Afficher la notice abrégée

dc.contributorFacultad de Veterinariaes_ES
dc.contributor.authorPanera Martínez, Sarah
dc.contributor.authorCapita González, Rosa María 
dc.contributor.authorGarcía Fernández, María del Camino 
dc.contributor.authorAlonso Calleja, Carlos 
dc.contributor.otherNutricion y Bromatologiaes_ES
dc.date2023
dc.date.accessioned2024-05-02T08:42:25Z
dc.date.available2024-05-02T08:42:25Z
dc.identifier.citationPanera Martínez, S., Capita, R., García Fernández, C., & Alonso Calleja, C. (2023). Viability and Virulence of Listeria monocytogenes in Poultry. Microorganisms, 11(9), Article e2232. https://doi.org/10.3390/MICROORGANISMS11092232es_ES
dc.identifier.otherhttps://www.mdpi.com/2076-2607/11/9/2232es_ES
dc.identifier.urihttps://hdl.handle.net/10612/20242
dc.descriptionCopyright: © 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/)es_ES
dc.description.abstract[EN] The prevalence of Listeria monocytogenes in 30 samples of poultry was determined using culture-dependent (isolation on OCLA and confirmation by conventional polymerase chain reaction -PCR-, OCLA&PCR) and culture-independent (real-time polymerase chain reaction, q-PCR) methods. L. monocytogenes was detected in 15 samples (50.0%) by OCLA&PCR and in 20 (66.7%) by q-PCR. The concentrations (log10 cfu/g) of L. monocytogenes (q-PCR) ranged from 2.40 to 5.22 (total cells) and from <2.15 to 3.93 (viable cells). The two methods, q-PCR using a viability marker (v-PCR) and OCLA&PCR (gold standard), were compared for their capacity to detect viable cells of L. monocytogenes, with the potential to cause human disease. The values for sensitivity, specificity and efficiency of the v-PCR were 100%, 66.7% and 83.3%, respectively. The agreement between the two methods (kappa coefficient) was 0.67. The presence of nine virulence genes (hlyA, actA, inlB, inlA, inlC, inlJ, prfA, plcA and iap) was studied in 45 L. monocytogenes isolates (three from each positive sample) using PCR. All the strains harbored between six and nine virulence genes. Fifteen isolates (33.3% of the total) did not show the potential to form biofilm on a polystyrene surface, as determined by a crystal violet assay. The remaining strains were classified as weak (23 isolates, 51.1% of the total), moderate (one isolate, 2.2%) or strong (six isolates, 13.3%) biofilm producers. The strains were tested for susceptibility to a panel of 15 antibiotics. An average of 5.11 ± 1.30 resistances per isolate was observed. When the values for resistance and for reduced susceptibility were taken jointly, this figure rose to 6.91 ± 1.59. There was a prevalence of resistance or reduced susceptibility of more than 50.0% for oxacillin, cefoxitin, cefotaxime, cefepime ciprofloxacin, enrofloxacin and nitrofurantoin. For the remaining antibiotics tested, the corresponding values ranged from 0.0% for chloramphenicol to 48.9% for rifampicin. The high prevalence and level of L. monocytogenes with numerous virulence factors in poultry underline how crucial it is to follow correct hygiene procedures during the processing of this foodstuff in order to reduce the risk of human listeriosis.es_ES
dc.languageenges_ES
dc.publisherMDPIes_ES
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectTecnología de los alimentoses_ES
dc.subject.otherListeria monocytogeneses_ES
dc.subject.otherQuantificationes_ES
dc.subject.otherViable non-culturable cellses_ES
dc.subject.otherVirulencees_ES
dc.subject.otherBiofilmes_ES
dc.subject.otherAntibiotic resistancees_ES
dc.titleViability and Virulence of Listeria monocytogenes in Poultryes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.identifier.doi10.3390/MICROORGANISMS11092232
dc.description.peerreviewedSIes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Programa Estatal de I+D+i Orientada a los Retos de la Sociedad/RTI2018- 098267-R-C33/ES/ALTERNATIVAS AL USO DE DESINFECTANTES EN LA INDUSTRIA ALIMENTARIA DIRIGIDAS A REDUCIR LA SUPERVIVENCIA DE LISTERIA MONOCYTOGENES Y SALMONELLA ENTERICA SOBRE LAS SUPERFICIESes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Programa Estatal para Impulsar la Investigación Científico-Técnica y su Transferencia/PID2022-142329OB-C31/ES/CARACTERIZACION DE LA MICROBIOTA EN SUPERFICIES DE INDUSTRIAS ALIMENTARIAS: EFECTO DE NUEVOS BIOCIDAS SOBRE LA RESISTENCIA A ANTIBIOTICOS Y LOS BIOFILMS DE L. MONOCYTOGENES//es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn2076-2607
dc.journal.titleMicroorganismses_ES
dc.volume.number11es_ES
dc.issue.number9es_ES
dc.page.initial2232es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.unesco2414.04 Bacteriologíaes_ES
dc.description.projectThis research was funded by the Junta de Castilla y León (Consejería de Educación, Spain, grant number LE018P20) and the Ministerio de Ciencia e Innovación (Spain, grant numbers RTI2018- 098267-R-C33 and PID2022-142329OB-C31). Sarah Panera-Martínez is the recipient of a predoctoral research fellowship from the Junta de Castilla y León (Consejería de Educación, Spain) co-financed by the European Social Fund.es_ES


Fichier(s) constituant ce document

Thumbnail

Ce document figure dans la(les) collection(s) suivante(s)

Afficher la notice abrégée

Atribución 4.0 Internacional
Excepté là où spécifié autrement, la license de ce document est décrite en tant que Atribución 4.0 Internacional