Rayamajhi M B, Pratt P D, Klopfenstein N B, Ross-Davis A L, Rodgers L
USDA-ARS, Invasive Plant Research Laboratory, Fort Lauderdale, FL.
USDA Forest Service, Rocky Mountain Research Station, Moscow, ID.
Plant Dis. 2013 Oct;97(10):1379. doi: 10.1094/PDIS-03-13-0225-PDN.
Rhodomyrtus tomentosa (Aiton) Hassk. (downy-rose myrtle, family: Myrtaceae), of South Asian origin, is an invasive shrub that has formed monotypic stands in Florida (3). During the winter and spring of 2010 through 2012, a rust disease of epiphytotic proportion was observed on young foliage, stem terminals, and immature fruits of this shrub in natural areas of Martin and Lee counties, Florida. Expanding leaves and succulent stems developed chlorotic flecks on the surface that developed into pustules and ruptured to discharge urediniospores. Symptomatic leaves and stems developed severe necrotic spots and resulted in tissue distortion, defoliation, and stem dieback. Based on symptoms and urediniospore morphology and dimensions (17.7 to 26.1 [22.1 ± 0.3] × 14.7 to 21.1 [17.7 ± 0.2] μm; n = 51) (4), the causal agent was identified as Puccinia psidii Winter; teliospores were not observed in samples since it does not produce these spore stages below 20°C ambient temperature (1). This identification was confirmed by a GenBank BLAST of internal transcribed spacer (ITS) sequences (Accession Nos. KC607876 and KC607877) that showed 99% identity with 42 sequences of P. psidii from diverse host species and locations. P. psidii is believed to be of neotropical origin and has a host range of 129 species in 33 genera within Myrtaceae (2). However, P. psidii caused disease of downy-rose myrtle has not been previously reported in Florida, even though severe infections occurred on another invasive tree, Melaleuca quinquenervia (Cav.) S.F. Blake (3), growing in adjacent areas. In December 2011, urediniospores were collected from downy-rose myrtle, established in aqueous suspension (45,000 spores/ml), and spray inoculated on potted downy-rose myrtle plants (n = 3), which were maintained in 100% ambient humidity, at 20°C, with a 12-h light cycle for 72 h. Plants mock-inoculated with water served as the negative control. Disease symptoms, including chlorotic flecks and raised surfaces, appeared on leaf lamina in 3 to 6 days on P. psidii-inoculated plants, while control plants remained symptomless. Raised surfaces developed into distinct pustules and eventually erupted to discharge urediniospores within 6 to 12 days of inoculation. Tests were repeated once during March and April of 2012 with the same results. The latent and incubation periods reported herein are within the previously reported range for P. psidii (2,4). To our knowledge, this is the first confirmed report of P. psidii epiphytotic on downy-rose myrtle populations in Florida. The recent occurrence of P. psidii epiphytotic on downy-rose myrtle raises critical questions as to why this myrtle rust disease is so severe and widespread on this host after decades of presumed exposure to P. psidii in Florida. Because this rust pathogen has emerged as a major invasive threat to many myrtaceous species around the world, further genotyping and cross-inoculation studies are needed to determine the host specificity and potential origin of the P. psidii isolates derived from downy-rose myrtle (2). References: (1) A. C. Alfenas et al. Australas. Plant Pathol. 32:325, 2003. (2) A. J. Carnegie and J. R. Lidbetter. Australas. Plant Pathol. 41:13, 2012. (3) K. A. Langeland and C. K Burks, eds. Identification and biology of non-native plants in Florida's natural areas. University of Florida, Gainesville, 1998. (4) M. B. Rayachhetry et al. Biol. Contr. 22:38, 2001.
桃金娘(Rhodomyrtus tomentosa (Aiton) Hassk.,桃金娘科,绒毛番樱桃)原产于南亚,是一种入侵灌木,已在佛罗里达州形成单一优势种群(3)。在2010年至2012年的冬季和春季,在佛罗里达州马丁县和李县的自然区域中,这种灌木的幼叶、茎尖和未成熟果实上观察到了具有流行规模的锈病。展开的叶片和多汁的茎干表面出现褪绿斑点,这些斑点发展成脓疱并破裂,释放出夏孢子。有症状的叶片和茎干出现严重的坏死斑点,导致组织变形、落叶和茎干枯死。根据症状以及夏孢子的形态和尺寸(17.7至26.1 [22.1 ± 0.3] × 14.7至21.1 [17.7 ± 0.2] μm;n = 51)(4),确定病原菌为桉叶锈菌(Puccinia psidii Winter);由于该菌在环境温度低于20°C时不产生这些孢子阶段(1),因此在样本中未观察到冬孢子。通过对内部转录间隔区(ITS)序列进行GenBank BLAST(登录号KC607876和KC607877),确认了该鉴定结果,该序列与来自不同寄主物种和地点的42个桉叶锈菌序列显示出99%的同一性。桉叶锈菌被认为原产于新热带地区,寄主范围包括桃金娘科33个属中的129个物种(2)。然而,此前在佛罗里达州,尽管相邻区域生长的另一种入侵树木——五脉白千层(Melaleuca quinquenervia (Cav.) S.F. Blake)(3)受到了严重感染,但桉叶锈菌引起绒毛番樱桃病害的情况尚未见报道。2011年12月,从绒毛番樱桃上采集夏孢子,制成水悬浮液(45,000个孢子/毫升),并喷雾接种到盆栽绒毛番樱桃植株(n = 3)上,这些植株保持在100%的环境湿度、20°C条件下,光照周期为12小时,持续72小时。用水进行模拟接种的植株作为阴性对照。接种桉叶锈菌的植株在3至6天内在叶片上出现了包括褪绿斑点和隆起表面在内的病害症状,而对照植株仍然无症状。隆起表面发展成明显的脓疱,并在接种后6至12天内最终破裂释放出夏孢子。在2012年3月和4月重复进行了测试,结果相同。本文报道的潜伏期和潜育期在桉叶锈菌先前报道的范围内(2,4)。据我们所知,这是佛罗里达州绒毛番樱桃种群上首次确认的桉叶锈菌流行的报道。桉叶锈菌近期在绒毛番樱桃上的流行引发了关键问题,即为何在佛罗里达州假定接触桉叶锈菌数十年后,这种桃金娘锈病在该寄主上如此严重和广泛。由于这种锈病病原菌已成为对全球许多桃金娘科物种的主要入侵威胁,因此需要进一步进行基因分型和交叉接种研究,以确定从绒毛番樱桃分离出的桉叶锈菌菌株的寄主特异性和潜在来源(2)。参考文献:(1)A. C. Alfenas等人,《澳大利亚植物病理学》32:325,2003年。(2)A. J. Carnegie和J. R. Lidbetter,《澳大利亚植物病理学》41:13,2012年。(3)K. A. Langeland和C. K Burks编,《佛罗里达州自然区域非本土植物的鉴定与生物学》,佛罗里达大学,盖恩斯维尔,1998年。(4)M. B. Rayachhetry等人,《生物防治》22:38,2001年。