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<正>马铃薯病毒毒源是马铃薯病毒检测中抗血清制备及ELISA检测中必备的材料,也是马铃薯抗病育种和马铃薯病毒学研究所需的材料。我国1987年以来就开展了采用试管封闭保存毒源法的研究,结果表明利用烟草、洋酸浆、番茄等植物做为马铃薯不同病毒试管保毒植物,其试管小植株可单节切断繁殖,均可正常成长发育,移栽到土壤中小植株发育正常,并仍具有浸染力,此法一直沿用至今。 相似文献
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本文报道了1987~1990年对马铃薯主要病毒毒源试管封闭保存的研究结果.保毒植物为普通烟草、心叶烟、德伯尼烟、番茄、千日红,洋酸浆等.在无菌条件下,温度为20~25℃,2000~3000m烛光照,取其0.5~1cm大茎尖消毒后扦插在试管培养基上培养,因保毒植物种类不同,其成活率为57.6%~100%,平均为87.1%,进管20~26天生根发育正常.在试管内发育成株时,可进行单节切段更新繁殖,其生长发育比大茎尖初次进管时速度快,一般6~12天生根发育正常,并保持试管毒源纯度和含毒量. 相似文献
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马铃薯普通花叶病毒(PVX)抗血清的制备和不同酶联免疫吸附检测法的对比试验 总被引:3,自引:0,他引:3
从一东农 30 3马铃薯的重花叶症状病株 ,经用千日红 (Gomphrenaglobosa)两次单斑分离获得一马铃薯普通花叶病毒 (PVX)毒源株 ,用普通烟 (Nicotianatabacum )繁殖病毒 ,参照S .M .PaulKhurana等人的方法提纯病毒 ,免疫家兔 ,获得了效价达 1∶5 12 ,非专化反应为 1∶4的马铃薯X病毒抗血清。把PVX抗血清用过碘酸钠氧化法制备成辣根过氧化物酶的结合物 ,其工作浓度可达到 1∶10 0 0以上。在这一基础上进行了直接酶联检测法 (DirectImmunosorbentAssay) ,间接酶联检测法 (IndirectImmunosorbentAssay)的对比试验。 相似文献
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二季作区脱毒马铃薯种薯繁殖技术规程 总被引:4,自引:0,他引:4
1 前 言马铃薯脱毒只是脱除了已经侵染到块茎内的各种病毒 ,但并不能解决植株遭受病毒再侵染的问题。事实上 ,脱毒马铃薯在繁殖过程中 ,只要接触毒源或遭到传毒介体的侵害 ,就会重新感染病毒而再次发生退化。因此 ,在繁殖脱毒种薯的过程中 ,必须采取严格的隔离措施以防止病毒的再侵染。脱毒种薯的繁殖过程包括脱毒试管苗快繁、脱毒微型薯 (原原种 )工厂化生产、一代原种生产和二、三代原种生产及一级脱毒种薯生产等过程。2 脱毒试管苗快繁保存的脱毒试管苗在进行大量扩繁时 ,首先要进行病毒检测 ,确信不含各种病毒后再开始切繁。基础苗在… 相似文献
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本文报道了1987 ̄1990年对马铃薯主要病毒毒源试管封闭保存的研究结果,保毒植物为普通烟草,心叶烟,德伯尼烟,番茄、千日红,洋酸浆等,在无菌条件下,温度为20 ̄25℃,2000 ̄3000m烛光照,取其0.5 ̄1cm,大茎尖消毒后扦插在试管培养苦上培养,因保毒植物种类不同,其成活率为57.6% ̄100%,平均为87.1%。进管20 ̄26天生根发育正常,在试管内发育成株时,可进行单节切段更新繁殖,其 相似文献
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病毒病是制约马铃薯产量和质量的重要因素。马铃薯脱毒试管苗、微型薯是生产脱毒种薯的重要环节。本研究于2010~2013年对收集自云南省的试管苗274个、微型薯356个,共计630个样品。应用电子显微镜观察,并采用DAS-ELISA检测了8种病毒:马铃薯S病毒、马铃薯卷叶病毒、马铃薯Y病毒、马铃薯X病毒、马铃薯A病毒、马铃薯M病毒、番茄斑萎病毒和烟草环斑病毒,发现试管苗和微型薯中马铃薯S病毒检出率最高(21.27%),其次是PLRV(5.71%);还检测到了新出现的侵染马铃薯的番茄斑萎病毒和烟草环斑病毒。研究结果为马铃薯种薯生产过程中病毒病的检测防控提供了参考。 相似文献
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J. F. J. M. van den Heuvel J. A. A. M. Dirven G. J. van Os D. Peters 《Potato Research》1993,36(2):89-96
Summary The acquisition of potato leafroll virus (PLRV) byMyzus persicae nymphs from the top leaves of potato plants was studied throughout a growing season in relation to the antigen titre in those
leaves and the feeding behaviour of the aphid. Secondarily-infected plants of eight potato genotypes with different levels
of field resistance served as virus sources. Early in the growing season, plants were efficient sources for virus acquisition.
