Publications by authors named "J Travis Brawner"

Fusarium ear rot (FER), caused by the fungal pathogen Fusarium verticillioides, stands as one of the most economically burdensome and pervasive diseases affecting maize worldwide. Its impact on food security is particularly pronounced due to the production of fumonisins, toxic secondary metabolites that pose serious health risks, especially for livestock. FER disease severity is complex and polygenic, with few resistance (R) genes being identified for use in breeding resistant varieties.

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Modern diagnostic techniques based on DNA sequence similarity are currently the gold standard for the detection of existing and emerging pathogens. Whilst individual assays are inexpensive to use, assay development is costly and carries risks of not being sensitive or specific enough to capture an increasingly diverse range of targets. Sequencing can provide the entire nucleic acid content of a sample and may be used to identify all pathogens present in the sample when the depth of coverage is sufficient.

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Integrating disease screening data and genomic data for host and pathogen populations into prediction models provides breeders and pathologists with a unified framework to develop disease resistance. Developing disease resistance in crops typically consists of exposing breeding populations to a virulent strain of the pathogen that is causing disease. While including a diverse set of pathogens in the experiments would be desirable for developing broad and durable disease resistance, it is logistically complex and uncommon, and limits our capacity to implement dual (host-by-pathogen)-genome prediction models.

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Article Synopsis
  • A draft genome assembly of isolate GEV 3550 has been completed.
  • This isolate was obtained from Florida, USA.
  • The report highlights progress in understanding the genetic makeup of this particular isolate.
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Article Synopsis
  • Rapid pathogen identification is crucial for managing diseases, and targeted sequencing can focus on important genes for better accuracy than single-gene methods.
  • A new tool was developed for high-throughput Nanopore sequencing, extracting targeted genes from 386 fungal species to create 26,000 DNA probes aimed at enhancing identification efficiency.
  • The resulting sequencing demonstrated a significant increase in coverage and allowed for clearer phylogenetic trees, proving effective for fungal identification and potentially applicable to other pathogens.
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