dc.creatorMoreno, Luisa Zanolli
dc.creatorPaixao, Renata
dc.creatorGobbi, Debora Dirani
dc.creatorRaimundo, Daniele Cristine
dc.creatorFerreira, Thais Porfida
dc.creatorHofer, Ernesto
dc.creatorMatte, Maria Helena
dc.creatorMoreno, Andrea Micke
dc.date.accessioned2013-10-03T12:23:56Z
dc.date.accessioned2018-07-04T15:57:10Z
dc.date.available2013-10-03T12:23:56Z
dc.date.available2018-07-04T15:57:10Z
dc.date.created2013-10-03T12:23:56Z
dc.date.issued2012
dc.identifierResearch in Microbiology, v. 163, n. 4, pp. 268-271, may, 2012
dc.identifier0923-2508
dc.identifierhttp://www.producao.usp.br/handle/BDPI/33982
dc.identifier10.1016/j.resmic.2012.02.004
dc.identifierhttp://dx.doi.org/10.1016/j.resmic.2012.02.004
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1629631
dc.description.abstractAtypical Listeria innocua strains presenting phenotypic characteristics similar to those of Listeria monocyto genes were recently isolated from food and the environment. These isolates also tested positive for virulence genes specific to L. monocytogenes. Here we report the isolation of atypical hemolytic L. innocua strains from the environment of pork processing plants in Brazil. The strains were positive for L. monocytogenes virulence genes hly, inlA and inlB by PCR and presented genotypic similarities with human isolates of L. monocytogenes via the AFLP technique using HindIII single enzyme protocol. Phenotypic and genotypic similarities suggest that these atypical L. innocua may be pathogenic strains. (C) 2012 Institut Pasteur. Published by Elsevier Masson SAS. All rights reserved.
dc.languageeng
dc.publisherElsevier Science
dc.publisherAmsterdam
dc.relationResearch in Microbiology
dc.rightsCopyright Elsevier Science
dc.rightsclosedAccess
dc.subjectListeria innocua
dc.subjectListeria monocytogenes
dc.subjectPork
dc.subjectAFLP
dc.subjectPCR
dc.subjectVirulence genes
dc.titleCharacterization of atypical Listeria innocua isolated from swine slaughterhouses and meat markets
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución