Detection of human Coronavirus 229E in nasal specimens in large scale studies using an RT-PCR hybridization assay

被引:16
作者
Vallet, S
Gagneur, A
Talbot, PJ
Legrand, MC
Sizun, J
Picard, B
机构
[1] Ctr Hosp Univ Morvan, Dept Microbiol, Virol Lab, F-29200 Brest, France
[2] Univ Hosp, Dept Pediat, Pediat Intens Care Unit, Brest, France
[3] Univ Quebec, Inst Armand Frappier, INRS, Lab Neuroimmunovirol, Laval, PQ, Canada
关键词
human Coronavirus; neonates; reverse transcription-PCR; nosocornial respiratory viral infections;
D O I
10.1016/j.mcp.2003.09.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A novel human Coronavirus (HCoV) was this year recognized as the etiological agent of the Severe Acute Respiratory Syndrome. Two other HCoV (HCoV-229E and HCoV-OC43) have been known for 30 years. HCoV-229E has been recently involved in nosocomial respiratory viral infections in high-risk children. However, their diagnosis is not routinely performed. Currently, reliable immunofluorescence and cell culture methodologies are not available. As part of a four-year epidemiological study in a Pediatric and Neonatal Intensive care unit, we have performed and demonstrated the reliability of a reverse transcription-PCR-hybridization assay to detect HCoV of the 229E antigenic group in 2028 clinical respiratory specimens. In hospitalized children (children and newborns) and staff members we found a high incidence of HcoV-229E infection. This reverse transcription-PCR-hybridization assay gave a high specificity and a sensitivity of 0.5 50% Tissue Culture Infective Dose per ml. This technique is reliable and its application for screening large number of clinical samples would improve the diagnosis of HCoVs respiratory infection and our knowledge of these viruses epidemiology. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:75 / 80
页数:6
相关论文
共 29 条
[1]   Neuroinvasion by human respiratory coronaviruses [J].
Arbour, N ;
Day, R ;
Newcombe, J ;
Talbot, PJ .
JOURNAL OF VIROLOGY, 2000, 74 (19) :8913-8921
[2]   COMPARISON OF NASAL BRUSH AND NASOPHARYNGEAL ASPIRATE TECHNIQUES IN OBTAINING SPECIMENS FOR DETECTION OF RESPIRATORY SYNCYTIAL VIRAL-ANTIGEN BY IMMUNOFLUORESCENCE [J].
BARNES, SD ;
LECLAIR, JM ;
FORMAN, MS ;
TOWNSEND, TR ;
LAUGHLIN, GM ;
CHARACHE, P .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1989, 8 (09) :598-601
[3]   DETECTION OF RESPIRATORY SYNCYTIAL VIRUS BY REVERSE TRANSCRIPTION PCR AND HYBRIDIZATION WITH A DNA ENZYME-IMMUNOASSAY [J].
FREYMUTH, F ;
EUGENE, G ;
VABRET, A ;
PETITJEAN, J ;
GENNETAY, E ;
BROUARD, J ;
DUHAMEL, JF ;
GUILLOIS, B .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (12) :3352-3355
[4]   Detection of viral, Chlamydia pneumoniae and Mycoplasma pneumoniae infections in exacerbations of asthma in children [J].
Freymuth, F ;
Vabret, A ;
Brouard, J ;
Toutain, F ;
Verdon, R ;
Petitjean, J ;
Gouarin, S ;
Duhamel, JF ;
Guillois, B .
JOURNAL OF CLINICAL VIROLOGY, 1999, 13 (03) :131-139
[5]   Coronavirus-related nosocomial viral respiratory infections in a neonatal and paediatric intensive care unit: a prospective study [J].
Gagneur, A ;
Sizun, J ;
Vallet, S ;
Legrand, MC ;
Picard, B ;
Talbot, PJ .
JOURNAL OF HOSPITAL INFECTION, 2002, 51 (01) :59-64
[6]   Nosocomial infection by human coronaviruses in neonates. [J].
Gagneur, A ;
Legrand, MC ;
Picard, B ;
Baron, R ;
Talbot, PJ ;
de Parscau, L ;
Sizun, J .
ARCHIVES DE PEDIATRIE, 2002, 9 (01) :61-69
[7]  
GAGNEUR AVS, 2002, PED AC SOC ANN M
[8]   DETECTION OF ENTEROVIRUSES AND RHINOVIRUSES IN CLINICAL SPECIMENS BY PCR AND LIQUID-PHASE HYBRIDIZATION [J].
HALONEN, P ;
ROCHA, E ;
HIERHOLZER, J ;
HOLLOWAY, B ;
HYYPIA, T ;
HURSKAINEN, P ;
PALLANSCH, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (03) :648-653
[9]  
HAMRE D, 1966, P SOC EXP BIOL MED, V121, P190, DOI 10.3181/00379727-121-30734
[10]   SURVIVAL CHARACTERISTICS OF AIRBORNE HUMAN CORONAVIRUS-229E [J].
IJAZ, MK ;
BRUNNER, AH ;
SATTAR, SA ;
NAIR, RC ;
JOHNSONLUSSENBURG, CM .
JOURNAL OF GENERAL VIROLOGY, 1985, 66 :2743-2748