Atypical EnteropathogenicEscherichia coliSecretes Plasmid Encoded Toxin
Author(s) -
Rita C. Ruiz,
Keyde Cristina Martins de Melo,
Sarita S. Rossato,
Camila M. Barbosa,
Lívia M. Corrêa,
Waldir P. Elias,
Roxane Maria Fontes Piazza
Publication year - 2014
Publication title -
biomed research international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.772
H-Index - 126
eISSN - 2314-6141
pISSN - 2314-6133
DOI - 10.1155/2014/896235
Subject(s) - microbiology and biotechnology , enteroaggregative escherichia coli , escherichia coli , enteropathogenic escherichia coli , serine protease , biology , cytotoxic t cell , toxin , plasmid , enterotoxin , diarrhea , virology , protease , enterobacteriaceae , in vitro , medicine , dna , biochemistry , enzyme , gene
Plasmid encoded toxin (Pet) is a serine protease originally described in enteroaggregative Escherichia coli (EAEC) prototype strain 042 whose entire characterization was essentially obtained from studies performed with the purified toxin. Here we show that Pet is not exclusive to EAEC. Atypical enteropathogenic Escherichia coli (aEPEC) strains, isolated from diarrhea cases, express Pet and its detection in supernatants of infected HEp-2 cells coincides with the appearance of cell damage, which, in turn, were similar to those described with purified Pet. Pet secretion and the cytotoxic effects are time and culture medium dependent. In presence of DMEM supplemented with tryptone cell rounding and detachment were observed after just 5 h of incubation with the bacteria. In the absence of tryptone, the cytotoxic effects were detected only after 24 h of infection. We also show that, in addition to the prototype EAEC, other pet + EAEC strains, also isolated from diarrhea cases, induce cellular damage in the same degree as the aEPEC. The cytotoxic effects of EAEC and aEPEC strains were significantly reduced in the presence of a serine protease inhibitor or anti-Pet IgG serum. Our results show a common aspect between the aEPEC and EAEC and provide the first evidence pointing to a role of Pet in aEPEC pathogenesis.
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