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  <controlfield tag="005">20251017144626.0</controlfield>
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    <subfield code="2">doi</subfield>
    <subfield code="a">10.1093/jac/dkaf104</subfield>
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  <datafield tag="024" ind1="8" ind2=" ">
    <subfield code="2">sideral</subfield>
    <subfield code="a">143923</subfield>
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  <datafield tag="037" ind1=" " ind2=" ">
    <subfield code="a">ART-2025-143923</subfield>
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  <datafield tag="041" ind1=" " ind2=" ">
    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Campaña-Burguet, Allelen</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Changing epidemiology of MRSA-CC398 in Spanish hospitals located in areas with different pig farming densities: a 2023 multicentre study</subfield>
  </datafield>
  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2025</subfield>
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  <datafield tag="520" ind1="3" ind2=" ">
    <subfield code="a">Background: Livestock-associated (LA)-MRSA of CC398 lineage is related to the pig environment, although it also colonizes/infects humans. Tetracycline resistance (TETR) is a phenotypic marker of LA-MRSA-CC398.

Objectives: To determine the prevalence and changing epidemiology of LA-MRSA-CC398 in seven Spanish hospitals (H1-H7) located in areas with different pig farming densities (PFDs) (extremely high, very high, medium, and very low: EH/VH/M/VL), and to identify other non-CC398-LA-MRSA clones.

Methods: MRSA-TETR isolates (n = 165) obtained from hospitals H1-H7 over 6 months in 2023 were characterized with respect to genetic lineages/antimicrobial resistance and virulence/immune evasion cluster of CC398 and non-CC398. Results were compared with a previous multicentre study from 2016.

Results: We identified 86/165 MRSA-TETR isolates (52.1%) as being MRSA-CC398. A significant difference in MRSA-CC398/MRSA prevalence was detected between hospitals located in EH-PFD areas (H1 and H2, > 25%) and the one in a VL-PFD area (H7, 0%). Prevalences in the range 6.4%-12.2% were found in hospitals in M- and VH-PFD areas (H3-H6). Fourteen spa-types were identified among MRSA-CC398 isolates, with t011/t034 predominating (68.3%), followed by t1451/t1255 (13%). All but two MRSA-CC398 isolates were scn-negative (human adaptation marker). Among the 79 non-CC398-MRSA-TETR isolates, CC5, CC1 and CC8 predominated (45.6%, scn-negative). The prevalences of the scn gene among non-CC398-MRSA-TETR isolates in hospitals of EH-, VH-, M- and VL-PFD areas were 77.8%, 50%, 18.75% and 0%, respectively (significant correlation, P &lt; 0.05). This study shows that MRSA-CC398 isolates are prevalent in hospitals located in EH-PFD areas but absent in the hospital of the VL-PFD area. Moreover, an increase in both PFD and prevalence of MRSA-CC398/MRSA in hospitals H3-H6 was observed in the 2023 study compared with the 2016 study.

Conclusions: A significant increase and more genetic diversity of predominant lineages of CC398-MRSA-TETR were observed in hospitals located in M- to VH-PFD areas.</subfield>
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    <subfield code="9">info:eu-repo/grantAgreement/ES/AEI/PID2022-139591OB-I00</subfield>
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    <subfield code="9">info:eu-repo/semantics/closedAccess</subfield>
    <subfield code="a">All rights reserved</subfield>
    <subfield code="u">http://www.europeana.eu/rights/rr-f/</subfield>
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    <subfield code="a">info:eu-repo/semantics/article</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Latorre-Fernández, Javier</subfield>
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    <subfield code="a">Eguizábal, Paula</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Bellés-Bellés, Alba</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Mormeneo-Bayo, Saray</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Alonso, Carla Andrea</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Arregui, Irati</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">López-Calleja, Ana Isabel</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Rezusta, Antonio</subfield>
    <subfield code="0">(orcid)0000-0001-7294-245X</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Seral, Cristina</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-9742-1463</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Castillo, Francisco Javier</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-2519-701X</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Vilamala, Anna</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Navarro, María</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Aspiroz, Carmen</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Cebollada, Rocío</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Cercenado, Emilia</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Zarazaga, Myriam</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Lozano, Carmen</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Torres, Carmen</subfield>
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    <subfield code="1">1011</subfield>
    <subfield code="2">630</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Microb.Ped.Radio.Sal.Pú.</subfield>
    <subfield code="c">Área Microbiología</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">(2025), [10 pp.]</subfield>
    <subfield code="p">J. antimicrob. chemother.</subfield>
    <subfield code="t">The Journal of antimicrobial chemotherapy</subfield>
    <subfield code="x">0305-7453</subfield>
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    <subfield code="a">2025-10-17-14:24:26</subfield>
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