Agreement of SpO2, SaO2 and ScO2 in anesthetized cynomolgus monkeys (Macaca fascicularis)

Objective To assess the agreement between three measurements of arterial oxygen saturation (SpO₂, SaO₂ and ScO₂) in anesthetized cynomolgus monkeys. Study Design Prospective study. Animals Eleven mature, male cynomolgus monkeys (Macaca fasicularis). Methods Monkeys were anesthetized with intramuscular ketamine followed by intravenous propofol. The trachea of each was intubated and the lungs ventilated. Arterial oxygen saturation was measured with a Nonin 8500 V pulse oximeter, using a lingual clip on the cheek. Arterial blood samples were taken from an indwelling catheter. Inspired oxygen concentration was varied from 12 to 20%, and 88 paired arterial blood samples and saturation measurements were taken. Arterial oxygen saturation in the blood samples was measured using a cooximeter. The saturation was also calculated from the arterial oxygen tension using the Adair equation. The results were compared using Bland and Altman's method. Results The pulse oximeter readings were 2.7% higher than that of the cooximeter, with a limit of agreement of ?3.9 to 9.3%. The pulse oximeter readings were 1.8% higher than the calculated saturation, with a limit of agreement of ?6.5% to 10.1%. The cooximeter readings were 0.9% lower than the calculated saturation, with a limit of agreement of ?5.6% to 3.8%. Conclusions The agreement between SpO₂ and other measurements of arterial oxygen saturation in this study is typical for this technique. The bias and limits of agreement are consistent with reports in other species. Clinical relevance The Nonin 8500 V is a useful pulse oximeter for clinical use in primates.     

猪2型圆环病毒Cap蛋白在伪狂犬病病毒中的表达

用EcoR Ⅰ酶切伪狂犬病病毒疫苗株Tk-/gE-/LacZ 基因组,与含有猪2型圆环病毒(PCV2)ORF2基因的重组转移载体pIEORF2共转染IBRS-2细胞.收集病变细胞,经空斑纯化和PCR鉴定,获得了新的重组病毒Tk-/gE-/ORF2 .用Southern blot杂交证明该重组病毒构建正确,用间接免疫荧光法和Western blot证日月该重组病毒可表达PCV2的主要免疫原性蛋白Cap蛋白.重组病毒在IBRS-2细胞上连续传15代后,遗传稳定.该重组病毒在IBRS-2细胞上增殖滴度为10-7.1 TCID50/0.1mL,在鸡胚成纤维细胞上增殖滴度为10-4.8 TCID50/0.1mL,在Marc-145细胞上增殖滴度为10-6.8 TCID50/0.1mL.     

犊牛常见病的诊治体会

犊牛的健康关系着牛场的未来生产。本文介绍了几种犊牛常见病的辨别及诊断方法,帮助牛场快速进行疾病判断。作者对几种疾病的病因、临床症状、诊断方式、治疗方法进行综述,旨在为犊牛的常见病的防控和选择治疗药物提供参考依据。     

郏县红牛皮肤真菌病的流行性调查及治疗体会

本文以场内生产情况为例,记录了牛皮肤真菌病的症状、治疗及诊断和防治措施,以期给同行提供参考,共同探讨。     

山东省减抗背景下的中兽药产业调研分析

基于对山东省兽药生产企业和养殖企业中兽药生产和使用情况的调研,本文深入分析了我省中兽药发展现状和存在的问题,针对性地提出了中兽药产业发展的对策建议。需着力构建全产业链发展格局;不断释放市场创新创业活力;快速实现我省中兽药产业现代化;充分发挥好政策对产业引领作用;着力打造专业化人才队伍。并不断推进兽用抗菌药减量化示范行动等综合措施,从根本上遏制兽用抗菌药滥用,提倡使用中兽药等绿色高效产品的减抗行动,以期降低细菌耐药性的发生和发展,保障畜禽产品质量安全。     

猪流感病毒（A／swine／Jiangsu／2／2006（H3N2）NS1基因表达产物分析

采用RT—PCR方法克隆猪流感病毒H3N2亚型NS1全长基因,构建NS1基因原核表达质粒pET-28a—NS1和真核表达质粒p3XFLAG—CMV—NS1,在大肠杆菌和真核细胞内表达NS1基因,制备抗NS1多克隆抗体。用所制备的抗体分析p3xFLAG—CMV—NS1转染表达NS1蛋白和病毒感染细胞内的NS1蛋白。经终浓度为1mmol／L的IPTG诱导后,重组蛋白NS1在大肠杆菌中得到表达。表达蛋白纯化后免疫Wistar大鼠制备抗NS1蛋白多克隆抗体,Western—blot分析表明抗NS1多克隆抗体可以识别大肠杆菌表达的NS1蛋白、转染Veio细胞表达的NS1蛋白和病毒感染细胞内的NS1蛋白。间接免疫荧光发现NS1蛋白主要定位于细胞核。结果显示,本试验成功构建了NS1基因原核和真核表达系统,获得了NS1特异性多克隆抗体,分析了NS1细胞定位,为进一步研究NS1蛋白在病毒复制过程中的生物学功能和猪流感病毒的复制机理奠定基础。     

