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41.
萨马丽汗·阿帕克 《畜牧兽医科学(电子版)》2021,(5):119-120
牛肺疫又被称为牛传染性胸膜肺炎,是由肺炎支原体感染引发的急慢性呼吸道疾病,临床上主要表现为呼吸急促,呼吸困难,从鼻腔中流出脓性分泌物,主要对患病牛的肺脏、胸膜和淋巴结造成危害,典型的临床特征是肺小叶浆液性肺炎和肺实质纤维素性肺炎,被国际兽医局划归为A类动物疫病,我国将其划归为一类重大动物疫病,发生流行后,需要执行严格的扑杀、无害化处理制度,逐渐净化牛群,避免疫情进一步扩展蔓延到造成更为严重的经济损失。该文主要论述牛肺疫的临床症状和综合防治措施。 相似文献
42.
In order to detect the clinical efficacy of oligosaccharide sulfate(DEAE) and dextran sulfate (DS-4000) against bovine mastitis,56 cows with bovine mastitis were divided into 5 groups (DEAE group,DS-4000 group,DEAE+penicillin group,DS-4000+penicillin group and penicillin group),and their breasts were perfusion with different drugs twice one day for 3 days.The effective rates of drugs were observed by clinic symptoms.Milk samples were collected before and after treatment of drugs,and the bacterial negative conversion rate of each group were detected by microbial examination.The results showed that total effective rates of 5 groups were 10.00%,20.00%,58.33%,75.00% and 50.00%,respectively,and the bacterial negative conversion rates were 0,12.50%,50.00%,54.55% and 44.44%,respectively.In conclusion,the curative efficiencies of the polysaccharides against bovine mastitis were weak,but it could be improved by combination with penicillin. 相似文献
43.
ZHANG Hai ZHOU Bi-jun YANG Zhong-cheng LIAO Mei WANG Kai-gong WEN Ming CHENG Zhen-tao WANG Wei FENG Xu-fang 《中国畜牧兽医》2016,43(11):2834-2843
In order to study and analyze L1 gene of bovine papillomavirus(BPV)in Guizhou province,the L1 gene of BPV-GZ01 strain was amplified,cloned and sequenced using bioinformatic softwares and methods,and the secondary structure,tertiary structure,B-cell preponderant epitope,conserved domains analysis, transmembrane domain and signal peptide of L1 gene were predicted.The results showed that the length of L1 gene was 1 494 bp,encoding 497 amino acids.The L1 gene of BPV-GZ01 strain shared an amino acid identities of 98.6%,99.4%,98.4%,94.4% and 91.3%,and a nucleotide identities of 99.1%,99.8%,99.4%,87.6% and 82.8% with those of BPV2,BPV2-SW01,BPV2-AKS01,BPV13 and BPV1 strains,respectively.The results of phylogenetic tree analysis indicated that there was a close relationship between BPV-GZ01 and BPV2-SW01 strains.The prediction of secondary structure of L1 protein indicated that the random coil,extended strand and alphahelix took a higher percentage.The L1 protein was supposed contain 6 potential antigen epitopes.And no transmembrane domains and no signal peptide were found.The tertiary structure of L1 protein was curved spiral structure.These results provided a theoretical basis for immunologic diagnosis and further research of nucleic acid vaccine of BPV. 相似文献
44.
Xiao-ying He Li-bing Ma Xiao-ning He Wan-tong Si Yue-Mao Zheng 《Journal of veterinary science (Suw?n-si, Korea)》2016,17(2):145-152
Previous studies have established a bovine mammary gland epithelia cells in vitro model by the adenovirus-mediated telomerase (hTERT-bMGEs). The present study was conducted to confirm whether hTERT-bMGEs were effective target cells to improve the efficiency of transgenic expression and somatic cell nuclear transfer (SCNT). To accomplish this, a mammary-specific vector encoding human lysozyme and green fluorescent protein was used to verify the transgenic efficiency of hTERT-bMGEs, and untreated bovine mammary gland epithelial cells (bMGEs) were used as a control group. The results showed that the hTERT-bMGEs group had much higher transgenic efficiency and protein expression than the bMGEs group. Furthermore, the nontransgenic and transgenic hTERT-bMGEs were used as donor cells to evaluate the efficiency of SCNT. There were no significant differences in rates of cleavage or blastocysts or hatched blastocysts of cloned embryos from nontransgenic hTERT-bMGEs at passage 18 and 28 groups (82.8% vs. 81.9%, 28.6% vs. 24.8%, 58.6% vs. 55.3%, respectively) and the transgenic group (80.8%, 26.5% and 53.4%); however, they were significantly higher than the bMGEs group (71.2%, 12.8% and 14.8%), (p < 0.05). We confirmed that hTERT-bMGEs could serve as effective target cells for improving development of somatic cell cloned cattle embryos. 相似文献
45.
Anna Bassols José Angel Robles-Guirado Laura Arroyo Lourdes Soler Natalia García Raquel Pato Raquel Peña Yolanda Saco Ramon Armengol Fermín Lampreave María A. Alava Francesca Canalias Matilde Piñeiro 《Veterinary clinical pathology / American Society for Veterinary Clinical Pathology》2023,52(Z1):64-74
46.
