Muniz Carla Caroline Santana, Ferreira Rivanildo Junior, Nascimento Daniel Dalvan, Souza Pollo Andressa, Silva Edicleide Macedo da, Andrade Francisco Laurimar Nascimento, Melo Raylane Monteiro, Gomes Rafaelle Fazzi, Santos Lucas Silva, Soares Pedro Luiz Martins
Universidade Federal Rural da Amazonia - Campus Capanema, Capanema, Pará, Brazil;
Universidade Estadual Paulista Julio de Mesquita Filho Faculdade de Ciencias Agrarias e Veterinarias Campus de Jaboticabal, Department of Plant Health, Jaboticabal, São Paulo, Brazil;
Plant Dis. 2025 Jun 24. doi: 10.1094/PDIS-03-25-0613-PDN.
Eryngium foetidum L. (Apiaceae) is a pungent leafy herb known as culantro. It is native to tropical America and the West Indies. In 2025, E. foetidum is widely present throughout Asia, tropical Africa, the Pacific Islands, and the warmer areas of southern Europe. It is used for gastronomy, medicinal applications, and other purposes in the pharmaceutical industry (Paul et al. 2011). In February 2019, a farm cultivating culantro in the municipality of Ananindeua (01°19'26.6" S 048°23'06.3" W), state of Pará, Brazil, reported a 5% incidence of plants affected (20 plants) by severe symptoms of nematode parasitism within a 20 m² area. The symptoms included underdevelopment of the shoot system, leaf yellowing followed by necrosis, and a high number of galls on the roots. Three symptomatic plants, along with the roots and surrounding soil, were randomly sampled and sent to the Nematology Laboratory (LabNema) at São Paulo State University (UNESP) for nematode identification. A total of 3,120 second-stage juveniles (J2) of Meloidogyne spp. were present in 100 cm³ of soil, and a total of 21,052 eggs and J2 were recovered per gram of root. The nematodes collected from the roots and rhizosphere of culantro were analyzed using morphological, biochemical and molecular methods. The perineal pattern of females (n = 15) exhibited a high dorsal arch with thick stripes and a trapezoidal shape. The labial region in males (n = 15) displayed a trapezoidal shape with distinct rings, prominent labial disc, transverse striations present, and basal nodules taller than wide (Taylor and Netscher 1974; Eisenback and Hirschmann 1981). The morphological characteristics of the adults were compatible to those originally described for M. incognita (Kofoid and White 1919) Chitwood 1949. The profile of 16 female obtained through isoenzyme electrophoresis was consistent with the I1 phenotype, which is characteristic of M. incognita (Esbenshade and Triantaphyllou 1985). Additionally, DNA was extracted from six females individually, in separate tubes. Amplification was performed using species-specific primers for M. incognita (Zijlstra et al. 2000) and for the 18S rDNA region (Holterman et al. 2006). Only 1,200 bp amplicons generated with the M. incognita-specific primers were obtained. Sequencing of 18S rDNA region confirmed the species as M. incognita with 100% of identity (haplotypes accession numbers OR001655 and OR001656). Koch's postulate confirmation research was conducted in a greenhouse under a temperature of 23°C, 73% relative humidity, and a 12-hour photoperiod. Seven culantro seedlings were individually transplanted into 5-liter pots filled with autoclaved substrate composed of sand, soil, and manure (4:1:1). Six seedlings were inoculated with 10 mL of a suspension containing 3,000 eggs and J2 juveniles (initial population density, Pi) from the original M. incognita population, whereas four seedlings served as uninoculated controls. After 90 days, the inoculated plants exhibited symptoms similar to those initially observed in the field, including numerous root galls and a substantial egg mass, in contrast to the healthy nonincubated plants. The average number of recovered J2 and eggs from seedlings roots and in 100 cm³ of soil was 209,700 (final population density, Pf), with a reproduction factor (Pf/Pi) of 69.90. Culantro is typically grown in succession with other vegetable host plants of M. incognita, such as lettuce, which facilitate the multiplication and dissemination of the nematode. This is the first report of M. incognita parasitizing E. foetidum in the Amazon region, serving as an alert for the practice of crop rotation.
刺芫荽(伞形科)是一种有刺激性气味的多叶草本植物,被称为刺芹。它原产于热带美洲和西印度群岛。到2025年,刺芫荽在亚洲、热带非洲、太平洋岛屿以及南欧较温暖的地区广泛分布。它用于烹饪、医药应用以及制药行业的其他用途(保罗等人,2011年)。2019年2月,巴西帕拉州阿纳尼德乌市(南纬01°19'26.6",西经048°23'06.3")一个种植刺芫荽的农场报告称,在20平方米的区域内,有5%的植株(20株)受到线虫寄生严重症状的影响。症状包括地上部系统发育不良、叶片发黄随后坏死,以及根部大量虫瘿。随机选取了三株有症状的植株,连同其根部和周围土壤,送往圣保罗州立大学(UNESP)的线虫学实验室(LabNema)进行线虫鉴定。每100立方厘米土壤中共有3120条南方根结线虫属的二期幼虫(J2),每克根中总共回收了21052个卵和J2。从刺芫荽的根部和根际收集的线虫采用形态学、生化和分子方法进行分析。雌性(n = 15)的会阴花纹呈现高背弓,有粗条纹且呈梯形。雄性(n = 15)的唇区呈梯形,有明显的环,突出的唇盘,有横向条纹,基部瘤高于宽(泰勒和内切尔,1974年;艾森巴克和赫希曼,1981年)。成虫的形态特征与最初描述的南方根结线虫(科福伊德和怀特,1919年)奇伍德,1949年相符。通过同工酶电泳获得的16只雌性的图谱与I1表型一致,这是南方根结线虫的特征(埃斯本沙德和特里安塔菲洛,1985年)。此外,从六只雌性个体中分别在单独的试管中提取DNA。使用南方根结线虫的种特异性引物(齐尔斯特拉等人,2000年)和18S rDNA区域的引物(霍尔特曼等人,2006年)进行扩增。仅获得了用南方根结线虫特异性引物产生的1200 bp扩增子。18S rDNA区域的测序证实该物种为南方根结线虫,同一性为100%(单倍型登录号OR001655和OR001656)。科赫法则的验证研究在温度为23°C、相对湿度为73%、光周期为12小时的温室中进行。将七株刺芫荽幼苗分别移栽到装有由沙子、土壤和粪肥(4:1:1)组成的经高压灭菌基质的5升花盆中。六株幼苗接种了10毫升含有来自原始南方根结线虫种群的3000个卵和J2幼虫的悬浮液(初始种群密度,Pi),而四株幼苗作为未接种的对照。90天后,接种的植株表现出与最初在田间观察到的类似症状,包括大量根瘤和大量卵块,与健康未接种的植株形成对比。从幼苗根部和100立方厘米土壤中回收的J2和卵的平均数量为209700(最终种群密度,Pf),繁殖系数(Pf/Pi)为69.90。刺芫荽通常与南方根结线虫的其他蔬菜寄主植物如莴苣轮作种植,这有利于线虫的繁殖和传播。这是亚马逊地区南方根结线虫寄生刺芫荽的首次报告,为作物轮作实践敲响了警钟。