Suppr超能文献

澳大利亚昆士兰州植原体相关番木瓜病害的流行病学

Epidemiology of Phytoplasma-Associated Papaya Diseases in Queensland, Australia.

作者信息

Guthrie J N, White D T, Walsh K B, Scott P T

机构信息

Plant Sciences Group, School of Biological and Environmental Sciences, Central Queensland University, Rockhampton Queensland 4702 Australia.

出版信息

Plant Dis. 1998 Oct;82(10):1107-1111. doi: 10.1094/PDIS.1998.82.10.1107.

Abstract

Three phytoplasma-related diseases of papaya (Carica papaya), dieback, yellow crinkle, and mosaic, are recognized within Australia. Immature leaf material was sampled every week for 8 months from a cohort of 60 female plants, located within a commercial papaya plantation, to determine the minimum time between infection and symptom expression. Phytoplasma DNA was detected using the polymerase chain reaction (PCR) with primers specific for phytoplasmas in general, and for the stolbur group of phytoplasmas. The dieback-associated phytoplasma was detected 1 week prior to (four cases) or the same week (nine cases) as symptom expression, while phytoplasma DNA was detected between 3 and 11 weeks prior to expression of mosaic symptom (six cases). Lateral shoot regrowth on the lower stem of plants which had suffered dieback disease failed to generate stolbur-specific PCR products in 15 cases. A dual infection with dieback and yellow crinkle or mosaic was diagnosed in a further two cases, using restriction fragment length polymorphism digests, and both cases were interpreted as secondary infections by the dieback-associated phytoplasma. Regrowth in three of seven cases of yellow crinkle- and three of nine cases of mosaic-affected plants tested positive for phytoplasma-specific DNA. Ratooning of dieback-affected plants and removal of yellow crinkle- or mosaic-affected plants is suggested for the management of these diseases.

摘要

在澳大利亚确认了三种与植原体相关的番木瓜病害,即枝枯病、黄皱病和花叶病。在一个商业番木瓜种植园内,从60株雌株群体中,连续8个月每周采集未成熟叶片材料,以确定感染与症状表现之间的最短时间。使用聚合酶链反应(PCR),采用针对一般植原体以及针对植原体 stolbur 组的特异性引物,检测植原体DNA。在症状表现前1周(4例)或同一周(9例)检测到与枝枯病相关的植原体,而在花叶症状表现前3至11周检测到植原体DNA(6例)。在15例遭受枝枯病的植株下部茎上,侧枝再生长未能产生 stolbur 特异性PCR产物。另外两例通过限制性片段长度多态性消化诊断为枝枯病与黄皱病或花叶病双重感染,这两例均被解释为由与枝枯病相关的植原体引起的二次感染。在7例黄皱病植株中的3例以及9例花叶病植株中的3例再生长,检测到植原体特异性DNA呈阳性。建议对受枝枯病影响的植株进行宿根处理,并清除受黄皱病或花叶病影响的植株,以管理这些病害。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验