我国近年来水稻重大病虫害可持续控制技术重要研究进展——非化学控害技术研究

针对水稻病虫害防治中长期存在控害保产与生产无公害稻米矛盾比较突出的问题,研究提出了几种效果显著的非化学控害增产技术。其中,利用水稻遗传背景、对病虫抗感水平等差异显著的水稻品种多样性种植,控制稻瘟病的效果达42.12％～76.68％,抑制白背飞虱若虫数量增长效果明显,增产糯稻或优质稻600～1050 kg／hm²,平均增收约1 500元／hm²;稻鱼共育控制稻飞虱的效果为63.77％～86.89％,对纹枯病病株抑制率70.52％,控制稻田杂草效果为89.57％,平收获鲜鱼319.5～1 177.5 kg／hm²,水稻产量比对照区增产7.05％～10.11％;稻鸭共育控制稻飞虱效果63.73％～77.18％,控制稻螟效果30.11％,控制纹枯病效果19.33％～67.03％,对稻田杂草控制效果91.96％,减少施肥30.6％、农药59.3％,减少投入1 987.05元／hm²。     

百合病毒病的发生与症状类型

百合病毒病症状类型可归纳为7种类型,轻花叶型(Mm),重花叶型(Sm),矮化型(Stu),丛簇矮化型(Rstu)。黄化矮化型(Ys),扁茎簇叶型(Fsbl),花变叶型(Phy),其中轻花叶型和重花叶型发生普遍,花变叶型出现较少。病害发生的轻重与种球种龄有关,种龄越大,发病越重。前茬种植百合的地块较种植小麦的地块发病重,低洼积水地发病重。不同百合品种对病毒病的抗性有差异。     

Advances in studying the differentiation into neurons of mesenchymal stem cells and their application

Mesenchymal stem cells (MSCs) are a population of multipotent cells that can proliferate and differentiate into marrow and non-marrow cell types, such as adipocytes, chondrocytes, myocytes, and so on. In recent years, many researchers have studied whether MSCs are capable of differentiation into neurons in vivo and ex vivo. The result that MSCs-derived neurons express NSE and NF, but don't express GFAP suggests MSCs can differentiate into neurons, some researchers have achieved success in promoting functional recovery in Pakinsons and transactional spinal cord injury rat models by use of MSCs-derived neurons. Therefore, MSCs-derived neurons will play an important role in the therapy for a variety of diseases of the nervous system.     

中国苜蓿育成品种遗传多样性及亲缘关系研究

以苜蓿的种子贮藏蛋白的多态性为研究指标,对中国14个审定登记的苜蓿育成品种的遗传多样性及亲缘关系进行了研究。研究结果表明:蛋白单体的分子量介于21.2～85.1kD之间,蛋白单体电泳图谱多态性品种间无显著的特异性;在参试的14个育成品种中,品种内基因多样性平均值(HS)为0.3136,总基因多样度(HT)为0.3741,基因分化系数(GST)为0.162;以λ=3.700为标准划分,14个育成品种划分为六个组群,各组群划分结果主要与参试品种的亲本来源有关,而与其种植地、育种地关系不大。     

控制鸡场呼吸道病的初步研究

江苏某鸡场饲养的蛋鸡，呼吸道病很严重，用药物和现有的疫苗控制效果都不够理想。为此，将该鸡场发生呼吸道病病鸡的病料进行收集，制成油佐剂灭活苗对鸡进行免疫接种，结果获得满意的效果。     

草地生态系统碳循环研究进展

随着全球气候变化和陆地生态系统碳循环研究的发展,碳循环正成为草地生态系统研究的热点.本文在介绍其研究发展过程、主体内容和方向的同时,对目前的研究动态和研究方法进行系统的概述,重点分析了目前国内外草地生态系统碳循环过程研究、机制研究、研究方法及模型的发展动态,并对今后草地生态系统碳循环和相关研究提出了建议.     

茶黄酮对无角多赛特羊生长和呼吸道疾病的影响

选择平均体重为26．6kg的无角多赛特断奶大羔羊22只．平均体重为49．3kg的无角多赛特育成羊48只，分别分为对照组和试验组，试验组羊只精料补充料中添加300mg／kg的茶黄酮，研究茶黄酮对羊只生长和呼吸道疾病的影响。结果表明，添加茶黄酮可提高羔羊和育成羊的增重效果．和对照组比较羔羊提高增量9．8%（P〉0．05），育成羊提高增重6．1%（P〉0．05）；在饲料中添加茶黄酮可使羔羊呼吸道疾病发病率降低64%，使育成羊呼吸道疾病发病率降低50%，可有效预防羊的呼吸道疾病。     

Canine GM2‐Gangliosidosis Sandhoff Disease Associated with a 3‐Base Pair Deletion in the HEXB Gene

Background

GM2‐gangliosidosis is a fatal neurodegenerative lysosomal storage disease (LSD) caused by deficiency of either β‐hexosaminidase A (Hex‐A) and β‐hexosaminidase B (Hex‐B) together, or the GM2 activator protein. Clinical signs can be variable and are not pathognomonic for the specific, causal deficiency.

Objectives

To characterize the phenotype and genotype of GM2‐gangliosidosis disease in an affected dog.

Animals

One affected Shiba Inu and a clinically healthy dog.

Methods

Clinical and neurologic evaluation, brain magnetic resonance imaging (MRI), assays of lysosomal enzyme activities, and sequencing of all coding regions of HEXA, HEXB, and GM2A genes.

Results

A 14‐month‐old, female Shiba Inu presented with clinical signs resembling GM2‐gangliosidosis in humans and GM1‐gangliosidosis in the Shiba Inu. Magnetic resonance imaging (MRI) of the dog's brain indicated neurodegenerative disease, and evaluation of cerebrospinal fluid (CSF) identified storage granules in leukocytes. Lysosomal enzyme assays of plasma and leukocytes showed deficiencies of Hex‐A and Hex‐B activities in both tissues. Genetic analysis identified a homozygous, 3‐base pair deletion in the HEXB gene (c.618‐620delCCT).

Conclusions and Clinical Importance

Clinical, biochemical, and molecular features are characterized in a Shiba Inu with GM2‐gangliosidosis. The deletion of 3 adjacent base pairs in HEXB predicts the loss of a leucine residue at amino acid position 207 (p.Leu207del) supporting the hypothesis that GM2‐gangliosidosis seen in this dog is the Sandhoff type. Because GM1‐gangliosidosis also exists in this breed with almost identical clinical signs, genetic testing for both GM1‐ and GM2‐gangliosidosis should be considered to make a definitive diagnosis.