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Different Cellular Origins and Functions of Extracellular Proteins from Escherichia coli O157:H7 and O104:H4 as Determined by Comparative Proteomic Analysis.
Islam, Nazrul; Nagy, Attila; Garrett, Wesley M; Shelton, Dan; Cooper, Bret; Nou, Xiangwu.
Affiliation
  • Islam N; Environmental Microbial and Food Safety Laboratory, USDA Agricultural Research Service, Beltsville, Maryland, USA.
  • Nagy A; Department of Nutrition and Food Science, University of Maryland, College Park, Maryland, USA.
  • Garrett WM; Environmental Microbial and Food Safety Laboratory, USDA Agricultural Research Service, Beltsville, Maryland, USA.
  • Shelton D; Animal Biosciences and Biotechnology Laboratory, USDA Agricultural Research Service, Beltsville, Maryland, USA.
  • Cooper B; Environmental Microbial and Food Safety Laboratory, USDA Agricultural Research Service, Beltsville, Maryland, USA.
  • Nou X; Soybean Genomics and Improvement Laboratory, USDA Agricultural Research Service, Beltsville, Maryland, USA bret.cooper@ars.usda.gov xiangwu.nou@ars.usda.gov.
Appl Environ Microbiol ; 82(14): 4371-4378, 2016 07 15.
Article in En | MEDLINE | ID: mdl-27208096
ABSTRACT
UNLABELLED Extracellular proteins play important roles in bacterial interactions with the environmental matrices. In this study, we examined the extracellular proteins from Escherichia coli O157H7 and O104H4 by tandem mass spectrometry. We identified 500 and 859 proteins from the growth media of E. coli O157H7 and O104H4, respectively, including 371 proteins common to both strains. Among proteins that were considered specific to E. coli O157H7 or present at higher relative abundances in O157H7 medium, most (57 of 65) had secretion signal sequences in their encoding genes. Noticeably, the proteins included locus of enterocyte effacement (LEE) virulence factors, proteins required for peptidyl-lipoprotein accumulation, and proteins involved in iron scavenging. In contrast, a much smaller proportion of proteins (37 of 150) that were considered specific to O104H4 or presented at higher relative abundances in O104H4 medium had signals targeting them for secretion. These proteins included Shiga toxin 2 subunit B and O104H4 signature proteins, including AAF/1 major fimbrial subunit and serine protease autotransporters. Most of the abundant proteins from the growth medium of E. coli O104H4 were annotated as having functions in the cytoplasm. We provide evidence that the extensive presence of cytoplasmic proteins in E. coli O104H4 growth medium was due to biological processes independent of cell lysis, indicating alternative mechanisms for this potent pathogen releasing cytoplasmic contents into the growth milieu, which could play a role in interaction with the environmental matrices, such as pathogenesis and biofilm formation. IMPORTANCE In this study, we compared the extracellular proteins from two of the most prominent foodborne pathogenic E. coli organisms that have caused severe outbreaks in the United States and in Europe. E. coli O157H7 is a well-studied Shiga toxigenic foodborne pathogen of the enterohemorrhagic pathotype that has caused numerous outbreaks associated with various contaminated foods worldwide. E. coli O104H4 is a newly emerged Shiga toxigenic foodborne pathogen of the enteroaggregative pathotype that gained notoriety for causing one of the most deadly foodborne outbreaks in Europe in 2011. Comparison of proteins in the growth medium revealed significant differences in the compositions of the extracellular proteins for these two pathogens. These differences may provide valuable information regarding the cellular responses of these pathogens to their environment, including cell survival and pathogenesis.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Proteome / Escherichia coli Proteins / Escherichia coli / Serogroup Type of study: Prognostic_studies Language: En Journal: Appl Environ Microbiol Year: 2016 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Proteome / Escherichia coli Proteins / Escherichia coli / Serogroup Type of study: Prognostic_studies Language: En Journal: Appl Environ Microbiol Year: 2016 Document type: Article Affiliation country: United States