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Long-Read Sequencing Genome Assembly of Ceratocystis fimbriata Enables Development of Molecular Diagnostics for Sweetpotato Black Rot.
Stahr, M N; Parada-Rojas, C; Childs, K L; Alfenas, R F; Fernandes, F M; Avila, K; Quesada-Ocampo, L M.
Affiliation
  • Stahr MN; Department of Entomology and Plant Pathology and NC Plant Sciences Initiative, North Carolina State University, Raleigh, NC 27695-7825, U.S.A.
  • Parada-Rojas C; Department of Entomology and Plant Pathology and NC Plant Sciences Initiative, North Carolina State University, Raleigh, NC 27695-7825, U.S.A.
  • Childs KL; Department of Plant Biology, Michigan State University, East Lansing, MI 48824, U.S.A.
  • Alfenas RF; Department of Plant Pathology, Universidade Federal de Viçosa, Minas Gerais State, 36570-900, Brazil.
  • Fernandes FM; Department of Plant Pathology, Universidade Federal de Viçosa, Minas Gerais State, 36570-900, Brazil.
  • Avila K; Department of Entomology and Plant Pathology and NC Plant Sciences Initiative, North Carolina State University, Raleigh, NC 27695-7825, U.S.A.
  • Quesada-Ocampo LM; Department of Entomology and Plant Pathology and NC Plant Sciences Initiative, North Carolina State University, Raleigh, NC 27695-7825, U.S.A.
Phytopathology ; 114(6): 1411-1420, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38264989
ABSTRACT
Ceratocystis fimbriata is a destructive fungal pathogen of sweetpotato (Ipomoea batatas) that leads to losses at all stages of sweetpotato production. Accurate detection of C. fimbriata would allow for more efficient deployment of management tactics in sweetpotato production. To develop a diagnostic assay, a hybrid genome assembly of C. fimbriata isolate AS236 was generated. The resulting 31.7-MB assembly was near-chromosome level, with 18 contigs, 6,481 predicted genes, and a BUSCO completion score of 98.4% when compared with the fungus-specific lineage database. Additional Illumina DNA reads from C. manginecans, C. platani, and a second C. fimbriata isolate (C1421) were then mapped to the assembled genome using BOWTIE2 and counted using HTSeq, which identified 148 genes present only within C. fimbriata as molecular diagnostic candidates; 6 single-copy and 35 highly multi-copy (>40 BLAST hits), as determined through a self-BLAST-P alignment. Primers for PCR were designed in the 200-bp flanking region of the first exon for each candidate, and the candidates were validated against a diverse DNA panel containing Ceratocystis species, sweetpotato pathogens, and plants. After validation, two diagnostic candidates amplified only C. fimbriata DNA and were considered to be highly specific to the species. These genetic markers will serve as valuable diagnostic tools with multiple applications including the detection of C. fimbriata in seed, soil, and wash water in sweetpotato production.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Plant Diseases / Ascomycota / Genome, Fungal / Ipomoea batatas Type of study: Diagnostic_studies / Prognostic_studies Language: En Journal: Phytopathology Journal subject: BOTANICA Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Plant Diseases / Ascomycota / Genome, Fungal / Ipomoea batatas Type of study: Diagnostic_studies / Prognostic_studies Language: En Journal: Phytopathology Journal subject: BOTANICA Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States