Serveur d'exploration H2N2

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The immunogenicity of reassortants of the cold-adapted influenza A master strain A/Ann Arbor/6/60 is determined by both the genes for cold-adaptation and the haemagglutinin gene

Identifieur interne : 000123 ( PascalFrancis/Curation ); précédent : 000122; suivant : 000124

The immunogenicity of reassortants of the cold-adapted influenza A master strain A/Ann Arbor/6/60 is determined by both the genes for cold-adaptation and the haemagglutinin gene

Auteurs : G. A. Tannock [Australie] ; J. R. Romanova ; J. A. Paul

Source :

RBID : Pascal:95-0141912

Descripteurs français

English descriptors

Abstract

Two surface antigen segregants were prepared by co-infection of chicken embryo kidney cell cultures with reassortants of the cold-adapted influenza A master strain A/Ann Arbor/6/60-ca (H2N2) possessing the surface antigens of A/Queensland /6 /72 (H3N2) and A/Hong Kong/123/77 (H1N1) and other genes that were common to the master strain. The segregants were shown by serological tests to possess H3N1 and H1N2 surface antigens but it was not possible to determine the presence of HI or NI genes by single-stranded RNA polyacrylamide gel electrophoresis. The immunogenic properties of A/Queensland /6/72-ca and H3N1 segregant CR6/35/2/9 were compared by immunising mice intranasally with graded doses of each virus twice at an interval of 3 weeks and then challenging with the wild-type A/Queensland/6/72 (H3N2). Clearance of the challenge virus occurred in mice immunised with the same vaccinating dose, indicating that the immunogenicity of both the ca H3N2 and H3N1 viruses was identical and similar findings were obtained for mice immunised with A/Hong Kong/123/77-ca and the H1N2 segregant CR6/35/1/19 and challenged with the wild-type A/Hong Kong/123/77. Therefore, there appears to be a good correlation between immunogenicity and the inheritance of the haemagglutinin gene
pA  
A01 01  1    @0 0304-8608
A03   1    @0 Arch. virol.
A05       @2 140
A06       @2 1
A08 01  1  ENG  @1 The immunogenicity of reassortants of the cold-adapted influenza A master strain A/Ann Arbor/6/60 is determined by both the genes for cold-adaptation and the haemagglutinin gene
A11 01  1    @1 TANNOCK (G. A.)
A11 02  1    @1 ROMANOVA (J. R.)
A11 03  1    @1 PAUL (J. A.)
A14 01      @1 Royal Melbourne inst. technology, dep. applied biotechnology @2 Melbourne Victoria 3001 @3 AUS @Z 1 aut.
A20       @1 201-209
A21       @1 1995
A23 01      @0 ENG
A43 01      @1 INIST @2 6355 @5 354000059268530180
A44       @0 0000
A45       @0 9 ref.
A47 01  1    @0 95-0141912
A60       @1 P @3 CC
A61       @0 A
A64 01  1    @0 Archives of virology
A66 01      @0 AUT
C01 01    ENG  @0 Two surface antigen segregants were prepared by co-infection of chicken embryo kidney cell cultures with reassortants of the cold-adapted influenza A master strain A/Ann Arbor/6/60-ca (H2N2) possessing the surface antigens of A/Queensland /6 /72 (H3N2) and A/Hong Kong/123/77 (H1N1) and other genes that were common to the master strain. The segregants were shown by serological tests to possess H3N1 and H1N2 surface antigens but it was not possible to determine the presence of HI or NI genes by single-stranded RNA polyacrylamide gel electrophoresis. The immunogenic properties of A/Queensland /6/72-ca and H3N1 segregant CR6/35/2/9 were compared by immunising mice intranasally with graded doses of each virus twice at an interval of 3 weeks and then challenging with the wild-type A/Queensland/6/72 (H3N2). Clearance of the challenge virus occurred in mice immunised with the same vaccinating dose, indicating that the immunogenicity of both the ca H3N2 and H3N1 viruses was identical and similar findings were obtained for mice immunised with A/Hong Kong/123/77-ca and the H1N2 segregant CR6/35/1/19 and challenged with the wild-type A/Hong Kong/123/77. Therefore, there appears to be a good correlation between immunogenicity and the inheritance of the haemagglutinin gene
C02 01  X    @0 002A05C07
C03 01  X  FRE  @0 Influenzavirus A @2 NW @5 01
C03 01  X  ENG  @0 Influenzavirus A @2 NW @5 01
C03 01  X  SPA  @0 Influenzavirus A @2 NW @5 01
C03 02  X  FRE  @0 Souche atténuée @5 02
C03 02  X  ENG  @0 Attenuated strain @5 02
C03 02  X  SPA  @0 Cepa atenuada @5 02
C03 03  X  FRE  @0 Adaptation @5 03
C03 03  X  ENG  @0 Adaptation @5 03
C03 03  X  SPA  @0 Adaptación @5 03
C03 04  X  FRE  @0 Froid @5 04
C03 04  X  ENG  @0 Cold @5 04
C03 04  X  SPA  @0 Frío @5 04
C03 05  X  FRE  @0 Hémagglutinine @5 05
C03 05  X  ENG  @0 Hemagglutinin @5 05
C03 05  X  SPA  @0 Hemoaglutinina @5 05
C03 06  X  FRE  @0 Relation structure propriété @5 06
C03 06  X  ENG  @0 Property structure relationship @5 06
C03 06  X  SPA  @0 Relación estructura propiedad @5 06
C03 07  X  FRE  @0 Immunogénicité @5 07
C03 07  X  ENG  @0 Immunogenicity @5 07
C03 07  X  SPA  @0 Inmunogenicidad @5 07
C03 08  X  FRE  @0 Immunisation @5 08
C03 08  X  ENG  @0 Immunization @5 08
C03 08  X  SPA  @0 Inmunización @5 08
C03 09  X  FRE  @0 Souris @5 09
C03 09  X  ENG  @0 Mouse @5 09
C03 09  X  SPA  @0 Ratón @5 09
C03 10  X  FRE  @0 Voie intranasale @5 10
C03 10  X  ENG  @0 Intranasally administration @5 10
C03 10  X  SPA  @0 Vía intranasal @5 10
C03 11  X  FRE  @0 Réassortiment génétique @4 CD @5 96
C03 11  X  ENG  @0 Genetic reassortment @4 CD @5 96
C07 01  X  FRE  @0 Influenzavirus @2 NW
C07 01  X  ENG  @0 Influenzavirus @2 NW
C07 01  X  SPA  @0 Influenzavirus @2 NW
C07 02  X  FRE  @0 Orthomyxoviridae @2 NW
C07 02  X  ENG  @0 Orthomyxoviridae @2 NW
C07 02  X  SPA  @0 Orthomyxoviridae @2 NW
C07 03  X  FRE  @0 Virus @2 NW
C07 03  X  ENG  @0 Virus @2 NW
C07 03  X  SPA  @0 Virus @2 NW
C07 04  X  FRE  @0 Rodentia @2 NS
C07 04  X  ENG  @0 Rodentia @2 NS
C07 04  X  SPA  @0 Rodentia @2 NS
C07 05  X  FRE  @0 Mammalia @2 NS
C07 05  X  ENG  @0 Mammalia @2 NS
C07 05  X  SPA  @0 Mammalia @2 NS
C07 06  X  FRE  @0 Vertebrata @2 NS
C07 06  X  ENG  @0 Vertebrata @2 NS
C07 06  X  SPA  @0 Vertebrata @2 NS
C07 07  X  FRE  @0 Glycoprotéine @5 27
C07 07  X  ENG  @0 Glycoproteins @5 27
C07 07  X  SPA  @0 Glicoproteina @5 27
N21       @1 088

