Establishment of highly specific and quantitative immunoassay systems for staphylococcal enterotoxin A, B, and C using newly-developed monoclonal antibodies

被引:19
作者
Sasaki, T
Terano, Y
Shibata, T
Kawamoto, H
Kuzuguchi, T
Kohyama, E
Watanabe, T
Ohyama, T
Gemba, M
机构
[1] Osaka Univ Pharmaceut Sci, Div Pharmacol, Takatsuki, Osaka 5691094, Japan
[2] Osaka Prefectural Inst Publ Hlth, Div Food Microbiol, Osaka, Osaka 5370025, Japan
[3] Gifu Prefectural Inst Bioind Technol, Dept Mol Microbiol, Gifu 5050004, Japan
[4] Tokyo Univ Agr, Fac Bioind, Dept Food Sci & Technol, Abashiri, Hokkaido 0992493, Japan
关键词
staphylococcal food poisoning; staphylococcal enterotoxins; avidin-biotin sandwich ELISA;
D O I
10.1111/j.1348-0421.2005.tb03650.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Staphylococcal enterotoxin (SE) activities remain after boiling or treating with proteases. The main symptoms such as vomiting and diarrhea, are caused by the ingestion of SEs. Among SEs, SEA has been reported to be the major and most toxic protein. A highly specific and simple assay system is required to diagnose staphylococcal food poisoning. Therefore, the development of a suitable assay system is strongly anticipated. In this study, we have established a highly specific and sensitive avidin-biotin sandwich ELISA (ABS-ELISA) system for SEA, SEB, and SECI using newly-developed monoclonal antibodies. The linearity of these systems obtained was in the range of 0.78-25 ng/ml for each SE, and furthermore, the lower concentrations of SEs could also be detected. The recoveries of SEs from murine serum, skim milk solution, and raw milk were found to be over 90%, suggesting that our systems could detect SEs without any interventions, such as these from milk or serum proteins. We were also able to quantify SEs in 22 specimens of culture supernatants of S. aureus isolated in past occurrences. Our established system should be very useful not only in the clinical field but also in various fields of investigation because of its quantification and simplicity in detecting SEs.
引用
收藏
页码:589 / 597
页数:9
相关论文
共 51 条
[11]   Bovine mammary immune response to an experimental intramammary infection with a Staphylococcus aureus strain containing a gene for staphylococcal enterotoxin C1 [J].
Ebling, TL ;
Fox, LK ;
Bayles, KW ;
Bohach, GA ;
Byrne, KM ;
Davis, WC ;
Ferens, WA ;
Hillers, JK .
JOURNAL OF DAIRY SCIENCE, 2001, 84 (09) :2044-2050
[12]   QUANTITATIVE-DETERMINATION OF STAPHYLOCOCCAL ENTEROTOXIN-A BY AN ENZYME-LINKED IMMUNOSORBENT-ASSAY USING A COMBINATION OF POLYCLONAL AND MONOCLONAL-ANTIBODIES AND BIOTIN-STREPTAVIDIN INTERACTION [J].
EDWIN, C .
JOURNAL OF CLINICAL MICROBIOLOGY, 1989, 27 (07) :1496-1501
[13]   Characterization of a putative pathogenicity island from bovine Staphylococcus aureus encoding multiple superantigens [J].
Fitzgerald, JR ;
Monday, SR ;
Foster, TJ ;
Bohach, GA ;
Hartigan, PJ ;
Meaney, WJ ;
Smyth, CJ .
JOURNAL OF BACTERIOLOGY, 2001, 183 (01) :63-70
[14]   ENZYME-LINKED IMMUNOSORBENT-ASSAY FOR DETECTION OF STAPHYLOCOCCAL ENTEROTOXINS IN FOODS [J].
FREED, RC ;
EVENSON, ML ;
REISER, RF ;
BERGDOLL, MS .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1982, 44 (06) :1349-1355
[15]   DIRECT BINDING OF SECRETED T-CELL RECEPTOR BETA CHAIN TO SUPERANTIGEN ASSOCIATED WITH CLASS-II MAJOR HISTOCOMPATIBILITY COMPLEX PROTEIN [J].
GASCOIGNE, NRJ ;
AMES, KT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (02) :613-616
[16]   DOUBLE-SANDWICH ENZYME-LINKED-IMMUNOSORBENT-ASSAY (ELISA) WITH MURINE MONOCLONAL-ANTIBODIES FOR DETECTION OF STAPHYLOCOCCAL-ENTEROTOXIN-B [J].
GOYACHE, J ;
ORDEN, JA ;
BLANCO, JL ;
DOMENECH, A ;
SUAREZ, G ;
GOMEZLUCIA, E .
JOURNAL OF VETERINARY MEDICINE SERIES B-ZENTRALBLATT FUR VETERINARMEDIZIN REIHE B-INFECTIOUS DISEASES AND VETERINARY PUBLIC HEALTH, 1994, 41 (10) :639-644
[17]   BIOLOGICAL-ACTIVITIES OF STAPHYLOCOCCAL-ENTEROTOXIN TYPE-A MUTANTS WITH N-TERMINAL SUBSTITUTIONS [J].
HARRIS, TO ;
BETLEY, MJ .
INFECTION AND IMMUNITY, 1995, 63 (06) :2133-2140
[18]  
HERTEL A, 1990, NUKLEARMED, V29, P221
[19]   Emesis in the shrew mouse (Suncus murinus) induced by peroral and intraperitoneal administration of staphylococcal enterotoxin A [J].
Hu, DL ;
Omoe, K ;
Shimura, H ;
Ono, K ;
Sugii, S ;
Shinagawa, K .
JOURNAL OF FOOD PROTECTION, 1999, 62 (11) :1350-1353
[20]   Epitope analysis of staphylococcal enterotoxin A using different synthetic peptides [J].
Hu, DL ;
Imai, A ;
Ono, K ;
Sasaki, S ;
Nakane, A ;
Sugii, S ;
Shinagawa, K .
JOURNAL OF VETERINARY MEDICAL SCIENCE, 1998, 60 (09) :993-996