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Infection and Immunity, July 2004, p. 3724-3732, Vol. 72, No. 7
0019-9567/04/$08.00+0     DOI: 10.1128/IAI.72.7.3724-3732.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Mycobacterium avium subsp. paratuberculosis Fibronectin Attachment Protein Facilitates M-Cell Targeting and Invasion through a Fibronectin Bridge with Host Integrins

T. E. Secott,{dagger} T. L. Lin, and C. C. Wu*

Department of Veterinary Pathobiology, Purdue University, West Lafayette, Indiana 47907

Received 11 July 2003/ Returned for modification 23 September 2003/ Accepted 9 March 2004

Efficient attachment and ingestion of Mycobacterium avium subsp. paratuberculosis by cultured epithelial cells requires the expression of a fibronectin (FN) attachment protein homologue (FAP-P) which mediates FN binding by M. avium subsp. paratuberculosis. Invasion of Peyer's patches by M. avium subsp. paratuberculosis occurs through M cells, which, unlike other intestinal epithelial cells, express integrins on their luminal faces. We sought to determine if the interaction between FAP-P of M. avium subsp. paratuberculosis and soluble FN enabled targeting and invasion of M cells by M. avium subsp. paratuberculosis in vivo via these surface integrins. Wild-type and antisense FAP-P mutant M. avium subsp. paratuberculosis strains were injected alone or coinjected with blocking peptides or antibodies into murine gut loops, and immunofluorescence microscopy was performed to assess targeting and invasion of M cells by M. avium subsp. paratuberculosis. Nonopsonized M. avium subsp. paratuberculosis preferentially invaded M cells in murine gut loops. M-cell invasion was enhanced 2.6-fold when M. avium subsp. paratuberculosis was pretreated with FN. Invasion of M cells by the antisense FAP-P mutant of M. avium subsp. paratuberculosis was reduced by 77 to 90% relative to that observed for the control strains. Peptides corresponding to the RGD and synergy site integrin recognition regions of FN blocked M. avium subsp. paratuberculosis invasion of M cells by 75 and 45%, respectively, whereas the connecting segment 1 peptide was noninhibitory. Antibodies against the {alpha}5, {alpha}V, ß1, and ß3 integrin subunits inhibited M-cell invasion by 52 to 73%. The results indicate that targeting and invasion of M cells by M. avium subsp. paratuberculosis in vivo is mediated primarily by the formation of an FN bridge formed between FAP-P of M. avium subsp. paratuberculosis and integrins on M cells.


* Corresponding author. Mailing address: Department of Veterinary Pathobiology, Purdue University, 406 S. University St., West Lafayette, IN 47907. Phone: (765) 494-7459. Fax: (765) 494-9181. E-mail: wuc{at}purdue.edu.

Editor: S. H. E. Kaufmann

{dagger} Present address: Department of Biological Sciences, Minnesota State University, Mankato, MN 56001.


Infection and Immunity, July 2004, p. 3724-3732, Vol. 72, No. 7
0019-9567/04/$08.00+0     DOI: 10.1128/IAI.72.7.3724-3732.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.




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