activity in Staphylococcus lugdunensis isolates are associated with its genotypes. PG - e0129823 LID - 10.1128/spectrum.01298-23 [doi] LID - e01298-23 AB - Lugdunin produced by Staphylococcus lugdunensis has been shown to have broad inhibitory activity against Gram-positive bacteria; however, lugdunin activity among S. lugdunensis isolates and its association with different agr, SCCmec, and sequence types remain unclear. We used matrix-assisted laser desorption ionization-time-of-flight mass spectrometry to identify S. lugdunensis and collected 202 S. lugdunensis samples for further assays. Agar spot tests were performed to characterize S. lugdunensis lugdunin production and activity. Multilocus sequence typing, SCCmec, and agr genotyping were performed on S. lugdunensis. In all, 91 Staphylococcus aureus strains with varying vancomycin susceptibilities were used to examine lugdunin activity in S. lugdunensis. In total, 48 S. lugdunensis strains (23.8%) were found to be oxacillin-resistant S. lugdunensis (ORSL), whereas 154 (76.2%) were classified as oxacillin-sensitive S. lugdunensis (OSSL). Moreover, 16 (33.3%) ORSL and 35 (22.7%) OSSL strains showed antibacterial activity against S. aureus. Our data showed that most lugdunin-producing ORSL strains (14/48, 29.2%) were of ST3-SCCmec V-agr II genotypes, whereas most lugdunin-producing OSSL strains (15/154, 9.7%) were of ST3-agr II, followed by ST1-agr I (10/154, 6.5%). Our data also revealed that lugdunin exhibited weak inhibitory activity against the VISA ST239 isolate. In addition, we observed that ST239 VSSA was more resistant to lugdunin than ST5, ST59, and ST45 VSSA. Taken together, our data pioneered the epidemiology of lugdunin production in S. lugdunensis isolates and revealed its association with genotypes. However, further molecular and bioinformatics investigations are needed to elucidate the regulatory mechanisms of lugdunin production and activity. IMPORTANCE Lugdunin is active against both methicillin-resistant Staphylococcus aureus and vancomycin-resistant enterococci by dissipating their membrane potential. However, the association of lugdunin activity with the genotypes of Staphylococcus lugdunensis has not been addressed. Here, we show the high prevalence of lugdunin-producing strains among ST1 (83.3%), ST2 (66.7%), and ST3 (53.3%) S. lugdunensis. Moreover, we identified the antibacterial activity of lugdunin-producing strains against VISA and hVISA. These results shed light on the potential application of lugdunin for the treatment of drug-resistant pathogens. FAU - Chang, Shih-Cheng AU - Chang SC AUID- ORCID: 0000-0001-5921-7974 AD - Department of Laboratory Medicine, Linkou Chang Gung Memorial Hospital , Taoyuan, Taiwan. AD - Department of Medical Biotechnology and Laboratory Science, College of Medicine, Chang Gung University , Taoyuan, Taiwan. FAU - Kao, Cheng-Yen AU - Kao CY AD - Institute of Microbiology and Immunology, College of Life Sciences, National Yang Ming Chiao Tung University , Taipei, Taiwan. FAU - Lin, Lee-Chung AU - Lin LC AD - Department of Laboratory Medicine, Linkou Chang Gung Memorial Hospital , Taoyuan, Taiwan. FAU - Hidrosollo, Jazon Harl AU - Hidrosollo JH AD - Institute of Microbiology and Immunology, College of Life Sciences, National Yang Ming Chiao Tung University , Taipei, Taiwan. FAU - Lu, Jang-Jih AU - Lu JJ AD - Department of Laboratory Medicine, Linkou Chang Gung Memorial Hospital , Taoyuan, Taiwan. AD - Department of Medical Biotechnology and Laboratory Science, College of Medicine, Chang Gung University , Taoyuan, Taiwan. AD - Department of Medicine, College of Medicine, Chang Gung University , Taoyuan, Taiwan. LA - eng PT - Journal Article DEP - 20230921 PL - United States TA - Microbiol Spectr JT - Microbiology spectrum JID - 101634614 SB - IM PMC - PMC10580833 OTO - NOTNLM OT - S. aureus OT - Staphylococcus lugdunensis OT - genotype OT - lugdunin COIS- The authors declare no conflict of interest. EDAT- 2023/09/21 12:42 MHDA- 2023/09/21 12:42 PMCR- 2023/09/21 CRDT- 2023/09/21 09:13 PHST- 2023/09/21 12:42 [medline] PHST- 2023/09/21 12:42 [pubmed] PHST- 2023/09/21 09:13 [entrez] PHST- 2023/09/21 00:00 [pmc-release] AID - 01298-23 [pii] AID - spectrum.01298-23 [pii] AID - 10.1128/spectrum.01298-23 [doi] PST - aheadofprint SO - Microbiol Spectr. 2023 Sep 21;11(5):e0129823. doi: 10.1128/spectrum.01298-23.