First Report of Paramyrothecium roridum Causing Leaf Blight on Water Hyacinth (Eichhornia crassipes) in Malaysia.

Abstract

Water hyacinth (Eichhornia crassipes) is a free-floating aquatic plant and is also widely cultivated as an aquatic ornamental plant in Malaysia. In June 2018, a severe foliar disease with typical leaf blight symptoms were observed on leaves of water hyacinth plants (approximately 50%) in waterways adjacent to two rice fields located at Tanjung Karang and Sungai Besar, Selangor province, Malaysia. Symptoms appeared irregular necrotic lesions with concentric rings, later lesions expanded to entire leaves and became blighted. Twenty symptomatic leaves were collected from two sampling locations. Symptomatic leaf tissue was cut into small pieces (5 × 5 mm), surface sterilized with 0.5% sodium hypochlorite (NaOCl) for 2 min, rinsed three times with sterile distilled water, plated on potato dextrose agar (PDA), and incubated at 25 °C with a 12-h light/dark cycle for 7 days. Twenty single-spore isolates were recovered from sampled leaves, all isolates exhibited Paramyrothecium-like morphology and two representative isolates, PR1 and PR2 were used for further studies. Fungal colonies were initially white aerial mycelia with sporodochia bearing olivaceous green conidial masses formed on PDA after 5 days of incubation. Conidiogenous cells were phialidic, hyaline, smooth, straight to slightly curved, 13 to 20 × 1.0 to 1.8 μm and setae were absent. Conidia were aseptate, hyaline to pale green, smooth, cylindrical to ellipsoidal with rounded ends, and measured 5.8 to 8.0 μm × 1.8 to 2.2 μm (n=50). These morphological characteristics were consistent with the description of Paramyrothecium roridum (Tode) L. Lombard & Crous (Lombard et al. 2016). Total genomic DNA of the isolates was extracted from fresh mycelium using DNeasy Plant Mini kit (Qiagen, USA). The internal transcribed spacer (ITS) and calmodulin (cmdA) gene regions were amplified using the ITS5/ITS4 (White et al.1990) and CAL-228F/CAL2Rd primer sets (Carbone and Kohn 1999; Groenewald et al., 2013), respectively. BLASTn analysis showed that the ITS and cmdA sequences of the isolates were 100% identity with Paramyrothecium roridum ex-epitype strain CBS 357.89 (GenBank accession nos. KU846300 and KU846270), respectively. The resulting sequences were deposited in GenBank (ITS: Accession nos. MW850370, MW850371; cmdA Accession nos. MW854363, MW854364). Pathogenicity tests of the two isolates were performed by spray inoculation on healthy leaves of each five potted water hyacinth plants using a 3-ml conidial suspension (1 × 106 conidia/ml) produced on 7-day-old PDA cultures incubated at 25 °C with a 12-h light/dark cycle. Five potted water hyacinth plants inoculated with sterile water served as controls. Inoculated plants were covered with plastic bags for 48 h to maintain high humidity and kept in a growth chamber for 2 weeks at 25 ± 1°C, 95% relative humidity and a 12-h light/dark period. The experiment was repeated twice. Eight days post-inoculation, symptoms on inoculated leaves developed necrotic brown lesions similar to those observed in the field, while control leaves remained asymptomatic. After 2 weeks of inoculation, lesions enlarged into severe blighting until all leaves died. Paramyrothecium roridum was re-isolated from randomly selected symptomatic tissues and verified by morphology and sequencing of ITS (MZ675387, MZ706462) and cmdA (MZ686706, MZ712041) loci, confirming Koch's postulates. The fungus was not re-isolated from non-inoculated control plants. Pa. roridum is distributed on a wide range of plants (Farr and Rossman 2021) and has been reported to cause leaf spot of water hyacinth in Nigeria (Okunowo et al. 2013) and Sri Lanka (Adikaram and Yakandawala 2020). To our knowledge, this is the first report of Pa. roridum causing leaf blight of water hyacinth in Malaysia. This disease is an emerging threat to water hyacinth and it reduces the leaf quality, therefore, appropriate management should be developed to control this disease.