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ARS Home » Midwest Area » Ames, Iowa » National Animal Disease Center » Food Safety and Enteric Pathogens Research » Research » Publications at this Location » Publication #301921

Title: Molecular insights into the unique phenotypes exhibited by super shed shiga toxin producing Escherichia coli O157

item MOREAU, MATHEW - Pennsylvania State University
item KATANI, ROBAB - Pennsylvania State University
item COTE, REBECCA - Pennsylvania State University
item Kudva, Indira
item Brandl, Maria
item Carter, Michelle
item Arthur, Terrance
item DEBROY, CHITRITA - Pennsylvania State University
item GOODFIELD, LAURA - Pennsylvania State University
item LI, LINGLING - Pennsylvania State University
item KAPUR, VIVEK - Pennsylvania State University

Submitted to: Meeting Abstract
Publication Type: Abstract Only
Publication Acceptance Date: 2/21/2014
Publication Date: 5/18/2014
Citation: Moreau, M.R., Katani, R., Cote, R., Kudva, I.T., Brandl, M., Carter, M.Q., Arthur, T.M., Debroy, C., Goodfield, L., Li, L., Kapur, V. 2014. Molecular insights into the unique phenotypes exhibited by super shed shiga toxin producing Escherichia coli O157 [abstract]. American Society for Microbiology. Abstract No. 179.

Interpretive Summary:

Technical Abstract: Shiga toxin producing Escherichia coli (STEC) serovar O157:H7 is a major foodborne pathogen that can cause bloody diarrhea and life threatening hemolytic uremic syndrome in humans. Asymptomatic cattle are colonized with E. coli O157:H7 at the mucosal interface of the recto-anal junction (RAJ). Super shedding (SS) is a phenomenon that has been reported in some cattle shedding O157:H7 at an amount greater than 104 CFU/g of feces, 100-1000 times greater than commonly observed. To better understand the molecular genetic mechanisms associated with this unique phenotype and, in the long-term, investigate the phenomenon of super-shedding, our laboratory recently sequenced and characterized the complete genome of SS17, a representative SS-isolate that shows a strongly adherent and aggregated phenotype on recto-anal squamous epithelial (RSE) cells. Subsequently, genes selected for study in SS17 were selected for their potential functions and/or the presence of non-synonymous SNPs and other genetic alterations. The results of our analysis show that deletions of ompA, eivA, yfaL, and wzzB in the reference strain EDL933 resulted in a phenotypic switch from diffuse and moderate adherence in the RSE model to strong adherence and aggregation, similar to SS17. Furthermore, SS17 exhibited enhanced attachment to the surface of spinach leaves and biofilm formation in spinach leaf lysates compared with EDL933. The genes ompA, cah, and yfaL are all required for SS17’s enhanced biofilm formation in spinach extract. Together, these investigations are beginning to help establish the functional role of various genes and their contribution to animal colonization, adherence to produce, environmental survival, transmission and eventual infection of human hosts by SS isolates of E. coli.