New hepatitis B virus of cranes that has an unexpected broad host range

被引:46
作者
Prassolov, A
Hohenberg, H
Kalinina, T
Schneider, C
Cova, L
Krone, O
Frölich, K
Will, H
Sirma, H
机构
[1] Univ Hamburg, Heinrich Pette Inst Expt Virol & Immunol, D-20251 Hamburg, Germany
[2] Inst Zool & Wildlife Res, Berlin, Germany
[3] Engelhardt Inst Mol Biol, Moscow, Russia
[4] INSERM U271, Lyon, France
关键词
D O I
10.1128/JVI.77.3.1964-1976.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
All hepadnaviruses known so far have a very limited host range, restricted to their natural hosts and a few closely related species. This is thought to be due mainly to sequence divergence in the large envelope protein and species-specific differences in host components essential for virus propagation. Here we report an infection of cranes with a novel hepadnavirus, designated CHBV, that has an unexpectedly broad host range and is only distantly evolutionarily related to avihepadnaviruses of related hosts. Direct DNA sequencing of amplified CHBV DNA as well a sequencing of cloned viral genomes revealed that CHBV is most closely related to, although distinct from, Ross'goose hepatitis B virus (RGHBV) and slightly less closely related to duck hepatitis B virus (DHBV). Phylogenetically, cranes are very distant from geese and ducks and are most closely related to herons and storks. Naturally occurring hepadnaviruses in the last two species are highly divergent in sequence from RGHBV and DHBV and do not infect ducks or do so only marginally. In contrast, CHBV from crane sera and recombinant CHBV produced from LMH cells infected primary duck hepatocytes almost as efficiently as DHBV did. This is the first report of a rather broad host range of an avihepadnavirus. Our data imply either usage of similar or identical entry pathways and receptors by DHBV and CHBV, unusual host and virus adaptation mechanisms, or divergent evolution of the host genomes and cellular components required for virus propagation.
引用
收藏
页码:1964 / 1976
页数:13
相关论文
共 33 条
[11]   MYRISTYLATION OF A DUCK HEPATITIS-B VIRUS ENVELOPE PROTEIN IS ESSENTIAL FOR INFECTIVITY BUT NOT FOR VIRUS ASSEMBLY [J].
MACRAE, DR ;
BRUSS, V ;
GANEM, D .
VIROLOGY, 1991, 181 (01) :359-363
[12]   EXPERIMENTAL TRANSMISSION OF DUCK HEPATITIS-B VIRUS TO PEKIN DUCKS AND TO DOMESTIC GEESE [J].
MARION, PL ;
CULLEN, JM ;
AZCARRAGA, RR ;
VANDAVELAAR, MJ ;
ROBINSON, WS .
HEPATOLOGY, 1987, 7 (04) :724-731
[13]   VIRUS OF PEKIN DUCKS WITH STRUCTURAL AND BIOLOGICAL RELATEDNESS TO HUMAN HEPATITIS-B VIRUS [J].
MASON, WS ;
SEAL, G ;
SUMMERS, J .
JOURNAL OF VIROLOGY, 1980, 36 (03) :829-836
[14]   Sequence heterogeneity of heron hepatitis B virus genomes determined by full-length DNA amplification and direct sequencing reveals novel and unique features [J].
Netter, HJ ;
Chassot, S ;
Chang, SF ;
Cova, L ;
Will, H .
JOURNAL OF GENERAL VIROLOGY, 1997, 78 :1707-1718
[15]   DUCK HEPATITIS-B VIRUS-INFECTION OF MUSCOVY DUCK HEPATOCYTES AND NATURE OF VIRUS-RESISTANCE IN-VIVO [J].
PUGH, JC ;
SIMMONS, H .
JOURNAL OF VIROLOGY, 1994, 68 (04) :2487-2494
[16]   Identification and analysis of a new hepadnavirus in white storks [J].
Pult, I ;
Netter, HJ ;
Bruns, M ;
Prassolov, A ;
Sirma, H ;
Hohenberg, H ;
Chang, SF ;
Frölich, K ;
Krone, O ;
Kaleta, EF ;
Will, H .
VIROLOGY, 2001, 289 (01) :114-128
[17]   Primate hepatitis B viruses - genetic diversity, geography and evolution [J].
Robertson, BH ;
Margolis, HS .
REVIEWS IN MEDICAL VIROLOGY, 2002, 12 (03) :133-141
[18]  
SCHAFER S, 1998, ANIMAL MODELS EXPT S
[19]   THE DUCK HEPATITIS-B VIRUS PRE-C REGION ENCODES A SIGNAL SEQUENCE WHICH IS ESSENTIAL FOR SYNTHESIS AND SECRETION OF PROCESSED CORE PROTEINS BUT NOT FOR VIRUS FORMATION [J].
SCHLICHT, HJ ;
SALFELD, J ;
SCHALLER, H .
JOURNAL OF VIROLOGY, 1987, 61 (12) :3701-3709
[20]   MECHANISM, KINETICS, AND ROLE OF DUCK HEPATITIS-B VIRUS E-ANTIGEN EXPRESSION INVIVO [J].
SCHNEIDER, R ;
FERNHOLZ, D ;
WILDNER, G ;
WILL, H .
VIROLOGY, 1991, 182 (02) :503-512