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61.
Deanna L. Funnell Christopher B. Lawrence Jeffrey F. Pedersen Christopher L. Schardl 《Physiological and Molecular Plant Pathology》2004,65(6):285-296
Systemic acquired resistance (SAR) is induced following inoculation of Peronospora tabacina sporangia into the stems of Nicotiana tabacum plants highly susceptible to the pathogen. Previous results have shown that accumulation of acidic β-1,3-glucanases (PR-2's) following induction of SAR by P. tabacina may contribute to resistance to P. tabacina. We showed that up-regulation of the PR-2 gene, PR-2d, following stem inoculation with P. tabacina, is associated with SAR. Studies using plants transformed with GUS constructs containing the full length promoter from PR-2d or promoter deletions, provided evidence that a previously characterized regulatory element that is involved in response to salicylic acid (SA), may be involved in regulation of PR-2d following induction of SAR with P. tabacina. This work provides evidence that regulation of PR-2 genes during P. tabacina-induced SAR may be similar to regulation of these genes during infection of N-gene tobacco by TMV or following exogenous application of SA, and provides further support for the role of SA in regulation of genes during P. tabacina-induced SAR. 相似文献
62.
Trichoderma Biocontrol of Colletotrichum acutatum and Botrytis cinerea and Survival in Strawberry 总被引:1,自引:2,他引:1
Stanley Freeman Dror Minz Inna Kolesnik Olga Barbul Aida Zveibil Marcel Maymon Yehuda Nitzani Benny Kirshner Dalia Rav-David Alon Bilu Arnon Dag Sharoni Shafir Yigal Elad 《European journal of plant pathology / European Foundation for Plant Pathology》2004,110(4):361-370
Trichoderma isolates are known for their ability to control plant pathogens. It has been shown that various isolates of Trichoderma, including T. harzianum isolate T-39 from the commercial biological control product TRICHODEX, were effective in controlling anthracnose (Colletotrichum acutatum) and grey mould (Botrytis cinerea) in strawberry, under controlled and greenhouse conditions. Three selected Trichoderma strains, namely T-39, T-161 and T-166, were evaluated in large-scale experiments using different timing application and dosage rates for reduction of strawberry anthracnose and grey mould. All possible combinations of single, double or triple mixtures of Trichoderma strains, applied at 0.4% and 0.8% concentrations, and at 7 or 10 day intervals, resulted in reduction of anthracnose severity; the higher concentration (0.8%) was superior in control whether used with single isolates or as a result of combined application of two isolates, each at 0.4%. Only a few treatments resulted in significant control of grey mould. Isolates T-39 applied at 0.4% at 2 day intervals, T-166 at 0.4%, or T-161 combined with T-39 at 0.4% were as effective as the chemical fungicide fenhexamide. The survival dynamics of populations of the Trichoderma isolates (T-39, T-105, T-161 and T-166) applied separately was determined by dilution plating and isolates in the mixtures calculated according to the polymerase chain reaction (PCR) using repeat motif primers. The biocontrol isolates were identified to the respective species T. harzianum (T-39), T. hamatum (T-105), T. atroviride (T-161) and T. longibrachiatum (T-166), according to internal transcribed spacer sequence analysis. 相似文献
63.
64.
西安荷斯坦奶牛群5个基因座位遗传多态性的PCR-RFLP分析 总被引:6,自引:0,他引:6
应用PCR-RFLP方法对西安荷斯坦牛的κ-en、β-lg、β-lg5′侧翼区、CSN1S2、IGFBP-3共5个基因座位进行了多态性分析。结果表明,在西安荷斯坦牛群中,没有发现携带CSN1S2^P等位基因的个体,其多态信息含量为0。κ-en基因座位呈现低度多态(PIC=0.2366),β-lg、β-lg5′侧翼区、IGFBP-3基因座位的多态信息含量分别为0.3168、0.3689、0.4439,均呈现中度多态。κ-en、β-lg、β-lg5′侧翼区、IGFBP-3、CSNIS2基因座位的杂合度和DNA多态度分别为0.2742、0.3947、0.4879、0.4891、0和0.0255、0.0116、0.0333、0.0112、0。而且,在西安荷斯坦牛群中,κ-en、β-lg、β-lg5′侧翼区、IGFBP-3共4个基因座位均处于Hardy-Weinberg平衡状态,CSN1S2基因座位处于纯合状态。 相似文献
65.
66.
亚洲璃眼蜱唾液腺一新功能基因的克隆与测序 总被引:1,自引:0,他引:1
HaB1是亚洲璃眼蜱雌成蜱唾液腺差异表达基因文库中的一个片段,根据其序列设计引物HaB1-GSP1和HaB1-GSP2,以唾液腺总RNA为模板,RACE法扩增获得HaB1的未知3′-末端。测定该末端序列,进行序列拼接,设计全长引物5-′CCAGTCCGAAGGAAGGGCG-3′和5-′TCTC-CGGGCACGTGAAGTGTC-3′。以cDNA第一链为模板,扩增获得基因全长。经核查表明,该基因为一新基因(登录号AY803896)。 相似文献
67.
随机抽取荷斯坦奶牛 472头 (1~ 11胎 )进行奶牛隐性乳房炎的检测 ,乳用特征性状 (楞角性、尻宽、尻角度、后肢侧视、蹄角度 )的线性评定 ,以及隐性乳房炎与乳用特征的相关性分析。结果表明 :奶牛隐性乳房炎的乳区阳性率与楞角性、尻宽、尻角度、后肢侧视、蹄角度的相关系数分别为 0 1171、0 10 3 0、0 0 681、0 0 180、-0 12 65 ,其中与楞角性、尻宽分别达到显著水平 (P <0 0 5 )的正相关 ,与蹄角度达极显著 (P <0 0 1)的负相关。奶牛阳性率与楞角性、尻宽、尻角度、后肢侧视、蹄角度的相关系数分别为 0 0 967、0 0 5 61、0 0 2 82、0 0 12 7和 -0 0 670 ,其中除与楞角性为显著水平 (P <0 0 5 )的正相关 (0 0 967)外 ,其余均不显著 (P >0 0 5 )。 相似文献
68.
69.
Canine GM2‐Gangliosidosis Sandhoff Disease Associated with a 3‐Base Pair Deletion in the HEXB Gene 下载免费PDF全文
P. Wang P.S. Henthorn E. Galban G. Lin T. Takedai M. Casal 《Journal of veterinary internal medicine / American College of Veterinary Internal Medicine》2018,32(1):340-347
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. 相似文献70.
Familial Congenital Methemoglobinemia in Pomeranian Dogs Caused by a Missense Variant in the NADH‐Cytochrome B5 Reductase Gene 下载免费PDF全文
H. Shino Y. Otsuka‐Yamasaki T. Sato K. Ooi O. Inanami R. Sato M. Yamasaki 《Journal of veterinary internal medicine / American College of Veterinary Internal Medicine》2018,32(1):165-171