First Detection of Ehrlichia canis in Cerebrospinal Fluid From a Nonthrombocytopenic Dog with Meningoencephalitis By Broad‐Range PCR          下载免费PDF全文

G. Kaewmongkol  P. Maneesaay  N. Suwanna  B. Tiraphut  T. Krajarngjang  A. Chouybumrung  S. Kaewmongkol  T. Sirinarumitr  S. Jittapalapong  S.G. Fenwick 《Journal of veterinary internal medicine / American College of Veterinary Internal Medicine》2016,30(1):255-259

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金针菇异戊烯基焦磷酸异构酶基因的克隆及表达分析     

刘建雨  刘建辉  徐珍  于海龙  宋春艳  尚晓冬 《食用菌学报》2016,(3):10-14

PCR扩增了金针菇(Flammulina velutipes)异戊烯基焦磷酸异构酶基因(FvIDI)的DNA全长和开放阅读框序列.该基因的ORF全长753 bp,DNA全长923 bp,含有3个内含子和4个外显子,编码250个氨基酸,金针菇异戊烯基焦磷酸异构酶相对分子质量为28450,等电点为5.05.采用实时荧光定量PCR技术研究FvIDI基因在不同发育时期和不同温度下的表达量,结果显示,FvIDI基因在采收期菌盖中表达量最高,4℃诱导处理2～4 h和37℃诱导处理2～6 h的表达量明显高于常规温度21℃处理.  相似文献   

Assessing the within-herd prevalence of Coxiella burnetii milk-shedder cows using a real-time PCR applied to bulk tank milk     

Guatteo R  Beaudeau F  Joly A  Seegers H 《Zoonoses and public health》2007,54(5):191-194

Thirty-seven bulk tank milk (BTM) and individual milk samples of all contributing cows were tested for Coxiella burnetii detection by a real-time PCR assay and used to assess the relationship between the BTM PCR-response and (i) the within-herd prevalence of milk-shedder cows and (ii) the proportion of heavy milk-shedder cows. The within-herd prevalence of milk-shedder cows (i) was found to be significantly higher in herds with a positive BTM and (ii) increased significantly with the estimated titre in Coxiella burnetii obtained in positive BTM. The proportion of heavy milk-shedder cows among the milk-shedder cows increased significantly with an increased estimated titre in Coxiella burnetii in positive BTM. Therefore, a real-time PCR assay applied to BTM samples collected repeatedly over time appears to be a valuable tool to assess on a larger scale the status of herds towards Coxiella shedding, and to evaluate the efficiency of control actions aimed at controlling and/or preventing Coxiella shedding in dairy herds.  相似文献   

甜瓜黄斑病毒SYBR Green Ⅰ实时荧光定量PCR方法     

孙晓辉  潘睿婧  刘永光  王丹  石朝鹏  乔宁  孙作文  竺晓平 《植物病理学报》2023,53(1):119-125

为建立检测甜瓜黄斑病毒(melon yellow spot virus, MYSV)的SYBR Green Ⅰ实时荧光定量PCR(qPCR)方法。基于MYSV核衣壳蛋白基因保守序列设计qPCR特异性引物对,针对引物退火温度、引物浓度、特异性和敏感性进行系列优化。结果显示,优化后的qPCR方法最适退火温度为61.3℃,最适引物浓度为0.65μmol·L^-1,特异性强,灵敏度高,比PCR高100倍。以携带目的基因片段的重组质粒为标准品,构建的qPCR标准曲线循环阈值与模板浓度呈良好的线性关系,相关系数为0.999 7。实验样品验证表明建立的qPCR方法可用于MYSV的定量检测。  相似文献   

薄壳山核桃疮痂病菌TaqMan荧光定量PCR检测方法的建立及应用     

赵玉强  卓可儿  郭云  朱灿灿  王行军  陆小美  田艳丽  胡白石 《植物保护》2023,49(3):193-198

疮痂病是薄壳山核桃上最具毁灭性的病害,带菌植物材料是传播疮痂病的重要来源。准确、灵敏、快速的检测方法可为该病害流行规律调查和防控提供有力的依据。本文通过比较薄壳山核桃疮痂病菌Venturia effusa及其近似种之间的ITS序列差异,设计了特异性引物和TaqMan探针,建立了薄壳山核桃疮痂病菌的荧光定量PCR检测方法。特异性检测结果表明,该方法可以检测不同地区的薄壳山核桃疮痂病菌菌株,而对其近似种以及薄壳山核桃上的其他真菌均没有信号。本研究建立的检测方法对薄壳山核桃疮痂病菌DNA的最低检测限可达0.5 pg/μL。该方法用于田间样品检测时,检测时间仅需1 h,远快于常规的分离培养法。本研究建立的基于TaqMan探针的荧光定量PCR检测方法为薄壳山核桃疮痂病菌的快速检测和监测提供了有力工具。  相似文献   

