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首页> 外文期刊>New Agriculturist >DAC-ELSSA AND INFECTIVITY ASSAY BASED IDENTIFICATION OF PEANUT BUD NECROSIS VIRUS (PBNV) AS INCITANT OF MUNG AND URDBEAN LEAF CURL DISEASES IN ALLAHABAD
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DAC-ELSSA AND INFECTIVITY ASSAY BASED IDENTIFICATION OF PEANUT BUD NECROSIS VIRUS (PBNV) AS INCITANT OF MUNG AND URDBEAN LEAF CURL DISEASES IN ALLAHABAD

机译:基于DAC-ELSSA和传染病分析的花生芽孢杆菌病毒(PBNV)诱发阿拉哈巴德的绿豆和城市叶卷曲病

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Preliminary survey was conducted during kharif 2004 and 2005 to detect the natural infection of vira! diseases in standing crops of urd and mungbean in experimental trials at AAI-DU and farmer's fields in the vicinity of AAI-DU. Young tissue samples collected from suspected plants in crop wise were subjected to bioassay and DAC-ELISA. For bioassay, the samples were mechanically inoculated on to cowpea cv.152 (local lesion host) and to respective host plants under glass house conditions. Symptoms, physical properties of buffered sap like dilution end point (DEP), thermal inactivation point (TIP) and longevity in vitro (LIV) were studied separately for each crop isolate. Direct antigen linked immunosorbent assay (DAC-ELISA) was done by using PBNV antiserum diluted to 1:5000. All the mechanically inoculated cowpea leaves showed chlorotic spots from 6-8 days, which subsequently turned irregular chlorotic lesions from 11-12 days and finally the lesioned portions of leaves turned necrotic and dried within 16-17 days after inoculation. Glasshouse inoculated mung and urdbean from cowpea single lesion inoculations produced similar symptoms with negligible variations from natural infection, the DEP, TIP and LIV was found to be 10~(-2) (mung) 10~(-3) (urd),40-50°C (for both mung and urd) and 4 hrs (for both mung and urd). All the bioassayed samples were tested positive in ELISA. In the light of the present investigation involving serology, symptomatology and physical properties of buffered sap, the virusis confirmed as peanut bud necrosis virus (PBNV) inciting of leaf curl in mung and urdbean.
机译:在2004年和2005年的Kharif期间进行了初步调查,以检测病毒的自然感染!在AAI-DU和AAI-DU附近的农民田间进行的试验性试验中,发现了腐殖质和绿豆类作物的主要病害。从可疑植物中以作物方式收集的年轻组织样品经过生物测定和DAC-ELISA。为了进行生物测定,将样品在温室条件下机械接种到cow豆cv.152(本地病原体宿主)和各自的宿主植物上。对每种农作物分离物分别研究了症状,缓冲液的物理性质,如稀释终点(DEP),热失活点(TIP)和体外寿命(LIV)。通过使用稀释至1:5000的PBNV抗血清进行直接抗原连接免疫吸附测定(DAC-ELISA)。所有机械接种的cow豆叶片在6-8天都显示出褪绿斑点,随后在11-12天后变成不规则的褪绿病损害,最后叶片的病变部分在接种后16-17天内变成坏死并干燥。温室cow豆单病菌接种的绿豆和urdbean产生了类似的症状,自然感染的变化可忽略不计,发现DEP,TIP和LIV为10〜(-2)(绿豆)10〜(-3)(urd),40 -50°C(对于绿豆和乌德)和4小时(对于绿豆和乌德)。所有生物测定的样品在ELISA中均呈阳性。根据涉及缓冲液的血清学,症状学和物理特性的当前研究,该病毒被证实为花生芽坏死病毒(PBNV),引起绿豆和乌豆叶片卷曲。

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