Seroprevalence,associated risk factors analysis and first molecular characterization of chlamydia abortus among Egyptian sheep     

《Comparative immunology, microbiology and infectious diseases》2021

Chlamydia abortus is one of the most common abortive agents worldwide in sheep. Few studies have been reported C. abortus infection among sheep in Egypt but the available data is scarce. The objective of the present study was to determine the seroprevalence of C. abortus among sheep, the associated risk factors and its molecular characterization. The present study was conducted on 675 sheep in six Governorates at Northern Egypt. Data analysis confirmed the presence of antibodies against C. abortus in 93 out of 675 sheep. The logistic regression model was fitted to identify the associated risk factors with C. abortus infection. The results revealed that C. abortus increased significantly in ewes (OR = 4.04, 95 %CI: 1.44−11.28) during autumn season (OR = 3.6, 95 %CI: 1.64–8.28), in ewes with a history of abortion (OR = 1.4, 95 %CI: 0.87–2.50) and in farm where no lambing pen (OR = 2.2, 95 %CI: 1.30–3.94) or abscence of post abortion measures (OR = 1.96, 95%CI: 1.23-3.12). In addition, age, flock size and exchange of breeding ram had no significant effect on prevalence of chlamydiosis. Also, PCR assay was confirmed presence of C. abortus as accusative pathogen in aborted ewe and the genetic characterization of Egyptian C. abortus strain revealed 100 % identity with another strain from Iraq. A control program should be applied to reduce economic losses and risk of human infection.  相似文献   

猪瘟野毒感染抗体阻断ELISA检测方法的建立与初步评价     

周景云  刘百红  刘雪微  杨欣艳  李宝春  陈西钊 《畜牧与兽医》2021,(2):82-87

以猪瘟野毒E2蛋白为包被抗原、辣根过氧化物酶标记的猪瘟野毒单抗作为酶标抗体,建立检测猪瘟野毒抗体的阻断ELISA方法。猪瘟野毒E2最适包被浓度为0.03μg/mL,待检血清最适稀释度为1∶4,酶标猪瘟野毒单抗稀释度为1∶1 000。用建立的阻断ELISA方法检测369份临床阴性血清,计算阻断率,确定临界值,阻断率>40%为猪瘟野毒抗体阳性,阻断率≤40%为猪瘟野毒抗体阴性。用建立的ELISA方法检测84份血清,其中78份为免疫猪瘟疫苗的血清,6份为猪瘟病毒感染血清。结果显示,78份免疫血清均检测为猪瘟野毒抗体阴性,6份猪瘟感染血清均检测为猪瘟野毒抗体阳性。因此可初步判定该方法可用于鉴别诊断猪瘟病毒自然感染动物和C株疫苗免疫动物的血清抗体,并为临床检测猪瘟野毒抗体提供便捷、快速,精准的检测工具,对猪瘟的临床诊断、预防以及猪瘟净化工作具有非常重要的参考意义。  相似文献   

Effect of calf age on bovine viral diarrhea virus tests     

Scott McDougall 《Journal of veterinary diagnostic investigation》2021,33(3):528

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绒山羊皮肤毛囊兴盛前期组织形态、chi-miR-107-3p与RHBDF2基因表达分析     

王立忠  吴铁成  马跃军  李玉荣  乌亚罕  何托雅  赵生国  刘斌 《中国畜牧兽医》2021,48(6):1918-1926

为了探究chi-miR-107-3p和菱形家族蛋白2（rhomboid family member 2,RHBDF2）基因在不同品种（系）和光控增绒绒山羊兴盛前期（5~7月份）皮肤毛囊重建时的表达差异,本试验在7月份采集内蒙古阿拉善型绒山羊、敏盖绒山羊和光控增绒技术处理的阿尔巴斯型绒山羊体侧皮肤毛囊组织,采用组织切片技术对组织形态比较分析,实时荧光定量PCR法检测chi-miR-107-3p和RHBDF2基因的表达量。结果显示,在皮肤毛囊兴盛前期,阿拉善型绒山羊次级毛囊正处于重建阶段,敏盖绒山羊和阿尔巴斯型绒山羊（光控增绒）次级毛囊重建已基本完成;在阿拉善型绒山羊皮肤组织中chi-miR-107-3p表达量极显著高于敏盖绒山羊和阿尔巴斯型绒山羊（光控增绒）（P<0.01）,而RHBDF2基因表达量极显著低于其他两品种（系）（P<0.01）,且RHBDF2基因表达量在敏盖绒山羊皮肤组织中显著低于阿尔巴斯型绒山羊（P<0.05）。不同品种（系）和光控增绒绒山羊皮肤毛囊兴盛前期组织显微结构与chi-miR-107-3p、RHBDF2基因在皮肤组织中的表达差异分析结果相一致,次级毛囊重建初期chi-miR-107-3p表达量较高,而RHBDF2基因表达量极低,随着次级毛囊重建完成,chi-miR-107-3p表达量明显降低,RHBDF2基因表达量逐渐增高,且在不同品种（系）内蒙古绒山羊绒毛生长发育过程中的表达机制基本相同。因此,chi-miR-107-3p和RHBDF2基因是绒山羊皮肤毛囊生长发育的重要调控因子。  相似文献   

