锌对几种淋巴类细胞生长和功能影响的研究

本文研究比较了锌和螯合剂ＥＤＴＡ对淋巴类细胞株ＰＤｃ－Ｂ－１、Ｊｕｒｋａｔ、ＢｏＬｃＬ、６Ｃ９和奶牛ＰＢＭＣ增殖及功能的影响。除奶牛ＰＢＭＣ之外，锌对各株细胞的增殖和功能均无促进作用，在浓度为１０￣１００μｍｏｌ／Ｌ时有明显抑制甚至毒性作用。ＥＤＴＡ对各株细胞的增殖只有抑制作用，在同一浓度时对杂交瘤细胞增殖和抗体分泌的抑制作用基本一致，而对ＰＢＭＣ增殖和Ｉｇ分泌程度不同的抑制作用，是因为不同功能的     

禽腺病毒血清4型贵州株全基因序列分析

为了解禽腺病毒血清4型(FAdV-4)地方流行毒株的分子进化情况,基于实验室分离的2株FAdV-4贵州株GZ-BJ株和GZ-QL株,分别对2株FAdV-4毒株进行PCR分段扩增,扩增产物克隆至载体,提取质粒进行PCR和双酶切鉴定后筛选出重组质粒进行测序,将测序结果依次拼接得到病毒的全基因组,获得FAdV-4贵州株的全基因序列,并对其进行序列和遗传进化分析。结果显示,通过PCR分段扩增成功获得了2株FAdV-4贵州株(GZ-BJ株和GZ-QL株)的全基因序列,长度分别为43352、43723 bp,FAdV-4 GZ-BJ株全基因序列长度比FAdV-4 GZ-QL株短371 bp,少6个ORF(22K、putative 9.1 ku、u-exon、ORF17、ORF28、ORF42),二者的氨基酸同源性为57.1%。2株FAdV-4贵州株同国内外不同地区FAdV-4毒株核苷酸同源性在88.7%~100%,与FAdV-4经典毒株ON1比对,2株FAdV-4贵州株和国内FAdV-4分离株均缺失ORF19、ORF27、ORF30。系统进化树分析显示,2株FAdV-4贵州株GZ-BJ株和GZ-QL株仍属于Ⅰ群C种FAdV。研究结果表明,2株贵州株FAdV-4 GZ-BJ株和FAdV-4 GZ-QL株较国内外FAdV-4毒株均存在进化与突变,且FAdV-4 GZ-BJ株变化较大,但尚未改变其血清型,这为探索FAdV-4致病机理的分子机制研究提供依据。     

猪伪狂犬病病毒gE抗体胶体金免疫层析检测方法的建立及应用

以纯化的抗人红细胞单链抗体(ScFv)-猪伪狂犬病病毒(PRV)gE蛋白双功能融合蛋白为诊断抗原和胶体金标记物,以羊抗猪IgG包被硝酸纤维膜作为质控带,制作检测猪伪狂犬病毒gE抗体的双抗原胶体金试纸条。利用方阵滴定试验筛选出金标抗原最佳工作浓度为17.6μg,检测线诊断抗原最佳标记量为1.76μg,血清最佳稀释度为1∶10,作用时间15 min,与猪瘟病毒(CSFV)、猪细小病毒(PPV)、猪繁殖与呼吸综合征病毒(PRRSV)、猪乙型脑炎病毒(JEV)、猪布鲁菌(Brucella)阳性血清和PRVgE缺失疫苗接种的猪免疫血清检测线均不出现红色条带,与PRV标准阳性血清反应检测线出现红色条带。试纸条操作简单,肉眼于15 min内可判定结果;试纸条在室温保存6个月,其特异性和敏感性没有明显变化;与美国IDEXX和法国LSI gE-ELISA抗体检测诊断试剂盒检测结果比较,1 164份猪血清的符合率均为90.55%。制备的胶体金试纸条具有操作简便、敏感性和特异性较高的特点,可用于PRV野毒感染的快速筛查。     

含PRRS病毒ORF5的伪狂犬病病毒TK基因缺失转移载体的构建

提取伪狂犬病病毒（ＰＲＶ）ＢａｒｔｈａＫ６１株基因组ＤＮＡ,用限制性内切酶ＫｐｎＩ充分消化,回收５．９ｋｂ片段（Ｊ片段）,将其克隆于质粒ｐＵＣ１１９ ＫｐｎＩ位点上,获得ｐＢＫＪ。用两对针对ＰＲＶ ＴＫ基因的特异性引物对重组质粒进行ＰＣＲ鉴定,证明其中含有ＰＲＶ ＴＫ基因。然后用ＫｐｎＩ、ＰｓｔＩ和ＢａｍＨＩ等限制性内切酶对其进行酶切分析,确定了克隆片段的物理图谱。进一步研究证实ＴＫ基因位于其中的     

