副猪嗜血杆菌病的临床症状与防治

副猪嗜血杆菌病是一种急性、典型猪传染病,对生猪生长发育的各个阶段都会产生不良影响,对膘情较好的保育阶段仔猪影响最为严重。由于副猪嗜血杆菌血清型多且细菌易产生耐药性,导致诊治困难。目前该病发病率日渐上升,为避免养猪生产因此造成巨大经济损失,需要结合日常预防和治疗,避免此病出现并进一步发展。文章综合叙述了副猪嗜血杆菌病原学、流行病学、临床病变及综合防治,以期为该病的防控与治疗提供参考。     

HSP90 gene expression induced by aspirin is associated with damage remission in a chicken myocardial cell culture exposed to heat stress

1. To understand the potential protection of heat shock protein 90 (HSP90) induced by aspirin against heat stress damage in chicken myocardial cells, enzyme activities related to stress damage, cytopathological changes, the expression and distribution of HSP90, and HSP90 mRNA levels in the myocardial cells exposed to heat stress (42°C) for different durations with or without aspirin administration (1 mg/ml, 2 h prior) in vitro were investigated.

2. Significant increase of enzyme levels in the supernatant of heat-stressed myocardial cells and cellular lesions characterised by acute degeneration, karyopyknosis and karyorrhexis were observed, compared to non-treated cells. However, the lesions of cells treated with aspirin were milder, characterised by earlier recovery of enzyme levels to the control levels and no obvious heat stress-related cellular necrosis.

3. Stronger positive signals in the cytoplasm and longer retention of HSP90 signal in nuclei were observed in aspirin-treated myocardial cells than those of only heat-stressed cells. HSP90 level in the aspirin-treated myocardial cells was 11.1-fold higher than that in non-treated cells, and remained at a high level at the early stage of heat stress, whereas it was just 4.1-fold higher in only heat-stressed cells and returned rapidly to a low level.

4. Overexpression of HSP90 mRNA in aspirin-treated cells was observed throughout the experiment, whereas HSP90 mRNA decreased significantly only in heat-stressed cells.

5. The early higher HSP90 expression induced by aspirin during heat stress was accompanied by decreased heat stress damage, suggesting that aspirin might play an important role in preventing myocardial cells from heat stress damage in vitro.

     

利用香菇菌糠栽培罗勒初探

以香菇菌糠为试材,采用不同比例的香菇菌糠和花园土、砂土的混合基质种植罗勒,测定其发芽率、形态指标以及生理指标,研究了香菇菌糠对罗勒幼苗生长的影响。结果表明:适宜种植罗勒的菌糠配方为花园土、菌糠、砂子=6∶1∶1;不同比例的菌糠配方对罗勒的发芽率有一定影响,随着菌糠比例的不断增加,罗勒的发芽率也不断提高,发芽时间也随菌糠的增加有一定缩短;该试验为菌糠的循环利用开辟了一条新的途径。     

外源乙烯和1-甲基环丙烯处理对采后胡萝卜品质的影响

以胡萝卜为试材,采用乙烯及乙烯受体抑制剂(1-甲基环丙烯)处理,通过对贮藏60d后胡萝卜的品质劣变率(长须根率、腐烂指数、出薹率)、外观指数、可溶性糖含量及多酚氧化酶活性进行测定,研究了1-MCP对胡萝卜采后贮藏品质的影响。结果表明:1-MCP结合手洗贮藏可抑制胡萝卜贮藏期间的品质劣变率、抑制可溶性糖含量的损失、保持较高的外观指数及抑制多酚氧化酶(PPO)活性。手洗后贮藏则可有效改善胡萝卜贮藏期间的表皮褐变问题。     

Synthetic Assessment of Power Transformer Condition Based on Matter-element Theory

Condition assessment on power transformer is an important approach to improve reliability of transformer and provide proper decision-making for condition-based maintenance. For long, static assessment method used in the past has already not adapted to the development of modem electricity transmission and distribution technology. So based on the deficiency of fuzzy synthetic assessment method, matter-element synthetic assessment method is introduced. The method can evaluate transformer condition not only in quality but also in quantity. Because each index weight can be given fairly and fast through improved analytic hierarchy process, which need not carry on consistency chec accuracy of assessment can be improved. Examples analysis has proved that assessment method of power transformer condition based on matter-element theory is rational and effective.     

