請用此 Handle URI 來引用此文件: http://hdl.handle.net/11455/81012
標題: Development+of+a+Medium+for+Detecting+Ophiostoma+querci+on+China+Fir+and+Its+Application
廣葉杉萎凋病菌的偵測培養基研發與應用
作者: Wu, Yi-Yan
吳宜晏
Lin, Tsung-Chun
Jian, Israel Bau-Jen
Liao, Tien-Szu
Huang, Jenn-Wen
林宗俊
姜保真
廖天賜
黃振文
關鍵字: ITS
選擇性培養基
LLCFC medium
ITS
Ophiostoma querci
Selective medium
廣葉杉萎凋病菌
Ophiostoma querci
LLCFC培養基
出版社: 臺中巿: 國立中興大學農學院
摘要: A semiselective medium, Leionian-lactosecasein-flutolanil-cyclohexmide (LLCFC) medium, for detecting Ophiostoma querci, the causal agent of China fir wilt, was developed in this study. The LLCFC medium consisting of 6.25g malt extract, 1.25g K2HPO4, 0.625g MgSO4, 5g lactose, 1g casein, 20g agar, 200mg/L flutolanil, 100mg/L cycloheximide and 100mg/L streptomycin sulfate in 1L distilled water was formulated for detecting O. querci. Recovery efficacy of the pathogen was evaluated by introducing spore-infested sawdust into five testing media, namely PDAS, YMCS, YMCSC, MEAC, and LLCFC. LLCFC medium was most effective in detecting the pathogen from the infested sawdust. The infested wood chips baked in the oven at 90℃ for 1 hour or treated separately with five different pesticides for 1 hour were used for the evaluation of the treatment efficacy by the LLCFC medium. The names and concentrations of each pesticide used were Carbendazim 500 mg/L, Benomyl 500 mg/L, Mertect 1000 mg/L, Prochloraz-Mn 250 mg/L and Prochloraz 400 mg/L. Both treatment methods were proved to be effective in controlling the pathogen. In addition, the pathogens isolated by LLCFC medium, were identified and confirmed as O. querci by using a modified Dellaporta Plant DNA Minipreparatio method in combination with the ITS primers (ITS1-F, 5'-CTTGGTCATTTAGAGGAAGTAA-3' and ITS4, 5'-TCCTCCGCTTATTGATATGC-3').
本研究主要目的在於研發廣葉杉萎凋病菌Ophiostoma querci的偵測培養基,首先將麥芽抽出物6.25g、磷酸氫鉀1.25g、硫酸鎂0.625g、乳糖5g、酪蛋白1g、洋菜粉20g及蒸餾水1公升均勻混合,經高溫高壓滅菌(121℃,15lb,15 min.)後,逐一加入福多寧(flutolanil)200 mg/L、亞胺環己酮(cycloheximide)100mg/L及鏈黴素(streptomycin sulfate)100mg/L,即製成偵測本病菌的Leonian-乳糖-酪蛋白-福多寧-亞胺環己酮(LLCFC)培養基。將接種本病原菌的木屑分別置於LLCFC(Leonian-乳糖-酪蛋白-福多寧-亞胺環己酮培養基)、PDAS(在馬鈴薯葡萄糖瓊脂培養基添加200 mg/L鏈黴素)、MEAC(在麥芽萃取物瓊脂培養基添加100 mg/L亞胺環己酮)、YMCS(在酵母及麥芽萃取物瓊脂培養基添加200 mg/L氯黴素與100 mg/L 鏈黴素)及YMCSC(在酵母及麥芽萃取物瓊脂培養基添加200 mg/L氯黴素、100 mg/L鏈黴素及400mg/L亞胺環己酮)等五種培養基平板上,進行評估它們分離本病原菌的效果,結果發現LLCFC培養基偵測本病原菌的效果最佳。進一步利用LLCFC培養基評估乾熱與化學藥劑處理木片防治本病原菌的效果,發現以高溫處理病原菌孢子懸浮液(50℃)或帶菌木片(90℃),可有效抑制病原菌的生長。此外,以貝芬替500mg/L、免賴得500 mg/L、腐絕1000 mg/L、撲克拉錳250 mg/L 及撲克拉400 mg/L 等五種化學藥劑處理帶菌木片一小時後,亦可有效抑制病原菌的存活。此外,以修正之Dellaporta PlantDNA Minipreparation 法搭配ITS引子對(ITS1-F,5’-CTTGGTCATTTAGAGGAAGTAA-3’及ITS4,5’-TCCTCCGCTTATTGATATGC-3’),證實LLCFC培養基分離到的菌類確為O.querci。
URI: http://hdl.handle.net/11455/81012
顯示於類別:第60卷 第03期
農業暨自然資源學院

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