Genomic characterization of antimicrobialresistance and virulence factors in Salmonella isolates obtained from pig farms in Antioquia, Colombia

dc.audienceInvestigadorspa
dc.audience.contentCientíficospa
dc.contributor.authorGarcía Álvarez, María Isabel
dc.contributor.authorVidal, Juana L.
dc.contributor.authorDonado Godoy, Pilar
dc.contributor.authorSmith, Jared
dc.contributor.authorShariat, Nikki
dc.contributor.authorValencia, María Fernanda
dc.contributor.authorGómez Osorio, Luis M.
dc.contributor.authorLópez Osorio, Sara
dc.contributor.authorChaparro Gutiérrez, Jenny J.
dc.coverage.countryColombiaspa
dc.coverage.researchcenterC.I Tibaitatáspa
dc.date.accessioned2025-08-28T19:44:35Z
dc.date.available2025-08-28T19:44:35Z
dc.date.created2025-01
dc.date.issued2025
dc.description.abstractOccurrence of antimicrobial-resistant Salmonella strains has been reported worldwide, because of inappropriate use of antimicrobial products in either humans or animals. The presence of multidrug resistant Salmonella in pig production systems had been reported in Antioquia, Colombia. Aim: To identify antimicrobial resistance genes (ARG) in different Salmonella spp. strains isolated from pig productions in Antioquia, Colombia. Methods: Samples were received at the Diagnostic Unit of the Faculty of Agrarian Sciences at the University of Antioquia, from January 1, 2019, to January 2021. A total of 28 isolates of Salmonella spp. were included, which presented phenotypic resistance to more than one antibiotic used in pig farms. Whole genome sequencing (WGS) was performed in the Unit of Genomic of Agrosavia using an automated pipeline from the GHRU- Sanger Institute, employing the Illumina MiSeq platform. Results: WGS revealed 34 ARGs among these isolates. In 25 isolates (89%) more than two ARGs were found. Genes encoding resistance were found for 10 different groups of antibiotics (beta-lactam, aminoglycosides, chloramphenicol, rifampicins, lincosamides, fluoroquinolones, tetracyclines, sulfonamides and trimethoprim). The most frequently observed MDR profile in Typhimurium isolates was AMP-CEX-CEP-CEF-EFT-CEQ-FLU-ENR-TE-FFC-SXT.spa
dc.description.productionsystemsPorciculturaspa
dc.format.mimetypeapplication/pdf
dc.identifierhttps://pubmed.ncbi.nlm.nih.gov/39888971/spa
dc.identifier.doi10.1371/journal.pntd.0012830spa
dc.identifier.instnameinstname:Corporación colombiana de investigación agropecuaria AGROSAVIA
dc.identifier.issn1935-2727
dc.identifier.reponamereponame:Biblioteca Digital Agropecuaria de Colombia
dc.identifier.urihttp://hdl.handle.net/20.500.12324/41148
dc.language.isoengspa
dc.publisherPublic Library of Sciencespa
dc.publisher.placeBogotá (Colombia)spa
dc.relation.citationendpage18spa
dc.relation.citationissue1spa
dc.relation.citationstartpage1spa
dc.relation.citationvolume19spa
dc.relation.ispartofjournalPLoS Neglected Tropical Diseasesspa
dc.relation.referencesWibisono FM, Wibisono FJ, Effendi MH, Plumeriastuti H, Hidayatullah AR, Hartadi EB, et al. A review of salmonellosis on poultry farms: Public health importance. Syst Rev Pharm. 2020;11(9):481–6.spa
dc.relation.referencesAndino A, Hanning I. Salmonella enterica: survival, colonization, and virulence differences among serovars. Sci World J. 2015;2015:520179. https://doi.org/10.1155/2015/520179 PMID: 25664339spa
