| Literature DB >> 29754819 |
Felipe A Pinho-Ribeiro1, Buket Baddal2, Rianne Haarsma1, Maghnus O'Seaghdha3, Nicole J Yang1, Kimbria J Blake1, Makayla Portley1, Waldiceu A Verri4, James B Dale5, Michael R Wessels2, Isaac M Chiu6.
Abstract
The nervous system, the immune system, and microbial pathogens interact closely at barrier tissues. Here, we find that a bacterial pathogen, Streptococcus pyogenes, hijacks pain and neuronal regulation of the immune response to promote bacterial survival. Necrotizing fasciitis is a life-threatening soft tissue infection in which "pain is out of proportion" to early physical manifestations. We find that S. pyogenes, the leading cause of necrotizing fasciitis, secretes streptolysin S (SLS) to directly activate nociceptor neurons and produce pain during infection. Nociceptors, in turn, release the neuropeptide calcitonin gene-related peptide (CGRP) into infected tissues, which inhibits the recruitment of neutrophils and opsonophagocytic killing of S. pyogenes. Botulinum neurotoxin A and CGRP antagonism block neuron-mediated suppression of host defense, thereby preventing and treating S. pyogenes necrotizing infection. We conclude that targeting the peripheral nervous system and blocking neuro-immune communication is a promising strategy to treat highly invasive bacterial infections. VIDEO ABSTRACT.Entities:
Keywords: CGRP; botulinum neurotoxin; infection; neuroimmune; neuroimmunology; neutrophil; nociceptor; pain; streptococcus pyogenes; streptolysin
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Year: 2018 PMID: 29754819 PMCID: PMC5959783 DOI: 10.1016/j.cell.2018.04.006
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582