Abstracts
Pathogenesis
of rotavirus gastroenteritis
Mary K. Estes, Gagandeep
Kang, Carl Q.-Y. Zeng, Sue E. Crawford and Max Ciarlet
Division of Molecular Virology
and Microbiology, Baylor College of Medicine, Houston, TX 77030, USA
The outcome of intestinal
infection with rotaviruses is more complex than initially appreciated, and it
is affected by a complex interplay of host and viral factors. Rotaviruses infect
intestinal enterocytes, and the early events in infection are mediated by virus-epithelial
cell interactions. Diarrhoea may be caused by several mechanisms including (i)
malabsorption that occurs secondary to the destruction of enterocytes, (ii)
villus ischaemia and activation of the enteric nervous system that may be evoked
by release of a vasoactive agent from infected epithelial cells in the absence
of significant pathologic lesions or enterocyte damage, and (iii) intestinal
secretion stimulated by the intracellular or extracellular action of the rotavirus
non-structural protein, NSP4, a novel enterotoxin and secretory agonist with
pleiotropic properties. New studies of rotavirus infection of polarized intestinal
epithelial cells show that rotaviruses infect cells differently depending on
whether or not they require sialic acid for initial binding, and infection alters
epithelial cell functions. NSP4 also affects epithelial cell function and interactions.
NSP4 (i) induces an age- and dose-dependent diarrhoeal response in young rodents
that is similar to virus-induced disease, (ii) stimulates a Ca2+-dependent cell
permeability where the secretory response is age-dependent, and (iii) alters
epithelial cell integrity. Antibody to NSP4 protects mouse pups from diarrhoea
induced by homotypic and heterotypic viruses. These data support a new mechanism
of rotavirus-induced diarrhoea whereby a viral enterotoxin triggers a signal
transduction pathway that alters epithelial cell permeability and chloride secretion.
This new information about how a gastrointestinal virus causes disease demonstrates
common pathogenic mechanisms for viral and bacterial pathogens not previously
appreciated. These results also suggest new approaches to prevent or treat rotavirus-induced
diarrhoea.
Return
to contents of the Symposium on Gastroenteritis viruses (held at the Novartis Foundation, London, 16-18 May 2000)
©2001 The Novartis Foundation
(close window to return to Alimentary System Physiology lectures)