Correction to: Predation on glass eels of Japanese eel <Emphasis Type="Italic">Anguilla japonica</Emphasis> in the Tone River Estuary,Japan     

Yoichi Miyake  Aigo Takeshige  Hikaru Itakura  Hajime Itoh  Hiroaki Onda  Akira Yamaguchi  Akihito Yoneta  Kohma Arai  Yulina V. Hane  Shingo Kimura 《Fisheries Science》2018,84(6):1015-1016

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Differential regulation on C5 expression in goose versus mammals by glucose/palmitate provides a potential protection for goose fatty liver     

Zidi Jin  Long Liu  Cheng Xu  Chunchi Yan  Shuo Li  Tuoyu Geng  Daoqing Gong 《Animal Science Journal》2021,92(1):e13672

Goose fatty liver is a specific type of nonalcoholic fatty liver that is protected from harmful effects associated with severe steatosis. Our previous findings suggest that suppression of the complement C5 may be relevant, but the mechanism is unclear. Therefore, in this study, we first verified the expression pattern of complement genes (including C5) during goose fatty liver formation and then determined the liver fat content and fatty acid composition by high-performance liquid chromatography (HPLC), followed by selecting the differential metabolites to treat HepG2, goose and mouse primary hepatocytes, aiming to explore the mechanism of C5 and inflammation suppression in goose fatty liver. The data confirmed the suppression of complement genes (including C5) in goose fatty livers. Moreover, fat content was significantly higher in fatty liver versus normal ones, with oleic acid and palmitic acid dominantly accounting for the difference. In line with this, high concentration of palmitate led to down regulation of C5 expression in goose primary hepatocytes whereas upregulation in mouse primary hepatocytes and HepG2 cells. In conclusion, regulation on C5 expression by fatty liver related factors including high level of palmitic acid may contribute to the protection of goose liver from severe hepatic steatosis.  相似文献   

Alessandro Bonanno and Lawrence Busch (eds): Handbook of the international political economy of agriculture and food     

Marie Louise Ryan 《Agriculture and Human Values》2018,35(3):731-732

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金秋橘飘香 黄岩采橘忙——中国蜜橘之乡采访记实     

耿国彪 《绿色中国(综合版)》2005,(11):72-73

在一个秋风送爽的日子，伴随着秋风中飘动的甜甜橘香，我来到了位于浙江省东部沿海的台州市黄岩区。黄岩蜜橘的名字在小时候就听说过，是橘子中的魁首。这次来到黄岩，想到要与心仪已久的蜜橘谋面，心中就充满了期待和兴奋。  相似文献   

聚焦绿色建筑：揭开绿色建筑的面纱     

耿国彪 《绿色中国(综合版)》2005,(10):22-29

2005年是中国“绿色地产年”，谈起绿色地产、绿色楼盘，不少人的头脑中立即就会反映出小区的绿化、花草树木与楼房的搭配和比例。把绿色理解成绿化的消费者不在少数．如果不是经过半个月的采访．就是记者本身也存在着相同的认识。“安得广厦千万间．大庇天下寒士俱欢颜”这是唐代大诗人杜甫对人需要居住的慨叹。时光过去了一千余年，人类仅需要遮风挡雨的草堂时代．早已成为了历史。现在人们不仅要求有房子住．而且要住的舒适惬意。而绿色建筑就是符合人们现代居住需求的房子。在2005“绿色地产年”接近尾声的时候．本刊记者用半个月的时间走访了相关的政府部门．建筑设计者、开发商以及消费者，对绿色建筑进行了一次全方位的调查。本期特别策划，我们汇集了记者、专家、开发商三方的见解，力图为读者立体地揭开绿色建筑的神秘面纱。  相似文献   

犬腺病毒SY-45株不同大小蚀斑特性研究     

范泉水  夏咸柱  邱薇  黄耕  何洪彬  余春  乔军  武银莲  殷震 《动物医学进展》2001,22(4):86-87,99

应用蚀斑方法将SY－45毒株经过3次蚀斑纯化直到蚀斑大小相对稳定。从不同大小的蚀斑中挑选出三种蚀斑，大斑直径约3mm(简称LP）、中斑约2mm(简称MP）、小斑约1mm(简称SP）。分别在MDCK细胞上增殖并进行了三种不同大小斑毒对犬的毒力、免疫原性和在MDCK细胞上产毒量比较，以筛选最佳的疫苗株，试验结果表明用不同大小蚀斑病毒大剂量人工感染易感犬后，所有的试验犬临床症状和病理解剖学和病理组织学表现均正常；对挑选的4窝CAV HI抗体效价小于等于1：2的健康幼犬进行免疫试验，测定血清的中和抗体效价和血凝抑制抗体效价，结果表明：大斑毒的免疫原性要稍高于中斑毒，而明显高于小斑毒；不同大小蚀斑毒在MDKC细胞上产毒量差异很大，大斑毒可达10^7TCID50／mL、小斑毒达10^6TCID50／ml、小斑毒达10^4.5TCID^50/mL。综合所有试验结果表明：大斑毒株具有产毒量高、安全性好、免疫原性强的优点，是较为理想的疫苗株。  相似文献   

