Identification of phytoplasmas associated with a decline of European hackberry (Celtis australis)

被引:21
作者
Bertaccini, A [1 ]
Mittempergher, L [1 ]
Vibio, M [1 ]
机构
[1] CNR, CTR STUDIO PATOL SPECIE LEGNOSE MONTANE, I-50144 FLORENCE, ITALY
关键词
Celtis australis; decline; phytoplasma; polymerase chain reaction; restriction fragment length polymorphism;
D O I
10.1111/j.1744-7348.1996.tb07320.x
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
The presence of phytoplasmas in declining trees of European hackberry was demonstrated for the first time using polymerase chain reaction assays with primers amplifying phytoplasma 16S rDNA regions. Restriction fragment length polymorphism analysis of these DNA fragments together with PCR, employing primers specific for particular phylogenetic groups of phytoplasmas, made it possible to detect the presence of aster yellows group (16SrI) related phytoplasmas. These were classified into two different subgroups (I-B and I-C) and were present in both symptomatic and asymptomatic hackberry plants. Aster yellows-related phytoplasmas were found in all the root samples collected during the winter, In addition, phytoplasmas from the peach X disease group (16SrIII) were found in four out of 10 root samples; in live root samples phytoplasmas of the elm yellows group (16SrV) were also present.
引用
收藏
页码:245 / 253
页数:9
相关论文
共 29 条
[1]  
AHRENS U, 1994, EUR J FOREST PATHOL, V24, P55
[2]  
Anselmi N., 1980, Informatore Fitopatologico, V30, P11
[3]  
Bertaccini A., 1995, Phytopathologia Mediterranea, V34, P137
[4]  
CHA B, 1991, Arboricultural Journal, V15, P323
[5]  
CONTI M, 1987, P 7 C MED PHYT UN GR, P202
[6]   CLUSTER-SPECIFIC POLYMERASE CHAIN-REACTION AMPLIFICATION OF 16S RDNA SEQUENCES FOR DETECTION AND IDENTIFICATION OF MYCOPLASMALIKE ORGANISMS [J].
DAVIS, RE ;
LEE, IM .
PHYTOPATHOLOGY, 1993, 83 (09) :1008-1011
[7]  
KIRKPATRICK BC, 1990, INT J MED MICROB A S, V20, P288
[8]  
LEDERER W, 1991, EUR J FOREST PATHOL, V21, P90
[9]  
Lee I. M., 1988, Molecular Plant-Microbe Interactions, V1, P303, DOI 10.1094/MPMI-1-303
[10]   USE OF MYCOPLASMALIKE ORGANISM (MLO) GROUP-SPECIFIC OLIGONUCLEOTIDE PRIMERS FOR NESTED-PCR ASSAYS TO DETECT MIXED-MLO INFECTIONS IN A SINGLE HOST-PLANT [J].
LEE, IM ;
GUNDERSEN, DE ;
HAMMOND, RW ;
DAVIS, RE .
PHYTOPATHOLOGY, 1994, 84 (06) :559-566