Publications by authors named "C Travis Rappleye"

Article Synopsis
  • - The dimorphic fungus thrives inside host phagocytic cells and scavenges for nutrients, mainly relying on amino acids, particularly for gluconeogenesis.
  • - Growth assays show that the fungus can use most amino acids as nitrogen sources, but efficiently breaks down only specific ones like glutamine and alanine for carbon.
  • - An analysis identified 28 potential amino acid transporters, with three key transporters (Dip5, Gap3, and Gai1) significantly affecting growth on amino acids, yet the fungus remains virulent even without them, suggesting it utilizes different nutrient sources inside phagocytes during infection.
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During the infectious process, pathogenic microorganisms must obtain nutrients from the host in order to survive and proliferate. These nutritional sources include the metallic nutrient copper. Despite its essentiality, copper in large amounts is toxic.

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Peroxisomes are versatile eukaryotic organelles essential for many functions in fungi, including fatty acid metabolism, reactive oxygen species detoxification, and secondary metabolite biosynthesis. A suite of Pex proteins (peroxins) maintains peroxisomes, while peroxisomal matrix enzymes execute peroxisome functions. Insertional mutagenesis identified peroxin genes as essential components supporting the intraphagosomal growth of the fungal pathogen .

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The rapid development of CRISPR/CRISPR-associated (Cas) systems has revolutionized the ability to produce genetic mutations in a desired locus, particularly in organisms with low rates of homologous recombination. is an important respiratory and systemic fungal pathogen that has few reverse genetic options. We describe an optimized CRISPR/Cas system for the efficient generation of mutations in desired genes.

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Histoplasma capsulatum yeasts reside and proliferate within the macrophage phagosome during infection. This nutrient-depleted phagosomal environment imposes challenges to yeasts for nutrition acquisition. yeasts require all 20 amino acids, which can be formed by biosynthesis and/or acquired directly from the phagosomal environment.

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