抗病毒药物在兽医上的应用与存在的问题

病毒的生物学特性、生活和繁殖方式，给防治病毒病造成了困难。本文介绍了抗病毒药物的作用机制、分类和种类，得出抗病毒药物在应用中存在的问题。     

用卡片PCR法检测卡耶他环孢子虫

使用FTA卡片法提取卡耶他环孢子虫DNA,利用特异性引物组F1E/R2B、CC719/CRP999进行巢式PCR,得到1条298bp的特异条带。并以柔嫩艾美尔球虫、贝氏隐孢子虫等作为对照,结果显示,除卡耶他环孢子虫外,均无特异性条带。用卡耶他环孢子虫卵囊进行巢式PCR敏感性试验,结果显示敏感度最高达1.0×100个/mL。     

常态下景天科室内观赏植物释放负离子的研究

目的为景天科拟石莲花属植物规模化繁殖和生产提供依据。方法以景天科拟石莲花属植物雪莲种子、红边月影、女雏、花乃井和小蓝衣叶片以及3种播种基质(V_{泥炭土422#}∶V_珍珠岩=3∶2、V_{泥炭土680#}∶V_珍珠岩=3∶2和V_{本地红壤土}∶V_珍珠岩=3∶2)为试材,测定了3种基质的理化性质及其对红边月影、女雏、花乃井和小蓝衣叶插生根率、新芽直径以及对雪莲种子发芽率的影响。结果3种基质的容重、总孔隙度、通气孔隙度、持水孔隙度、有机质和有效氮磷钾元素均存在差异,pH值和EC值均符合拟石莲花属植物的生长要求。3种基质对拟石莲花属植物叶插生根率影响不显著(P>0.05),对新芽直径和种子发芽率影响显著(P<0.05),拟石莲花属植物物种间的叶插生根率和新芽直径存在显著(P<0.05)或极显著(P<0.01)差异,拟石莲花属植物物种和基质间存在互作效应。基质理化性质中,对拟石莲花属植物发芽率和生根率均为显著影响的共性因素为基质中有机质含量、氮元素含量和持水孔隙度,而对生长速度有极显著影响的因素为通气孔隙度。结论泥炭和珍珠岩复配较适宜作为拟石莲花属植物的叶插和播种繁殖基质,针对不同拟石莲花属植物品种筛选不同性质的泥炭,并且在不同生长期选用不同理化性质的基质,可获得更好的繁育效果。     

基于乌金猪深度发掘的优质高效新品种选育

目的揭示宣和猪PRKAG3基因外显子5多态性及其与肉质性状的关联。方法采用PCR产物直接测序法检测了120头宣和猪PRKAG3基因外显子5区域的SNP位点,借助最小二乘模型分析了各位点不同基因型及合并基因型对6个肉质性状的影响。结果宣和猪PRKAG3基因外显子5区域检出3个SNP位点,包括2个同义突变位点(T579C、T580C)和1个错义突变位点(G595A),分别以TT、TT、GA基因型和T、T、G等位基因的频率最高,且都处于Hardy-Weinberg平衡状态。T579C、T580C位点的TT和TC基因型可显著提高大理石纹(P<0.05)和降低失水率(P<0.01),分别呈显著的加性效应及加性—显性效应(P<0.05或P<0.01);G595A位点的AA基因型失水率最低(P<0.05)、熟肉率最高(P<0.05),呈显著的加性效应(P<0.05);3个位点的合并基因型TTTTGG、TCTCGG和TTTTAA分别具有最高的大理石纹、pH₁和最低的失水率(P<0.05或P<0.01),CCCCGG基因型的大理石纹和pH₁最低、失水率最高(P<0.05或P<0.01)。结论研究结果进一步确认宣和猪PRKAG3基因外显子5多态性与肌肉大理石纹、pH值和失水率显著关联,T579C、T580C位点的CC基因型和G595A位点的GG基因型具有协同降低猪肉品质的效应。     

