|
|
||||||||
Laboratoire de Virologie de la Faculté de Médecine de l'Université Louis Pasteur et Unité I.N.S.E.R.M. U 74, 3, rue Koeberlé, 67000 Strasbourg, France
Infection with mouse hepatitis virus type 3 (MHV 3) of primary cultures of Kupffer and endothelial cells from the livers of resistant (A/J) and susceptible (BALB/c) mice was followed by the appearance of typical syncytia and comparable yields of virus. Using cells from A/J mice there was a delay of about 24 to 36 h in the appearance of the first particles detected by electron microscopy, the maximum viral titre and the number and size of syncytia. The partial resistance to MHV 3 multiplication expressed by cells from A/J mice was also observed when they were infected with a strain of low virulence (JHM strain). The delay in MHV multiplication found in the sinusoidal liver cells, mainly in the endothelial cells, may be an important factor in their resistance, by allowing time for the local and systemic responses to clear the infective particles as well as in determining their degree of hepatotropism.
Keywords: MHV 3, JHMV, sinusoidal liver cell, replication
Received 13 January 1984;
accepted 21 May 1984.
This article has been cited by other articles:
![]() |
S. Navas and S. R. Weiss Murine Coronavirus-Induced Hepatitis: JHM Genetic Background Eliminates A59 Spike-Determined Hepatotropism J. Virol., April 15, 2003; 77(8): 4972 - 4978. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Navas, S.-H. Seo, M. M. Chua, J. D. Sarma, E. Lavi, S. T. Hingley, and S. R. Weiss Murine Coronavirus Spike Protein Determines the Ability of the Virus To Replicate in the Liver and Cause Hepatitis J. Virol., March 1, 2001; 75(5): 2452 - 2457. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| INT J SYST EVOL MICROBIOL | MICROBIOLOGY | J GEN VIROL |
| J MED MICROBIOL | ALL SGM JOURNALS | |