A COMPARATIVE-STUDY OF THE FDA AND USDA METHODS FOR THE DETECTION OF LISTERIA-MONOCYTOGENES IN FOODS

被引:42
作者
WARBURTON, DW
FARBER, JM
ARMSTRONG, A
CALDEIRA, R
HUNT, T
MESSIER, S
PLANTE, R
TIWARI, NP
VINET, J
机构
[1] MANITOBA RES COUNCIL,WINNIPEG,MANITOBA,CANADA
[2] AGR CANADA,HYG VET LAB,ST HYACINTHE,QUEBEC,CANADA
[3] COMMUNAUTE URBAINE MONTREAL,SERV ENVIRONNEMENT,MONTREAL,QUEBEC,CANADA
[4] ALBERTA DEPT AGR,FOOD LAB SERV BRANCH,EDMONTON,ALBERTA,CANADA
[5] HLTH & WELF CANADA,HLTH PROTECT BRANCH,BUR MICROBIAL HAZARDS,DIV RES,OTTAWA K1A 0L2,ONTARIO,CANADA
[6] HLTH & WELF CANADA,HLTH PROTECT BRANCH,FOOD STAT & OPERAT PLANNING,VANIER,ONTARIO,CANADA
[7] INSPECT POISSON LAB,LONGUEIUIL,QUEBEC,CANADA
关键词
LISTERIA-MONOCYTOGENES; FRASER BROTH; INCUBATION TIME; SELECTIVE MEDIA;
D O I
10.1016/0168-1605(91)90053-R
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Nineteen laboratories across Canada took part in a comparative study of the 'FDA' and 'USDA' methods for the detection of Listeria monocytogenes in foods and environmental samples. The results show that the enrichment period of the FDA method can be shortened from 7 to 2 days without substantially reducing the number of positive samples. With a limited number of samples, the USDA method proved to be slightly more efficient in isolating L. monocytogenes than the FDA method. Fraser broth, in principle, proved to be useful as a screening tool but is not very selective. Oxford agar and lithium chloride-phenylethanol-moxalactam medium were better than modified McBride's agar in isolating this microorganism.
引用
收藏
页码:105 / 117
页数:13
相关论文
共 19 条
[1]   RECOVERY AND SEROTYPE DISTRIBUTION OF LISTERIA-MONOCYTOGENES FROM BROILER-CHICKENS IN THE SOUTHEASTERN UNITED-STATES [J].
BAILEY, JS ;
FLETCHER, DL ;
COX, NA .
JOURNAL OF FOOD PROTECTION, 1989, 52 (03) :148-150
[2]  
CASSIDAY P K, 1989, Food Microbiology (London), V6, P113, DOI 10.1016/S0740-0020(89)80045-0
[3]   EVALUATION OF 3 NEWLY DEVELOPED DIRECT PLATING MEDIA TO ENUMERATE LISTERIA-MONOCYTOGENES IN FOODS [J].
CASSIDAY, PK ;
BRACKETT, RE ;
BEUCHAT, LR .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1989, 55 (06) :1645-1648
[4]   QUANTITATIVE-EVALUATION OF 3 SELECTIVE ENRICHMENT BROTHS AND AGARS USED IN RECOVERING LISTERIA MICROORGANISMS [J].
FERNANDEZGARAYZABAL, J ;
GENIGEORGIS, C .
JOURNAL OF FOOD PROTECTION, 1990, 53 (02) :105-110
[5]   RAPID DETECTION OF LISTERIA SPP IN FOOD AND ENVIRONMENTAL-SAMPLES BY ESCULIN HYDROLYSIS [J].
FRASER, JA ;
SPERBER, WH .
JOURNAL OF FOOD PROTECTION, 1988, 51 (10) :762-765
[6]   EVALUATION OF SELECTIVE DIRECT PLATING MEDIA FOR THEIR SUITABILITY TO RECOVER UNINJURED, HEAT-INJURED, AND FREEZE-INJURED LISTERIA-MONOCYTOGENES FROM FOODS [J].
GOLDEN, DA ;
BEUCHAT, LR ;
BRACKETT, RE .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1988, 54 (06) :1451-1456
[7]   LISTERIA SPP FOUND ON FRESH-MARKET PRODUCE [J].
HEISICK, JE ;
WAGNER, DE ;
NIERMAN, ML ;
PEELER, JT .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1989, 55 (08) :1925-1927
[8]   COMPARISON OF 4 PROCEDURES TO DETECT LISTERIA SPP IN FOODS [J].
HEISICK, JE ;
HARRELL, FM ;
PETERSON, EH ;
MCLAUGHLIN, S ;
WAGNER, DE ;
WESLEY, IV ;
BRYNER, J .
JOURNAL OF FOOD PROTECTION, 1989, 52 (03) :154-157
[9]  
LAMMERDING AM, 1989, INT J FOOD MICROBIOL, V9, P249, DOI [10.1016/0168-1605(89)90094-9, 10.1016/S0168-1605(00)00363-9]
[10]   IMPROVED LISTERIA-MONOCYTOGENES SELECTIVE AGAR [J].
LEE, WH ;
MCCLAIN, D .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1986, 52 (05) :1215-1217