Luongo L, Haegi A, Galli M, Berti S, Vitale S, Belisario A
Consiglio Nazionale per la Ricerca e la Sperimentazione in Agricoltura, Centro di Ricerca per la Patologia Vegetale (CRA-PAV), 00156 Roma, Italy.
Umbraflor srl, 06038 Perugia, Italy.
Plant Dis. 2015 Jan;99(1):155. doi: 10.1094/PDIS-05-14-0534-PDN.
European hackberry (Celtis australis L.) is a popular shade tree mainly planted in southern Europe and known to be tolerant to dry and poor soils. In early autumn 2013, hackberry plants grown in soil in a commercial nursery located in the floodplain in Umbria region showed symptoms of wilting, dieback, and death. Up to 100% of the canopy was affected, and over 60% of the plants were symptomatic or dead. A Phytophthora species was consistently isolated from symptomatic 6-year-old plants by plating small pieces of collar and root tissues, cut from the margin of dark-brown necrotic lesions, onto PARPH selective medium (4). Pure cultures were obtained by single-hyphal transfers on potato dextrose agar (PDA). Sporangia, produced on pepper seeds in soil extract solution (3), were nonpapillate and noncaducous, measuring 34.0 to 85.0 × 22.0 to 50.0 μm. Oospores had an average diameter of 44 μm with mostly paragynous antheridia. On the basis of morphological features, the isolates were identified as P. megasperma Drech. (2). The identity was confirmed by sequencing the cytochrome c oxidase subunit II (Cox II) (5), which gave 100% identity with P. megasperma sequences available in GenBank (GU222070), and by sequencing the internal transcribed spacer (ITS) using the universal primers ITS4 and ITS6, which gave 99% identity with the AF266794 sequence from Cooke et al. (1). The sequences of one isolate (AB239) were deposited in the European Nucleotide Archive (ENA) with accession numbers HG973451 and HG973450 for Cox II and ITS, respectively. Pathogenicity tests were conducted in the greenhouse with isolate AB239 on eight 2-year-old potted European hackberry plants. Mycelial plugs (5 mm diameter) cut from the margins of actively growing 8-day-old cultures on PDA were inserted through the epidermis to the phloem at the collar level. Two plants were used as controls and treated as described above except that sterile PDA plugs replaced the inoculum. Inoculated plants were kept for 4 weeks in a greenhouse at 24 ± 2°C. During that period, inoculated plants showed wilting symptoms similar to those observed in the field. Lesions were evident at all the inoculation points progressing downward to the roots. Colonies of Phytophthora were isolated from the margins of lesions and identified as P. megasperma, thus fulfilling Koch's postulates. Controls remained symptomless. P. megasperma taxonomy is rather complex since it embraces different subgroups, including host specialized forms (formae speciales), some of which are recognized as biological species. Based on morphological and molecular data presented here, the Phytophthora isolates from hackberry belong to P. megasperma sensu stricto, which is included in the "pathogenic to a broad range of hosts" (BHR) group (1). This pathogen is rather polyphagous, attacking mainly fruit and ornamental woody plants, commonly Prunus spp., Malus spp., and Actinidia deliciosa. Like other homothallic Phytophthora species, it is particularly dangerous due to its abundant production of thick-walled resting oospores that enable long-term survival in the soil. To our knowledge this is the first report of P. megasperma sensu stricto (1) on C. australis and its family Ulmaceae/Cannabaceae. References: (1) D. E. L. Cooke et al. Fungal Genet. Biol. 30:17, 2000. (2) D. C. Erwin and O. K. Ribeiro, American Phytopathological Society, St. Paul, MN, 1996. (3) E. Ilieva et al. Eur. J. Plant Path. 101:623, 1995. (4) S. N. Jeffers and S. B. Martin. Plant Dis. 70:1038, 1986. (5) F. N. Martin and P. W. Tooley. Mycologia 95:269, 2003.
欧洲朴树(Celtis australis L.)是一种常见的行道树,主要种植于欧洲南部,已知其耐干旱和土壤贫瘠。2013年秋初,位于翁布里亚地区洪泛平原的一家商业苗圃中,种植在土壤里的朴树出现了萎蔫、枯枝和死亡症状。高达100%的树冠受到影响,超过60%的植株出现症状或死亡。通过将从深褐色坏死病斑边缘切下的小块根颈和根组织接种到PARPH选择性培养基(4)上,从有症状的6年生植株中持续分离出一种疫霉属真菌。通过在马铃薯葡萄糖琼脂(PDA)上进行单菌丝转移获得纯培养物。在土壤提取液(3)中的辣椒种子上产生的孢子囊无乳突且不脱落,大小为34.0至85.0×22.0至50.0μm。卵孢子平均直径为44μm,雄器大多为侧生。根据形态特征,分离物被鉴定为大孢疫霉(P. megasperma Drech.)(2)。通过对细胞色素c氧化酶亚基II(Cox II)进行测序(5),与GenBank中可用的大孢疫霉序列(GU222070)有100%的一致性,以及使用通用引物ITS4和ITS6对内部转录间隔区(ITS)进行测序,与Cooke等人(1)的AF266794序列有99%的一致性,从而确认了其身份。一个分离物(AB239)的序列分别以登录号HG973451和HG973450存入欧洲核苷酸档案馆(ENA),用于Cox II和ITS。在温室中对分离物AB239在8株2年生盆栽欧洲朴树上进行了致病性测试。从在PDA上活跃生长8天的培养物边缘切下的菌丝块(直径5mm)通过表皮插入到根颈水平的韧皮部。将两株植物作为对照,除用无菌PDA块代替接种物外,处理方式与上述相同。接种的植物在24±2°C的温室中保存4周。在此期间,接种的植物出现了与田间观察到的类似的萎蔫症状。在所有接种点都出现了病斑,并向下蔓延至根部。从病斑边缘分离出疫霉菌落,并鉴定为大孢疫霉,从而满足了柯赫氏法则。对照植株无症状。大孢疫霉的分类相当复杂,因为它包含不同的亚组,包括寄主专化型(专化型),其中一些被认为是生物学种。根据此处提供的形态和分子数据,从朴树分离出的疫霉分离物属于严格意义上的大孢疫霉,它被归入“对多种寄主致病”(BHR)组(1)。这种病原菌食性较广,主要攻击果树和观赏木本植物,常见的有李属、苹果属和美味猕猴桃。与其他同宗配合的疫霉物种一样,由于其大量产生厚壁休眠卵孢子,能够在土壤中长期存活,因此特别危险。据我们所知,这是首次关于严格意义上的大孢疫霉(1)对欧洲朴树及其所属的榆科/大麻科的报道。参考文献:(1)D. E. L. Cooke等人,《真菌遗传学与生物学》30:17,2000年。(2)D. C. Erwin和O. K. Ribeiro,美国植物病理学会,明尼苏达州圣保罗,1996年。(3)E. Ilieva等人《欧洲植物病理学杂志》101:623,1995年。(4)S. N. Jeffers和S. B. Martin,《植物病害》70:103,8,1986年。(5)F. N. Martin和P. W. Tooley,《真菌学》95:269,2003年。