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Identification of a potential neutralizing linear epitope of hemagglutinin-neuraminidase in Newcastle disease virus
by
Liu, Haijin
, Huo, Na
, Chen, Hongjun
, Jin, Zhongyuan
, Yang, Zengqi
, Li, Yongshan
, Mou, Sujing
, Xiao, Sa
, Wei, Qiaolin
, Bi, Youkun
, Wang, Wenbin
in
Amino acids
/ Antibodies
/ Antigenic determinants
/ Antigens
/ Antisera
/ Avian orthoavulavirus 1
/ B-lymphocytes
/ Biomedical and Life Sciences
/ Biomedicine
/ Care and treatment
/ chickens
/ Development and progression
/ Epitopes
/ Exo-a-sialidase
/ fluorescent antibody technique
/ Genetic aspects
/ Health aspects
/ Hemagglutinin-neuraminidase
/ Hemagglutinins
/ HN protein
/ Immune response
/ Immunodominance
/ Immunodominant epitope
/ immunodominant epitopes
/ Immunofluorescence
/ Immunogenicity
/ LaSota strain
/ Lymphocytes B
/ mice
/ neutralization tests
/ Newcastle disease
/ Newcastle disease virus
/ Pathogens
/ Pepscan
/ Peptides
/ Plasmids
/ Poultry
/ Protective antigen
/ Proteins
/ Strains (organisms)
/ Vaccines
/ Veterinary RNA viruses
/ Virology
/ virulence
/ Viruses
/ Western blotting
2021
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Identification of a potential neutralizing linear epitope of hemagglutinin-neuraminidase in Newcastle disease virus
by
Liu, Haijin
, Huo, Na
, Chen, Hongjun
, Jin, Zhongyuan
, Yang, Zengqi
, Li, Yongshan
, Mou, Sujing
, Xiao, Sa
, Wei, Qiaolin
, Bi, Youkun
, Wang, Wenbin
in
Amino acids
/ Antibodies
/ Antigenic determinants
/ Antigens
/ Antisera
/ Avian orthoavulavirus 1
/ B-lymphocytes
/ Biomedical and Life Sciences
/ Biomedicine
/ Care and treatment
/ chickens
/ Development and progression
/ Epitopes
/ Exo-a-sialidase
/ fluorescent antibody technique
/ Genetic aspects
/ Health aspects
/ Hemagglutinin-neuraminidase
/ Hemagglutinins
/ HN protein
/ Immune response
/ Immunodominance
/ Immunodominant epitope
/ immunodominant epitopes
/ Immunofluorescence
/ Immunogenicity
/ LaSota strain
/ Lymphocytes B
/ mice
/ neutralization tests
/ Newcastle disease
/ Newcastle disease virus
/ Pathogens
/ Pepscan
/ Peptides
/ Plasmids
/ Poultry
/ Protective antigen
/ Proteins
/ Strains (organisms)
/ Vaccines
/ Veterinary RNA viruses
/ Virology
/ virulence
/ Viruses
/ Western blotting
2021
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Identification of a potential neutralizing linear epitope of hemagglutinin-neuraminidase in Newcastle disease virus
by
Liu, Haijin
, Huo, Na
, Chen, Hongjun
, Jin, Zhongyuan
, Yang, Zengqi
, Li, Yongshan
, Mou, Sujing
, Xiao, Sa
, Wei, Qiaolin
, Bi, Youkun
, Wang, Wenbin
in
Amino acids
/ Antibodies
/ Antigenic determinants
/ Antigens
/ Antisera
/ Avian orthoavulavirus 1
/ B-lymphocytes
/ Biomedical and Life Sciences
/ Biomedicine
/ Care and treatment
/ chickens
/ Development and progression
/ Epitopes
/ Exo-a-sialidase
/ fluorescent antibody technique
/ Genetic aspects
/ Health aspects
/ Hemagglutinin-neuraminidase
/ Hemagglutinins
/ HN protein
/ Immune response
/ Immunodominance
/ Immunodominant epitope
/ immunodominant epitopes
/ Immunofluorescence
/ Immunogenicity
/ LaSota strain
/ Lymphocytes B
/ mice
/ neutralization tests
/ Newcastle disease
/ Newcastle disease virus
/ Pathogens
/ Pepscan
/ Peptides
/ Plasmids
/ Poultry
/ Protective antigen
/ Proteins
/ Strains (organisms)
/ Vaccines
/ Veterinary RNA viruses
/ Virology
/ virulence
/ Viruses
/ Western blotting
2021
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Identification of a potential neutralizing linear epitope of hemagglutinin-neuraminidase in Newcastle disease virus
Journal Article
Identification of a potential neutralizing linear epitope of hemagglutinin-neuraminidase in Newcastle disease virus
2021
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Overview
Background
The hemagglutinin-neuraminidase (HN) protein of Newcastle disease virus (NDV) is a major antigen that can induce protective antibodies in poultry. However, its antigenic epitopes have not been fully elucidated. Therefore, defining the linear epitopes of HN, especially neutralizing epitopes, will be useful for revealing its antigenic characterization.
Methods
In this study, we analyzed B-cell immunodominant epitopes (IDEs) of the HN protein from the vaccine strain LaSota using pepscan technology with LaSota-specific chicken hyperimmune antisera. We constructed IDEs-RFP plasmids and prepared anti-IDEs peptide mouse sera to identify IDEs through immunological tests. At last, the different diluted anti-IDE antisera were used in BHK-21 cells to perform the neutralization test.
Results
Five IDEs of the HN were screened and further verified by indirect immunofluorescence assays, dot blots and Western blots with NDV- and IDEs-specific antisera. All five IDEs showed good immunogenicity. IDE5 (328–342 aa) could recognize only class II NDV but did not react with the class I strain. Most of the IDEs are highly conserved among the different strains. A neutralization test in vitro showed that the peptide-specific mouse antisera of IDE4 (242–256 aa) and HN341-355, a reported neutralizing linear epitope, could partially neutralize avirulent LaSota as well as virulent strains at similar levels, suggesting that IDE4 might be a potential neutralizing linear epitope.
Conclusion
The HN protein is a major protective antigen of NDV that can induce neutralizing antibodies in animals. We identified five IDEs of the HN using a pepscan approach with NDV-specific chicken hyperimmune antisera. The five IDEs could elicit specific antibodies in mice. IDE4 (242–256 aa) was identified as a novel potential neutralizing linear epitope. These results will help elucidate the antigenic epitopes of the HN and facilitate the development of NDV vaccines.
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