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Journal of Virology, January 2000, p. 1045-1050, Vol. 74, No. 2
Department of Medical Microbiology,
Cardiovascular Research Institute Maastricht, University of
Maastricht, 6202 AZ Maastricht, The Netherlands
Received 24 June 1999/Accepted 14 October 1999
The rat cytomegalovirus (RCMV) r144 gene encodes a polypeptide
homologous to major histocompatibility complex class I heavy chains. To
study the role of r144 in virus replication, an RCMV r144 null mutant
strain (RCMV
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
The r144 Major Histocompatibility Complex Class
I-Like Gene of Rat Cytomegalovirus Is Dispensable for both Acute and
Long-Term Infection in the Immunocompromised Host
r144) was generated. This strain replicated with
efficiency similar to that of wild-type (WT) RCMV in vitro.
Additionally, WT RCMV and RCMV
r144 were found not to differ in their
replication characteristics in vivo. First, the survival rate was
similar among groups of immunosuppressed rats infected with either
RCMV
r144 or WT RCMV. Second, the dissemination of virus did not
differ in either RCMV
r144- or WT RCMV-infected, immunosuppressed
rats, either in the acute phase of infection or approximately 1 year
after infection. These data indicate that the RCMV r144 gene is
essential neither for virus replication in the acute phase of infection
nor for long-term infection in immunocompromised rats. Interestingly,
in a local infection model in which footpads of immunosuppressed rats
were inoculated with virus, a significantly higher number of
infiltrating macrophage cells as well as of CD8+ T cells
was observed in WT RCMV-infected paws than in RCMV
r144-infected paws. This suggests that r144 might function in the interaction with
these leukocytes in vivo.
*
Corresponding author. Mailing address: Department of
Medical Microbiology, University of Maastricht, P.O. Box 5800, 6202 AZ Maastricht, The Netherlands. Phone: 31 43 3876669. Fax: 31 43 3876643. E-mail: kvi{at}lmib.azm.nl.
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