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      Opposing Effects of Fasting Metabolism on Tissue Tolerance in Bacterial and Viral Inflammation

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          Summary

          Acute infections are associated with a set of stereotypic behavioral responses, including anorexia, lethargy, and social withdrawal. Although these so called sickness behaviors are the most common and familiar symptoms of infections, their roles in host defense are largely unknown. Here we investigated the role of anorexia in models of bacterial and viral infections. We found that anorexia was protective while nutritional supplementation was detrimental in bacterial sepsis. Furthermore, glucose was necessary and sufficient for these effects. In contrast, nutritional supplementation protected against mortality from influenza infection and viral sepsis, while blocking glucose utilization was lethal. In both bacterial and viral models, these effects were largely independent of pathogen load and magnitude of inflammation. Instead, we identify opposing metabolic requirements tied to cellular stress adaptations critical for tolerance of differential inflammatory states.

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          Author and article information

          Journal
          0413066
          2830
          Cell
          Cell
          Cell
          0092-8674
          1097-4172
          7 July 2017
          08 September 2016
          08 September 2017
          : 166
          : 6
          : 1512-1525.e12
          Affiliations
          [1 ]Department of Immunobiology, Yale University School of Medicine, New Haven, CT 06520, USA
          [2 ]Department of Medicine (Rheumatology), Yale University School of Medicine, New Haven, CT 06520, USA
          [3 ]Department of Medicine (Nephrology), Yale University School of Medicine, New Haven, CT 06520, USA
          [4 ]Yale PET Center, Department of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, CT 06520, USA
          [5 ]Section of Comparative Medicine, Yale University School of Medicine, New Haven, CT 06520, USA
          [6 ]Howard Hughes Medical Institute
          Author notes
          [7]

          These authors contributed equally to this work

          Article
          PMC5555589 PMC5555589 5555589 nihpa889505
          10.1016/j.cell.2016.07.026
          5555589
          27610573
          86c8f584-bee5-4e9d-9684-bdd18543a745
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