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Cytokines Expression Profile and Kinetics of Peste des petits ruminants Virus Antigen and Antibody in Infected and Vaccinated Goats
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作者 Arun Patel Kaushal Kishor Rajak +5 位作者 Vinayagamurthy Balamurugan Arnab Sen Shashi Bhusan Sudhakar Veerakyathappa Bhanuprakash Raj Kumar Singh Awadh Bihari Pandey 《Virologica Sinica》 CAS CSCD 2012年第4期265-271,共7页
The present study deals with the co-ordination of cytokine (IL-4 and IFN-7) expression and kinetics of peste des petits ruminants (PPR) virus antigen and antibody in PPRV infected and vaccinated goats. The infecte... The present study deals with the co-ordination of cytokine (IL-4 and IFN-7) expression and kinetics of peste des petits ruminants (PPR) virus antigen and antibody in PPRV infected and vaccinated goats. The infected animals exhibited mixed cytokine (both TH1 and TH2) responses in the initial phase of the disease. The infected and dead goats had increased IFN-T response before their death; while IL-4 remained at the base level. The cytokine expression in recovered animals was almost similar to that of vaccinated ones, where a unique biphasic response of IL-4 expression was observed with an up-regulation of IFN-T on 7th days post vaccination (dpv). Analysis of PPR virus antigen and antibody kinetics in different components of blood from infected and vaccinated animais revealed that the PPR virus antigen load was highest in plasma followed by serum and blood of the infected animals, whereas vaccinated animals showed only marginal positivity on 9th dpv. The antibody titer was high in serum followed by plasma and blood in both vaccinated and infected animals. Therefore, it is inferred that the presence of antigen and antibody were significant with the expression of cytokine, and that a decreased response of IL-4 was noticed during intermediate phase of the disease i.e., 7 to 12m days post infection (dpi). This indicates the ability to mount a functional TH2 response after 14th dpi could be a critical determinant in deciding the survival of the PPR infected animal. 展开更多
关键词 Peste despetits ruminants (PPR) GOAT CYTOKINES Real time RT-PCR ELISA
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小反刍兽疫疫苗毒株与强毒株的鉴别性荧光RT-PCR检测方法的建立 被引量:7
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作者 袁向芬 吴绍强 林祥梅 《中国动物检疫》 CAS 2012年第7期30-34,共5页
对GenBank已公布的小反刍兽疫病毒N基因序列进行分析,设计引物与探针,建立PPRV通用型与Ⅱ系疫苗毒特异型二重实时荧光RT-PCR方法,同时建立针对PPRVⅣ系强毒株的特异型荧光PCR方法。特异性试验和灵敏度试验表明:建立的二重荧光RT-PCR方... 对GenBank已公布的小反刍兽疫病毒N基因序列进行分析,设计引物与探针,建立PPRV通用型与Ⅱ系疫苗毒特异型二重实时荧光RT-PCR方法,同时建立针对PPRVⅣ系强毒株的特异型荧光PCR方法。特异性试验和灵敏度试验表明:建立的二重荧光RT-PCR方法可特异性检测PPRV病毒,其HEX信号通道(通用型)和TAMRA信号通道(Ⅱ系疫苗毒特异型)的检测灵敏度分别可达101TCID50/mL和102TCID50/mL,完全满足PPRV的检测要求。用二重荧光RT-PCR方法对西藏采集的14份羊血清样品进行检测,并用建立的Ⅳ系强毒株特异型荧光PCR方法对二重荧光RT-PCR的检测效果进行评估,结果显示,该方法可有效甄别PPRV强毒株和疫苗毒株,避免假阳性结果的出现。 展开更多
关键词 小反刍兽疫病毒 鉴别 疫苗毒与感染毒 二重 荧光RT-PCR
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小反刍兽疫病毒(PPRV)与蓝舌病病毒(BTV)双重荧光RT-PCR快速检测方法的建立 被引量:3
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作者 李儒曙 苏惠龙 +5 位作者 罗宝正 赵福振 薄清如 邵建宏 邓湘辉 黄铮 《病毒学报》 CAS CSCD 北大核心 2017年第6期886-891,共6页
为了研制小反刍兽疫病毒(PPRV)与蓝舌病病毒(BTV)双重荧光RT-PCR快速检测试剂盒,根据GenBank公布的小反刍兽疫病毒、蓝舌病病毒的基因序列,设计两套特异性的引物和探针,建立基于Taqman探针的双重荧光RT-PCR快速检测小反刍兽疫病毒与蓝... 为了研制小反刍兽疫病毒(PPRV)与蓝舌病病毒(BTV)双重荧光RT-PCR快速检测试剂盒,根据GenBank公布的小反刍兽疫病毒、蓝舌病病毒的基因序列,设计两套特异性的引物和探针,建立基于Taqman探针的双重荧光RT-PCR快速检测小反刍兽疫病毒与蓝舌病病毒的方法。实验结果表明,该方法特异性好、灵敏度高,检测最低浓度为10拷贝/μL数量级阳性标准品。通过对临床样品的检测,证实本研究建立的检测方法具有较好的临床应用价值。 展开更多
关键词 小反刍兽疫病毒(PPRV) 蓝舌病病毒(BTV) 双重荧光RT-PCR
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