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Enhancement of porcine in vitro embryonic development through luteolin‑mediated activation of the Nrf2/Keap1 signaling pathway
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作者 Se-Been Jeon Pil-Soo Jeong +5 位作者 Min Ju Kim Hyo-Gu Kang Bong-Seok Song Sun-Uk Kim Seong-Keun Cho Bo-Woong Sim 《Journal of Animal Science and Biotechnology》 SCIE CAS CSCD 2024年第2期600-613,共14页
Background Oxidative stress,caused by an imbalance in the production and elimination of intracellular reactive oxygen species(ROS),has been recognized for its detrimental effects on mammalian embryonic development.Lut... Background Oxidative stress,caused by an imbalance in the production and elimination of intracellular reactive oxygen species(ROS),has been recognized for its detrimental effects on mammalian embryonic development.Luteolin(Lut)has been documented for its protective effects against oxidative stress in various studies.However,its specific role in embryonic development remains unexplored.This study aims to investigate the influence of Lut on porcine embryonic development and to elucidate the underlying mechanism.Results After undergoing parthenogenetic activation(PA)or in vitro fertilization,embryos supplemented with 0.5μmol/L Lut displayed a significant enhancement in cleavage and blastocyst formation rates,with an increase in total cell numbers and a decrease in the apoptosis rate compared to the control.Measurements on D2 and D6 revealed that embryos with Lut supplementation had lower ROS levels and higher glutathione levels compared to the control.Moreover,Lut supplementation significantly augmented mitochondrial content and membrane potential.Intriguingly,activation of the Nrf2/Keap1 signaling pathway was observed in embryos supplemented with Lut,leading to the upregulation of antioxidant-related gene transcription levels.To further validate the relationship between the Nrf2/Keap1 signaling pathway and effects of Lut in porcine embryonic development,we cultured PA embryos in a medium supplemented with brusatol,with or without the inclusion of Lut.The positive effects of Lut on developmental competence were negated by brusatol treatment.Conclusions Our findings indicate that Lut-mediated activation of the Nrf2/Keap1 signaling pathway contributes to the enhanced production of porcine embryos with high developmental competence,and offers insight into the mechanisms regulating early embryonic development. 展开更多
关键词 LUTEOLIN Mitochondrial function Nrf2/Keap1 signaling pathway Oxidative stress porcine embryo development
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Recent Advances in Epidemiology of Porcine Circovirus Type 2 and Diagnosis of Porcine Circovirus-Associated Diseases
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作者 LIU Gang JIANG Yan-bin +3 位作者 YU Lei REN Wen-kai WANG Hai YIN Yu-long 《Animal Husbandry and Feed Science》 CAS 2011年第3期25-28,共4页
