Irish B M, Goenaga R, Park S, Kang S
USDA-ARS Tropical Agriculture Research Station, Mayaguez, Puerto Rico.
Department of Plant Pathology, Pennsylvania State University, University Park.
Plant Dis. 2007 Aug;91(8):1051. doi: 10.1094/PDIS-91-8-1051B.
Black pod or Phytophthora pod rot is the most economically important and widespread disease of cacao, Theobroma cacao L. Total losses due to Phytophthora exceed $400 million worldwide (1), and several species are known to attack cacao with P. palmivora (E.J. Butler) E. J. Butler as the most common. All plant parts are infected, but pod infections are particularly damaging. Symptoms resembling those of black pod disease were observed at the National Plant Germplasm Collection System of cacao at the USDA-ARS Tropical Agriculture Research Station (TARS) in Mayaguez, Puerto Rico for a number of years. During May of 2005, to determine the etiology of the disease, small, surface disinfested sections of pod lesions were placed on water agar and incubated for 4 days. The formation of papillate, deciduous, ellipsoidal to ovoid sporangia produced on sympodial sporangiophores on fruits, fit the description of P. palmivora and the identification was confirmed on cultures on water agar (2). Chlamydospores were readily observed in diseased pods and observed in pure cultures on V8 agar (2). Eight, single hyphal tips were transferred to potato dextrose agar (PDA) (Sigma-Aldrich, St. Louis, MO) and maintained as stock cultures. For pathogenicity tests, healthy mature pods were surface disinfested and placed in a humidity chamber lined with moist paper towels. Eight isolates were tested on four fruits per isolate and the pathogenicity test was repeated once. Inoculum was prepared by growing each isolate on PDA for 5 days with irradiation at 24°C, adding approximately 3.0 ml of water to each plate, dislodging the sporangia with a glass rod, mixing the suspension, estimating spore numbers with a hemacytometer, and adjusting to 10 sporangia per ml. A small, sterile scalpel was used to make an approximately 20.0 mm cut on the fruit epidermis, and approximately 0.2 ml of inoculum was placed on the wound. Pods were evaluated daily for 2 weeks. For molecular analysis, each of the eight cultures were grown in 50% potato dextrose broth to produce mycelia for DNA extraction using the FastDNA kit (Q-Biogen1, Irvine, CA). The internal transcribed spacer (ITS) region of the ribosomal RNA gene cluster was amplified, purified, and sequenced for all eight isolates. The ITS sequences of GenBank Accession Nos. DQ987915 to DQ987922 were identical and exhibited strong similarity (>99% identity) to that of three previously described isolates of P. palmivora from cacao (GenBank Accession Nos. AF 228097, AF467093, and AF467089). P. palmivora has been reported on citrus, coconut, black pepper, and Arracacia xanthorrhiza in Puerto Rico (2,3) and inoculum may have originated from these host or imported on cacao planted into the cacao collection before 2000. USDA-ARS-TARS is the official site for the cacao germplasm collection, thus, a detailed integrated pest management plan that includes the evaluation for resistance, sanitation measures, and use of fungicides to reduce disease levels has been implemented. Decreasing incidence and severity of this disease is a top priority. To our knowledge, this is the first report of P. palmivora on cacao in Puerto Rico. References: (1) M. C. T. Braga et al. Agrotropica 1:108, 1989. (2) D. Erwin and O. K. Ribeiro. Phytophthora Diseases Worldwide. The American Phytopathological Society. St. Paul, MN, 1996. (3) E. Rosa-Marquez. J. Agric. Univ. P. R. 84:53, 2000.
黑荚病或疫霉荚腐病是可可树(Theobroma cacao L.)最具经济重要性且分布广泛的病害。全球因疫霉造成的总损失超过4亿美元(1),已知有几种疫霉会侵害可可树,其中棕榈疫霉(Phytophthora palmivora (E.J. Butler) E. J. Butler)最为常见。可可树的所有部位都会被感染,但荚果感染造成的损害尤为严重。多年来,在位于波多黎各马亚圭斯的美国农业部农业研究局热带农业研究站(TARS)的国家可可植物种质收集系统中,都观察到了类似黑荚病的症状。2005年5月,为确定该病的病因,将荚果病斑上经表面消毒的小块组织放在水琼脂上,培养4天。在果实上的合轴孢子囊梗上产生的乳头状、脱落性、椭圆形至卵形的孢子囊,符合棕榈疫霉的描述,并且在水琼脂培养基上的培养物中得到了确认(2)。在患病荚果中很容易观察到厚垣孢子,在V8琼脂纯培养物中也能观察到(2)。将8个单菌丝尖端转移到马铃薯葡萄糖琼脂(PDA)(Sigma-Aldrich,密苏里州圣路易斯)上,并作为保藏培养物保存。进行致病性测试时,将健康的成熟荚果进行表面消毒,然后放在衬有湿纸巾的湿度箱中。对8个分离株进行测试,每个分离株在4个果实上进行测试,致病性测试重复一次。通过在24°C下对每个分离株在PDA上培养5天并进行辐照来制备接种物,向每个平板中加入约3.0毫升水,用玻璃棒使孢子囊脱落,混合悬浮液,用血球计数板估计孢子数量,并调整至每毫升10个孢子囊。用一把小的无菌手术刀在果实表皮上切一个约20.0毫米的切口,在伤口上放置约0.2毫升接种物。对荚果进行为期2周的每日评估。进行分子分析时,将8个培养物中的每一个在50%马铃薯葡萄糖肉汤中培养以产生菌丝体,使用FastDNA试剂盒(Q-Biogen1,加利福尼亚州欧文)提取DNA。对所有8个分离株的核糖体RNA基因簇的内部转录间隔区(ITS)进行扩增、纯化和测序。GenBank登录号DQ987915至DQ987922的ITS序列相同,并且与之前描述的来自可可树的3个棕榈疫霉分离株(GenBank登录号AF 228097、AF467093和AF467089)具有高度相似性(>99%同一性)。在波多黎各,柑橘、椰子、黑胡椒和黄根刺芹上都报道过棕榈疫霉(2,3),接种物可能源自这些寄主,或者是在2000年之前种植到可可收集区的可可树上带入的。美国农业部农业研究局热带农业研究站是可可种质收集的官方地点,因此,已经实施了一项详细的综合虫害管理计划,包括抗性评估、卫生措施以及使用杀菌剂来降低病害水平。降低这种病害的发病率和严重程度是首要任务。据我们所知,这是棕榈疫霉在波多黎各可可树上的首次报道。参考文献:(1)M. C. T. Braga等人,《Agrotropica》1:108,1989年。(2)D. Erwin和O. K. Ribeiro,《世界疫霉病》,美国植物病理学会,明尼苏达州圣保罗,1996年。(3)E. Rosa-Marquez,《波多黎各农业大学学报》84:53,2000年。