以粮温实测数据为例探讨低温储粮的可行性

通过对高大平房仓粮温进行跟踪检测，分析比较了粮温变化情况，并探讨了低温储粮的可行性。     

凋落物分解酶的研究进展

森林凋落物分解是陆地生态系统物质循环和能量流动的重要环节,凋落物和土壤中的酶在凋落物分解过程中起着关键的调节作用.该研究综述了凋落物分解酶的生态学作用、种类以及影响酶活性的主要因素,为深入研究凋落物分解机理及其在森林可持续经营中的作用提供参考.未来该领域应注重全球变化背景下凋落物分解过程中酶的反馈调节机制探索,需将植物、凋落物和土壤作为一个整体,并结合新的检测技术和方法,对不同类型生态系统开展长期性、系统性的研究.     

基于形态性状和SSR标记的克氏原螯虾养殖群体遗传多样性分析

为客观评估广西南宁周边地区克氏原螯虾养殖群体的遗传多样性,采集来自南宁的3个克氏原螯虾群体——埃及群体（AJ）、良庆群体（LQ）和上林群体（SL）,以及湖北荆州（JZ）和江西湖口（HK）的群体各1个,采用形态学结合微卫星分子标记的方法分析其遗传多样性水平。形态分析结果显示,雌性群体的综合判别准确率为68.59%,雄性群体的综合判别准确率为73.60%;3个南宁群体（AJ,LQ,SL）与JZ群体聚为一类,3个南宁群体间具有较高的形态相似度。微卫星分析结果显示,AJ群体和LQ群体的遗传多样性最高,SL群体和HK群体次之;LQ群体与SL群体的遗传分化系数和遗传距离最小。结果表明广西南宁克氏原螯虾群体具有较高的遗传多样性,从国外引种或国内不同地理来源群体的杂交可能是提高克氏原螯虾群体遗传多样性的重要途径。     

Roles of protein phosphatase 4 in down-regulation of eNOS Ser633 phosphorylation induced by palmitic acid in human umbilical vein endotheli?al cells

AIMTo investigate the roles of protein phosphatase 4 (PP4) in down-regulation of endothelial nitric oxide synthase (eNOS) Ser633 phosphorylation induced by palmitic acid (PA). METHODSHuman umbilical vein endothelial cells (HUVECs) were treated with PA at 25 μmol/L, 50 μmol/L, 100 μmol/L and 200μmol/L for 36 h, or treated with PA at 100 μmol/L for 12 h, 24 h, 36 h and 48 h. Protein phosphatase 2A (PP2A) family inhibitor fostriecin (FST, 20 nmol/L) or okadaic acid (OA, 5 nmol/L) was selected to pretreat the HUVECs for 30 min. Protein phosphatase 4 catalytic subunit (PP4c) siRNA or protein phosphatase 2A catalytic subunit (PP2Ac) siRNA was transfected into the HUVECs. The protein expression levels of of eNOS, PP4c and PP2Ac, as well as the level of eNOS Ser633 phosphorylation, were detected by Western blot. The intracellular nitric oxide (NO) content was measured by DAF-FM DA. RESULTS(1) Compared with control group, the levels of eNOS Ser633 phosphorylation were decreased in PA groups in which the HUVECs were treated with 25 μmol/L, 50 μmol/L, 100 μmol/L and 200 μmol/L PA for 36 h (P<0.05) and 100 μmol/L PA for 24 h, 36 h and 48 h (P<0.05). No significant difference in the level of total eNOS protein expression among all the groups was observed. (2) Compared with control group, both FST and OA pretreatment reversed the reduction of eNOS Ser633 phosphorylation (P<0.05) and the decrease in intracellular NO content (P<0.05) induced by PA. No significant difference in the level of total eNOS protein expression among all the groups was observed. (3) Compared with si-Control group, the PP4c protein expression was significantly reduced (P<0.05), while the level of eNOS Ser633 phosphorylation was significantly increased in si-PP4c group (P<0.05). Although the levels of PP2Ac protein expression declined significantly (P<0.05), the level of eNOS Ser633 phosphorylation remained unchanged in si-PP2Ac group. No significant differencein the level of total eNOS protein expression among all the groups was found. CONCLUSION PA significantly reduces the level of eNOS Ser633 phosphorylation and the content of NO in the HUVECs, which may be due to PA inducing the activation of the PP2A family member PP4 rather than PP2A.