Shaw R D, Hempson S J, Mackow E R
Research Service, Northport V.A. Medical Center, 11768, USA.
J Virol. 1995 Oct;69(10):5946-50. doi: 10.1128/JVI.69.10.5946-5950.1995.
Rotaviruses infect the villous epithelium of the small intestine and cause severe diarrhea in young children. The mechanism by which rotavirus causes diarrhea has not been elucidated. It has been hypothesized that rotavirus replication in the intestinal epithelium causes a loss of viable absorptive cells, leading to an imbalance of intestinal secretion and absorption. Cell destruction has generally been thought to result from rotavirus transcription and replication. However, the widely used heterologous murine model of rotavirus infection demonstrates minimal viral replication and histological changes limited to epithelial vacuolation on the distal villus despite the simultaneous occurrence of voluminous liquid diarrhea. We have genetically inactivated rotaviruses to test the importance of viral replication in the pathogenesis of rotavirus-induced diarrhea. We present direct evidence that transcription- and replication-defective rotaviruses cause diarrhea in an animal model. These findings suggest that rotavirus attachment or entry into cells is sufficient for the induction of diarrhea. The mechanism of rotavirus-induced diarrhea is therefore consistent with a viral toxin-like effect exerted during virus-cell contact.
轮状病毒感染小肠绒毛上皮,导致幼儿严重腹泻。轮状病毒引起腹泻的机制尚未阐明。据推测,轮状病毒在肠道上皮中的复制会导致有活力的吸收细胞丧失,从而导致肠道分泌和吸收失衡。一般认为细胞破坏是由轮状病毒转录和复制引起的。然而,广泛使用的轮状病毒感染异源小鼠模型显示,尽管同时出现大量液体腹泻,但病毒复制极少,组织学变化仅限于远端绒毛上皮空泡化。我们通过基因手段使轮状病毒失活,以测试病毒复制在轮状病毒诱导腹泻发病机制中的重要性。我们提供了直接证据,表明转录和复制缺陷的轮状病毒在动物模型中会导致腹泻。这些发现表明,轮状病毒附着或进入细胞足以引发腹泻。因此,轮状病毒诱导腹泻的机制与病毒 - 细胞接触过程中发挥的病毒毒素样作用一致。