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111.
低聚木糖和酸化剂对断奶仔猪生产性能的影响 总被引:6,自引:0,他引:6
本试验研究了低聚木糖及其与酸化剂合用对断奶仔猪生产性能的影响。选择72头35±1日龄、平均断奶体重(10.33±0.34)kg的健康三元(杜×长×大)杂交仔猪,按体重和性别分成4个处理组,每处理组3个重复。第1组为对照组,饲喂玉米-豆粕型基础日粮;第2组为低聚木糖(200mg/kg)组;第3组为酸化剂(8g/kg)组;第4组为合用组,添加低聚木糖(200mg/kg)和酸化剂(8g/kg)。研究结果表明,各试验组日增重、料重比得到显著改善(P<0.05),腹泻率显著下降(P<0.01)。 相似文献
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114.
Brajesh C. Varshney N.M. Ponnanna Pranati A. Sarkar Pragna Rehman Jigar H. Shah 《Journal of veterinary science (Suw?n-si, Korea)》2007,8(1):57-64
Escherichia coli (E. coli) strains were collected from young diarrheic calves in farms and field. Strains that expressed the K99 (F5) antigen were identified by agglutination tests using reference antibodies to K99 antigen and electron microscopy. The K99 antigen from a selected field strain (SAR-14) was heat-extracted and fractionated on a Sepharose CL-4B column. Further purification was carried out by sodium deoxycholate treatment and/or ion-exchange chromatography. Monoclonal antibodies to purified K99 antigen were produced by the hybridoma technique, and a specific clone, NEK99-5.6.12, was selected for propagation in tissue culture. The antibodies, thus obtained, were affinity-purified, characterized and coated onto Giemsa-stained Cowan-I strain of Staphylococcus aureus (S. aureus). The antibody-coated S. aureus were used in a co-agglutination test to detect K99+ E. coli isolated from feces of diarrheic calves. The specificity of the test was validated against reference monoclonal antibodies used in co-agglutination tests, as well as in ELISA. Specificity of the monoclonal antibodies was also tested against various Gram negative bacteria. The developed antibodies specifically detected purified K99 antigen in immunoblots, as well as K99+ E. coli in ELISA and co-agglutination tests. The co-agglutination test was specific and convenient for large-scale screening of K99+ E. coli isolates. 相似文献
115.
This study was aimed to isolate a mutant strain of porcine epidemic diarrhea virus and prepare a PEDV inactivated vaccine with high valence by suspension culture process for immunizing against PEDV effectively in China.200 small intestines and theirs contents of diarrhea piglets died of diarrhea,collected from many large-scale pig farms in China,were detected by RT-PCR and sequenced,a mutant strain of porcine epidemic diarrhea virus was selected and put on the suspension-cultured Vero cells in a 2 L reactor for virus isolation and continuous cell culture,the harvested virus suspension,which was identified and determined TCID50,was inactivated by formaldehyde and mixed with aluminum hydroxide gel adjuvant to prepare PEDV inactivated vaccine.After its physical behavior,stability viscosity,sterility test were checked out,the safety and immune efficacy were studied by immunizing the pregnant pigs and theirs piglets.The results were as follows:86 samples were detected positive in 200 samples,cytopathy occurred after the mutant strain samples screened were passaged to 5th generation,the virus suspension was harvested in 10th generation and identified as a mutant strain of PEDV,named PEDV-GF10 strain.The virus titer of harvested virus suspension was measured up to 1×108.0 TCID50/mL after concentrated.After the vaccine was checked out,the sows,40 and 25 days before delivery in experimental groups,were injected into Xuehai acupoint with 4 mL vaccine and the pigs in blank group were free of immunifications.The results showed that there were no obvious differences in the production status of the sows in experimental groups and blank group and the temperature of theirs 3-day-old healthy piglets injected different doses of vaccine,and the vaccine was safe to the sows and piglets.Forty 3-day-old piglets producted by pregnant sows in experimental groups and blank group were randomly selected and taken 4 mL 1×108.0TCID50/mL F10 virus culture.The PEDV morbidity of piglets in blank group was 100% after injection and the antibodies were negative;10% piglets in blank group had mild diarrhea symptoms,the protection rate was up to 90%,antibody of passive immunity in piglets lasted for more than 35 days.Virus titer of mutant strain of PEDV-GF10 improved a lot by suspension cell culture,the PEDV-GF10 inactivated vaccine was safe,and could effectively prevent and control the variation strain of PEDV in China. 相似文献
116.