气肿疽梭菌CctA基因的原核表达及其间接ELISA检测方法的建立     

李新苹  陈晓洁  赵兵  刘强德  丁占强  张飞  唐慧芬  曹剑  侯凤  刘洋  王钢 《中国畜牧兽医》2021,48(5):1876-1882

研究旨在原核表达气肿疽梭菌细胞毒素A （CctA）基因,用纯化的重组蛋白建立其间接ELISA检测方法,a。利用大肠杆菌密码子的偏爱性优化CctA基因序列,克隆至原核表达载体pET-28a （+）,双酶切鉴定原核表达质粒pET28a-CctA并测序。将重组质粒转入大肠杆菌,经IPTG诱导得到高表达的重组CctA包涵体蛋白。包涵体蛋白变性后经镍（Ni）柱纯化,SDS-PAGE检测其纯化效果。以豚鼠抗气肿疽梭菌抗血清为一抗,用Western blotting方法检测重组CctA蛋白的反应原性。用棋盘滴定法建立间接ELISA检测方法,以复性后的重组CctA蛋白作为检测抗原,摸索抗原包被浓度、封闭液的种类及浓度、抗体的最适稀释度和反应条件等。选用3批气肿疽灭活疫苗免疫豚鼠后采集血清,同时用攻毒和间接ELISA两种方法验证疫苗的免疫效力。质粒双酶切结果显示,得到大小约853 bp的条带,与预期相符,且测序结果正确。SDS-PAGE结果表明,成功表达并纯化大小为35 ku的重组CctA蛋白。Western blotting结果显示,豚鼠抗气肿疽梭菌抗血清与重组CctA蛋白具有良好的反应原性。建立的间接ELISA法的最适条件为：抗原的包被浓度为0.5 μg/mL,于4 ℃包被过夜;封闭液选择10%胎牛血清,37 ℃孵育2 h;二抗的稀释度为1：8 000;室温避光显色10 min后终止反应,测定D_{450 nm}值。当P/N>4.6时,间接ELISA法检测结果与豚鼠攻毒试验结果拟合度较好。本研究成功表达CctA基因并纯化了重组CctA蛋白,建立的以重组CctA蛋白为检测抗原的间接ELISA检测方法,有望成为气肿疽灭活疫苗免疫效果验证的替代方法。  相似文献   

2020年新疆地区猪繁殖与呼吸综合征病毒抗体检测与分析     

王紫阳  屈勇刚  孙琼飞  党瑞莹  周海琴  张小玉  张家瑞  常军帅  李岩 《中国猪业》2021,16(3):58-61

为了解2020年新疆地区猪繁殖与呼吸障碍综合征病毒（PRRSV）抗体水平及其消长规律,本试验采用间接酶联免疫吸附试验（ELISA）法对1 218份血清中PRRSV免疫抗体水平进行检测和分析。结果显示,PRRSV抗体平均阳性率为78.49%（956/1218）,高于国家规定标准（70%）。S/P的平均值为1.22±0.84,变异系数为69.45%。不同类别猪群抗体平均阳性率在59.19%~91.50%之间,有一定的差异。在调查的10个规模化养殖场中,9个场PRRSV免疫抗体阳性率达到国家标准。不同类别猪群PRRSV变异系数较高,需进一步对现有的免疫程序进行调整和完善,确保各猪群健康。  相似文献   

