Ginetti B, Uccello A, Bracalini M, Ragazzi A, Jung T, Moricca S
Dipartimento di Biotecnologie Agrarie, Sezione Protezione delle Piante. Piazzale delle Cascine, 28, I-50144, Florence, Italy.
Phytophthora Research and Consultancy, Thomastrasse 75, D-83098 Brannenburg, Germany.
Plant Dis. 2012 Nov;96(11):1694. doi: 10.1094/PDIS-05-12-0451-PDN.
High mortality was noticed in a 10-year-old stand of Pinus pinea in the Alberese area (Grosseto, central Italy, elev. 40 m, 42° 39' 46″ N, 11° 06' 25″ E) in July 2010. Aerial symptoms of trees included chlorosis, crown thinning, stunted growth, bark lesions at the stem base with resinous exudations, and extensive necroses of the underlying xylem tissue. Woody roots of two uprooted trees exhibited bark necroses and a high proportion of fine roots was destroyed. Soil around necrotic roots was baited using apple fruits (cv. Gala). After 1 week of incubation at 24°C, typical firm fruit rot developed and small tissue samples were transferred to clarified V8 agar (V8A) amended with 5 ml/l PARPNH and incubated at 24°C. After 7 days, stellate to rosaceous, finely lobed cottony colonies arose that were transferred to FPM medium and incubated at 24°C. Within 7 days, spherical oogonia with a smooth surface and predominantly paragynous antheridia formed; sporadic amphyginous antheridia could be observed. Colony squares (1 cm) were then placed in filtered and sterilized pond water. After 48 h, ovoid, obpyriform, or clavate, nonpapillate, persistent sporangia with internal nested and extended proliferation were formed. Fifty oogonia and 30 sporangia were measured. The diameter of the 50 spherical oogonia varied from 33.6 to 44.9 μm (avg. 39 μm); dimensions of the 30 sporangia were 42.6 to 59.8 × 28.9 to 47.8 μm (avg. 52.95 × 38.98 μm; 1:b ratio 1.37). The isolate was identified as Phytophthora humicola W. H. Ko & Ann on the basis of colony type, size and morphology of oogonia and sporangia, average length/width ratio of sporangia, the homothallic formation of oogonia (4), and ITS rDNA sequence information (GenBank Accession No. JQ757060). A BLAST search of the ITS sequence of P. humicola isolate B33 revealed a 99% identity with the Phytophthora ITS Clade 6 species P. humicola and P. inundata (2). This latter species could be ruled out, however, since it is self-sterile, whereas our isolate B33 was self-fertile (3). A strain of P. humicola was deposited in the CBS-KNAW Fungal Biodiversity Centre, strain no. CBS129249. Pathogenicity tests were conducted on 10 one-year-old twigs of Pinus pinea. A bark portion was removed aseptically and a V8A disc (0.5 cm diam.) of P. humicola mycelium was placed on the wound. Control twigs (3) received sterile V8A discs. Inoculated and control twigs were incubated at 20°C in the dark. Clearly noticeable necrotic lesions (avg. length 2.2 × 0.68 cm) were observed after 15 days on inoculated twigs. Control twigs showed no symptoms. Reisolations on selective V8-PARPNH-agar confirmed P. humicola as the causal agent. P. humicola is mainly associated with woody horticultural crops (1, 3), while the other taxa grouped with this species in Clade 6 are mainly found in forest and riparian ecosystems (1). These aquatic Phytophthora species normally have a saprophytic lifestyle, but under favourable environmental circumstances can act as opportunistic pathogens, attacking susceptible trees and causing scattered mortality in forest stands and natural ecosystems (3). To our knowledge, this is the first report of P. humicola from a pine stand. It is supposed that the pathogen reached the stand through infected plant material or infested soil introduced into the stand. References: (1) C. M. Brasier et al. Mycol. Res. 107:277, 2003. (2) D. E. L. Cooke et al. Fungal Genet. Biol. 30:17, 2000. (3) T. Jung et al. Persoonia 26:13, 2011. (4) W. H. Ko and P. J. Ann. Mycologia 77:631, 1985.
2010年7月,在阿尔贝雷塞地区(意大利中部格罗塞托,海拔40米,北纬42°39′46″,东经11°06′25″)一片10年生的意大利松林中发现了高死亡率现象。树木的地上症状包括褪绿、树冠变稀、生长受阻、树干基部树皮损伤并伴有树脂状渗出物,以及下层木质部组织广泛坏死。两棵被连根拔起的树的木质根出现树皮坏死,且大量细根被破坏。在坏死根周围的土壤中用苹果果实(品种为嘎啦)进行诱捕。在24°C下培养1周后,出现典型的坚实果实腐烂,将小组织样本转移至添加了5毫升/升PARPNH的澄清V8琼脂(V8A)上,并在24°C下培养。7天后,形成星状至蔷薇状、具细裂片的棉絮状菌落,将其转移至FPM培养基上并在24°C下培养。7天内,形成表面光滑的球形藏卵器,雄器主要为侧生;偶尔可观察到周生雄器。然后将1平方厘米的菌落方块置于经过滤和灭菌的池塘水中。48小时后,形成卵形、倒梨形或棒状、无乳头状突起、持久的孢子囊,内部有嵌套和扩展的增殖结构。测量了50个藏卵器和30个孢子囊。50个球形藏卵器的直径在33.6至44.9微米之间(平均3�微米);30个孢子囊的尺寸为42.6至59.8×28.9至47.8微米(平均52.95×38.98微米;长宽比1.37)。根据菌落类型、藏卵器和孢子囊的大小及形态、孢子囊的平均长宽比、藏卵器的同宗配合形成(4)以及ITS rDNA序列信息(GenBank登录号JQ757060),该分离物被鉴定为Humicola疫霉W. H. Ko & Ann。对Humicola疫霉分离株B33的ITS序列进行BLAST搜索发现,它与疫霉ITS进化枝6中的Humicola疫霉和淹水疫霉的序列一致性为99%(2)。然而,可以排除后一个物种,因为它是自交不育的,而我们的分离株B33是自交可育的(3)。一株Humicola疫霉保藏于CBS - KNAW真菌生物多样性中心,菌株编号为CBS129249。对10根一年生意大利松嫩枝进行了致病性测试。无菌去除树皮部分,在伤口处放置一片直径0.5厘米的Humicola疫霉菌丝体V8A圆盘。对照嫩枝(3根)放置无菌V8A圆盘。接种和对照嫩枝在20°C黑暗条件下培养。接种15天后,接种嫩枝上观察到明显的坏死病斑(平均长度2.2×0.68厘米)。对照嫩枝无任何症状。在选择性V8 - PARPNH琼脂上进行再分离,证实Humicola疫霉为致病因子。Humicola疫霉主要与木本园艺作物相关(1, 3),而在进化枝6中与该物种归为一类 的其他分类群主要存在于森林和河岸生态系统中(1)。这些水生疫霉物种通常具有腐生生活方式,但在有利的环境条件下可作为机会性病原菌,攻击易感树木并在林分和自然生态系统中导致散发性死亡(3)。据我们所知,这是Humicola疫霉在松林的首次报道。推测该病原菌是通过引入林分的受感染植物材料或受侵染土壤传播到该林分的。参考文献:(1)C. M. Brasier等人,《真菌学研究》107:277,2003年。(2)D. E. L. Cooke等人,《真菌遗传学与生物学》30:17,2000年。(3)T. Jung等人,《真菌学报》26:13,2011年。(4)W. H. Ko和P. J. Ann,《真菌学》77:631,1985年。