Immunopathology of the eye: Purification of canine retinal “S” antigen

Canine retinal S antigen has been purified to study the retinal progressive atrophy of the dog. The purified antigen will be used to detect, by the ELISA technique, specific autoantibody in dogs with ocular diseases.     

The pond's shape matters: differential growth,physiological condition and survival of epibenthic Farfantepenaeus aztecus postlarvae

As a function of the water quality provided by square, circular and oval experimental ponds, the growth, survival and oxygen requirements in epibenthic postlarvae of Farfantepenaeus aztecus were analysed in relation to their routine metabolism and apparent heat increment. Temperature, oxygen concentration, pH and salinity were measured daily in two experimental ponds of each shape. The postlarvae oxygen consumption during two 24‐h cycles, their growth, physiological condition and survival and the productivity in the ponds were estimated. Low values of pH, oxygen concentration and phytobenthos productivity, and reduced postlarvae relative growth and survival were observed in the square ponds. We suggest that the latter results from a deficient water circulation related to the effect of the pond's shape on dissolved oxygen levels and, consequently, on growth and survival. The postlarvae routine metabolism, including feeding, varied between 1.91 and 2.25 mg O₂ h^?1 g^?1 wet weight, whereas the minimum oxygen concentration needed in the ponds is approximately 4.25 mg O₂ L^?1. These conditions were achieved in the oval ponds concurrent with higher survival and growth values, in which individuals distributed randomly, for which we suggest that oval‐shaped ponds could be the most adequate for the culture of this and other penaeid species.     

北海道9号苹果在冀北山地引种初报

为探讨北海道９号苹果在冀北山地推广的可能性，于１９９５￣１９９７年进行了引种观察，积累了试验数据。结果表明，北海道９号苹果抗寒性较强，丰产性能好，果实着色好，品质优良，可在冀北平泉县中部及其以南的区域进一步进行生产示范，建园方式采用以国光／海棠作基砧，用高接换头方法较好。     

基于ARM-Linux的生物发酵智能控制系统

介绍了基于ARM-Linux的生物发酵智能控制系统.ARM9使用方便,有利于复杂系统的控制,同时在软件设计上采用了嵌入式Linux,方便了编程,缩短了软件的开发周期,提高了开发效率.针对生物发酵控制过程中的时变性、非线性、延时性和随机性等特点,提出了采用基于遗传算法的模糊神经网络控制方法.该控制方法结合了遗传算法、模糊理论及神经网络的优点,在一定程度上解决了传统控制方法不易得到精确的数学模型和难于对系统进行有效控制的不足.实践表明:该系统具有较强的鲁棒性,能够达到预期的控制效果,可以实现对发酵系统进行有效的控制.     

Interleukin 1, a mediator of immunoadjuvant peptidoglycans

Bacterial peptidoglycans and the synthetic analog muramyl dipeptide possess various immunomodulating properties (adjuvant effect, increase of resistance to infectious agents and to tumor growth). They are able to induce B cell activation and to stimulate macrophages to produce monokines such as Interleukin 1 (IL 1). IL 1 plays an essential role in immune response. It promotes thymocytes maturation and Interleukin 2 secretion by antigen sensitive T cells, which in turn triggers regulatory T cells. Moreover, it is involved in the proliferation and differentiation of B cells.

There is a correlation between the immunoenhancing effect of PG of a definite structure and their ability to induce IL 1 secretion. Non-adjuvant PG were inactive. This suggests that one of the major mechanisms of action of adjuvant PG could be the stimulation of IL 1 synthesis.     

Adenovirus-mediated mPPARγ1 gene overexpression inhibits IFN-γ-induced galectin-9 gene and protein expression in ECV304

AIM:To investigate whether adenovirus-mediated mPPARγ1 gene overexpression inhibits IFN-γ-induced galectin-9 gene and protein expression in ECV304. METHODS:A replication-deficient recombinant adenovirus expression vector of mPPARγ1 was constructed by using the AdEasy system. ECV304 were incubated for 24 h with 1×104 U/L, 5×104 U/L, 1×105 U/L and 2×105 U/L IFN-γ, respectively. ECV304 stimulated with 1×105 U/L IFN-γ were divided into 4 groups in random: P group (PPARγ1 gene overexpression), T group (treated with troglitazone 40 μmol/L in DMSO), PT group (PPARγ1 gene overexpression+troglitazone treatment) and control group. Changes of PPARγ and galectin-9 in mRNA and protein levels in different groups and subgroups were investigated by RT-PCR and immunoblotting. RESULTS: Galectin-9 expression was very few in normal ECV304. IFN-γ induced the expression of galectin-9 in ECV304. Degree of galectin-9 expression increased with the dose of IFN-γ. PPARγ1 gene overexpression inhibited IFN-γ-induced galectin-9 expression in ECV304. Galectin-9 mRNA and protein expressions from PT group and P group were inhibited in similar degree (P>0.05). However, this effect was not observed in troglitazone intervention (P>0.05). PPARγ expression was also very few in normal ECV304. PPARγ1 gene overexpression/activation had no effect on endogenous mPPARγ expression. CONCLUSION: This may partly contributed to the anti-inflammatory and immuno-regulatory effect of PPARγ1 gene overexpression by inhibiting IFN-γ-induced galectin-9 gene and protein expression in ECV304.     