倍他米松ELISA检测方法的建立     

郭璐  张晶  沙芳芳  赵兴然  王敬  王向红 《动物医学进展》2016,(12):50-54

为建立倍他米松(BET)ELISA检测方法,先使BET与琥珀酸酐反应,再采用活化酯法与牛血清白蛋白(BSA)偶联制备免疫原;其次,利用免疫动物获得多克隆抗体,经Sephrose 4B-proteinA方法对抗体进行纯化;最后,建立倍他米松ELISA检测方法。结果表明,免疫抗原偶联成功,获得了亲和力较高的多克隆抗血清,间接竞争ELISA测定其滴度为102 400、IC15为6.60×10-5 ng/mL和IC50为0.97ng/mL。该方法适用于残留在动物性食品中的BET现场大批量检测。  相似文献   

Evaluation of truncated LipL32 expressed by Escherichia coli and Pichia pastoris for serodiagnosis of Leptospira infection in rodents     

Kanae SHIOKAWA  Chandika D. GAMAGE  Nobuo KOIZUMI  Yoshihiro SAKODA  Kenta SHIMIZU  Yoshimi TSUDA  Kumiko YOSHIMATSU  Jiro ARIKAWA 《The Journal of veterinary medical science / the Japanese Society of Veterinary Science》2016,78(2):221-230

The applicability of the recombinant LipL32 for serodiagnosis of leptospiral infection in field rodents was assessed in this study. An immunodominant region of LipL32 was determined by monoclonal antibodies, and then, truncated LipL32 (tLipL32) was designed to contain the region (87–188th amino acid). The tLipL32 was compared between two recombinant expression hosts Escherichia coli and Pichia pastoris in ELISA. With field rat sera, tLipL32 expressed by P. pastoris (tLipL32p) had high antigenicity without background reactions, while tLipL32 expressed by E. coli (tLipL32e) showed high background reactions, which were reduced by pre-adsorption of sera with E. coli. To evaluate tLipL32-ELISA, field rat sera were tentatively divided into a Leptospira infection positive (12 sera) and a negative group (12 sera) based on the results from flaB gene PCR of kidney samples and WB with whole Leptospira cell. Consequently, the sensitivity of tLipL32p-ELISA for field rat sera was 83% . A similar result was obtained from tLipL32e-ELISA with adsorbed sera, (92%). However, sensitivity of tLipL32e-ELISA using sera without an adsorption treatment was 50%. Regardless of the expression host, tLipL32-ELISA had 100% specificity and sensitivity in experimentally infected laboratory rats. These results suggest that recombinant LipL32 expressed by P. pastoris is more applicable for serodiagnosis in field rats due to a lack of background reaction.  相似文献   

Improvement of an enzyme-linked immunosorbent assay for equine herpesvirus type 4 by using a synthetic-peptide 24-mer repeat sequence of glycoprotein G as an antigen     

Hiroshi BANNAI  Manabu NEMOTO  Koji TSUJIMURA  Takashi YAMANAKA  Ken MAEDA  Takashi KONDO 《The Journal of veterinary medical science / the Japanese Society of Veterinary Science》2016,78(2):309-311

To increase the sensitivity of an enzyme-linked immunosorbent assay (ELISA) for equine herpesvirus type 4 (EHV-4) that uses a 12-mer peptide of glycoprotein G (gG4-12-mer: MKNNPIYSEGSL) [4], we used a longer peptide consisting of a 24-mer repeat sequence (gG4-24-mer: MKNNPIYSEGSLMLNVQHDDSIHT) as an antigen. Sera of horses experimentally infected with EHV-4 reacted much more strongly to the gG4-24-mer peptide than to the gG4-12-mer peptide. We used peptide ELISAs to test paired sera from horses naturally infected with EHV-4 (n=40). gG4-24-mer ELISA detected 37 positive samples (92.5%), whereas gG4-12-mer ELISA detected only 28 (70.0%). gG4-24-mer ELISA was much more sensitive than gG4-12-mer ELISA.  相似文献   

美国军事司法禁止强制性自证其罪规则解读     

张山新  兰晓晖 《信阳农业高等专科学校学报》2007,17(4):1-4

美国军事司法禁止强制性自证其罪规则,与"米兰达规则"有着本质区别。尽管二者在法源上相同,但建立的规则不同。美国军事司法禁止强制性自证其罪规则确立了禁止刑讯逼供原则、预先告知原则和非法证据排除规则,但虐囚事件充分暴露了美国军事司法禁止强制性自证其罪规则的本质。  相似文献