Construction and application of a bovine immune-endocrine cDNA microarray

A variety of commercial DNA arrays specific for humans and rodents are widely available; however, microarrays containing well-characterized genes to study pathway-specific gene expression are not as accessible for domestic animals, such as cattle, sheep and pigs. Therefore, a small-scale application-targeted bovine immune-endocrine cDNA array was developed to evaluate genetic pathways involved in the immune-endocrine axis of cattle during periods of altered homeostasis provoked by physiological or environmental stressors, such as infection, vaccination or disease. For this purpose, 167 cDNA sequences corresponding to immune, endocrine and inflammatory response genes were collected and categorized. Positive controls included 5 housekeeping genes (glyceraldehydes-3-phosphate dehydrogenase, hypoxanthine phosphoribosyltransferase, ribosomal protein L19, beta-actin, beta2-microglobulin) and bovine genomic DNA. Negative controls were a bacterial gene (Rhodococcus equi 17-kDa virulence-associated protein) and a partial sequence of the plasmid pACYC177. In addition, RNA extracted from un-stimulated, as well as superantigen (Staphylococcus aureus enterotoxin-A, S. aureus Cowan Pansorbin Cells) and mitogen-stimulated (LPS, ConA) bovine blood leukocytes was mixed, reverse transcribed and PCR amplified using gene-specific primers. The endocrine-associated genes were amplified from cDNA derived from un-stimulated bovine hypothalamus, pituitary, adrenal and thyroid gland tissues. The array was constructed in 4 repeating grids of 180 duplicated spots by coupling the PCR amplified 213-630 bp gene fragments onto poly-l-lysine coated glass slides. The bovine immune-endocrine arrays were standardized and preliminary gene expression profiles generated using Cy3 and Cy5 labelled cDNA from un-stimulated and ConA (5 microg/ml) stimulated PBMC of 4 healthy Holstein cows (2-4 replicate arrays/cow) in a time course study. Mononuclear cell-derived cytokine and chemokine (IL-2, IL-1alpha, TNFalpha, IFN-gamma, TGFbeta-1, MCP-1, MCP-2 and MIP-3alpha) mRNA exhibited a repeatable and consistently low expression in un-stimulated cells and at least a two-fold increased expression following 6 and 24 h ConA stimulation as compared to 0 h un-stimulated controls. In contrast, expression of antigen presenting molecules, MHC-DR, MHC-DQ and MHC-DY, were consistently at least two-fold lower following 6 and 24 h ConA stimulation. The only endocrine gene with differential expression following ConA stimulation was prolactin. Additionally, due to the high level of genetic homology between ovine, swine and bovine genes, RNA similarly acquired from sheep and pigs was evaluated and similar gene expression patterns were noted. These data demonstrate that this application-targeted array containing a set of well characterized genes can be used to determine the relative gene expression corresponding to immune-endocrine responses of cattle and related species, sheep and pigs.     

单播草坪匍匐翦股颖溶磷菌筛选及溶磷能力的初步研究

对西安地区单播草坪匍匐翦股颖根际联合固氮菌进行分离的基础上,采用PKO无机磷培养基和蒙金娜有机 培养基对匍匐翦股颖根际分离的联合固氮菌(共获得188种分离物)中具有溶磷能力的菌株(占29.3％),通过对菌株溶 磷圈大小的测定,最终筛选出溶磷能力较强菌株4株,分离物溶解无机磷D/d值在1.324~3.014之间;而溶解有机磷的能力 在1.239~2.156之间。     

Expression and Bioinformatic Analysis of ADIPOQ Gene in Hanper Sheep

The aim of this study was to investigate the expression and biological characteristics of adiponectin (ADIPOQ) gene in longissimus dorsi muscle of Hanper sheep at different months of age.The ADIPOQ gene mRNA expression was detected in longissimus dorsi muscle of Hanper sheep at 3 different growth periods (1,7 and 13 months old) by Real-time quantitative PCR.The bioinformatics method was used to analyze the nucleotide and amino acid sequences of ADIPOQ gene,protein characteristics and network interaction protein.The results showed that ADIPOQ gene was expressed in longissimus dorsi muscle of Hanper sheep,which showed an increasing trend with the growth of the months age without significant difference (P>0.05).There was higher homology of ADIPOQ gene with Capra hircus (98.60%,99.00%) and Bos taurus (98.60%,87.00%) in nucleotide and amino acid sequences.The results of physical and chemical properties analysis showed that the molecular formula of ADIPOQ protein was C₁₁₇₂H₁₇₇₆N₃₁₄O₃₄₉S₅,the molecular mass was 26.00 ku,and the theoretical isoelectric point (pI) was 5.88,which suggested that the protein was acidic.The average value of ADIPOQ hydrophilic protein (GRAVY) was －0.403,which indicated that the protein was hydrophilic and didn’t belong to transmembrane protein.In addition,the signal peptide sequence was Met¹-Ala¹⁷,and the cleavage site was between Ala¹⁷ and Arg¹⁸.ADIPOQ existed collagen structure domain and C1Q conserved structure domain at position 45－101 and 101－237,respectively.The secondary structure mainly composed of random coil (66.95%).The construction of protein interaction network indicated that ADIPOQ might interact with ADIPOR1,ADIPOR2,CDH13 and LEP.The results provided a theoretical basis for further exploring the molecular biological functions of ADIPOQ gene in the process of muscle development in Hanper sheep.     

