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DOI 10.1016/j.jmoldx.2011.09.004

Медицинская библиотека · The Journal of molecular diagnostics : JMD · 2011

Genotype variability and clinical features of human metapneumovirus isolated from Korean children, 2007 to 2010.

Kim Hye Ryoun, Cho Ah Ra, Lee Mi-Kyung, Yun Sin Weon, Kim Tae-Hyoung

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

This study was undertaken to determine the genotype variability of human metapneumovirus (hMPV) and its circulation pattern over a 3.5-year period, and to evaluate its clinical characteristics in Korean children. We investigated 4599 pediatric patients who were referred for a routine respiratory virus test by RT-PCR. hMPV genotype analyses were performed using a nested PCR-restriction fragment length polymorphism assay. Clinical and laboratory data obtained from medical records were reviewed retrospectively. Of the 4599 samples tested, 325 (7.1%) were positive for hMPV, and the co-infection rate among these 325 was 16%. Nested PCR-restriction fragment length polymorphism analysis clearly identified four of the five hMPV genotypes (A2a, A2b, B1, and B2) in 97.8%. The predominant genotype of hMPV changed over the 3.5-year study period from genotype A2a to B2 and then back to A2a. The most common genotype was A2a (214/325, 65.8%). Evidence of recurrent infection was obtained in one child only. Lymphocytosis was more frequent in children with a co-infection, but sputum production was less frequent than in children with a single infection. In genotype A2a hMPV-infected children, sneezing and neutrophilia were more frequent than in genotype B1 or B2 hMPV-infected children. This study broadens knowledge regarding the prevalence, the seasonal incidence, the occurrences of co-infection and re-infection, and the genotype diversity of hMPV in Korea.

Для цитирования: Kim Hye Ryoun, Cho Ah Ra, Lee Mi-Kyung, Yun Sin Weon, Kim Tae-Hyoung. Genotype variability and clinical features of human metapneumovirus isolated from Korean children, 2007 to 2010.. The Journal of molecular diagnostics : JMD. 2011. DOI: 10.1016/j.jmoldx.2011.09.004.

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