First Report of <i>Neopestalotiopsis vaccinii</i> in Delaware and <i>Neopestalotiopsis rosae</i> in Virginia Associated with Similar Disease Symptoms in Strawberry (<i>Fragaria × ananassa</i>)

During the 2023 harvest, 2-5% of strawberry plants in two commercial fields in Virginia Beach, Virginia (cv. 'Chandler' and 'Sweet Charlie'), and one in Kent County, Delaware (cv. 'Ruby June') showed tan to dark brown leaf spots, dark brown internal crown necrosis, or fruit rot. Pathogen isolation was performed on 2-3 symptomatic plants per variety per field. Infected tissues were surface sterilized in 75% ethanol, rinsed in sterile distilled water (sdH₂O), air-dried, and incubated on potato dextrose agar (PDA) at 28°C for 7 days. Hyphal tips of isolates were transferred to fresh PDA for morphological identification. After 15 days, Virginia isolates (n=3) showed white to pale yellow colonies with lobate edges and brown pigmentation. Their conidia were fusoid to ellipsoid, straight or slightly curved, four-septate, dolioform, and versicolored (17.2 ± 1.7 × 8.5 ± 0.8 μm; n=30), with 2-4 apical and 1 basal appendage. Delaware isolates (n=2) formed white cottony colonies in radial wave-like patterns with yellowish pigmentation. Their conidia were fusoid to ellipsoid, 3-4 septate, versicolored (15.5 ± 1.7 × 6.0 ± 0.6 μm; n=30), with 2-3 apical and 1 basal appendage. These isolates were identified as <i>Neopestalotiopsis</i> spp. (Maharachchikumbura et al. 2014; Santos et al. 2022). For molecular identification, internal transcribed spacer (ITS), β-tubulin (<i>βt</i>), and translation elongation factor 1-alpha (<i>tef-1α</i>) were amplified from <i>Neopestalotiopsis</i> DNA extracted using the Qiagen's AllPrep® Fungal kit and sequenced with ITS4/ITS5, Bt2b/T1, and EF1-728/EF1-986 primers (Hidrobo-Chavez et al. 2022). BLASTn searches showed VB3-1 (<i>βt</i>: PP239405, ITS: PP259539, <i>tef-1α</i>: PP239403) was 99.8-100% identical to <i>N. rosae</i> CBS 101057 (KM199429, KM199359, KM199523), and DE2-1 (<i>βt</i>: PP239404, ITS: PP259538, <i>tef-1α</i>: PP239402) was 99.6-100% identical to <i>N. vaccinii</i> CAA1059/MUM 21.36 (MW934610, MW969747, MW959099). Isolates from the same field had identical sequences, so VB3-1 and DE2-1 were used for phylogenetic analysis and clustered with <i>N. rosae</i> and <i>N. vaccinii</i>, respectively. Pathogenicity assays were conducted on leaves and crowns of 'Sweet Charlie' and 'Chandler' plants. Leaflets of two-month-old 'Sweet Charlie' were surface-sterilized, wounded, and treated with 100 µl of a 10⁴ conidia suspension of VB3-1, while control plants received 100 µl sdH₂O. Crowns of four-month-old 'Sweet Charlie' were wounded and injected with 50 µl of VB3-1 (10⁴ conidia) or sdH₂O. Isolate DE2-1 was used to inoculate 'Chandler' using the same method. For fruit inoculation, 10-mm deep wounds were created on surface-sterilized fruit and filled with 100 µl of VB3-1 or DE2-1 suspension (10⁴ conidia) or sdH₂O. All plants were kept at 25 ± 3 °C in a greenhouse with a 12 h photoperiod, and fruits at 24 ± 2 °C in the lab. Each experiment consisted of three plants or fruits per isolate and was repeated twice. Dark brown lesions appeared on leaves 24 h post-inoculation and fully developed in 3-5 days. Internal crown necrosis was observed 15 days post-inoculation. Fruits showed dry, sunken lesions at 48 h and fully developed in 5 days. Control plants/fruits remained symptomless. Koch's postulates were fulfilled by reisolating the pathogens from inoculated tissues but not controls. This is the first report of <i>N. vaccinii</i> and <i>N. rosae</i> causing leaf spot, crown rot, and fruit rot on strawberries in Virginia or Delaware. Previously, a new strain of <i>Neopestalotiopsis</i> sp. was reported to cause outbreaks in Florida and Georgia (Baggio et al. 2021; Jimenez Madrid et al. 2024). Given the diversity of <i>Neopestalotiopsis</i> spp. associated with strawberries, accurate pathogen identification is essential for understanding the epidemiology of <i>Neopestalotiopsis</i> diseases.