dc.relation.referencesConsumo per cápita de carne de cerdo en Colombia. Porkcolombia. 2022.spa
dc.relation.referencesFerrari RG, Rosario DKA, Cunha-Neto A, Mano SB, Figueiredo EES, Conte-Junior CA, et al. Worldwide Epidemiology of Salmonella Serovars in Animal-Based Foods: a Meta-analysis. Appl Environ Microbiol. 2019;85(14):e00591–19. https://doi.org/10.1128/AEM.00591-19 PMID: 31053586spa
dc.relation.referencesInstituto Colombiano Agropecuario. Censos pecuarios nacional. 2023.spa
dc.relation.referencesMinisterio de Agricultura y Desarrollo Rural. Cadena Cárnica porcina. 2021.spa
dc.relation.referencesComunicado de prensa: Consumo de carne de cerdo en Colombia llegó a 13 kg por persona en 2022. Porkcolombia. 2023.spa
dc.relation.referencesEl valor de la actividad porcícola. Porkcolombia. 2022.spa
dc.relation.referencesShang K, Wei B, Cha S-Y, Zhang J-F, Park J-Y, Lee Y-J, et al. The Occurrence of Antimicrobial-Resistant Salmonellaenterica in Hatcheries and Dissemination in an Integrated Broiler Chicken Operation in Korea. Animals (Basel). 2021;11(1):154. https://doi.org/10.3390/ani11010154 PMID: 33440890spa
dc.relation.referencesBrown A, Grass J, Richardson L, Nisler A, Bicknese A, Gould L, et al. Antimicrobial resistance in salmonella that caused foodborne disease outbreaks: United States, 2003–2012. Epidemiol Infect. 2017;145:766–74. https://doi.org/10.1017/S0950268816002867 PMID: 27919296spa
dc.relation.referencesVanderWaal K, Deen J. Global trends in infectious diseases of swine. Proc Natl Acad Sci U S A. 2018;115(45):11495–500. https://doi.org/10.1073/pnas.1806068115 PMID: 30348781spa
dc.relation.referencesVan TTH, Yidana Z, Smooker P, Coloe P. Antibiotic use in food animals in the world with focus on Africa: pluses and minuses. J Glob Antimicrob Resist. 2019. https://doi.org/10.1016/j.jgar.2019.07.031 PMID: 31401170spa
dc.relation.referencesChokshi A, Sifri Z, Cennimo D, Horng H. Global contributors to antibiotic resistance. J Glob Infect Dis. 2019;11(1):36–42. https://doi.org/10.4103/jgid.jgid_110_18 PMID: 30814834spa
dc.relation.referencesVidal J, Clavijo V, Castellanos L, Kathiresan J, Kumar A, Mehta K, et al. Multidrug-resistant Salmonella spp. in fecal samples of pigs with suspected salmonellosis in Antioquia, Colombia, 2019–2021. Rev Panam Salud Publica. 2023;47:2023. https://doi.org/10.26633/RPSP.2023.46 PMID: 37082540spa
dc.relation.referencesGiraldo-Cardona J, Gualdrón-Ramírez D, Chamorro-Tobar I, Pulido-Villamarín A, Santamaría-Durán N, Castañeda-Salazar R, et al. Salmonella spp. prevalence, antimicrobial resistance and risk factor determination in Colombian swine farms. Pesquisa Veterinária Brasileira. 2019;39:816–22.spa
dc.relation.referencesAbraham S, O’Dea M, Page SW, Trott DJ. Current and future antimicrobial resistance issues for the Australian pig industry. Anim Prod Sci. 2017;57(12):2398. https://doi.org/10.1071/an17358spa
dc.relation.referencesMoreno-Switt A, Pezoa D, Sepúlveda V, González I, Rivera D, Retamal P, et al. Transduction as a potential dissemination mechanism of a clonal qnrB19-carrying plasmid isolated from Salmonella of multiple serotypes and isolation sources.. Fron Microbiol. 2019;10:2503.spa
dc.relation.referencesMANUAL DE. OIE sobre animales terrestres. 2004. Brucelosis (en línea) Consult. 12.spa
