Sequence polymorphism of the predicted human metapneumovirus G glycoprotein

被引:58
作者
Peret, TCT
Abed, Y
Anderson, LJ
Erdman, DD [1 ]
Boivin, G
机构
[1] Ctr Dis Control & Prevent, Resp & Enter Viruses Branch, Div Viral & Rickettsial Dis, Natl Ctr Infect Dis, Atlanta, GA 30333 USA
[2] Task Force Child Survival & Dev, Atlanta, GA USA
[3] Univ Laval, Dept Microbiol, Quebec Univ Hosp Ctr, Res Ctr Infect Dis, Quebec City, PQ G1V 4G2, Canada
关键词
D O I
10.1099/vir.0.19504-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The putative G glycoprotein genes of 25 human metapneumovirus (hMPV) field isolates obtained during five consecutive epidemic seasons (1997 to 2002) were sequenced. Sequence alignments identified two major genetic groups, designated groups 1 and 2, and two minor genetic clusters within each major group, designated subgroups A and B. Extensive nucleotide and deduced amino acid sequence variability was observed, consisting of high rates of nucleotide substitutions, use of alternative transcription-termination codons and insertions that retained the reading frame. Deduced amino acid sequences showed the greatest variability, with most differences located in the extracellular domain of the protein: nucleotide and amino acid sequence identities for the entire open reading frame ranged from 52 to 58% and 31 to 35 respectively, between the two major groups. Like the closely related avian pneumovirus and human and bovine respiratory syncytial viruses, the predicted G protein of hMPV shared the basic features of a type II mucin-like glycosylated protein. However, differences from these related viruses were also observed, e.g. lack of conserved cysteine clusters as seen in human respiratory syncytial virus and avian pneumovirus. The displacement of genetic groups of hMPV observed during the study period suggests that potential antigenic; differences in the G glycoprotein, which have evolved in response to immune-mediated pressure, may influence the circulation patterns of hMPV strains.
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页码:679 / 686
页数:8
相关论文
共 34 条
[1]   Nucleotide and predicted amino acid sequence-based analysis of the avian metapneumovirus type C cell attachment glycoprotein gene: Phylogenetic analysis and molecular epidemiology of US pneumoviruses [J].
Alvarez, R ;
Lwamba, HM ;
Kapczynski, DR ;
Njenga, MK ;
Seal, BS .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (04) :1730-1735
[2]   Sequence analysis of the N, P, M and F genes of Canadian human metapneumovirus strains [J].
Bastien, N ;
Normand, S ;
Taylor, T ;
Ward, D ;
Peret, TCT ;
Boivin, G ;
Anderson, LJ ;
Li, Y .
VIRUS RESEARCH, 2003, 93 (01) :51-62
[3]  
Bäyon-Auboyer MH, 2000, J GEN VIROL, V81, P2723, DOI 10.1099/0022-1317-81-11-2723
[4]   Genetic diversity between human metapneumovirus subgroups [J].
Biacchesi, S ;
Skiadopoulos, MH ;
Boivin, G ;
Hanson, CT ;
Murphy, BR ;
Collins, PL ;
Buchholz, UJ .
VIROLOGY, 2003, 315 (01) :1-9
[5]  
Boivin G, 2003, EMERG INFECT DIS, V9, P634
[6]   Virological features and clinical manifestations associated with human metapneumovirus:: A new paramyxovirus responsible for acute respiratory-tract infections in all age groups [J].
Boivin, G ;
Abed, Y ;
Pelletier, G ;
Ruel, L ;
Moisan, D ;
Côte, S ;
Peret, TCT ;
Erdman, DD ;
Anderson, LJ .
JOURNAL OF INFECTIOUS DISEASES, 2002, 186 (09) :1330-1334
[7]   EVOLUTION OF SUBGROUP-A RESPIRATORY SYNCYTIAL VIRUS - EVIDENCE FOR PROGRESSIVE ACCUMULATION OF AMINO-ACID CHANGES IN THE ATTACHMENT PROTEIN [J].
CANE, PA ;
PRINGLE, CR .
JOURNAL OF VIROLOGY, 1995, 69 (05) :2918-2925
[8]  
CANE PA, 1994, J CLIN MICROBIOL, V32, P1
[9]  
Elena SF, 2000, IUBMB LIFE, V49, P5, DOI 10.1080/152165400306296
[10]   Genetic and antigenic analysis of the G attachment protein of bovine respiratory syncytial virus strains [J].
Elvander, M ;
Vilcek, S ;
Baule, C ;
Uttenthal, Å ;
Ballagi-Pordány, A ;
Belák, S .
JOURNAL OF GENERAL VIROLOGY, 1998, 79 :2939-2946