The amount of viral antigen detected inM. persicae nymphs fed on the top leaves was strongly correlated with the titres of viral antigen in these leaves. Virus acquisition
from the top leaves of older potato plants was markedly impaired and could not be correlated with their virus titre. With
increasing age of the potato plants and the development of virus symptoms, the virus titre in the leaves declined and the
initial weak correlation between the virus titre and field resistance ratings disappeared. Thus, screening secondarily-infected
potato plants for field resistance to PLRV based on the concentration of viral antigen in leaves or in aphids fed on them
should be avoided later in the growing season. The feeding rate ofM. persicae, measured by the number of honeydew droplets excreted, did not account for the reduced uptake of virus from older plants
since it was not influenced by the age of the plant. Throughout the growing season, the feeding rate ofM. persicae nymphs on PLRV-infected plants was higher on genotypes with low levels of field resistance to PLRV than on genotypes with
high ones. 相似文献
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The concentration of potato virus Y (PVY) was determined, using ELISA values (A405 nm), in twenty-six potato cultivars belonging to five resistance groups, grown in the field and in the greenhouse. On the basis of virus concentration, potato cultivars of group A, B, and C did not differ significantly and constitute the most susceptible group; those of group D and E differ significantly with each other and with group A, B, C, and constitute moderate and highly resistant groups, respectively. In the second year of infection, virus concentration was higher in each group, irrespective of resistance level. Thus, the infected plants of resistant groups, in a second year of growth, could be as rich sources of virus to aphids as plants from susceptible groups. 相似文献
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Volunteer potatoes were investigated as infection sources for potato leafroll virus (PLRV) and potato virus X (PVX) in a high elevation seed potato growing area of eastern Idaho. Population densities ofMyzus persicae were assessed. Percentage of PLRV and PVX infection of the volunteers and seed potato crops was determined, as well as density of volunteers and certain parameters of volunteer growth and reproduction. Volunteers apparently harbored no more PLRV than the potato crop from which they originated. But they were found to be an important reservoir of PVX with the infection increasing as much as 12.43% in one year. No aphids capable of transmitting PLRV were found although one species that can transmit potato virus Y was recorded. The mean density of volunteers varied from 0 to 84,880 stems/ha. The number of tubers remaining in the field after harvest and winter weather conditions appeared to be the only factors affecting volunteer density. Volunteer plants arising from seed pieces at an average depth of 6.1 cm were found to set an average of 2.1 new tubers per plant at an average depth of 4.0 cm. These results suggest that volunteer potatoes are a significant source of PVX infection in subsequent seed potato crops. 相似文献
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Summary Conditions necessary for the detection of potato leafroll virus (PLRV) and potato virus Y (PVY) in tubers from primary and
secondary infected plants were investigated. Tubers were analysed before and after breaking dormancy by rindite treatment.