dc.relation.referencesDíaz CA, Est MNR, MV VJV, Ramírez G, Casas GA, Mogollón JD, et al. Revista Colombiana de Ciencias Pecuarias. Revista Colombiana de Ciencias Pecuarias. 2011;24(2):131–44.spa
dc.relation.referencesClinical and Laboratory Standards Institute (CLSI). Performance Standards for Antimicrobial Susceptibility Testing. 31st Edition. Published 2021. cited 2021 July 22.spa
dc.relation.referencesWingett SW, Andrews S. FastQ Screen: A tool for multi-genome mapping and quality control. F1000Res. 2018;7:1338. https://doi.org/10.12688/f1000research.15931.2 PMID: 30254741spa
dc.relation.referencesUnderwood A. BactInspector. Available from: https://gitlab.com/antunderwood/bactinspector.spa
dc.relation.referencesLow AJ, Koziol AG, Manninger PA, Blais B, Carrillo CD. ConFindr: rapid detection of intraspecies and cross-species contamination in bacterial whole-genome sequence data. PeerJ. 2019;7:e6995. https:// doi.org/10.7717/peerj.6995 PMID: 31183253spa
dc.relation.referencesBolger AM, Lohse M, Usadel B. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics. 2014;30(15):2114–20. https://doi.org/10.1093/bioinformatics/btu170 PMID: 24695404spa
dc.relation.referencesOndov B, Treangen T, Melsted P, Mallonee A, Bergman N, Koren S, et al. Mash: fast genome and metagenome distance estimation using MinHash. Geno Biol. 2016;17(132). https://doi.org/10.1186/ s13059-016-0997-x PMID: 27323842spa
dc.relation.referencesLi H. Seqtk;. Available from: https://github.com/lh3/seqtk.spa
dc.relation.referencesMagoč T, Salzberg SL. FLASH: fast length adjustment of short reads to improve genome assemblies. Bioinformatics. 2011;27(21):2957–63. https://doi.org/10.1093/bioinformatics/btr507 PMID: 21903629spa
dc.relation.referencesSong L, Florea L, Langmead B. Lighter: fast and memory-efficient sequencing error correction without counting. Geno Biol. 2014;15(509).spa
dc.relation.referencesBankevich A, Nurk S, Antipov D, Gurevich AA, Dvorkin M, Kulikov AS, et al. SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. J Comput Biol. 2012;19(5):455–77. https://doi.org/10.1089/cmb.2012.0021 PMID: 22506599spa
dc.relation.referencesGurevich A, Saveliev V, Vyahhi N, Tesler G. QUAST: quality assessment tool for genome assemblies. Bioinformatics. 2013;29(8):1072–5. https://doi.org/10.1093/bioinformatics/btt086 PMID: 23422339spa
dc.relation.referencesHunt M, Mather AE, Sánchez-Busó L, Page AJ, Parkhill J, Keane JA, et al. ARIBA: rapid antimicrobial resistance genotyping directly from sequencing reads. Microb Genom. 2017;3(10):e000131. https://doi. org/10.1099/mgen.0.000131 PMID: 29177089spa
dc.relation.referencesZankari E, Hasman H, Cosentino S, Vestergaard M, Rasmussen S, Lund O, et al. Identification of acquired antimicrobial resistance genes. J Antimicrob Chemother. 2012;67(11):2640–4. https://doi. org/10.1093/jac/dks261spa
dc.relation.referencesCarattoli A, Zankari E, García-Fernández A, Voldby Larsen M, Lund O, Villa L, et al. In silico detection and typing of plasmids using PlasmidFinder and plasmid multilocus sequence typing. Antimicrob Agents Chemother. 2014;58(7):3895–903. https://doi.org/10.1128/AAC.02412-14 PMID: 24777092spa
