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parvovirus相关的网络例句

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Porcine parvovirus is a major cause of reproductive failure in swine, manifested as embryonic resorption, fetal mummification, abortion and stillbirths .The virus is ubiquitous among swine throughout the world and is enzootic in most herds that have been tested.

猪细小病毒(porcine parvovirus,PPV)为引起母猪繁殖障碍的主要病原之一,猪细小病毒感染的主要特征是孕猪在怀孕前容易受到感染,可引起胚胎或胎儿的感染和死亡,导致母猪发生流产、死胎、胎儿木乃伊化及新生仔猪的死亡。

Waterfowl parvovirus infection is caused by goose parvovirus and Muscovy duck parvovirus and might lead to severe economic losses.

中文摘要水禽小病毒感染症由Goose parvovirus与Muscovy duck parvovirus所引起,此二病毒经常造成养禽业重大的经济损失。

Key words: Muscovy duck parvovirus;goose parvovirus;PCR;differential diagnosis

番鸭细小病毒;鹅细小病毒;聚合酶链式反应;鉴别诊断

In order to diagnose disease caused by muscovy duck parvovirus rapidly and accurately, and at same time, further study the taxonomic relationship between muscovy duck parivovirus and goose parvovirus, two pairs of PCR primers (LHMP1/LHMP2 and LHGP1/LHGP2) were designed respectively base on complete nucleotide sequences of Muscovy duck and Goose parvoviruses registered in the GenBank, The LHMP1 for the upper one and the LHMP2 for the lower one, corresponding to the specific nucleotides sequence 454-472 and 1173-1155 respectively in MDPV, and the LHGP1 for the the upper one and the LHGP2 for the lower one, corresponding to the specific nucleotides sequence 454-472 and 1173-1155 respectively in GPV.

为了能快速、准确地对番鸭细小病毒病进行诊断,同时为了能进一步弄清番鸭细小病毒与鹅细小病毒在分类学上是一种怎样的关系,比较GenBank中MDPV和GPV的基因序列,针对这两种病毒左阅读框编码非结构蛋白基因序列的相同区段,分别构建两对PCR引物。第一对引物LHMP1/LHMP2是根据MDPV的基因序列设计的,上游引物针对MDPV基因序列的454~472;下游引物针对基因序列的1173~1155,为19个碱基,扩增跨幅为719bp。

To establish a method to differentiate Muscovy duck parvovirus from goose parvovirus, primers GPVF/R1 and MDPVF1/R1 were designed according to the genomic sequences of GPV and MDPV to amplify the virus culture and nucleotide of GPV, MDPV, duck plague virus, duck hepatitis virus, duck reovirus, canine parvovirus and feline panleucopenia virus.

根据番鸭细小病毒和鹅细小病毒基因组的非同源序列各设计了1对引物MDPVF1/R1和GPVF1/R1,建立了一种PCR方法,用该PCR方法分别对GPV、MDPV、鸭瘟病毒、鸭肝炎病毒、鸭呼肠孤病毒、犬细小病毒和猫泛白细胞减少症病毒的病毒培养物及其核酸进行扩增。

The VP2 gene of Canine parvovirus isolated from a raccoon dog was amplified by PCR and cloned into the vector pMD18-T.

用PCR方法扩增犬细小病毒(Canine parvovirus,CPV)貉分离株(PV/貉/CC/1/86)的VP2蛋白基因,并将其克隆入pMD18-T,命名为pTCPV,进行测序分析。

In this study, we refer to the NCBI database to design primers which are used for amplification of the gene fragment of hepatopancreatic parvovirus、infectious hypodermal and hematopoietic necrosis virus and taura syndrome virus.

本研究从NCBI database资料中,分别在肝胰小病毒(hepatopancreatic parvovirus, HPV)、传染性皮下及造血组织坏死病毒(infectious hypodermal and hematopoietic necrosis virus, IHHNV)和桃拉病毒(taura syndrome virus, TSV)等三种常见之虾病毒中,各选出一段壳蛋白基因,利用重组蛋白的方式,在大肠杆菌中大量表现。

The materials including small intestines,large intestines,heart,lymph node,spleen,lungs,liver,kidneys,etc.obtained from a baby dog that were diagnosed to be canine parvovirus in the lab,were studied by freezing section and HE staining.

犬细小病毒病,又称犬细小病毒性肠炎,是由犬细小病毒(Canine parvovirus,CPV)引起的一种高度接触性传染病[1],临床上以剧烈呕吐、排血样粪便和心肌炎为特征[2]。

Canine parvovirus is a very hardy virus, and this is one of the reasons that parvovirus is so dangerous.

犬细小病毒是一个非常坚强的病毒,这是一个原因,细小病毒非常危险。

Objective To investigate human parvovirus B19 infection in children with a variety of clinical manisfestations.

目的 了解人类微小病毒B19(human parvovirus, B19在儿童中的感染情况。

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