کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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3378078 | 1220062 | 2013 | 6 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Clinical features of different genotypes/genogroups of human metapneumovirus in hospitalized children Clinical features of different genotypes/genogroups of human metapneumovirus in hospitalized children](/preview/png/3378078.png)
Background/Purpose(s)To explore the clinical features of different human metapneumovirus (hMPV) genotypes/genogroups in hospitalized children.MethodsFrom January 2005 to April 2010, 3313 children's respiratory specimens sent for the detection of respiratory syncytial virus antigen were also tested for hMPV by real time-polymerase chain reaction. Demographics, clinical presentations, and laboratory findings of patients infected with different genotypes/genogroups of hMPV were compared.ResultsA total of 725 samples were positive for hMPV (positive rate, 23%). The F gene was sequenced for 279 isolates; of these, genotype A was identified in 51% (A1, 6.1%; A2, 45%) and genotype B in 49% (B1, 19%; B2, 30%). Medical records of 152 hospitalized children were reviewed. Co-infection with other pathogens was 25.7% (39/152). Excluding co-pathogens other than respiratory syncytial virus, a total of 124 children were analyzed. The most common symptoms included cough, fever, rhinorrhea, wheezing and respiratory distress with accessory muscle usage. The main diagnosis was bronchiolitis. The most common chest radiographic findings were increased perihilar infiltrates. No significant difference was found in terms of demographics, clinical manifestations, and laboratory findings among the children infected with different serogroups of hMPV.ConclusionhMPV accounted for a substantial proportion of hospitalized children with lower respiratory tract infection with a high co-infection rate. The A2 subgroup was the most frequently observed, followed by B2. No significant difference was found among patients infected with different genotypes/genogroups of hMPV in terms of clinical manifestations.
Journal: Journal of Microbiology, Immunology and Infection - Volume 46, Issue 5, October 2013, Pages 352–357