Department of Virology, Norwegian Institute of Public Health, Oslo, Norway.
Euro Surveill. 2013 Jan 17;18(3):20369.
The association between a particular mutation in the HA1 subunit of the influenza virus haemagglutinin, D222G, and severe and fatal disease in cases of influenza A(H1N1)pdm09 in Norway during the 2009 pandemic was investigated using pyrosequencing. The prevalence of the variant among fatal cases was 8/26 and among severe non-fatal cases 5/52. No D222G mutations were found among the 381 mild cases. This difference could not be attributed to sampling differences, such as body location of sampling, or duration of illness. In cases with mutant virus where clinical specimens from different days of illness were available, transition from wild-type to mutant virus was commonly observed (4/5), indicating that the mutant virus emerged sporadically in individual patients. In patients with paired samples from both the upper and lower respiratory tract (n=8), the same viral genotypes were detected in both locations. In most of the D222G cases (11/13), the mutant virus was found as a quasispecies.
使用焦磷酸测序技术研究了流感病毒血凝素 HA1 亚单位中的特定突变 D222G 与 2009 年大流行期间挪威甲型 H1N1pdm09 流感中严重和致命病例之间的关联。在死亡病例中,该变异体的流行率为 26 例中的 8 例,在严重非致命病例中为 52 例中的 5 例。在 381 例轻症病例中未发现 D222G 突变。这种差异不能归因于采样差异,例如采样的身体部位或疾病持续时间。在有突变病毒的病例中,如果有不同发病日的临床标本可用,则通常观察到从野生型到突变型病毒的转变(4/5),表明突变病毒在个别患者中零星出现。在来自上呼吸道和下呼吸道的配对样本(n=8)的患者中,在两个部位均检测到相同的病毒基因型。在大多数 D222G 病例(11/13)中,发现突变病毒为准种。