You need JavaScript to view this

An immunological analysis of natural resistance to moise hepatitis virus (JHMV strain) infection in C3H mice

Abstract

Since the development of resistance against mouse hepatitis virus (JHMV strain) coincides with the maturation of the immune system, we studied the possible role of distinct immunological components in the resistance of adult mice during JHMV infection. Adult C3H mice naturally resistant to JHMV were rendered susceptible to infection by lethal {sup 60}Co-irradiation and were subsequently reconstituted with limiting numbers of syngeneic bone marrow cells or spleen cells. Resistance or susceptibility dependend on the number of cells used for reconstitution and the interval between reconsitution and infection. Spleen cells from suckling mice affected neither resistance nor susceptibility and peritoneal cells from adult mice and thymus cells reduced resistance. Persistence of JHMV was demonstrated by virus reactivation. Animals infected with JHMV only once before being rendered immunoincompetent showed a different pattern of resistance. One to four months after infection, 15 to 35% of the animals died after reconstitution without having been reinfected, and persisting JHMV was found in their liver, spleen and peritoneal exudate. The survivors (47 to 87%) were resistant to further JHMV infection during immunodeficiency. Animals immunized 3 times with JHMV before irradiation did not show virus reactivation and were fully resistant to JHMV reinfection after reconstitution. The level  More>>
Authors:
Pereira, C A; Pickel, K [1] 
  1. Wurzburg Univ. (Germany, F.R.). Inst. fuer Virologie und Immunbiologie
Publication Date:
Jan 01, 1987
Product Type:
Journal Article
Reference Number:
AIX-21-078845; EDB-90-149320
Resource Relation:
Journal Name: Revista Brasileira de Pesquisas Medicas e Biologicas (Brazilian Journal of Medical and Biological Research); (Brazil); Journal Volume: 20:1
Subject:
63 RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT.; COBALT 60; HEPATITIS; MICE; GAMMA RADIATION; VIRAL DISEASES; ANIMALS; BETA DECAY RADIOISOTOPES; BETA-MINUS DECAY RADIOISOTOPES; COBALT ISOTOPES; DIGESTIVE SYSTEM DISEASES; DISEASES; ELECTROMAGNETIC RADIATION; INFECTIOUS DISEASES; INTERMEDIATE MASS NUCLEI; INTERNAL CONVERSION RADIOISOTOPES; IONIZING RADIATIONS; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; MAMMALS; MINUTES LIVING RADIOISOTOPES; NUCLEI; ODD-ODD NUCLEI; RADIATIONS; RADIOISOTOPES; RODENTS; VERTEBRATES; YEARS LIVING RADIOISOT; 560162* - Radionuclide Effects, Kinetics, & Toxicology- Animals, Plants, Microorganisms, & Cells
OSTI ID:
6864649
Country of Origin:
Brazil
Language:
English
Other Identifying Numbers:
Journal ID: ISSN 0034-7310; CODEN: RBPMB
Submitting Site:
INIS
Size:
Pages: 115-123
Announcement Date:
Oct 15, 1990

Citation Formats

Pereira, C A, and Pickel, K. An immunological analysis of natural resistance to moise hepatitis virus (JHMV strain) infection in C3H mice. Brazil: N. p., 1987. Web.
Pereira, C A, & Pickel, K. An immunological analysis of natural resistance to moise hepatitis virus (JHMV strain) infection in C3H mice. Brazil.
Pereira, C A, and Pickel, K. 1987. "An immunological analysis of natural resistance to moise hepatitis virus (JHMV strain) infection in C3H mice." Brazil.
@misc{etde_6864649,
title = {An immunological analysis of natural resistance to moise hepatitis virus (JHMV strain) infection in C3H mice}
author = {Pereira, C A, and Pickel, K}
abstractNote = {Since the development of resistance against mouse hepatitis virus (JHMV strain) coincides with the maturation of the immune system, we studied the possible role of distinct immunological components in the resistance of adult mice during JHMV infection. Adult C3H mice naturally resistant to JHMV were rendered susceptible to infection by lethal {sup 60}Co-irradiation and were subsequently reconstituted with limiting numbers of syngeneic bone marrow cells or spleen cells. Resistance or susceptibility dependend on the number of cells used for reconstitution and the interval between reconsitution and infection. Spleen cells from suckling mice affected neither resistance nor susceptibility and peritoneal cells from adult mice and thymus cells reduced resistance. Persistence of JHMV was demonstrated by virus reactivation. Animals infected with JHMV only once before being rendered immunoincompetent showed a different pattern of resistance. One to four months after infection, 15 to 35% of the animals died after reconstitution without having been reinfected, and persisting JHMV was found in their liver, spleen and peritoneal exudate. The survivors (47 to 87%) were resistant to further JHMV infection during immunodeficiency. Animals immunized 3 times with JHMV before irradiation did not show virus reactivation and were fully resistant to JHMV reinfection after reconstitution. The level of neutralizing anti JHMV serum antibodies in the group of mice immunized only once was comparable with the level of those immunized 3 times. The role of macrophage activation and cell-mediated immunity in this model are discused as an explanation for the resistance to, and persistence of, JHMV. (author).}
journal = []
volume = {20:1}
journal type = {AC}
place = {Brazil}
year = {1987}
month = {Jan}
}