猪传染性胃肠炎病毒S基因核酸疫苗免疫小鼠体液免疫功能变化的研究

本实验对TGEV S基因核酸疫苗免疫后体液免疫功能变化进行了研究,同时比较了两种核酸疫苗单独免疫小鼠后体液免疫应答的变化,证明重组核酸疫苗诱导小鼠产生体液免疫应答。     

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。     

仔猪产气荚膜梭菌肠毒血症病原诊断及疫苗研究IV．肠毒血症C型疫苗生产用菌种的确定

试验证明用单一菌株C59-2生产C型产气荚膜梭菌肠毒血症干粉灭活疫苗,其效力可以达到《规程》要求,并且简化了生产工艺,降低了生产成本,提高了生产效率。疫苗免疫的兔血清可分别中和原来3个制苗用菌株所产生的外毒素。     

Sortase anchored proteins of Streptococcus uberis play major roles in the pathogenesis of bovine mastitis in dairy cattle

Streptococcus uberis, strain 0140J, contains a single copy sortase A (srtA), encoding a transamidase capable of covalently anchoring specific proteins to peptidoglycan. Unlike the wild-type, an isogenic mutant carrying an inactivating ISS1 insertion within srtA was only able to infect the bovine mammary gland in a transient fashion. For the first 24 h post challenge, the srtA mutant colonised at a similar rate and number to the wild type strain, but unlike the wild type did not subsequently colonise in higher numbers. Similar levels of host cell infiltration were detected in response to infection with both strains, but only in those mammary quarters infected with the wild type strain were clinical signs of disease evident. Mutants that failed to express individual sortase substrate proteins (sub0135, sub0145, sub0207, sub0241, sub0826, sub0888, sub1095, sub1154, sub1370, and sub1730) were isolated and their virulence determined in the same challenge model. This revealed that mutants lacking sub0145, sub1095 and sub1154 were attenuated in cattle. These data demonstrate that a number of sortase anchored proteins each play a distinct, non-redundant and important role in pathogenesis of S. uberis infection within the lactating bovine mammary gland.     

兽用生物制品的运输、贮存与使用

对兽用生物制品的命名作了概述,并对免疫预防用制品、诊断用制品、治疗用制品的运输、贮存与使用分别进行了阐述,同时对改善我国兽用生物制品的监管提出了建议。     

不同纯化浓缩方法制备的新城疫疫苗对SPF鸡免疫效果的研究

为研究利用不同纯化浓缩方法制备的新城疫疫苗对SPF鸡免疫效果的影响,试验取经过纯化浓缩的新城疫抗原制备的疫苗、经离心未经浓缩的抗原制备成的疫苗和经浓缩未离心的抗原制备成的疫苗分别免疫30日龄SPF鸡,免疫后分别在第7d、14 d、21 d、28 d、35 d、45 d、70 d、90 d采集血清检测新城疫抗体水平。结果表明,经浓缩纯化后抗原制备的疫苗与其他两组抗原制备的疫苗相比,物理外观性状基本相同,浓缩纯化后抗原制备的疫苗其单位抗原含量更高、杂质更少,抗体水平更高,统计数据显示差异显著。因此研究得出,浓缩倍数(即抗原含量)越高,抗体水平越高,持续的时间也越长。     

兔病毒性出血症、多杀性巴氏杆菌病、产气荚膜梭菌病(A)型三联灭活疫苗研制

对 5批兔病毒性出血症、多杀性巴氏杆菌病、产气荚膜梭菌病三联灭活疫苗进行了动物试验 ,结果表明该疫苗安全有效。近期效检对兔病毒性出血症的保护率为 1 0 0 % ,对兔多杀性巴氏杆菌病保护率为 92 % ,对产气荚膜梭菌病 (A)型保护率为 88%。在免疫期试验中 ,免疫 6个月后 ,对兔病毒性出血症保护率为 1 0 0 % ,对多杀性巴氏杆菌病的保护率为 79% ,对产气荚膜梭菌病 (A)型的保护率为 88%。在保存期试验中 ,4～ 8℃保存 1年仍有效。     

羊痘研究概况

羊痘病毒基因组庞大,约有150 kb,包括中间编码区和两端相同的反向末端重复序列;绵羊痘病毒和山羊痘病毒基因组彼此十分相似,约有96%的核苷酸完全相同.p32蛋白是目前世界各地分离鉴定的所有羊痘病毒株共有的且特异性很强的结构蛋白,在诊断和预防方面具有重要的应用价值.虽然羊疸从临床症状和宿主特异性上很客易做出诊断,但进一步的实验室确诊还是必要的,现已有多种检测方法和诊断试剂.控制该病最有效的方法是使用疫苗对易感动物进行免疫接种.文章从病原学、诊断和预防控制等方面对羊痘进行综述.     

Vaccination of Poultry Workers: Delivery and Uptake of Seasonal Influenza Immunization

Avian influenza is a highly infectious disease in poultry and although the risk of human infection is low, concerns exist that it could evolve into a new human strain of pandemic potential if reassortment with a human influenza virus occurs. In January 2007, the UK government introduced a programme to vaccinate poultry workers to reduce the potential of such an event. This study evaluates the delivery, uptake and costs of the programme in three counties of England. A questionnaire survey was completed by consultants in public health in all the Primary Care Trusts in Norfolk, Suffolk and Cambridgeshire in May 2007. The delivery of the programme varied between Primary Care Trusts, including being delivered in some cases by clinics in primary care, by general practitioners and occupational health services in others. The uptake of vaccination was low ranging from 7% to 29% at a cost of £29 to £132 per person vaccinated. Vaccination of poultry workers as a public health measure to prevent an influenza pandemic is likely to be ineffective with the level of coverage found in this evaluation in our region.