松嫩平原艾蒿无性系种群根茎的年龄结构研究

将艾蒿根茎划分为不同年龄级,按长度和生物量统计其年龄结构,分析各龄根茎数量特征的变化规律.结果表明:艾蒿根茎的最大存活年龄为4龄;其根茎长度年龄结构为增长型;生物量年龄结构为稳定型;开花期根茎累积长度为6984.8 cm·m-2,根茎生物量为103.7 g·m-2;单位长度根茎的干物质贮存量随着龄级的增加而不断增大;高龄根茎具有较强的生活力;根茎长度比根茎生物量具有更大的生态可塑性.     

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。     

黄芩地膜露头栽培密度研究

目的:探索地膜露头栽培模式下陇西同类地区黄芩栽培的最佳密度。方法:采用35 cm黑膜覆盖露头栽培模式,在控制统一行距的条件下,设计4种不同的株距进行田间栽培试验,通过观测黄芩地上部分、地下药用部位的生长量、试验区药材产量和种子产量等生物经济指标,结合经济效益分析,优选黄芩地膜露头栽培的最佳密度。结果:株距5 cm栽培的鲜药产量较高,但药材商品规格、产籽量均低,增产不增收;株距15 cm栽培的鲜药商品规格较高,但产量和产籽量均偏低,经济效益低;株距10 cm栽培的出苗率、鲜药产量、产籽量、田间长势、药材商品规格表现好。结论:黄芩35 cm黑膜覆盖露头栽培,在陇西同类地区的最佳密度为行距30 cm、株距10 cm,即亩保苗22 000-22 500株。     

颈静脉灌注不同模式的氨基酸混合物对泌乳奶牛乳蛋白合成的影响

本试验旨在比较颈静脉灌注酪蛋白模式和理想模式的氨基酸混合物对泌乳中期荷斯坦奶牛乳产量、乳成分以及乳腺对氨基酸摄取利用的影响。选择8头泌乳中期[泌乳天数:(82±11)d]荷斯坦奶牛作为试验动物,试验采用随机区组设计,将试验牛随机分为2组,分别颈静脉灌注160g/d酪蛋白模式(Casein组)和理想模式的氨基酸混合物(R组)。2个试验组分别以各自灌注前作为空白对照组(C1组为Casein组的空白对照组,C2组为R组的空白对照组)。预试期14d,灌注期5d。试验采用全混合日粮(TMR)饲喂,以玉米、豆粕、棉籽粕、玉米青贮、苜蓿干草和羊草为主要原料,参照NRC(2001)奶牛饲养标准配制。结果表明:灌注酪蛋白模式的氨基酸混合物后,乳蛋白产量和含量较灌注前呈上升趋势(乳蛋白产量上升7.14%,P=0.078;乳蛋白含量上升3.27%,P=0.072);并且,奶牛动脉血浆中异亮氨酸(Ile)、亮氨酸(Leu)、赖氨酸(Lys)和组氨酸(His)的浓度较灌注前有不同程度的上升(Ile的浓度提高31.5%,P=0.097;Leu的浓度提高65.9%,P=0.041;Lys的浓度提高36.9%,P=0.088;His的浓度提高40.1%,P=0.010),而苏氨酸(Thr)、缬氨酸(Val)、蛋氨酸(Met)、苯丙氨酸(Phe)和精氨酸(Arg)的浓度在数值上虽较灌注前高但无显著差异(P0.05)。灌注酪蛋白模式的氨基酸混合物后,奶牛乳腺对天冬氨酸(Asp)和半胱氨酸(Cys)的摄取率显著升高(Asp的摄取率提高95.2%,P=0.031;Cys的摄取率提高49.6%,P=0.031),而奶牛乳腺对甘氨酸(Gly)的摄取率显著降低(降低158.3%,P=0.041)。灌注理想模式的氨基酸混合物后,乳蛋白含量比灌注前有上升趋势(提高5.78%,P=0.064),而乳脂产量显著低于灌注前(降低8.57%,P=0.015);并且,奶牛动脉血浆中Arg的浓度有上升趋势(提高18.0%,P=0.093),而酪氨酸(Tyr)的浓度呈下降趋势(降低47.8%,P=0.074)。灌注理想模式的氨基酸混合物后,奶牛乳腺对谷氨酸(Glu)、Cys和Ile的摄取率显著上升(Glu的摄取率提高118.7%,P=0.015;Cys的摄取率提高77.4%,P=0.032;Ile的摄取率提高46.0%,P=0.012),而奶牛乳腺对Ser的摄取率呈下降趋势(降低56.2%,P=0.052)。灌注氨基酸混合物后,Casein组乳脂产量增量显著高于R组(P=0.012),且Casein组的乳产量增量(P=0.095)和乳糖产量增量(P=0.091)较R组有升高的趋势,而2组间其他指标增量无显著差异(P0.05)。由此得出,在本试验条件下,颈静脉灌注酪蛋白模式和理想模式的氨基酸混合物均可提高泌乳奶牛的乳蛋白含量,而灌注酪蛋白模式氨基酸混合物同时可以促进乳蛋白产量的升高,因此,颈静脉灌注酪蛋白模式氨基酸混合物的效果优于灌注理想模式氨基酸混合物。     

