杨梅优良基因型对毛角鼻虫的遗传抗性

Dawa Méndez-Álvarez, Yorleny Badilla-Valverde, Olman Murillo-Gamboa, Rafael Ferreira Alfenas
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介绍。在哥斯达黎加,据报道,由毛状角鼻虫引起的一种疾病在该国种植面积第二大的森林树种小木兰花(melina arborea)的商业种植园中发病率接近40%。因此,迫切需要探索对这种病原体具有抗性的遗传物质。目标。目的评价两种不同的菌根接种方法及其对melina优良基因型的影响,为国际森林遗传改良合作组织GENFORES melina遗传改良项目提供参考。材料和方法。在哥斯达黎加圣克拉拉,圣卡洛斯的温室条件下,利用CIF 001分离物建立了C. fibriata的致病性试验。2019年10月至2020年1月,对5个优秀基因型的两种接种方法进行了评估。通过测定植株的总高、基部直径、叶片数、发病率和内伤来评价病原菌的影响。评估分别在30、60、90和120天进行。结果。从第38天开始观察到死亡率,到第120天死亡率达到26.7%。固体培养基处理的发病率最高。基因型15N和58对CIF 001表现出高敏感性,而基因型1和57表现出高耐受性。综上所述,可以在90 d后对黑螺旋体的致病性进行评价。结论。用固体培养基接种黑螺旋体(CIF - 001)是最有效的方法。评估显示需要在接种后至少90天评估结果。根据内部病变的分析,基因1型被确定为对病原体的影响具有高度抗性。将该基因型纳入评估技术将大大提高对病原体耐受性的评估方案。
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Genetic resistance to Ceratocystis fimbriata in elite genotypes of Gmelina arborea
Introduction. In Costa Rica, an incidence of nearly 40 % has been reported for a disease caused by Ceratocystis fimbriata in commercial plantations of Gmelina arborea (melina), which is the second most widely planted forest tree species in the country. Consequently, there is a pressing need to explore genetic material that exhibit resistance to this pathogen. Objective. To evaluate two methods of C. fimbriata inoculation and their effect on elite genotypes of melina, for their use within the melina genetic improvement program at the international forest genetic improvement cooperative GENFORES. Materials and methods. A pathogenicity test was established using the CIF 001 isolate of C. fimbriata under greenhouse conditions, in Santa Clara, San Carlos, Costa Rica. Two inoculation methods were evaluated in five elite genotypes from October 2019 to January 2020. The effect of the pathogen was evaluated by measuring total height development, basal diameter, number of leaves, incidence, and internal injury within the plant. The assessment was conducted at 30, 60, 90, and 120 days. Results. Mortality was observed from day 38 and reached an incidence of 26.7 % at 120 days. The treatment using solid medium displayed the highest incidence percentage. Genotypes 15N and 58 exhibited high susceptibility to the CIF 001 isolate, whereas genotypes 1 and 57 exhibited high tolerance. Based on the results, it was determined that the pathogenicity test of C. fimbriata on melina can be evaluated at 90 days. Conclusion. Solid medium was the most effective method for inoculating melina with C. fimbriata (isolate CIF 001). Evaluations showed the need to assess results at least 90 days after inoculation. Based on the analysis of the internal lesion, genotype 1 was identified as highly resistant to the effect of the pathogen. The inclusion of this genotype as an evaluation technique will substantially enhance the protocol for assessing tolerance to the pathogen.
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