CIDR PMSG FSH联合处理不同品种绵羊效果的研究

CIDR、PMSG、FSH联合使用对初产供体羊Borderdale(波德代)3♂15♀、Poll Dorset(无角陶赛特)5♂18♀和Ger-man Mutton Merino(德国肉毛兼用美利奴—德美)3♂15♀进行同期发情和超数排卵。同期化发情波德代、无角陶赛特和德美分别为100.00%、88.89%和93.33%,羊只同期化发情时间经历和各时间点分布3个品种各有特点。超数排卵效果品种间存在差异,波德代、无角陶赛特、德美分别为6.60±2.97(枚)、3.63±2.25(枚)、5.50±3.32(枚),波德代极显著地高于无角陶赛特(P<0.01)。超排有效率波德代、无角陶赛特、德美分别为100.00%、87.50%、92.86%。未受精卵波德代极显著地高于德美羊和无角陶赛特羊(P<0.01)。胚胎总数德美羊极显著地高于波德代(P<0.01)。有效胚胎波德代羊、无角陶赛特羊、德美羊分别为2.40±2.31、2.75±2.05、4.07±3.79,德美极显著地高于波德代(P<0.01)。同一方法进行同期化发情,羊只经历时间和各时间点均衡分布能否有效控制是同期发情的焦点问题,是有效胚胎数目差异的主导因素之一。     

Genetic diversity of herbicide-resistant and -susceptible Avena fatua populations in North Dakota and Minnesota

Genetic diversity within and among 20 herbicide-resistant (HR) and 16 herbicide-susceptible (HS) Avena fatua multi-field populations was determined using 82 polymorphic loci resulting from two intersimple sequence repeat (ISSR) primers and one long-primer random amplified polymorphic DNA (LP-RAPD) primer. Collections from the Red River Valley of North Dakota and Minnesota, sampled in 1964 and 2000, represented A. fatua populations before and after intensive exposure to herbicides. A 1995 collection from south-west North Dakota represented A. fatua exposed to low herbicide selection. Despite differences in years of herbicide exposure among collections, both HR and HS populations from every collection maintained nearly similar levels of ISSR and RAPD diversity. Genetic differentiation among populations (G_ST) varied from 11% to 13% among HR populations and from 9% to 16% among HS populations, indicating that 84–91% of total variation remained within HS or within HR populations. Minimal difference in gene diversity between HR and HS is consistent with multiple origins of resistance, where HR A. fatua most likely evolved from diverse founding individuals.     

标记抗体染色法检查布氏杆菌的研究

为了建立一种快速、简便、敏感、特异地检测动物病理材料中布氏杆菌的方法,选用四种标记抗体法,对5种共15个生物型的布氏杆菌,以及大量与流产有关或常常污染病理材料的对照细菌,分别进行了纯菌、感染实验动物及牦牛组织材料的染色检查,并与柯氏染色法及细菌分离培养法进行了比较。结果表明,四种方法对于各种材料中的布氏杆菌(粗糙型犬布氏菌除外)均呈阳性反应,而绝大多数对照菌均呈阴性反应。其中尤以SPA法染色背景更为清晰,非特异性反应更少。这些方法既简便、快速,检出率也较高。对于布氏杆菌病的诊断和疫情监测,是很有价值的。     

Ultrasonographic and Gross Pathological Findings in the Mammary Glands of Weaned Sows Having Suffered Recidiving Mastitis Metritis Agalactia

In a large pig breeding herd with high prevalence of post-parturient diseases of the sows, weaned sows of different parity groups with (n = 663) or without (n = 1125) recidiving mastitis metritis agalactia (MMA) in their previous history were subjected to ultrasonography. A total of 114 of 663 sows with recidiving MMA in their previous history and with ultrasonographic visible mammary gland changes, and 157 of sows without recidiving MMA in their previous history were culled and subjected to gross pathological and bacteriological examination of their mammary glands. The sows having suffered MMA had more (p < 0.001) hyperechogenic images in their mammary glands compared with the sow having suffered no recidiving MMA. Abdominal glands were more (p < 0.01) prone to pathological changes compared with the pectoral ones. Sows of high parity had more hyperechogenic images and gross pathological changes in their mammary glands compared with the sows of low parity.     

Individual antigens of cattle. Bovine CD2 (BoCD2).

The data obtained in the workshop provide further evidence that CH128A and IL-A26 and the 12 new mAbs that form a cluster recognise the bovine orthologue of CD2. The mAbs inhibit rosetting with SRBC, stain cells in primary and secondary lymphoid organs in patterns consistent with those obtained in humans with anti-CD2 mAbs, and the 11 IgG mAbs all immunoprecipitate a peptide with a Mr of 58-62 kDa. It is not clear from the studies whether the epitopes defined by the mAbs correspond with the region I and II epitopes present on CD2. None of the data suggest that any of the mAbs recognise the region III (CDD2R) epitope (Peterson and Seed, 1987; Knapp et al., 1989). Further studies are now needed to define the physical and functional relation of the epitopes and establish whether antibody-mediated activation corresponds with that noted in humans. Data reported in one study (Baldwin et al., 1988) with IL-A26 suggest possible differences in the requirements for activation. In addition, further studies are needed to demonstrate how many cell types express BoCD2. In mice, evidence has been presented which shows the mouse orthologue is expressed on some B cells (Yagitta et al., 1989). Studies in cattle have clearly shown CD2 is present on the majority of CD4+ and CD8+ T-cells and a small population of CD4-/CD8- cells (Baldwin et al., 1988; Davis, unpublished observations). Evidence presented in this workshop has shown that some CD2+ cells express a WC2 molecule (Sopp et al., 1991).(ABSTRACT TRUNCATED AT 250 WORDS)     

Culture of bovine bone marrow progenitor cells in vitro.

In vitro methylcellulose cultures of bovine bone marrow progenitor cells were developed. An existing technique described for bovine species was compared to a method for human tissue and further adapted during subsequent experiments. Bovine bone marrow samples were collected at the slaughterhouse, and mononuclear cells were separated by gradient centrifugation (1.077 g/ml specific density and 400 g). The use of 3% bovine leucocyte-conditioned medium, produced by stimulation of blood lymphocytes with 4 microg/ml concanavalin A and harvested on day 4 of culture, gave better results than the use of supernatant of the human bladder carcinoma 5637, which is widely used in human bone marrow cultures. However, bovine leucocyte-conditioned medium was not added to erythroid cultures because inhibitory effects were observed. Erythroid colonies were stimulated with erythropoietin, and hemin was added to enable microscopic identification. Reduced oxygen tension was necessary to induce growth of erythroid colonies. This was not necessary for myeloid cultures. In conclusion, the results of this study show that the growth of myeloid and erythroid colonies in methylcellulose-based medium requires different culture conditions, which are different from the culture conditions for human cells.