肯尼亚谷子稻瘟霉多样性及致病性的研究

Jayo Manyasi Tracyline, P. Kimurto, J. Mafurah
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摘要

稻瘟病菌的鉴定是物种分化和了解其病理系统、进化和多样性的先决条件。本研究的目的是确定稻瘟病菌分离株的形态变异、致病菌毒力和分子多样性。2019年在Bomet、Nakuru、Baringo、Busia和machaos县采集了5株受感染的指谷穗分离株。样品在实验室中培养,用于表征和制备孢子悬浮液。形态学表征数据包括菌落直径、分生孢子颜色和形状。采用kne741基因型、易感基因型和疾病数据评分,采用随机完全区组设计在温室中进行致病性试验。分子鉴定涉及使用7个SSR标记。数据分析包括使用AUDPC、Power Maker、GeneAlex和Darwin等软件。结果表明,稻瘟病菌分离株在菌落颜色、菌落直径和分生孢子形状等方面具有不同的生长模式。致病性试验显示,各位点对试验基因型的毒力差异极显著(P<0.01)。生理成熟时,Koibatek和Bomet品系的颈瘟病表现突出,而Bomet和Alupe品系的叶瘟病表现严重。分子分析结果显示,na范围为1.30 (MGM 437) ~ 1.99 (Pyrm 61 ~ 62),平均为1.71。引物MGM 437和Pyrm 61 ~ 62的PIC变化范围分别为0.20 ~ 0.37。析因分析和系统发育分析表明,稻瘟病菌分离株具有多样性,没有地理分组。AMOVA分析表明,多样性发生在种群内(87%),而不是种群间(13%)。研究中发现的稻瘟病菌高变异性清楚地表明,在肯尼亚主要种植区收集的菌株之间存在高性重组。关键词:多样性,形态,致病性,稻瘟病菌
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Characterization of diversity and pathogenecity of Pyricularia grisea affecting finger millet in Kenya
Pyricularia grisea characterization is a prerequisite for species differentiation and understanding of the pathosystem, evolution and diversity of species. The aim of this study is to determine the morphological variation, pathogen virulence and molecular diversity of P. grisea isolates. Five isolates from infected heads of finger millet were collected from Bomet, Nakuru, Baringo, Busia and Machakos counties in 2019. The samples were cultured in the lab for both characterization and spore suspension preparation. Data on morphological characterization included colony diameter, color and shape of conidia. Pathogenicity test was done in the greenhouse in a randomized complete block design using KNE 741, a susceptible genotype and disease data scored. Molecular characterization involved the use of seven SSR markers. Data analyses included use of softwares such as AUDPC, Power Maker, GeneAlex and Darwin. Results showed that P. grisea isolates had different growth pattern with respect to color, colony diameter and conidia shape. Pathogenicity test revealed that all sites had significant different (P<0.01) virulence on the test genotype. Neck blast, scored at physiological maturity was prominent in Koibatek and Bomet strains while leaf blast was severe in Bomet and Alupe strains. Molecular analysis showed that ENA ranged from 1.30 (MGM 437) -1.99 (Pyrm 61-62) with an average of 1.71. PIC varied between 0.20-0.37 for primers MGM 437 and Pyrm 61-62, respectively. Factorial and phylogenetic analysis revealed that P. grisea isolates were diverse with no geographical grouping. AMOVA indicated diversity occurred within populations (87%) as opposed to among populations (13%). The high P. grisea variability found in the study is a clear indication of the high sexual recombination among strains collected in major growing areas of Kenya.   Key words: Diversity, morphology, pathogenecity, Pyricularia grisea.
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