Division of Influenza Virus, Center for Infectious Diseases, Korea National Institute of Health, Osong, Chungcheongbuk-do 363-951, South Korea.
Division of Influenza Virus, Center for Infectious Diseases, Korea National Institute of Health, Osong, Chungcheongbuk-do 363-951, South Korea.
Virus Res. 2014 Jun 24;185:41-6. doi: 10.1016/j.virusres.2014.03.014. Epub 2014 Mar 19.
Oseltamivir, a neuraminidase (NA) inhibitor, has been widely used for the treatment of patients infected with the pandemic (H1N1) 2009 influenza virus. With the increasing use of oseltamivir, drug-resistant mutants emerged rapidly and 11 cases of resistant viruses were detected during the 2009 H1N1 pandemic in South Korea. To better understand the differences between oseltamivir-susceptible and oseltamivir-resistant virus, we compared the replication and pathogenesis of the NA H275Y mutant virus, A/Gyeongnam/1820/2009, in ferrets and mice with those of oseltamivir-susceptible A/Korea/01/2009 virus. Oseltamivir-resistant virus infected ferrets showed mild clinical signs and the virus replicated well in the upper respiratory tract and slightly in the lower respiratory tract. No virus was detected in the extrapulmonary organs. Severe bronchopneumonia and thickening of alveolar walls were detected in the lungs. Viral antigens were detected mainly in the bronchiolar epithelial cells, cells present in the interstitial septa, pneumocytes and peribronchial glands with severe peribronchitis. A/Gyeongnam/1820/2009 virus-infected mice showed weight loss and the virus replicated in lungs with high titer. Histopathologically, the mice showed mild to moderate alveolitis, interstitial pneumonia and perivascular lymphoid tissue hyperplasia. In lungs, bronchiolar epithelial cells, pneumocytes and interstitial inflammatory cells were infected by influenza virus and trachea epithelial cells were the sites of infection. When compared with the results of A/Korea/01/2009 oseltamivir-susceptible pandemic influenza virus, an oseltamivir-resistant virus isolated in South Korea showed fewer pathogenic properties in ferrets and similar fitness in mice.
奥司他韦是一种神经氨酸酶(NA)抑制剂,已广泛用于治疗感染大流行(H1N1)2009 流感病毒的患者。随着奥司他韦的使用增加,耐药突变体迅速出现,在韩国 2009 年 H1N1 大流行期间检测到 11 例耐药病毒。为了更好地了解奥司他韦敏感病毒和奥司他韦耐药病毒之间的差异,我们比较了神经氨酸酶 H275Y 突变病毒 A/Gyeongnam/1820/2009 在雪貂和小鼠中的复制和发病机制,与奥司他韦敏感病毒 A/Korea/01/2009 病毒相比。感染奥司他韦耐药病毒的雪貂表现出轻微的临床症状,病毒在上呼吸道和下呼吸道均良好复制。在肺外器官中未检测到病毒。在肺部检测到严重的支气管肺炎和肺泡壁增厚。病毒抗原主要在细支气管上皮细胞、间质隔室中的细胞、肺泡细胞和支气管周围腺中检测到,伴有严重的细支气管炎。感染 A/Gyeongnam/1820/2009 病毒的小鼠出现体重减轻,病毒在肺部以高滴度复制。组织病理学检查显示,小鼠出现轻度至中度肺泡炎、间质性肺炎和血管周围淋巴组织增生。在肺部,细支气管上皮细胞、肺泡细胞和间质炎症细胞感染流感病毒,气管上皮细胞是感染部位。与奥司他韦敏感的 A/Korea/01/2009 大流行流感病毒的结果相比,韩国分离的奥司他韦耐药病毒在雪貂中表现出较少的致病性,在小鼠中具有相似的适应性。