牛病毒性腹泻病毒(Bovine viral diarrhoea virus,BVDV)在我国发现有20多年,而在世界范珏来讲已有近100年的历史。由于牛病毒性腹泻病毒造成奶牛生产性能下降、繁殖障碍、持续感染等,是导劐集约化奶牛场严重亏损的重要原因。且牛病毒性腹泻导致的黏膜病致死率几乎1000A,已经严重阻碍养斗业的发展,但目前我国对牛病毒性腹泻还没有好的防控措施。文章对牛病毒性腹泻的发生历史总结,便于石牛病毒性腹泻病毒的诊断和预防中参考。 相似文献
117.
徐州地区鸭传染性浆膜炎的病原分离鉴定及药敏试验 总被引:16,自引:0,他引:16
从徐州地区临床疑似鸭传染性浆膜炎发病鸭中分离到细菌21株,通过细菌形态、培养特怔、生化试验和动物试验,鉴定为鸭疫里默氏杆菌菌株,对不同地区分离到的21株菌进行了24种常用抗菌药物的药敏试验,结果该24个菌株对头孢类药物、红霉素、链霉素、妥布霉素、新霉素、氯霉素、泰乐菌素、痢特灵等几种药物敏感性较高,对喹诺酮类、强力霉素、丁安卡那霉素、林肯霉素、庆大霉素、氟苯尼考、利福平、复方新诺明等均不同程度地产生了耐药性。不同地区分离到的鸭疫里默氏杆菌对不同抗菌药的敏感程度存在较大差异性,研究结果为该地区鸭传染性浆膜炎的药物防治提供了很好的理论依据. 相似文献
118.
对近年来山东省内鸡沙门氏菌病进行了调查,并对典型的沙门氏菌做了生化鉴定和药物敏感试验。调查表明沙门氏菌病在小规模养殖场的发生呈上升趋势,常与大肠杆菌病、新城疫和鸡球虫病混合感染。对所分离的沙门氏菌株鉴定表明,70%为副伤寒沙门氏菌,也有鸡白痢沙门氏菌的存在。药敏试验结果表明沙门氏菌对传统的防治细菌性药物产生了多重耐药性,这说明细菌耐药性的产生和发展与抗生素长期反复使用和盲目使用有密切的关系。本文为更有效地防控细菌性疫病提供科学依据。 相似文献
119.
猪繁殖与呼吸综合征病毒感染对猪肺泡巨噬细胞外源性抗原加工递呈相关分子和共刺激分子的影响 总被引:1,自引:1,他引:1
采用定量竞争PCR技术对猪繁殖与呼吸综合征病毒(PRRSV)感染后不同时相猪肺泡巨噬细胞(PAM)中外源性抗原加工递呈相关分子SLA-DR、Ii链和SLA-DM分子及共刺激分子CD40、CD80、CD86的mRNA转录动态进行了定量检测。结果表明,PRRSV感染后PAM的SLA-DR mRNA转录水平在3、7和14 d下调,低于对照组;感染后3 d,Ii链、SLA-DM和CD40的mRNA转录水平极显著下调(P〈0.01);CD80和CD86mRNA转录水平也在感染后3 d明显下调(P〈0.05)。用流式细胞术检测PAM表面的SLA-DR抗原的结果表明,在感染后3 d短暂上升,7 d之后一直低于对照组。由此说明,PRRSV感染早期对猪肺泡巨噬细胞的外源性抗原加工和递呈功能产生显著影响,导致其外源性抗原递呈功能下降,进而影响机体的体液免疫应答。 相似文献
120.
抗猪流行性腹泻病毒单克隆抗体的研制及其特性鉴定 总被引:1,自引:1,他引:0
以新生乳猪增殖猪流行性腹泻病毒(PEDV),通过蔗糖密度梯度离心将其纯化,获得较为完整的病毒颗粒。病毒ELISA效价为1∶3×105,蛋白含量为3.96g/L。将提纯的PEDV免疫BALB/c小鼠,取免疫鼠脾细胞与SP2/0骨髓瘤细胞进行融合,融合率为95.6%。用间接ELISA进行筛选,共检出38个阳性孔,阳性率为28.8%。对其中15个阳性值较高的孔进行3次再克隆,阳性率达100%,最后获得15株稳定分泌特异性抗PEDV单抗(McAb)的杂交瘤细胞。ELISA阻断试验与交叉试验证明,其分泌的抗体具有高度特异性。腹水和细胞培养上清的ELISA效价分别为1∶103~1∶106和1∶128~1∶512。经鉴定,15株McAb的分子类型均为IgG,均无免疫沉淀特性。杂交瘤细胞的染色体数目为90~110,平均95。尤为重要的是,这些杂交瘤细胞所分泌的抗体,有的对PEDV具有中和作用,能够阻断病毒对猪只的侵害作用。 相似文献