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Delayed presence of alternatively activated macrophages during a Francisella tularensis infection
Affiliation:1. Biomedical Sciences, Dstl Porton Down, Salisbury SP4 0JQ, UK;2. Pathology Department, Animal Health and Veterinary Laboratories Agency – Weybridge, Woodham Lane, New Haw, Addlestone KT15 3NB, UK;1. Department of Immunology, Army Medical Research Institute of Infectious Diseases, Frederick, MD, USA;2. Department of Bacteriology, Army Medical Research Institute of Infectious Diseases, Frederick, MD, USA;1. Department of Anesthesiology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China;2. Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, China;3. Department of Pathology, Sun Yat-sen University Cancer Center, Guangzhou, China;4. Department of Anesthesiology, Guangdong Cardiovascular Institute and Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China;5. Department of Medical Laboratory, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China;6. Department of Anesthesiology, Nanfang Hospital, Southern Medical University, Guangzhou, China;1. Division of Pharmacy, Ehime University Hospital, 454 Shitsukawa, Toon, Ehime 791-0295, Japan;2. Integrated Center for Sciences, Ehime University, 454 Shitsukawa, Toon, Ehime 791-0295, Japan;3. School of Pharmacy, Shujitsu University, 1-6-1 Nishigawara, Naka-ku, Okayama, Okayama 703-8516, Japan
Abstract:Francisella tularensis is an intracellular bacterium that has the ability to multiply within the macrophage. The phenotype of a macrophage can determine whether the infection is cleared or the host succumbs to disease. Previously published data has suggested that F. tularensis LVS actively induces the alternative phenotype as a survival mechanism. In these studies we demonstrate that this is not the case for the more virulent strain of F. tularensis SCHU-S4. During an intranasal mouse model of infection, immuno-histochemistry identified that iNOS positive (“classical”) macrophages are present at 72 h post-infection and remain high (supported by CCL-5 release) in numbers. In contrast, arginase/FIZZ-1 positive (“alternative”) cells appear later and in low numbers during the development of the disease tularemia.
Keywords:Francisella  Tularensis  Macrophages  Activation  Classical  Alternative  Immunohistochemistry
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