首页> 外文期刊>Journal of Fish Diseases >Macrobrachium rosenbergii nodavirus infection in M. rosenbergii (de Man) with white tail disease cultured in Taiwan.
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Macrobrachium rosenbergii nodavirus infection in M. rosenbergii (de Man) with white tail disease cultured in Taiwan.

机译:罗氏沼虾罗氏沼虾诺达病毒感染台湾养殖的白尾病。

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White tail disease (WTD) is a serious problem in Macrobrachium rosenbergii hatcheries and nursery ponds in Asia. The causative agents have been identified as M. rosenbergii nodavirus (MrNV) and its associated extra small virus. This is the first report demonstrating MrNV virus in M. rosenbergii displaying WTD signs in Taiwan by reverse transcriptase-polymerase chain reaction (RT-PCR). Amplified fragments of 850 and 425 bp for RNA-1 and RNA-2 of MrNV, respectively, were obtained by RT-PCR. RT-PCR products of about 850 and 1121 bp for RNA-1 and RNA-2 of MrNV were also obtained using different primer pairs. The amplicons were individually cloned into pGEM-T vector and sequenced. Using this recombinant plasmid of MrNV RNA-2 as DNA template, the non-radioactive DNA probes were prepared by PCR amplification with DIG-11-dUTP. The probes were used to successfully detect MrNV infection in the striated muscle tissues of WTD-diseased prawns using in situ hybridization. The 1121 bp genomic fragment of RNA-2 of MrNV consisted of a unique open reading frame with 1116 nucleotides, and it encoded a structural protein with 371 amino acids. The nucleotide sequence of the partial genome of MrNV RNA-2 revealed a 97% identity with an Indian isolate. A phylogenetic tree constructed using the nucleotide sequence of the viral capsid gene from insect and fish nodaviruses revealed that the MrNV Taiwan isolate could be interpreted as a new genus within the family Nodaviridae. However, its position showed more affinity with Alphanodavirus than with Betanodavirus. The study confirmed the presence of MrNV infection in freshwater prawns cultured in Taiwan suffering from WTD.
机译:在亚洲罗氏沼虾孵化场和苗圃池塘中,白尾病(WTD)是一个严重的问题。病原已被鉴定为罗氏沼虾诺达病毒(MrNV)及其相关的特小病毒。这是第一份证明罗氏沼虾中的MrNV病毒通过逆转录聚合酶链反应(RT-PCR)在台湾显示出WTD征象的报告。通过RT-PCR获得了MrNV的RNA-1和RNA-2的分别为850和425bp的扩增片段。还使用不同的引物对获得了针对MrNV的RNA-1和RNA-2的约850和1121 bp的RT-PCR产物。将扩增子分别克隆到pGEM-T载体中并测序。以MrNV RNA-2的重组质粒为DNA模板,通过DIG-11-dUTP的PCR扩增制备了非放射性DNA探针。探针用于通过原位杂交成功检测WTD病性对虾横纹肌组织中的MrNV感染。 MrNV的RNA-2的1121 bp基因组片段由一个独特的开放阅读框组成,具有1116个核苷酸,并编码具有371个氨基酸的结构蛋白。 MrNV RNA-2的部分基因组的核苷酸序列与印度分离株显示97%的同一性。使用昆虫和鱼类诺达病毒的病毒衣壳基因的核苷酸序列构建的系统树表明,MrNV台湾分离株可被解释为诺达病毒科的一个新属。但是,它的位置显示出与Alphanodavirus的亲和力大于Betanodavirus。这项研究证实了台湾患有WTD的淡水虾养殖中存在MrNV感染。

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