Clinical and Diagnostic Laboratory Immunology, July 1998, p. 446-451, Vol. 5, No. 4
1071-412X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Histology Unit1 and
Experimental Immunology Unit,
Received 1 October 1997/Returned for modification 25 November
1997/Accepted 6 April 1998
We have previously described the cloning and sequencing of a gene
portion coding for the terminal part of a 34-kDa protein of
Mycobacterium avium subsp. paratuberculosis,
the etiological agent of Johne's disease (P. Gilot, M. De Kesel,
L. Machtelinckx, M. Coene, and C. Cocito, J. Bacteriol. 175:4930-4935,
1993). The recombinant polypeptide (a362) carries species-specific
B-cell epitopes which do not cross-react with other mycobacterial
pathogens (M. De Kesel, P. Gilot, M.-C. Misonne, M. Coene, and C. Cocito, J. Clin. Microbiol. 31:947-954, 1993). The present work
describes the preparation of polyclonal and monoclonal antibodies
directed against a362 and the use of these immunoglobulins for
histopathological diagnosis of Johne's disease. The new
immunohistological procedures herewith detailed proved to be able to
identify M. avium subsp. paratuberculosis antigens in the intestinal tissues and
lymph nodes of cattle affected by either the paucibacillary or
pluribacillary form of the disease. They yielded negative responses not
only with healthy animals but also with those affected by tuberculosis (Mycobacterium bovis). Both immunohistological procedures
proved to be as sensitive as or more sensitive than
Ziehl-Neelsen staining and, in addition, to be endowed with species
specificity.
*
Corresponding author. Mailing address:
GEMO-ISTO-UCL-5225, Ave. Mounier 52, Brussels 1200, Belgium. Phone and
fax: 32-2-764-5225.
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