Lipid A Variants Activate Human TLR4 and the Noncanonical Inflammasome Differently and Require the Core Oligosaccharide for Inflammasome Activation

Author:

Alexander-Floyd Jasmine1,Bass Antonia R.1,Harberts Erin M.2,Grubaugh Daniel3,Buxbaum Joseph D.456,Brodsky Igor E.3ORCID,Ernst Robert K.2ORCID,Shin Sunny1ORCID

Affiliation:

1. Department of Microbiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA

2. Department of Microbial Pathogenesis, University of Maryland, School of Dentistry, Baltimore, Maryland, USA

3. Department of Pathobiology, University of Pennsylvania School of Veterinary Medicine, Philadelphia, Pennsylvania, USA

4. Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, New York, USA

5. Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, USA

6. Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, New York, USA

Abstract

Detection of Gram-negative bacterial lipid A by the extracellular sensor, myeloid differentiation 2 (MD2)/Toll-like receptor 4 (TLR4), or the intracellular inflammasome sensors, CASP4 and CASP5, induces robust inflammatory responses. The chemical structure of lipid A, specifically its phosphorylation and acylation state, varies across and within bacterial species, potentially allowing pathogens to evade or suppress host immunity.

Funder

HHS | NIH | National Institute of Allergy and Infectious Diseases

HHS | NIH | National Institute of General Medical Sciences

National Science Foundation

Burroughs Wellcome Fund

HHS | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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