硝基咪唑类药物检测技术研究进展

本文介绍了硝基咪唑类药物的理化性质、作用、应用现状及检测方法,重点论述了动物组织,产品及排泄物中药物残留和饲料中原药的检测技术。     

脂肪细胞膜免疫技术研究进展

脂肪细胞膜免疫技术是从以动物脂肪细胞膜分离得到的膜蛋白作为抗原,通过被动免疫或主动免疫来破坏脂肪细胞,使脂肪组织中的细胞数量减少,限制其贮存脂肪的能力,从而达到调控动物生长和降低动物脂肪的目的。本文将对脂肪细胞膜蛋白抗体的制备、作用机制及在动物上的使用效果进行阐述,并对此技术尚需解决的问题和发展方向进行综述。     

水分胁迫和复水对紫花苜蓿幼苗叶绿素荧光特性的影响

利用PEG-6000模拟水分胁迫(ψs=-0.2MPa,胁迫时间:48 h,复水48 h),研究了紫花苜蓿(Medicago sativa L)品种陇东苜蓿和阿尔冈金叶片叶绿素荧光特性和光合色素含量的变化,旨在探讨紫花苜蓿水分胁迫条件下的光合反应机制.结果表明:光化学淬灭系数(qP)和PSII线性电子传递的有效量子产额(YIELD)以及非光化学淬灭系数(qN)和表观光合电子传递效率(ETR)在胁迫前后随光合有效辐射(PAR)的变化规律分别可用公式:Y=aLn(X) b(Y:qP或YIELD,X:PAR,X≠0)和Y=aX2 bX c(Y:qN或ETR,X:PAR)来表示;在受到干旱胁迫后,PSII最大光能转化效率(Fv/Fm)、PSII潜在活性(Fv/Fo)和光合色素含量均明显低于对照,在任意光强下的qP、YIELD和ETR值也极显著低于对照的相应值,qN值则极显著高于对照的相应值;同时,和对照相比,qN和ETR光响应曲线顶点所对应的光强值在受到胁迫后亦明显下降,表明光抑制初始点的降低和最大光保护能力的减弱,甚至光抑制的提前到来.干旱胁迫使得PSⅡ反应中心结构和功能遭到破坏而部分关闭,光合电子传递受阻,光能利用与光化学转化与能力下降,吸收的光能更多的以热能形式耗散.复水后,虽然有光保护机制的存在,但除陇东苜蓿光合色素含量及阿尔冈金类胡萝卜素外,各参数均未能恢复到对照水平,因此旱后复水不能完全解除干旱对PSII反应中心所带来的伤害.紫花苜蓿幼苗对干旱胁迫较为敏感.供试品种相比,陇东苜蓿耐旱性优于阿尔冈金.     

人工模拟高温环境下白三叶草相对生理指标测定

研究了高温胁迫条件下白三叶叶片相对含水量、膜透性、脯氨酸含量和叶绿素含量的变化规律。结果表明:25~35℃处理0.5 h后,白三叶的膜透性、脯氨酸含量逐渐上升,相对含水量、叶绿素含量逐渐下降,但幅度不大;45℃以上高温处理后,以上生理指标均有显著性大幅度的变化。与CK比较,温度每升高5℃,白三叶细胞质膜透性、脯氨酸含量平均增加50.62%、59.89%,而相对含水量、叶绿素含量分别下降34.22%、4.61%。在实验条件下,白三叶能适应35℃的高温,40~45℃为其忍耐高温的临界温度范围,50℃为致死温度上限。     

中国部分地区猪圆环病毒2型的基因型分析

对中国11个省(市)部分猪场收集的812份病料,应用ORF2-PCR进行检测,发现有235份为PCV2阳性病料.利用鉴别PCR方法从235份阳性病料中,检出10份PCV2a基因型和133份PCV2b基因型,检出率分别为4.2%、56.6%.进一步对ORF2-PCR检测阳性的部分模板进行全基因组扩增,构建阳性重组质粒,对插入质粒的片段进行测序鉴定,利用DNAStar进行同源性分析,同GenBank参考毒株绘制系统发育树,从系统发育树中也可分出PCV2a、PCV2b 2种基因型.鉴别PCR和测序结果说明,我国部分地区流行的猪圆环病毒2型以PCV2b基因型为主,少数为PCV2a基因型,也有既非PCV2a又非PCV2b的基因型(PCV2c?).     