维生素A、E对獭兔繁殖性能的影响

将 2 8只繁殖獭兔随机均分 2组 ,基础日粮相同 ,但试验组在配种前 3天妊娠第 7天于日粮中添加VA8mg/kg、VE10 0mg/kg。结果与对照组相比 :试验组产活仔数提高了 2 0 2 3 %(P <0 0 5 ) ,育成率提高了 6 5 8%(P <0 0 5 ) ,增重速度提高 7 11%(P <0 0 5 )。     

四川省猪繁殖与呼吸综合征病毒分子流行病学调查

为了解2012-2013年四川省猪繁殖与呼吸综合征病毒(PRRSV)流行毒株的遗传变异背景和分子流行病学情况,对PRRSV阳性病料中的Nsp2、ORF5基因进行RT-PCR扩增和序列测定,所获得的序列分别与美洲型代表株(VR2332)、欧洲型代表株(LV)、标准毒株和变异毒株进行相似性分析。结果本研究成功获得8条Nsp2基因序列和17条ORF5基因序列,序列分析表明所有PRRSV流行毒株均属于美洲型,其中8株Nsp2基因序列与标准毒株和变异毒株的核苷酸相似性分别为75.2%~88.6%和94.8%~97.1%,推导的氨基酸相似性分别为58.7%~79.2%和92.8%~94.8%;17株ORF5基因序列与标准毒株和变异毒株的核苷酸相似性分别为90.1%~96.6%和95.6%~99.4%,推导的氨基酸相似性为77.2%~93.0%和88.0%~96.8%;与标准毒株相比,8株Nsp2基因有30个不连续氨基酸缺失,17株ORF5基因序列有点突变。从遗传进化分析看,所有流行毒株均属于PRRSV亚群Ⅲ。     

断奶日龄对仔猪血液生理指标的影响

选取15窝日龄相近的三元杂交仔猪 ,按14、21、28、35日龄断奶和不断奶随机分为5组 (14E、21E、28E、35E和C) ,每组3窝。主要研究断奶与不同断奶日龄对仔猪血液生理指标的影响。主要结果为 :①哺乳仔猪从21日龄后血液中白细胞水平基本稳定 ,但14日龄时血液中白细胞水平显著低于正常水平 ;21日龄前断奶可显著降低血液中白细胞数量 ,1周后迅速提高 ,但14日龄断奶仔猪直至42日龄血液中白细胞计数(WBC)仍低于正常水平。②仔猪28日龄血液红细胞计数 (RBC)、红细胞中血红蛋白浓度 (HGB)、血液血球比容 (HCT)均达到高峰值 ,RBC、HGB、HCT均不受断奶及断奶日龄影响。③哺乳仔猪14～42日龄间血液平均红血球容积 (MCV)、红血球血红蛋白量 (MCH)呈线性下降的趋势 ,断奶对MCV、MCH测值无明显影响。     

Effect of different hand-milking techniques on milk production and teat treatment in Zebu dairy cattle

The aim of the study was to test three different hand-milking techniques (“pull down”, “thumb in”, and “full hand grip”) and their effects on milk production and teat treatment. This is important since milk production in many tropical areas still rely on hand-milking. The study was carried out at a peri-urban farm in the Bobo-Dioulasso area in Burkina Faso. Twelve indigenous Zebu cows in early lactation were used in the study. The sequences of the treatments (hand-milking techniques) and the milkers were balanced for carry-over effects between successive periods and days, respectively. The sequences were constructed by using special Latin squares. Yield and composition of saleable milk was not affected by milking technique but there were differences between the milkers in milk yield. There was also a significant interaction for saleable milk yield between milker and milking technique. Hemoglobin in milk was measured as an indicator of teat damage. The hemoglobin content was numerically higher in post-milking strip milk samples than in saleable milk. It was concluded that the amount of milk removed depends mainly on the milker and how well the milking technique works for the individual milker. No effect of milking technique was observed on teat treatment.     

A novel dendrimeric peptide induces high level neutralizing antibodies against classical swine fever virus in rabbits

The amino acid sequence (TAVSPTTLR, 829-837aa) on the glycoprotein E2 of classical swine fever virus (CSFV) is a conserved and linear neutralizing epitope. In the present study, two peptides were constructed based the core sequence of this neutralizing epitope, the dendrimeric peptide (Th-B(4)) containing four copies of B cell epitope fused to one copy of promiscuous T helper (Th) cell epitope and the peptide Th-B containing a single copy of B cell epitope fused to one copy of Th cell epitope. The dendrimeric peptide Th-B(4) elicited high titers of neutralizing antibodies as detected in an indirect ELISA, blocking ELISA and neutralization test and induced a complete protection against CSFV C strain in rabbits. The Th-B elicited low titers of neutralizing antibodies and did not induce a protection in rabbits. These results suggest that the dendrimeric peptide Th-B(4) may be a promising marker vaccine candidate against CSFV and the multimerization is a requirement for development of a peptide vaccine.