Klemsdal S S, Elen O
The Norwegian Crop Research Institute, Plant Protection Centre, Norway.
Lett Appl Microbiol. 2006 May;42(5):544-8. doi: 10.1111/j.1472-765X.2006.01880.x.
The aim of the study was to develop a sensitive detection method of Fusarium culmorum contamination in cereal samples.
A nested-PCR method using a single closed tube was developed for the detection of F. culmorum in infected cereal samples. The concentrations of the first primer pair was diluted 10,000 times compared to the concentration used for the second primer pair. Differing annealing temperatures allowed both first and second polymerase chain reaction (PCR) reactions to be performed subsequently in the same closed tube. The detection limit was 5-50 fg of purified target DNA and allowed the detection of 1% infected seeds of wheat in a mixture with uninfected grains.
F. culmorum can be specifically detected in cereal samples by the highly sensitive method of nested-PCR in a single closed tube.
This work describes the detection of F. culmorum in cereal samples that is approximately 100 times more sensitive than previous PCR methods, involves low risk of cross contaminations between samples, low costs and reduced hands-on time as compared to standard nested-PCR protocols.
本研究的目的是开发一种灵敏的检测谷物样品中禾谷镰刀菌污染的方法。
开发了一种使用单个封闭管的巢式PCR方法,用于检测受感染谷物样品中的禾谷镰刀菌。与用于第二对引物的浓度相比,第一对引物的浓度稀释了10000倍。不同的退火温度使得第一和第二次聚合酶链反应(PCR)能够随后在同一封闭管中进行。检测限为5-50 fg的纯化靶DNA,能够在与未感染谷物的混合物中检测出1%受感染的小麦种子。
通过在单个封闭管中进行巢式PCR的高灵敏方法,可以在谷物样品中特异性检测出禾谷镰刀菌。
这项工作描述了在谷物样品中检测禾谷镰刀菌的方法,其灵敏度比以前的PCR方法高约100倍,与标准巢式PCR方案相比,样品间交叉污染风险低、成本低且实际操作时间减少。