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Comparative Study
. 2001 Jun;39(6):2233-6.
doi: 10.1128/JCM.39.6.2233-2236.2001.

Detection of herpes simplex virus DNA in genital and dermal specimens by LightCycler PCR after extraction using the IsoQuick, MagNA Pure, and BioRobot 9604 methods

Affiliations
Comparative Study

Detection of herpes simplex virus DNA in genital and dermal specimens by LightCycler PCR after extraction using the IsoQuick, MagNA Pure, and BioRobot 9604 methods

M J Espy et al. J Clin Microbiol. 2001 Jun.

Abstract

We evaluated two automated systems, MagNA Pure (Roche Molecular Biochemicals, Indianapolis, Ind.) and BioRobot 9604 (Qiagen, Inc., Chatsworth, Calif.) as effective replacements for the manual IsoQuick method (Orca Research, Inc., Bothell, Wash.) for extraction of herpes simplex virus (HSV) DNA from dermal and genital tract specimens prior to analysis by LightCycler PCR. Of 198 specimens (152 genital, 46 dermal), 92 (46.2%) were positive for HSV DNA by LightCycler PCR after automated extraction of specimens with either the MagNA Pure or BioRobot 9604 instrument. The manual IsoQuick method yielded HSV DNA (total n = 95) from three additional specimens that were negative by the automated method (P = 0.25, sign test). Although the mean numbers of LightCycler PCR cycles required to reach positivity differed statistically significantly among all three of the methods of extraction, the estimated means differed by no more than 1.5 cycles (P < 0.05). Seventy (76%) of the 92 specimens that were LightCycler PCR positive by all three extraction methods were also positive by shell vial cell culture assay. HSV DNA was detected by a lower LightCycler PCR cycle number (26.1 cycles) in specimens culture positive for the virus than in culture-negative samples (33.3 cycles) (P < 0.0001). The manual IsoQuick and automated MagNA Pure and BioRobot 9604 methods provide standardized, reproducible extraction of HSV DNA for LightCycler PCR. The decision to implement a manual versus an automated procedure depends on factors such as costs related to the number of specimens processed rather than on the minimal differences in the technical efficiency of extraction of nucleic acids among these methods.

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Figures

FIG. 1
FIG. 1
Numbers of LightCycler PCR cycles required for the detection of HSV DNA by three nucleic acid extraction methods.
FIG. 2
FIG. 2
Numbers of LightCycler PCR cycles required for the detection of HSV DNA by the IsoQuick, MagNA Pure, and BioRobot 9604 extraction methods with regard to shell vial cell culture results. There were shell vial cell culture-positive samples.

References

    1. Bancroft T A. Topics in intermediate statistical methods. 2nd ed. Vol. 1. Ames, Iowa: The Iowa State University Press; 1968. pp. 100–113.
    1. Casas I, Powell L, Klapper P E, Cleator G M. New method for the extraction of viral RNA and DNA from cerebrospinal fluid for use in the polymerase chain reaction assay. J Virol Methods. 1995;53:25–36. - PubMed
    1. Cloud J L, Carroll K C, Pixton P, Erali M, Hillyard D R. Detection of Legionella species in respiratory specimens using PCR with sequencing confirmation. J Clin Microbiol. 2000;38:1709–1712. - PMC - PubMed
    1. Espy M J, Patel R, Paya C V, Smith T F. Comparison of three methods for extraction of viral nucleic acids from blood cultures. J Clin Microbiol. 1995;33:41–44. - PMC - PubMed
    1. Espy M J, Ross T K, Teo R, Svien K A, Wold A D, Uhl J R, Smith T F. Evaluation of LightCycler PCR for implementation of laboratory diagnosis of herpes simplex virus infections. J Clin Microbiol. 2000;38:3116–3118. - PMC - PubMed

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