Porcine cimovirus (PCV) is the smallest animal virus so far and has two serotypes. PCV1 is nonpathogenic, but PCV2 is pathogenic and causes post-weaning multisystemic wasting syndrome ( PMWS). Factors to induce PM... Porcine cimovirus (PCV) is the smallest animal virus so far and has two serotypes. PCV1 is nonpathogenic, but PCV2 is pathogenic and causes post-weaning multisystemic wasting syndrome ( PMWS). Factors to induce PMWS include immunity and infection status of sows, infec- tion time, mixed infection, PCV2 variants, physical status of gilts, and feeding management. For final diagnosis, histopathological changes and ex- istence of PCV2 in lymphoid tissues are professional standards, because fluorescence quantitative RT-PCR is not enough specific or sensitive. The commemial PCV2 vaccines can reduce occurrence of PMWS and PCV-related diseases. This paper reviews recent advances in epidemiology of PCV2 as well as diagnosis and control of PMWS. 展开更多
关键词 porcine circovirus type 2 Post-weaning multisystemic wasting syndrome EPIDEMIOLOGY DIAGNOSIS
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鉴别猪圆环病毒2型和3型双重TaqMan MGB探针FQ-PCR检测方法研究
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作者 赵雪丽 闫若潜 +8 位作者 王华俊 王淑娟 马震原 谢彩华 柴茂 杨海波 王翠 刘影 王东方 《中国动物传染病学报》 CAS 北大核心 2024年第2期165-173,共9页
建立一种快速、特异鉴别检测猪圆环病毒2型(PCV2)和猪圆环病毒3型(PCV3)的双重TaqMan MGB探针FQ-PCR方法,本研究以PCV2的Rep蛋白和PCV3的Cap蛋白基因作为靶基因,各设计1对特异性引物和1条TaqMan MGB探针,经优化各反应条件和进行敏感性... 建立一种快速、特异鉴别检测猪圆环病毒2型(PCV2)和猪圆环病毒3型(PCV3)的双重TaqMan MGB探针FQ-PCR方法,本研究以PCV2的Rep蛋白和PCV3的Cap蛋白基因作为靶基因,各设计1对特异性引物和1条TaqMan MGB探针,经优化各反应条件和进行敏感性、特异性、重复性和干扰性试验,建立鉴别检测PCV2/PCV3的双重FQ-PCR方法。结果显示:该方法可特异性扩增PCV2、PCV3核酸,与猪伪狂犬病病毒(PRV)等8种病原及阴性对照无交叉反应,特异性较强;对PCV2和PCV3阳性质粒标准品的最低检出限均可达10 copies/μL,敏感性较高;PCV2/PCV3批内/批间重复试验变异系数(CV)值均在3%以下,表明方法稳定性、重复性较好;干扰性试验表明在两种病毒阳性质粒起始模板相差较大时该方法不会影响对其中任一病毒核酸的检出和准确定量。对42份临床疑似PCV感染样品检测结果与PCV2、PCV3基因测序结果符合率100%。本研究建立的双重FQ-PCR方法具有敏感性高达10 copies/μL、特异性强、在同一反应体系中能同时快速鉴别检测PCV2、PCV3等优点,可用于临床PCV2/PCV3感染的快速鉴别检测。 展开更多
关键词 猪圆环病毒2 rep基因 猪圆环病毒3型 cap基因 双重TaqMan MGB FQ-PCR
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猪圆环病毒2型疫苗及其效力评价方法比较研究
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作者 徐嫄 彭国瑞 +8 位作者 徐小艾 吴睿智 赵启祖 朱元源 李翠 王团结 邹兴启 李琰 刘业兵 《中国兽药杂志》 2024年第1期87-94,共8页
为探索对不同猪圆环病毒2型(Porcine circovirus type2,PCV2)疫苗产品进行统一质量评价的可行性,对国内该类疫苗产品及其现有效力评价方法进行了归纳和比较研究。结果发现,目前猪圆环病毒2型疫苗类产品种类有25个,且疫苗毒株数量多达10... 为探索对不同猪圆环病毒2型(Porcine circovirus type2,PCV2)疫苗产品进行统一质量评价的可行性,对国内该类疫苗产品及其现有效力评价方法进行了归纳和比较研究。结果发现,目前猪圆环病毒2型疫苗类产品种类有25个,且疫苗毒株数量多达10余个,效力检验方法包括传统的免疫攻毒法、血清学方法和多种不同的替代方法,但尚没有统一的效力评价体系。本研究可为进一步完善PCV2疫苗效力评价方法、统一评价疫苗效力、提高产品质量提供参考。 展开更多
关键词 猪圆环病毒2 疫苗 效力评价方法
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保育仔猪猪圆环病毒2型和副猪嗜血杆菌混合感染的诊疗
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作者 薛翼鹏 吴忻 《天津农业科学》 CAS 2024年第6期44-48,共5页
为查清山西省吕梁市中阳县某猪场从山东购买的保育仔猪大量出现的急性死亡、关节发炎、呼吸困难、高热等症状的病原,无菌采集病猪并带回实验室进行临床剖检,随后采集血液、淋巴结、肺、肾脏和脾脏进行实验室诊断,做出初步判断,制定综合... 为查清山西省吕梁市中阳县某猪场从山东购买的保育仔猪大量出现的急性死亡、关节发炎、呼吸困难、高热等症状的病原,无菌采集病猪并带回实验室进行临床剖检,随后采集血液、淋巴结、肺、肾脏和脾脏进行实验室诊断,做出初步判断,制定综合防治策略,病情得到控制。本研究采用灵敏度和准确度较高的实时荧光PCR技术定性检测病料样品中的猪繁殖与呼吸综合征病毒(PRRSV)、非洲猪瘟病毒(ASFV)、猪圆环病毒2型(PCV2)、猪瘟病毒(CSFV)、猪伪狂犬病毒(PRV)和副猪嗜血杆菌(HPS)。结果表明:中阳县某猪场保育仔猪为PCV2与HPS混合感染。基于诊断结论对保育猪免疫治疗程序和消毒进行合理调整,综合防治13 d后,猪群无新增发病率和新增死亡率,最大程度地减少了经济损失。本研究为猪场后续的治疗与预防提供了诊断依据。 展开更多
关键词 保育仔猪 猪圆环病毒2型(PCV2) 副猪嗜血杆菌病(HPS) 混合感染 诊疗
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猪圆环病毒2型ORF1部分位点突变对病毒复制能力的影响 被引量:1
