荧光定量PCR检测人巨细胞病毒的方法学建立

目的建立人巨细胞病毒（HCMV）的TaqMan MGB探针荧光定量PCR（FQ—PCR）检测方法。方法选取HCMV MIE exon4为PCR扩增靶序列,经TA克隆构建重组质粒作为定量标准品,经FQ—PCR反应条件的优化及方法学评价,再将其应用于临床检测。结果FQ—PCR最适循环参数为：95℃ 5 min;95℃ 20 s,60℃ 60 s（40 cycles）,20μl最适反应体系为：2．0mmol／L Mg^2＋、0．5μmol／L引物、1．5μmol／L探针、200μmol／L dNTP、2110×buffer、1．0 U Taq酶、2．0μl DNA模板。检测批内CV（变异系数）值为1．32％,批间CV值为1．96％;特异性较好;线性范围为10^2-10^8copies／μl。结论成功地建立了检测HCMV的FQ—PCR法,完全适用于临床检测。     

猕猴结核分枝杆菌PCR检测方法的建立与初步应用

目的建立猕猴结核分枝杆菌PCR快速检测方法。方法根据GenBank中报道的人型结核分枝杆菌标准株H37RV全基因序列,针对其中致病性结核分枝杆菌所特有的保守区域ESAT-6设计一对引物进行TouchdownPCR反应,利用此方法对100份野生来源猕猴全血标本进行检测,并与传统的PPD实验和咽拭子抗酸染色实验结果作比对。结果抽取33份野生来源猕猴的外周血,提取DNA进行扩增,扩增片段经纯化、回收克隆测序后用BLAST软件进行同源性对比,与GenBank中报道的序列基本相同,检测标本中有4份（4／33）为阳性,其中3份（3／33）标本与结核菌素试验和咽拭子抗酸染色试验结果相符合。结论建立了从猴全血中直接检测猴结核分枝杆菌DNA的TouchdownPCR方法,具有敏感性和特异性高,且简便的优点。     

猕猴逆转录病毒多重套式PCR检测方法的建立

分别针对编码STLV-1和SRV/D-1两种逆转录病毒膜蛋白的env基因进行引物设计,通过优化、调整PCR条件,建立一种能同时检测猕猴STLV-1和SRV/D-1两种逆转录病毒的多重PCR方法,用于猕猴种群逆转录病毒的常规监测。结果显示多重套式PCR产物片段大小与预期结果一致,进一步测序证实为目的产物,说明建立的多重套式PCR方法能同时检测出猕猴体内可能存在的STLV-1和SRV/D-1两种逆转录病毒。这种方法具有灵敏度高、特异性强、省时、试剂用量少和检测费用低等优点,因此可以作为一种新方法用于猕猴种群逆转录病毒的定性监测。     

一次PCR扩增单纯疱疹和巨细胞病毒基因的检测方法

宫内感染是影响优生优育质量的一个重要因素,由病毒引起的宫内感染主要有以下四类病原：ＨＳＶ、ＣＭＶ、ＴＯＸＯ和风疹病毒（ＲＶ）,其中ＨＳＶ和ＣＭＶ的感染率较高。孕期这两种病原的感染会影响胎儿的正常发育,严重的可导致流产甚至胎儿畸形。目前已有针对这两种病...     

猕猴血清B病毒抗体三种检测方法的比较

目的对B病毒（B virus）抗体检测的3种方法进行比较,寻求准确、可靠、经济的检疫方法。方法对以HSV-1为抗原的玻片酶免疫法、B病毒为抗原的玻片酶法（EIA）和酶联免疫吸附法（ELISA）的猕猴血清B病毒抗体检测结果进行比较。结果HSV-1为抗原的EIA与B病毒为抗原的EIA、ELISA检测结果符合率分别为97.7%和95.5%。结论HSV-1为抗原EIA的检测结果与B病毒抗原EIA和ELISA的检测结果一致性较好,可以做为初筛手段,且检测效果较好,投入资金相对最低,达到节约成本的目的。     

