新城疫病毒结构蛋白功能及检测技术研究进展

新城疫是一种由新城疫病毒引起的烈性传染病,病死率很高,严重危害家禽养殖业,被世界动物卫生组织列为必须报告的动物传染病。在我国,新城疫的暴发和流行虽然已得到了控制,但病毒的变异给新城疫的防控工作带来了困难。新城疫病毒的隐性感染也对我国禽类产品的质量及出口造成了一定影响。因此,明确新城疫病毒各结构蛋白的功能、改进现有检测技术以及开发新的检测技术平台是目前新城疫防控工作的重点。论文对新城疫病毒结构蛋白功能及检测技术的进展进行了系统的阐述。     

亚洲1型口蹄疫病毒L蛋白缺失株的构建及其生物学定性

为确定口蹄疫病毒(FMDV)L蛋白缺失对其生物学特性的影响,本研究在已建立的Asia1型FMDV反向遗传操作平台基础上,利用融合PCR方法缺失L蛋白基因编码区,构建了缺失L蛋白的重组Asia1型FMDV(rFMDV-ΔL)。拯救病毒的一步生长曲线结果表明,rFMDV-ΔL与亲本病毒相比在BHK-21细胞中的复制水平下降10倍,乳鼠毒力试验表明rFMDV-ΔL的毒力比亲本毒株下降6倍。另外,rFMDV-ΔL在BHK-21细胞上产生病变的速度明显变慢,形成蚀斑的时间延长,致乳鼠死亡所需时间也比亲本毒株明显延长。本研究是关于亚洲1型FMDVL蛋白结构与功能研究的首次报道,为亚洲1型FMDVL蛋白结构与功能的研究奠定了基础。     

猪繁殖与呼吸综合征病毒GP5、M蛋白基因的克隆及其基因疫苗构建

参照GenBank中猪繁殖与呼吸综合征病毒(PRRSV)美洲型代表株VR2332 GP5和M蛋白基因序列,设计并合成2对引物,用RT-PCR方法分别扩增出PRRSV野毒株GP5和M蛋白基因603,525bp片段,并将其分别克隆到pMD18-T载体。测序正确后,将GP5和M蛋白基因分别克隆到真核表达载体pEGFP-C1上,成功构建基因疫苗表达载体pEGP5-C1和pEM-C1。小鼠免疫试验证实,这些基因疫苗质粒可以诱导小鼠产生特异性抗体,并在二免后1周开始检测到特异性淋巴细胞增殖反应。     

IMC10200株ALV-J实验诱发禽骨髓性白血病的研究

对分离自肉种鸡群亚临床感染的J亚群禽白血病病毒IMC1o200株进行了实验感染诱发禽骨髓性白血病的病理学研究.IMC10200株J亚群禽白血病病毒尿囊腔接种11日龄肉鸡胚和SPF蛋鸡胚,孵出后跟踪观察.9周龄时随机抽检感染鸡,感染肉鸡特异引物PCR检测全部为阳性;组织病理学观察感染鸡无明显病变.至21周龄时感染肉鸡出现第一例典型骨髓性白血病病例;感染SPF蛋鸡未见明显J亚群禽白血病相关病变.     

Antibody prevalence of low-pathogenicity avian influenza and evaluation of management practices in Minnesota backyard poultry flocks

Low‐pathogenicity avian influenza (LPAI) viruses have caused illness in poultry and humans with poultry contact. To determine whether there is evidence of exposure to avian influenza viruses (AIV) among backyard poultry in Minnesota and their human caretakers, 150 flocks of backyard birds were sampled for antibodies to AIV from August 2007 through December 2008. One hundred flocks were tested through routine slaughter surveillance by the Minnesota Board of Animal Health and an additional 50 flocks were contacted and sampled by study investigators. Blood was collected from 10 to 13 birds from each flock and a survey of biosecurity and management practices was administered to the flock owner. Blood samples were tested by agar gel immunodiffusion (AGID) for influenza A antibodies. Tested flocks had a median flock size of 100 birds (range: 12–800 birds), and were most commonly owned for meat for personal use (81% of respondents), fun or hobby (58%) and eggs for personal use (56%). Although 7% of flock owners reported that their birds had shown respiratory signs in the previous 3 months, only 1 of 150 flocks tested positive for influenza by AGID. Antibodies to LPAI H6N1 were detected in the positive flock. The owner of the positive flock did not have antibodies to H6 or other common AIV. Based on the findings of this study, the risk of transmission of LPAI viruses from backyard poultry to owners in Minnesota appears to be low under current conditions and management practices.     

