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Study of microRNA expression in Salmonella Typhimurium-infected porcine ileum reveals miR-194a-5p as an important regulator of the TLR4-mediated inflammatory response.

dc.contributor.authorHerrera-Uribe, Juber
dc.contributor.authorZaldivar-Lopez, Sara
dc.contributor.authorAguilar, Carmen
dc.contributor.authorEntrenas-Garcia, Carmen
dc.contributor.authorBautista, Rocío
dc.contributor.authorClaros, M Gonzalo
dc.contributor.authorGarrido, Juan J
dc.contributor.funderSpanish Ministry of Economy and Competitiveness
dc.contributor.funderFPI Research Program of the Spanish Ministry of Economy and Competitiveness
dc.contributor.funderPostdoctoral Trainee Program of the Spanish Ministry of Economy and Competitiveness
dc.date.accessioned2023-05-03T13:35:10Z
dc.date.available2023-05-03T13:35:10Z
dc.date.issued2022-03-08
dc.description.abstractInfection with Salmonella Typhimurium (S. Typhimurium) is a common cause of food-borne zoonosis leading to acute gastroenteritis in humans and pigs, causing economic losses to producers and farmers, and generating a food security risk. In a previous study, we demonstrated that S. Typhimurium infection produces a severe transcriptional activation of inflammatory processes in ileum. However, little is known regarding how microRNAs regulate this response during infection. Here, small RNA sequencing was used to identify 28 miRNAs differentially expressed (DE) in ileum of S. Typhimurium-infected pigs, which potentially regulate 14 target genes involved in immune system processes such as regulation of cytokine production, monocyte chemotaxis, or cellular response to interferon gamma. Using in vitro functional and gain/loss of function (mimics/CRISPR-Cas system) approaches, we show that porcine miR-194a-5p (homologous to human miR-194-5p) regulates TLR4 gene expression, an important molecule involved in pathogen virulence, recognition and activation of innate immunity in Salmonella infection.
dc.description.versionSi
dc.identifier.citationHerrera-Uribe J, Zaldívar-López S, Aguilar C, Entrenas-García C, Bautista R, Claros MG, et al. Study of microRNA expression in Salmonella Typhimurium-infected porcine ileum reveals miR-194a-5p as an important regulator of the TLR4-mediated inflammatory response. Vet Res. 2022 May 21;53(1):35
dc.identifier.doi10.1186/s13567-022-01056-7
dc.identifier.essn1297-9716
dc.identifier.pmcPMC9123658
dc.identifier.pmid35598011
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9123658/pdf
dc.identifier.unpaywallURLhttps://veterinaryresearch.biomedcentral.com/track/pdf/10.1186/s13567-022-01056-7
dc.identifier.urihttp://hdl.handle.net/10668/20367
dc.issue.number1
dc.journal.titleVeterinary research
dc.journal.titleabbreviationVet Res
dc.language.isoen
dc.organizationInstituto Maimónides de Investigación Biomédica de Córdoba-IMIBIC
dc.page.number13
dc.publisherBioMed Central
dc.pubmedtypeJournal Article
dc.relation.projectIDAGL2014-54089-R and AGL2017-87415-R
dc.relation.projectIDBES-2012-058642
dc.relation.projectIDFPDI-2013-15619 and IJCI-2017-31382
dc.relation.publisherversionhttps://veterinaryresearch.biomedcentral.com/articles/10.1186/s13567-022-01056-7
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectCRISPR-Cas9
dc.subjectSalmonellosis
dc.subjectToll-like receptor
dc.subjectIleum
dc.subjectImmunity
dc.subjectInfection
dc.subjectInflammation
dc.subjectMiRNA-seq
dc.subjectMicroRNAs
dc.subjectPig
dc.subject.decsAnimales
dc.subject.decsMicroARNs
dc.subject.decsPorcinos
dc.subject.decsReceptor toll-like 4
dc.subject.decsSalmonelosis animal
dc.subject.decsÍleon
dc.subject.meshAnimals
dc.subject.meshIleum
dc.subject.meshMicroRNAs
dc.subject.meshSalmonella Infections, Animal
dc.subject.meshSalmonella typhimurium
dc.subject.meshSwine
dc.subject.meshToll-Like Receptor 4
dc.titleStudy of microRNA expression in Salmonella Typhimurium-infected porcine ileum reveals miR-194a-5p as an important regulator of the TLR4-mediated inflammatory response.
dc.typeResearch article
dc.type.hasVersionVoR
dc.volume.number53
dspace.entity.typePublication

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