同时检测人多瘤病毒和巨细胞病毒PCR技术的建立及在肾移植受者中的初步应用

建立同时检测人多瘤病毒(BKV)和巨细胞病毒(CMV)载量的实时定量荧光PCR技术(FQ-PCR),并探讨其在肾移植术后感染监测中的应用。选择BKV和CMV核酸保守性序列作为靶基因,PCR扩增靶片段与质粒pcD-NA3.1(+)连接。通过测序技术对进行克隆筛选。提取质粒并采用10倍梯度稀释(5×103～107拷贝/mL)作为BKV和CMV核酸序列的标准品,并评价其灵敏度;采用对比正常人DNA、BKV阳性质控和CMV阳性质控评价其特异性;通过对标准品DNA分别进行批内和批间各20次重复实验,以其循环阈值(Ct)的变异系数(CV)评价其精密度。对480例肾移植受者外周血样本,进行FQ-PCR检测BKV和CMV DNA拷贝数,检测FK506血药浓度,并对两者进行相关性分析。重组质粒经测序检测显示含有靶BKV和CMV核酸序列。所建立的FQ-PCR方法,其最低检测下限均为5.0×103拷贝/mL的DNA标准品。正常人DNA的BKV和CMV拷贝数检测为阴性,而阳性对照能够发现荧光值显著变化,证实为针对靶DNA的特异性扩增;重复性检测显示批内差异分别为3.44%(BKV)和2.23%(CMV),批间差异分别为4.98%(BKV)和3.76%(CMV)。肾移植患者CMV感染的阳性率为27.08%(130/480),明显高于BKV的阳性率(13.33%,64/480,P<0.05),并且感染程度与免疫抑制剂FK506用量呈正相关。建立的同时检测BKV和CMV两种病毒载量的FQ-PCR方法具有快速、重复性好、灵敏的优点,可为临床监测肾移植术后病毒感染提供技术平台。     

RT—PCR检测蓝舌病毒技术的建立

蓝舌病毒 (ＢｌｕｅｔｏｎｇｕｅＶｉｒｕｓ,ＢＴＶ)是呼肠孤病毒科 (Ｒｅｏｖｉｒｉｄａｅ)环状病毒属 (Ｏｒｂｉｖｉｒｕｓ)的代表种 ,含10个节段的双链ＲＮＡ(ｄｓＲＮＡ)作基因组。其中 ,Ｌ2节段编码ＢＴＶ型特异性抗原ＶＰ2 ,Ｌ3节段和Ｓ7节段编码群特异性抗原多肽ＶＰ3和ＶＰ7。其中 ,ＶＰ7是ＢＴＶ粒子的主要结构多肽之一 ,其编码基因序列保守。ＶＰ7具有高度的抗原性 ,能刺激被感机体产生强的群特异性免疫反应[1] 。蓝舌病毒的易感宿主是牛、羊及野生反刍动物 ,死亡率高达 6 0 %～ 70 %以上 ,并且至今仍无有效的防治措施 ,对畜牧业…     

多重PCR同时检测人乳头瘤病毒、巨细胞病毒和沙眼衣原体

为了应用聚合酶链反应同时检测人巨细胞病毒（CMV）、人乳头瘤病毒（HPV）、沙眼衣原体（CT）,参照文献报道的基因序列,设计合成了三对能扩增370bp、450bp、510bp基因片段的引物,并对PCR扩增条件进行了优化。0.1fgHPV－DNA、CMV－DNA、CT－DNA即可被检出,得到了与设计片段相同的产物,且不扩增大肠杆菌、白色念球菌、解尿支原体等病原的核酸。对395例标本进行检查,各病原体的检出率分别是：HPV19.2%、CMV14.9%、CT5.1%。其中混合感染42例。PCR同时检测CMV、HPV、CT经济、快速、敏感、特异,可用于临床诊断和实验研究。     

