First report of Diaporthe ueckeri and Diaporthe longicolla as the causal agent of pod and grain rot of soybean in Brazil.

IF 4.4 2区 农林科学 Q1 PLANT SCIENCES Plant disease Pub Date : 2024-12-14 DOI:10.1094/PDIS-10-24-2255-PDN
Cosma Raissa Bezerra do Nascimento, Rafael Souza Anjos, Raphael Rosa Barboza, Hiago Antonio Oliveira da Silva, Iris Carolina Henrique de Lima Leite, Daniel Yuri Xavier Sousa, Miller da Silva Lehner, Juliano Martins Diniz, Eduardo S G Mizubuti
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Here, we report Diaporthe ueckeri and D. longicolla as the causal agents of PGR. A total of 118 isolates were obtained from symptomatic grains, pods, and stems, across five Brazilian states other than SC: Mato Grosso (n = 62), Paraná (n = 20), Minas Gerais (n = 19), Goiás (n = 14), and Rio Grande do Sul (n = 3) during the 2022/23 and 2023/24 seasons. Infected grains and pods usually had necrotic lesions and were poorly developed. Symptomatic plant parts (stems, pods, and grains) were collected and maintained under high relative humidity conditions in the laboratory. Pycnidia or cirri were transferred from infected tissues onto PDA at 25 °C and monoconidial isolates were obtained, thereafter. Colonies were light gray with a dense and fluffy appearance. Pycnidia were erumpent, with elongated necks and cirri were observed. Alpha conidia were aseptate, hyaline, and biguttulate, measuring 6.6 to 8.6 μm length × 1.6 to 2.2 μm width, similar to those of Diaporthe spp. (Udayanga et al. 2015). Isolates were considered pathogenic when depressed necrotic lesions with or without pycnidia were formed after inoculation of 'Williams 82' at the V2 growth stage by the toothpick method which consisted of the insertion of a toothpick colonized by the fungus 1 cm below the cotyledonary node. Insertion of a non-infested, sterilized toothpick, was used as control. Partial sequences of the internal transcribed spacer (ITS) (White et al. 1990), translation elongation factor 1-α (TEF) (Carbone and Kohn 1999), calmodulin (CAL) (Carbone and Kohn 1999), and beta-tubulin (TUB) (Glass and Donaldson 1995) were amplified. GenBank accessions codes for UFVDUS-20 and UFVDLS-67 are ITS: PQ331841 and PQ331842; TEF: PQ37542 and PQ375427; CAL: PQ375426 and PQ375428; TUB: PQ375429 and PQ375430, respectively. Sequences of TEF of UFVDUS-20 and UFVDLS-67 were 100% similar to D. ueckeri strain 17-DIA-079 (MK941298.1) and D. longicolla D15.1 (MN584786.1), respectively. Bayesian inferences with the concatenated dataset grouped UFVDUS-20 and UFVDLS-67 with the reference strains of D. ueckeri or D. longicolla, respectively. Isolates UFVDUS-20 (D. ueckeri from MT) and UFVDLS-67 (D. longicolla from Goiás) were used for inoculation of soybean plants and detached pods with a 1×106 conidia/mL suspension. Sterile distilled water with Tween was used as control. Five pots (replicates) each with two 'L93-3312' plants at the V4 and R5 stages were used for inoculation until the runoff point and incubated at 28 °C, > 95% RH, and 12h-photoperiod. Plants were assessed until R8, and the experiment was conducted twice. Pod rot symptoms and pycnidia were observed in plants inoculated in both phenological stages. Moreover, detached pods at the R5 stage of 'L93-3312' were submerged in the conidial suspension while those of 'BMX Olimpo IPRO' were drop-inoculated with 10 μl of the conidial suspension. The treatments (immersion or drop-inoculation) were applied to 10 replicates, each composed of a humid chamber (11 x 11 x 3 cm plastic box) containing 5 pods. Rot symptoms with erumpent pycnidia with cirri were visible in all inoculated pods after seven days. Fungal colonies were reisolated, and identity was confirmed by morphological and molecular analysis. This is the first report fulfilling Koch's postulates, unequivocally establishing D. ueckeri and D. longicolla as the causal agents of soybean PGR. This establishes the correct etiology of PGR in Brazil, providing valuable information for disease management strategies.