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A variation of the amplified-fragment length polymorphism (AFLP) technique using three restriction endonucleases, and assessment of the enzyme combination Bg/II-MfeI for AFLP analysis of Salmonella enterica subsp enterica isolates
被引:21
作者:
Lindstedt, BA
[1
]
Heir, E
Vardund, T
Kapperud, G
机构:
[1] Natl Inst Publ Hlth, Dept Bacteriol, N-0403 Oslo, Norway
[2] Norwegian Sch Vet Sci, Dept Pharmacol Microbiol & Food Hyg, N-0033 Oslo, Norway
关键词:
amplified-fragment length polymorphism;
capillary electrophoresis;
Salmonella;
D O I:
10.1016/S0378-1097(00)00245-7
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
We have performed amplified-fragment length polymorphism (AFLP) fingerprinting on a collection of Salmonella enterica subsp. enterica serovar typhimurium strains with a restriction endonuclease combination (BglII and MfeI) that has previously been used successfully for typing Campylobacter jejuni isolates with high resolution. Additionally, a variation of the AFLP assay in which two rare cutting restriction enzymes (XbaI and BsrGI) in combination with the frequent cutter (HinP1I) was examined. The BglII and MfeI enzyme combination offered low resolution for genotyping Salmonella typhimurium isolates and is not recommended for this common serovar. The three-enzyme combination gave a higher discrimination, and is thus a new alternate way of performing AFLP fingerprinting of S. typhimurium. (C) 2000 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
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页码:19 / 24
页数:6
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