PLRV was reliably detected indormant tubers whereas PVY was readily detected only when tubers had been rindite-treated and
held for two to three weeks at 22°C and high humidity in the dark. PLRV occurred in higher concentration at the heel end than
at the rose end of infected tubers and the concentration remained nearly unchanged during the experimental period of 35 days,
whereas PVY was found to be more concentrated at the rose end and was rapidly accumulating in the tubers after the break of
dormancy. In dormant tubers PVY concentration dropped during storage at 22°C. The use of ELISA for tuber indexing is discussed. 相似文献
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E. A. Simakov B. V. Anisimov I. M. Yashina A. I. Uskov S. M. Yurlova E. V. Oves 《Potato Research》2008,51(3-4):313-326
First, an extensive literature review was performed with respect to Potato virus Y (PVY) resistance sources and their further utilization in a breeding programme. On the basis of that review we present a scheme of backcrossing and new cultivar creation on the basis of five detected sources of PVY resistance and one source of Potato virus X resistance. Some cultivar pedigrees are presented reflecting the differences in the breeding strategies. Moreover, results of investigations on some polygenic traits such as field resistance against late blight and starch content are presented. For these purposes progenies were screened for suitable recombinant genotypes which were used in further crossings. Also the results of investigations on resistance to the potato golden nematode and on the selection of cultivars suitable for processing are briefly analysed. We also describe a programme of parallel evaluation of identical hybrid populations in different soils and climatic zones. The development of seed potato production systems facilitated the conditions to improve the quality of potato seed material, to increase potato production and to allow Russia to participate in the international potato market. Systems of virus detection, norms and methods of laboratory tests as well as requirements for quality and tolerance levels of different seed classes (generations) were unified and harmonized with European systems. 相似文献
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Summary The diploid clone DW.84-1457 which has outstanding resistance to potato leafroll virus (PLRV), has been selected at the Mlochów
Centre of the Institute for Potato Research. It has in its pedigree PLRV-resistant clones from the Max Planck Institute nos.
MPI 44.1016/10, MPI 44.335/130 and MPI 49.540/2. Its behaviour in the field and response to aphid inoculation indicate high
resistance to infection, and the low concentration of the virus in graft-inoculated plants indicates high resistance to multiplication.
This combination within one genotype of two aspects of resistance is not connected with hypersensitivity, and is heritable.
Clone DW.84-1457 has other desirable characters such as extreme resistance to potato virus X (PVX), high resistance to potato
virus M (PVM) and good table and processing quality. It is being utilized in the development of parental lines, both at the
diploid and tetraploid level. 相似文献
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脱毒马铃薯试管苗营养液栽培试验 总被引:1,自引:1,他引:1
对马铃薯试管苗液体培养过程中所需的温度、光照、营养液浓度等条件进行了研究。结果表明:马铃薯试管苗适应用清水生根,在无机盐离子浓度0.05%~1.25%营养液中生长。在昼夜温度变幅为20~35℃的智能温室中,采用自然光照,脱毒马铃薯试管苗3d开始生长,5d根生齐,在适合的营养液培养条件下,7d达到根长4.5~5.0cm,根数15~22根,茎长6.0~8.0cm,茎粗1.4~2.2cm,叶片数7片,一株可剪顶,切段扦插2~3株,母苗可在侧芽生长后移栽结薯。该法繁殖速度快,成本低,省人力,对技术人员要求不高,是脱毒马铃薯试管苗繁殖的最为有效的途径。 相似文献
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PVYCP基因导入加工型马铃薯甘农薯1号的研究 总被引:1,自引:0,他引:1
利用整合有马铃薯Y病毒外壳蛋白基 (PVYCP基因 )的改建质粒PEY3,以土壤农杆菌为载体转化加工型马铃薯新品种甘农薯 1号叶盘 ,细菌侵染 14d后用 10 0ml/LKM在愈伤组织水平上选择 ,转化率最高可达 2 1 3%。转化效率与细菌生理状态、NAA浓度、叶盘预培养天数有关。转化体分化 2株再生植株。冠瘿碱分析证明转化体整合了PVYCP基因。 相似文献