葛根对奶牛脂肪肝细胞生化指标的影响

为探讨葛根对奶牛脂肪肝细胞的作用机制,采用胶原酶二步灌流法分离病牛的肝细胞,并观察细胞形态。用不同浓度的葛根水提物处理肝细胞,生化法检测细胞上清液中丙氨酸氨基转移酶（ALT）、天门冬氨酸氨基转移酶（AST）活性,并测定细胞裂解液中甘油三酯（TG）、胆固醇（TC）、丙二醛（MDA）、超氧化物歧化酶（SOD）的活性及含量。结果显示,50、100、500 μg/mL葛根水提物能极显著降低肝细胞中ALT、AST、TG、TC、MDA活性及含量,增加SOD活性（P < 0.01）。葛根水提物能显著改善肝细胞的相关生化指标,其机制可能与调节脂质代谢、抗脂质过氧化作用相关。     

沿河山羊舍饲养殖试验研究

通过对沿河山羊进行舍饲养殖试验研究,结果表明沿河山羊在舍饲环境条件下其发情规律、怀孕期均与放牧山羊基本一致.舍饲母羊胎均产羔率为187.88%,略高于放牧母羊产羔率(184.85%).舍饲羔羊断奶成活率为88.71%,比放牧羔羊断奶成活率(81.97%)提高8.22%.舍饲山羊发病死亡率为12.50%,比放牧山羊低76.54%.舍饲羔羊公母平均初生重为1.71±0.57kg,2月龄体重为8.88±1.64kg,6月龄体重为17.85±2.69 kg,9月龄体重为27.37±3.32kg,比放牧羔羊分别提高1.79%、27.95%、26.78%和26.16%,除羔羊初生重相接近外,其余各月龄阶段的体重差异均极显著(P＜0.01).舍饲羔羊各月龄阶段的体高变化不大,体斜长、胸围均有明显提高,增长幅度在10%以上,差异显著(P＜0.05).可见,沿河山羊在舍饲环境条件下具有良好的适应能力,而且舍饲还有利于疫病的防治,促进生长发育,值得在全县范围内推广.     

萨杜湖杂交羊生长性能、羊毛品质及血液生理生化指标测定

为研究萨福克羊×杜泊羊×湖羊杂交羊(萨杜湖杂交羊)生长发育情况及其对当地生态环境的适应能力,采用生产性能常规测定、显微测定和全自动血液生理生化分析仪分别测定了不同年龄阶段萨杜湖杂交羊的体重、体尺指标、羊毛品质(包括不同部位羊毛的净毛率、细度、有髓毛和无髓毛占比、自然长度和伸直长度等指标)和成年羊血液生理生化指标。结果表明:萨杜湖杂交羊早期生长速度较快,初生阶段及周岁时公羊体斜长均显著高于母羊(P<0.05);3月龄时公羊体高、体斜长和胸围均显著高于母羊(P<0.05);6月龄时母羊体重极显著高于公羊(P<0.01),成年时期公羊体重和体高均显著高于母羊(P<0.05);其余各生长阶段内,公母羊间体重及体尺差异不显著(P>0.05)。其成年时平均净毛率较低,为45.21%;长度适中:平均自然长度为4.55cm,伸直长度为6.22cm;细度良好,为17.60μm。公母羊血液生理生化指标及其同国内绵羊参考值相比存在一定的差异,其中母羊血小板总数(PLT)和血小板压积(PCT)均极显著高于公羊(P<0.01),公羊甘油三酯(TG)和白蛋白(ALB)含量显著高于母羊(P<0.05),其余各项指标均无显著差异(P>0.05)。综上所述,萨杜湖杂交羊在生长发育等方面都有不同程度的改进和提高,本试验结果可为该品种杂交羊进一步开发利用提供参考依据。