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1 May 2011 Histopathology of Experimental Myiasis in Mice as a Result of Infestation and Experimental Implantation of Dermatobia hominis Larvae
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Abstract

A laboratory model of myiasis as a result of Dermatobia hominis (L.) larvae was developed using mice as hosts. Mice in three groups were each infested with one newly hatched larva and skin biopsies processed for histopathology at 4, 12, and 20 d postinfestation (dpi). Mice in three other groups were each subjected to implantation of one larva collected from an infested (donor) mouse at 4, 12, and 20 dpi. Skin lesions of these receptor mice were then assessed at 10, 14, and 6 d postimplantation (dpimp), respectively. The inflammatory process in infested mice at 4 dpi was discrete, consisting of a thin necrotic layer around the larva, edema, many neutrophils, few eosinophils, mast cells, and proliferation of fibroblasts. At 12 dpi, there was a thicker necrotic layer, edema, many neutrophils and eosinophils, few mast cells, neoformation of capillaries, proliferation of the endothelium and fibroblasts, and early stages of fibrosis. These histopathological characteristics together with fibrosis were observed over a large area of the lesion at 20 dpi. Mice submitted to larval implantations demonstrated similar skin histopathology to that seen in the infested rodents, 10 dpimp corresponding to 12 dpi and 6 or 14 dpimp to 20 dpi. In all mice, the progressive acute inflammatory process followed a sequence linked to factors such as size of larvae and presence of secretory-excretory products. Both infested mice and those implanted experimentally with D. hominis larvae were shown to be suitable models for the study of the parasite-host relationship in this important zoonotic myiasis.

© 2011 Entomological Society of America
A.C.R. Leite, M.F.A. Nascimento, L.H.R. Leite, and V.H.R. Leite "Histopathology of Experimental Myiasis in Mice as a Result of Infestation and Experimental Implantation of Dermatobia hominis Larvae," Journal of Medical Entomology 48(3), 680-686, (1 May 2011). https://doi.org/10.1603/ME10237
Received: 29 October 2010; Accepted: 1 January 2011; Published: 1 May 2011
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