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首页> 外文期刊>Virus Genes >Identification of recombination in novel goose parvovirus isolated from domesticated Jing-Xi partridge ducks in South China
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Identification of recombination in novel goose parvovirus isolated from domesticated Jing-Xi partridge ducks in South China

机译:在华南驯化京溪鹧鸭子中分离出新型鹅剖腹产的重组鉴定

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Outbreaks of short beak and dwarfism syndrome (SBDS), caused by a novel goose parvovirus (NGPV), have occurred in China since 2015. This rapidly spreading, infectious disease affects ducks in particular, with a high morbidity and low mortality rate, causing huge economic losses. This study analyzed the evolution of NGPV isolated from Jing-Xi partridge duck with SBDS in South China. Complete genome sequences of the NGPV strains GDQY1802 and GDSG1901 were homologous with other GPV/NGPV and Muscovy duck parvovirus (MDPV) strains. Phylogenetic analysis showed that the NGPV isolated from mainland China was related to the Taiwan 82-0321v strain of GPV. In contrast to 82-0321v and the SDLC01 strain, which was first isolated from China, the two isolates showed no deletions in the inverted terminal repeat (ITR) region. Further, in these isolates, 24 amino acid sites of the replication protein were different compared to that of GPV live vaccine strain 82-0321v, and 12 sites were unique across all NGPV isolates. These isolates also showed differences in 17 amino acid sites of the capsid protein from that of 82-0321v, two of which were the same as those in MDPV. Recombination analysis identified the major parents of GDSG1901 and GDQY1802 as the NGPV-GD and NGPV-Hun18 strains, and the minor parents as the classical GPV 06-0329 and GPV LH strains, respectively. GDQY1802 and GDSG1901 are recombinant GPV-related parvovirus isolated from domesticated partridge duck. Recombination is evident in the evolution of NGPV, and as such, the use of live attenuated vaccines for NGPV requires further study.
机译:自2015年以来,由新型鹅细小病毒(NGPV)引起的短喙和侏儒综合征(SBDS)在中国暴发。这种迅速传播的传染病尤其影响鸭子,发病率高,死亡率低,造成巨大的经济损失。本研究分析了我国南方产SBDS的京西鹧鸪鸭NGPV的进化。NGPV株GDQY1802和GDSG1901的全基因组序列与其他GPV/NGPV和番鸭细小病毒(MDPV)株同源。系统发育分析表明,从中国大陆分离的NGPV与台湾的GPV 82-0321v株有关。与82-0321v和首次从中国分离的SDLC01菌株相比,这两个菌株在倒末端重复序列(ITR)区域没有缺失。此外,在这些分离株中,复制蛋白的24个氨基酸位点与GPV活疫苗株82-0321v不同,在所有NGPV分离株中有12个位点是唯一的。这些分离物在衣壳蛋白的17个氨基酸位点上与82-0321v的衣壳蛋白存在差异,其中两个与MDPV中的相同。重组分析确定GDSG1901和GDQY1802的主要亲本分别为NGPV-GD和NGPV-Hun18菌株,次要亲本分别为经典GPV 06-0329和GPV LH菌株。GDQY1802和GDSG1901是从家养鹧鸪鸭中分离的重组GPV相关细小病毒。重组在NGPV的进化中很明显,因此,NGPV减毒活疫苗的使用需要进一步研究。

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