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作者 李荷然 肖琦 +3 位作者 温立斌 朱雪蛟 芮荣 何孔旺 《畜牧与兽医》 CAS 北大核心 2024年第1期71-76,共6页
猪圆环病毒2型(PCV2)可引起断奶仔猪多系统衰竭综合征,导致仔猪逐渐消瘦。PCV2 ORF1表达的Rep蛋白及其剪切体Rep′是PCV2复制所需的重要蛋白。为了研究PCV2 ORF1部分位点对PCV2复制能力的影响,本试验通过构建PCV2 ORF1区域点突变双拷贝... 猪圆环病毒2型(PCV2)可引起断奶仔猪多系统衰竭综合征,导致仔猪逐渐消瘦。PCV2 ORF1表达的Rep蛋白及其剪切体Rep′是PCV2复制所需的重要蛋白。为了研究PCV2 ORF1部分位点对PCV2复制能力的影响,本试验通过构建PCV2 ORF1区域点突变双拷贝感染性克隆质粒,在无PCV2污染的PK-15细胞中进行病毒拯救,使用荧光定量PCR检测不同位点突变病毒培养不同代次上清液的Ct值。结果:将PCV2 Rep的17 aa、19 aa、20 aa和21 aa突变为丙氨酸后病毒无法成功拯救,2 aa突变后严重影响病毒的复制能力,3 aa、5 aa和18 aa突变后病毒的复制能力增强且细胞病毒载量高于PCV2原毒株,推测17 aa、19 aa、20 aa和21 aa是影响PCV2复制的关键作用位点。本研究结果为未来PCV2复制相关研究提供了试验依据。 展开更多
关键词 猪圆环病毒2 REP蛋白 病毒复制
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Porcine Interleukin-2 Expression in Insect Cells and Its Enhancement of Pig Immunity to Swine Influenza Virus Inactivated Vaccine 被引量:3
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作者 CHEN Hong-ying ZHANG Hong-ying HUANG Yan-quan CUI Bao-an WANG Zhen-ya WANG Yan-bin LIU Jin-peng CHAO An-jun 《Agricultural Sciences in China》 CAS CSCD 2010年第8期1211-1220,共10页
Mature porcine interleukin-2 (pIL-2) gene was amplified by PCR from the plasmid pGEM-T-pIL2 and cloned into the baculovirus pFastBacTM Dual vector of the Bac-to-Bac baculovirus expression system under the control of... Mature porcine interleukin-2 (pIL-2) gene was amplified by PCR from the plasmid pGEM-T-pIL2 and cloned into the baculovirus pFastBacTM Dual vector of the Bac-to-Bac baculovirus expression system under the control of the PH promoter. Recombinant plL-2 (rpIL-2) expressed in Sf9 insect cells was detected by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and immunofluorescence assay. Western blot analysis confirmed that the rpIL-2 protein had a molecular mass of 20 kDa, which was larger than the molecular mass of the mature protein predicted based on its peptide sequence. The rpIL-2 protein induced in vitro proliferation of ConA-stimulated porcine splenocytes and enhanced in vivo protective immune responses induced by vaccinating the pigs with inactivated oil emulsion vaccine against swine influenza virus. The results showed that the rpIL-2 expressed in Sf9 insect cells has immunoenhancement effects; the finding lays the foundation for the preparation of a specific recombinant IL-2 protein and the development of a novel immune adjuvant of vaccines against various infectious porcine pathogens to increase the immunoprotective efficacy of vaccines. 展开更多
关键词 porcine interleukin-2 Sf9 insect cells EXPRESSION inactivated vaccine swine influenza virus
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表达CSFV E2线性表位的PCV2病毒样颗粒的制备及免疫原性研究
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作者 李岩岩 张帅 +5 位作者 赵云环 任晓祥 李思琪 王文钊 左玉柱 范京惠 《中国预防兽医学报》 CAS CSCD 北大核心 2024年第1期70-77,共8页
