Comparison of seven commercial DNA extraction kits for the recovery of Brucella DNA from spiked human serum samples using real-time PCR

被引:0
作者
M. I. Queipo-Ortuño
F. Tena
J. D. Colmenero
P. Morata
机构
[1] Universidad de Málaga,Biochemistry and Molecular Biology Department, Faculty of Medicine
[2] Carlos Haya University Hospital,Infectious Diseases Service
来源
European Journal of Clinical Microbiology & Infectious Diseases | 2008年 / 27卷
关键词
Polymerase Chain Reaction Assay; Brucellosis; Human Brucellosis; Brucella Melitensis; Temperature Change Rate;
D O I
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中图分类号
学科分类号
摘要
We compared the relative recovery of extraction of bacterial DNA from serum using seven commercial kits (UltraClean DNA BloodSpin Kit, Puregene DNA Purification System, Wizard Genomic DNA Purification Kit, High Pure PCR Template Preparation Kit, GFX™ Genomic Blood DNA Purification Kit, NucleoSpin Tissue Kit, and QIAamp DNA Blood Mini Kit). Human serum samples were spiked with known concentrations of Brucella melitensis Rev 1; the DNA was extracted and tested in genus-specific LightCycler polymerase chain reaction (PCR). The UltraClean DNA BloodSpin Kit proved to be as sensitive as the QIAamp DNA Blood Mini Kit isolation method and could detect down to 100 fg of DNA, though only the former had no contamination. All the other procedures yielded DNA isolation results that were less sensitive and were always contaminated. Our results show that the UltraClean DNA Blood Spin Kit was the commercially available assay tested that yielded the best sensitivity, purity, and lack of contamination for Brucella DNA isolation from serum.
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页码:109 / 114
页数:5
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共 73 条
  • [1] Pappas G(2005)Brucellosis N Engl J Med 352 2325-2336
  • [2] Akritidis N(2000) bacteraemia: clinical and laboratory observations in 160 patients J Infect 40 59-63
  • [3] Bosilkovski M(1991)Serologic diagnosis of human brucellosis: analysis of 214 cases by agglutination tests and review of the literature Rev Infect Dis 13 359-372
  • [4] Tsianos E(1993)Factors affecting detection of J Clin Microbiol 31 3200-3203
  • [5] Memish Z(1999) by BACTEC NR730, a nonradiometric system for hemocultures Biotechniques 27 248-252
  • [6] Mah MW(2001)Hydrogen peroxide improves the efficiency of a peripheral blood PCR assay for diagnosis of human brucellosis J Clin Microbiol 39 1661-1664
  • [7] Al Mahmoud S(2001)Serum is the preferred clinical specimen for the diagnosis of human brucellosis by PCR Mol Pathol 54 86-90
  • [8] Al Shaalan M(2005)Recovery efficiencies of nucleic acid extraction kits as measured by quantitative LightCycler™ PCR Clin Microbiol Infect 11 713-718
  • [9] Khan MY(2005)Rapid diagnosis of human brucellosis by SYBR Green I-based real-time PCR assay and melting curve analysis serum samples Clin Infect Dis 40 260-264
  • [10] Young EJ(1992)Comparison between LightCycler Real-Time Polymerase Chain Reaction (PCR) assay with serum and PCR-enzyme-linked immunosorbent assay with whole blood samples for the diagnosis of human brucellosis J Trop Med Hyg 95 271-275