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AbstractLingonberry (Vaccinium vitis-idaea L.) is a dwarf shrub that is native to Northern climates. The berries are harvested from wild plants and the disease incidence in the crop is generally low. However, disease pressure may increase since the surface area dedicated to the crop is expected to expand in the future. In 2021 and 2022, brown necrotic leaves and stem dieback symptoms were observed on lingonberry plants grown at the St. John’s Research and Development Center, Newfoundland and Labrador, Canada. Pathogens were isolated from the diseased plant tissues and identified as Neopestalotiopsis rosae (n = 2) and Neopestalotiopsis zimbabwana (n = 2) using colony and conidia morphology as well as sequencing of the Internal Transcribed Spacer (ITS), beta-tubulin gene (ß-tub), and the translation elongation factor 1-alpha gene (tef1). Pathogenicity assays in detached lingonberry and strawberry leaves as well as lingonberry plants indicated that all four isolates were able to cause disease. This is the first report of N. rosae and N. zimbabwana causing leaf spot and stem dieback of lingonberry. Further monitoring of this disease is important to understand its prevalence in berry crops, as Neopestalotiopsis spp. in Canada have been reported to occur since 2018 in strawberry and other small fruits. Control measures and strategies are required to mitigate the potential risk from the disease, as there are no registered fungicides available to the growers. [ABSTRACT FROM AUTHOR]

Salmonberry (Rubus spectabilis) and thimbleberry (Rubus nutkanus) are important native berry plants for Indigenous communities and restoration sites in the coastal region of British Columbia (BC). Compared to cultivated berry plants, information on the diseases impacting native berry plant species is limited. In late August 2022, powdery mildew symptoms and signs were observed on field plots of salmonberry and thimbleberry plants at the Agassiz Research and Development Centre, BC. The disease symptoms progressed until the end of September. The morphology of conidiophores and conidia when examined under a compound and scanning electron microscope showed they matched with those of Podosphaera aphanis. DNA from diseased foliage was subjected to PCR amplification with primers representing the internal transcribed spacer (ITS) region of rDNA followed by sequencing. The corresponding sequences from both hosts showed >99% similarity to P. aphanis in GenBank and grouped with several accessions of P. aphanis following phylogenetic analysis. In artificially inoculated trials conducted in the greenhouse, powdery mildew symptoms developed within 3−4 weeks post-inoculation and P. aphanis isolates from salmonberry and thimbleberry were cross-pathogenic to each host. To our knowledge, this is the first study characterizing the powdery mildew pathogen infecting salmonberry and thimbleberry and demonstrating cross-pathogenicity to both hosts. The outcomes from this study provide insight into the biology of the powdery mildew pathogen infecting native Rubus spp. [ABSTRACT FROM AUTHOR]

Potato and tomato are grown in all Canadian provinces and contribute billions of dollars in exports and sales. Late blight, caused by Phytophthora infestans, is a destructive disease of potato and tomato worldwide and is responsible for millions of dollars in losses annually. Changes in pathogen strains were reported to be associated with late blight epidemics in several regions and pose challenges to late blight management. In British Columbia (BC), diverse strains of P. infestans were reported. Using multiplex microsatellite or simple sequence repeat (SSR) markers, we identified the new genotype US17 of P. infestans from samples of potato and tomato with late blight in BC. All isolates were of the A1 mating type. One, five, and one isolates were sensitive, moderately resistant, and highly resistant to metalaxyl-m, respectively. This is the first report of the occurrence of the US17 genotype in BC and Canada. The US17 strain was also able to cause tuber rot and foliar blight symptoms in potato in pathogen-inoculated assays. [ABSTRACT FROM AUTHOR]

Monilinia vacccinii-corymbosi (phylum Ascomycota, family Sclerotiniaceae) causes fruit disease 'mummy berry' on berry crops and responsible for yield losses and quality of fruits. We reported mummy berry disease of black huckleberry (Vaccinium membranaceum) first time in British Columbia, Canada. We have performed sequencing and genome assembly of M. vacccinii-corymbosi from infected fruits of huckleberry. The resulting genome was 33.8 Mbp in size and consisted of 2,437 scaffolds with an N50 of 33,816 bp. To our best knowledge, this is the first report of resource announcement of whole genome sequence of mummy berry pathogen ( M. vacccinii-corymbosi ) infecting black huckleberry. The genome resource will be valuable for future studies to understand the genomic structure of pathogen, and mechanisms associated with black huckleberry- M. vacccinii-corymbosi interactions., Competing Interests: Competing Interests: The authors have declared that no competing interest exists., (© His Majesty the King in Right of Canada, as represented by the Minister of Agriculture and Agri-Food Canada, 2024.)

Phytophthora root rot and wilting complex (PRRW) of red raspberry, caused primarily by Phytophthora rubi , is an economically important disease in British Columbia (BC) and in raspberry producing regions globally. Reliable, rapid, and efficient screening methods are lacking for evaluating germplasm for potential disease resistance in raspberry breeding programs as well as for screening pathogen isolates for virulence. The objective of this study was to compare various screening methods for efficiency and rapidity in inducing symptoms of disease to identify the most suitable approach. We compared several intact plant root inoculation (IPRI) assays, detached stem assays, and an intact plant stem inoculation (IPSI) assay. A virulent isolate of P. rubi was inoculated in two commercial cultivars: 'Chemainus' (susceptible to PRRW) and 'Cascade Bounty' (moderately resistant to PRRW). For IPRI assays, days to first symptom development, plant wilt progression, and root assessment were recorded. For detached stem tissue and IPSI assays, days to first visible lesions and lesion size were assessed. Experiments were arranged in a completely randomized design with three replications in each experiment. Three IPRI assays produced reliable symptoms in both cultivars. Among the detached stem assays, a node inoculation method performed better than other methods. Detached stem assays are useful for rapid pathogenicity testing of P. rubi , whereas IPRI assays are better for screening germplasm for disease resistance. Overall, this study identified several assays that can be used for conducting studies on pathogen phenotypic diversity (pathogenicity and virulence tests) and screening raspberry cultivars, germplasm, and breeding materials for response to PRRW.