Kauffman R S, Wolf J L, Finberg R, Trier J S, Fields B N
Virology. 1983 Jan 30;124(2):403-10. doi: 10.1016/0042-6822(83)90356-2.
After intragastric inoculation of adult mice, type 1 reovirus was initially concentrated in Peyer's patches over the first 4 hr after inoculation, then spread sequentially to the mesenteric lymph nodes and spleen. For type 3 reovirus, however, initial entry into Peyer's patches in adult mice was followed by loss of viral infectivity so that by 4 hr after inoculation virtually no infectious virus was detected in the intestine, and spread to extraintestinal tissues did not occur. In 10-day-old mice, type 3 was capable of spread to the mesenteric lymph nodes but not the spleen. Thus, as animals aged there was a greater restriction of the spread of type 3 from the intestine. Studies using a field isolate of type 3 reovirus that is resistant to intestinal proteases, and genetic studies utilizing type 1 x type 3 viral reassortants, revealed that the viral sigma 1 protein determined the capacity of reovirus to spread from the intestine in both adult and 10-day-old mice. Thus, the interaction of reovirus with host defense mechanisms, and the age-dependent restriction of spread of type 3 reovirus from the intestine are mediated by the viral sigma 1 protein.
成年小鼠经胃内接种后,1型呼肠孤病毒在接种后的最初4小时内最初集中在派尔集合淋巴结,然后依次扩散到肠系膜淋巴结和脾脏。然而,对于3型呼肠孤病毒,成年小鼠最初进入派尔集合淋巴结后病毒感染性丧失,以至于接种后4小时在肠道中几乎检测不到感染性病毒,并且未发生向肠外组织的扩散。在10日龄小鼠中,3型能够扩散到肠系膜淋巴结,但不能扩散到脾脏。因此,随着动物年龄的增长,3型从肠道扩散的限制更大。使用对肠道蛋白酶有抗性的3型呼肠孤病毒田间分离株进行的研究,以及利用1型×3型病毒重配体进行的遗传学研究表明,病毒σ1蛋白决定了呼肠孤病毒在成年和10日龄小鼠中从肠道扩散的能力。因此,呼肠孤病毒与宿主防御机制的相互作用,以及3型呼肠孤病毒从肠道扩散的年龄依赖性限制是由病毒σ1蛋白介导的。