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Pascal:95-0141912

Le document en format XML

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<div type="abstract" xml:lang="en">Two surface antigen segregants were prepared by co-infection of chicken embryo kidney cell cultures with reassortants of the cold-adapted influenza A master strain A/Ann Arbor/6/60-ca (H2N2) possessing the surface antigens of A/Queensland /6 /72 (H3N2) and A/Hong Kong/123/77 (H1N1) and other genes that were common to the master strain. The segregants were shown by serological tests to possess H3N1 and H1N2 surface antigens but it was not possible to determine the presence of HI or NI genes by single-stranded RNA polyacrylamide gel electrophoresis. The immunogenic properties of A/Queensland /6/72-ca and H3N1 segregant CR6/35/2/9 were compared by immunising mice intranasally with graded doses of each virus twice at an interval of 3 weeks and then challenging with the wild-type A/Queensland/6/72 (H3N2). Clearance of the challenge virus occurred in mice immunised with the same vaccinating dose, indicating that the immunogenicity of both the ca H3N2 and H3N1 viruses was identical and similar findings were obtained for mice immunised with A/Hong Kong/123/77-ca and the H1N2 segregant CR6/35/1/19 and challenged with the wild-type A/Hong Kong/123/77. Therefore, there appears to be a good correlation between immunogenicity and the inheritance of the haemagglutinin gene</div>
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<s0>Rodentia</s0>
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<fC07 i1="04" i2="X" l="ENG">
<s0>Rodentia</s0>
<s2>NS</s2>
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<s0>Vertebrata</s0>
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<fC07 i1="06" i2="X" l="ENG">
<s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="07" i2="X" l="FRE">
<s0>Glycoprotéine</s0>
<s5>27</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>Glycoproteins</s0>
<s5>27</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Glicoproteina</s0>
<s5>27</s5>
</fC07>
<fN21>
<s1>088</s1>
</fN21>
</pA>
</standard>
</inist>
</record>

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   |flux=    PascalFrancis
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   |texte=   The immunogenicity of reassortants of the cold-adapted influenza A master strain A/Ann Arbor/6/60 is determined by both the genes for cold-adaptation and the haemagglutinin gene
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