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Journal of Clinical Microbiology, April 2001, p. 1633-1637, Vol. 39, No. 4
School of Pharmacy and Medical Sciences,
University of South Australia,1 and
Infectious Diseases Laboratories, Institute of Medical and
Veterinary Science,2 Adelaide 5000, Australia
Received 9 October 2000/Returned for modification 19 December
2000/Accepted 29 January 2001
Linear B-cell epitopes of the Rhodococcus equi
virulence-associated protein (VapA) were mapped using a synthetic
peptide bank in this study. The peptides were screened in an
enzyme-linked immunosorbent assay (ELISA) with a total of 70 sera from
foals with current R. equi disease (51 sera), as well as
from foals that had either recovered from R. equi infection
10 months previously (3 sera) or that had no known history of R. equi disease (16 sera). An epitope with the sequence
NLQKDEPNGRA was identified and was universally recognized by
all 51 sera from foals with R. equi disease and was not
recognized by any of the other sera. There was poor reactivity between
all sera and peptides relating to other areas of the VapA protein. It
is proposed that an ELISA based upon a defined peptide epitope may be
used in an improved serological diagnostic test for R. equi
infection in foals.
0095-1137/01/$04.00+0 DOI: 10.1128/JCM.39.4.1633-1637.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
B-Cell Epitope Mapping of the VapA Protein of
Rhodococcus equi: Implications for Early Detection of
R. equi Disease in Foals
*
Corresponding author. Mailing Address: Infectious
Diseases Laboratories, Institute of Medical and Veterinary Science,
Adelaide 5000, Australia. Phone: (08) 8222-3275. Fax: (08) 8222-3543. E-mail: heuzenroeder{at}imvs.sa.gov.au.
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