</p>","PeriodicalId":20063,"journal":{"name":"Plant disease","volume":" ","pages":""},"PeriodicalIF":4.4000,"publicationDate":"2024-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant disease","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1094/PDIS-10-24-2255-PDN","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Epidemics of pod and grain rot (PGR) of soybean (Glycine max (L.) Merr.), popularly referred to as "pod anomaly", have economically impacted Brazilian farmers, especially in Mato Grosso (MT), Brazil's largest producer state, where incidence varies from 10 to 40%. Although Diaporthe ueckeri was reported causing soybean seed decay in Santa Catarina state (SC), a disease similar to PGR, no pod inoculation was attempted and no rot symptoms reproduced. Here, we report Diaporthe ueckeri and D. longicolla as the causal agents of PGR. A total of 118 isolates were obtained from symptomatic grains, pods, and stems, across five Brazilian states other than SC: Mato Grosso (n = 62), Paraná (n = 20), Minas Gerais (n = 19), Goiás (n = 14), and Rio Grande do Sul (n = 3) during the 2022/23 and 2023/24 seasons. Infected grains and pods usually had necrotic lesions and were poorly developed. Symptomatic plant parts (stems, pods, and grains) were collected and maintained under high relative humidity conditions in the laboratory. Pycnidia or cirri were transferred from infected tissues onto PDA at 25 °C and monoconidial isolates were obtained, thereafter. Colonies were light gray with a dense and fluffy appearance. Pycnidia were erumpent, with elongated necks and cirri were observed. Alpha conidia were aseptate, hyaline, and biguttulate, measuring 6.6 to 8.6 μm length × 1.6 to 2.2 μm width, similar to those of Diaporthe spp. (Udayanga et al. 2015). Isolates were considered pathogenic when depressed necrotic lesions with or without pycnidia were formed after inoculation of 'Williams 82' at the V2 growth stage by the toothpick method which consisted of the insertion of a toothpick colonized by the fungus 1 cm below the cotyledonary node. Insertion of a non-infested, sterilized toothpick, was used as control. Partial sequences of the internal transcribed spacer (ITS) (White et al. 1990), translation elongation factor 1-α (TEF) (Carbone and Kohn 1999), calmodulin (CAL) (Carbone and Kohn 1999), and beta-tubulin (TUB) (Glass and Donaldson 1995) were amplified. GenBank accessions codes for UFVDUS-20 and UFVDLS-67 are ITS: PQ331841 and PQ331842; TEF: PQ37542 and PQ375427; CAL: PQ375426 and PQ375428; TUB: PQ375429 and PQ375430, respectively. Sequences of TEF of UFVDUS-20 and UFVDLS-67 were 100% similar to D. ueckeri strain 17-DIA-079 (MK941298.1) and D. longicolla D15.1 (MN584786.1), respectively. Bayesian inferences with the concatenated dataset grouped UFVDUS-20 and UFVDLS-67 with the reference strains of D. ueckeri or D. longicolla, respectively. Isolates UFVDUS-20 (D. ueckeri from MT) and UFVDLS-67 (D. longicolla from Goiás) were used for inoculation of soybean plants and detached pods with a 1×106 conidia/mL suspension. Sterile distilled water with Tween was used as control. Five pots (replicates) each with two 'L93-3312' plants at the V4 and R5 stages were used for inoculation until the runoff point and incubated at 28 °C, > 95% RH, and 12h-photoperiod. Plants were assessed until R8, and the experiment was conducted twice. Pod rot symptoms and pycnidia were observed in plants inoculated in both phenological stages. Moreover, detached pods at the R5 stage of 'L93-3312' were submerged in the conidial suspension while those of 'BMX Olimpo IPRO' were drop-inoculated with 10 μl of the conidial suspension. The treatments (immersion or drop-inoculation) were applied to 10 replicates, each composed of a humid chamber (11 x 11 x 3 cm plastic box) containing 5 pods. Rot symptoms with erumpent pycnidia with cirri were visible in all inoculated pods after seven days. Fungal colonies were reisolated, and identity was confirmed by morphological and molecular analysis. This is the first report fulfilling Koch's postulates, unequivocally establishing D. ueckeri and D. longicolla as the causal agents of soybean PGR. This establishes the correct etiology of PGR in Brazil, providing valuable information for disease management strategies.

