Further investigation on the mode of entry of human rotavirus into cells |
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Authors: | H. Suzuki S. Kitaoka T. Sato T. Konno Y. Iwasaki Y. Numazaki N. Ishida |
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Affiliation: | (1) Department of Microbiology and Parasitology, Royal Veterinary College, London, UK |
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Abstract: | Summary Monoclonal antibodies (MAbs) to 2 epitopes on the haemagglutininneuraminidase (HN) protein of the Ulster strain of Newcastle disease virus neutralized synergistically: MAbs to HN-1 and HN-2 neutralized 1.2 and 1.7 log10 infectious units (i. u.) of virus when single as compared to 4.1 when combined. Although MAb to HN-1 but not to HN-2 inhibited haemagglutination they both neutralized more virus on desialized cells compared to normal cells and were considered to have interfered with viral attachments in a cooperative manner when combined. A third MAb to fusion (F) protein reduced infectivity by five log10 i. u. HN-1, HN-2 and F were not the only immunodominant epitopes because mutants, which simultaneously lacked all 3 epitopes, were indistinguishable from wild type when neutralized by polyclonal mouse, rabbit or chicken antiserum to whole virus.With 2 Figures |
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