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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1016/j.fm.2025.104823</dc:identifier><dc:language>eng</dc:language><dc:creator>Tavares da Silva, Ruthchelly</dc:creator><dc:creator>García-Penas, Ivo</dc:creator><dc:creator>Espina, Laura</dc:creator><dc:creator>García-Gonzalo, Diego</dc:creator><dc:creator>Magnani, Marciane</dc:creator><dc:creator>Pagán, Rafael</dc:creator><dc:title>Meropenem-induced cross-protection in Salmonella enterica resistant variants: Insights from adaptive laboratory evolution and whole genome sequencing</dc:title><dc:identifier>ART-2025-144305</dc:identifier><dc:description>Adaptive laboratory evolution (ALE) assay provides a deep understanding of the genetic mechanisms and processes involved in bacterial responses. This study aimed to obtain resistant-variants (RVs) of Salmonella enterica subsp. enterica Typhimurium (SeT) and Enteritidis (SeE) after ALE assays with meropenem (MPM); to identify genetic modifications of RVs responsible for their increased resistance; and to evaluate their cross-protection against antibiotics and food preservatives (heat and carvacrol). Five MPM-RVs from SeT (SeT_M1-5) and one from SeE (SeE_M5) showed a 100 % increase in MPM minimum inhibitory concentrations (from 0.0312 to 0.0625 μg/mL). MPM-RVs had lower maximum growth rates and/or longer lag times, except in SeT_M5 and SeE_M3, which maintained or even improved growth fitness in the presence of MPM. Whole genome sequencing of RVs revealed single mutations in AMR-related and -unrelated genes in most MPM-RVs: spoT in SeT_M1, glnA in SeT_M2, thrS in SeT_M4 and SeE_M2, and mrdA in SeT_M5, SeE_M3 and SeE_M5. Two mutations were identified in SeT_M3 and SeE_M4: spoT and znuA in SeT_M3 and AWJ12_RS14025 and rfbF in SeE_M4. The individual mutations resulted in cross-protection to at least one of the antibiotics tested and/or heat (reductions of up to 3.8–4.3 cycles of inactivation for MPM-RVs in contrast to 4.7 and 5.3 cycles for SeE and SeT, respectively) and/or carvacrol (3.4–3.7 cycles for MPM-RVs in contrast to 4.4 cycles for SeT). These findings highlight the importance of preventing the emergence of resistant bacterial variants, considering the cross-protection to other antibiotics and food preservatives, which plays an important role in spreading resistance in food chain.</dc:description><dc:date>2025</dc:date><dc:source>http://zaguan.unizar.es/record/161079</dc:source><dc:doi>10.1016/j.fm.2025.104823</dc:doi><dc:identifier>http://zaguan.unizar.es/record/161079</dc:identifier><dc:identifier>oai:zaguan.unizar.es:161079</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/MCIU/PID2021-123404NB-I00</dc:relation><dc:identifier.citation>FOOD MICROBIOLOGY 132 (2025), 104823 [12 pp.]</dc:identifier.citation><dc:rights>by-nc</dc:rights><dc:rights>https://creativecommons.org/licenses/by-nc/4.0/deed.es</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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