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Glucocorticoid receptors on and in a unicellular organism,Cryptobia salmositica
Institution:1. Instituto de Ciencias Ambientales y Evolutivas, Facultad de Ciencias, Universidad Austral de Chile, Casilla 567, Isla Teja, Valdivia, Chile;2. Programa de Doctorado en Ciencias Aplicadas, Mención en Sistemas Marinos Costeros, Universidad de Antofagasta, Antofagasta, Chile;3. Department of Biology, Texas A&M University, 3258 TAMU, College Station, TX 77843, USA;4. Instituto de Ciencias Naturales “Alexander Von Humboldt”, Facultad de Ciencias del Mar y Recursos Biológicos, Universidad de Antofagasta, Av. Angamos 601, P.O. Box 170, Antofagasta, Chile;1. School of Biological Sciences, University of Queensland, St Lucia, Brisbane, Queensland 4072, Australia;2. Australian Army Malaria Institute, Brisbane, Queensland 4051, Australia;3. Queensland Tropical Health Alliance, James Cook University, Cairns, Australia;4. Eck Institute for Global Health, University of Notre Dame, IN, USA;5. Taman Damai, Jalan Fung Yei Teing, Kota Kinabalu, Sabah, Malaysia;6. CSIRO Ecosystem Sciences, Boggo Rd, Dutton Park, Queensland 4102, Australia;1. Institute of Parasitology, McGill University, Macdonald Campus, 21,111 Lakeshore Road, St Anne-de-Bellevue, QC H9X3V9, Canada;2. INRA, UMR1282 Infectiologie et Santé Publique, F-37380 Nouzilly, France;3. Université François Rabelais de Tours, UMR1282 Infectiologie et Santé Publique, F-37000 Tours, France;1. Hunan Institute of Parasitic Diseases, World Health Organisation Collaborating Centre for Research and Control of Schistosomiasis in Lake Region, Yueyang, Hunan Province, People’s Republic of China;2. Molecular Parasitology Laboratory, Infectious Diseases Division, Queensland Institute of Medical Research, Brisbane, Australia;3. School of Population Health, University of Queensland, Brisbane, Australia;4. Jiangxi Institute of Parasitic Diseases, Nanchang, Jiangxi, People’s Republic of China;5. College of Veterinary Medicine, University of Georgia, Athens, USA;6. Griffith Health Institute, Griffith University, Gold Coast, Australia;7. National Institute of Parasitic Diseases, Chinese Centre for Disease Control and Prevention, Shanghai, People’s Republic of China
Abstract:This is the first report to our knowledge that demonstrates a functional steroid hormone receptor in a protozoon. The study used Cryptobia salmositica, a pathogenic haemoflagellate found in salmonid fishes. It has been previously shown that cortisol and dexamethasone (a synthetic glucocorticoid) enhanced the multiplication of C. salmositica under in vitro conditions indicating the presence of glucocorticoid receptors on/in the parasite. Also, the glucocorticoid receptor antagonist, mifepristone (RU486), inhibited the stimulatory effect of the two glucocorticoids on parasite multiplication. In the present study, we used an antibody (produced in a rabbit against glucocorticoid receptor protein) agglutination test and confocal microscopy with immunohistofluorescence staining to demonstrate cortisol-glucocorticoid receptor-like protein receptors on the plasma membrane and in the cytoplasm of the parasite. In two in vitro studies, the addition of 50 ng ml−1 of RU486 was more effective in inhibiting parasite replication in cultures with 7,000 parasites ml−1 than in cultures with 14,000 parasites ml−1. Also, 100 ng ml−1 of RU486/ml was more effective than 50 ng ml−1 in inhibiting parasite multiplication in the 14,000 parasites ml-1 cultures. These in vitro studies indicate that the number of binding sites on/in the parasite is finite. The findings may be important in future studies especially on steroid receptor signalling pathways and dissection of ligand–receptor interactions, and for evaluating the adaptations that develop in pathogens as part of the host–parasite interaction.
Keywords:Glucocorticoid receptor (GR)  Protozoan  Cortisol  RU486  In vitro culture  Host–parasite interaction
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