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Infection and Immunity, October 2001, p. 6044-6054, Vol. 69, No. 10
0019-9567/01/$04.00+0   DOI: 10.1128/IAI.69.10.6044-6054.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Molecular Cloning of a Bacteroides caccae TonB-Linked Outer Membrane Protein Identified by an Inflammatory Bowel Disease Marker Antibody

Bo Wei,1 Harnisha Dalwadi,1 Lynn K. Gordon,2 Carol Landers,3 David Bruckner,1 Stephan R. Targan,3,4 and Jonathan Braun1,5,*

Departments of Pathology and Laboratory Medicine,1 Ophthalmology,2 and Medicine4 and Molecular Biology Institute,5 University of California, Los Angeles, California 90095, and Inflammatory Bowel Disease Research Center, Cedars-Sinai Medical Center, Los Angeles, California 900483

Received 13 October 2000/Returned for modification 7 December 2000/Accepted 10 July 2001

Commensal enteric bacteria are a required pathogenic factor in inflammatory bowel disease (IBD), but the identity of the pertinent bacterial species is unresolved. Using an IBD-associated pANCA monoclonal antibody, a 100-kDa protein was recently characterized from an IBD clinical isolate of Bacteroides caccae (p2Lc3). In this study, consensus oligonucleotides were designed from 100-kDa peptides and used to identify a single-copy gene from the p2Lc3 genome. Sequence analysis of the genomic clone revealed a 2,844-bp (948 amino acid) open reading frame encoding features typical of the TonB-linked outer membrane protein family. This gene, termed ompW, was detected by Southern analysis only in B. caccae and was absent in other species of Bacteroides and gram-negative coliforms. The closest homologues of OmpW included the outer membrane proteins SusC of Bacteroides thetaiotaomicron and RagA of Porphyromonas gingivalis. Recombinant OmpW protein was immunoreactive with the monoclonal antibody, and serum anti-OmpW immunoglobulin A levels were elevated in a Crohn's disease patient subset. These findings suggest that OmpW may be a target of the IBD-associated immune response and reveal its structural relationship to a bacterial virulence factor of P. gingivalis and periodontal disease.


* Corresponding author. Mailing address: Department of Pathology and Lab Medicine, UCLA School of Medicine, CHS 13-222, Los Angeles, CA 90095-1732. Phone: (310) 794-7953. Fax: (310) 825-5674. E-mail: jbraun{at}mednet.ucla.edu.


Infection and Immunity, October 2001, p. 6044-6054, Vol. 69, No. 10
0019-9567/01/$04.00+0   DOI: 10.1128/IAI.69.10.6044-6054.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



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