Evaluation of the performance of LNA and MGB probes in 5′-nuclease PCR assays

被引:66
作者
Letertre, C
Perelle, S
Dilasser, F
Arar, K
Fach, P
机构
[1] AFSSA, Lab Etud & Rech Hyg & Qual Aliments, Unite Atelier Biotechnol, F-94700 Maisons Alfort, France
[2] Proligo, F-75011 Paris, France
关键词
Minor Groove Binder; Locked Nucleic Acids; TaqMan probes; 5 '-nuclease PCR;
D O I
10.1016/j.mcp.2003.08.004
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The aim of this study was to evaluate the use of Locked Nucleic Acids (LNA) probes in 5'-nuclease PCR, by comparison with Minor Groove Binder (MGB) probes routinely practiced in laboratories on ABI Prism 7700. The comparison was made using a collection of Staphylococcus aureus strains that have already been characterized by MGB 5'-nuclease PCR assays in a previous study [Mol Cell Probes, submitted for publication]. The sensitivity and specificity of 5'-nuclease PCR assays targeting the Staphylococcal enterotoxin genes sea to see were compared and showed that the LNA and MGB methods were equivalent. In conclusion, the LNA 5'-nuclease PCR assays developed in this work provide a specific and sensitive alternative to the well-established MGB 5'-nuclease PCR assays used for the rapid detection of bacterial pathogens genes on ABI Prism 7700. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:307 / 311
页数:5
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