犬瘟热病毒的静水压灭活   总被引：4，自引：1，他引：3  

池元斌  夏咸柱  王雪梅  余春  王琰第  何洪彬  范泉水  黄耕  王允海  刘海涛  张春红 《中国兽医学报》2001,21(1):35-37

以250MPa的静水压力对犬瘟热病毒（CDV）处理30min之后，CDV被灭活，由其制成的灭活疫苗诱导犬产生中和抗体的能力明显优于传统的福尔马林灭活疫苗，免疫保护率达90％。电镜观察显示，经不同程度静水压力处理后的CDV粒子均发生变形，表面呈现凸起，但CDV H基因部分片段的RT－PCR扩增结果揭示，高达510MPa的静水压力作用30min也未能使其基因片段受到破坏。  相似文献   

迪卡配套系猪RYR1的PCR分析及其利用的研究   总被引：1，自引：0，他引：1  

李馨  耿忠诚  袁子国  李晓敏  刘太红 《黑龙江畜牧兽医》2003,(7):15-16

试验从鸡东县永安猪场随机抽取迪卡配套系猪B系和E系42头，通过PCR扩增技术和酶切鉴定．采用克隆技术进行测序，来检测是否含有氟烷基因序列。经过以上技术检测这42头猪均没有氟烷基因。  相似文献   

通过病毒分离鉴定和基因检测首次发现虎流感   总被引：21，自引：1，他引：20  

夏咸柱  高玉伟  扈荣良  王立刚  刘丹  邹啸环  黄耕  贺文琦  王玮  苏伟林  刘文良 《中国兽医学报》2003,23(2):107-110

应用F81猫肾传代细胞，从高热、拒食和间有神经症状的死亡率病科中分离获得1株病毒，经形态学、理化学、生物学和血清学系统鉴定，证明为流感病毒。采用流感病毒核蛋白基因引物，对分离病毒及该虎病科进行RT－PCR扩增和序列分析，结果从分离病毒和虎病科中均扩增出与理论值大小相符的464bp基因片段；其序列与A、B、C3型流感病毒相比较，同源性分别为84．9％、35．0％、24．8％。由此说明，所分离病毒为A型流感病毒，命名为/蘧／哈尔滨（中国）／01／2002。用此分离病毒静脉接种于3月龄家猫3号，均出现与病虎相似的临床症状，其中1号耐过，2只死亡。死亡猫剖检变化与死虎相似，主要是呈肺炎病变，并可从病科中回收到所接种病毒。从此分离病毒为HA抗原，进行虎与猫血清的HI抗体检测，结果康复虎血清比其病初血清、康复猫血清比其接种前血清HI抗体均增高4倍以上，表明该病毒具有致病性，是引起该虎与试验猫发病甚至死亡的病原。  相似文献   

‘Plantibodies’: a flexible approach to design resistance against pathogens     

A. Schots  J. De Boer  A. Schouten  J. Roosien  J. F. Zil Verentant  H. Pomp  L. Bouwman-Smits  H. Overmars  F. J. Gommers  B. Visser  W. J. Stiekema  J. Bakker 《European journal of plant pathology / European Foundation for Plant Pathology》1992,98(2):183-191

Engineering resistance against various diseases and pests is hampered by the lack of suitable genes. To overcome this problem we started a research program aimed at obtaining resistance by transfecting plants with genes encoding monoclonal antibodies against pathogen specific proteins. The idea is that monoclonal antibodies will inhibit the biological activity of molecules that are essential for the pathogenesis. Potato cyst nematodes are chosen as a model and it is thought that monoclonal antibodies are able to block the function of the saliva proteins of this parasite. These proteins are, among others, responsible for the induction of multinucleate transfer cells upon which the nematode feeds. It is well documented that the ability of antibodies to bind molecules is sufficient to inactivate the function of an antigen and in view of the potential of animals to synthesize antibodies to almost any molecular structure, this strategy should be feasible for a wide range of diseases and pests.Antibodies have several desirable features with regard to protein engineering. The antibody (IgG) is a Y-shaped molecule, in which the domains forming the tips of the arms bind to antigen and those forming the stem are responsible for triggering effector functions (Fc fragments) that eliminate the antigen from the animal. Domains carrying the antigen-binding loops (Fv and Fab fragments) can be used separately from the Fc fragments without loss of affinity. The antigen-binding domains can also be endowed with new properties by fusing them to toxins or enzymes. Antibody engineering is also facilitated by the Polymerase Chain Reaction (PCR). A systematic comparison of the nucleotide sequence of more than 100 antibodies revealed that not only the 3′-ends, but also the 5′-ends of the antibody genes are relatively conserved. We were able to design a small set of primers with restriction sites for forced cloning, which allowed the amplification of genes encoding antibodies specific for the saliva proteins ofGlobodera rostochiensis. Complete heavy and light chain genes as well as single chain Fv fragments (scFv), in which the variable parts of the light (V_L) and heavy chain (V_H) are linked by a peptide, will be transferred to potato plants. A major challenge will be to establish a correct expression of the antibody genes with regard to three dimensional folding, assembly and intracellular location.  相似文献