López-Corrales Rosalia, Michereff Sami Jorge, Garcia-Estrada Raymundo Saul, Leon-Felix Josefina, C Correia Kamila, Rabago-Zavala Karen, Tovar-Pedraza Juan Manuel
Centro de Investigación en Alimentación y Desarrollo, Coordinación Culiacán, Culiacán, Sinaloa, Mexico;
Universidade Federal do Cariri, Centro de Ciências Agrárias e da Biodiversidade, Rua Ícaro de Sousa Moreira, s/n, Crato, Ceará, Brazil, 63130-025;
Plant Dis. 2023 Jan 23. doi: 10.1094/PDIS-11-22-2661-PDN.
, is the causal agent of black scurf and stem canker of potatoes ( L.) throughout the world. In November 2021, stem canker symptoms were observed in two potato fields located in Ahome, Sinaloa, Mexico. The disease incidence was estimated up to 15%. For fungal isolation, fragments of symptomatic stems were surface sterilized with 2% sodium hypochlorite for 2 min, rinsed with sterilized distilled water, and blotted dry on sterile filter paper. Fragments were placed on PDA medium and incubated at 25°C in darkness for 4 days. -like colonies were consistently obtained and 12 isolates were purified by the hyphal-tip method. Fungal colonies on PDA were white initially and then turned brown, raised, and with entire or undulate edges. Septate hyphae were hyaline, smooth, and branched at right angles with a septum near the point of branching. Microscopic examination by staining with 1% safranin O and 3% KOH solution showed multinucleate cells. The morphological features of the isolates resembled those of (Sneh et al. 1991). Four representative isolates were selected for molecular analysis and pathogenicity tests. The isolates were deposited in the Culture Collection of Phytopathogenic Fungi at the Research Center for Food and Development (Culiacán, Sinaloa) under accession nos. CCLF267, CCLF274, CCLF277, and CCLF279. For molecular identification, genomic DNA from each of the four isolates was extracted, and the internal transcribed spacer (ITS) region was amplified, and sequenced with the primer pair ITS5/ITS4 (White et al. 1990). The sequences were deposited in GenBank (accession nos. OP784258 to OP784261). Phylogenetic analyses were performed using the Maximum Likelihood method with ITS sequences for anastomosis groups (AG) of The phylogenetic tree grouped the four isolates within the AG-7 clade with high bootstrap support (100%). For pathogenicity tests, certified pathogen-free potato mini-tuber (cv. Fianna) were placed in a polystyrene pot (1 L) filled with a 5 cm layer of a sterile substrate composed of soil and peat moss (2:1 w/w). One rice grain (20 mg) colonized with each isolate was placed 10 mm above the uppermost sprout tip and covered with the sterile substrate (Inokuti et al. 2019). Control plants were inoculated with sterile rice grains. All pots were transferred to a greenhouse where the temperature ranged from 20 to 32°C. Stem necrosis symptoms were observed on all inoculated plants 25 days after emergence, whereas control plants remained symptomless. Pathogenicity test was performed twice with similar results. Fungi were reisolated from the infected stems and found to be morphologically identical to the isolates used for inoculation, thus fulfilling Koch's postulates. The AG-7 has been previously reported to cause potato diseases in South Africa (Truter and Wehner 2004). In Mexico, Carling et al. (1998) reported the presence of an isolate of R. solani AG-7 obtained from a potato tuber-borne sclerotium in Toluca; however, there is no information about the methodology used for the characterization of that isolate. To our knowledge, this is the first confirmed report of AG-7 causing potato stem canker in Mexico. Our findings improve knowledge about AGs occurring in potato fields in Mexico. So, further studies should be conducted to investigate the diversity, prevalence, and fungicide sensitivity of AGs distributed in the main potato-producing states in Mexico.
是全球马铃薯黑胫病和茎溃疡病的致病因子。2021年11月,在墨西哥锡那罗亚州阿霍梅的两块马铃薯田中观察到茎溃疡症状。病害发生率估计高达15%。为了进行真菌分离,将有症状的茎段用2%次氯酸钠进行表面消毒2分钟,用无菌蒸馏水冲洗,然后在无菌滤纸上吸干。将茎段置于马铃薯葡萄糖琼脂(PDA)培养基上,在25°C黑暗条件下培养4天。持续获得类似的菌落,并通过菌丝尖端法纯化了12个分离株。PDA培养基上的真菌菌落最初为白色,然后变为褐色,凸起,边缘完整或呈波浪状。有隔菌丝透明、光滑,在分枝点附近有隔膜且呈直角分枝。用1%番红O和3%氢氧化钾溶液染色的显微镜检查显示有多核细胞。分离株的形态特征与(斯内赫等人,1991年)描述的相似。选择四个代表性分离株进行分子分析和致病性测试。这些分离株保藏于食品与发展研究中心(锡那罗亚州库利亚坎)的植物病原真菌培养物保藏中心,保藏编号分别为CCLF267、CCLF274、CCLF277和CCLF279。为了进行分子鉴定,提取了四个分离株的基因组DNA,扩增了内转录间隔区(ITS),并用引物对ITS5/ITS4(怀特等人,1990年)进行测序。序列保藏于GenBank(登录号OP784258至OP784261)。使用最大似然法对立枯丝核菌融合群(AG)的ITS序列进行系统发育分析。系统发育树将这四个分离株聚类在AG - 7分支内,自展支持率很高(100%)。为了进行致病性测试,将经过认证无病原菌的马铃薯微型块茎(品种Fianna)置于一个聚苯乙烯盆(1升)中,盆中装有一层5厘米厚的由土壤和泥炭藓(2:1重量比)组成的无菌基质。将每个分离株定殖的一粒水稻种子(20毫克)放置在最上部芽尖上方10毫米处,并用无菌基质覆盖(井口等人,2019年)。对照植株接种无菌水稻种子。所有花盆转移到温度为20至32°C的温室中。出苗后25天,在所有接种植株上观察到茎坏死症状,而对照植株无症状。致病性测试重复进行了两次,结果相似。从感染的茎中重新分离出真菌,发现其形态与用于接种的分离株相同,从而满足了柯赫氏法则。此前已报道AG - 7在南非引起马铃薯病害(特鲁特和韦纳,2004年)。在墨西哥,卡林等人(1998年)报道从托卢卡的一个马铃薯块茎传播的菌核中获得了一株立枯丝核菌AG - 7分离株;然而,没有关于该分离株鉴定所使用方法的信息。据我们所知,这是AG - 7在墨西哥引起马铃薯茎溃疡病的首次确诊报道。我们的研究结果增进了对墨西哥马铃薯田中存在的立枯丝核菌融合群的了解。因此,应进一步开展研究,调查分布在墨西哥主要马铃薯生产州的融合群的多样性、流行情况和对杀菌剂的敏感性。