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dc.contributor.authorNeupane, Mahesh
dc.contributor.authorAbu-Ali, Galeb S.
dc.contributor.authorMitra, Avishek
dc.contributor.authorLacher, David W.
dc.contributor.authorManning, Shannon D.
dc.contributor.authorRiordan, James T.
dc.date.accessioned2023-02-16T16:48:46Z
dc.date.available2023-02-16T16:48:46Z
dc.date.issued2011-12
dc.identifier.citationNeupane, M., Abu-Ali, G. S., Mitra, A., Lacher, D. W., Manning, S. D., Riordan, J. T. (2011). Shiga toxin 2 overexpression in Escherichia coli O157:H7 strains associated with severe human disease. Microbial Pathogenesis, 51(6), pp. 466-470. https://doi.org/10.1016/j.micpath.2011.07.009
dc.identifier.issn0882-4010
dc.identifier.urihttps://hdl.handle.net/11244/337044
dc.description.abstractVariation in disease severity among Escherichia coli O157:H7 infections may result from differential expression of Shiga toxin 2 (Stx2). Eleven strains belonging to four prominent phylogenetic clades, including clade 8 strains representative of the 2006 U.S. spinach outbreak, were examined for stx2 expression by real-time PCR and western blot analysis. Clade 8 strains were shown to overexpress stx2 basally, and following induction with ciprofloxacin when compared to strains from clades 1-3. Differences in stx2 expression generally correlated with Stx2 protein levels. Single-nucleotide polymorphisms identified in regions upstream of stx2AB in clade 8 strains were largely absent in non-clade 8 strains. This study concludes that stx2 overexpression is common to strains from clade 8 associated with hemolytic uremic syndrome, and describes SNPs which may affect stx2 expression and which could be useful in the genetic differentiation of highly-virulent strains.
dc.formatapplication/pdf
dc.languageeng
dc.publisherElsevier
dc.relation.ispartofMicrobial Pathogenesis, 51 (6)
dc.relation.urihttps://www.ncbi.nlm.nih.gov/pubmed/21864671
dc.relation.urihttp://dx.doi.org/10.1016/j.micpath.2011.07.009
dc.rightsThis material has been previously published. In the Oklahoma State University Library's institutional repository this version is made available through the open access principles and the terms of agreement/consent between the author(s) and the publisher. The permission policy on the use, reproduction or distribution of the material falls under fair use for educational, scholarship, and research purposes. Contact Digital Resources and Discovery Services at lib-dls@okstate.edu or 405-744-9161 for further information.
dc.subject.meshCluster Analysis
dc.subject.meshDisease Outbreaks
dc.subject.meshEscherichia coli Infections
dc.subject.meshEscherichia coli O157
dc.subject.meshGene Expression
dc.subject.meshHemolytic-Uremic Syndrome
dc.subject.meshHumans
dc.subject.meshMolecular Typing
dc.subject.meshPolymorphism, Single Nucleotide
dc.subject.meshShiga Toxin 2
dc.subject.meshSpinacia oleracea
dc.subject.meshUnited States
dc.subject.meshVirulence
dc.titleShiga toxin 2 overexpression in Escherichia coli O157:H7 strains associated with severe human disease
dc.date.updated2023-02-15T23:01:59Z
dc.noteopen access status: Green OA
dc.identifier.doi10.1016/j.micpath.2011.07.009
dc.description.departmentMicrobiology and Molecular Genetics
dc.type.genreArticle
dc.type.materialText
dc.subject.keywordsRare Diseases
dc.subject.keywordsImmunization
dc.subject.keywordsVaccine Related
dc.subject.keywordsGenetics
dc.subject.keywordsEmerging Infectious Diseases
dc.subject.keywordsKidney Disease
dc.subject.keywordsBiotechnology
dc.subject.keywordsDigestive Diseases
dc.subject.keywordsInfectious Diseases
dc.subject.keywordsFactors relating to the physical environment
dc.subject.keywordsAetiology
dc.subject.keywordsInfection
dc.subject.keywordsMicrobiology
dc.subject.keywordsImmunology
dc.subject.keywordsMedical Microbiology
dc.relation.oaurlhttps://pubmed.ncbi.nlm.nih.gov/21864671/
dc.identifier.authorORCID: 0000-0003-0243-2045 (Mitra, Avishek)
dc.identifier.essn1096-1208


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