为制备携带猪瘟病毒(CSFV)E2蛋白的猪圆环病毒2型(PCV2)病毒样颗粒(VLP),并在小鼠体内评价其免疫原性,本研究采用PCR扩增PCV2 Cap基因,利用重叠延伸PCR将PCV2 Cap蛋白的诱饵表位(aa169~aa180)替换成编码两个连续的CSFV E2蛋白线性表位(a... 为制备携带猪瘟病毒(CSFV)E2蛋白的猪圆环病毒2型(PCV2)病毒样颗粒(VLP),并在小鼠体内评价其免疫原性,本研究采用PCR扩增PCV2 Cap基因,利用重叠延伸PCR将PCV2 Cap蛋白的诱饵表位(aa169~aa180)替换成编码两个连续的CSFV E2蛋白线性表位(aa829~aa837)的融合基因(PCV2-Cap^(169~180)-E2^(829~837))经测序鉴定正确后克隆至载体pET-32a(+)中,构建重组质粒p-Cap-E2并采用PCR方法鉴定正确后转化大肠杆菌BL21(DE3),经IPTG诱导表达重组蛋白(PCV2-Cap-E2),采用改良的镍亲和层析法纯化重组蛋白,并利用SDS-PAGE与western blot对重组蛋白的表达形式及反应原性鉴定;利用透射电镜观察纯化的重组蛋白能否形成VLP;利用本研究制备的VLP、PCV2及CSFV商品化疫苗分别免疫小鼠,采用ELISA方法检测免疫后不同时间小鼠体内的抗体水平及细胞因子含量。SDS-PAGE结果显示,在49 ku处出现目的条带,且重组蛋白主要以可溶性形式表达,纯化得到单一的目的蛋白;western blot结果显示,重组蛋白能够与猪源PCV2多克隆抗体(PAb)、猪源CSFV PAb及HRP标记的6×His-Tag小鼠单克隆抗体(MAb)发生特异性反应,在49 ku处出现特异性条带;电镜观察可见重组蛋白形成规则的VLP;抗体的ELISA结果显示,与PBS对照相比,VLP能够诱导小鼠产生较高的PCV2及CSFV抗体水平(P<0.01),与各商品化疫苗均无显著差异。细胞因子的ELISA结果显示,与PBS对照组相比,VLP能够诱导小鼠产生较高水平的细胞因子(P<0.01)。体外病毒中和试验结果显示,VLP免疫的小鼠血清中具有中和PCV2的活性。综上所述,本实验首次在大肠杆菌中可溶性表达并获得了纯化的重组蛋白(PCV2-Cap-E2),且其能够在体外自组装成VLP,并可刺激小鼠产生针对PCV2 Cap蛋白及CSFV E2蛋白的特异性抗体,为研制针对PCV2和CSFV的新型二联VLP疫苗提供了物质基础。 展开更多
关键词 猪圆环病毒2 病毒样颗粒 猪瘟病毒E2蛋白 CAP蛋白
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ACE2对猪流行性腹泻病毒体外感染传代猪小肠上皮细胞的影响
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作者 任莉鑫 张静怡 +3 位作者 徐沙沙 杨柳 张兴翠 宋振辉 《畜牧兽医学报》 CAS CSCD 北大核心 2024年第3期1238-1248,共11页
为探究血管紧张素转换酶2(angiotensin converting enzyme 2,ACE2)在猪流行性腹泻病毒(porcine epidemic diarrhea virus, PEDV)感染仔猪过程中发挥的作用,本研究通过转录组学分析仔猪肠道ACE2在PEDV感染前后表达的变化情况,然后利用猪... 为探究血管紧张素转换酶2(angiotensin converting enzyme 2,ACE2)在猪流行性腹泻病毒(porcine epidemic diarrhea virus, PEDV)感染仔猪过程中发挥的作用,本研究通过转录组学分析仔猪肠道ACE2在PEDV感染前后表达的变化情况,然后利用猪小肠上皮细胞(porcine intestinal epithelial cells, IPEC-J2细胞)模型,通过RT-qPCR、Western blot检测PEDV感染后ACE2的mRNA、蛋白表达水平的变化。过表达与抑制表达ACE2后通过RT-qPCR、Western blot、TCID50检测PEDV复制水平。结果显示,PEDV感染IPEC-J2后ACE2的mRNA及蛋白表达水平均显著下调,与转录组学结果一致。过表达ACE2组PEDV感染量显著上升,抑制表达ACE2组PEDV感染量显著下降。本研究在细胞水平上验证了ACE2在PEDV感染过程中的作用,即PEDV感染能够使ACE2表达量下降,在IPEC-J2细胞中过表达ACE2能提高PEDV复制水平,抑制ACE2的表达可降低PEDV复制水平。 展开更多
关键词 血管紧张素转换酶2 ACE2 猪流行性腹泻病毒 猪小肠上皮细胞
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表达PCV2 ORF2的重组T7噬菌体在猪体内的存留分析
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作者 杨柳 牟豪 +5 位作者 吕林丹 胡霞 许国洋 郑华 张邑帆 沈克飞 《中国兽医杂志》 CAS 北大核心 2024年第8期38-43,共6页
为了检测经颈部肌肉注射入猪体的、表达猪圆环病毒2型(PCV2)衣壳蛋白(ORF2)的重组T7噬菌体(T7-ORF2)在体内的存留情况,本试验将PCV2抗原和抗体均为阴性的20日龄仔猪随机分为试验组和对照组,每组5只;试验组猪只以1.5mL/只剂量颈部肌肉注... 为了检测经颈部肌肉注射入猪体的、表达猪圆环病毒2型(PCV2)衣壳蛋白(ORF2)的重组T7噬菌体(T7-ORF2)在体内的存留情况,本试验将PCV2抗原和抗体均为阴性的20日龄仔猪随机分为试验组和对照组,每组5只;试验组猪只以1.5mL/只剂量颈部肌肉注射增殖收获的T7-ORF2,对照组猪只以相同途径注射等体积的洗脱液;于注射前1 d、注射后10 h、1~7 d测量体温,观察猪只的临床症状和死亡情况;分别于注射后1 h、3 h、5 h、10 h、1 d、3 d、5 d和7 d采集猪只的血液和粪便样品,注射后10 h、1 d、3 d、5 d和7 d采集肝脏、脾脏和腹股沟淋巴结样品;将收集的各样品处理上清与宿主菌(大肠埃希菌BLT5403株)混合培养,通过细菌裂解分析T7-ORF2的感染性;以细菌裂解液提取的基因组DNA为模板进行PCR,检测ORF2基因;通过免疫组织化学检测T7-ORF2在肝脏、脾脏和腹股沟淋巴结中的分布和存留时间。结果显示,试验组猪只在试验期体温、采食、饮水和精神状态正常,无不良症状和死亡发生;注射后5 d能从血清和粪便中检测到感染性的T7-ORF2;注射后3 d能从肝脏、脾脏和腹股沟淋巴结中检测到感染性的T7-ORF2;从细菌裂解液中可扩增检测到PCV2 ORF2基因片段;免疫组织化学切片观察结果显示,T7-ORF2在机体中逐渐被清除,在脾脏中存留至少5 d,在肝脏和腹股沟淋巴结中存留至少7 d。结果表明,T7-ORF2可进入猪只的血液循环、肝脏、脾脏和腹股沟淋巴结中,并随粪便排出体外。本试验为利用T7-ORF2深入开发PCV2新型疫苗提供数据支撑。 展开更多
关键词 重组T7噬菌体 猪圆环病毒2型(PCV2) 肌肉注射 检测 疫苗
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猪圆环病毒2型感染性克隆的构建及拯救病毒的双抗体夹心ELISA鉴定
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作者 贺紫琴 宁李纳 +6 位作者 范杰 凌同 刘甜甜 李欣 陈志雄 黎满香 葛猛 《畜牧与兽医》 CAS 北大核心 2024年第7期95-101,共7页
旨在构建猪圆环病毒2型(PCV2)感染性克隆,并利用双抗体夹心ELISA对拯救病毒进行鉴定。通过PCR从阳性病料中扩增出PCV2两种基因型2b与2d的全基因组DNA,并分别克隆入pMD-19T载体,获得2个重组质粒,命名为p19T-PCV2b与p19T-PCV2d。利用Sac... 旨在构建猪圆环病毒2型(PCV2)感染性克隆,并利用双抗体夹心ELISA对拯救病毒进行鉴定。通过PCR从阳性病料中扩增出PCV2两种基因型2b与2d的全基因组DNA,并分别克隆入pMD-19T载体,获得2个重组质粒,命名为p19T-PCV2b与p19T-PCV2d。利用SacⅡ酶切获得l 767 bp的PCV2全基因组,并在体外分别用T4连接酶连接而环化,将环状基因组转染至PK-15细胞,传至P6代,利用间接免疫荧光试验(IFA)对拯救病毒进行鉴定,结果表明PCV2b与PCV2d感染性克隆可拯救出病毒。利用PCV2单克隆抗体(单抗)作为捕获抗体,用辣根过氧化酶(HRP)标记的PCV2多抗作为检测抗体,建立检测PCV2病毒粒子的双抗体夹心ELISA方法,用于PCV2拯救病毒的鉴定。将该检测方法与IFA和半数组织细胞感染量(TCID_(50))结果进行对比分析,结果显示,ELISA检测值与Image-J所计算的IFA荧光强度及TCID_(50)的相关系数分别达到0.7和0.8以上,说明该方法与IFA及TCID_(50)检测结果均具有较强的一致性,可以用于PCV2拯救病毒的快速鉴定。 展开更多
