Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 1986;91(3-4):247-56.
doi: 10.1007/BF01314284.

Mouse hepatitis virus nasoencephalopathy is dependent upon virus strain and host genotype

Comparative Study

Mouse hepatitis virus nasoencephalopathy is dependent upon virus strain and host genotype

S W Barthold et al. Arch Virol. 1986.

Abstract

Mouse hepatitis virus (MHV) S induced typical MHV spongiform lesions in brainstem 28 days following intranasal inoculation of adult A/J, BALB/cByJ, CBA/J, C 3 H/HeJ and C 3 H/RV, but not SJL mice. In all but SJL mice, brain lesions occurred at or near the infectious dose level, based on seroconversion by the indirect immunofluorescence assay. During the acute phase of infection (day 5), lesions were limited to the nose and brain in most genotypes. Exceptions were BALB mice, which had mild hepatitis and SJL mice, which had lesions restricted to the nose. No mortality occurred in any genotype. Following intranasal inoculation of adult mice, MHV-1, -3, -A 59, -JHM and -S all caused brain lesions at 28 days after inoculation. MHV-1 and -3 caused lesions that were usually restricted to the anterior olfactory tracts, while MHV-A 59, -S and -JHM also caused more generalized and pronounced lesions involving the midbrain and pons. These studies suggest that avirulent MHV-S given intranasally to most mouse genotypes is a good model for induction of brain infection in the absence of mortality. They also confirm observations made by others in which MHV-JHM, -S and -A 59 are relatively more neurotropic than other MHV strains, such as MHV-1 and -3.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Bailey OT, Pappenheimer AM, Cheever FS, Daniels JB. A murine virus (JHM) causing disseminated encephalomyelitis with extensive destruction of myelin. II. Pathology. J Exp Med. 1949;90:195–221. - PMC - PubMed
    1. Bang FB, Warwick A. Mouse macrophages as host cells for the mouse hepatitis virus and the genetic basis of their susceptibility. Proc Natl Acad Sci U.S.A. 1960;46:1065–1075. - PMC - PubMed
    1. Barthold SW. Research complications and state of knowledge of rodent coronaviruses. In: TE Hamm., editor. Complications of viral and mycoplasmal infections in rodents to toxicology research testing. Washington, D C: Hemisphere Publishing Corp; 1986. pp. 53–89.
    1. Barthold SW, Smith AL. Mouse hepatitis virus S in weanling Swiss mice following intranasal inoculation. Lab Anim Sci. 1983;33:355–360. - PubMed
    1. Barthold SW, Smith AL. Mouse hepatitis virus strain-related patterns of tissue tropism in suckling mice. Arch Virol. 1984;81:103–112. - PMC - PubMed

Publication types

LinkOut - more resources