Genetic diversity and epidemiology of infectious hematopoietic necrosis virus in Alaska

被引:70
作者
Emmenegger, EJ
Meyers, TR
Burton, TO
Kurath, G
机构
[1] US Geol Survey, Western Fisheries Res Ctr, Biol Resources Div, Seattle, WA 98115 USA
[2] Alaska Dept Fish & Game, Juneau Fish Pathol Lab, Juneau, AK 99802 USA
[3] Alaska Dept Fish & Game, Anchorage Fish Pathol Lab, Anchorage, AK 99518 USA
关键词
IHNV; salmon; Alaska; diversity; epidemiology; phylogeny;
D O I
10.3354/dao040163
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Forty-two infectious hematopoietic necrosis virus (IHNV) isolates from Alaska were analyzed using the ribonuclease protection assay (RPA) and nucleotide sequencing. RPA analyses, utilizing 4 probes, N5, N3 (N gene), GF (G gene), and NV (NV gene), determined that the haplotypes of all 3 genes demonstrated a consistent spatial pattern. Virus isolates belonging to the most common haplotype groups were distributed throughout Alaska, whereas isolates in small haplotype groups were obtained from only 1 site (hatchery, lake, etc.). The temporal pattern of the GF haplotypes suggested a 'genetic acclimation' of the G gene, possibly due to positive selection on the glycoprotein. A pairwise comparison of the sequence data determined that the maximum nucleotide diversity of the isolates was 2.75% (10 mismatches) for the NV gene, and 1.99% (6 mismatches) for a 301 base pair region of the G gene, indicating that the genetic diversity of IHNV within Alaska is notably lower than in the more southern portions of the IHNV North American range. Phylogenetic analysis of representative Alaskan sequences and sequences of 12 previously characterized IHNV strains from Washington. Oregon, Idaho, California (USA) and British Columbia (Canada) distinguished the isolates into clusters that correlated with geographic origin and indicated that the Alaskan and British Columbia isolates may have a common viral ancestral lineage. Comparisons of multiple isolates from the same site provided epidemiological insights into viral transmission patterns and indicated that viral evolution, viral introduction, and genetic stasis were the mechanisms involved with IHN virus population dynamics in Alaska. The examples of genetic stasis and the overall low sequence heterogeneity of the Alaskan isolates suggested that they are evolutionarily constrained. This study establishes a baseline of genetic fingerprint patterns and sequence groups representing the genetic diversity of Alaskan IHNV isolates. This information could be used to determine the source of an IHN outbreak and to facilitate decisions in fisheries management of Alaskan salmonid stocks.
引用
收藏
页码:163 / 176
页数:14
相关论文
共 44 条
[31]  
2.0.CO
[32]  
2
[33]   MOLECULAR EPIZOOTIOLOGY AND EVOLUTION OF THE GLYCOPROTEIN AND NON-VIRION PROTEIN GENES OF INFECTIOUS HEMATOPOIETIC NECROSIS VIRUS, A FISH RHABDOVIRUS [J].
NICHOL, ST ;
ROWE, JE ;
WINTON, JR .
VIRUS RESEARCH, 1995, 38 (2-3) :159-173
[34]   BACTERIALLY EXPRESSED NUCLEOPROTEIN OF INFECTIOUS HEMATOPOIETIC NECROSIS VIRUS AUGMENTS PROTECTIVE IMMUNITY INDUCED BY THE GLYCOPROTEIN VACCINE IN FISH [J].
OBERG, LA ;
WIRKKULA, J ;
MOURICH, D ;
LEONG, JC .
JOURNAL OF VIROLOGY, 1991, 65 (08) :4486-4489
[35]   THE GENETIC DIVERSITY AND EPIZOOTIOLOGY OF INFECTIOUS HEMATOPOIETIC NECROSIS VIRUS [J].
OSHIMA, KH ;
ARAKAWA, CK ;
HIGMAN, KH ;
LANDOLT, ML ;
NICHOL, ST ;
WINTON, JR .
VIRUS RESEARCH, 1995, 35 (02) :123-141
[36]  
PASCUAL MA, 1993, HOMING STRAYING SALM, V25, P17
[37]   Ecological factors rather than temporal factors dominate the evolution of vesicular stomatitis virus [J].
Rodriguez, LL ;
Fitch, WM ;
Nichol, ST .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (23) :13030-13035
[38]  
ROSE J, 1987, RHABDOVIRUSES, P129
[39]   Evolution and probable transmission of intersubtype recombinant human immunodeficiency virus type 1 in a Zambian couple [J].
Salminen, MO ;
Carr, JK ;
Robertson, DL ;
Hegerich, P ;
Gotte, D ;
Koch, C ;
SandersBuell, E ;
Gao, F ;
Sharp, PM ;
Hahn, BH ;
Burke, DS ;
McCutchan, FE .
JOURNAL OF VIROLOGY, 1997, 71 (04) :2647-2655
[40]  
Sambrook J., 2002, MOL CLONING LAB MANU