中国羊肚菌栽培真菌病害的流行鉴定

Xiaofei Shi, Dong Liu, Xinhua He, Wei Liu, Fuqiang Yu
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摘要

真正的羊肚菌(Morchella, Pezizales)是世界著名的食用菌(ascocarps),在国际市场上需求量很大。自2012年以来,羊肚菌在中国已成功人工培育,并迅速成为一个新的食用菌产业,在2021-2022年期间占地16466公顷。然而,每年有近25%的种植面积遭受真菌疾病。虽然已经报道了各种各样的羊肚菌致病真菌,但它们的流行特征尚不清楚,特别是在区域或国家范围内。本文对中国18个省32个地点的morel ascocarp病变进行了ITS扩增子测序和显微镜检查。结果表明:Diploöspora长孢子菌(75.48%)、梭氏梭菌(5.04%)、gamsimortierella(0.83%)、amoeboidea Mortierella(0.37%)和kongipenicillium(0.15%)是推定的病原真菌。所有子囊上均可见长卵形的分生孢子。在高ITS reads丰度的茄茄菌感染样品中还检测到卵圆形的无性孢子和产孢结构,如Clonostachys孢子。从7个子囊皮损中分离到7株长孢子虫。这些分离物的纯培养物的显微特征与子囊蛇皮病变的形态学特征一致。Diploöspora longispora在93.75%的样品中扩增丰度最高,而C. solani在其余2个采样点的6个生物样品中扩增丰度最高(6.25%)。结果表明,长孢霉是羊粪真菌病害的主犯。其他低丰度的非宿主真菌似乎是在长孢霉感染后的腐生真菌。本研究为虫草真菌病害的形态学和分子鉴定及防治提供了依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Epidemic Identification of Fungal Diseases in <i>Morchella</i> Cultivation across China.

Epidemic Identification of Fungal Diseases in <i>Morchella</i> Cultivation across China.

Epidemic Identification of Fungal Diseases in <i>Morchella</i> Cultivation across China.

Epidemic Identification of Fungal Diseases in Morchella Cultivation across China.

True morels (Morchella, Pezizales) are world-renowned edible mushrooms (ascocarps) that are widely demanded in international markets. Morchella has been successfully artificially cultivated since 2012 in China and is rapidly becoming a new edible mushroom industry occupying up to 16,466 hectares in the 2021-2022 season. However, nearly 25% of the total cultivation area has annually suffered from fungal diseases. While a variety of morel pathogenic fungi have been reported their epidemic characteristics are unknown, particularly in regional or national scales. In this paper, ITS amplicon sequencing and microscopic examination were concurrently performed on the morel ascocarp lesions from 32 sites in 18 provinces across China. Results showed that Diploöspora longispora (75.48%), Clonostachys solani (5.04%), Mortierella gamsii (0.83%), Mortierella amoeboidea (0.37%) and Penicillium kongii (0.15%) were the putative pathogenic fungi. The long, oval, septate conidia of D. longispora was observed on all ascocarps. Oval asexual spores and sporogenic structures, such as those of Clonostachys, were also detected in C. solani infected samples with high ITS read abundance. Seven isolates of D. longispora were isolated from seven selected ascocarps lesions. The microscopic characteristics of pure cultures of these isolates were consistent with the morphological characteristics of ascocarps lesions. Diploöspora longispora had the highest amplification abundance in 93.75% of the samples, while C. solani had the highest amplification abundance in six biological samples (6.25%) of the remaining two sampling sites. The results demonstrate that D. longispora is a major culprit of morel fungal diseases. Other low-abundance non-host fungi appear to be saprophytic fungi infecting after D. longispora. This study provides data supporting the morphological and molecular identification and prevention of fungal diseases of morel ascocarps.

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