Coronaviridae, pathogenetic and clinical aspects: An update

A review is given about pathogenetic and clinical aspects of the well-known as well as of recently detected members of the family Coronaviridae. Special attention is paid to coronavirus infections of domestic cattle and pets, whereas avian, murine, rat and human coronaviruses are summarized briefly.     

Use of differently enriched rotifers,Brachionus plicatilis,during larviculture of haddock,Melanogrammus aeglefinus: effects on early growth,survival and body lipid composition

We evaluated the effects of enriched rotifers on growth, survival and on the lipid composition of haddock larvae. The treatments tested were (1) AlgaMac 2000^®, (2) AquaGrow^® Advantage and (3) Pavlova sp. paste and AlgaMac 2000^®. The treatments did not influence larval growth rate throughout the experimental period (P = 0.70). Larvae from all treatments grew approximately 8% of their dry weight per day between 1 and 29 days post hatch (dph). Treatment 3 resulted in the best survival, estimated to be 3 on a scale from 0 to 5, whereas for the two other groups the survival estimates were 0 and 2. Rotifers from treatment 1 had low sterol concentrations, high eicosapentaenoic acid/arachidonic acid ratio and their feeding resulted in high larval mortality. Rotifers enriched with Pavlova sp. had the lowest proportions of the sum of saturated fatty acids, docosahexaenoic acid and sum of ω3 and the highest proportions of the sum of monounsaturated fatty acids (ΣMUFA). This was partially reflected in larvae from treatment 3 in that they had the highest proportions of ΣMUFA and the lowest proportions of Σω3 (P < 0.0001 for both analyses). In addition, these larvae had the highest and lowest ΣC₂₀ and ΣC₂₂ polyunsaturated fatty acids (PUFA) respectively (P < 0.0001 for both analyses). We suggest that more research with ω3 and ω6 PUFA can lead to improvements in the rearing of haddock larvae produced in hatcheries.     

史氏鲟精子超微结构

利用扫描和透射电镜观察了史氏鲟精子形态和超微结构。精子具有顶体、头部、中段和单鞭毛等部分。顶体长0.99±0.06μm,宽0.87±0.09μm。细胞核从后往前逐渐变细,前端宽度为0.88±0.04μm,后端宽度为1.26±0.06μm,细胞核长7.29±0.32μm。核内含有3条核管(E),核管上行至顶体下行至植入窝而止。中段紧接头后部,长为0.51±0.12μm,宽0.91±0.05μm。中段含有线粒体、中心粒复合体和鞭毛的起始部分。线粒体分2~3层排列,线粒体中可见髓样嵴结构。在细胞核与中段接合部细胞核向内凹陷形成植入窝,纤维体位于植入窝内,其后是中心粒复合体。中段后缘延长为袖套,袖套腔中含有线粒体、脂质空泡。鞭毛从袖套中伸出,由轴丝组成,为典型的"9+2"微管结构。     

PK-15细胞的ISG15基因敲除促进PRV的复制

本试验旨在研究干扰素刺激基因15（interferon-stimulated gene 15,ISG15）敲除对猪伪狂犬病病毒（PRV）复制的影响。通过CRISPR/Cas9技术构建猪ISG15基因敲除猪肾上皮（PK-15）细胞系,利用CCK-8试剂盒检测PK-15敲除ISG15基因对细胞活力的影响,采用间接免疫荧光技术检测PK-15以及PK15-ISG15^-/-细胞感染PRV的增殖差异,通过RT-qPCR检测PRV-EP0、PRV-gE、PRV-VP16和IFN-β的转录水平,Western blot检测PRV-gE和ISG15的蛋白表达水平,以及通过病毒噬斑检测对子代病毒感染力的影响。结果表明,sgRNA1和sgRNA2均成功敲除ISG15基因;CCK-8试剂盒检测细胞活力结果表明,敲除ISG15基因对PK-15细胞活力无影响;间接免疫荧光检测结果表明,PRV感染后,PK15-ISG15^-/-细胞中的荧光强度明显高于PK-15细胞;RT-qPCR和Western blot结果表明,敲除ISG15可以促进PRV的转录和蛋白表达;病毒噬斑试验进一步显示,敲除ISG15可以促进PRV的复制。另外,RT-qPCR结果显示,敲除ISG15可以抑制PRV感染引起的IFN-β转录上调。本研究成功构建了PK15-ISG15^-/-细胞系,并通过PRV感染试验证实ISG15基因可以抑制PRV在PK-15细胞中的增殖,并推测这种抑制作用可能与IFN通路有关。