Detection of Zucchini Yellow Mosaic Virus-Infected Squash Plants in Egypt

Rokaia Nabil, Ahmed Abdelkhalek, S. Behiry, H. Younes
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Abstract

Background: The Zucchini yellow mosaic virus (ZYMV) is well recognized as a very significant viral pathogen that causes substantial yield reductions in cucurbitaceous crops on a global scale. Methods: To detect and identify ZYMV in squash plants we used the serology reaction, transmission electron microscope, and molecular methods. Results: ZYMV was first isolated from naturally infected squash plants in the Alexandria governorate of Egypt, where it caused mosaic, yellowing, and deformation of the leaves. In addition to a molecular diagnosis utilizing RT-PCR, the identification relied on serological responses with antisera to CMV, SqMV, and ZYMV. Using centrifugation and PEG, the virus was cleaned. The A260/280 and A280/260 ratios of the purified virus were 1.38 and 0.72, respectively, which are consistent with those of a nucleoprotein. 2.36 mg of pure virus was recovered from per 100g of infected leaf material. The virus particles, as seen under an electron microscope after a partial purification preparation technique, have a flexuous filamentous structure and measure around 750 nm in length and 12 nm in diameter. Finally, the molecular investigation established the identification of the ZYMV isolate after a specific antiserum with a titer of 1:2.56×10 4 was generated and tested at the third week.
检测埃及受西葫芦黄花叶病毒感染的瓜类植物
背景:西葫芦黄镶嵌病毒(Zucchini yellow mosaic virus,ZYMV)被公认为是一种非常重要的病毒病原体,在全球范围内导致葫芦科作物大幅减产。研究方法为了检测和鉴定南瓜植株中的 ZYMV,我们使用了血清反应、透射电子显微镜和分子方法。结果ZYMV 最初是从埃及亚历山大省自然感染的南瓜植株中分离出来的,该病毒会导致叶片马赛克、黄化和变形。除了利用 RT-PCR 进行分子诊断外,鉴定还依赖于 CMV、SqMV 和 ZYMV 抗血清反应。利用离心和 PEG 清除病毒。纯化病毒的 A260/280 和 A280/260 比率分别为 1.38 和 0.72,与核蛋白的比率一致。从每 100 克受感染的叶片材料中回收了 2.36 毫克纯病毒。经过部分纯化制备技术后,在电子显微镜下观察到的病毒颗粒具有弯曲的丝状结构,长度约为 750 nm,直径约为 12 nm。最后,在第三周生成并测试了滴度为 1:2.56×10 4 的特异性抗血清后,分子研究确定了 ZYMV 分离物的身份。
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