猴副流感病毒SV5 PCR检测方法的建立与初步应用

目的建立检测SV5的PCR方法并加以初步应用。方法根据GenBank中报道的SV5序列,针对其中的SH基因设计引物进行PCR反应,扩增产物进行测序并用BLAST软件进行同源性比对,同时利用限制性内切酶的酶切反应以证实此PCR反应的特异性。在此基础上设计巢式PCR提高此方法的灵敏度。利用此方法对20份猴肾源细胞培养物和40份血清标本进行检测。结果利用设计的引物扩增出的序列测序结果证实与报道的SV5SH基因相对位置的序列一致。AccⅢ限制性内切酶可对PCR产物进行特异性酶切。巢式PCR比一次PCR的敏感度有所提高。用此方法检测的20份猴肾源细胞培养物和40份血清标本结果为阴性。结论初步建立了检测SV5病毒的PCR方法,排除实验室用20份猴肾源细胞培养物和40份血清标本SV5的污染。     

Nested real-time PCR for hepatitis A detection

Aims:  The hepatitis A virus (HAV) is one of the most important human foodborne pathogens causing a number of worldwide outbreaks each year. The detection of HAV in food samples remains a complex issue, because commonly used detection tools, such as conventional or even real-time PCR assays, are often unable to detect HAV with sufficient sensitivity. The aims of this study were to develop highly sensitive and specific nested real-time PCR (NRT-PCR)-based method for HAV detection in food and to compare it with currently available methods.
Methods and Results:  By combining conventional PCR, nested PCR and real-time PCR techniques, we have developed a specific NRT-PCR assay for the detection of HAV. The procedure involves two consecutive PCRs, the first of which is performed as a conventional RT-PCR using primers specific for HAV 5' noncoding region. The second reaction involves a real-time PCR using a nested primer pair specific for the first PCR product and a TaqMan probe.
Conclusions:  We have developed a novel NRT-PCR method capable of detecting as little as 0·2 PFU of HAV, which is significantly more sensitive than any other PCR technique tested in our system.
Significance and Impact of the Study:  NRT-PCR provides a potentially useful method for detecting HAV at extremely low levels, as frequently found in food samples, and can be potentially adopted as a regulatory method to ensure food safety.     

猴腺病毒（SAdV）PCR检测方法的建立及初步应用

目的建立SAdV特异的PCR检测方法并研究实验猴群和猴源性生物制品中SAdV感染或污染情况。方法比对分析多株SAdV序列,设计SAdV特异引物,优化PCR实验条件,建立的PCR方法经验证后检测实验猴群和猴源性生物制品,阳性产物测序并构建进化树。结果经特异性和敏感性鉴定,在设计的5对引物中确定一对最佳引物,可以区分SAdV和MAD,ICH,CELO且可以检测到的最小DNA量为47.9 pg/mL。PCR方法检测实验猴群,阳性率49.2%,测序及进化分析表明,SAdV感染型别呈广泛基因多样性。主要分布在G亚属和以SAdV-49为代表的分支。结论经测序验证,PCR检测方法具有很好准确性,初步应用表明我国实验猴群中SAdV高度流行,应加强实验猴群及相关生物制品中SAdV的监测,避免人类感染SAdV的潜在风险。     

Detection of Plasmodium vivax by Nested PCR and Real-Time PCR

Malaria is endemic in the Cukurova region while it is sporadic in other regions of Turkey. Therefore, the laboratory and clinical diagnosis of malaria is important for the treatment of malaria. In this study, 92 blood samples that were taken from the suspected malaria patients for routine diagnosis in a period of 10 years between 1999 and 2009 were analyzed. All of these blood samples were examined by microscopic examinations using Giemsa-stained thick blood films, nested PCR, and real-time PCR. The sensitivity-specificity and positive-negative predictive values for these diagnostic tests were then calculated. It was found that the positive predictive values of microscopic examination of thick blood films, nested PCR, and real-time PCR were 47.8%, 56.5%, and 60.9% for malaria, respectively. The real-time PCR was found to have a specificity of 75% and sensitivity of 100%, while specificity and sensitivity of nested PCR was found 81.2% and 97.7% according to the microscopic examination of thick blood films, respectively.     

