StcE, a metalloprotease secreted by Escherichia coli O157:H7, specifically cleaves C1 esterase inhibitor

StcE — металлопротеаза, секретируемая Escherichia coli O157:H7, специфически расщепляющая ингибитор эстеразы C1
Wyndham W. Lathem, Thomas E. Grys, Sarah E. Witowski, Alfredo G. Torres, James B. Kaper, Phillip I. Tarr, Rodney A. Welch
2002-07-01

C1 esterase inhibitor cleavageEscherichia coli O157:H7StcE metalloproteaseT-cell aggregationtype II secretion pathway
Escherichia coli O157:H7 causes diarrhoea, haemorrhagic colitis, and the haemolytic uraemic syndrome. We have identified a protein of previously unknown function encoded on the pO157 virulence plasmid of E. coli O157:H7, which is the first described protease that specifically cleaves C1 esterase inhibitor (C1-INH), a member of the serine protease inhibitor family. The protein, named StcE for secreted protease of C1 esterase inhibitor from EHEC (formerly Tagn), cleaves C1-INH to produce (unique) approximately 60-65 kDa fragments. StcE does not digest other serine protease inhibitors, extracellular matrix proteins or universal protease targets. We also observed that StcE causes the aggregation of cultured human T cells but not macrophage-like cells or B cells. Substitution of aspartic acid for glutamic acid at StcE position 435 within the consensus metalloprotease active site ablates its abilities to digest C1-INH and to aggregate T cells. StcE is secreted by the etp type II secretion pathway encoded on pO157, and extracellular StcE levels are positively regulated by the LEE-encoded regulator, Ler. StcE antigen and activity were detected in the faeces of a child with an E. coli O157:H7 infection, demonstrating the expression of StcE during human disease. Cleavage of C1-INH by StcE could plausibly cause localized pro-inflammatory and coagulation responses resulting in tissue damage, intestinal oedema and thrombotic abnormalities.
1
C1-INH cleavage by StcE may promote localized pro-inflammatory and coagulation responses, potentially contributing to tissue damage, intestinal oedema, and thrombotic abnormalities.
2
Replacing glutamic acid with aspartic acid at position 435 in StcE’s consensus metalloprotease active site abolishes both C1-INH cleavage and T-cell aggregation.
3
StcE cleaves C1-INH into distinctive approximately 60–65 kDa fragments while sparing other serine protease inhibitors, extracellular matrix proteins, and universal protease substrates.
4
StcE induces aggregation of cultured human T cells but not macrophage-like cells or B cells.
5
StcE is a previously uncharacterized E. coli O157:H7 virulence-plasmid protein and the first protease reported to specifically cleave C1 esterase inhibitor.
6
StcE is secreted through the pO157-encoded Etp type II secretion pathway, positively regulated by the LEE regulator Ler, and its antigen and activity are detectable in infected human faeces.

StcE metalloprotease secreted by Escherichia coli O157:H7

Its specific cleavage of C1 esterase inhibitor, associated T-cell aggregation, metalloprotease catalytic activity, secretion, regulation, and potential inflammatory and coagulation effects

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2002-07-01
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Wyndham W. Lathem
Thomas E. Grys
Sarah E. Witowski
Alfredo G. Torres
James B. Kaper
Phillip I. Tarr
Rodney A. Welch
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