鼠源细胞TaqMan实时荧光定量PCR检测方法的建立     

苏佳  赵炜  秦义娴  邓永  高月异  白洪旭  薛青红  陈晓春  吴华伟 《中国兽药杂志》2023,57(3):10-16

为对鼠源细胞进行鉴别检测,以鼠线粒体16S rRNA基因序列为靶位点设计特异性引物及探针,建立实时荧光定量PCR检测方法,并评价该方法的特异性及敏感性。结果显示,所建立的检测方法特异性好,针对鼠源细胞基因组荧光定量PCR扩增曲线良好,其他物种来源细胞基因组及生物制品原辅材料未出现特异性扩增曲线;敏感性高,基因拷贝数检出限度为45.3拷贝。本试验建立的荧光定量PCR检测方法能够有效地对鼠源细胞进行快速检测,为细胞质量控制提供了有效方法。  相似文献   

植物基因启动子的克隆方法及其应用   总被引：1，自引：0，他引：1  

尹辉　李丹张毅  李秋莉 《分子植物育种》2006,4(Z1):85-91

植物基因的表达调控已成为分子生物学研究热点,启动子是基因表达调控的重要顺式元件,启动子的克隆对于研究基因表达调控、构建基因工程载体、表达目的蛋白有着重要的意义。启动子克隆的方法很多,从常用的启动子陷阱技术筛选启动子到PCR方法的应用,此后相继问世的一些基于PCR的克隆启动子技术,如载体锚定PCR、反向PCR、接头PCR、交错热不对称PCR等,为克隆启动子提供了更可靠,更合理的方法。本文着重介绍了几种植物基因启动子的克隆方法,分析了它们的优缺点,并展望了今后的研究前景。  相似文献   

Determination of vc and mating types of Cryphonectria parasitica isolates by multiplex PCR and their genetic diversity in 13 chestnut-growing provinces of Turkey     

Deniz Çakar  Göksel Özer  Seçil Akıllı Şimşek  Salih Maden 《Forest Pathology》2023,53(3):e12813

Vegetative compatibility (vc) and mating types and genetic diversity of Cryphonectria parasitica isolates were determined using 183 isolates obtained from 215 infected chestnut trees growing in 13 provinces of Turkey. Based on the cultural aspects, 143 of these isolates were evaluated as virulent whereas the remaining 40 isolates were hypovirulent. When vc types of 183 isolates were classically differentiated, 135 of them matched to EU-1 (82.3%), 29 of them to EU-12 (17.6%) vc type, whereas 19 of them did not match to the two. When molecular vic markers were used, all the isolates were assigned to two EU vc types; 149 to EU-1 (81.4%) and 34 (18.5%) to EU-12. Of the majority of the isolates, 134 (73.2%) had mating-type MAT-1, while 44 (24%) isolates had MAT-2 and 5 (2.8%) isolates had both mating types. The population analysis based on two DNA marker systems, Inter-Primer Binding Site and Start Codon Targeted Polymorphism, showed no intraspecific genetic variation among the C. parasitica isolates. The prevalence of two dominant vc types revealed by this study shows that biological control with hypovirulent EU-1 and EU-12 isolates will be significant for the country. The results might be helpful to chestnut breeders carrying out resistance breeding studies to manage this disease based on hypovirulence attributed to Cryphonectria hypovirus 1.  相似文献   

玉米样品中转基因玉米Bt176含量检测     

吴明生  田雷  云晓敏  贾希海  律宝春 《分子植物育种》2007,5(5):715-719

根据其检测特异性,转基因产品检测技术可分为筛选、基因、构建和转化体特异性检测四类.由于转化体特异性检测方法的具有高度特异性,目前,一些发达国家对于转基因产品检测方法正逐步过渡到转化体特异性序列的检测方法.本研究针对转基因玉米Bt176的外源基因3'端与玉米基因组DNA相接区序列设计具有转化体特异性的引物和荧光探针.利用实时荧光定量PCR,以已知Bt176含量样品为标准样品建立内外源基因标准曲线,利用该标准曲线对多个玉米样品Bt176玉米成分含量进行检测,结果显示该方法检测结果准确,检测特异性强,Bt176玉米检测极限浓度达到0.001 ng/μL.同时该方法操作简单,适合转基因样品大批量检测.  相似文献   

数字PCR技术在动物疫病检测中的应用     

数字PCR技术在动物疫病检测中的应用 《畜牧与饲料科学》2021,42(6):124-128

为了支持动物疫病流行地区的控制及消除计划,以及在动物疫病非流行地区进行有效筛查,必须使用更加准确灵敏的诊断手段。数字PCR可实现绝对定量及痕量核酸的检测,与传统检测方法相比具有不依赖参考物或标准品、对抑制剂具有较高耐受性、灵敏度和精准度更高的优点。数字PCR作为一种定量分析的核酸检测新方法,在动物疫病检测中得到了应用,围绕数字PCR技术的原理、应用、存在的问题及发展趋势等进行综述及分析,为数字PCR在动物疫病检测中的进一步应用提供参考。  相似文献