First report of Calonectria pseudopteridis causing brown spot on Eriocaulon buergerianum in Zhejiang province, China.

Abstract

Eriocaulon buergerianum is a traditional Chinese herb, used to treat eye diseases. In July 2020, a severe brown spot disease occurred on E. buergerianuim in Yongjia county (120°19'E, 27°58'N), Zhejiang province, China. Seventy-three plants from a survey of about 150 plants showed brown leaf spots. The spots were yellowish-brown to brown, and primarily affected leaves. As the disease progressed, the spots expanded, and fused. Sixty of the 150 plants wilted (Fig. 1 A-D). Diseased tissues were surface-sterilized in 75% ethanol (30 s), rinsed three times with sterile distilled water, air-dried (5 min), placed on potato dextrose agar (PDA) at 26°C (12-h light/dark cycle), and cultured for 4 days. Hyphal tip technique was used to obtain five isolates, which were transferred to malt extract agar (MEA), oatmeal agar (OA), and PDA. After seven days of growth at 26°C, the colonies had light, yellowish-brown centers with gray-white edges; the reverse sides had reddish- to yellowish-brown centers. Seven-day-old colonies grown on oatmeal agar (OA) produced a sparse aerial mycelium with yellowish-brown centers, and light yellowish-brown centers on the reverse side. Seven-day-old colonies grown on PDA exhibited yellowish-brown, floccose, aerial mycelia with reddish-brown to yellowish-brown pigment on the back (Fig. 1 E-G). The colonies also produced microsclerotia on OA and PDA media. On carnation leaf agar (CLA) and water agar (WA), only macroconidia were produced. Macroconidiophores comprised a stipe bearing penicillate, fertile branches, and a clavate vesicle. Macroconidia were cylindrical, rounded at both ends, colorless, hyaline, 1- to 2-septate, but mainly one, and 71.86 to 96.11 µm (mean = 82.27 µm, n = 50) × 4.13 to 5.21 µm (mean = 4.63 µm, n = 50) (Fig. 1 H-K). Morphological characteristics of the isolate on CLA or WA medium were similar to the Calonectria petridis species complex (Alfenas et al. 2015; Liu et al. 2020). The actin (Act), calmodulin (Cal), internal transcribed spacer (ITS), Histone3 (His3), a fragment of the large subunit nuclear ribosomal DNA (LSU), RNA polymerase II subunit 2 (Rpb2), translation elongation factor 1α (Tef1), and β-tubulin 2 (Tub2) genes were sequenced. The sequences were deposited in GenBank as: His3: Not detected; Act, OM933603, MZ770831, OM933604-OM933606; Cal, OM933607, MZ770832, OM933608-OM933610; ITS, OM955624, MZ720794, OM955625-OM955627; LSU, OM955640, MZ720792, OM955641-OM955643; Rpb2, OM933615, MZ770834, OM933616-OM933618; Tef1, OM933611, MZ770833, OM933612-OM933614; and Tub2, OM933619, MZ770835, OM933620-OM933622. Sequences of the Act, Cal, ITS, LSU, Rpb2, and Tef1 genes of these strains show a 99% match to the ex-type strain Ca. pteridis CBS111793 and Ca. pseudopteridis CBS163.28 (Act, GQ280494, MT335112; Cal, GQ267413, MT335347; ITS, GQ280616, MT359808; LSU, GQ280738, MT359568; Rpb2, KY653438, MT412640; Tef1, FJ918563, MT412878). The Tub2 sequences showed 99% identity with sequences of the ex-holotype Ca. pteridis CBS111793 (Tub2, DQ190578) (Alfenas et al. 2015; Liu et al. 2020; Lombard et al. 2016). Phylogenetic analysis showed that these strains and Ca. pseudopteridis CBS163.28 were clustered in a high-support bootstrap value clade (bootstrap = 85) (Fig. 2). In August 2020, healthy E. buergerianum plants in the blooming-fruiting stage were used to test the pathogenicity of the isolates. The mycelium of isolate GJC3 was cultured on CLA medium at 26°C (12-h light/dark cycle) for ten days. Eight healthy plants were inoculated by spraying with a conidial suspension (10 mL of 1 × 105 conidia/mL). Another eight plants were sprayed with sterilized water 10 mL of sterilized water as controls. The experiment was repeated three times. Pathogenicity tests were performed in the greenhouse (60% relative humidity, 28 to 20°C day/night, temperature range, and natural sunlight). After 15 days, inoculated plants showed yellowish-brown to brown spots and withering of the leaves, whereas the control plants remained healthy (Fig. 1 L-N). Ca. pseudopteridis was reisolated from the inoculated plants, and its morphology and gene sequences were similar to the original isolate GJC3. Ca. pseudopteridis was not isolated from the control plants. Morphological characteristics, molecular data and pathogenicity test identified these organisms as Ca. pseudopteridis. This report provides a basis for further research on biology and management of this disease.