Increasing evidence suggests that in hosts infected with parasites of the complex, transmission of infection to the sand fly vector is linked to parasite repositories in the host skin. However, a detailed understanding of the dispersal (the mechanism of spread) and dispersion (the observed state of spread) of these obligatory-intracellular parasites and their host phagocytes in the skin is lacking. Using endogenously fluorescent parasites as a proxy, we apply image analysis combined with spatial point pattern models borrowed from ecology to characterize dispersion of parasitized myeloid cells (including Man and CD11c cells) and predict dispersal mechanisms in a previously described immunodeficient model of infection. Our results suggest that after initial seeding of infection in the skin, heavily parasite-infected myeloid cells are found in patches that resemble innate granulomas. Spread of parasites from these initial patches subsequently occurs through infection of recruited myeloid cells, ultimately leading to self-propagating networks of patch clusters. This combination of imaging and ecological pattern analysis to identify mechanisms driving the skin parasite landscape offers new perspectives on myeloid cell behavior following parasitism by and may also be applicable to elucidating the behavior of other intracellular tissue-resident pathogens and their host cells.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8716623PMC
http://dx.doi.org/10.3389/fimmu.2021.795554DOI Listing

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