H1N1亚型猪流感病毒A/Swine/GD/2/12基因特征分析

2012年从广东省某猪场的疑似流感猪群采集鼻拭子样品,接种鸡胚并收集尿囊液,通过血凝、血凝抑制和RT-PCR,鉴定出1株H1N1亚型猪流感病毒,命名为A/Swine/GD/2/12。RT-PCR扩增得到全基因8个片段,与GenBank收录的参考毒株比对并构建进化树,发现本毒株可能是H1N1亚型重组株,其8个片段与我国猪源和北美地区1985—1992年间的猪源、禽源(A/turkey/IA/1992)和人源(A/Maryland/12/1991)流感毒株在同一个大分支上,其中与我国猪源参考株同源性在95.8%以上,与北美地区的H1N1参考株同源性在94%以上。HA受体位点分析表明,本毒株既具备结合Saα2,6Gal型人类流感病毒SA受体的特点,也有结合Saα2,3Gal型禽类流感病毒SA受体的可能。提示本毒株可能是由北美地区猪源、禽源和人源的H1N1亚型流感病毒重排形成的。HA蛋白裂解位点分析、NS和PB2蛋白位点分析表明,本毒株具备低致病性毒株的特点。小鼠致病性试验进一步证实本毒株能够引起小鼠运动减少、食欲欠佳、体重减轻等表现,但不会引起咳嗽和死亡等严重反应。     

猪圆环病毒2型感染的猪肺泡巨噬细胞TLR2/TLR4/CD16/CD18转录水平动态变化

为了解猪圆环病毒2型(porcine circovirus type 2,PCV2)感染对仔猪的肺泡巨噬细胞(PAM)免疫功能造成的影响,试验对PCV2感染40日龄左右健康仔猪PAM模式识别受体TLR2、TLR4、CD16、CD18 mRNA的动态变化进行了研究。结果发现,在病毒感染后TLR2、TLR4、CD16 mRNA的转录水平动态变化基本相似,3、7 d高于对照组,14 d低于对照组,28 d接近对照组,且3 d时TLR4、CD16差异极显著(P<0.01),14 d仅TLR2差异显著(P<0.05);CD18 mRNA的转录水平,3 d时显著低于对照组(P<0.05),而7 d时显著高于对照组(P<0.05),28 d接近正常。以上结果表明,PCV2感染PAM后可引起PAM对异物识别吞噬功能与吞噬后信号转导功能出现紊乱,影响了PAM吞噬和清除病原微生物的能力。     

Phase transformation and microstructure of Mo2FeB2 based cermets by spark plasma sintering

Mo2FeB2 based cermets were prepared by spark plasma sintering(SPS) The microstructure evolution and phase transformation were studied by using scanning electron microscopy(SEM) and X-ray diffraction analysis(XRD) in comparison with conventional vacuum sintering(CVS).It was found that the SPS remarkably accelerated phase transformation and decreased the end sintering temperature.A large amount of Mo2FeB2 hard phase occurred for the sintering temperature of 750℃ by SPS,and no Mo2FeB2 phase was detected for the sintering temperature below 900℃ by CVS.Almost full densification was obtained for the sintering temperature of 1050℃ by SPS,However,the microstructure was uneven,and a significant exudation of the liquid phase through the clearance between SPS punches and die was present in this stage.     

Low expression of cyclin D2 in G2/M-arrested and transformed proliferating Balb/3T3 cells

At present, the effect of cyclin D2 implicated in cell cycle regulation, differentiation, and oncogenic transformation is not fully confirmed. To better elucidate the role of cyclin D2 in controling the cell proliferation, cyclin D2 expression level was determined at the early initiation and promotion stages during the in vitro two-stage transformation process of Balb/3T3 A31 cells. N-methyl-N'-nitro-N-nitrosoguanidine (MNNG)-induced G2/M-arrested cells expressed low level of cyclin D2 mRNA, while the contact-inhibited nonproliferating cells expressed high level of cyclin D2 mRNA. In the transformed proliferating cells at the promotion stage, cyclin D2 mRNA was not expressed. These data suggest that cyclin D2 expression may be associated with the type of growth arrest and nonproliferating state, but not with the cell proliferation and transformation.     

中国首例兔出血症病毒2型(RHDV2/b/GI.2)的鉴定及病理学观察

本试验旨在鉴定四川金堂某兔场疑似兔出血症病毒2型（RHDV2）感染疫情的病原,并分析病兔的病理组织学变化。利用血凝试验和RT-PCR检测病死兔内脏组织中的病原,取病变组织制作病理切片,观察分析各组织的病理组织学变化,同时应用病兔肝脏悬液感染幼兔,分析该毒株的致病力。血凝试验结果显示,所采集病死兔肝脏样品能凝集人"O"型血红细胞;RT-PCR扩增及测序结果显示,多对引物均能从样品中扩增出RHDV2特异性条带;病理组织学观察结果显示,病兔多脏器严重出血、肿胀,淋巴细胞和中性粒细胞大量浸润,气管黏膜、肝脏、肺脏出血尤为严重;动物试验结果显示,该毒株毒力较强,含毒肝脏悬液能在24 h内迅速致死幼兔。本研究经临床诊断、核酸检测及测序证实了此次疫情确由RHDV2感染引起,动物试验和病理组织学观察表明该毒株毒力较强,可引发脏器严重出血,造成病兔急性死亡,RHDV2的出现提示病毒的跨境传播情况不容乐观,应引起更大的重视。