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中国引起枇杷根腐病的物种复合体的首次报道

First report of Species Complex Causing Root Rot of Loquat () in China.

作者信息

Wu Di, Zhang Danhua, Wang Caixia, Wei Yue, Timko Michael Paul, Liang Guolu

机构信息

University of Virginia, Department of Biology, 117 mimosa dr. Apt. 101, charlottesville, Chongqing, Virginia, United States, 400716.

Southwest University, College of horticulture and landscape architecture, Tiansheng Road. No. 2, Beibei, Chongqing, chongqing, Chongqing, China, 400716;

出版信息

Plant Dis. 2021 Jan 6. doi: 10.1094/PDIS-09-20-2003-PDN.

Abstract

Loquat (), a native fruit tree to China, is a popular edible fruit with medicinal properties (Badenes et al. 2013). A 2016-2019 field survey of ~13,000 loquat trees in two orchards in Chongqing and Fujian provinces showed about 5 to 10% root rot disease incidence. The disease symptoms included leaf yellowing, wilting, rotting of main root, and cracking of lateral roots, eventually leading to defoliation and death. To determine the causative agent, diseased roots from six trees were collected, washed in tap water, cut into 2-3 mm pieces, and disinfected for 3 min in 75% (v/v) EtOH. After rinsing in sterilized water, the root pieces were soaked in 10% NaClO (w/v) for 5-10 min, rinsed thrice in sterile water, and plated on potato dextrose agar (PDA). After 7 days of incubation at 25°C, individual spores were collected from the fungal colonies and replated. Single spore cultures growing on PDA gave rise to woolly-cottony, cream-white colored aerial mycelium and a yellowish pigmented mycelium. The average colony growth rate was 8.6 mm day (n=3). Microscopic observation of the mycelium revealed septate and hyaline hyphae and long cylindrical monophialides. Macroconidia were moderately curved, stout, 3-4 septate, measuring 20.79-48.70 μm × 4.16-10.14 μm (n=50). Microconidia produced from long phialides were kidney-shaped, 0-2 septate, and 5.72-17.28 μm × 2.29-6.51 μm (n=50) in size. The mycelial characteristics and reproductive structures of the isolates fit the morphological description of sp. (Summerell et al. 2003). To confirm this identification, translation elongation factor () and RNA polymerase I beta subunit () and RNA polymerase II beta subunit () regions of the genome were PCR amplified from 3 separate isolates (R2, R4 and R5) using EF1/ EF2, RPB1-Fa/G2R, RPB2-5f2/7cR & RPB2-7cF/11aR primer pairs (O'Donnell et al. 2010) and sequenced. BLASTn comparison of the EF-1α (MT976167), RPB1 (MT967271) and RPB2 (MW233052) regions from isolate R4 showed 99% identity with the (GU170620, 675/676 bp), (KC808270, 1543/1545 bp) and (MK4419902, 1637/1638 bp) sequences of species complex (FSSC) in GenBank database. The same species level identification was also found using FUSARIUM-ID and FUSARIUM-MLDT databases. Two-year-old seedlings (n=3) of two different cultivars, 'Hunanzaoshu' and 'Huabai No. 1', growing in pots indoors at 25-27 °C were inoculated by drenching the soil with a conidial suspension of isolate R4 (40 mL, 10 conidia mL obtained from 6-10 day old cultures). Control plants (n=3) were inoculated with sterilized water. At 20 days after inoculation (DAI) the leaves of inoculated plants became chlorotic and wilted, defoliated over time, and by 53 DAI 91.67% of plants died. The taproot and lateral roots of inoculated plants appeared brown to black in color and most lateral roots died and decomposed at 53 DAI, whereas the control plant roots remained healthy. All control plants remained symptomless. Based on morphological and molecular characters (, and ), the re-isolated pathogen from diseased plants was identical to the R4 isolate used for inoculation and the disease assays were repeated thrice. FSSC was recently reported to cause fruit rot disease on loquat in Pakistan (Abbas et al. 2017). Identifying species complex as a disease agent in Chinese loquat will assist in future development of improved germplasm for this important worldwide tree crop.

