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Volume 35, Issue 2, Pages 141-146 (February 2006)


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QIAamp MinElute Virus kit effectively extracts viral nucleic acids from cerebrospinal fluids and nasopharyngeal swabs

Susan E. Sefersa, Jamie Rickmyreb, Amondrea Blackmanb, Haijing Lib, Kathryn Edwardsc, Yi-Wei TangabCorresponding Author Informationemail address

Received 10 March 2005; received in revised form 23 May 2005; accepted 25 May 2005. published online 22 July 2005.

Abstract 

Background

Nucleic acid preparation from a variety of clinical specimens requires efficient target recovery and amplification inhibitor removal and is critical for successful molecular diagnosis. The QIAamp MinElute Virus kit (Qiagen Inc., Valencia, CA) was compared to the two existing methods currently used in our laboratory, IsoQuick (Orca Research Inc., Bothell, WA) for DNA extraction and RNAzol B (Leedo Laboratories Inc., Houston, TX) for RNA extraction, of viral nucleic acids.

Study design

A total of 150 clinical specimens, including cerebrospinal fluid (CSF) and nasopharyngeal swabs (NPS), were used to determine the extraction efficiency of the MinElute compared to the other two methods. Nucleic acid recovery, hands-on time, turn-around-time and cost were compared across all kits.

Results

There was complete concordance between the MinElute and IsoQuick/RNAzol kits when herpes simplex virus (HSV), Epstein–Barr virus (EBV), varicella-zoster virus (VZV), influenza A virus or enteroviruses were detected using a colorimetric microtiter plate PCR system. The kits were equivalent in their ability to detect either DNA or RNA with superior ability to recover a high quality and quantity of RNA. With the potential to process larger specimen volumes, the MinElute kit can significantly shorten processing time from 2h to 50–55min.

Conclusions

Although relatively high test kit costs were noted, the MinElute kit provides another rapid and user-friendly specimen processing tool in the diagnostic molecular microbiology laboratory.

a Department of Pathology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA

b Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN 37232, USA

c Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN 37232, USA

Corresponding Author InformationCorresponding author at: Molecular Infectious Disease Laboratory, Vanderbilt University Hospital, 4605 TVC, Nashville, TN 37232-5310, USA. Tel.: +1 615 322 2035; fax: +1 615 343 8420.

 This study was presented in part at the 20th Annual Meeting of the Pan American Society for Clinical Virology, Clearwater Beach, FL, USA, 25–28 April 2004.

PII: S1386-6532(05)00152-6

doi:10.1016/j.jcv.2005.05.011


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