Moody N J G, Horwood P F, Reynolds A, Mahony T J, Anderson I G, Oakey H J
Tropical and Aquatic Animal Health Laboratory, Department of Primary Industries and Fisheries, 180-202 River Boulevard, Townsville, Queensland 4810, Australia.
Dis Aquat Organ. 2009 Dec 3;87(3):151-60. doi: 10.3354/dao02130.
In Australia, disease caused by betanodavirus has been reported in an increasing number of cultured finfish since the first report of mortalities in 1990. Partial coat protein gene sequences from the T2 or T4 regions of 8 betanodaviruses from barramundi Lates calcarifer, sleepy cod Oxyeleotris lineolata, striped trumpeter Latris lineata, barramundi cod Cromileptes altivelis, Australian bass Macquaria novemaculata and gold-spotted rockcod Epinephelus coioides from several Australian states were determined. Analysis of the 606 bp nucleotide sequences of the T2 region of 4 isolates demonstrated the close relationship with isolates from the red-spotted grouper nervous necrosis virus (RGNNV) genotype and the Cluster Ia subtype. Comparison of a smaller 289 bp sequence from the T4 region identified 2 distinct groupings of the Australian isolates within the RGNNV genotype. Isolates from barramundi from the Northern Territory, barramundi, sleepy cod, barramundi cod and gold-spotted rockcod from Queensland, and striped trumpeter from Tasmania shared a 96.2 to 99.7% nucleotide identity with each other. These isolates were most similar to the RGNNV genotype Cluster Ia. Isolates from Australian bass from New South Wales and from barramundi from South Australia shared a 98.6% sequence identity with each other. However, these isolates only shared an 85.8 to 87.9% identity with the other Australian isolates and representative RGNNV isolates. The closest nucleotide identity to sequences reported in the literature for the New South Wales and South Australian isolates was to an Australian barramundi isolate (Ba94Aus) from 1994. These 2 Australian isolates formed a new subtype within the RGNNV genotype, which is designated as Cluster Ic.
在澳大利亚,自1990年首次报告鱼类死亡病例以来,由β-诺达病毒引起的疾病在养殖的有鳍鱼类中报告的数量不断增加。测定了来自澳大利亚几个州的尖吻鲈、细纹鳢、条纹笛鲷、驼背鲈、澳大利亚黑鲈和点带石斑鱼的8种β-诺达病毒T2或T4区域的部分衣壳蛋白基因序列。对4株分离株T2区域606 bp核苷酸序列的分析表明,它们与红斑石斑鱼神经坏死病毒(RGNNV)基因型和Cluster Ia亚型的分离株关系密切。对T4区域较小的289 bp序列进行比较,确定了RGNNV基因型内澳大利亚分离株的2个不同分组。来自北领地的尖吻鲈、昆士兰的尖吻鲈、细纹鳢、驼背鲈和点带石斑鱼,以及塔斯马尼亚的条纹笛鲷的分离株彼此之间的核苷酸同一性为96.2%至99.7%。这些分离株与RGNNV基因型Cluster Ia最相似。来自新南威尔士州的澳大利亚黑鲈和南澳大利亚州的尖吻鲈的分离株彼此之间的序列同一性为98.6%。然而,这些分离株与其他澳大利亚分离株和代表性RGNNV分离株的同一性仅为85.8%至87.9%。新南威尔士州和南澳大利亚州分离株与文献中报道的序列最接近的核苷酸同一性是与1994年的一株澳大利亚尖吻鲈分离株(Ba94Aus)。这2株澳大利亚分离株在RGNNV基因型内形成了一个新的亚型,被指定为Cluster Ic。