A highly sensitive and subspecies-specific surface antigen enzyme-linked immunosorbent assay for diagnosis of Johne's disease

被引:52
作者
Eda, Shigetoshi
Bannantine, John P.
Waters, W. R.
Mori, Yasuyuki
Whitlock, Robert H.
Scott, M. Cathy
Speer, C. A.
机构
[1] Univ Tennessee, Ctr Wildlife Hlth, Dept Forestry Wildlife & Fisheries, Knoxville, TN 37901 USA
[2] USDA, Bacterial Dis Liverstock Res Unit, Natl Anim Dis Ctr, Agr Res Serv, Ames, IA 50010 USA
[3] Natl Inst Anim Hlth, Paratuberculosis Res Team, Tsukuba, Ibaraki 3050856, Japan
[4] Univ Penn, New Bolton Ctr, Kennett Sq, PA 19348 USA
关键词
D O I
10.1128/CVI.00148-06
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Johne's disease (JD), or paratuberculosis, caused by Mycobacterium avium subsp. paratuberculosis, is one of the most widespread and economically important diseases of livestock and wild ruminants worldwide. Control of JD could be accomplished by diagnosis and good animal husbandry, but this is currently not feasible because commercially available diagnostic tests have low sensitivity levels and are incapable of diagnosing prepatent infections. In this study, a highly sensitive and subspecies-specific enzyme-linked immunosorbent assay was developed for the diagnosis of JD by using antigens extracted from the surface of M. avium subsp. paratuberculosis. Nine different chemicals and various intervals of agitation by vortex were evaluated for their ability to extract the surface antigens. Various quantities of surface antigens per well in a 96-well microtiter plate were also tested. The greatest differences in distinguishing between JD-positive and JD-negative serum samples by ethanol vortex enzyme-linked immunosorbent assay (EVELISA) were obtained with surface antigens dislodged from 50 mu g/well of bacilli treated with 80% ethanol followed by a 30-second interval of agitation by vortex. The diagnostic specificity and sensitivity of the EVELISA were 97.4% and 100%, respectively. EVELISA plates that had been vacuum-sealed and then tested 7 weeks later (the longest interval tested) had diagnostic specificity and sensitivity rates of 96.9 and 100%, respectively. In a comparative study involving serum samples from 64 fecal culture-positive cattle, the EVELISA identified 96.6% of the low-level fecal shedders and 100% of the midlevel and high-level shedders, whereas the Biocor ELISA detected 13.7% of the low-level shedders, 25% of the mid-level shedders, and 96.2% of the high-level shedders. Thus, the EVELISA was substantially superior to the Biocor ELISA, especially in detecting low-level and midlevel shedders. The EVELISA may form the basis for a highly sensitive and subspecies-specific test for the diagnosis of JD.
引用
收藏
页码:837 / 844
页数:8
相关论文
共 18 条
[1]  
BROWN WJ, 1989, METHOD CELL BIOL, V31, P553
[2]   A COLORIMETRIC METHOD FOR THE DETERMINATION OF SUGARS [J].
DUBOIS, M ;
GILLES, K ;
HAMILTON, JK ;
REBERS, PA ;
SMITH, F .
NATURE, 1951, 168 (4265) :167-167
[3]   New method of serological testing for Mycobacterium avium subsp paratuberculosis (Johne's disease) by flow cytometry [J].
Eda, S. ;
Elliott, B. ;
Scott, M. C. ;
Waters, W. R. ;
Bannantine, J. P. ;
Whitlock, R. H. ;
Speer, C. A. .
FOODBORNE PATHOGENS AND DISEASE, 2005, 2 (03) :250-262
[4]   Development of an ELISA technique for serodiagnosis of bovine paratuberculosis [J].
Jark, U ;
Ringena, I ;
Franz, B ;
Gerlach, GF ;
Beyerbach, M ;
Franz, B .
VETERINARY MICROBIOLOGY, 1997, 57 (2-3) :189-198
[5]   Differential changes in heat shock protein-, lipoarabinomannan-, and purified protein derivative-specific immunoglobulin G1 and G2 isotype responses during bovine Mycobacterium avium subsp paratuberculosis infection [J].
Koets, AP ;
Rutten, VPMG ;
de Boer, M ;
Bakker, D ;
Valentin-Weigand, P ;
van Eden, W .
INFECTION AND IMMUNITY, 2001, 69 (03) :1492-1498
[6]   The complete genome sequence of Mycobacterium avium subspecies paratuberculosis [J].
Li, LL ;
Bannantine, JP ;
Zhang, Q ;
Amonsin, A ;
May, BJ ;
Alt, D ;
Banerji, N ;
Kanjilal, S ;
Kapur, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (35) :12344-12349
[7]   Evaluation of three ELISAs for Mycobacterium avium subsp paratuberculosis using tissue and fecal culture as comparison standards [J].
McKenna, SLB ;
Keefe, GP ;
Barkema, HW ;
Sockett, DC .
VETERINARY MICROBIOLOGY, 2005, 110 (1-2) :105-111
[8]  
National Research Council, 2003, DIAGN CONTR JOHN DIS
[9]   Comparison of serological tests and faecal culture for the detection of Mycobacterium avium subsp. paratuberculosis infection in cattle and analysis of the antigens involved [J].
Reichel, MP ;
Kittelberger, R ;
Penrose, ME ;
Meynell, RM ;
Cousins, D ;
Ellis, T ;
Mutharia, LM ;
Sugden, EA ;
Johns, AH ;
de Lisle, GW .
VETERINARY MICROBIOLOGY, 1999, 66 (02) :135-150
[10]   EVALUATION OF 4 SEROLOGICAL TESTS FOR BOVINE PARATUBERCULOSIS [J].
SOCKETT, DC ;
CONRAD, TA ;
THOMAS, CB ;
COLLINS, MT .
JOURNAL OF CLINICAL MICROBIOLOGY, 1992, 30 (05) :1134-1139