Changes in the haemagglutinin and the neuraminidase genes prior to the emergence of highly pathogenic H7N1 avian influenza viruses in Italy

被引:263
作者
Banks, J [1 ]
Speidel, ES
Moore, E
Plowright, L
Piccirillo, A
Capua, I
Cordioli, P
Fioretti, A
Alexander, DJ
机构
[1] VLA Weybridge, Addlestone KT15 3NB, Surrey, England
[2] Ist Zooprofilatt Sperimentale Venezie, Padua, Italy
[3] Ist Zooprofilatt Lombardia & Emilia Romagna, Brescia, Italy
[4] Univ Naples Federico II, Naples, Italy
关键词
D O I
10.1007/s007050170128
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Outbreaks of avian influenza due to an H7N1 virus of low pathogenicity occurred in domestic poultry in northern Italy from March 1999 until December 1999 when a highly pathogenic avian influenza (HPAI) virus emerged. Nucleotide sequences were determined for the HA1 and the stalk region of the neuraminidase (NA) for viruses from the outbreaks. The HPAI viruses have an unusual multibasic haemagglutinin (HA) cleavage site motif, PEIPKG (SRVR) under bar RGLF. Phylogenetic analysis showed that the HPAI viruses arose from low pathogenicity viruses and that they are most closely related to a wild bird isolate, A/teal/Taiwan/98. Additional glycosylation sites were present, at amino acid position 149 of the HA for two separate lineages, and at position 123 for all HPAI and some low pathogenicity viruses. Other viruses had no additional glycosylation sites. All viruses examined from the Italian outbreaks had a 22 amino acid deletion in the NA stalk that is not present in the N1 genes of the wild bird viruses examined. We conclude that the Italian HPAI viruses arose from low pathogenicity strains, and that a deletion in the NA stalk followed by the acquisition of additional glycosylation near the receptor binding site of HA1 may be an adaptation of H7 viruses to a new host species i.e. domestic poultry.
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页码:963 / 973
页数:11
相关论文
共 31 条
[1]  
[Anonymous], 1992, OFFICE J EUROPEAN CO, VL167, P1
[2]   Characterisation of an avian influenza A virus isolated from a human - is an intermediate host necessary for the emergence of pandemic influenza viruses? [J].
Banks, J ;
Speidel, E ;
Alexander, DJ .
ARCHIVES OF VIROLOGY, 1998, 143 (04) :781-787
[3]   Phylogenetic analysis of H7 haemagglutinin subtype influenza A viruses [J].
Banks, J ;
Speidel, EC ;
McCauley, JW ;
Alexander, DJ .
ARCHIVES OF VIROLOGY, 2000, 145 (05) :1047-1058
[4]   PROTEOLYTIC CLEAVAGE OF INFLUENZA-VIRUS HEMAGGLUTININS - PRIMARY STRUCTURE OF THE CONNECTING PEPTIDE BETWEEN HA1 AND HA2 DETERMINES PROTEOLYTIC CLEAVABILITY AND PATHOGENICITY OF AVIAN INFLUENZA-VIRUSES [J].
BOSCH, FX ;
GARTEN, W ;
KLENK, HD ;
ROTT, R .
VIROLOGY, 1981, 113 (02) :725-735
[5]  
Coffin J. M., 1990, Applied Virology Research, V2, P11
[6]  
Domingo Esteban, 1994, P161
[7]   EVOLUTIONARY TREES FROM DNA-SEQUENCES - A MAXIMUM-LIKELIHOOD APPROACH [J].
FELSENSTEIN, J .
JOURNAL OF MOLECULAR EVOLUTION, 1981, 17 (06) :368-376
[8]  
FELSENSTEINJ, 1994, EVOLUTION, V38, P16
[9]   Long term trends in the evolution of H(3) HA1 human influenza type A [J].
Fitch, WM ;
Bush, RM ;
Bender, CA ;
Cox, NJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (15) :7712-7718
[10]   Evolution of H5 subtype avian influenza A viruses in North America [J].
Garcia, M ;
Suarez, DL ;
Crawford, JM ;
Latimer, JW ;
Slemons, RD ;
Swayne, DE ;
Perdue, ML .
VIRUS RESEARCH, 1997, 51 (02) :115-124