西安地区鸵鸟养殖现状调查

简述了国内外鸵鸟养殖概况 ,通过对西安地区 5个公司的鸵鸟养殖场中的饲养管理、繁育、疾病防治及产品开发等的调查和分析 ,提出了西安地区在鸵鸟养殖方面存在的问题及我国鸵鸟养殖业的发展对策     

镉中毒解毒机理的研究：硒化合物的预防和治疗作用初探

对大鼠组织胞液(Cytosol)的体外试验结果表明:亚硒酸钠、硒酸钠及硒化钠以明显影响[~(109)Cd]标记的氯化镉在组织胞液中的分布。硒酸钠、亚硒酸钠有较强的封闭金属硫蛋白(MT)与镉结合部位、激活分子量较大的蛋白质,捕获胞液中[~(109)Cd]的作用,还可使已经和MT结合的[~(109)Cd]被剥离,随后,[~(109)Cd]转入分子量较大的蛋白质上;亚硒酸钠还可使[~(109)Cd]转入分子量为32000～35000的蛋白质上。硒化钠仅有较弱的剥离与MT结合的镉,使之转入分子量较大的蛋白质上,但几乎不能阻止镉与MT结合。镉与大、中分子量蛋白质结合力远较它与MT的结合力弱,因而以能有利于镉被排出体外。     

EM发酵鸡粪喂猪试验

为开发鸡粪再生饲料资源、降低饲料成本和研究EM微生物制剂发酵鸡粪的功效，我们对45～90kg阶段的肉猪进行了EM发酵鸡粪饲喂试验。使用25％发酵鸡粪的试验猪的效果及与对照猪(用100％的饲料)的比较如下：1kg增重耗料3.1kg(除去鸡粪)，降低11.4％，日增重638.9g，降低5.7％，1kg增重饲料成本3.88元，降低7.6％，头均增重饲料成本182.94元，降低了43.38元。使用50％发酵鸡粪的试验猪的效果与对照猪的比较如下：1kg增重耗料2.4kg(除去鸡粪)，降低31.4％，日增重551.4g，降低18.6％，1kg增重饲料成本3.48元，降低17.1％，头均饲料成本138.07元，降低85.83元。此外，试验猪舍蝇蚊减少，臭味减轻。     

巴比妥类镇静剂的检测研究进展

本文对巴比妥类安眠镇静剂检测方法的研究进展进行了综述。重点讨论了样品前处理方法及各种衍生化方法,GC、GC-MS、HPLC、HPLC-MS等检测方法。     

基层动物防疫人员职业风险因素分析与防护

以2011年通过的《关于修改〈中华人民共和国职业病防治法〉的决定》提出的相关内容为指导,从环境、物理、化学、生物、心理等方面分析了危害基层动物防疫人员的职业因素,提出从提高自我保护意识、强化防护措施、做好人员健康监测、完善法律保障体系等方面采取措施,加强对基层动物防疫人员的防护和管理,以保证基层兽医人员的职业安全。     

Cartilage proteoglycans from normal and osteochondrotic porcine joints.

Modern pigs grow fast but are highly susceptible to degenerative joint abnormalities, including osteochondrosis. Normal and osteochondrotic humeri and femurs were obtained from five normal and ten lame adolescent boars to study cartilage proteoglycans. Histological examination of joints indicated a locally-reduced intensity of proteoglycan staining by safranin-O in lesion areas of cartilage. Cartilage proteoglycans extracted with 4.0 M guanidinium chloride were studied using Sepharose 2B gel chromatography. The proteoglycans from severely osteochondrotic joints were less (P less than 0.05) aggregated and contained a greater (P less than 0.05) proportion of smaller monomers than those from normal joints. Loss or damage of core protein, including its hyaluronic acid-binding regions, may account for the greater proportion of small monomers. The results also indicated that the proportion of hyaluronic acid in the total glycosaminoglycan uronic acid fraction, estimated by Sephadex G-200 chromatography and cellulose acetate electrophoresis, was lower (P less than 0.05) for the extracted proteoglycans than for the residual or the whole cartilage proteoglycans in all joints studied.     

