Dry cotton or flocked respiratory swabs as a simple collection technique for the molecular detection of respiratory viruses using real-time NASBA

被引:70
作者
Moore, Catherine [1 ]
Corden, Sally [1 ]
Sinha, Jaisi [1 ]
Jones, Rachel [1 ]
机构
[1] Univ Wales Hosp, Wales Specialist Virol Ctr, Cardiff CF14 4XW, S Glam, Wales
关键词
Respiratory Viruses; Real-time NASBA; Dry respiratory swab;
D O I
10.1016/j.jviromet.2008.08.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This paper describes the molecular detection of influenza A, influenza B, respiratory syncytial virus and human metapneumovirus using real-time nucleic acid sequence based amplification (NASBA) from respiratory samples collected on simple dry cotton swabs, non-invasively and in the absence of transport medium. Viral RNA was detectable on dry cotton and flocked swabs for at least 2 weeks at room temperature and was readily extracted using magnetic silica extraction methods. Dry cotton respiratory swabs were matched with traditionally collected respiratory samples from the same patient, and results of traditional laboratory techniques and real-time NASBA were compared for all four viral targets. The results not only showed a significant increase in the detection rate of the viral targets over traditional laboratory methods of 46%, but also that dry swabs did not compromise their recovery. Over two subsequent winter seasons, 736 dry cotton respiratory swabs were collected from symptomatic patients and tested using real-time NASBA giving an overall detection rate for these respiratory virus targets of 38%. The simplicity of the method together with the increased detection rate observed in the study proves that transporting a dry respiratory swab to the laboratory for respiratory virus diagnosis using molecular methods is a suitable and robust alternative to traditional sample types. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:84 / 89
页数:6
相关论文
共 29 条
[1]   Hepatitis C virus RNA in dried serum spotted onto filter paper is stable at room temperature [J].
Abe, K ;
Konomi, N .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (10) :3070-3072
[2]   High correlation of human immunodeficiency virus type-1 viral load measured in dried-blood spot samples and in plasma under different storage conditions [J].
Alvarez-Muñoz, MT ;
Zaragoza-Rodríguez, S ;
Rojas-Montes, O ;
Palacios-Saucedo, G ;
Vázquez-Rosales, G ;
Gómez-Delgado, A ;
Torres, J ;
Muñoz, O .
ARCHIVES OF MEDICAL RESEARCH, 2005, 36 (04) :382-386
[3]   Multiplex real-time PCR assay for detection of influenza and human respiratory syncytial viruses [J].
Boivin, G ;
Côté, S ;
Déry, P ;
De Serres, G ;
Bergeron, MG .
JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (01) :45-51
[4]   Quantification of human immunodeficiency virus type 1 RNA from dried plasma spots collected on filter paper [J].
Cassol, S ;
Gill, MJ ;
Pilon, R ;
Cormier, M ;
Voigt, RF ;
Willoughby, B ;
Forbes, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (11) :2795-2801
[5]   Raid and highly sensitive qualitative real-time assay for detection of respiratory syncytial virus A and B using NASBA and molecular beacon technology [J].
Deiman, B. ;
Schrover, C. ;
Moore, C. ;
Westmoreland, D. ;
van de Wiel, P. .
JOURNAL OF VIROLOGICAL METHODS, 2007, 146 (1-2) :29-35
[6]   Point-of-care testing for community-acquired pneumonia: do we have all the answers? [J].
Dwyer, Dominic E. ;
Sintchenko, Vitali .
MEDICAL JOURNAL OF AUSTRALIA, 2007, 187 (01) :40-42
[7]   Surveillance of measles in the Sudan using filter paper blood samples [J].
El Mubarak, HS ;
Yüksel, S ;
Mustafa, OM ;
Ibrahim, SA ;
Osterhaus, ADME ;
de Swart, RL .
JOURNAL OF MEDICAL VIROLOGY, 2004, 73 (04) :624-630
[8]   Rapid diagnosis of respiratory syncytial virus infections in immunocompromised adults [J].
Englund, JA ;
Piedra, PA ;
Jewell, A ;
Patel, K ;
Baxter, BB ;
Whimbey, E .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (07) :1649-1653
[9]   Respiratory syncytial virus infection in adults [J].
Falsey, Ann R. .
SEMINARS IN RESPIRATORY AND CRITICAL CARE MEDICINE, 2007, 28 (02) :171-181
[10]  
HALL CB, 1976, J PEDIAT, V131, P1