Sclerotium rolfsii Sacc. is a soil-borne fungus that causes southern blight on many crops in the tropical and subtropical regions. In 2018, southern blight was reported as the most prevalent bean root rot in Uganda. Earlier studies ascertained the morphological and pathogenic diversity of S. rolfsii, but a limited understanding of its genetic diversity exists. Knowledge of S. rolfsii genetic diversity is a critical resource for pathogen surveillance and developing common bean varieties with durable resistance. A total of 188 S. rolfsii strains from infected common bean plants were collected from seven agro-ecological zones of Uganda in 2013, 2020 and 2021, and characterized morphologically and pathogenically. The genetic diversity of the strains was assessed using single-nucleotide polymorphisms (SNPs) obtained from whole-genome sequencing. The growth rate of the strains ranged between 1.1 and 3.6 cm per day, while the number of sclerotia produced ranged from 0 to 543 per strain. The strains had fluffy, fibrous, and compact colony texture. The strains were pathogenic on common bean and caused disease severity indices ranging from 10.1% to 93.3%. Average polymorphic information content across all chromosomes was 0.27. Population structure analysis identified five genetically distinct clusters. The results of analysis of molecular variance revealed that 54% of the variation was between clusters while 46% of variation was within clusters. Pairwise comparison of Wright’s fixation indices between genetic clusters ranged from 0.31 to 0.78. The findings of this study revealed moderate genetic diversity among S. rolfsii strains, which should be taken into consideration when selecting strains for germplasm screening.

Recently, Fusarium root rot (FRR)-like symptoms were observed in Uganda’s agroecology zones, prompting the National Agricultural Organisation (NARO) to conduct a disease survey. The survey reports indicated FRR as the second most prevalent root rot disease of common bean in Uganda after Southern blight. Ninety nine Fusarium spp. strains were obtained from samples collected during the surveys. The strains were morphologically and pathogenically characterised and confirmed to cause Fusarium root rot as observed in the field. However, molecular characterization of the strains was not conducted. In this study, therefore, 80 of the strains were characterized using partial sequences of translation elongation factor 1-alpha (TEF-1α) gene, beta tubulin (β tubulin) gene and internal transcribed spacers (ITS) region of ribosomal RNA to determine species diversity. High-quality Sanger sequences from the target genes were compared to the sequences from Fusarium species available in the National Centre for Biotechnology Information coding sequences (NCBI-CDS) database to determine the most likely species the strains belonged. The sequences from our strains were deposited into the NCBI gene bank under ID#288420, 2883276, 2873058 for TEF-1α, β tubulin and ITS respectively. The Fusarium species identified included; F. oxysporum, F. solani, F. equiseti F. delphinoides, F. commune, F. subflagellisporum, F. fabacearum, F. falciforme, F. brevicaudatum, F. serpentimum, F. fredkrugeri and F. brachygibbosum. The diversity of these Fusarium species needs to be taken into consideration when developing breeding programs for management of the disease since currently there is no variety of common bean resistant to FRR in Uganda.

Recently, Fusarium root rot (FRR)-like symptoms were observed in Uganda’s agroecology zones, prompting the National Agricultural Organisation (NARO) to conduct a disease survey. The survey reports indicated FRR as the second most prevalent root rot disease of common bean in Uganda after Southern blight. Ninety nine Fusarium spp. strains were obtained from samples collected during the surveys. The strains were morphologically and pathogenically characterised and confirmed to cause Fusarium root rot as observed in the field. However, molecular characterization of the strains was not conducted. In this study therefore, 80 of the strains were characterized using partial sequences of translation elongation factor 1-alpha (TEF-1α) gene, beta tubulin (β tubulin) gene and internal transcribed spacers (ITS) region of ribosomal RNA to determine species diversity. High quality Sanger sequences from the target genes were compared to the sequences from Fusarium species available in the National Centre for Biotechnology Information coding sequences (NCBI-CDS) database to determine the most likely species the strains belonged. The sequences from our strains were deposited into the NCBI gene bank under ID#288420, 2883276, 2873058 for TEF-1α, β tubulin and ITS respectively. The Fusarium species identified included; F. Oxysporum, F. solani, F. equiseti F. delphinoides, F. commune, F. subflagellisporum, F. fabacearum, F. falciforme, F. brevicaudatum, F. serpentimum, F. fredkrugeri and F. brachygibbosum. The diversity of these Fusarium species needs to be taken into consideration when developing breeding programs for management of the disease since currently there is no variety of common bean resistant to FRR in Uganda.

Sclerotium rolfsi Sacc. is a soil born fungus that causes southern blight to many crops in the tropical and subtropical regions. In 2018, Southern blight was reported to be the most prevalent bean root rot in Uganda. Earlier studies ascertained the morphological and pathogenic diversity of S. rolfsii , but limited understanding of its genetic diversity exists. Knowledge of S. rolfsii genetic diversity is a critical resource in the development of common bean varieties with durable resistance to the pathogen. A total of 188 S. rolfsii strains were collected from seven agro-ecological zones of Uganda in 2013, 2020 and 2021, and characterized for pathogenecity, growth rate, the number and colour of sclerotia produced and colony texture. The genetic diversity of the 188 strains was assessed using single nucleotide polymorphisms (SNPs) obtained from whole genome sequencing. The growth rate of the strains ranged between 1.1 to 3.6 cm/day while the number of sclerotia produced ranged between 0 to 543 per strain. The strains had fluffy, fibrous and compact colony texture. The sclerotia were either brown or dark brown. The analyzed strains were pathogenic on common bean and caused a disease severity indices between 10.1% and 93.3%. Average polymorphic information content across all chromosomes was 0.322 with a minimum of 0.145 and maximum of 0.525. Average observed heterozygosity across all the chromosomes was 0.782. Population structure analysis identified five genetically distinct groups. The results of analysis of molecular variance revealed that 0.39% of the variation was between population while 11.98% was between samples within population and 87.62% between samples across populations. The average genetic distances between the isolates from different agro-ecological zones was 0.038 while the average similarity coefficient was 0.968 There were significant differences in the morphological traits and pathogenicity across the different genetic clusters. This high levels of genetic diversity within strains needs to be taken into consideration while selecting strains for screening breeding lines. Key word: Pathogenicity, genetic diversity, Characterisation, Southern blight, common bean