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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Archives of virology 114 (1990), S. 121-136 
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary An antigenic analysis was carried out on 145 duck influenza virus isolates of the H3 haemagglutinin subtype obtained over five years continuous surveillance from the region of southern China, a hypothetical influenza epicentre. This was done using a panel of twelve monoclonal antibodies raised to an early human strain of the H3 subtype. We demonstrate the existence of an extensive range of antigenic profiles, broadly similar but not identical to the human H3 strain, which persisted over the five year period. This variability was as great during discrete twelve month periods as over the whole five years. Hierarchic progression (observed with human strains) was not evident and no correlation of antigenic drift, in either positive or negative direction, was observed with the domestic duck isolates over time. Changing dominant antigenic profiles were, however, observed in faecal isolates with time within a single farm. The much broader range of profiles detected in pond water samples from the same farm suggested the existence of a heterogeneous antigenic reservoir. Local switching of dominant profiles may occur due to changes of cohorts as birds are taken to market. In vitro and in vivo passage experiments revealed a high degree of heterogeneity in antigenic profiles in progeny of uncloned isolates, whereas the profiles of cloned isolates were largely conserved. These results suggested that particular antigenic profiles in primary isolates may result from mixtures of subpopulations of the wild type virus in natural duck infections. Switching between reactivity profiles of different progeny is likely to be largely a result of regrouping of these subpopulations with lesser effects due to mutation. Hypervariability in some of the cloned isolates was observed with a few monoclonal antibodies recognising a region of HA reported to be hypervariable in swine influenza virus. Reactivity with one particular antibody was correlated with passage in chicken eggs. The ability of this enormously varied pool of duck influenza H3 strains to cross the species barrier to man and give rise to viruses with hierarchic capabilities was considered.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] A highly pathogenic avian influenza virus, H5N1, caused disease outbreaks in poultry in China and seven other east Asian countries between late 2003 and early 2004; the same virus was fatal to humans in Thailand and Vietnam. Here we demonstrate a series of genetic reassortment events traceable ...
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The nucleotide sequences of the HA1 domain of the H1 hemagglutinin genes of A/duck/Hong Kong/36/76, A/duck/Hong Kong/196/77, A/sw/North Ireland/38, A/sw/Cambridge/39 and A/Yamagata/120/86 viruses were determined, and their evolutionary relationships were compared with those of previously sequenced hemagglutinin (H1) genes from avian, swine and human influenza viruses. A pairwise comparison of the nucleotide sequences revealed that the genes can be segregated into three groups, the avian, swine and human virus groups. With the exception of two swine strains isolated in the 1930s, a high degree of nucleotide sequence homology exists within the group. Two phylogenetic trees constructed from the substitutions at the synonymous site and the third codon position showed that the H1 hemagglutinin genes can be divided into three host-specific lineages. Examination of 21 hemagglutinin genes from the human and swine viruses revealed that two distinct lineages are present in the swine population. The swine strains, sw/North Ireland/38 and sw/Cambridge/39, are clearly on the human lineage, suggesting that they originate from a human A/WSN/33-like variant. However, the classic swine strain, sw/Iowa/15/30, and the contemporary human viruses are not direct descendants of the 1918 human pandemic strain, but did diverge from a common ancestral virus around 1905. Furthermore, previous to this the above mammalian viruses diverged from the lineage containing the avian viruses at about 1880.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Newcastle disease virus vaccine strain (La Sota) specific monoclonal antibody (La-1) was produced by immunizing mice with isolated glycoproteins of strain La Sota. This antibody was recognized only in the ELISA test in which it bound exclusively to La Sota strain out of a range of over 300 lentogenic, mesogenic and velogenic strains examined.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Archives of virology 25 (1968), S. 148-159 
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In this paper evidence is presented to show that the non-specific inhibitor of adenovirus type 5 haemagglutination is associated with a very labile, low molecular weight α1-globulin. This inhibitor flocculates the whole particle and a mixture of its soluble antigens. The data suggest that the inhibitor attaches directly to the haemagglutination sites on the virus and electron microscope evidence is produced to support this idea. Electron microscopy of the flocculated virus revealed that the particles appeared to be joined at the vertex projections. It is hoped that the study of the interaction of serum inhibitors and viruses could serve as a means of elucidating the nature of the virus surface.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Archives of virology 29 (1970), S. 1-24 
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Adenovirus type 5 was degraded by 8m urea to release three readily identifiable internal components and three species of surface hexon component each of which appeared to be associated with minor constituents which were lacking in the “soluble” hexon antigens. The vertex projection was destroyed. All components were recognized serologically. Whole virus antiserum appeared to contain antibody to both external and internal components. Any breakdown product that reacted with this antiserum and not “soluble” hexon antiserum was regarded as an internal component. The major internal component was estimated to be 170Å×23Å and of molecular weight (MW) 280,000. Two minor internal components were of approximate MW 5,000. The individual hexons, as well as “soluble” hexons were estimated to be 160Å×33Å and of MW 380,000. The three species were ascribed various positions in the virus particle. 1. Hexons surrounding the vertex capsomere — peripentons. 2. Hexons that lie along the adjacent sides — adjacent hexons. 3. Hexons occurring in triangular facets of six lying in the one plane — hexons proper. It is suggested that the central hole of the hexons plays a role in attaching them to the virus particle. This attachment may be mediated by the major internal component which could occur as a radial array around the DNA base structure.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Archives of virology 52 (1976), S. 181-186 
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Trypsinization rendered human group 0 erythrocytes highly susceptible to agglutination by chagres virus possibly due to the exposure of underlying lipid receptor groups to give rise to haemagglutination patterns firmer than those observed with gander cells.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Archives of virology 60 (1979), S. 105-113 
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The morphological, bio-physical and growth properties of the isolate duck/Hong Kong/D3/75 (D3/75) were consistent with this virus being a member of the paramyxovirus group. Using haemagglutination inhibition and neuraminidase inhibition tests no serological relationships between D3/75 and other paramyxoviruses could be demonstrated. The structural polypeptides of D3/75 were also typical of paramyxoviruses, consisting of 6–7 polypeptides ranging in molecular weight from 46,000–200,000 under reduced conditions. Two polypeptides were glycosylated.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Archives of virology 30 (1970), S. 238-244 
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In this paper evidence is presented to show that the non-specific inhibitor of adenovirus haemagglutination combines with hexons (soluble and viral) as well as with the haemagglutinating entities to produce flocculation. Therefore the haemagglutination inhibition test is best performed using either penton or fibre antigen as indicator and because of its stability the fibre is preferred. Of the hexons, the inhibitor appears to combine specifically with the hexons proper. It is concluded that the adjacent hexons and/or peripentons are responsible for attachment of virus to the host cell. The nature of these interactions is discussed. These results underline the importance of the use of serum inhibitors in the elucidation of the nature of the viral surface and the relationship of that surface to red blood cell and host cell systems. It is hoped that chemical identification of the active groupings involved will shed light on the fundamentals of the infective process.
    Type of Medium: Electronic Resource
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