AI Article Synopsis

  • This study compares two species from the same genus, highlighting that one causes invasive lung infections while the other is linked to superficial infections.
  • The analysis showed that the conidia of the invasive species elicit a stronger inflammatory response in healthy mice and have different structural and immunological properties compared to the other species’ conidia.
  • Findings suggest that targeting the unique conidial cell wall structures could lead to more effective, species-specific treatments for infections caused by these fungi.

Article Abstract

Although belong to the same genus, is primarily involved in invasive pulmonary infection, whereas is a common cause of superficial infection. In this study, we compared conidia (the infective propagules) of these two species. In immunocompetent mice, intranasal inoculation with conidia of resulted in significantly higher inflammatory responses in the lungs compared to mice inoculated with conidia. assays revealed that the dormant conidia of , unlike dormant conidia, are immunostimulatory. The conidial surface of was covered by a rodlet-layer, while that of were presented with exposed polysaccharides. harbored significantly higher number of proteins in its conidial cell wall compared to conidia. Notably, β-1,3-glucan in the conidial cell-wall showed significantly higher percentage of branching compared to that of . The polysaccharides ensemble of conidial cell wall stimulated the secretion of proinflammatory cytokines, and conidial cell wall associated proteins specifically stimulated IL-8 secretion from the host immune cells. Furthermore, the two species exhibited different sensitivities to antifungal drugs targeting cell wall polysaccharides, proposing the efficacy of species-specific treatment strategies. Overall, the species-specific organization of the conidial cell wall could be important in establishing infection by the two species.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7950546PMC
http://dx.doi.org/10.3389/fcimb.2021.643312DOI Listing

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