Comparative expression profile of microRNAs and piRNAs in three ruminant species testes using next‐generation sequencing

microRNA (miRNA) and piwi‐interacting RNA (piRNA) are two classes small non‐coding regulatory RNAs that play crucial roles in multiple biological processes such as spermatogenesis. However, there are no published studies on conjoint analysis of miRNA and piRNA profiles among cattle, yak and their interspecies (the dzo) using sequencing technology. Next‐generation sequencing technology was used to profile miRNAs and piRNAs among those three ruminants to elucidate their functions. A total of 119, 14 and six differentially expressed miRNAs were obtained in cattle vs. dzo, cattle vs. yak and yak vs. dzo comparison groups, while there were 873, 1,065 and 1,158 differentially expressed piRNAs in those three comparison groups. The expression of three miRNAs was validated in the three ruminants, and the results suggested that the miRNA expression profiles data could represent actual miRNA expression levels. Moreover, the putative targets of differentially expressed miRNAs were predicted by their own genome, it is worth to note that both the cattle and yak genome were used for dzo, then the targets were subjected to GO enrichment and KEGG pathway analysis, revealing the likely roles for these differentially expressed miRNAs in spermatogenesis. In conclusion, this study provided a useful resource for further elucidation of the miRNAs and piRNAs regulatory roles in spermatogenesis. It may also facilitate the development of therapeutic strategies for dzo reproduction research.     

NHLRC1 repeat expansion in two beagles with Lafora disease

Lafora disease is a fatal genetic disorder characterised by neurotoxic deposits of malformed insoluble glycogen. In humans it is caused by mutation in the EPM2A or NHLRC1 genes. There is a known mutation in miniature wirehaired dachshunds which has not been documented in other dog breeds, including beagles, in which the disease is relatively commonly reported. This case report describes the causative defect in two affected beagles, namely the same massive expansion as in miniature wirehaired dachshunds of a 12‐nucleotide repeat sequence that is unique to the canine NHLRC1 gene. This is the first mutation described in beagles with Lafora disease, and so far the only Lafora disease genetic variant in dogs.     

山羊脑包虫病的手术治疗

2006年8月5日,仁怀市坛厂镇桅杆养殖场的一只波尔山羊发病。经畜主介绍,此羊是人工授精的一代杂交后备母羊,年龄1周岁,体重25kg,全身毛呈白色,头部黑色。该羊最近食欲下降,反应迟钝,长时间沉郁不动,当遇障碍物时则奋力前冲,并抵物不动,两眼视力模糊,其眼内瞳孔上附有一层白膜。     

Construction and immunogenicity studies of recombinant fowl poxvirus containing the S1 gene of Massachusetts 41 strain of infectious bronchitis virus

The spike 1 (S1) surface glycoprotein of infectious bronchitis virus (IBV) is the major inducer of the generation of virus neutralizing antibodies, and the administration of purified S1 has been shown to elicit a protective immune response against virulent virus challenge. On the basis of these observations, recombinant fowl poxvirus (rFPV) containing a cDNA copy of the S1 gene of IBV Mass 41 (rFPV-S1) was constructed and its immunogenicity and vaccine potential were evaluated. Initially, rFPV-S1 was shown to express the S1 in vito by indirect immunofluorescence staining and western blot analyses. Later, in vivo expression was demonstrated by the detection of IBV-specific serum immunoglobulin G and neutralization antibodies in the sera of chickens immunized with rFPV-S1. That the recombinant virus elicited anti-IBV protective immunity was indicated by the manifested, relatively mild clinical signs of disease, decreased titers of recovered challenge virus, and less severe histologic changes of the tracheas in virulent IBV Mass 41-challenged chickens previously receiving rFPV-S1 as compared with parental fowl poxvirus (FPV)-vaccinated control birds. In contrast, chickens immunized with either recombinant or parental FPV were resistant to a subsequent virulent FPV challenge. As to a preferred method of immunization, wing web administration appeared to be superior to the subcutaneous route because a greater percentage of birds vaccinated by the former protocol exhibited an anti-IBV humoral immune response. Thus, rFPV-S1 has potential as a poultry vaccine against both fowl pox and infectious bronchitis.