我国小麦茎基腐病菌致病力比较分析

为明确我国不同种、地理来源和毒素化学型小麦茎基腐病菌的致病力分化情况,采用纸塔法对来自全国9个省市80个采样点分离的224株小麦茎基腐病菌进行致病力分析。结果表明,不同种镰刀菌的致病力不同,黄色镰刀菌Fusarium culmorum,禾谷镰刀菌F.graminearum,假禾谷镰刀菌F.pseudograminearum及亚洲镰刀菌F.asiaticum致病力强于其他种。F.culmorum致病力显著高于F.pseudograminearum和F.asiaticum,而F.pseudograminearum,F.graminearum及F.asiaticum三者之间无显著性差异。中华镰刀菌F.sinensis,木贼镰刀菌F.equiseti,锐顶镰刀菌F.acuminatum致病力较弱,三者间苗期致病力无显著性差异;多数省份F.pseudograminearum群体间致病力无显著差异,仅山东F.pseudograminearum群体的致病性显著低于河南群体;此外,产毒类型为3ADON的F.pseudograminearum群体致病力显著高于15ADON群体。     

No effect of exogenous melatonin on development of cryopreserved metaphase II oocytes in mouse

Background

This study was conducted to investigate effect of exogenous melatonin on the development of mouse mature oocytes after cryopreservation.

Results

First, mouse metaphase II (MII) oocytes were vitrified in the open-pulled straws (OPS). After warming, they were cultured for 1 h in M₂ medium containing melatonin at different concentrations (0, 10⁻⁹, 10⁻⁷, 10⁻⁵, 10⁻³ mol/L). Then the oocytes were used to detect reactive oxygen species (ROS) and glutathione (GSH) levels (fluorescence microscopy), and the developmental potential after parthenogenetic activation. The experimental results showed that the ROS level and cleavage rate in 10⁻³ mol/L melatonin group was significantly lower than that in melatonin-free group (control). The GSH levels and blastocyst rates in all melatonin-treated groups were similar to that in control. Based on the above results, we detected the expression of gene Hsp90aa1, Hsf1, Hspa1b, Nrf2 and Bcl-x1 with qRT-PCR in oocytes treated with 10⁻⁷, or 10⁻³ mol/L melatonin and untreated control. After warming and culture for 1 h, the oocytes showed higher Hsp90aa1 expression in 10⁻⁷ mol/L melatonin-treated group than in the control (P < 0.05); the Hsf1, Hsp90aa1 and Bcl-x1 expression were significantly decreased in 10⁻³ mol/L melatonin-treated group when compared to the control. Based on the above results and previous research, we detected the development of vitrified-warmed oocytes treated with either 10⁻⁷ or 0 mol/L melatonin by in vitro fertilization. No difference was observed between them.

Conclusions

Our results indicate that the supplementation of melatonin (10⁻⁹ to 10⁻³ mol/L) in culture medium and incubation for 1 h did not improve the subsequent developmental potential of vitrified-warmed mouse MII oocytes, even if there were alteration in gene expression.     

Effects of day and night temperature on photosynthesis,antioxidant enzyme activities,and endogenous hormones in tomato leaves during the flowering stage

To study the effects of day and night temperature difference (DIF) on tomato growth, a controlled experiment using Solanum lycopersicum L., cv. Jinguan 5 was conducted. The daily mean temperature (T_m) was maintained at 18°C and 25°C, and the DIF was set at 0°C, 6°C, and 12°C. The results indicated that chlorophyll a (Chl a) and chlorophyll b (Chl b) gradually increased as DIF rose. At 18°C T_m, the carotenoid content reached a maximum at 12°C DIF. The Chl a/Chl b, net photosynthetic rate (P_N), photosynthetic rate at irradiation saturation (P_max), stomatal conductance (g_s), intercellular CO₂ concentration (C_i), stomatal limitation value, the maximum assimilation rate (A_max), apparent quantum efficiency (A_q), carboxylation efficiency (C_e), superoxide dismutase (SOD), peroxidase (POD), catalase (CAT), gibberellin A₃ (GA₃), and indole-3-acetic acid (IAA) were highest, while malondialdehyde (MDA) was lowest at 6°C DIF. At 25°C T_m, P_N, P_max, A_max, A_q, C_e, g_s, C_i, CAT, POD, GA₃, IAA, and zeatin reached the maximum under 6°C DIF, while SOD and MDA reached the maximum under 12°C DIF. Furthermore, the morphological index peaked at 6°C DIF under 18°C and 25°C T_m. The results suggested that 6°C DIF improved the growth and development of tomato during the flowering stage. ABBREVIATIONS: Aq – apparent quantum efficiency; Amax – the maximum assimilation rate; CAT – Catalase; Chl a(b) – chlorophyll a(b); Ca – ambient CO₂ concentration; Ce – carboxylation efficiency; Ci – intercellular CO₂ concentration; DIF – difference between day temperature (TD) and night temperature(TN); FM – fresh mass; gs – stomatal conductance; GA₃ – gibberellin A₃; IAA – indole-3-acetic acid; Ls – stomatal limitation value; MDA – malondialdehyde; Pmax – photosynthetic rate at irradiation saturation; PN – net photosynthetic rate; POD – peroxidase; ROS – reactive oxygen species; SOD – superoxidedismutase; Tm – daily mean temperature; ZT – zeatin.     

