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        <identifier>oai:figshare.com:article/33936181</identifier>
        <datestamp>2026-09-18T14:24:00Z</datestamp>
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          <dc:title>Aspergillus fumigatus and Cryptic Species Exhibit Distinct Strategies for Adaptation to Host-Relevant Conditions</dc:title>
          <dc:creator>Alexandre Mendonça (24209241)</dc:creator>
          <dc:subject>Biological adaptation</dc:subject>
          <dc:subject>Mycology</dc:subject>
          <dc:subject>Infectious agents</dc:subject>
          <dc:subject>Biological network analysis</dc:subject>
          <dc:subject>Proteomics and metabolomics</dc:subject>
          <dc:subject>Sequence analysis</dc:subject>
          <dc:subject>Section Fumigati</dc:subject>
          <dc:subject>Comparative Genomics</dc:subject>
          <dc:subject>Genotype-Phenotype Relationships</dc:subject>
          <dc:subject>Host Adaptation</dc:subject>
          <dc:subject>Antifungal Resistance</dc:subject>
          <dc:description>&lt;p dir="ltr"&gt;&lt;i&gt;Aspergillus fumigatus&lt;/i&gt; is the leading cause of invasive aspergillosis however, cryptic species within section &lt;i&gt;Fumigati&lt;/i&gt; are emerging pathogens due to antifungal resistance and misidentification in routine clinical practice. We investigated whether divergence in virulence-associated proteins accompanies phenotypic diversification across section &lt;i&gt;Fumigati&lt;/i&gt;. Forty virulence-associated proteins were analyzed across 71 genomes, while 16 random representative isolates were evaluated under host-relevant conditions. Protein-based multidimensional scaling revealed species-specific divergence in virulence-associated proteins, most prominently for host interactions, and secondary metabolism.&lt;/p&gt;&lt;p dir="ltr"&gt;Phenotype-based principal component analysis reproduced the species-level clustering observed in protein-based analyses, separating &lt;i&gt;A. fumigatus&lt;/i&gt; from cryptic species. Cryptic species displayed enhanced metabolic activity and biomass production on alternative respiratory carbon sources, reduced macrophage damage, and higher frequency of pan-azole resistance. &lt;i&gt;A. fumigatus&lt;/i&gt; exhibited faster germination, greater metabolic activity and biomass under thermal, osmotic, cell wall and oxidative stress, and enhanced fungal persistence following macrophage interaction. Category-specific protein phylogenies and phenotypic heatmaps demonstrated broad genotype-phenotype concordance.&lt;/p&gt;&lt;p dir="ltr"&gt;Together, these findings demonstrate that divergence in virulence-associated proteins accompanies species-specific metabolic, stress-responses and host-pathogen adaptations across section &lt;i&gt;Fumigati&lt;/i&gt;.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-18T14:24:00Z</dc:date>
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          <dc:identifier>10.6084/m9.figshare.33936181.v1</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Aspergillus_fumigatus_and_Cryptic_Species_Exhibit_Distinct_Strategies_for_Adaptation_to_Host-Relevant_Conditions/33936181</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
          <dc:rights>Open Access after 2027-01-31</dc:rights>
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