H5N1亚型禽流感病毒A/Guangxi/1/2005株抗药机制的研究

为研究H5N1亚型禽流感病毒(AIV)的抗药机制,本研究选取Clade2.3.4亚群中一株对金刚烷胺敏感的人源AIV A/Guangxi/1/2005(H5N1)(S-GX05),用抗流感病毒药物金刚烷胺对其进行定向诱导,筛选出一株抗药性病毒株,命名为R-A/Guangxi/1/2005(R-GX05)。通过全基因测序并与S-GX05全基因序列进行对比,结果显示S-GX05只在其M2蛋白中有一个氨基酸位点发生突变,即A30P;抗药性鉴定这两株病毒的半数药物抑制浓度(IC50)分别为0.9μM和48.9μM,表明R-GX05对金刚烷胺表现出一定程度的抗性。动物实验证实,这两株病毒对BALB/c小鼠的致病性基本一致,均表现出高致病性,其MLD50分别为4.7 log10 EID50和5.0 log10 EID50,两株病毒在小鼠体内各组织脏器中的分布及增殖能力也基本相同。这些结果表明,S-GX05在药物压力下产生抗药性后,并未引起其它生物学特性的改变。A30P的发现为进一步从分子水平上研究H5N1亚型AIV的抗药机制及新型抗流感新药的研发奠定了基础。     

传染性喉气管炎病毒WG株糖蛋白gJ基因的克隆与表达

根据GenBank中已发表的传染性喉气管炎病毒全基因组序列（NC006233）设计引物,以传染性喉气管炎病毒WG株基因组为模板,PCR扩增糖蛋白gJ基因,并对其进行序列分析。用DNAStar软件分析酣蛋白的抗原性,选择抗原性强的140aa-483aa片段,克隆并连接到原核表达载体pET-32a（＋）中,转化BL21（DE3）菌株。经IPTG诱导后,获得大小为65．2ku的重组蛋白,命名为卜出,表达量占菌体蛋白总量的60．8％;Westernblot分析表明r-gJ具有较强的抗原性。     

M148R and M149R are two virulence factors for myxoma virus pathogenesis in the European rabbit

Myxoma virus (MYXV), a member of the Poxviridae family, is the agent responsible for myxomatosis, a fatal disease in the European rabbit (Oryctolagus cuniculus). MYXV has a linear double-stranded DNA genome that encodes several factors important for evasion from the host immune system. Among them, four ankyrin (ANK) repeat proteins were identified: M148R, M149R, M150R and M-T5. To date, only M150R and M-T5 were studied and characterized as critical virulence factors. This article presents the first characterization of M148R and M149R. Green Fluorescent Protein (GFP) fusions allowed us to localize them in a viral context. Whereas M149R is only cytoplasmic, interestingly, M148R is in part located in the nucleolus, a unique feature for an ANK repeat poxviral protein. In order to evaluate their implication in viral pathogenicity, targeted M148R, M149R, or both deletions were constructed in the wild type T1 strain of myxoma virus. In vitro infection of rabbit and primate cultured cells as well as primary rabbit cells allowed us to conclude that M148R and M149R are not likely to be implicated in cell tropism or host range functions. However, in vivo experiments revealed that they are virulence factors since after infection of European rabbits with mutant viruses, a delay in the onset of clinical signs, an increase of survival time and a dramatic decrease in mortality rate were observed. Moreover, histological analysis suggests that M148R plays a role in the subversion of host inflammatory response by MYXV.     

Immune responses and protective efficacy of a recombinant swinepox virus co-expressing HA1 genes of H3N2 and H1N1 swine influenza virus in mice and pigs

The recombinant swine poxvirus rSPV/H3-2A-H1 co-expressing HA1 genes of H3N2 and H1N1 subtype SIV has been constructed and identified. Inoculations of rSPV/H3-2A-H1 yielded ELISA and neutralization antibodies against SIV H1N1 and H3N2, and elicited potent H1N1 and H3N2 SIV-specific INF-γ response from T-lymphocytes in mice and pigs in this study. Complete protection against SIV H1N1 or H3N2 challenge in pigs was observed.     

禽流感病毒分子生物学的研究进展

禽流行性感冒(av ian in fluenza,A I,简称禽流感)是由A型禽流感病毒(av ian in fluenza v irus,A IV)引起的禽类烈性传染病。作为被世界动物卫生组织(O IE)定为A类的传染病,A I不仅给世界养禽业造成了巨大的经济损失,而且对人类健康和生命安全构成了严重威胁。因此,A I已经成为人们关注的焦点,国内外学者也对其进行了大量研究。作者从病原基因组及其编码的蛋白质、致病力、变异性以及对人类感染A IV的分子机制等角度就A IV的分子生物学研究作一综述,为防制A I提供理论基础,并在此基础上探讨了人类禽流感的防治措施,加深人们对A I的认识。