dc.relation.referencesChen L, Zheng D, Liu B, Yang J, Jin Q. VFDB 2016: hierarchical and refined dataset for big data analysis--10 years on. Nucleic Acids Res. 2016;44(D1):D694-7. https://doi.org/10.1093/nar/gkv1239 PMID: 26578559spa
dc.relation.referencesJolley KA, Bray JE, Maiden MCJ. Open-access bacterial population genomics: BIGSdb software, the PubMLST.org website and their applications. Wellcome Open Res. 2018 Sep 24;3:124. https://doi. org/10.12688/wellcomeopenres.14826.1 PMID: 30345391spa
dc.relation.referencesYoshida CE, Kruczkiewicz P, Laing CR, Lingohr EJ, Gannon VPJ, Nash JHE, et al. The salmonella in silico typing resource (SISTR): an open web-accessible tool for rapidly typing and subtyping draft salmonella genome assemblies. PLoS One. 2016;11(1):e0147101. https://doi.org/10.1371/journal. pone.0147101 PMID: 26800248spa
dc.relation.referencesZhang S, den Bakker HC, Li S, Chen J, Dinsmore BA, Lane C, et al. SeqSero2: rapid and improved salmonella serotype determination using whole-genome sequencing data. Appl Environ Microbiol. 2019;85(23):e01746-19. https://doi.org/10.1128/AEM.01746-19 PMID: 31540993spa
dc.relation.referencesZhou Z, Alikhan N-F, Mohamed K, Fan Y, Achtman M. The EnteroBase user’s guide, with case studies on Salmonella transmissions, Yersinia pestis phylogeny, and Escherichia core genomic diversity. Genome Res. 2019;30(1):138–52. https://doi.org/10.1101/gr.251678.119spa
dc.relation.referencesPrice MN, Dehal PS, Arkin AP. FastTree 2--approximately maximum-likelihood trees for large alignments. PLoS One. 2010;5(3):e9490. https://doi.org/10.1371/journal.pone.0009490 PMID: 20224823spa
dc.relation.referencesZhou Z, Alikhan N-F, Sergeant MJ, Luhmann N, Vaz C, Francisco AP, et al. GrapeTree: visualization of core genomic relationships among 100,000 bacterial pathogens. Genome Res. 2018;28(9):1395–404. https://doi.org/10.1101/gr.232397.117 PMID: 30049790spa
dc.relation.referencesZeng Y-B, Xiong L-G, Tan M-F, Li H-Q, Yan H, Zhang L, et al. Prevalence and antimicrobial resistance of salmonella in pork, chicken, and duck from retail markets of China. Foodborne Pathog Dis. 2019;16(5):339–45. https://doi.org/10.1089/fpd.2018.2510 PMID: 31013442spa
dc.relation.referencesÁvila E, Cardona L, Fandiño L, Barragán I. Prevalencia de Salmonella spp. en carne porcina, plantas de beneficio y expendios del Tolima. Orinoquia. 2013;17(1):59–68.spa
dc.relation.referencesAyala-Romero C, Ballen-Parada C, Rico-Gaitan M, Chamorro-Tobar I, Zambrano-Moreno D, Poutou-Piñales R, et al. Prevalencia de Salmonella spp., en ganglios mesentéricos de porcinos en plantas de beneficio Colombianas. Rev MVZ Córdoba. 2018;23(1):6447–86. https://doi.org/10.21897/ rmvz.1242spa
dc.relation.referencesGiraldo-Cardona JP, Gualdrón-Ramírez D, Chamorro-Tobar I, Pulido-Villamarín A, Santamaría-Durán N, Castañeda-Salazar R, et al. Salmonella spp. prevalence, antimicrobial resistance and risk factor determination in Colombian swine farms. Pesq Vet Bras. 2019;39(10):816–22. https://doi. org/10.1590/1678-5150-pvb-6156spa
dc.relation.referencesCampos J, Mourão J, Peixe L, Antunes P. Non-typhoidal Salmonella in the Pig Production Chain: A Comprehensive Analysis of Its Impact on Human Health. Pathogens. 2019;8(1):19. https://doi. org/10.3390/pathogens8010019 PMID: 30700039spa
