黄萎病菌培养适宜营养培养基的选择

G. Volkova, Y. Yakhnik, O. Kremneva, E. N. Merzlikina
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引用次数: 0

摘要

网斑病(Pyrenophora teres Drechsler)是世界范围内大麦叶病的主要致病复合体。研究控制半生物营养真菌的各种方法需要精心制备和开发足够数量的致病接种物。本研究的目的是选择合适的营养培养基,以获得具有最大侵袭性参数(菌落生长率、产孢量、潜伏期短)和制备过程中符合人体工程学的球芽甘蓝接种物。采用胡萝卜-甜菜琼脂(CBA)、马铃薯-葡萄糖琼脂(PGA)和Czapek培养基作为标准方法和培养条件。每种培养基筛选10株菌株,各实验变异间差异有统计学意义。结果表明,在胡萝卜-甜菜琼脂培养基上培养第6天,可获得生长速率(5.3±0.5 mm/d)、菌落直径(53.4±1.1 mm)、潜伏期(4 d)、产孢强度(4100个分生孢子/ 1 ml)等适宜的参数组合。在马铃薯-葡萄糖琼脂培养基上培养时,真菌的生长速度(5.2±0.8 mm/d)、菌落直径(52.0±2.9 mm)、产孢强度(3700个分生孢子/ 1 ml)较高,潜伏时间最长,第6天开始产孢。在使用标准Czapek培养基的情况下,P. teres分离株的侵袭性最低(生长速度- 3.2±0.3 mm/d;菌落直径- 31.6±1.9 mm;潜伏期- 1杯第4天出现孢子;产孢强度为500个分生孢子/ 1 ml。值得注意的是,在胡萝卜-甜菜琼脂上菌落的形态类型范围更大,包括在其他培养基上生长的分离株的形态类型。几乎所有在CBA培养基上培养的实验变异体菌丝体结构清晰,颜色深,表明培养基中营养物质的可利用性充足。因此,在使用标准培养方法时,为了获得具有最大侵袭性参数和较低人工成本的红鲌接种物,使用胡萝卜-甜菜琼脂是合理的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SELECTION OF APPROPRIATE NUTRIENT MEDIUM FOR CULTIVATION OF PYRENOPHORA TERES DRECHSLER
Net blotch (Pyrenophora teres Drechsler) is the dominant pathogenic complex of barley leaf diseases worldwide. The study of various methods of controlling hemibiotrophic fungus requires careful preparation and development of a sufficient amount of pathogenic inoculum. The aim of our research was to select appropriate nutrient medium for obtaining P. teres inoculum with maximum aggressiveness parameters (colony growth rate, sporulation, short latency period) and ergonomics in preparation. Three nutrient media were used: carrot-beet agar (CBA), potato-glucose agar (PGA), Czapek's medium for standard methods and cultivation conditions. The selection consisted of 10 isolates for each nutrient medium and had statistically significant differences among the experimental variants. It was found that appropriate combination of parametres such as growth rate (5.3±0.5 mm/day), colony diameter (53.4±1.1 mm), latent period (4 days), sporulation intensity (4100 conidia in 1 ml) was observed in case of cultivation of P. teres isolates on carrot-beet agar on the 6th day. When cultivating the fungus on potato-glucose agar, rather high growth rates (5.2±0.8 mm/day), colony diameter (52.0±2.9 mm), sporulation intensity (3700 conidia per 1 ml) were revealed, the latent period was the longest among the studied variants, the first sporulation was detected on the 6th day. In case of usage of the standard Czapek medium, the minimum aggressiveness of P. teres isolates was revealed (growth rate - 3.2 ± 0.3 mm/day; colony diameter - 31.6 ± 1.9 mm; latent period - spores were revealed on the 4th day in 1 cup; the intensity of sporulation was 500 conidia per 1 ml). It was noted that there is a larger range of morphological types of colonies on carrot-beet agar, including morphotypes of isolates which grow on other media. Almost all experimental variants cultivated on CBA medium had a clear structured mycelium with a dark color, which indicates a sufficient availability of nutrients in the culture medium. Thus, it is reasonable to use carrot-beet agar in order to obtain P. teres inoculum with maximum aggressiveness parameters and low labor costs when using standard cultivation methods.
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