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1.
Rinsho Byori ; 51(11): 1061-7, 2003 Nov.
Article in Japanese | MEDLINE | ID: mdl-14679783

ABSTRACT

The isothermal and chimeric primer-initiated amplification of nucleic acids (ICAN) is a new isothermal DNA amplification method composed of exo Bca DNA polymerase, RNaseH and DNA-RNA chimeric primers. We developed the simultaneous detection system for Chlamydia trachomatis/Neisseria gonorrhoeae DNA, combined with luminescence detection by a probe hybridization. In the performance tests, this system was able to detect 10 to 100 copies of C. trachomatis/N. gonorrhoeae DNA for only 3.5 hours, and was highly specific to C. trachomatis/N. gonorrhoeae without any cross-reaction to C. pneumoniae, N. lactamica, N. sicca or N. meningitidis. When we tested 60 clinical samples of urine and cervical swabs, the interpretive results were completely consistent with those obtained by Roche PCR system. Of 13 positive samples by the ICAN and PCR systems for C. trachomatis, four were negative by EIA method(IDEIA Chlamydia). These results indicate that the ICAN system is an efficient and sensitive system to simultaneously detect C. trachomatis/N. gonorrhoeae DNA.


Subject(s)
Chlamydia trachomatis/genetics , DNA, Bacterial/analysis , Neisseria gonorrhoeae/genetics , Nucleic Acid Amplification Techniques/methods , Chlamydia trachomatis/isolation & purification , Neisseria gonorrhoeae/isolation & purification , Sensitivity and Specificity
2.
Rinsho Byori ; 50(5): 528-32, 2002 May.
Article in Japanese | MEDLINE | ID: mdl-12078054

ABSTRACT

The isothermal and chimeric primer-initiated amplification of nucleic acids(ICAN) is a new isothermal DNA amplification method composed of exo- Bca DNA polymerase, RNaseH and DNA-RNA chimeric primers. We developed the detection system, combined the ICAN with luminescence detection by a probe hybridization, for Mycobacterium tuberculosis DNA targeting the IS6110 insertion element. We examined performance tests of the system. This system was able to detect one copy of Mycobacterium tuberculosis DNA for only 3.5 hours, and performance of the system was equivalent or better to the Roche PCR system. We also examined a detection system by using magnetic beads, which system could shorten detection time for 2.5 hours. It was shown that the ICAN system was an efficient and sensitive detection system for Mycobacterium tuberculosis DNA from mass samples.


Subject(s)
DNA, Bacterial/isolation & purification , Mycobacterium tuberculosis/genetics , Nucleic Acid Amplification Techniques , Humans , Mycobacterium tuberculosis/isolation & purification , Sensitivity and Specificity
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