Evaluation of NucliSens easyMAG for automated nucleic acid extraction from various clinical specimens

被引:101
作者
Loens, K. [1 ]
Bergs, K. [1 ]
Ursi, D. [1 ]
Goossens, H. [1 ]
Ieven, M. [1 ]
机构
[1] Univ Antwerp, UIA, Dept Microbiol, B-2020 Antwerp, Belgium
关键词
D O I
10.1128/JCM.00894-06
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The objectives of this study were to evaluate the performance of the NucliSens easyMAG platform for nucleic acid extraction from different clinical specimens compared to NucliSens miniMAG platform and manual QIAGEN extraction. The NucliSens easyMAG and the NucliSens miniMAG showed equal performance on 215 throat swabs since real-time nucleic acid sequence-based amplification scored the same samples positive for Mycoplasma pneumoniae (n = 9) and Chlamydia pneumoniae (n = 5) RNAs, although internal control RNA was slightly better detected with the NucliSens easyMAG (99.3% versus 96.8%). NucliSens easyMAG extracted nucleic acids more efficiently (higher recovery and/or fewer inhibitors) compared to QIAGEN extraction by showing, on average, lower Ct values in real-time LightCycler PCR, although 4 individual specimen out of 45 were found positive only with QIAGEN. For nine M. pneumoniae-positive throat swabs, the mean difference in Ct values between NucliSens easyMAG extraction and QIAGEN extraction was -2.26 (range, -5.77 to +0.60); for the detection of five C. pneumoniae-positive throat swabs, the average difference in Ct values between the two methods was -3.38 (range, -6.62 to -2.02); and for the detection of cytomegalovirus in 24 blood samples, the mean difference in Ct values between the two methods was -0.95 (range, -5.51 to +1.68). The NueliSens easyMAG is considerably easier to perform, efficiently extracts nucleic acids from throat swabs and whole blood, is automated, and has high throughput.
引用
收藏
页码:421 / 425
页数:5
相关论文
共 25 条
  • [1] Automated extraction of viral-pathogen RNA and DNA for high-throughput quantitative real-time PCR
    Beuselinck, K
    van Ranst, M
    van Eldere, J
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (11) : 5541 - 5546
  • [2] CLINICAL UTILITY OF THE POLYMERASE CHAIN-REACTION TO DIAGNOSE MYCOPLASMA-PNEUMONIAE INFECTION
    BLACKMORE, TK
    REZNIKOV, M
    GORDON, DL
    [J]. PATHOLOGY, 1995, 27 (02) : 177 - 181
  • [3] RAPID AND SIMPLE METHOD FOR PURIFICATION OF NUCLEIC-ACIDS
    BOOM, R
    SOL, CJA
    SALIMANS, MMM
    JANSEN, CL
    WERTHEIMVANDILLEN, PME
    VANDERNOORDAA, J
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (03) : 495 - 503
  • [4] Detection of enterovirus RNA in cerebrospinal fluid (CSF) using NucliSens EasyQ Enterovirus assay
    Capaul, SE
    Gorgievski-Hrisoho, A
    [J]. JOURNAL OF CLINICAL VIROLOGY, 2005, 32 (03) : 236 - 240
  • [5] Isolation and detection of Borrelia burgdorferi DNA from cerebral spinal fluid, synovial fluid, blood, urine, and ticks using the Roche MagNA Pure system and real-time PCR
    Exner, MM
    Lewinski, MA
    [J]. DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2003, 46 (04) : 235 - 240
  • [6] Immunohistostaining assays for detection of Chlamydia pneumoniae in atherosclerotic arteries indicate cross-reactions with nonchlamydial plaque constituents
    Hoymans, VY
    Bosmans, JM
    Ursi, D
    Martinet, W
    Wuyts, FL
    Van Marck, E
    Altwegg, M
    Vrints, CJ
    Ieven, MM
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (07) : 3219 - 3224
  • [7] Comparison of automated and manual nucleic acid extraction methods for detection of enterovirus RNA
    Knepp, JH
    Geahr, MA
    Forman, MS
    Valsamakis, A
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (08) : 3532 - 3536
  • [8] Comparison of DNA and RNA extraction methods for mummified tissues
    Konomi, N
    Lebwohl, E
    Zhang, D
    [J]. MOLECULAR AND CELLULAR PROBES, 2002, 16 (06) : 445 - 451
  • [9] Development and verification of an automated sample processing protocol for quantitation of human immunodeficiency virus type 1 RNA in plasma
    Lee, BG
    Fiebelkorn, KR
    Caliendo, AM
    Nolte, FS
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (05) : 2062 - 2067
  • [10] LEVEN M, 1996, J INFECT DIS, V173, P1445