Ji Pingsheng, Allen Caitilyn, Sanchez-Perez Amilcar, Yao Jian, Elphinstone John G, Jones Jeffrey B, Momol M Timur
North Florida Research and Education Center, University of Florida, IFAS, Quincy 32351.
Department of Plant Pathology, University of Wisconsin-Madison, 53706.
Plant Dis. 2007 Feb;91(2):195-203. doi: 10.1094/PDIS-91-2-0195.
In 2003 and 2004, 15 isolates of Ralstonia solanacearum were obtained from wilting plants of field-grown pepper (Capsicum annuum) in south Florida and from pot-grown hydrangea (Hydrangea paniculata and H. macrophylla) and geranium (Pelargonium × hortorum) in commercial nurseries and retention ponds in north Florida. Diagnostic immunoassays and polymerase chain reaction (PCR) analyses identified all the isolates as R. solanacearum but not race 3 biovar 2. Pathogenicity studies on tomato, pepper, and tobacco revealed that all 15 strains had similar high virulence on tomato and all caused wilting of tobacco, although there were significant differences among the strains in aggressiveness on tobacco. An indigenous Florida tomato strain, race 1 biovar 1 (Rs5), caused no disease on tobacco and little or none on pepper. The three pepper strains were more aggressive than Rs5 or two hydrangea strains on all three pepper cultivars studied. Phylogenetic analysis based on an endoglucanase gene sequence indicated that these strains had three distinct origins. The three pepper strains belonged to phylotype I biovar 3 and clustered with strains from diverse hosts in Asia belonging to sequevar 13. The six geranium strains and four of the hydrangea strains were closely related to strains in sequevar 5, a distinct subcluster of phylotype II biovar 1 strains isolated from the French West Indies and Brazil. Two other biovar 1 strains from hydrangea and strains K60, AW, and Rs5 belonged to sequevar 7 in phylotype II and probably are native to North America. None of the Florida isolates belong to the highly regulated Select Agent race 3 biovar 2 subgroup, according to both the DNA sequence analysis and the biovar phenotypic test results. However, the race 3 biovar 2-specific B2 primers weakly amplified a product from some race 1 biovar 1 strains in real-time PCR, indicating that this assay may give false positives under some conditions. Given the high cost of a misdiagnosis, it seems advisable to use at least two independent diagnostic methods to confirm that a suspect isolate is R. solanacearum R3B2. This is the first report of the presence of R. solanacearum race 1 biovar 3 or phylotype I strains in North America, and the first report confirming R. solanacearum causing natural infection of hydrangea in Florida. Thus, R. solanacearum strains that are quite distinct from presumably indigenous strains are present and can infect diverse hosts in Florida.
2003年和2004年,从佛罗里达州南部田间种植的辣椒(辣椒属)萎蔫植株以及佛罗里达州北部商业苗圃和滞留池塘中盆栽的绣球花(圆锥绣球和大叶绣球)和天竺葵(天竺葵属)上获得了15株青枯雷尔氏菌分离株。诊断免疫分析和聚合酶链反应(PCR)分析确定所有分离株均为青枯雷尔氏菌,但不是3号小种2型生物变种。对番茄、辣椒和烟草的致病性研究表明,所有15个菌株对番茄均具有相似的高毒力,并且都能导致烟草萎蔫,尽管这些菌株在对烟草的侵袭力上存在显著差异。佛罗里达州本地的一个番茄菌株,1号小种1型生物变种(Rs5),对烟草不致病,对辣椒致病轻微或不致病。在所研究的所有三个辣椒品种上,三个辣椒菌株比Rs5或两个绣球花菌株更具侵袭力。基于内切葡聚糖酶基因序列的系统发育分析表明,这些菌株有三个不同的起源。三个辣椒菌株属于I型菌系3型生物变种,与亚洲不同寄主的属于序列变种13的菌株聚类。六个天竺葵菌株和四个绣球花菌株与序列变种5中的菌株密切相关,序列变种5是从法属西印度群岛和巴西分离的II型菌系1型生物变种的一个独特亚群。另外两个来自绣球花的1型生物变种菌株以及K60、AW和Rs5菌株属于II型菌系中的序列变种7,可能原产于北美。根据DNA序列分析和生物变种表型测试结果,佛罗里达州的分离株均不属于高度受管制的选择性病原体3号小种2型生物变种亚群。然而,3号小种2型特异性B2引物在实时PCR中从一些1号小种1型生物变种菌株中微弱扩增出一个产物,表明该检测在某些条件下可能会产生假阳性。鉴于误诊成本高昂,似乎建议至少使用两种独立的诊断方法来确认可疑分离株为青枯雷尔氏菌R3B2。这是北美首次报道存在青枯雷尔氏菌1号小种3型或I型菌系菌株,也是首次报道确认青枯雷尔氏菌在佛罗里达州导致绣球花自然感染。因此,与推测的本地菌株截然不同的青枯雷尔氏菌菌株在佛罗里达州存在,并且可以感染多种寄主。