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J. Virol., 06 1997, 4829-4831, Vol 71, No. 6
JT Guo and JC Pugh
As an approach to identifying hepatocyte receptors for the avian
hepadnavirus duck hepatitis B virus (DHBV), hybridomas were prepared from
mice immunized with permissive duck hepatocytes. Monoclonal antibodies
(MAbs) were screened for the ability to inhibit binding of DHBV particles
to primary duck hepatocytes and to block infection. We identified two MAbs
which partially blocked binding and caused marked inhibition of infection
of primary duck hepatocytes with DHBV. Lack of cross-reactivity with DHBV
envelope proteins suggested that inhibition of infection was due to
specific interaction between the antibodies and a host cell surface
molecule. Both MAbs immunoprecipitated a 55-kDa protein (p55) expressed in
duck liver and several other duck tissues. p55 homologs were also
identified in other birds and mammals. We predict from our data that only a
small proportion of total cellular p55 molecules are expressed at the
surfaces of hepatocytes and that p55 is involved in some early step in the
infectious pathway.
Copyright © 1997, American Society for Microbiology
Monoclonal antibodies to a 55-kilodalton protein present in duck liver inhibit infection of primary duck hepatocytes with duck hepatitis B virus
Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111, USA.
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