scholarly journals Antigenic variation of influenza A virus nucleoprotein detected with monoclonal antibodies.

1980 ◽  
Vol 35 (1) ◽  
pp. 24-30 ◽  
Author(s):  
K L van Wyke ◽  
V S Hinshaw ◽  
W J Bean ◽  
R G Webster
2009 ◽  
Vol 90 (7) ◽  
pp. 1730-1733 ◽  
Author(s):  
Natalia L. Varich ◽  
Konstantin S. Kochergin-Nikitsky ◽  
Evgeny V. Usachev ◽  
Olga V. Usacheva ◽  
Alexei G. Prilipov ◽  
...  

The locations of amino acid positions relevant to antigenic variation in the nucleoprotein (NP) of influenza virus are not conclusively known. We analysed the antigenic structure of influenza A virus NP by introducing site-specific mutations at amino acid positions presumed to be relevant for the differentiation of strain differences by anti-NP monoclonal antibodies. Mutant proteins were expressed in a prokaryotic system and analysed by performing ELISA with monoclonal antibodies. Four amino acid residues were found to determine four different antibody-binding sites. When mapped in a 3D X-ray model of NP, the four antigenically relevant amino acid positions were found to be located in separate physical sites of the NP molecule.


2011 ◽  
Vol 85 (24) ◽  
pp. 13463-13467 ◽  
Author(s):  
M. Terajima ◽  
J. Cruz ◽  
M. D. T. Co ◽  
J.-H. Lee ◽  
K. Kaur ◽  
...  

2017 ◽  
Vol 91 (12) ◽  
Author(s):  
Netanel Tzarum ◽  
Ryan McBride ◽  
Corwin M. Nycholat ◽  
Wenjie Peng ◽  
James C. Paulson ◽  
...  

ABSTRACT Influenza A H15 viruses are members of a subgroup (H7-H10-H15) of group 2 hemagglutinin (HA) subtypes that include H7N9 and H10N8 viruses that were isolated from humans during 2013. The isolation of avian H15 viruses is, however, quite rare and, until recently, geographically restricted to wild shorebirds and waterfowl in Australia. The HAs of H15 viruses contain an insertion in the 150-loop (loop beginning at position 150) of the receptor-binding site common to this subgroup and a unique insertion in the 260-loop compared to any other subtype. Here, we show that the H15 HA has a high preference for avian receptor analogs by glycan array analyses. The H15 HA crystal structure reveals that it is structurally closest to H7N9 HA, but the head domain of the H15 trimer is wider than all other HAs due to a tilt and opening of the HA1 subunits of the head domain. The extended 150-loop of the H15 HA retains the conserved conformation as in H7 and H10 HAs. Furthermore, the elongated 260-loop increases the exposed HA surface and can contribute to antigenic variation in H15 HAs. Since avian-origin H15 HA viruses have been shown to cause enhanced disease in mammalian models, further characterization and immune surveillance of H15 viruses are warranted. IMPORTANCE In the last 2 decades, an apparent increase has been reported for cases of human infection by emerging avian influenza A virus subtypes, including H7N9 and H10N8 viruses isolated during 2013. H15 is the other member of the subgroup of influenza A virus group 2 hemagglutinins (HAs) that also include H7 and H10. H15 viruses have been restricted to Australia, but recent isolation of H15 viruses in western Siberia suggests that they could be spread more globally via the avian flyways that converge and emanate from this region. Here we report on characterization of the three-dimensional structure and receptor specificity of the H15 hemagglutinin, revealing distinct features and specificities that can aid in global surveillance of such viruses for potential spread and emerging threat to the human population.


Virology ◽  
2009 ◽  
Vol 385 (1) ◽  
pp. 218-226 ◽  
Author(s):  
Tong-Ming Fu ◽  
Daniel C. Freed ◽  
Melanie S. Horton ◽  
Jiang Fan ◽  
Michael P. Citron ◽  
...  

Hybridoma ◽  
2010 ◽  
Vol 29 (4) ◽  
pp. 321-326 ◽  
Author(s):  
Alexandra Nordmann ◽  
Ludmilla Wixler ◽  
Stephan Ludwig ◽  
Viktor Wixler

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