dc.relation.referencesZhou Z, Jin X, Zheng H, Li J, Meng C, Yin K, et al. The prevalence and load of Salmonella, and key risk points of Salmonella contamination in a swine slaughterhouse in Jiangsu province, China. Food Control. 2018;87:153–60. https://doi.org/10.1016/j.foodcont.2017.12.026spa
dc.relation.referencesBearson SMD. Salmonella in Swine: Prevalence, Multidrug Resistance, and Vaccination Strategies. Annu Rev Anim Biosci. 2022;10:373–93. https://doi.org/10.1146/annurev-animal-013120-043304 PMID: 34699256spa
dc.relation.referencesSun H, Wan Y, Du P, Bai L. The Epidemiology of Monophasic Salmonella Typhimurium. Foodborne Pathog Dis. 2019. https://doi.org/10.1089/fpd.2019.2676 PMID: 31532231spa
dc.relation.referencesMultistate CDC. Outbreak of human Salmonella Altona and Salmonella johannesburg infections linked to chicks and ducklings (final update). CDC. 2011.spa
dc.relation.referencesHirai N, Kasahara K, Yoshihara S, Nishimura T, Ogawa Y, Ogawa T. Spinal epidural abscess caused by non-typhoidal Salmonella: a case report and literature review. J Infect Chemother. 2020. https://doi. org/10.1016/j.jiac.2020.05.016 PMID: 32591325spa
dc.relation.referencesQin X, Yang M, Cai H, Liu Y, Gorris L, Aslam MZ, et al. Antibiotic resistance of salmonella typhimurium monophasic variant 1,4,[5],12:i:-in China: a systematic review and meta-analysis. Antibiotics (Basel). 2022;11(4):532. https://doi.org/10.3390/antibiotics11040532 PMID: 35453283spa
dc.relation.referencesElnekave E, Hong S, Taylor A, Boxrud D, Rovira A, Alvarez J. Tracing the evolutionary history of an emerging Salmonella 4,[5],12:i:- clone in the United States.. Virus Evolution. 2019;5:19–20.spa
dc.relation.referencesYang X, Wu Q, Zhang J, Huang J, Chen L, Wu S, et al. Prevalence, bacterial load, and antimicrobial resistance of salmonella serovars isolated from retail meat and meat products in China. Front Microbiol. 2019;10:2121. https://doi.org/10.3389/fmicb.2019.02121 PMID: 31608021spa
dc.relation.referencesPossebon F, Tiba Casas M, Nero L, Yamatogi R, Araújo Jr. J, Pinto J de A. Prevalence, antibiotic resistance, PFGE and MLST characterization of Salmonella in swine mesenteric lymph nodes. Prev Vet Med. 2020;179:105024. https://doi.org/10.1016/j.prevetmed.2020.105024 PMID: 32417637spa
dc.relation.referencesWang R, Chen M, Feng F, Zhang J, Sui Q, Tong J, et al. Effects of chlortetracycline and copper on tetracyclines and copper resistance genes and microbial community during swine manure anaerobic digestion. Bioresour Technol. 2017;238:57–69. https://doi.org/10.1016/j.biortech.2017.03.134 PMID: 28432950spa
dc.relation.referencesRicker N, Trachsel J, Colgan P, Jones J, Choi J, Lee J, et al. Toward antibiotic stewardship: route of antibiotic administration impacts the microbiota and resistance gene diversity in swine feces. Front Vet Sci. 2020;7:255. https://doi.org/10.3389/fvets.2020.00255 PMID: 32509805spa
dc.relation.referencesDebroy R, Miryala SK, Naha A, Anbarasu A, Ramaiah S. Gene interaction network studies to decipher the multi-drug resistance mechanism in Salmonella enterica serovar Typhi CT18 reveal potential drug targets. Microb Pathog. 2020;142:104096. https://doi.org/10.1016/j.micpath.2020.104096 PMID: 32097747spa
