Rotavirus nonstructural glycoprotein NSP4 alters plasma membrane permeability in mammalian cells

K Newton, JC Meyer, AR Bellamy, JA Taylor - Journal of virology, 1997 - Am Soc Microbiol
K Newton, JC Meyer, AR Bellamy, JA Taylor
Journal of virology, 1997Am Soc Microbiol
The endoplasmic reticulum-localized transmembrane glycoprotein NSP4 of rotavirus is a
key protein involved in rotavirus cytopathology. We have used a dual-recombinant vaccinia
virus system to express NSP4 in monkey kidney epithelial cells at a level comparable to that
observed during rotavirus infection. Expression of NSP4 results in loss of plasma membrane
integrity, which can be demonstrated by release of both 51Cr and lactate dehydrogenase
into the medium. The cytotoxic behavior of NSP4 is dose dependent, and morphological …
The endoplasmic reticulum-localized transmembrane glycoprotein NSP4 of rotavirus is a key protein involved in rotavirus cytopathology. We have used a dual-recombinant vaccinia virus system to express NSP4 in monkey kidney epithelial cells at a level comparable to that observed during rotavirus infection. Expression of NSP4 results in loss of plasma membrane integrity, which can be demonstrated by release of both 51Cr and lactate dehydrogenase into the medium. The cytotoxic behavior of NSP4 is dose dependent, and morphological analysis reveals gross changes to cell ultrastructure, indicative of cell death. Thus, intracellular expression of a single rotavirus protein which localizes to the endoplasmic reticulum membrane has profound effects on the stability of the plasma membrane and cell viability. Analysis of NSP4 deletion mutants indicates that a membrane-proximal region located within the cytoplasmic domain may mediate cytotoxicity.
American Society for Microbiology
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