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dc.contributor.authorLópez de Egea, Guillem
dc.contributor.authorGonzález-Díaz, Aida
dc.contributor.authorAragon, Virginia
dc.contributor.authorCabezón, Oscar
dc.contributor.authorGuédon, Gérard
dc.contributor.authorBerbel, Dàmaris
dc.contributor.authorCadenas-Jiménez, Irene
dc.contributor.authorEspunyes, Johan
dc.contributor.authorPlanellas, Marta
dc.contributor.authorDomínguez, M. Ángeles
dc.contributor.authorLeblond-Bourget, Nathalie
dc.contributor.authorArdanuy, Carmen
dc.contributor.otherProducció Animalca
dc.date.accessioned2026-03-20T10:43:35Z
dc.date.available2026-03-20T10:43:35Z
dc.date.issued2026-03-16
dc.identifier.issn2165-0497ca
dc.identifier.urihttp://hdl.handle.net/20.500.12327/5163
dc.description.abstractThe increasing macrolide resistance in Streptococcus spp. causing human and animal infections in the last decades is a concern for global health. The objectives of this study were to analyze the macrolide resistance rates of Streptococcus spp. from animals and their resistance determinants. We conducted a retrospective study of an animal Streptococcus collection (307 isolates) from farm, wild animals, and pets in Catalonia, Northeast Spain. Identification was done by MALDI-TOF, and antimicrobial susceptibility to erythromycin and clindamycin was assessed by disk diffusion (EUCAST). Resistant strains were further tested for susceptibility to other antimicrobial agents using disk diffusion and microdilution methods. Selected isolates (n = 50) were subjected to whole-genome sequencing (WGS). Mobile genetic elements (MGEs), such as integrative and conjugative elements (ICEs) and integrative and mobilizable elements (IMEs), were identified using ICEscreen. Streptococcal strains were mainly isolated from domestic swine (50.5%) and wild boars (19.2%), with S. suis (54.4%) and S. hyovaginalis (14%) the predominant species. The macrolide resistance phenotypes found were MLSB (n = 145), M (n = 6), and L (n = 30). Macrolide (84.5%) and lincosamide (94.8%) resistance rates from swine strains were higher than those from other animals (13.2% and 18.4%, respectively, P < 0.001). The predominant resistant genes found were erm(B) (n = 38), tet(O) (n = 28), vga(F) (n = 20), and lnu(B)-lsa(E) (n = 10), and were mostly associated with ICEs or defective ICEs (dICEs) belonging to the Tn5252 family. Animal streptococci presented high macrolide resistance rates, especially concerning swine strains, associated with a variety of resistance determinants. MGEs were the main carriers of resistance determinants and contributors to its spread.ca
dc.description.sponsorshipWe thank the past and present staff of the microbiology departments who contributed to this project on a daily basis. We thank CReSA-IRTA and Universitat Autònoma de Barcelona for their bacterial collections. We thank the CERCA Program/Generalitat de Catalunya for institutional support. This study was supported in part through the Projects PI21/01000 and INT22/00096, “Centro de Investigación Biomédica en Red (CIBER) de Enfermedades Respiratorias (CB06/06/0037)” and “CIBER de Enfermedades Infecciosas (CB21/13/0009),” an initiative of the Instituto de Salud Carlos III, Madrid, Spain. It was co-funded by the European Regional Development Fund/European Social Fund (ERDF/ESF, “Investing in your future”).
dc.format.extent12ca
dc.language.isoengca
dc.publisherAmerican Society for Microbiologyca
dc.relation.ispartofMicrobiology Spectrumca
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleMacrolide resistance determinants and their associations in streptococci from selected livestock and wildlife species from Catalonia, Northeast Spainca
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/publishedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.termscapca
dc.relation.projectIDISCIII/ /PI21/01000/Una perspectiva global de las enfermedades neumocócicas y la resistencia en tiempos de pandemia por COVID-19 y vacunación universal en pediatría/
dc.relation.projectIDISCIII/ /INT22/00096/ES/ /
dc.relation.projectIDFEDER/ / /EU/ /
dc.relation.projectIDFSE/ / /EU/ /
dc.subject.udc619ca
dc.identifier.doihttps://doi.org/10.1128/spectrum.02567-25ca
dc.contributor.groupSanitat Animalca


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