RN Zadoks E Scholz SM Rowe JM Norris HB Pooley J House 《Australian veterinary journal》2023,101(4):142-152
Numerous culture-based diagnostics are available on the Australian and international markets for on-farm detection of bacterial pathogens in milk. Use of such diagnostics may provide an opportunity to improve the prudent use of antimicrobials in udder health management. Farms are low-resource settings in terms of diagnostic microbiology capacity. The World Health Organisation has identified criteria for the evaluation of diagnostic tests in low resource settings based on Accuracy, Sensitivity, Specificity, User-friendliness, being Rapid or Robust, Equipment-free and being Deliverable (ASSURED). Here, we review how those criteria can be interpreted in the context of microbiological diagnosis of mastitis pathogens, and how on-farm diagnostics that are currently available in Australia perform relative to ASSURED criteria. This evaluation identifies multiple trade-offs, both with regard to scientific criteria and with regards to convenience criteria. More importantly, the purpose of testing may differ between farms, and test performance should be evaluated relative to its intended use. The ability of on-farm mastitis diagnostics to inform mastitis treatment decision-making in a timely and cost-effective manner depends not just on test characteristics but also on farm-specific pathogen prevalence, and on the farm enterprise's priorities and the farm manager's potential courses of action. With most assay evaluations to date conducted in professional laboratories, there is a surprising dearth of information on how well any of the diagnostic tests perform on-farm and, indeed, of the on-farm decision-making processes that they aim to inform. 相似文献
47.
《Journal of Cereal Science》2014,59(3):451-456
Brans of 23 traditional and 12 improved (both red and white) rice varieties in Sri Lanka were screened for anti-amylase and anti-glycation activities in vitro. Varieties which showed the highest inhibitory activities at screening were further investigated for anti-glucosidase and glycation reversing as anti-diabetic properties. The same varieties were studied for selected antioxidant properties. Significantly high anti-amylase and anti-glycation activities were observed for bran extracts of red varieties compared to white varieties at screening. Traditional red rice varieties, Masuran, Sudu Heeneti, Dik Wee and Goda Heeneti, exhibited significant and dose dependent anti-amylase, anti-glycation and glycation reversing activities. These varieties also showed marked antioxidant properties. It is concluded that brans of Sri Lankan traditional red rice varieties Masuran, Sudu Heeneti, Dik Wee and Goda Heeneti may be potential food supplements for diabetes. 相似文献
48.
整合位点的侧翼序列是外源基因表型研究和功能探讨的前提条件,对目的基因的正常转录和表达有着重要影响。本试验利用热不对称交措式PCR(Thermal Asymmetric Interlaced PCR,TAIL-PCR)的方法克隆了目的基因。结果表明:外源基因整合到牛的12号染色体基因组克隆(NW_003104315.1)中。分析了整合位点的纯合性发现转基因牛为整合位点杂合子。TAIL-PCR法能够有效、快速的鉴定外源基因在基因组中的整合位置,具有良好的应用前景。 相似文献
49.
酶解工艺参数不仅会影响畜禽骨蛋白的酶解效率,而且会改变骨胶原肽产物的肽分子量分布、氨基酸组成和微结构性能,从而影响其高值高效化利用。以制备均一性低分子量骨胶原肽为目的,以牛骨粉为研究对象,以水解度为主要评价指标,考察碱性蛋白酶、中性蛋白酶、复合蛋白酶和风味蛋白酶对牛骨粉的酶解效果,探究双酶分步酶解工艺、脂肪酶预处理的单独与组合应用对酶解效果的提升作用,选定最优的低分子量骨胶原肽制备工艺;结合酶解过程中各项指标的变化、产物表征分析和Person相关系数法分析不同复合酶解工艺对产物特性的影响及作用机制。研究发现:经脂肪酶预处理-碱性蛋白酶-复合蛋白酶酶解工艺制备的骨胶原肽产物具有最佳的理化性质,优化的工艺参数为:底物质量浓度为0.09 g/mL、初始pH值7.5的牛骨粉溶液加入碱性脂肪酶(加酶量0.08%)在40℃下反应4 h,再加入碱性蛋白酶(加酶量0.36 U/g)在60℃下反应5 h后,最后加入复合蛋白酶(加酶量0.36 U/g)在55℃下反应5 h,此时,水解度可达16.12%,总游离氨基酸含量可达171.571 mg/g,其Mw、Mw/... 相似文献
50.
牛体外受精卵的二步法培养体系的研究 总被引:1,自引:0,他引:1
以CR1aa为基础培养液,采用二步法对牛体外受精卵进行体外培养,完善牛体外受精卵的培养体系.实验一:对照组连续7 d均为CR1aa 50 mL/L FBS培养,处理组前3 d为CR1aa 3 mg/mLBSA培养,后4 d换为CR1aa 50 mL/L FBS.处理组的囊胚率显著高于对照组,但卵裂率和囊胚孵化率无显著差异.实验二:对照组连续7 d均为CR1aa 50 mL/L FBS培养,处理组前3 d为CR1aa培养,后4 d换为CR1aa 50 mL/L FBS.处理组的卵裂率显著高于对照组,但囊胚率和囊胚孵化率差异不显著.实验三:对照组连续7 d均为CR1aa 50 mL/L FBS 0.1mmol/L GSH培养,处理组前3 d为CR1aa 0.1 mmol/L GSH培养,后4 d换为CR1aa 50 mL/L FBS 0.1 mmol/L GSH.处理组的卵裂率显著高于对照组,囊胚率极显著高于对照组,但囊胚孵化率差异不显著.结果表明,GSH与二步法培养系统结合相对于传统的一步法培养系统更适于牛体外受精卵的体外培养. 相似文献