A total of 40 A. butzleri strains (see Table S1 in the Supplemental Material) were included in this study. All strains were collected and identified at the species level using molecular methods (multiplex polymerase chain reaction [PCR] and rpoB sequencing) during a previous Arcobacter prevalence study in Kaunas, Lithuania [20 (link)]. All 40 strains were also previously tested for susceptibility to six antimicrobial agents (ampicillin, ciprofloxacin, gentamicin, tetracycline, azithromycin, and erythromycin) using the gradient strip diffusion method [20 (link)]. Half of A. butzleri strains were isolated from different food products obtained from local retail markets: raw cow milk (n = 11), chicken meat (n = 7) and ready-to-eat (RTE) salad mixes (n = 2). The remaining strains originated from human stool (n = 10) and environmental water samples (n = 10, including lake and river-water samples). All 40 strains were stored at −80 °C in a brain–heart infusion broth (BHI) (Oxoid, Thermo Fisher Scientific, Basingstoke, UK) containing 30% (v/v) glycerol (Stanlab, Lublin, Poland). Before genomic DNA (gDNA) extraction, A. butzleri strains were cultured on Mueller–Hinton agar (Oxoid, Thermo Fisher Scientific) plates supplemented with 5% (v/v) defibrinated sheep blood (MHB) (Oxoid, Thermo Fisher Scientific) at 30 °C for 48 h under microaerobic conditions.
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