Detection of Mycobacterium bovis lymphocyte stimulating antigens in culture filtrates of a recombinant Mycobacterium smegmatis cosmid library

被引:9
作者
Gormley, E
Fray, L
Sandall, L
Ke, GP
Dupont, C
Carpenter, E
机构
[1] Massey Univ, Dept Vet Pathol & Publ Hlth, Bovine TB Res Lab, Palmerston North, New Zealand
[2] ILRI, Nairobi, Kenya
关键词
Mycobacterium bovis BCG; vaccines; lymphocytes; antigens; bovine tuberculosis;
D O I
10.1016/S0264-410X(99)00091-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Culture filtrates derived from a Mycobacterium bovis cosmid library in Mycobacterium smegmatis were screened for bovine lymphocyte stimulatory antigens using peripheral blood mononuclear cells (PBMC) from cattle vaccinated with a low dose of Mycobacterium bovis BCG. Lymphocyte proliferation and interferon-gamma (IFN-gamma) production were used as cellular response markers for antigen recognition. In the primary screen, approximately 28% of all culture filtrates (CF) stimulated responses by PBMC from at least two out of four vaccinated cattle. In one of these CF, the M. bovis Ag85-B antigen was detected by Western-blot analysis. Despite heterogeneous lymphocyte responses of the animals, twenty-four of the culture filtrates stimulated lymphocyte proliferation and IFN-gamma production from at least six out of eight vaccinated animals in a secondary screen. Analysis of the cosmid DNA associated with these positive CF demonstrated that several contained homologous DNA sequences. It appears that the lymphocyte screening has detected M. bovis antigens that are immuno-dominant in cattle vaccinated with,M. bovis BCG. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2792 / 2801
页数:10
相关论文
共 45 条
[31]   Predominant recognition of the ESAT-6 protein in the first phase of infection with Mycobacterium bovis in cattle [J].
Pollock, JM ;
Andersen, P .
INFECTION AND IMMUNITY, 1997, 65 (07) :2587-2592
[32]  
ROBERTS AD, 1995, IMMUNOLOGY, V85, P502
[33]   Expression of Mycobacterium tuberculosis MPT64 in recombinant Myco-smegmatis: Purification, immunogenicity and application to skin tests for tuberculosis [J].
Roche, PW ;
Winter, N ;
Triccas, JA ;
Feng, CG ;
Britton, WJ .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 1996, 103 (02) :226-232
[34]   A SANDWICH ENZYME-IMMUNOASSAY FOR BOVINE INTERFERON-GAMMA AND ITS USE FOR THE DETECTION OF TUBERCULOSIS IN CATTLE [J].
ROTHEL, JS ;
JONES, SL ;
CORNER, LA ;
COX, JC ;
WOOD, PR .
AUSTRALIAN VETERINARY JOURNAL, 1990, 67 (04) :134-137
[35]  
Sambrook J., 1989, MOL CLONING
[36]   HETEROGENEITY OF THE REPERTOIRE OF T-CELLS OF TUBERCULOSIS PATIENTS AND HEALTHY CONTACTS TO MYCOBACTERIUM-TUBERCULOSIS ANTIGENS SEPARATED BY HIGH-RESOLUTION TECHNIQUES [J].
SCHOEL, B ;
GULLE, H ;
KAUFMANN, SHE .
INFECTION AND IMMUNITY, 1992, 60 (04) :1717-1720
[37]   Definition of Mycobacterium tuberculosis culture filtrate proteins by two-dimensional polyacrylamide gel electrophoresis, N-terminal amino acid sequencing, and electrospray mass spectrometry [J].
Sonnenberg, MG ;
Belisle, JT .
INFECTION AND IMMUNITY, 1997, 65 (11) :4515-4524
[38]  
SORENSEN AL, 1995, INFECT IMMUN, V63, P1710
[39]  
SURCEL HM, 1994, IMMUNOLOGY, V81, P171
[40]   COMPLETE NUCLEOTIDE-SEQUENCE OF IMMUNOGENIC PROTEIN-MPB70 FROM MYCOBACTERIUM-BOVIS BCG [J].
TERASAKA, K ;
YAMAGUCHI, R ;
MATSUO, K ;
YAMAZAKI, A ;
NAGAI, S ;
YAMADA, T .
FEMS MICROBIOLOGY LETTERS, 1989, 58 (2-3) :273-276