Yan H J, Gaskins V L, Vico I, Luo Y G, Jurick W M
Key Lab of Food Quality and Safety of Jiangsu Province-State Key Laboratory Breeding Base, Nanjing, China.
USDA-ARS, Food Quality Laboratory, Beltsville, MD.
Plant Dis. 2014 Jul;98(7):1004. doi: 10.1094/PDIS-12-13-1214-PDN.
Apples in the United States are stored in low-temperature controlled atmospheres for 9 to 12 months and are highly susceptible to blue mold decay. Penicillium spp. cause significant economic losses worldwide and produce mycotoxins that contaminate processed apple products. Blue mold is managed by a combination of cultural practices and the application of fungicides. In 2004, a new postharvest fungicide, pyrimethanil (Penbotec 400 SC, Janseen PMP, Beerse, Belgium) was registered for use in the United States to control blue mold on pome fruits (1). In this study, 10 blue mold symptomatic 'Red Delicious' apples were collected in May 2011 from wooden bins at a commercial facility located in Pennsylvania. These fruit had been treated with Penbotec prior to controlled atmosphere storage. Ten single-spore Penicillium spp. isolates were analyzed for growth using 96-well microtiter plates containing Richards minimal medium amended with a range of technical grade pyrimethanil from 0 to 500 μg/ml. Conidial suspensions adjusted to 1 × 10 conidia/ml were added to three 96-well plates for each experiment; all experiments were repeated three times. Nine resistant isolates had prolific mycelial growth at 500 μg/ml, which is 1,000 times the discriminatory dose that inhibited baseline sensitive P. expansum isolates from Washington State (1). However, one isolate (R13) had limited conidial germination and no mycelial proliferation at 0.5 μg/ml and was categorized as sensitive. One resistant (R22) and one sensitive (R13) isolate were selected on the basis of their different sensitivities to pyrimethanil. Both isolates were identified as P. expansum via conventional PCR using β-tubulin gene-specific primers according to Sholberg et al. (2). Analysis of the 2X consensus amplicon sequences from R13 and R22 matched perfectly (100% identity and 0.0 E value) with other P. expansum accessions in GenBank including JN872743.1, which was isolated from decayed apple fruit from Washington State. To determine if pyrimethanil applied at the labeled rate of 500 μg/ml would control R13 or R22 in vivo, organic 'Gala' apple fruit were wounded, inoculated with 50 μl of a conidial suspension (1 × 10 conidia/ml) of either isolate, dipped in Penbotec fungicide or sterile water, and stored at 25°C for 7 days. Twenty fruit composed a replicate within a treatment and the experiment was performed twice. Non-inoculated water-only controls were symptomless, while water-dipped inoculated fruit had 100% decay with mean lesion diameters of 36.8 ± 2.68 mm for R22 and 38.5 ± 2.61 mm for R13. The R22 isolate caused 30% decay with 21.6 ± 5.44 mm lesions when inoculated onto Penbotec-treated apples, while the R13 isolate had 7.5% decay incidence with mean lesion diameters of 23.1 ± 3.41 mm. The results from this study demonstrate that P. expansum pyrimethanil-resistant strains are virulent on Penbotec-treated apple fruit and have the potential to manifest in decay during storage. To the best of our knowledge, this is the first report of pyrimethanil resistance in P. expansum from Pennsylvania, a major apple growing region for the United States. Moreover, these results illuminate the need to develop additional chemical, cultural, and biological methods to control this fungus. References: (1) H. X. Li and C. L. Xiao. Phytopathology 98:427, 2008. (2) P. L. Sholberg et al. Postharvest Biol. Technol. 36:41, 2005.
美国的苹果在低温控制气氛中储存9至12个月,极易受到青霉腐烂的影响。青霉属真菌在全球范围内造成重大经济损失,并产生污染加工苹果产品的霉菌毒素。青霉病通过综合栽培措施和施用杀菌剂进行管理。2004年,一种新型采后杀菌剂嘧霉胺(Penbotec 400 SC,扬森PMP,比利时贝尔瑟)在美国注册用于控制仁果类水果上的青霉病(1)。在本研究中,2011年5月从宾夕法尼亚州一家商业设施的木箱中收集了10个有青霉病症状的“红元帅”苹果。这些水果在气调贮藏前已用Penbotec处理过。使用含有Richards基本培养基的96孔微量滴定板分析了10个单孢子青霉属真菌分离株的生长情况,该培养基添加了一系列技术级嘧霉胺,浓度范围为0至500μg/ml。将调整至1×10⁶分生孢子/ml的分生孢子悬浮液加入每个实验的三个96孔板中;所有实验重复三次。九个抗性分离株在500μg/ml时菌丝生长旺盛,这是抑制华盛顿州基线敏感扩展青霉分离株的鉴别剂量的1000倍(1)。然而,一个分离株(R13)在0.5μg/ml时分生孢子萌发有限且没有菌丝增殖,被归类为敏感株。根据对嘧霉胺的不同敏感性,选择了一个抗性(R22)和一个敏感(R13)分离株。根据Sholberg等人(2)的方法,使用β-微管蛋白基因特异性引物通过常规PCR将两个分离株鉴定为扩展青霉。对R13和R22的2X共有扩增子序列分析与GenBank中包括从华盛顿州腐烂苹果果实中分离的JN872743.1在内的其他扩展青霉登录号完全匹配(100%同一性和0.0 E值)。为了确定以500μg/ml的标记剂量施用的嘧霉胺在体内是否能控制R13或R22,将有机“嘎啦”苹果果实划伤,接种50μl任一分离株的分生孢子悬浮液(1×10⁶分生孢子/ml),浸入Penbotec杀菌剂或无菌水中,并在25°C下储存7天。每个处理中20个果实构成一个重复,实验进行了两次。未接种的仅用水处理的对照无症状,而浸水处理的接种果实100%腐烂,R22的平均病斑直径为36.8±2.68mm,R13的平均病斑直径为38.5±2.61mm。当接种到Penbotec处理的苹果上时,R22分离株导致30%的腐烂,病斑大小为21.6±5.44mm,而R13分离株的腐烂发生率为7.5%,平均病斑直径为23.1±3.41mm。本研究结果表明,扩展青霉对嘧霉胺的抗性菌株在Penbotec处理的苹果果实上具有致病性,并且在储存期间有可能导致腐烂。据我们所知,这是美国主要苹果种植区宾夕法尼亚州扩展青霉对嘧霉胺抗性的首次报道。此外,这些结果表明需要开发额外的化学、栽培和生物学方法来控制这种真菌。参考文献:(1)H. X. Li和C. L. Xiao。植物病理学98:427,2008。(2)P. L. Sholberg等人。采后生物学与技术36:41,2005。