应用昆虫病原真菌 Akanthomyces muscarius 改良 GFP 研究内生菌

Q3 Agricultural and Biological Sciences
G. Mitina, A. Choglokova, Marina A. Cherepanova, S. Timofeev, V. Dolgikh
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引用次数: 0

摘要

Akanthomyces(原Lecanicillium)属昆虫病原真菌(EPF)是最常见和重要的昆虫病原真菌之一,主要感染半翅目吸血昆虫。这种真菌也可以寄生在植物病原真菌(锈病、白粉病)上。据报道,在自然条件下,这些属的昆虫病原体在各种植物中都是内生菌[1-2],有助于提高植物对病原体的免疫力,减少害虫对植物的定植。Akanthomyces lecanii真菌对植物的内生定殖可以抑制桃蚜的生长[3]。Akanthomyces muscarius菌株在食用被真菌定殖的卷心菜时导致飞蛾死亡[4]。采用绿色荧光蛋白荧光标记的A. muscarius (= Lecanicillium muscarium)菌株Vl 72-GFP评估内生特性[5]。利用含有eGFP基因的pBARGPE1载体电穿孔高毒力“野生”菌株Vl 72的萌发分生孢子,在不影响真菌生长和毒力的情况下表达荧光蛋白。以108孢子/ml的分生孢子悬浮液处理蚕豆叶片、无菌土壤和种子,研究了真菌对蚕豆生长速率的影响。第7天,将种子浸泡在真菌的孢子悬浮液中,观察到豆茎和根的生长受到刺激。喷叶时,只观察到茎伸长。被研究的菌株不规则地在豆类上定植。在处理种子时,真菌从根中分离出来的数量更多(26%),在喷洒叶子时从茎中分离出来(36%),在浇水时也从茎中分离出来(43%)。洒土侵染蕈类植物的效果最好。在蚜虫植物定殖14天后,内生作用对蚜虫数量没有影响。在圣彼得堡植物园的温室中,通过对开花作物(大蕉、非洲菊、棘果)土壤的脱落,将Vl 72-GFP菌株的孢子引入,一个月后从棘果叶片中分离出该菌株,证实了该菌株在温室条件下对植物的内生定殖能力。在AxioImager M1荧光显微镜上对该植物菌丝Vl 72-GFP进行分析,发现其荧光水平与在培养基上生长的a.m uscarius菌丝相同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The application of the entomopathogenic fungus Akanthomyces muscarius modified GFP to study endophytization
Entomopathogenic fungi (EPF) of the genus Akanthomyces (formerly Lecanicillium) are one of the most common and important fungal entomopathogens, infecting sucking insects of the order Hemiptera mainly. The fungi can also parasitize on phytopathogenic fungi (rust, powdery mildew). The entomopathogens from these genera reported as endophytes in various plants under natural conditions [1–2], contributing to an increase in plant immunity to pathogens, as well as a decrease in plant colonization by pests. Endophytic colonization of plants by the fungus Akanthomyces lecanii can suppress the growth of the peach aphid [3]. Akanthomyces muscarius strains caused the death of moth when feeding on cabbage colonized by the fungus [4]. Endophytic properties were assessed using the A. muscarius (= Lecanicillium muscarium) strain Vl 72-GFP fluorescently labeled with GFP [5]. The transformation was done by electroporation of germinated conidia of the high-virulent “wild” strain Vl 72 by the pBARGPE1 vector harboring an eGFP gene, showed an expression of fluorescent protein without affecting fungal growth and virulence. The influence of the fungus on the growth rates of beans was revealed when leaves, sterile soil and seeds were treated with a suspension of conidia of 108 spores/ml. On the 7th day, stimulation of the growth of the stems and roots of the beans was observed when the seeds were soaked in a spore suspension of the fungus. When spraying the leaves, only the stem’s elongation was observed. The studied strain colonizes beans irregularly. When treating the seeds, the fungus was isolated in greater quantities from the roots (26%), when spraying the leaves — from the stem (36%), when watering the soil — also from the stem (43%). Infection of A. muscarius plants by spilling the soil was most effective. No effect of endophytization was found on the number of aphids after 14 days of aphid plant colonization. As a result of the introduction of the spores of Vl 72-GFP strain by shedding the soil under flower crops (lantana, gerbera, acanthus) in the greenhouse of Saint Petersburg Botanical Garden, this strain was isolated from the leaves of the Acanthus mollis L. after one month, which confirms the ability of this species to endophytic colonization of plants in greenhouse conditions. Analysis of hyphae Vl 72-GFP in the plant performed on an AxioImager M1 fluorescent microscope demonstrated the same level of fluorescence as in A. muscarius hyphae growing on the media.
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来源期刊
Ecological genetics
Ecological genetics Environmental Science-Ecology
CiteScore
0.90
自引率
0.00%
发文量
22
期刊介绍: The journal Ecological genetics is an international journal which accepts for consideration original manuscripts that reflect the results of field and experimental studies, and fundamental research of broad conceptual and/or comparative context corresponding to the profile of the Journal. Once a year, the editorial Board reviews and, if necessary, corrects the rules for authors and the journal rubrics.
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