关键词 PCV2 感染性克隆 ELISA
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A survey on porcine circovirus type 2 infection and phylogenetic analysis of its ORF2 gene in Hangzhou,Zhejiang Province,China 被引量:13
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作者 Zong-zhao YANG Jiang-bing SHUAI +1 位作者 Xian-jun DAI Wei-huan FANG 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2008年第2期148-153,共6页
Porcine circovirus type 2 (PCV2) is closely related to the postweaning multisystemic wasting syndrome (PMWS). In this study, the pig serum and tissue samples collected from different regions of Hangzhou District in Zh... Porcine circovirus type 2 (PCV2) is closely related to the postweaning multisystemic wasting syndrome (PMWS). In this study, the pig serum and tissue samples collected from different regions of Hangzhou District in Zhejiang Province of China between 2003 and 2005 were analyzed by enzyme-linked immunosorbent assay (ELISA) for PCV2 antibody and by polymerase chain reaction (PCR) for ORF2 gene. The results show that out of 1250 randomly collected serum samples, 500 sera (40%) were seropositive for PCV2. PCR results demonstrate that Hangzhou PCV2 with more than 50% Chinese PCV2 strains and French PCV2 formed Cluster A. Only one PCV2 from Hangzhou belonged to Cluster B with some other Chinese PCV2 and Netherlands’s isolates. Cluster C consisted of PCV2 isolates from China, US, Canada, UK and Germany. The results indicate that the PCV2 infection was widespread in Hangzhou. 展开更多
关键词 PCV2 动植物分析 遗传基因 中国
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猪圆环病毒2型感染性克隆构建
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作者 辛子琪 杨明珠 +3 位作者 张晓茜 靳继惠 陈晓春 李俊平 《中国兽药杂志》 2024年第5期1-9,共9页
基于PCV2滚环复制原理,在分析PCV2不同基因亚型代表毒株基因组结构和序列的基础上,设计2对引物用于PCR扩增PCV2基因组序列。以从收集到的疑似PCV2感染的10份猪血清样品中提取的DNA为模板,用设计的引物扩增目的片段,并进行测序分析,1株为... 基于PCV2滚环复制原理,在分析PCV2不同基因亚型代表毒株基因组结构和序列的基础上,设计2对引物用于PCR扩增PCV2基因组序列。以从收集到的疑似PCV2感染的10份猪血清样品中提取的DNA为模板,用设计的引物扩增目的片段,并进行测序分析,1株为PCV2a型,4株为PCV2b型,5株为PCV2d型。每种基因型毒株中各选取一个样本,利用上述2对引物进行PCR扩增,并将扩增产物克隆至pEASY-Blunt simple载体中,通过双酶切连接2个PCR片段,构建含有约1500 bp重叠序列的PCV2基因组的质粒。通过脂质体转染法将含PCV2全基因组的质粒转染至PK-15细胞进行病毒拯救,经PCR和IFA两种方法验证,证明成功拯救出3个基因型的PCV2毒株。通过对PCV2全基因组结构及序列分析,该方法同样适用于PCV2g、PCV2h基因型病毒的感染性克隆构建。本研究建立了一种基于反向遗传学技术的PCV2感染性克隆的构建方法,为开展PCV2的病原学研究提供了技术支持。 展开更多
关键词 猪圆环病毒2 感染性克隆 病毒拯救 遗传进化分析
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猪圆环病毒2型疫苗的应用和研发进展
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作者 王鹏 沈伟桢 周斌 《畜牧与兽医》 CAS 北大核心 2024年第4期139-146,共8页
猪圆环病毒2型(PCV2)是猪圆环病毒相关疾病(PCVAD)的主要病原,感染后会导致猪淋巴系统功能衰竭和免疫抑制,严重危害养猪业的正常生产。近年来,PCV2疫苗的研发一直备受关注,相关研究已取得一定进展,已上市了多种疫苗,包括灭活疫苗、亚单... 猪圆环病毒2型(PCV2)是猪圆环病毒相关疾病(PCVAD)的主要病原,感染后会导致猪淋巴系统功能衰竭和免疫抑制,严重危害养猪业的正常生产。近年来,PCV2疫苗的研发一直备受关注,相关研究已取得一定进展,已上市了多种疫苗,包括灭活疫苗、亚单位疫苗、嵌合疫苗和合成肽疫苗等。此外,研究人员还在疫苗的免疫机制和接种策略方面进行了深入探讨,为疫苗的研发和应用提供了重要的理论支持。然而,目前PCV2疫苗的研究仍面临着诸多挑战,如临床流行的主要毒株从PCV2b逐渐转变为PCV2d,疫苗安全性、长期免疫效果等,现有疫苗的免疫效果仍需进一步研究证实。本文对PCV2及其现有疫苗的生产现状、新型疫苗的研发进展、佐剂在疫苗中的应用、疫苗对不同基因型的保护能力等进行了综述,以期为我国有效防控PCVAD提供科学参考。 展开更多
