Author
Listed:
- Carissa K. Harvest
(Duke University School of Medicine
Duke University School of Medicine
University of North Carolina at Chapel Hill)
- Taylor J. Abele
(Duke University School of Medicine
Duke University School of Medicine)
- Chen Yu
(Duke University School of Medicine)
- Cole J. Beatty
(Duke University School of Medicine
Duke University School of Medicine)
- Megan E. Amason
(Duke University School of Medicine
Duke University School of Medicine
University of North Carolina at Chapel Hill)
- Zachary P. Billman
(Duke University School of Medicine
Duke University School of Medicine
University of North Carolina at Chapel Hill)
- Morgan A. DePrizio
(Duke University School of Medicine
Duke University School of Medicine)
- Fernando W. Souza
(Duke University School of Medicine
Duke University School of Medicine
Duke University School of Medicine)
- Carolyn A. Lacey
(Duke University School of Medicine
Duke University School of Medicine)
- Vivien I. Maltez
(University of North Carolina at Chapel Hill)
- Heather N. Larson
(Duke University School of Medicine
Duke University School of Medicine)
- Benjamin D. McGlaughon
(University of North Carolina at Chapel Hill)
- Daniel R. Saban
(Duke University School of Medicine
Duke University School of Medicine)
- Stephanie A. Montgomery
(University of North Carolina at Chapel Hill)
- Edward A. Miao
(Duke University School of Medicine
Duke University School of Medicine
Duke University School of Medicine
Duke University School of Medicine)
Abstract
Granulomas often form around pathogens that cause chronic infections. Here, we discover an innate granuloma model in mice with an environmental bacterium called Chromobacterium violaceum. Granuloma formation not only successfully walls off, but also clears, the infection. The infected lesion can arise from a single bacterium that replicates despite the presence of a neutrophil swarm. Bacterial replication ceases when macrophages organize around the infection and form a granuloma. This granuloma response is accomplished independently of adaptive immunity that is typically required to organize granulomas. The C. violaceum-induced granuloma requires at least two separate defense pathways, gasdermin D and iNOS, to maintain the integrity of the granuloma architecture. This innate granuloma successfully eradicates C. violaceum infection. Therefore, this C. violaceum-induced granuloma model demonstrates that innate immune cells successfully organize a granuloma and thereby resolve infection by an environmental pathogen.
Suggested Citation
Carissa K. Harvest & Taylor J. Abele & Chen Yu & Cole J. Beatty & Megan E. Amason & Zachary P. Billman & Morgan A. DePrizio & Fernando W. Souza & Carolyn A. Lacey & Vivien I. Maltez & Heather N. Larso, 2023.
"An innate granuloma eradicates an environmental pathogen using Gsdmd and Nos2,"
Nature Communications, Nature, vol. 14(1), pages 1-19, December.
Handle:
RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42218-1
DOI: 10.1038/s41467-023-42218-1
Download full text from publisher
References listed on IDEAS
- Kengo Nozaki & Vivien I. Maltez & Manira Rayamajhi & Alan L. Tubbs & Joseph E. Mitchell & Carolyn A. Lacey & Carissa K. Harvest & Lupeng Li & William T. Nash & Heather N. Larson & Benjamin D. McGlaugh, 2022.
"Caspase-7 activates ASM to repair gasdermin and perforin pores,"
Nature, Nature, vol. 606(7916), pages 960-967, June.
Full references (including those not matched with items on IDEAS)
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