Automated quantification of the phagocytosis of Aspergillus fumigatus conidia by a novel image analysis algorithm
Studying the pathobiology of the fungus Aspergillus fumigatus has gained a lot of attention in recent years. This is due to the fact that this fungus is a human pathogen that can cause severe diseases, like invasive pulmonary aspergillosis in immunocompromised patients. Because alveolar macrophages belong to the first line of defense against the fungus, here, we conduct an image-based study on the host-pathogen interaction between murine alveolar macrophages and A. fumigatus. This is achieved by an automated image analysis approach that uses a combination of thresholding, watershed segmentation and feature-based object classification. In contrast to previous approaches, our algorithm allows for the segmentation of individual macrophages in the images and this enables us to compute the distribution of phagocytosed and macrophage-adherent conidia over all macrophages. The novel automated image-based analysis provides access to all cell-cell interactions in the assay and thereby represents a framework that enables comprehensive computation of diverse characteristic parameters and comparative investigation for different strains. We here apply automated image analysis to confocal laser scanning microscopy images of the two wild-type strains ATCC 46645 and CEA10 of A. fumigatus and investigate the ability of macrophages to phagocytose the respective conidia. It is found that the CEA10 strain triggers a stronger response of the macrophages as revealed by a higher phagocytosis ratio and a larger portion of the macrophages being active in the phagocytosis process.
SEEK ID: https://funginet.hki-jena.de/publications/13
PubMed ID: 26106370
Projects: FungiNet A - Aspergillus projects, FungiNet B - Bioinformatics projects
Publication type: Not specified
Journal: Front Microbiol
Citation:
Date Published: 9th Jun 2015
Registered Mode: Not specified
Views: 2444
Created: 8th Mar 2016 at 08:59
Last updated: 17th Jan 2024 at 10:24
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