关键词 猪圆环病毒2 疫苗 佐剂 保护力
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Mouse models of porcine circovirus 2 infection 被引量:1
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作者 Ting Ouyang Xiao-hui Liu +1 位作者 Hong-sheng Ouyang Lin-zhu Ren 《Animal Models and Experimental Medicine》 2018年第1期23-28,共6页
PCV2 is considered the main pathogen of porcine circovirus diseases and porcine circovirus-associated diseases(PCVD/PCVAD). However, the exact mechanism underlying PCVD/PCVAD is currently unknown. Mouse models of PCV2... PCV2 is considered the main pathogen of porcine circovirus diseases and porcine circovirus-associated diseases(PCVD/PCVAD). However, the exact mechanism underlying PCVD/PCVAD is currently unknown. Mouse models of PCV2 are valuable experimental tools that can shed light on the pathogenesis of infection and will enable the evaluation of antiviral agents and vaccine candidates. In this review, we discuss the current state of knowledge of mouse models used in PCV2 research that has been performed to date, highlighting their strengths and limitations, as well as prospects for future PCV2 studies. 展开更多
关键词 ANIMAL model mouse(Mus musculus) porcine CIRCOVIRUS 2(PCV2)
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猪圆环病毒Ⅱ型感染3D4/2细胞的转录组学分析
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作者 陈虹伶 赵怡 +5 位作者 陈家骥 韦秋旭 李禧梦 冯国越 胡焜翔 胡庭俊 《中国畜牧兽医》 CSCD 北大核心 2024年第1期42-51,共10页
【目的】通过转录组测序筛选猪圆环病毒Ⅱ型(Porcine circovirus typeⅡ,PCV2)感染猪肺泡巨噬细胞系(3D4/2)差异表达基因,为了解PCV2感染宿主免疫细胞机制和抗PCV2感染药物研发奠定基础。【方法】用感染复数(multiplicity of infection,... 【目的】通过转录组测序筛选猪圆环病毒Ⅱ型(Porcine circovirus typeⅡ,PCV2)感染猪肺泡巨噬细胞系(3D4/2)差异表达基因,为了解PCV2感染宿主免疫细胞机制和抗PCV2感染药物研发奠定基础。【方法】用感染复数(multiplicity of infection, MOI)为1的PCV2 NJ2002株处理3D4/2细胞,利用Illumina NovaSeq 6000测序平台进行转录组测序。使用DeSeq 2.0软件进行差异表达基因分析,并对差异表达基因进行基因本体论(GO)、京都基因与基因组百科全书(KEGG)功能分析及转录因子靶向分析,选取免疫及凋亡相关基因进行实时荧光定量PCR验证,用Western blotting技术检测细胞内磷脂酰肌醇激酶(PI3K)及磷酸化胞内磷脂酰肌醇激酶(p-PI3K)、蛋白激酶B(Akt)和磷酸化蛋白激酶B(p-Akt)蛋白表达水平。【结果】转录组测序结果显示,与对照组相比,PCV2感染组共获得713个差异表达基因,其中313个上调,400个下调。GO功能和KEGG通路富集分析显示,差异表达基因与免疫应答等相关,主要富集在细胞外基质受体互作通路、新陈代谢通路、HIF-1信号通路、病毒致癌作用、PI3K-Akt等信号通路。实时荧光定量PCR结果与转录组测序的基因表达水平保持一致。Western blotting检测结果显示,PCV2感染3D4/2细胞24 h后PI3K和Akt蛋白磷酸化水平显著升高(P<0.05)。转录因子靶向分析表明,差异表达基因与核转录因子Y亚基β(NFYB)和ETS转录因子(ELK4)联系紧密。【结论】PCV2可能通过PI3K-Akt信号通路影响下游炎症信号通路和凋亡信号通路增强自身复制能力。NFYB和ELK4转录因子在PCV2感染过程中可能发挥重要作用,可考虑作为抗PCV2药物靶点。研究结果为深入了解PCV2感染宿主免疫细胞机制和相关药物开发提供了理论基础。 展开更多
关键词 猪圆环病毒Ⅱ型 3D4/2细胞 转录组测序 差异表达基因 转录因子
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Development of a Loop-Mediated Isothermal Amplification Assay for Porcine Circovirus Type 2 被引量:2
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作者 Ye-bing Liu Lei Zhang +2 位作者 Qin-hong Xue Yi-bao Ning Zhi-gang Zhang 《Virologica Sinica》 SCIE CAS CSCD 2011年第3期214-220,共7页