绵羊肺腺瘤病特异性PCR及套式PCR诊断方法的建立

绵羊肺腺瘤是由外源性反转录病毒JSRV引起的接触性传染的肺肿瘤性疾病。感染羊没有针对JSRV的循环抗体,但在感染羊的肺肿瘤组织、淋巴网状系统及外周血单核细胞中可检测到外源性前病毒exJSRV及JSRV转录产物。健康羊基因组中存在15~20拷贝的内源性前病毒enJSRV,内外源性前病毒的结构基因高度相似,而在U3区存在差别,因而,设计了针对exJSRVU3区的特异性引物并在国内首次建立了一步法特异性PCR检测法及套式PCR检测法。以700ng健康羊基因组DNA为背景,梯度稀释阳性质粒pJSRV-LTR作为模板,比较两种方法的敏感性,结果表明套式法的敏感性是一步法的10倍以上,套式法也是目前可用于检测感染羊血液样品的唯一方法,可望在绵羊肺腺瘤病的流行病学调查及防控方面起重要作用。     

巢式PCR检测食蟹猴和猕猴中SRV和SFV

目的利用巢式PCR方法检测圈养的食蟹猴（Macaca fascicularis）和猕猴（Macaca mulatta）中猴D型逆转录病毒（Simian Type D Retrovirus SRV）和猴泡沫病毒（Simian foamy virus SFV）。方法针对SRV-env和SFV-pol基因的保守区序列设计特异性外引物,然后再设计特异性内引物。将外引物扩增出的片段克隆到PJET1.2blunt载体中作为阳性对照,运用NCBI中BLAST软件比对测序结果。用巢式PCR方法分别检测食蟹猴和猕猴中SRV和SFV。结果发现食蟹猴中SFV感染率为65.2%,SRV感染率为9.5%,猕猴中SFV感染率为60.5%,SRV感染率为12.8%。结论圈养的食蟹猴和猕猴SFV的感染率均较高,SRV感染率很低。     

Examining the Species-Specificity of Rhesus Macaque Cytomegalovirus (RhCMV) in Cynomolgus Macaques

Cytomegalovirus (CMV) is a highly species-specific virus that has co-evolved with its host over millions of years and thus restricting cross-species infection. To examine the extent to which host restriction may prevent cross-species research between closely related non-human primates, we evaluated experimental infection of cynomolgus macaques with a recombinant rhesus macaque-derived CMV (RhCMV-eGFP). Twelve cynomolgus macaques were randomly allocated to three groups: one experimental group (RhCMV-eGFP) and two control groups (UV-inactivated RhCMV-eGFP or media alone). The animals were given two subcutaneous inoculations at week 0 and week 8, and a subset of animals received an intravenous inoculation at week 23. No overt clinical or haematological changes were observed and PBMCs isolated from RhCMV-eGFP inoculated animals had comparable eGFP- and IE-1-specific cellular responses to the control animals. Following inoculation with RhCMV-eGFP, we were unable to detect evidence of infection in any blood or tissue samples up to 4 years post-inoculation, using sensitive viral co-culture, qPCR, and Western blot assays. Co-culture of urine and saliva samples demonstrated the presence of endogenous cynomolgus CMV (CyCMV) cytopathic effect, however no concomitant eGFP expression was observed. The absence of detectable RhCMV-eGFP suggests that the CyCMV-seropositive cynomolgus macaques were not productively infected with RhCMV-eGFP under these inoculation conditions. In a continued effort to develop CMV as a viral vector for an HIV/SIV vaccine, these studies demonstrate that CMV is highly restricted to its host species and can be highly affected by laboratory cell culture. Consideration of the differences between lab-adapted and primary viruses with respect to species range and cell tropism should be a priority in evaluating CMV as vaccine vector for HIV or other pathogens at the preclinical development stage.