中蜂来源的微孢子虫对意蜂工蜂的侵染性研究

为探讨中蜂来源的微孢子虫对意蜂的侵染性,本试验将纯化自中蜂的微孢子虫,以每只蜂1×105个和5×105个孢子的接种量,分别给2日、5日、8日、11日龄无微孢子虫感染的意蜂成年工蜂接种,在30℃±0.5℃,65%～80%RH,黑暗中隔离饲养10日后,各日龄工蜂的平均感染率达86.3%～100%,每只蜂中肠的平均产孢量为5.60×105～3.39×106个。在两接种量下,2日、5日龄意蜂工蜂的产孢量均显著(P<0.05)高于8日、11日龄的产孢量。试验首次证实了中蜂来源的微孢子虫对意蜂成年工蜂具较强的侵染性。     

肯塔基,瓦巴斯草地早熟禾在青岛地区的引种栽培研究

青岛地区自１９８４年引种表塔基草地早熟禾，瓦巴斯草地早熟禾之后，经对其形态学，生物学特征和特性的观察和试验，确认该草不仅具有耐寒，耐瘠薄，抗旱，返青早，枯黄晚，绿期长（３００ｄ以上）的特点，而且色泽鲜艳，单层厚密，繁殖容易，栽培简单，是建造草坪的一种优良草种。在大量栽培试验和推广实践的基础上，总结了肯塔基，瓦巴斯草坪草的播种，移栽技术，并重点介绍了草坪形成后的除草，修剪，施肥，浇水等养护管理措施和     

Identification of lactic acid bacteria in the feces of dairy cows fed whole crop maize silage to assess the survival of silage bacteria in the gut

In order to assess the survival of lactic acid bacteria (LAB) in whole crop maize silage in the gut of dairy cows, one representative silage sample and three different feces samples were collected from dairy cows on three dairy farms in Hua Bei, China and three dairy farms in Kyushu, Japan. The composition of the bacterial community was examined by denaturing gradient gel electrophoresis and quantitative polymerase chain reaction. Lactobacillus acetotolerans was detected in all bunker‐made maize silage samples, regardless of the dairy farm or sampling region from which they were sourced. A total of eight LAB species were detected in the maize silage samples, of which three (L. acetotolerans, L. pontis and L. casei) appeared to survive digestion. The populations of L. acetotolerans in silage and feces were 10^6–7 and 10^3–4 copies/g, respectively, indicating that, even for the LAB species showing potential survival in the gut, competition in this niche may be harsh and the population may substantially decrease during the digestion process. It may be difficult for silage LAB to survive in the gut of silage‐fed dairy cows, because marked decrease in population can take place during the digestion process, even for surviving species.     

Detection and survival of group A rotavirus in a piggery

Samples of dust, faeces and effluent were collected from a piggery and examined for group A rotavirus, using a commercial ELISA test, electron microscopy and inoculation of MA-104 cells. Rotavirus antigen was demonstrated in samples collected from farrowing and weaner rooms but not from fattener and sow houses. Rotavirus antigen was also detected in samples collected from a weaner room which had been free of piglets for three months. A cytopathic porcine rotavirus (British isolate SW20/21) was kept at room temperature for four months; it survived with titres reduced by 2 log10. These observations suggest that the environment of commercial piggeries is an important source of rotaviral infection for young piglets.     

河北进境种用动物衣原体血清学检测

衣原体病是一种重要的人畜共患病,给养殖业带来巨大的经济损失,同时严重威胁从业人员的身体健康。本研究对河北辖区引进的2批种鸡、2批种鸭及2批种猪进行抽样,使用间接血凝试验（IHA）检测引进种用动物的衣原体抗体。结果表明：衣原体IHA抗体阳性率为15.7%。在种鸡、种鸭和种猪中均检测到衣原体IHA抗体,阳性率分别为18.1%、4.2%和20%。这说明在引进种用动物中存在着较高的衣原体抗体阳性率,需要加强对该病的检测。     

1株犬副流感病毒的分离鉴定及生物学特性研究

试验旨在分离鉴定犬副流感病毒(canine parainfluenza virus,CPIV),并对其生物学特性进行研究。用Vero细胞接种感染CPIV阳性犬肺脏组织,盲传4代,收集72 h病毒液进行RT-PCR鉴定、电镜观察、血凝试验、热敏性试验、紫外照射试验及病毒一步生长曲线的测定,同时扩增N基因进行序列分析,并构建系统进化树。结果显示,试验成功从出现咳嗽、流鼻涕等呼吸系统疾病症状的病犬肺脏中分离出1株CPIV,命名为CPIV-BJ01;RT-PCR扩增结果发现,在534 bp处有特异性目的条带。病毒电镜观察发现,其超微结构呈圆形、有囊膜、直径在80～200 nm之间;血凝试验显示,病毒在4和37℃均能凝集1%猪红细胞,与报道的CPIV血凝特性一致;病毒对热敏感,长时间高温下病毒毒价会随之下降;紫外照射可使病毒在短时间内对细胞的感染性急剧下降。病毒一步生长曲线测定结果显示,在12～48 h病毒高速增殖,细胞培养液中病毒滴度急剧上升,之后趋于稳定。CPIV N基因序列与19株有代表性的副流感病毒N基因相比,其核苷酸序列同源性为97.1%～99.8%。遗传进化分析表明,CPIV-BJ01与PIV5 1168-1(登录号:KC237064.1)和PIV5 ZJQ 221(登录号:KX100034.1)位于同一分支上,亲缘关系较近。     

基于Cap蛋白研制的猪圆环病毒2型疫苗研究进展

猪圆环病毒相关疾病(PCVAD)是危害世界养猪业的主要疫病之一,主要由猪圆环病毒2型(PCV-2)引起。该病毒可引起感染猪免疫系统的破坏,造成严重的免疫抑制,继而引发多种病毒/细菌的混合感染与继发感染,给世界养猪业造成了巨大经济损失。近年来疫苗免疫接种是防控PCVAD的有效手段,由于衣壳蛋白(capside,Cap)是PCV-2的主要免疫保护性抗原,因此常被用作研制PCV-2基因工程疫苗的理想靶抗原。论文就PCV-2Cap蛋白基因工程疫苗的研究进展进行综述,以期为今后PCV-2新型疫苗的研究提供参考。     

Development and characterization of monoclonal antibodies to subgroup A avian leukosis virus

Avian leukosis virus subgroup A (ALV‐A) is a retrovirus which infects egg‐type chickens and is the main pathogen of lymphoid leukosis (LL) and myeloid leukosis (ML). In order to greatly enhance the diagnosis and treatment of clinical avian leukemia, two monoclonal antibodies (MAbs) to ALV‐A were developed by fusion between SP2/0 and spleen cells from mice immunized with expressed ALV‐A env‐gp85 protein. Using immunofluorescence assay (IFA), two MAbs reacted with ALV‐A, but not with subgroups B and J of ALV. Western blot tests showed that molecular weight of ALV‐A envelope glycoprotein recognized by MAbs was about 53 kD. Isotyping test revealed that two MAbs (A5C1 and A4C8) were IgG1 isotypes. These MAbs can be used for diagnosis and epidemiology of ALV‐A.     

DNA Methylation Pattern in Pronuclear-Stage Mouse Embryos: Effect of Oocyte Vitrification

This study was conducted to investigate the pattern of DNA methylation in pronuclearstage mouse embryos derived from vitrified-warmed oocytes.Mouse oocytes at metaphase Ⅱ (MⅡ) stage of meiosis were all...