Analysis of Fusarium graminearum mycotoxins in different biological matrices by LC/MS

被引:43
作者
Bily, AC
Reid, LM
Savard, ME
Reddy, R
Blackwell, BA
Campbell, CM
Krantis, A
Durst, T
Philogène, BJR
Arnason, JT
Regnault-Roger, C
机构
[1] Univ Pau & Pays Adour, Inst Biol Environm Aquitaine Sud, Dept Sci Biol, Lab Ecol Mol, F-64000 Pau, France
[2] Univ Ottawa, Dept Biol, Ottawa, ON K1N 6N5, Canada
[3] Univ Ottawa, Dept Chem, Ottawa, ON K1N 6N5, Canada
[4] Agr & Agri Food Canada, Cent Expt Farm, Eastern Cereal & Oilseed Res Ctr, Ottawa, ON K1A 0C6, Canada
[5] Univ Ottawa, Dept Cell & Mol Med, Ottawa, ON K1H 8M5, Canada
关键词
LC/MS; Fusarium graminearum; matrices; deoxynivalenol; zearalenone; toxicokinetic;
D O I
10.1023/B:MYCO.0000012218.27359.ec
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The purpose of this study was to develop an LC/MS assay to accurately detect three mycotoxins produced by Fusarium graminearum in various matrices. Using different LC conditions, deoxynivalenol ( DON), 15-acetyldeoxynivalenol (15-ADON), and zearalenone (ZEN) were detected in four different matrices (fungal liquid cultures, maize grain, insect larvae and pig serum). The sensitivity of MS detection allowed us to detect concentrations as low as 8 ppb of DON and 12 ppb of ZEN. A very small quantity of matrix was therefore necessary for successful analysis of these toxins and a variety of experimental situations were successfully investigated using this technique. Production of 15-ADON and butenolide was monitored in a liquid culture of F. graminearum under controlled conditions. Using simple extraction procedures, the differential accumulation of DON and 15-ADON was followed in inoculated maize genotypes varying in susceptibility to F. graminearum. Toxicokinetic studies were carried out with maize insect pests reared continually on artificial diets containing ZEN and suggested that larvae may possess the ability to degrade ZEN. Finally, persistence of DON was assessed in pigs fed diet supplemented with DON, results indicated that DON accumulates quickly in pig blood and then levels decline progressively for 12 hours thereafter. The LC/MS study reported here is very useful and flexible for the detection of these mycotoxins in different media and at very low concentrations.
引用
收藏
页码:117 / 126
页数:10
相关论文
共 32 条
[1]   Quantitative determination and structure elucidation of type A- and B-trichothecenes by HPLC/ion trap multiple mass spectrometry [J].
Berger, U ;
Oehme, M ;
Kuhn, F .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1999, 47 (10) :4240-4245
[2]  
Duvick J, 1998, DEV PLANT PATHOL, V13, P369
[3]  
ELSHARKAWY S, 1987, J ORG CHEM, V53, P515
[4]  
Feng-Qin Li, 1999, Natural Toxins, V7, P93, DOI 10.1002/(SICI)1522-7189(199905/06)7:3<93::AID-NT45>3.0.CO
[5]  
2-5
[6]  
GUTHRIE WD, 1985, HDB INSECT REARING, V2, P78
[7]  
KUIPERGOODMAN T, 2001, P 2 CAN WORKSH FUS H, P6
[8]   Instrumental methods for determination of nonmacrocyclic trichothecenes in cereals, foodstuffs and cultures [J].
Langseth, W ;
Rundberget, T .
JOURNAL OF CHROMATOGRAPHY A, 1998, 815 (01) :103-121
[9]   Fusarium Tri8 encodes a trichothecene C-3 esterase [J].
McCormick, SP ;
Alexander, NJ .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2002, 68 (06) :2959-2964
[10]   FUSARIUM TOXINS IN FIELD CORN .1. TIME COURSE OF FUNGAL GROWTH AND PRODUCTION OF DEOXYNIVALENOL AND OTHER MYCOTOXINS [J].
MILLER, JD ;
YOUNG, JC ;
TRENHOLM, HL .
CANADIAN JOURNAL OF BOTANY-REVUE CANADIENNE DE BOTANIQUE, 1983, 61 (12) :3080-3087