In vitro Propagation of Phytoplasma-Free Strawberry Plants and Molecular Characterization of the Pathogen

S. Mokbel, A. Kheder
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引用次数: 1

Abstract

Multiplication of strawberry plants in tissue culture has advantages as reduced exposure to many insects and several various diseases. During 2019 growing season, strawberry (Fragaria x ananassa Duchesne cv. Festival) plants showing phyllody fruit symptoms, in which petals and sepals become leaf-like, were detected in planting fields in Ismailia governorate, Egypt. Phytoplasma associated with phyllody of fruit in strawberry plants was detected using phytoplasma universal primers, accurately identified at the molecular level, and the DNA sequence has been deposited in GenBank under accession number MT757900 with Isolate name SAMA. DNA from all symptomatic plants yielded PCR products of 1278 bp, whereas DNA from asymptomatic plants collected in the field yielded no products. The phylogenetic analysis of the 16S rDNA sequence of SAMA-isolate indicated that the 16S rDNA gene shared 100% identity with StrawbPhF-isolate classified in a group 16SrI (AY102275) that belonged to new subgroup R. Meristems (0.1-0.3 mm in size) were excised from the terminal and axillary buds of the strawberry-runners and then cultured on hormone-free medium. The two sizes (0.2 mm and 0.3 mm) of meristem had pronounced effects on the phytoplasma elimination (100%), and survival rates (66.6 % and 90%, respectively), but the smaller size of meristem had a deleterious effect to survival rate (0%). After approximately seven months and a half, rooted plantlets raised from meristem culture were confirmed for phytoplasma-free by a nested PCR assay. Therefore, the production of strawberry plantlets that needs no examination for their phytoplasma infection could be expected by applying the meristem culture method.
草莓无植浆体植株的离体繁殖及病原菌的分子特性研究
草莓植株在组织培养中繁殖的优点是减少了对许多昆虫和几种疾病的暴露。在2019年的生长季节,草莓(Fragaria x ananassa Duchesne cv。在埃及伊斯梅利亚省的种植地里发现了显示叶状果实症状(花瓣和萼片变成叶子状)的节日植物。利用植原体通用引物对草莓果实叶状学相关的植原体进行了检测,在分子水平上进行了准确的鉴定,DNA序列已存入GenBank,登录号为MT757900,分离物名称为SAMA。所有有症状植物的DNA都产生了1278 bp的PCR产物,而从田间收集的无症状植物的DNA没有产生产物。对sama分离物的16S rDNA序列进行系统发育分析,结果表明,该分离物的16S rDNA基因与隶属于新亚群r的16SrI (AY102275)群中的strawbphf分离物具有100%的同源性。0.2 mm和0.3 mm两种大小的分生组织对植原体消除率(100%)和成活率(66.6%和90%)均有显著影响,但较小大小的分生组织对成活率的影响较小(0%)。大约7个半月后,分生组织培养的有根植株通过巢式PCR检测证实无植物原体。因此,应用分生组织培养法可以生产出不需要进行植原体感染检测的草莓植株。
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