犬Ⅱ型腺病毒自然弱毒株的分离与鉴定

从一只３月龄病犬中分离出一株犬腺病毒（ＣＡＶ）,暂定名为ＹＣＡ１８。从一系列形态学、生理化学、生物学和分子病毒学实验证明这是一株Ⅱ型犬腺病毒自然弱毒。此毒株能在犬、猪肾原代细胞和传代细胞系上生长,能产生腺病毒感染的特征性细胞病变,细胞肿胀,变圆和呈“葡萄串样”。在细胞核内可见病毒粒子及其前本的晶格状排列,病毒粒子呈２０面体立体对称,表面有排列整齐的壳粒;能抵抗乙醚的处理,在ＰＨ３及５０℃温度中稳定     

磷矿周围环境镉污染情况调查研究

为掌握磷矿区周围镉污染情况,确保畜禽养殖生产安全,采用电感耦合等离子体质谱法对矿区周围环境中的水源、土壤、饲草和畜禽体内的镉污染程度展开调查。结果：矿区环境中土壤、地表水镉含量均超标;畜禽中牛肾脏、牛肠、牛肺脏、羊脾脏、羊肌肉镉含量超标。结论：磷矿周围环境以及饲养的牲畜存在较严重的镉污染,从公共卫生学角度应给予高度关注。     

哺乳与保育仔猪腹泻的综合防治

<正>我国仔猪腹泻现象十分普遍,导致饲料报酬较低、成活率下降、生长发育停滞。引起腹泻发生的病因往往是多因素相互作用,呈多重感染或交叉混合感染,临床诊断防治困难,严重威胁着养猪业的健康发展。     

家蚕丝素蛋白抗氧化肽的制备及其稳定性研究

利用碱性蛋白酶水解家蚕丝素蛋白制备抗氧化肽,考察水解pH、水解时间、加酶量、底物浓度、水解温度5个因素对水解产物DPPH自由基清除率的影响,在此基础上采用响应面试验优化水解工艺条件,并调查家蚕丝素蛋白抗氧化肽对热、酸、碱和体外肠道消化的稳定性,测定不同分子质量范围的家蚕丝素蛋白水解产物组分的抗氧化活性.结果 表明,碱性蛋白酶水解制备家蚕丝素蛋白抗氧化肽的最优工艺条件为水解pH 8.69、水解时间60 min、加酶量3035 U/g、底物(丝素蛋白)质量浓度26.80 g/L、水解温度53.89℃,在此条件下制备获得的家蚕丝素蛋白抗氧化肽对DPPH自由基的清除率为55.16％.家蚕丝素蛋白抗氧化肽具有良好的热稳定性;在中性环境中抗氧化活性很稳定,但在强酸和强碱环境中抗氧化活性明显降低;经体外模拟胃肠道消化后,对DPPH自由基的清除率比未消化处理对照组提高了9.43百分点.分子质量小于5 kD组分是家蚕丝素蛋白抗氧化肽的主要活性组分.研究结果为家蚕丝素蛋白功能产品的开发提供了试验依据.     

Phylogenetic analysis of S1 gene of infectious bronchitis virus isolates from China

Between 2006 and 2009, seven strains of infectious bronchitis (IB) virus (IBV) were isolated from vaccinated chicken flocks on different chicken farms in China. The pathogenic characters of seven IBV strains were assessed. Each of the seven strains was infective to the test chickens and could induce an immune response. The results from chicken embryo cross-neutralization assays showed that these strains were antigenically distinct from classic IBV strains of H120, M41, Conn, and Gray. Compared to H120 vaccine strain, point mutation, short insertion, and deletion occurred at many positions in the S1 protein of the seven strains. Five of the seven strains had the motif (HRRRR), which was identical to that of the epidemic IBV strains in China. Two new motifs (HRLRR and RRIRR) emerged in the isolated strains. The homology of the nucleotide and amino acid sequences of the S1 gene among the seven isolates was 81.7%-99.7% and 79.0%-99.4%, respectively. These seven strains were also genetically different from the vaccine strains and non-China IBV strains but closely related to large numbers of Chinese strains. The seven isolates and 36 reference IBV strains were clustered into six distinct groups (I-VI). The seven strains were categorized into groups I, II, and III, forming a big phylogenetic branch, which is closely related to Chinese IBVs, whereas the vaccine strains belonging to group VI are genetically distant from groups I, II, and III. The results from this study indicate that different IBV strains cocirculate in the chicken population in China.     

于娜与『大饼』

带犬女民警于娜,今年24岁,是北京市公安局刑侦总队警犬侦查训练大队的侦查员。     

奶牛隐性酮病的研究概况

本文将黑龙江省规模化奶牛场隐性酮病的多年研究进行小结,根据奶牛隐性酮病的发病特点,并结合国内外的文献,概述了黑龙江省奶牛隐性酮病的发生情况、病因学、临床病理学特征和检测及防治方面的研究状况,提出一些问题,旨在为今后的研究提供新的思路和方向,从而创造良好的经济价值.     

皖西南地区春播牧草的适应性研究

对皖西南地区春播的9个牧草品种的适应性,草产量和营养成分进行分析,结果表明:墨西哥玉米、菊苣、杂交狼尾草、甜高粱产量高,干草产量和鲜草产量均在95 t/hm2和15 t/hm2以上,适应性强,品质优良,适合在皖西南地区大面积推广种植。苦荬菜和籽粒苋产量中等,蛋白质含量高达22%以上,青绿多汁,适口性好,可以做为优质牧草在皖西南地区大面积推广种植。饲用玉米、皖草2号、苏丹草产量较低,鲜草产量均在70 t/hm2以下,饲用玉米无再生性,皖草2号、苏丹草在高温条件下病虫害严重,种植时应该注意病虫害防治。     

古巴非洲猪瘟根除的经验与借鉴

1971年非洲猪瘟首次传入古巴并于当年根除,1980年再次传入并在一年内又被根除。古巴能快速根除非洲猪瘟,主要与防控专业委员会的及时成立,协作机制的快速建立;全面扑杀措施的快速实施,健康猪产品的合理利用;民间团队的积极参与以及政府财政的大力支持密切相关。古巴的根除经验,可为我国非洲猪瘟的防控提供参考。     

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.