In this study, the loop-mediated isothermal amplification (LAMP) method was used to develop a rapid and simple detection system for porcine circovirus type 2 (PCV2). According to the PCV2 sequences published in GenBan... In this study, the loop-mediated isothermal amplification (LAMP) method was used to develop a rapid and simple detection system for porcine circovirus type 2 (PCV2). According to the PCV2 sequences published in GenBank, multiple LAMP primers were designed targeting conserved sequences of PCV2. Using the DNA extracted from PCV2 isolates HUN-09 and SD-09 as the template, LAMP reactions in a PCV2 LAMP system was performed, the amplification products were detected by adding SYBR Green I and could be observed directly by the naked eye. The results showed highly-efficient and specific amplification in 30 min at 63°C with a LAMP real-time turbidimeter. Furthermore, PCV2 DNA templates, with a detection limit of 5.5×10-5 ng of nucleic acid, indicated that this assay was highly sensitive. The results obtained with the naked eye after SYBR Green I staining were consistent with those detected by the real-time turbidimeter, showing the potential simplicity of interpretation of the assay results. The LAMP assay appeared to have greater accuracy than PCR and virus isolation for the analysis of 18 clinical samples. In addition it offers higher specificity and sensitivity, shorter reaction times and simpler procedures than the currently available methods of PCV2 detection. It is therefore a promising tool for the effective and efficient detection of PCV2. 展开更多
关键词 猪圆环病毒2 实验 等温 介导 DNA模板 PCV2 GENBANK 检测系统
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Genetic Diversity of Intragenomic Rearrangement of Porcine Circovirus Type 2 in vitro and in vivo 被引量:1
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作者 Libin WEN Fengzhi WANG +5 位作者 Bin LI Yang YU Zhengyu YU Aihua MAO Jianping XIE Kong-wang HE 《Agricultural Science & Technology》 CAS 2013年第12期1719-1722,共4页
We characterized the genome sequences of defective-interfering(DI) particle DNA of porcine circovirus type 2(PCV2) by sequencing and bioinformatics analyses. DI particles were both generated by serial passage of PCV2 ... We characterized the genome sequences of defective-interfering(DI) particle DNA of porcine circovirus type 2(PCV2) by sequencing and bioinformatics analyses. DI particles were both generated by serial passage of PCV2 in PK15 cells and obtained from sera of pigs with postweaning multisystemic wasting syndrome(PMWS). These subviral isolates ranged from 358 nt to 1 125 nt genomes. Investigating the complexity and diversity of PCV2 DI in vivo and in vitro can help elucidating the evolutionary history of PCV2. 展开更多
关键词 猪圆环病毒2 遗传多样性 猪断奶后多系统衰竭综合征 体内 体外 基因组序列 PCV2 重排
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Analysis of molecular variation in porcine reproductive and respiratory syndrome virus in China between 2007 and 2012 被引量:2
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作者 Yuhang Cao Hongsheng Ouyang +4 位作者 Mingjun Zhang Fuwang Chen Xin Yang Daxing Pang Linzhu Ren 《Virologica Sinica》 SCIE CAS CSCD 2014年第3期183-188,共6页
