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A method to induce significant production of conidia from Monilinia fructigena, Monilia polystroma, and Monilia yunnanensis

机译:一种诱导大果念珠菌,多生念珠菌和云南念珠菌分生孢子大量产生的方法

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Brown rot, caused by Monilinia fructicola, Monilinia fructigena, Monilinia laxa, Monilia polystroma, and Monilia yunnanensis, is an important disease of stone and pome fruits. The conidia of these fungi commonly form on infected tissues and serve as the main inoculum source throughout the growing season. Epidemiological research, such as fruit inoculation, often requires a large quantity of inocula. However, the sporulation of M. fructigena, M. polystroma, and M. yunnanensis on artificial media is inferior to that of M. fructicola and M. laxa. In this study we compared the sporulation of these species on potato dextrose agar (PDA), cherry juice agar (CA), oatmeal tomato agar (OTA), rye tomato juice agar (RTA) and apple fruits, and developed an efficient conidial production method on PDA for these fungi. In this method, a regular PDA plate was inoculated by spreading mycelial fragments of the fungi on the surface and incubated at 22 A degrees C for approximately 2.5 days in the dark. Then, the mycelia were scraped and washed off using sterilized distilled water. The surface of the medium was then covered with two layers of gauze and incubated at 22 A degrees C for between 36 and 48 h. Without scraping, the range of sporulation on PDA per plate was sparse to 10(3) conidia, while with scraping it increased to 10(6)-10(7) conidia per plate. On apple fruit, the range of sporulation was sparse to 10(5) conidia per fruit depending on the isolates used. This scraping method led to the abundant production of conidia from brown rot fungi on the medium.
机译:褐腐病(Monilinia fructicola),Monilinia fructigena,Monilinia laxa,Monilia polystroma和云南Monilia引起的腐烂病是核果和石榴果实的重要病害。这些真菌的分生孢子通常在受感染的组织上形成,并在整个生长季节中充当主要的接种源。诸如水果接种之类的流行病学研究通常需要大量接种。但是,M。fructigena,M. polystroma和M. yunnanensis在人工培养基上的孢子形成次于M. fructicola和M. laxa。在这项研究中,我们比较了马铃薯葡萄糖琼脂(PDA),樱桃汁琼脂(CA),燕麦番茄琼脂(OTA),黑麦番茄汁琼脂(RTA)和苹果果实上这些物种的孢子形成,并开发了一种有效的分生孢子生产方法在PDA上用于这些真菌。在这种方法中,通过在表面上散布真菌的菌丝体片段来接种常规的PDA平板,并在黑暗中于22 A孵育约2.5天。然后,刮除菌丝体,并用无菌蒸馏水洗净。然后用两层纱布覆盖培养基表面,并在22 A摄氏度下孵育36至48小时。在不刮擦的情况下,每块板上PDA的孢子形成范围稀疏到10(3)分生孢子,而在刮擦时,每块板上的孢子形成范围增加到10(6)-10(7)分生孢子。在苹果果实上,孢子形成的范围稀疏至每个果实10(5)分生孢子,具体取决于所使用的分离物。这种刮擦方法导致培养基上的褐腐真菌大量生产分生孢子。

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