dc.relation.referencesLi Q, Yin J, Li Z, Li Z, Du Y, Guo W, et al. Serotype distribution, antimicrobial susceptibility, antimicrobial resistance genes and virulence genes of Salmonella isolated from a pig slaughterhouse in Yangzhou, China. AMB Express. 2019;9(1):210. https://doi.org/10.1186/s13568-019-0936-9 PMID: 31884559spa
dc.relation.referencesWang W, Chen J, Shao X, Huang P, Zha J, Ye Y. Occurrence and antimicrobial resistance of Salmonella isolated from retail meats in Anhui, China. Food Sci Nutr. 2021;9(9):4701–10. https://doi. org/10.1002/fsn3.2266 PMID: 34531984spa
dc.relation.referencesLiu Q, Chen W, Elbediwi M, Pan H, Wang L, Zhou C, et al. characterization of salmonella resistome and plasmidome in pork production system in Jiangsu, China. Front Vet Sci. 2020;7:617. https://doi. org/10.3389/fvets.2020.00617 PMID: 33062654spa
dc.relation.referencesAdel WA, Ahmed AM, Hegazy Y, Torky HA, Shimamoto T. High prevalence of ESBL and plasmidmediated quinolone resistance genes in salmonella enterica isolated from retail meats and slaughterhouses in Egypt. Antibiotics (Basel). 2021;10(7):881. https://doi.org/10.3390/antibiotics10070881 PMID: 34356803spa
dc.relation.referencesPitout JDD, Laupland KB. Extended-spectrum beta-lactamase-producing Enterobacteriaceae: an emerging public-health concern. Lancet Infect Dis. 2008;8(3):159–66. https://doi.org/10.1016/S1473- 3099(08)70041-0 PMID: 18291338spa
dc.relation.referencesRiaño I, Moreno MA, Teshager T, Sáenz Y, Domínguez L, Torres C. Detection and characterization of extended-spectrum beta-lactamases in Salmonella enterica strains of healthy food animals in Spain. J Antimicrob Chemother. 2006;58(4):844–7. https://doi.org/10.1093/jac/dkl337 PMID: 16935865spa
dc.relation.referencesMąka Ł, Popowska M. Antimicrobial resistance of Salmonella spp. isolated from food. Rocz Panstw Zakl Hig. 2016;67(4):343–58. PMID: 27922740spa
dc.relation.referencesFernandes L, Centeno MM, Couto N, Nunes T, Almeida V, Alban L, et al. Longitudinal characterization of monophasic Salmonella Typhimurium throughout the pig’s life cycle. Vet Microbiol. 2016;192:231–7. https://doi.org/10.1016/j.vetmic.2016.07.018 PMID: 27527788spa
dc.relation.referencesMichael GB, Butaye P, Cloeckaert A, Schwarz S. Genes and mutations conferring antimicrobial resistance in Salmonella: an update. Microbes Infect. 2006;8(7):1898–914. https://doi.org/10.1016/j. micinf.2005.12.019 PMID: 16716631spa
dc.relation.referencesFrye JG, Jackson CR. Genetic mechanisms of antimicrobial resistance identified in Salmonella enterica, Escherichia coli, and Enteroccocus spp. isolated from U.S. food animals. Front Microbiol. 2013;4:135. https://doi.org/10.3389/fmicb.2013.00135 PMID: 23734150spa
dc.relation.referencesSerio AW, Magalhães ML, Blanchard JS, Connolly LE. Aminoglycosides: mechanisms of action and resistance. Antimicrobial Drug Resistance. 2017;213–29. https://doi. org/10.1007/978-3-319-46718-4_14spa
dc.relation.referencesde Melo ANF, Monte DFM, de Souza Pedrosa GT, Balkey M, Jin Q, Brown E, et al. Genomic investigation of antimicrobial resistance determinants and virulence factors in Salmonella enterica serovars isolated from contaminated food and human stool samples in Brazil. Int J Food Microbiol. 2021;343:109091. https://doi.org/10.1016/j.ijfoodmicro.2021.109091 PMID: 33639477spa
