| Literature DB >> 18718748 |
Kenichi Tadokoro1, Toshikazu Yamaguchi, Katsumi Kawamura, Hajime Shimizu, Toru Egashira, Masato Minabe, Toshiaki Yoshino, Hirokazu Oguchi.
Abstract
The Invader PLUS technology is a sensitive, rapid method for the detection and quantification of nucleic acid. While the original technology is based on the amplification by polymerase chain reaction (PCR) of the target sequence followed by its detection using the Invader technology, the current modification allows simultaneous PCR amplification and Invader reaction. The PCR primers and the Invader probes are designed to operate at the same temperature. This allows simpler design and faster results. This technology has been applied for the quantification of six periodontitis-related bacteria (Actinobacillus actinomycetemcomitans, Porphyromonas gingivalis, Prevotella intermedia, Toreponema denticola, Tannerella forsythensis and Fusobacterium nucleatum). Direct comparison of this modified Invader PLUS with real-time PCR demonstrated similar linear range. Furthermore, testing of 64 volunteers showed a good correlation between both technologies with correlation factors r2 spanning between 0.827 and 0.987. We demonstrated here that the proposed improvement of the Invader PLUS allows the detection and quantification of DNA sequences using a simple design and protocol that can be implemented in clinical testing.Entities:
Mesh:
Substances:
Year: 2008 PMID: 18718748 DOI: 10.1016/j.micres.2008.06.001
Source DB: PubMed Journal: Microbiol Res ISSN: 0944-5013 Impact factor: 5.415