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Investigation of the mechanism of adult-stage resistance to barley yellow dwarf virus associated with awheat-Thinopyrum intermedium translocation
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作者 Xindong Wang Wei Rong +2 位作者 Yan Liu Xifeng Wang Zengyan Zhang 《The Crop Journal》 SCIE CAS CSCD 2018年第4期394-405,共12页
Barley yellow dwarf virus(BYDV)can infect wheat(Triticum aestivum L.),leading to yield loss.Among four BYDV strains(GAV,GPV,PAV,and RMV)identified in China,BYDV-GAV is the prevailing isolate.YW642,a wheat–Thinopyrum ... Barley yellow dwarf virus(BYDV)can infect wheat(Triticum aestivum L.),leading to yield loss.Among four BYDV strains(GAV,GPV,PAV,and RMV)identified in China,BYDV-GAV is the prevailing isolate.YW642,a wheat–Thinopyrum intermedium translocation line,is resistant to BYDV isolates at both seedling and adult stages.Zhong 8601 is the wheat recurrent parent of YW642 and is susceptible to BYDV.In this study,we investigated the adult-stage resistance mechanism of YW642,measured BYDV titer and hydrogen peroxide(H_2O_2) in adult-stage leaves of YW642 and Zhong 8601 inoculated with BYDV-GAV,and identified transcriptional differences between YW642 and Zhong 8601 using microarray-based comparative transcriptomics.Enzyme-linked immunosorbent assay and H_2O_2assay showed that both BYDV titer and H_2O_2 content were markedly lower in YW642 than in Zhong 8601 at 21,28,35,and 40 days post-inoculation(dpi).The transcriptomic comparison revealed that many types of genes were significantly up-regulated at 35 dpi in adult-stage leaves of YW642 compared to Zhong 8601.The important up-regulated genes associated with the adult-stage resistance encoded 15 resistance-like proteins,pathogenesis-related proteins(such as defensin and lipid transfer proteins),protein kinase homologs,transcription factors,reactive oxygen species scavenging-related proteins,and jasmonic acid and gibberellic acid biosynthesis enzymes.These results suggest that precise expression regulation of these proteins plays a crucial role in adult-stage resistance of YW642 against BYDV infection. 展开更多
关键词 Barley yellow dwarf virus Reactive oxygen species Resistance at adult stage Defense-associated genes PHYTOHORMONE
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Comparison of methods of purification and identification of Verticillium dahliae toxins
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作者 JIA Zhi-qi SHI Fu-mei YUAN Hai-yong HOU Yan-yan LI Ying-zhang 《Journal of Life Sciences》 2007年第1期67-72,81,共7页
The complexes excreted by VerticiUium dahliae are phytotoxins, which are responsible for most of the symptoms associated with Verticillium wilt disease. Verticillium dahliae toxins (VD-toxins) can be purified by dif... The complexes excreted by VerticiUium dahliae are phytotoxins, which are responsible for most of the symptoms associated with Verticillium wilt disease. Verticillium dahliae toxins (VD-toxins) can be purified by different methods. In the present study, we reported a simpler, more effective method to purify VD-toxins. The supematant of V. dahliae culture was frozen, lyophilized and dialyzed by 1 kDa Dialysis Membranes (MWCO). We also partially identified the characteristics of the purified VD-toxins. The results showed that the components of VD-toxins include glycoprotein within 35.8-83.2 kDa. The phytotoxic activity of VD-toxins was remained after VD-toxins were pretreated by high temperature, Concanavalin-A, and proteinase E, respectively. These data suggest that VD-toxins are heat-stable, and the protein fraction and glycosyl are both important contributors to the phytotoxic activity. VD-toxins purified effectively from the culture filtrates of V. dahliae may help in further understanding the mechanisms of interactions between V. dahliae and plants. 展开更多
关键词 GLYCOPROTEIN PHYTOTOXICITY PURIFICATION Verticillium dahliae toxins
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荧光定量PCR检测鹅细小病毒体系的建立和应用 被引量:2
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作者 曹楠 杨舒展 +4 位作者 郭思璇 曾依翎 李冰心 田允波 许丹宁 《仲恺农业工程学院学报》 CAS 2018年第2期18-23,共6页
为解决在养殖过程中多种疫病混合感染造成鹅细小病毒(Goose parvovirus,GPV)的临床及实验室诊断困难的问题,利用分离得到的GPV GDGZh1设计合成1对特异性引物GPV-rt PCRF/GPV-rt PCRR,建立了GPV SYBR Green I实时荧光定量PCR检测方法,并... 为解决在养殖过程中多种疫病混合感染造成鹅细小病毒(Goose parvovirus,GPV)的临床及实验室诊断困难的问题,利用分离得到的GPV GDGZh1设计合成1对特异性引物GPV-rt PCRF/GPV-rt PCRR,建立了GPV SYBR Green I实时荧光定量PCR检测方法,并进行了临床样品及GPV在种鹅体内定植规律的检测.结果表明,该方法对质粒的检测灵敏度为3.5×10~2copies/μL,GPV具有组织广泛嗜性,种鹅的直肠、脾脏、心脏、肾脏和卵巢中病毒含量在攻毒后第5天最高,肝脏中病毒含量在攻毒后第9天最高,心脏和肾脏在攻毒后第17天检测不到病毒,直肠、肝脏、脾脏和卵巢在攻毒后第25天还能检测到病毒.这说明种鹅感染GPV后,病毒可以在其体内长期存在,并不断向外排毒,还能通过垂直传播的方式将病毒传递给雏鹅. 展开更多
关键词 鹅细小病毒(Goose parvoviruse) REAL-TIME PCR 临床检测 病毒定植
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