dc.relation.referencesCao G, Balkey M, Jin Q, Brown E, Allard M, de Melo ANF, et al. Genomic and phylogenetic analysis of Salmonella enterica serovar Enteritidis strains linked to multiple outbreaks in Brazil. Lett Appl Microbiol. 2023;76(1):ovac045. https://doi.org/10.1093/lambio/ovac045 PMID: 36688781spa
dc.relation.referencesSinwat N, Angkittitrakul S, Coulson KF, Pilapil FMIR, Meunsene D, Chuanchuen R. High prevalence and molecular characteristics of multidrug-resistant Salmonella in pigs, pork and humans in Thailand and Laos provinces. J Med Microbiol. 2016;65(10):1182–93. https://doi.org/10.1099/jmm.0.000339 PMID: 27542886spa
dc.relation.referencesHe J, Sun F, Sun D, Wang Z, Jin S, Pan Z, et al. Multidrug resistance and prevalence of quinolone resistance genes of Salmonella enterica serotypes 4,[5],12:i:- in China. Int J Food Microbiol. 2020;330:108692. https://doi.org/10.1016/j.ijfoodmicro.2020.108692 PMID: 32521291spa
dc.relation.referencesJacoby GA, Walsh KE, Mills DM, Walker VJ, Oh H, Robicsek A, et al. qnrB, another plasmidmediated gene for quinolone resistance. Antimicrob Agents Chemother. 2006;50(4):1178–82. https:// doi.org/10.1128/AAC.50.4.1178-1182.2006 PMID: 16569827spa
dc.relation.referencesRuiz J. Transferable mechanisms of quinolone resistance from 1998 onward. Clin Microbiol Rev. 2019;32(4): e00007–19. https://doi.org/10.1128/CMR.00007-19 PMID: 31413045spa
dc.relation.referencesDavies N, Jørgensen F, Willis C, McLauchlin J, Chattaway MA. Whole genome sequencing reveals antimicrobial resistance determinants (AMR genes) of Salmonella enterica recovered from raw chicken and ready-to-eat leaves imported into England between 2014 and 2019. J Appl Microbiol. 2022;133(4):2569–82. https://doi.org/10.1111/jam.15728 PMID: 35880358spa
dc.relation.referencesHughes D, Andersson DI. Environmental and genetic modulation of the phenotypic expression of antibiotic resistance. FEMS Microbiol Rev. 2017;41(3):374–91. https://doi.org/10.1093/femsre/fux004 PMID: 28333270spa
dc.relation.referencesMa F, Xu S, Tang Z, Li Z, Zhang L. Use of antimicrobials in food animals and impact of transmission of antimicrobial resistance on humans. Biosaf Health. 2020.spa
dc.relation.referencesVinayamohan PG, Pellissery AJ, Venkitanarayanan K. Role of horizontal gene transfer in the dissemination of antimicrobial resistance in food animal production. Curr Opin Food Sci. 2022;47:100882. https://doi.org/10.1016/j.cofs.2022.100882spa
dc.relation.referencesBaker KS, Dallman TJ, Field N, Childs T, Mitchell H, Day M, et al. Horizontal antimicrobial resistance transfer drives epidemics of multiple Shigella species. Nat Commun. 2018;9(1):1462. https://doi. org/10.1038/s41467-018-03949-8 PMID: 29654279spa
dc.relation.referencesPostma M, Vanderhaeghen W, Sarrazin S, Maes D, Dewulf J. Reducing antimicrobial usage in pig production without jeopardizing production parameters. Zoonoses Public Health. 2017;64(1):63–74. https://doi.org/10.1111/zph.12283 PMID: 27362766spa
dc.relation.referencesHarbarth S, Balkhy HH, Goossens H, Jarlier V, Kluytmans J, Laxminarayan R, et al. Antimicrobial resistance: one world, one fight! Antimicrob Resist Infect Control. 2015;4(1). https://doi.org/10.1186/ s13756-015-0091-2spa
