Literature DB >> 20093759

Novel high-speed real-time PCR method (Hyper-PCR): results from its application to adenovirus diagnosis.

Tsuguto Fujimoto1, Masami Konagaya, Miki Enomoto, Kunio Tsuboi, Kazuhiro Hashimoto, Kiyosu Taniguchi, Takashi Kodama, Nobuhiko Okabe.   

Abstract

PCR, including real-time PCR, usually requires at least 1 h to obtain results. To shorten this time, a novel real-time PCR method (Hyper-PCR) was developed. This method utilizes high-speed DNA polymerase and a thin disc-type reaction vessel that can quickly alter the temperature of the reaction mixture in a newly developed PCR machine. Reactions capable of amplifying adenovirus (Ad) DNA can be completed within 11 min (3 temperature steps, 55 cycles). Hyper-PCR can detect 3.1-18.0 DNA copies/reaction of Ad types 1-4, 7, 8, 11, 15, 19, and 37. Hyper-PCR and conventional real-time PCR were applied to diagnose 147 clinical samples, and the results were compared. Hyper-PCR had a sensitivity of 100% (73/73) and a specificity of 100% (74/74), using conventional real-time PCR as the gold standard. Our newly developed PCR method, Hyper-PCR, was able to diagnose Ad infection within 17 min (not including the time for genome extraction). The thermocycling time of the novel PCR is faster than that of previously available PCR applications, and this method is thought to be potentially applicable to clinical and environmental diagnostics, where rapid diagnosis is important.

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Year:  2010        PMID: 20093759

Source DB:  PubMed          Journal:  Jpn J Infect Dis        ISSN: 1344-6304            Impact factor:   1.362


  5 in total

1.  Rapid genome detection of Schmallenberg virus and bovine viral diarrhea virus by use of isothermal amplification methods and high-speed real-time reverse transcriptase PCR.

Authors:  Andrea Aebischer; Kerstin Wernike; Bernd Hoffmann; Martin Beer
Journal:  J Clin Microbiol       Date:  2014-03-19       Impact factor: 5.948

2.  Improved real-time PCR assay for detection and quantification of all 54 known types of human adenoviruses in clinical samples.

Authors:  Iwona Bil-Lula; Nicola De Franceschi; Krzysztof Pawlik; Mieczysław Woźniak
Journal:  Med Sci Monit       Date:  2012-06

3.  A new rapid method for detecting epidermal growth factor receptor mutations in non-small cell lung cancer.

Authors:  Miyako Takata; Hiroki Chikumi; Keiji Matsunami; Masahiro Kodani; Tomohiro Sakamoto; Kazuhiro Hashimoto; Masaki Nakamoto; Kensaku Okada; Tsuyoshi Kitaura; Shingo Matsumoto; Jun Kurai; Akira Yamasaki; Tadashi Igishi; Naoto Burioka; Eiji Shimizu
Journal:  Oncol Rep       Date:  2015-01-14       Impact factor: 3.906

4.  A novel point-of-care system for high-speed real-time polymerase chain reaction testing for epidermal growth factor receptor mutations in bronchial lavage fluids after transbronchial biopsy in patients with non-small cell lung cancer.

Authors:  Tomohiro Sakamoto; Masahiro Kodani; Miyako Takata; Hiroki Chikumi; Masaki Nakamoto; Shizuka Nishii-Ito; Yasuto Ueda; Hiroki Izumi; Haruhiko Makino; Hirokazu Touge; Kenichi Takeda; Akira Yamasaki; Masaaki Yanai; Natsumi Tanaka; Tadashi Igishi; Eiji Shimizu
Journal:  Int J Oncol       Date:  2015-02-04       Impact factor: 5.650

5.  Prescription surveillance and polymerase chain reaction testing to identify pathogens during outbreaks of infection.

Authors:  Hiroaki Sugiura; Tsuguto Fujimoto; Tamie Sugawara; Nozomu Hanaoka; Masami Konagaya; Kiyoshi Kikuchi; Eisuke Hanada; Nobuhiko Okabe; Yasushi Ohkusa
Journal:  Biomed Res Int       Date:  2013-02-07       Impact factor: 3.411

  5 in total

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