Geisbert T W, Jahrling P B
Pathology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD 21702-5011, USA.
Virus Res. 1995 Dec;39(2-3):129-50. doi: 10.1016/0168-1702(95)00080-1.
Cultured monolayers of MA-104, Vero 76, SW-13, and DBS-FRhL-2 cells were infected with Marburg (MBG), Ebola-Sudan (EBO-S), Ebola-Zaire (EBO-Z), and Ebola-Reston (EBO-R) viruses (Filoviridae, Filovirus) and examined by electron microscopy to provide ultrastructural details of morphology and morphogenesis of these potential human pathogens. Replication of each filovirus was seen in all cell systems employed. Filoviral particles appeared to enter host cells by endocytosis. Filoviruses showed a similar progression of morphogenic events, from the appearance of nascent intracytoplasmic viral inclusions to formation of mature virions budded through plasma membranes, regardless of serotype or host cell. However, ultrastructural differences were demonstrated between MBG and other filoviruses. MBG virions recovered from culture fluids were uniformly shorter in mean unit length than EBO-S, EBO-Z, or EBO-R particles. Examination of filovirus-infected cells revealed that intermediate MBG inclusions were morphologically distinct from EBO-S, EBO-Z, and EBO-R inclusions. No structural difference of viral inclusion material was observed among EBO-S, EBO-Z, and EBO-R. Immunoelectron microscopy showed that the filoviral matrix protein (VP40) and nucleoprotein (NP) accumulated in EBO-Z inclusions, and were closely associated during viral morphogenesis. These details facilitate the efficient and definitive diagnosis of filoviral infections by electron microscopy.
用马尔堡病毒(MBG)、苏丹埃博拉病毒(EBO - S)、扎伊尔埃博拉病毒(EBO - Z)和雷斯顿埃博拉病毒(EBO - R)(丝状病毒科,丝状病毒属)感染MA - 104、Vero 76、SW - 13和DBS - FRhL - 2细胞的培养单层,并用电子显微镜检查,以提供这些潜在人类病原体形态和形态发生的超微结构细节。在所使用的所有细胞系统中均观察到每种丝状病毒的复制。丝状病毒颗粒似乎通过内吞作用进入宿主细胞。无论血清型或宿主细胞如何,丝状病毒均显示出相似的形态发生事件进程,从新生的胞质内病毒包涵体出现到通过质膜出芽形成成熟病毒粒子。然而,MBG与其他丝状病毒之间存在超微结构差异。从培养液中回收的MBG病毒粒子平均单位长度比EBO - S、EBO - Z或EBO - R颗粒均匀地短。对感染丝状病毒的细胞检查发现,MBG中间包涵体在形态上与EBO - S、EBO - Z和EBO - R包涵体不同。在EBO - S、EBO - Z和EBO - R之间未观察到病毒包涵体物质的结构差异。免疫电子显微镜显示,丝状病毒基质蛋白(VP40)和核蛋白(NP)在EBO - Z包涵体中积累,并在病毒形态发生过程中紧密相关。这些细节有助于通过电子显微镜对丝状病毒感染进行高效和明确的诊断。