浅谈猪瘟免疫失败的原因

猪瘟是由猪瘟病毒(HCV)引起的一种高度接触性传染病。猪瘟具有高度接触传染性,流行广泛,发病率、死亡率高,是危害我国养猪业最重要的传染病之一。我国自1954年成功研制出猪瘟兔化弱毒疫苗以来,有效地控制了猪瘟在我国的急性发生和大流行。但是,近些年来,转变为周期性、波浪式的     

饲料中常见有害物质及处理方法概述

饲料中含有的一些有害物质阻碍饲料营养物质在动物体内的消化吸收,影响动物的生长发育,使用不当还可能导致动物中毒和死亡。文章叙述了这些有害物质的结构,以及消除和降低这些物质的技术和方法。     

基于LF-NMR及MRI 的2种速生材干燥过程中水分分布状态研究

为了解太阳能干燥过程中速生材内部水分状态及迁移规律,采用低场核磁共振及核磁共振成像检测桉、杨木干燥过程中水分分布、含量变化及迁移过程,借助扫描电镜在微观层面进行分析。结果表明：核磁共振信号强度与称重法所测含水率相关性系数高达0.99以上,因此低场核磁共振可准确测定木材中的水分含量;桉木和杨木饱水试样的核磁共振信号中均存在3种峰,桉木弛豫时间分别为1.32、32.75、403.70 ms,杨木为2.66、32.75、352.12 ms,对应着结合水及两种状态的自由水;随着干燥进行,不同状态水分的横向弛豫时间逐渐减小,木材对水分的束缚增加。当桉木含水率为27.28%,杨木含水率为35.71%左右时,水分散失转为以结合水为主。通过核磁共振成像中氢质子密度的不同可对水分含量进行区分,进而可观测干燥过程中木材内部水分移动状态。因此,通过低场核磁共振及核磁共振成像可研究速生材干燥过程中的内部水分状态及分布。     

应用滤波方法提高高山松地上生物量遥感估测精度的研究

基于1987年、1992年、1997年、2002年、2007年、2012年分布在香格里拉市的34个高山松固定样地数据,以及Landsat时间序列数据集,利用谷歌地球引擎和Python,通过3种滤波算法对时间序列数据进行重构,应用随机森林算法对森林地上生物量进行估测,根据模型评价指标对重构前后时间序列数据的估测效果进行分析。结果表明：采用3种不同滤波方法重构的时间序列数据训练的非参数模型,其拟合精度和预测精度均高于滤波前时间序列的预测精度,整体均方根误差和相对均方根误差指标均优于滤波前数据,其中ARMIA方法最佳。应用滤波方法在一定程度消除了影像自身所携带的大量噪声和不确定性,有效地提高了数据质量,提高了高山松地上生物量遥感估测的精度。     

不同种源刨花润楠苗期生长及叶片性状变异的研究

以刨花润楠主要分布区的14个种源为研究对象,在广州增城开展种源试验,通过对14个种源的刨花润楠苗高、地径、叶面积、叶周长等性状进行观测,分析不同种源苗期性状的遗传变异规律。结果表明：3个生长性状种源间和种源内变异系数相当,其种源间和种源内生长性状变异均较丰富;8个叶片性状种源间的变异系数为17.52%～44.71%,不同种源间叶片性状亦变异明显;生长性状的种源遗传力均大于0.750,说明在一定程度上刨花润楠的苗高、地径等苗期生长性状受自身遗传控制,且不同种源间变异明显,种源选择潜力较大。刨花润楠苗期生长性状的地理及气候变异趋势不明显,表现出随机现象;苗木生长性状与叶片大小呈负相关,即叶片越大、叶柄越长,苗木生长有变慢的趋势;对种源苗期性状进行聚类,可将刨花润楠14个种源划分为5个类群;刨花润楠苗期生长及叶片性状有一定的地理趋势,但也有一定的随机性。以地径为标准对刨花润楠优良种源进行筛选,初步选出永春、兴安、昭平3个种源作为适宜广东地区造林的优势种源。     

美洲黑杨基因资源收存及其遗传评价的研究

从１７个国家引进３３１个黑杨派无性系（其中５２个美洲黑杨无性系）,在山东省长清县营建我国第一个黑杨派无性系基因库。连续１０年对基因库内美洲黑杨无性系进行了多性状系统研究,结果表明各无性系间在物候期、生长、生根、抗寒和抗病虫等方面均存在着显著的差异,遗传变异丰富;系间的主要性状与无性系起源纬度及各性状间存在一定相关性。主要材料性状变异的研究结果表明,３８个８年生美洲黑杨无性系在木材基本密度、纤维长度无性系间变异达到极显著水平;木材密度和纤维长度与树高和胸径呈一定相关性;木材密度和纤维长度这两个性状在遗传上相互独立,受不同遗传机制控制。利用分子遗传标记ＲＡＰＤ技术研究库内美洲黑杨无性系ＤＮＡ多态性,结果表明本库美洲黑杨ＤＮＡ多态率为８６％,再次证明本库美洲黑杨遗传多样性高,可为我国杨树改良提供丰富的育种材料。     

Anatid herpesvirus 1 CH virulent strain induces syncytium and apoptosis in duck embryo fibroblast cultures

Anatid herpesvirus 1 (AHV-1) CH virulent strain was first isolated from an infected duck and it was found that this virus strain could induce cytopathic effect (CPE) in duck embryo fibroblast (DEF). Following AHV-1 infection, DEF showed morphological changes such as cell rounding, improved refractivity and detachment from the culture surface. However, its pathological characteristics were not adequately known. Related studies were performed and the results showed that syncytium formation could be observed as the other type of CPE in AHV-1 infection. Hematoxylin-eosin staining and 4’, 6-diamidino-2-phenylindole (DAPI) staining of infected DEF were each used to visualize the shape and distribution of chromatin within nuclei and nuclear fragmentation was observed. Chromatin condensation and margination, as well as formation of apoptotic bodies were observed by transmission electron microscopy (TEM). DNA ladder formation was detected in AHV-1 infected cells and apoptosis of the infected DEF was also detected by flow cytometry analysis of Annexin V-FITC/PI staining method. Therefore, it was suggested that AHV-1 virulent strain can induce syncytium and apoptosis in DEF. Syncytium formation and apoptosis observed in this study may contribute to the elucidation of AHV-1 pathogenesis.     

Molecular cloning and functional analysis of duck Toll-like receptor 5

Toll-like receptor 5 (TLR5) is responsible for the recognition of bacterial flagellin in vertebrates. In this study, we cloned the single-exon TLR5 gene of the Maya breed of Common Shelduck (Tadorna tadorna). The TLR5 open reading frame is 2580 bp in length and encodes an 859-amino acid protein. The putative amino acid sequence of duck TLR5 consisted of a signal peptide sequence, 11 leucine-rich repeat domains, a leucine-rich repeat C-terminal domain, a transmembrane domain, and an intracellular Toll-interleukin-1 receptor domain. The duck TLR5 gene was highly expressed in the lung, bone marrow, spleen, and liver; moderately expressed in kidney, small intestine, large intestine, and brain. A plasmid expressing duck TLR5 was constructed and transfected into HEK293T cells, and expression was confirmed by indirect immunofluorescence assay. HEK293T cells transfected with duck TLR5- and NF-κB-luciferase-containing plasmids significantly responded to flagellin from Salmonella typhimurium, indicating that it is a functional TLR5 homolog.