The role of inducible nitric oxide synthase in the host response to Coxsackievirus myocarditis

Proc Natl Acad Sci U S A. 1998 Mar 3;95(5):2469-74. doi: 10.1073/pnas.95.5.2469.

Abstract

The host response to Coxsackievirus infection is complex, including T lymphocytes, B lymphocytes, natural killer cells, and macrophages. Although Coxsackievirus infection induces expression of inducible nitric oxide synthase (NOS2; EC 1.14.13.39) in macrophages, the precise role of NOS2 in the host response to Coxsackievirus myocarditis has been unclear. We show, by using mice homozygous for a disrupted NOS2 allele, that Coxsackievirus replicates to higher titers in NOS2(-/-) mice, that the host lacking NOS2 clears virus more slowly than the wild-type host, and that myocarditis is much more severe in infected NOS2(-/-) mice. These data show that NOS2 is crucial for the host response to Coxsackievirus in the mouse.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Coxsackievirus Infections / immunology
  • Coxsackievirus Infections / physiopathology*
  • Enterovirus B, Human* / isolation & purification
  • Enzyme Induction
  • Heart / virology*
  • Mice
  • Mice, Inbred Strains
  • Myocarditis / pathology
  • Myocarditis / physiopathology*
  • Myocarditis / virology*
  • Myocardium / pathology
  • Nitric Oxide Synthase / biosynthesis*
  • Nitric Oxide Synthase Type II
  • Organ Specificity
  • Polymerase Chain Reaction
  • RNA, Viral / biosynthesis

Substances

  • RNA, Viral
  • Nitric Oxide Synthase
  • Nitric Oxide Synthase Type II
  • Nos2 protein, mouse