dc.relation.referencesDonado-Godoy P, Castellanos R, León M, Arevalo A, Clavijo V, Bernal J, et al. The Establishment of the colombian integrated program for antimicrobial resistance surveillance (COIPARS): a pilot project on poultry farms, slaughterhouses and retail market. Zoonoses Public Health. 2015;62 Suppl 1:58–69. https://doi.org/10.1111/zph.12192 PMID: 25903494spa
dc.relation.referencesAyukekbong JA, Ntemgwa M, Atabe AN. The threat of antimicrobial resistance in developing countries: causes and control strategies. Antimicrob Resist Infect Control. 2017;6:47. https://doi.org/10.1186/ s13756-017-0208-x PMID: 28515903spa
dc.relation.referencesBerndtson AE. Increasing globalization and the movement of antimicrobial resistance between countries. Surg Infect (Larchmt). 2020;21(7):579–85. https://doi.org/10.1089/sur.2020.145 PMID: 32434446spa
dc.relation.referencesHolmes AH, Moore LSP, Sundsfjord A, Steinbakk M, Regmi S, Karkey A, et al. Understanding the mechanisms and drivers of antimicrobial resistance. Lancet. 2016;387(10014):176–87. https://doi. org/10.1016/S0140-6736(15)00473-0 PMID: 26603922spa
dc.relation.referencesProroga Y, Mancusi A, Peruzy M, Carullo M, Montone A, Fulgione A. Characterization of Salmonella Typhimurium and its monophasic variant 1,4,[5],12:i:- isolated from different sources. Folia Microbiologica. 2019;64(6):711–8. https://doi.org/10.1007/s12223-019-00683-6 PMID: 30721446spa
dc.relation.referencesHernández-Ledesma A, Cabrera-Díaz E, Arvizu-Medrano SM, Gómez-Baltazar A, Hernández- Iturriaga M, Godínez-Oviedo A, et al. Virulence and antimicrobial resistance profiles of Salmonella enterica isolated from foods, humans, and the environment in Mexico. Int J of Food Microbiol. 2023;391:110135. https://doi.org/10.1016/j.ijfoodmicro.2023.110135 PMID: 36827747spa
dc.relation.referencesBalasubramanian R, Im J, Lee J-S, Jeon HJ, Mogeni OD, Kim JH, et al. The global burden and epidemiology of invasive non-typhoidal Salmonella infections. Hum Vaccin Immunother. 2019;15(6):1421–6. https://doi.org/10.1080/21645515.2018.1504717 PMID: 30081708spa
dc.rightsAtribución-NoComercial-CompartirIgual 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/spa
dc.sourcePLoS Neglected Tropical Diseases; Vol. 19, Núm. 1 (2025): PLoS Neglected Tropical Diseases (Jan.);p. 1 - 18.spa
dc.subject.agrovocSalmonellaspa
dc.subject.agrovocAntimicrobianospa
dc.subject.agrovocCerdo cebónspa
dc.subject.agrovocExplotación agrariaspa
dc.subject.agrovocurihttp://aims.fao.org/aos/agrovoc/c_6757spa
dc.subject.agrovocurihttp://aims.fao.org/aos/agrovoc/c_509spa
dc.subject.agrovocurihttp://aims.fao.org/aos/agrovoc/c_59e0f842spa
dc.subject.agrovocurihttp://aims.fao.org/aos/agrovoc/c_2809spa
dc.subject.faoEnfermedades de los animales - L73spa
dc.subject.redGanadería y especies menoresspa
dc.titleGenomic characterization of antimicrobialresistance and virulence factors in Salmonella isolates obtained from pig farms in Antioquia, Colombiaspa
dc.title.translatedGenomic characterization of antimicrobialresistance and virulence factors in Salmonella isolates obtained from pig farms in Antioquia, Colombiaspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.driverinfo:eu-repo/semantics/articlespa
dc.type.localArtículo científicospa
dc.type.localengarticleeng
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85

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