Faculty Opinions recommendation of Characterization and evidence of mobilization of the LEE pathogenicity island of rabbit-specific strains of enteropathogenic Escherichia coli.

Author(s):  
Gadi Frankel
2003 ◽  
Vol 48 (2) ◽  
pp. 507-521 ◽  
Author(s):  
Andrew J. Grant ◽  
Michele Farris ◽  
Peter Alefounder ◽  
Peter H. Williams ◽  
Martin J. Woodward ◽  
...  

2004 ◽  
Vol 53 (11) ◽  
pp. 1145-1149 ◽  
Author(s):  
Rosanna Mundy ◽  
Claire Jenkins ◽  
Jun Yu ◽  
Henry Smith ◽  
Gad Frankel

Enterohaemorrhagic (EHEC) and enteropathogenic (EPEC) Escherichia coli are important diarrhoeagenic pathogens; infection is dependent on translocation of a number of type III effector proteins. Until recently all the known effectors were encoded on the LEE pathogenicity island, which also encodes the adhesin intimin and the type III secretion apparatus. Recently, a novel non-LEE effector protein, EspI/NleA, which is required for full virulence in vivo and is encoded on a prophage, was identified. The aim of this study was to determine the distribution of espI among clinical EHEC and EPEC isolates. espI was detected in 86 % and 53 % of LEE+ EHEC and EPEC strains, respectively. Moreover, the espI gene was more commonly found in patients suffering from a more severe disease.


2010 ◽  
Vol 48 (4) ◽  
pp. 1452-1455 ◽  
Author(s):  
M. A. M. Vieira ◽  
F. A. Salvador ◽  
R. M. Silva ◽  
K. Irino ◽  
T. M. I. Vaz ◽  
...  

2016 ◽  
Vol 306 (4) ◽  
pp. 231-236 ◽  
Author(s):  
Erik H. Mercado ◽  
Cristian Piscoche ◽  
Carmen Contreras ◽  
David Durand ◽  
Maribel Riveros ◽  
...  

2001 ◽  
Vol 69 (1) ◽  
pp. 315-324 ◽  
Author(s):  
Jay L. Mellies ◽  
Fernando Navarro-Garcia ◽  
Iruka Okeke ◽  
Julie Frederickson ◽  
James P. Nataro ◽  
...  

ABSTRACT At least five proteins are secreted extracellularly by enteropathogenic Escherichia coli (EPEC), a leading cause of infant diarrhea in developing countries. However only one, EspC, is known to be secreted independently of the type III secretion apparatus encoded by genes located within the 35.6-kb locus of enterocyte effacement pathogenicity island. EspC is a member of the autotransporter family of proteins, and the secreted portion of the molecule is 110 kDa. Here we determine that the espC gene is located within a second EPEC pathogenicity island at 60 min on the chromosome of E. coli. We also show that EspC is an enterotoxin, indicated by rises in short-circuit current and potential difference in rat jejunal tissue mounted in Ussing chambers. In addition, preincubation with antiserum against the homologous Pet enterotoxin of enteroaggregative E. coli eliminated EspC enterotoxin activity. Like the EAF plasmid, the espCpathogenicity island was found only in a subset of EPEC, suggesting that EspC may play a role as an accessory virulence factor in some but not all EPEC strains.


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