夏季高温胁迫对紫花苜蓿光合生理机制的影响研究

通过研究紫花苜蓿（Medicago sativa）不同品种在夏季高温下叶绿素含量和电导率的变化特征, 计算出各品种的半致死温度,评价其对夏季高温的耐受力。结果表明：高温导致不同苜蓿品种叶绿素含量不同程度的降低（12.04%～34.87%）,高温对不同苜蓿的相对电导率影响较大。综合分析认为,赛迪、苜蓿王和CUF101为强抗热性品种,阿尔冈金和WL612为抗热较差品种。     

饲料用混合油脂中苯并(a)芘测定方法的比较与优化

文中分析比较了三种油脂中苯并(a)芘含量的测定方法,其中GB/T22509—2008《动植物油脂苯并(a)芘的测定》方法安全性高、可行性强。本试验对该方法存在的一些不足之处加以优化后,用以测定饲料用混合油脂中苯并(a)芘的残留。标准品苯并(a)芘在0.5～20μg/l范围内的线性回归方程为:Y=1.445 6X+0.004 1,R2=0.999 5。油脂样品添加苯并(a)芘10μg/kg水平时的平均回收率为102.2%(N=5,RSD=2.3%);添加5μg/kg水平时的平均回收率为95.5%(N=5,RSD=4.2%)。结果表明该方法稳定性好、分析准确度高,非常适合用以评价油脂中苯并(a)芘的残留情况。抽样检测结果表明我国饲料级混合油中苯并(a)芘都有检出而且含量高于美国进口饲料级混合油,具有一定安全隐患。     

影响家禽就巢性因素的研究进展

就影响就巢因素的环境、内分泌和遗传国内外最新的研究进行了概述,并对去除就巢的最新研究进行了展望。     

microRNA-146a通过靶向MAPK4和Myosin Va基因调控羊驼黑色素细胞增殖、迁移

旨在研究microRNA-146a(miR-146a)对羊驼黑色素细胞增殖和迁移的调控及其分子机制.本研究使用双荧光素酶试验验证MAPK4和Myosin Va是miR-146a的靶基因;利用荧光定量PCR和蛋白质免疫印迹试验检测在羊驼黑色素细胞中过表达miR-146a对相关下游基因表达的影响;利用CCK8和Transw...     

Major outer membrane proteins of Brucella spp.: past,present and future

The major outer membrane proteins (OMPs) of Brucella spp. were initially identified in the early 1980s and characterised as potential immunogenic and protective antigens. They were classified according to their apparent molecular mass as 36–38 kDa OMPs or group 2 porin proteins and 31–34 and 25–27 kDa OMPs which belong to the group 3 proteins. The genes encoding the group 2 porin proteins were identified in the late 1980s and consist of two genes, omp2a and omp2b, which are closely linked in the Brucella genome, and which share a great degree of identity (>85%). In the 1990s, two genes were identified coding for the group 3 proteins and were named omp25 and omp31. The predicted amino acid sequences of omp25 and omp31 share 34% identity. The recent release of the genome sequence of B. melitensis 16 M has revealed the presence of five additional gene products homologous to Omp25 and Omp31. The use of recombinant protein technology and monoclonal antibodies (MAbs) has shown that the major OMPs appear to be of little relevance as antigens in smooth (S) B. abortus or B. melitensis infections i.e. low or no protective activity in the mouse model of infection and low or no immunogenicity during host infection. However, group 3 proteins, in particular Omp31, appear as immunodominant antigen in the course of rough (R) B. ovis infection in rams and as important protective antigen in the B. ovis mouse model of infection. The major OMP genes display diversity and specific markers have been identified for Brucella species, biovars, and strains, including the recent marine mammal Brucella isolates for which new species names have been proposed. Recently, Omp25 has been shown to be involved in virulence of B. melitensis, B. abortus and B. ovis. Mutants lacking Omp25 are indeed attenuated in animal models of infection, and moreover provide levels of protection similar or better than currently used attenuated vaccine strain B. melitensis Rev.1. Therefore, these mutant strains appear interesting vaccine candidates for the future. The other group 3 proteins identified in the genome merit also further investigation related to the development of new vaccines.