摘要

枇杷(Eriobotrya japonica)是中国本土的果树,是一种具有药用价值的受欢迎的可食用水果(Badenes等人,2013年)。2016 - 2019年对重庆和福建省两个果园约13000棵枇杷树进行的田间调查显示,根腐病发病率约为5%至10%。病害症状包括叶片发黄、枯萎、主根腐烂和侧根开裂,最终导致落叶和死亡。为了确定病原体,从六棵树上采集了患病根系,用自来水冲洗,切成2 - 3毫米的片段,并在75%(v/v)乙醇中消毒3分钟。在无菌水中冲洗后,将根段浸泡在10%次氯酸钠(w/v)中5 - 10分钟,在无菌水中冲洗三次,然后接种到马铃薯葡萄糖琼脂(PDA)上。在25°C下培养7天后,从真菌菌落中收集单个孢子并重新接种。在PDA上生长的单孢子培养物产生了羊毛状 - 棉絮状、乳白色的气生菌丝体和淡黄色的色素菌丝体。平均菌落生长速率为8.6毫米/天(n = 3)。对菌丝体的显微镜观察显示有隔膜和透明的菌丝以及长圆柱形的单瓶梗。大分生孢子适度弯曲,粗壮,有3 - 4个隔膜,大小为20.79 - 48.70μm×4.16 - 10.14μm(n = 50)。从长瓶梗产生的小分生孢子呈肾形,有0 - 2个隔膜,大小为5.72 - 17.28μm×2.29 - 6.51μm(n = 50)。分离物的菌丝体特征和繁殖结构符合尖孢镰刀菌(Fusarium oxysporum)的形态描述(Summerell等人,2003年)。为了确认这一鉴定,使用EF1/EF2、RPB1 - Fa/G2R、RPB2 - 5f2/7cR和RPB2 - 7cF/11aR引物对(O'Donnell等人,2010年)从3个单独的分离物(R2、R4和R5)中PCR扩增基因组的翻译延伸因子(EF - 1α)、RNA聚合酶Iβ亚基(RPB1)和RNA聚合酶IIβ亚基(RPB2)区域并进行测序。分离物R4的EF - 1α(MT976167)、RPB1(MT967271)和RPB2(MW233052)区域与GenBank数据库中尖孢镰刀菌复合种(Fusarium oxysporum species complex,FSSC)的序列(GU170620,675/676 bp)、(KC808270,1543/1545 bp)和(MK4419902,1637/1638 bp)的BLASTn比较显示99%的同一性。使用FUSARIUM - ID和FUSARIUM - MLDT数据库也发现了相同的物种水平鉴定。将两个不同品种‘湖南早树’和‘华白1号’的两年生幼苗(n = 3)种植在室内25 - 27°C的花盆中,用分离物R4的分生孢子悬浮液(40毫升,从6 - 10天龄的培养物中获得10⁶个分生孢子/毫升)浇灌土壤进行接种。对照植物(n = 3)接种无菌水。接种后20天(DAI),接种植物的叶片变黄并枯萎,随着时间的推移落叶,到53 DAI时91.67%的植物死亡。接种植物的主根和侧根呈现褐色至黑色,在53 DAI时大多数侧根死亡并分解,而对照植物的根保持健康。所有对照植物均无症状。基于形态和分子特征(EF - 1α、RPB1和RPB2),从患病植物中重新分离的病原体与用于接种的R4分离物相同,并且病害测定重复了三次。最近报道尖孢镰刀菌复合种在巴基斯坦导致枇杷果实腐烂病(Abbas等人,2017年)。将尖孢镰刀菌复合种鉴定为中国枇杷的病害病原体将有助于未来为这种重要的全球树木作物开发改良种质。

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