In the present study, 89 porcine reproductive and respiratory syndrome virus(PRRSV) isolates in China during 2007 to 2012 were randomly selected from the GenBank genetic sequence database. Evolutionary characteristics... In the present study, 89 porcine reproductive and respiratory syndrome virus(PRRSV) isolates in China during 2007 to 2012 were randomly selected from the GenBank genetic sequence database. Evolutionary characteristics of these isolates were analyzed based on the sequences of non-struc-tural protein 2(Nsp2) and glycoprotein 5(GP5). The genetic variations of the isolates were also compared with six representative strains. The results showed that a high degree of genetic diversity exists among the PRRSV population in China. Highly pathogenic PRRSV isolates, with a discon-tinuous deletion of a 30 amino acid residue in the Nsp2 region, remained the most dominant virus throughout 2007–2012 in China. Owing to the extensive use of representative vaccine strains, natu-ral recombination events occurred between strains. Three isolates – HH08, DY, and YN-2011 – were more closely related to vaccine strains than the other isolates. Both YN-2011 and DY were the evolu-tionary products of recombination events between strains SP and CH-1R. The results of the present study provide useful information for the epidemiology of PRRSV as well as for vaccine development. 展开更多
关键词 猪繁殖与呼吸综合征病毒 中国 分子变异 PRRSV GENBANK 序列数据库 基因变异 遗传多样性
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Expression of Porcine Interleukin-2 and Porcine Interleukin-6 and Their Adjuvant Effects on Gene Deleted Vaccine of Pseudorabies Virus(TK^-/gG^-/LacZ^+)
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作者 YAN Lin, HE Qi-gai, CHEN Huan-chun, XIAO Shao-bo, WU Mei-zhou,LU Jian-qiang and HAN Li(Laboratory of Virology, College of Animal Science and Veterinary Medicine, Huazhong Agriculture University , Wuhan 430070 , P. R. China) 《Agricultural Sciences in China》 CAS CSCD 2003年第8期924-929,共6页
Porcine interleukin-2 and porcine interleukin-6 cDNA sequences were cloned into the expressing vectors pET-28a and pGEX-KG respectively. They were expressed in E. coli BL21(DE3)with high-level production. The gene del... Porcine interleukin-2 and porcine interleukin-6 cDNA sequences were cloned into the expressing vectors pET-28a and pGEX-KG respectively. They were expressed in E. coli BL21(DE3)with high-level production. The gene deleted vaccine of pseudorabies virus Ea strain(TK-/gG-/LacZ+)was mixed with the two different purified recombinant proteins each, or both, with the doses of 2, 5 or 10 μg ml-1. Ten groups of pseudorabies negative antibody swines were immuned twice with tested vaccines with different doses, or control vaccine, respectively. The antibody liters of the test groups were detected by neutralization test, and the daily weight gains of swines were calculated and analyzed statistically. In the study, all the neutralizing antibody ti-ters in test groups were higher than the control group, and the recombinant proteins appeared a dose dependent adjuvant effect. The tested vaccines with 2 μg ml-1 pIL-2 and with 10 μg ml-1 pIL-2/pIL-6 got significant and extremely significant differences, compared with the vaccines without pILs. The difference of the daily weight gain indicated the potential positive influence of pIL-2 and pIL-6 on immune protection. 展开更多
关键词 porcine interleukin-2 porcine interleukin-6 Expression Gene deleted vaccine of pseudora-bies virus(TK-/gG-/LacZ+) Adjuvant effect
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