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首次报告 Diaporthe ueckeri 和 Diaporthe longicolla 是巴西大豆豆荚和谷粒腐烂病的病原菌。
大豆(Glycine max (L.) Merr.)豆荚和谷粒腐烂病(PGR)流行,俗称 "豆荚异常",对巴西农民造成了经济影响,尤其是在巴西最大的生产州马托格罗索州(MT),发病率在 10% 到 40% 之间。尽管有报道称 Diaporthe ueckeri 会导致圣卡塔琳娜州(SC)的大豆种子腐烂(一种与 PGR 相似的疾病),但并未尝试接种豆荚,也未再现腐烂症状。在此,我们报告 Diaporthe ueckeri 和 D. longicolla 是 PGR 的病原菌。在 2022/23 和 2023/24 年度,我们从巴西除南卡罗来纳州以外的五个州(马托格罗索州(n = 62)、巴拉那州(n = 20)、米纳斯吉拉斯州(n = 19)、戈亚斯州(n = 14)和南里奥格兰德州(n = 3)有症状的谷粒、豆荚和茎上共获得 118 个分离株。受感染的谷粒和豆荚通常有坏死病变,发育不良。收集有症状的植物部分(茎、豆荚和谷粒),并将其保存在实验室的高相对湿度条件下。从受感染的组织中将菌丝体或菌丝圈转移到 25 °C 下的 PDA 上,然后获得单细胞分离物。菌落呈浅灰色,外观致密蓬松。分生孢子梗呈糜烂状,有拉长的颈部,并可观察到盘状菌丝。α分生孢子无菌、透明、大uttulate,长 6.6 至 8.6 μm × 宽 1.6 至 2.2 μm,与 Diaporthe 属的分生孢子相似(Udayanga 等人,2015 年)。在 V2 生长阶段,用牙签法接种'Williams 82',将带有真菌菌落的牙签插入子叶节下 1 厘米处,形成带或不带菌核的凹陷坏死病斑,则认为该菌株具有致病性。插入一根未受真菌侵染的消毒牙签作为对照。扩增了内部转录间隔(ITS)(White 等人,1990 年)、翻译延伸因子 1-α (TEF)(Carbone 和 Kohn,1999 年)、钙调素(CAL)(Carbone 和 Kohn,1999 年)和β-微管蛋白(TUB)(Glass 和 Donaldson,1995 年)的部分序列。UFVDUS-20 和 UFVDLS-67 的 GenBank 登录号分别为 ITS:PQ331841 和 PQ331842;TEF:PQ37542和PQ375427;CAL:分别为 ITS:PQ331841 和 PQ331842;TEF:PQ37542 和 PQ375427;CAL:PQ375426 和 PQ375428;TUB:PQ375429 和 PQ375430。UFVDUS-20和UFVDLS-67的TEF序列分别与D. ueckeri菌株17-DIA-079(MK941298.1)和D. longicolla D15.1(MN584786.1)100%相似。贝叶斯推断法将 UFVDUS-20 和 UFVDLS-67 分别归入 D. ueckeri 或 D. longicolla 的参考菌株。分离菌株 UFVDUS-20(来自 MT 的 D. ueckeri)和 UFVDLS-67(来自戈亚斯州的 D. longicolla)以 1×106 分生孢子/毫升的悬浮液接种大豆植株和脱落的豆荚。含吐温的无菌蒸馏水用作对照。在 V4 和 R5 阶段,用五盆(重复)各两株'L93-3312'植株进行接种,直至流点,并在 28 °C、> 95% 相对湿度和 12 小时光周期下培养。直到 R8 期才对植株进行评估,实验进行了两次。在两个物候期接种的植株中都观察到了荚腐病症状和菌核。此外,在分生孢子悬浮液中浸泡'L93-3312'在 R5 阶段脱落的豆荚,而在'BMX Olimpo IPRO'的豆荚中滴入 10 μl 的分生孢子悬浮液。处理(浸泡或滴注接种)适用于 10 个重复,每个重复由一个装有 5 个豆荚的湿室(11 x 11 x 3 厘米塑料箱)组成。七天后,所有接种的豆荚都出现了腐烂症状,糜烂的分生孢子梗上有圈状物。对真菌菌落进行了重新分离,并通过形态学和分子分析确认了真菌身份。这是第一份符合科赫假说的报告,明确确定了 D. ueckeri 和 D. longicolla 是大豆 PGR 的病原菌。这确立了巴西 PGR 的正确病原学,为病害管理策略提供了宝贵的信息。
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来源期刊
Plant disease
Plant disease 农林科学-植物科学
CiteScore
5.10
自引率
13.30%
发文量
1993
审稿时长
2 months
期刊介绍: Plant Disease is the leading international journal for rapid reporting of research on new, emerging, and established plant diseases. The journal publishes papers that describe basic and applied research focusing on practical aspects of disease diagnosis, development, and management.
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