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Journal of Clinical Microbiology, April 2008, p. 1274-1280, Vol. 46, No. 4
0095-1137/08/$08.00+0     doi:10.1128/JCM.01567-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Clinical Evaluation of NucliSENS Magnetic Extraction and NucliSENS Analyte-Specific Reagents for Real-Time Detection of Human Metapneumovirus in Pediatric Respiratory Specimens{triangledown} ,{dagger}

Christine C. Ginocchio,1,2* Ryhana Manji,1 Madhavi Lotlikar,2 and Fan Zhang1

North Shore-Long Island Jewish Health System Laboratories, Department of Laboratory Medicine, Lake Success, New York,1 North Shore University Hospital, Department of Laboratory Medicine, Manhasset, New York2

Received 6 August 2007/ Returned for modification 1 November 2007/ Accepted 1 February 2008

In this study, we evaluated the NucliSENS miniMAG (MM) and easyMAG (EM) nucleic acid extraction platforms (bioMérieux, Durham, NC) in combination with the NucliSENS EasyQ basic kit and analyte-specific reagents (ASRs) (bioMérieux) for the detection of human metapneumovirus (hMPV) in respiratory samples. Total nucleic acids from pediatric clinical samples (n = 653) and an hMPV-specific inhibition control (h-IC) were coextracted using the MM and/or the EM. Nucleic acid sequence-based amplification and real-time molecular beacon detection of hMPV were performed using a NucliSENS EasyQ analyzer (bioMérieux). Positive results were confirmed using an in-house-validated reverse transcriptase PCR ASR-based assay. The inclusion of the h-IC monitored the entire process, including the efficiency of nucleic acid extraction, amplification, and detection. The percentages of samples with inhibited amplification of the h-IC after initial NA extraction by EM and MM were 1.88% and 3.17%, respectively. After reprocessing of a new aliquot, the final h-IC inhibition rates were 0% (EM) and 1.06% (MM). The limit of detection of the assay was between 2 (EM extraction) and 10 (MM extraction) RNA copies/reaction, and specificity was 100% when testing viral respiratory isolates and clinical samples. hMPV was detected in 5.6% of pediatric samples tested and was also detected in three coinfections with respiratory syncytial virus (RSV). hMPV was the second most frequently detected respiratory virus in children of 0 to 2 years of age, after RSV. In summary, NucliSENS extraction and ASRs provided a sensitive and specific method for the detection of hMPV in respiratory samples.


* Corresponding author. Mailing address: North Shore-Long Island Jewish Health System Laboratories, Molecular Diagnostics, Department of Laboratory Medicine, 10 Nevada Drive, Lake Success, NY 11042. Phone: (516) 719-1079. Fax: (516) 719-1254. E-mail: cginocch{at}nshs.edu

{triangledown} Published ahead of print on 13 February 2008.

{dagger} Supplemental material for this article may be found at http://jcm.asm.org/.


Journal of Clinical Microbiology, April 2008, p. 1274-1280, Vol. 46, No. 4
0095-1137/08/$08.00+0     doi:10.1128/JCM.01567-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.







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