Cloning and Tissue Expression Analysis of PDK4 and FGF10 Genes in Guizhou Congjiang Xiang Pig

The objective of this study was to clone PDK4 and FGF10 genes, and investigate the expression level of PDK4 and FGF10 genes mRNA in different tissues of Large White pig and Congjiang Xiang pig. The PDK4 and FGF10 genes were cloned by RT-PCR and analyzed by bioinformatics, the relative expression of PDK4 and FGF10 genes were detected by Real-time PCR. The results showed that the coding region of PDK4 gene was 1 224 bp, encoding 407 amino acids; The coding region of FGF10 gene was 636 bp and encoded 211 amino acids. The homologies of nucleotide sequences of PDK4 gene with sheep, horse and human were 93%, 92% and 91%,respectively. The homologies of nucleotide sequences of FGF10 gene with sheep, cattle, human and mouse were 94%,93%, 93% and 90%, respectively. The phylogenetic tree of PDK4 gene showed that the genetic relationship of Congjiang Xiang pig, cattle and sheep were very close, the phylogenetic tree of FGF10 gene indicated that the genetic relationship of Congjiang Xiang pig, cattle, sheep, human and macaque were very close, but the genetic relationship of Congjiang Xiang pig, rat and chicken were far away. Real-time PCR results showed that, in different tissues of Congjiang Xiang pig,PDK4 gene expression in kidney tissue was higher than other tissues, with a higher expression in stomach and adipose as well,FGF10 gene expression in stomach tissue was higher than other tissues, with a higher expression in kidney and adipose as well, but both of PDK4 and FGF10 genes expression were the lowest in longissimus dorsi. In different tissues of Large White pig, both of PDK4 and FGF10 genes were expressed the highest in adipose than other tissues, PDK4 gene expression in longissimus dorsi was the lowest, while the FGF10 gene expression the lowest in heart. This study successfully cloned the PDK4 and FGF10 genes of Large White pig and Congjiang Xiang pig,and detected the relative expression of PDK4 and FGF10 genes in different tissues of Large White pig and Congjiang Xiang pig, and also provided scientific basis for further study on regulation of PDK4 and FGF10 genes on lipid metabolism and deposition.     

腐植酸浸种对盐碱胁迫下小麦根系抗氧化系统的影响

采用中性盐( NaCl)和碱性盐(NaHCO3)混合模拟不同浓度盐碱胁迫条件,对龙麦26和克旱16两种同基因型春小麦进行腐植酸浸种处理.分别测定根系氧离子自由基、丙二醛和谷胱甘肽含量,以及过氧化物酶超氧化物歧化酶活性,以探讨腐植酸对盐碱两种胁迫下小麦根系抗氧化系统的调控效应.结果表明:随着盐碱迫浓度的提高,小麦幼苗根系...     

农户舍饲奶牛血清钙及游离羟脯氨酸水平测定

采用氯胺T比色法和EDTANa_2滴定法,对重庆市农户舍饲奶牛不同泌乳阶段血清中游离羟脯氨酸与血清钙的水平进行 测定,旨在调查试验条件下奶牛血钙代谢情况以及骨营养不良发生的可能性。结果显示: 在农户全舍饲条件下,血清钙含量Ⅱ组显著低于Ⅴ组、Ⅵ组,其它各组间差异不显著;Ⅰ～ Ⅵ组血清羟脯氨酸含量分别为2.32±0.37μg/ml、2.36±0.59μg/ml、2.02±0.54μg/ml、1.90±0.44μg/ml、1.98±0.45μg/ml、1.79±0.18μg/ml,Ⅰ、Ⅱ组与Ⅵ组差异极显著。采样后2-3个月内进行临床观察,血清游离羟脯氨酸水平与骨营养不良发生率呈现一致性变化。而钙磷摄入不足,比例不当是主要原因。