Prevalence of human metapneumovirus and influenza virus infections among Japanese children during two successive winters

被引:29
作者
Sasaki, A
Suzuki, H
Saito, R
Sato, M
Sato, I
Sano, Y
Uchiyama, M
机构
[1] Niigata Univ, Sch Med, Dept Publ Hlth, Niigata, Japan
[2] Niigata Univ, Sch Med, Dept Pediat, Niigata, Japan
[3] Sano Clin, Niigata, Japan
[4] Yoiko Sato Clin, Niigata, Japan
关键词
metapneumovirus; influenza; surveillance; coinfection; epidemiology;
D O I
10.1097/01.inf.0000180984.61778.1e
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Human metapneumoviruses (hMPVs) are recognized as a leading cause of respiratory infections in young infants in many countries. The objective of this study was to identify links between hMPV and influenza virus infections among children with influenzalike illness. Method: This study was conducted in 2 influenza seasons (20022003 and 2003-2004) at 2 pediatric outpatient clinics in Niigata city, Japan. Nasopharyngeal swabs or aspirates were collected from influenza-like illness patients, and hMPV and influenza were detected by reverse transcription-polymerase chain reaction (RTPCR). A nucleotide sequence of 352 nucleotides segment of the IT gene was performed. Results: A total of 765 influenza viruses and 84 hMPV were identified from 1498 nasopharyngeal swabs or aspirates by virus isolation and RT-PCR, respectively. hMPV-positive rates in patients with influenza-like illness were 5.7 and 5.2% in the 2002-2003 and 2003-2004 seasons, respectively. Epidemic curves of influenza and hMPV patients showed similar patterns with peaks in February in 2 influenza seasons. hMPV infections occurred frequently in infants and school children. Approximately 46% of hMPV patients were coinfected with influenza A viruses, but those coinfected cases were not clinically distinct from the others. No coinfection with influenza B viruses was found. Phylogenetic analysis of the hMPV fusion gene sequences revealed that 2 distinct hMPV cocirculated and that completely identical strains in subgroup A were observed over 2 years. Conclusions: HMPV plays an important pathogenic role in patients with influenza-like illness in winter seasons, often in coinfections with influenza A viruses.
引用
收藏
页码:905 / 908
页数:4
相关论文
共 27 条
[1]   Human metapneumovirus infection in the Canadian population [J].
Bastien, N ;
Ward, D ;
Van Caeseele, P ;
Brandt, K ;
Lee, SHS ;
McNabb, G ;
Klisko, B ;
Chan, E ;
Li, Y .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (10) :4642-4646
[2]  
Boivin G, 2003, EMERG INFECT DIS, V9, P634
[3]   Detection of human metapneumovirus RNA sequences in nasopharyngeal aspirates of young French children with acute bronchiolitis by real-time reverse transcriptase PCR and phylogenetic analysis [J].
Bouscambert-Duchamp, M ;
Lina, B ;
Trompette, A ;
Moret, H ;
Motte, J ;
Andréoletti, L .
JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (03) :1411-1414
[4]  
Chan PKS, 2003, EMERG INFECT DIS, V9, P1058
[5]   Human metapneumovirus and respiratory syncytial virus, Brazil [J].
Cuevas, LE ;
Ben Nasser, AM ;
Dove, W ;
Gurgel, RQ ;
Greensill, J ;
Hart, CA .
EMERGING INFECTIOUS DISEASES, 2003, 9 (12) :1626-1628
[6]  
Dollner H, 2004, PEDIATR INFECT DIS J, V23, P436, DOI [10.1097/01.inf.0000126401.21779.74, 10.1097/01.inf.000126401.21779.7]
[7]   A 1-year experience with human Metapneumovirus in children aged <5 years [J].
Esper, F ;
Martinello, RA ;
Boucher, D ;
Weibel, C ;
Ferguson, D ;
Landry, ML ;
Kahn, JS .
JOURNAL OF INFECTIOUS DISEASES, 2004, 189 (08) :1388-1396
[8]   Aetiology -: Koch's postulates fulfilled for SARS virus [J].
Fouchier, RAM ;
Kuiken, T ;
Schutten, M ;
van Amerongen, G ;
van Doornum, J ;
van den Hoogen, BG ;
Peiris, M ;
Lim, W ;
Stöhr, K ;
Osterhaus, ADME .
NATURE, 2003, 423 (6937) :240-240
[9]   Human metapneumovirus in severe respiratory syncytial virus bronchiolitis [J].
Greensill, J ;
McNamara, PS ;
Dove, W ;
Flanagan, B ;
Smyth, RL ;
Hart, CA .
EMERGING INFECTIOUS DISEASES, 2003, 9 (03) :372-375
[10]   Human metapneumovirus: A new player among respiratory viruses [J].
Hamelin, ME ;
Abed, Y ;
Boivin, G .
CLINICAL INFECTIOUS DISEASES, 2004, 38 (07) :983-990