病毒性软化病是一种严重影响蚕业生产的流行病，其病原为家蚕传染性软化病病毒（Bombyx mori infectiousflacherie virus，BmIFV）。本实验室在浙江省收集到具有软化病症状的家蚕幼虫，并分离纯化获得一株病毒。电镜观察到病毒粒子为直...病毒性软化病是一种严重影响蚕业生产的流行病，其病原为家蚕传染性软化病病毒（Bombyx mori infectiousflacherie virus，BmIFV）。本实验室在浙江省收集到具有软化病症状的家蚕幼虫，并分离纯化获得一株病毒。电镜观察到病毒粒子为直径26nm左右、无包涵体的球状颗粒。病毒添食四龄起蚕和五龄起蚕，分别在3～4d和5～7d出现明显症状和病变。纯化病毒SDS-PAGE条带与BmIFV蛋白相仿。病毒核酸鉴定为RNA，并可用套式RT-PCR扩增出特异性片段，测序发现片段序列和BmIFV日本坂城株的同源性为99．5％。由此可确定该病毒为BmIFV，这是我国首次分离到该病毒，暂命名为BmIFV-CHN001。展开更多
运用Discovery Studio 4.5软件,通过同源建模及分子动力学优化获得柞蚕小吐白水软化病毒(Ap IV)3C蛋白酶的3D结构;通过分子对接对天然产物库进行虚拟筛选,得到1个Ap IV 3C蛋白酶的有效抑制剂3',4',5,7-四羟基异黄酮(Orobol).分...运用Discovery Studio 4.5软件,通过同源建模及分子动力学优化获得柞蚕小吐白水软化病毒(Ap IV)3C蛋白酶的3D结构;通过分子对接对天然产物库进行虚拟筛选,得到1个Ap IV 3C蛋白酶的有效抑制剂3',4',5,7-四羟基异黄酮(Orobol).分子对接和分子动力学(MD)模拟结果进一步证明Orobol能稳定结合于Ap IV 3C蛋白酶的结合口袋处.体内外的Ap IV病毒抑制实验结果表明,Orobol具有良好的抗病毒活性.展开更多
Malakoplakia is a rare granulomatous disease probably caused by infection and characterized histologically by Michaelis-Gutmann bodies.We report a more rarely seen case esophageal malakoplakia in a 54-year-old woman.S...Malakoplakia is a rare granulomatous disease probably caused by infection and characterized histologically by Michaelis-Gutmann bodies.We report a more rarely seen case esophageal malakoplakia in a 54-year-old woman.She presented with coughing while eating and drinking.Gastroscopy showed yellow nodules in the esophagus,and endoscopic ultrasonography showed a space-occupying lesion in the substratum of the esophageal mucosa.All findings highly resembled esophageal cancer.Histopathological examination finally indentified this space-occupying lesion as malakoplakia and not cancer.Immunohistochemistry showed that she had human papillomavirus(HPV) infection in the esophagus,which indicates that infection was responsible for the malakoplakia.This is believed to be the first case of malakoplakia in the esophagus,and more importantly,we established that HPV infection was the initiator of esophageal malakoplakia.展开更多
文摘病毒性软化病是一种严重影响蚕业生产的流行病，其病原为家蚕传染性软化病病毒（Bombyx mori infectiousflacherie virus，BmIFV）。本实验室在浙江省收集到具有软化病症状的家蚕幼虫，并分离纯化获得一株病毒。电镜观察到病毒粒子为直径26nm左右、无包涵体的球状颗粒。病毒添食四龄起蚕和五龄起蚕，分别在3～4d和5～7d出现明显症状和病变。纯化病毒SDS-PAGE条带与BmIFV蛋白相仿。病毒核酸鉴定为RNA，并可用套式RT-PCR扩增出特异性片段，测序发现片段序列和BmIFV日本坂城株的同源性为99．5％。由此可确定该病毒为BmIFV，这是我国首次分离到该病毒，暂命名为BmIFV-CHN001。
文摘运用Discovery Studio 4.5软件,通过同源建模及分子动力学优化获得柞蚕小吐白水软化病毒(Ap IV)3C蛋白酶的3D结构;通过分子对接对天然产物库进行虚拟筛选,得到1个Ap IV 3C蛋白酶的有效抑制剂3',4',5,7-四羟基异黄酮(Orobol).分子对接和分子动力学(MD)模拟结果进一步证明Orobol能稳定结合于Ap IV 3C蛋白酶的结合口袋处.体内外的Ap IV病毒抑制实验结果表明,Orobol具有良好的抗病毒活性.
文摘Malakoplakia is a rare granulomatous disease probably caused by infection and characterized histologically by Michaelis-Gutmann bodies.We report a more rarely seen case esophageal malakoplakia in a 54-year-old woman.She presented with coughing while eating and drinking.Gastroscopy showed yellow nodules in the esophagus,and endoscopic ultrasonography showed a space-occupying lesion in the substratum of the esophageal mucosa.All findings highly resembled esophageal cancer.Histopathological examination finally indentified this space-occupying lesion as malakoplakia and not cancer.Immunohistochemistry showed that she had human papillomavirus(HPV) infection in the esophagus,which indicates that infection was responsible for the malakoplakia.This is believed to be the first case of malakoplakia in the esophagus,and more importantly,we established that HPV infection was the initiator of esophageal malakoplakia.
