Affiliation:
1. Departments of Pathology and Laboratory Medicine
2. Molecular Biology Institute, University of California, Los Angeles, California 90095
3. Santarus, Inc., San Diego, California 92130
Abstract
ABSTRACT
Commensal bacteria have emerged as an important disease factor in human Crohn's disease (CD) and murine inflammatory bowel disease (IBD) models. We recently isolated I2, a novel gene segment of microbial origin that is associated with human CD and that encodes a T-cell superantigen. To identify the I2 microorganism, BLAST analysis was used to identify a microbial homologue, PA2885, a novel open reading frame (ORF) in the
Pseudomonas aeruginosa
genome. PCR and Southern analysis identified
Pseudomonas fluorescens
as the originating species of I2, with homologues detectable in 3 of 13 other
Pseudomonas
species. Genomic cloning disclosed a locus containing the full-length I2 gene (
pfiT
) and three other orthologous genes, including a homologue of the
pbrA/pvdS
iron response gene. CD4
+
T-cell responses to recombinant proteins were potent for I2 and
pfiT
, but modest for PA2885.
pfiT
has several features of a virulence factor: association with an iron-response locus, restricted species distribution, and T-cell superantigen bioactivity. These findings suggest roles for
pfiT
and
P. fluorescens
in the pathogenesis of Crohn's disease.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
114 articles.
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