The Fimbriae of Enteroaggregative Escherichia coli Induce Epithelial Inflammation In Vitro and in a Human Intestinal Xenograft Model

EJ Boll, C Struve, A Sander, Z Demma… - The Journal of …, 2012 - academic.oup.com
EJ Boll, C Struve, A Sander, Z Demma, JP Nataro, BA McCormick, KA Krogfelt
The Journal of infectious diseases, 2012academic.oup.com
Abstract Background. Enteroaggregative Escherichia coli (EAEC) are increasingly
recognized as an important agent of inflammatory and often persistent diarrhea. Although
previous studies report on the inflammatory aspects of EAEC pathogenesis, the mechanisms
by which EAEC trigger these events are not well understood. Methods. EAEC strains
harboring mutations in known EAEC virulence determinants were tested in an in vitro model
of transepithelial migration of polymorphonuclear neutrophils (PMNs) and in human …
Abstract
Background. Enteroaggregative Escherichia coli (EAEC) are increasingly recognized as an important agent of inflammatory and often persistent diarrhea. Although previous studies report on the inflammatory aspects of EAEC pathogenesis, the mechanisms by which EAEC trigger these events are not well understood.
Methods. EAEC strains harboring mutations in known EAEC virulence determinants were tested in an in vitro model of transepithelial migration of polymorphonuclear neutrophils (PMNs) and in human intestinal xenografts in severe-combined immunodeficient (SCID-HU-INT) mice, a novel model for studying EAEC disease in vivo.
Results. Expression of aggregative adherence fimbriae (AAFs), the principal adhesins of EAEC, was required for EAEC-induced PMN transepithelial migration in vitro. Moreover, constructed plasmids encoding AAF gene clusters demonstrated that the AAF adhesins are sufficient for triggering this event in a nonpathogenic E. coli background. Furthermore, with use of the SCID-HU-INT mouse model, severe tissue damage and infiltration of inflammatory cells was observed in the human tissue after EAEC infection. These pathological marks were strongly related to AAF expression, thus clearly confirming our in vitro findings.
Conclusions. The present work establishes EAEC as an important inflammatory pathogen and the AAF adhesins as inducers of potentially detrimental immune responses.
Oxford University Press