Journal article
Induction of neutrophil extracellular traps by Campylobacter jejuni
Cellular microbiology, Vol.22(8), pp.e13210-n/a
08/2020
DOI: 10.1111/cmi.13210
PMCID: PMC7354212
PMID: 32329205
Abstract
Campylobacter jejuni is the leading cause of bacterial-derived gastroenteritis worldwide and can lead to several post-infectious inflammatory disorders. Despite the prevalence and health impacts of the bacterium, interactions between the host innate immune system and C. jejuni remain poorly understood. To expand on earlier work demonstrating that neutrophils traffic to the site of infection in an animal model of campylobacteriosis, we identified significant increases in several predominantly neutrophil-derived proteins in the faeces of C. jejuni-infected patients, including lipocalin-2, myeloperoxidase and neutrophil elastase. In addition to demonstrating that these proteins significantly inhibited C. jejuni growth, we determined they are released during formation of C. jejuni-induced neutrophil extracellular traps (NETs). Using quantitative and qualitative methods, we found that purified human neutrophils are activated by C. jejuni and exhibit signatures of NET generation, including presence of protein arginine deiminase-4, histone citrullination, myeloperoxidase, neutrophil elastase release and DNA extrusion. Production of NETs correlated with C. jejuni phagocytosis/endocytosis and invasion of neutrophils suggesting that host- and bacterial-mediated activities are responsible for NET induction. Further, NET-like structures were observed within intestinal tissue of C. jejuni-infected ferrets. Finally, induction of NETs significantly increased human colonocyte cytotoxicity, indicating that NET formation during C. jejuni infection may contribute to observed tissue pathology. These findings provide further understanding of C. jejuni-neutrophil interactions and inflammatory responses during campylobacteriosis.
Details
- Title: Subtitle
- Induction of neutrophil extracellular traps by Campylobacter jejuni
- Creators
- Sean Callahan - University of Tennessee at KnoxvilleRyan S Doster - Vanderbilt University Medical CenterJoseph W Jackson - University of Tennessee at KnoxvilleBrittni R Kelley - University of Tennessee at KnoxvilleJennifer A Gaddy - Vanderbilt University Medical CenterJeremiah G Johnson - University of Tennessee at Knoxville
- Resource Type
- Journal article
- Publication Details
- Cellular microbiology, Vol.22(8), pp.e13210-n/a
- DOI
- 10.1111/cmi.13210
- PMID
- 32329205
- PMCID
- PMC7354212
- NLM abbreviation
- Cell Microbiol
- ISSN
- 1462-5814
- eISSN
- 1462-5822
- Grant note
- R01 HD090061 / NICHD NIH HHS P30 DK058404 / NIDDK NIH HHS IK2 BX001701 / BLRD VA UL1 RR024975 / NCRR NIH HHS P30 DK020593 / NIDDK NIH HHS R01 AI134036 / NIH HHS R01 AI134036 / NIAID NIH HHS P30 DK058404 / NIH HHS UL1 TR000445 / NCATS NIH HHS P30 CA068485 / NCI NIH HHS P30 EY008126 / NEI NIH HHS T32 CA082084 / NCI NIH HHS U24 DK059637 / NIDDK NIH HHS K08 AI151100 / NIAID NIH HHS U01 TR002398 / NCATS NIH HHS
- Language
- English
- Date published
- 08/2020
- Academic Unit
- Microbiology and Immunology
- Record Identifier
- 9984696570302771
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