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Unraveling Ascaris suum experimental infection in humans
Affiliation:1. Laboratory of Veterinary Parasitic Diseases, Department of Veterinary Sciences, Faculty of Agriculture, University of Miyazaki, 1-1, Gakuen-Kibanadai Nishi, Miyazaki 889-2192, Japan;2. Department of Parasitology, Faculty of Veterinary medicine, Vietnam National University of Agriculture, Trau Quy, Gia Lam, Ha Noi, Viet Nam;3. Centre for Animal Disease Control (CADIC), University of Miyazaki, 1-1, Gakuen-Kibanadai Nishi, Miyazaki 889-2192, Japan;4. Division of Parasitology, Department of Infectious Diseases, Faculty of Medicine, University of Miyazaki 5200 Kihara, Kiyotake-cho, Miyazaki 889-1692, Japan.
Abstract:Ascaris lumbricoides and Ascaris suum are two closely related parasites that infect humans and pigs. The zoonotic potential of A. suum has been a matter of debate for decades. Here we sought to investigate the potential human infection by A. suum and its immunological alterations. We orally infected five healthy human subjects with eggs embraced by A. suum. The infection was monitored for symptoms and possible respiratory changes, by an interdisciplinary health team. Parasitological, hematological analyses, serum immunoglobulin, cytokine profiles, and gene expression were evaluated during the infection. Our results show that A. suum is able to infect and complete the cycle in humans causing A. lumbricoides similar symptoms, including, cough, headache, diarrhea, respiratory discomfort and chest x-ray alterations coinciding with larvae migration in the lungs. We also observed activation of the immune system with production of IgM and IgG and a Th2/Th17 response with downregulation of genes related to Th1 and apoptosis. PCA (Principal componts analysis) show that infection with A. suum leads to a change in the immune landscape of the human host. Our data reinforce the zoonotic capacity of A. suum and bring a new perspective on the understanding of the immune response against this parasite.
Keywords:Larval migration  Ascariasis  Host–parasite relationships  Th2/Th17 responses  Human infection
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