First Report of Clonostachys rhizophaga Causing Root Rot on Lentil in France and Cross-Pathogenicity on Pea.

IF 4.4 2区 农林科学 Q1 PLANT SCIENCES
Elodie Gautheron, Nadim Tayeh, Nadine Gautheron, Angélique André, Simon Gibert, Christian Steinberg, Véronique Edel-Hermann
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引用次数: 0

Abstract

Root rot affects legumes such as lentil (Lens culinaris subsp. culinaris Medik.) and pea (Pisum sativum L.) (Chatterton et al. 2019). In France, legume root rot occurs in 65% of cultivated areas and cause up to 60% yield loss (Augagneur et al. 2021; Moussart el al. 2011). Soil was sampled from plots where root rot disease was previously observed. Samplings were conducted in April 2019 from two plots in central France (46.59 N, 2.05 E; 46.57 N, 2.3 E). Pre-germinated lentil (cv. Anicia) seeds were transplanted in both soils and symptomatic plants were collected after two months. They showed yellowing and wilting symptoms associated with necrotic spots on the root system. The light brown color on the roots turned to dark brown as the necrotic spots progress. Diseased root fragments were surface-disinfected by soaking for 30 s in 70% ethanol, rinsed with sterile water and placed on malt extract agar (MEA). Fungal colonies growing from the root fragments were purified by single-spore sub-culturing and preserved in the Microorganisms of Interest for Agriculture and Environment (MIAE) collection (INRAE Dijon, France). They were transferred to potato dextrose agar and carnation leaf agar for macroscopic and microscopic observations. The colonies developed a dense and cottony aerial mycelium, pearly in color with pink reflections (Fig. S1). From below, the colonies were orange-pink. Under the microscope, Verticillium-like conidiophores arising on the same whorl released asymmetrical ovoid single-celled conidia, from 4 to 7 µm long and 2.5 to 3 µm wide, similar to the description of Clonostachys rhizophaga by Schroers (2001). Isolates MIAE08192 and MIAE08209 were identified as Clonostachys sp. based on their internal transcribed spacer (ITS) sequences (GenBank accessions OR902030 and OR902031). They were further identified based on their sequence of the translation elongation factor 1-α gene (TEF-1α) (Moreira et al. 2016) (GenBank accessions OR947648 and OR947649). A BLAST search identified the two isolates as C. rhizophaga based on 100% identity of their sequences to the published sequence KX184992 (382 bp out of 382 bp and 377 bp out of 377 bp, respectively). A phylogenetic analysis combining ITS and TEF-1α sequences confirmed that the two isolates clustered within the C. rhizophaga species (Fig. S2). Two strains MIAE07881 and MIAE07884 of C. rhizophaga have been reported to cause root rot on pea (Gibert et al. 2022). Due to equivalent symptoms on lentil and pea, and the fact that the strains belonged to the same taxon led to test cross-pathogenicity on the two plant species with the two strains collected from lentil and the two strains collected from pea. Surface-disinfected lentil (cv. Anicia) and pea (cv. Firenza) seeds were placed on MEA, and after 72 h, the germinated seeds were transferred into sterile glass tubes containing 30 mL of Hoagland's No. 2 basal salt mixture at 1.6 g.L-1 added with agar 8 g.L-1. Three days later, they were inoculated with 1 mL of a conidial suspension at 105 conidia.mL-1 or sterile deionized water for the control plantlets. Twelve tubes per strain and twelve negative control tubes were prepared. The tubes were incubated in a growth chamber at 22°C day/18°C night and 12 h light for four weeks. The bioassay was performed twice. The control plants were asymptomatic. Whatever their origin, the four isolates inoculated on lentil or pea caused necrotic areas on 100% of the plants leading to strongly degraded root system. Koch's postulates were verified by reisolating the inoculated fungi from one symptomatic plant among the twelve replicates. Our results confirm the absence of specificity of this interaction and suggests the possible pathogenicity of C. rhizophaga on other legumes (Abang et al. 2009). To our knowledge, this is the first report of C. rhizophaga as a causal agent of root rot on lentil and of its cross-pathogenicity on lentil and pea.

