Jomantiene R, Davis R E, Maas J, Dally E L
Molecular Plant Pathology Laboratory, Agricultural Research Service-USDA, Beltsville, MD 20705, USA.
Int J Syst Bacteriol. 1998 Jan;48 Pt 1:269-77. doi: 10.1099/00207713-48-1-269.
Strawberry plants exhibiting symptoms of stunting and abnormally small leaves were observed in production fields in central Florida, USA. Since the symptoms were suggestive of phytoplasma infection, plants were assayed for presence of phytoplasma by PCR amplification of 16S rDNA and ribosomal protein (rp) gene sequences. Amplification of phytoplasma-specific DNA sequences by PCR indicated infection of the diseased strawberry plants by phytoplasmas. RFLP analyses of amplified 16S rDNA revealed that the plants were infected by two mutually distinct phytoplasmas that differed from strawberry green petal phytoplasma (group 16Srl-C). Both phytoplasmas were members of 16S rRNA gene group I (16Srl). Based on RFLP analysis of amplified 16S rDNA and rp gene sequences, one was classified in group 16Srl subgroup I and new rp subgroup 16Srl-l(rp); its 16S rRNA-rp subgroup was designated 16Srl-K(rr-rp). The second phytoplasma represented a previously undescribed subgroup, designated K, in 16S rRNA group I but belonged to rp subgroup 16Srl-J(rp); this phytoplasma's 16S rRNA-rp subgroup was designated 16Srl-J(rr-rp). Results of RFLP analyses agreed with putative restriction site maps based on nucleotide sequences determined for the amplified 16S rDNAs and rp gene operon DNAs. Further evidence indicated that the 16Srl-K(rr-rp) strawberry phytoplasma, Mexican periwinkle virescence phytoplasma and stolbur phytoplasma shared sequence homologies that enabled amplification of DNA from all three by PCR using primers previously designed as stolbur-specific.
在美国佛罗里达州中部的生产田中,观察到草莓植株出现发育迟缓以及叶片异常小的症状。由于这些症状提示可能感染了植原体,因此通过对16S rDNA和核糖体蛋白(rp)基因序列进行PCR扩增,来检测植株中是否存在植原体。PCR扩增植原体特异性DNA序列表明,患病草莓植株已被植原体感染。对扩增的16S rDNA进行RFLP分析显示,这些植株感染了两种互不相同的植原体,它们与草莓绿瓣植原体(16Srl - C组)不同。这两种植原体均为16S rRNA基因I组(16Srl)的成员。基于对扩增的16S rDNA和rp基因序列的RFLP分析,其中一种被归类为16Srl亚组I和新的rp亚组16Srl - I(rp);其16S rRNA - rp亚组被命名为16Srl - K(rr - rp)。第二种植原体代表了16S rRNA I组中一个先前未描述的亚组,命名为K,但属于rp亚组16Srl - J(rp);该植原体的16S rRNA - rp亚组被命名为16Srl - J(rr - rp)。RFLP分析结果与基于扩增的16S rDNAs和rp基因操纵子DNA测定的核苷酸序列推测的限制性酶切位点图谱一致。进一步的证据表明,16Srl - K(rr - rp)草莓植原体、长春花变绿植原体和帚状植原体具有序列同源性,使用先前设计为帚状植原体特异性的引物通过PCR可从这三种植原体中扩增出DNA。