法国首次报告 Clonostachys rhizophaga 在扁豆上引起根腐病以及在豌豆上的交叉致病性。
根腐病影响豆科植物如扁豆(Lens culinaris subsp)。culinaris Medik.)和豌豆(Pisum sativum L.) (Chatterton et al. 2019)。在法国,65%的耕地发生豆科植物根腐病,造成高达60%的产量损失(Augagneur et al. 2021;Moussart et al. 2011)。从以前观察到根腐病的地块取样土壤。2019年4月在法国中部的两个样地(北纬46.59度,东经2.05度;46.57北纬,2.3东经)。在两种土壤中移栽鸢尾种子,两个月后采集有症状的植株。它们表现出与根系坏死斑点相关的发黄和萎蔫症状。随着坏死斑的发展,根部的浅棕色变为深棕色。患病根碎片在70%乙醇中浸泡30 s,用无菌水冲洗,放在麦芽提取物琼脂(MEA)上进行表面消毒。从根片段生长的真菌菌落通过单孢子继代培养纯化,并保存在农业和环境兴趣微生物(MIAE)收藏(法国第戎INRAE)中。将它们转移到马铃薯葡萄糖琼脂和康乃馨叶琼脂上进行宏观和微观观察。菌落发育成致密的、棉质的空中菌丝,呈珍珠色,反射出粉红色(图S1)。从下面看,蜂群呈橙红色。在显微镜下,在同一轮上产生的Verticillium-like分生孢子释放出不对称的卵形单细胞分生孢子,长4 ~ 7µm,宽2.5 ~ 3µm,与Schroers(2001)对Clonostachys rhizophaga的描述相似。根据分离株MIAE08192和MIAE08209的内部转录间隔序列(GenBank检索号OR902030和OR902031)鉴定为Clonostachys sp.。根据翻译延伸因子1-α基因(TEF-1α)的序列进一步鉴定(Moreira et al. 2016) (GenBank收录OR947648和OR947649)。BLAST检索结果显示,这两株分离菌株与已发表的KX184992序列(382 bp中的382 bp和377 bp中的377 bp)完全一致,鉴定为C. rhizophaga。结合ITS和TEF-1α序列的系统发育分析证实,这两个分离株属于C. rhizophaga种(图S2)。据报道,C. rhizophaga的两株菌株MIAE07881和MIAE07884可引起豌豆根腐病(Gibert et al. 2022)。由于两株菌株在扁豆和豌豆上的症状相当,且属于同一分类群,因此我们采用采集自扁豆的两株菌株和采集自豌豆的两株菌株对两种植物进行了交叉致病性试验。表面消毒扁豆(cv。菊苣)和豌豆(cv。将Firenza)种子置于MEA上,72h后将发芽的种子移入含有30 mL 1.6 g Hoagland’s 2号基础盐混合物的无菌玻璃管中。L-1加入琼脂8 g.L-1。3天后,接种1 mL分生孢子悬浮液,接种105个分生孢子。mL-1或无菌去离子水用于对照植株。每个菌株制备12根试管和12根阴性对照试管。试管在22°C昼/18°C夜,光照12 h的生长室中孵育4周。进行2次生物测定。对照植物无症状。无论其来源如何,接种在扁豆或豌豆上的4个分离株在100%的植株上造成坏死区,导致根系严重退化。通过从12个重复中的一个有症状的植物中重新分离接种的真菌,验证了Koch的假设。我们的研究结果证实了这种相互作用缺乏特异性,并提示了C. rhizophaga对其他豆科植物可能具有致病性(Abang et al. 2009)。据我们所知,这是第一次报道C. rhizophaga作为扁豆根腐病的病原,以及它对扁豆和豌豆的交叉致病性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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