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How the microbiota controls neutrophil activity

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IMAGE: Neutrophils take their cue: A protein produced in the intestinal epithelium in response to the microbiome educates innate immune cells. High resolution in vivo imaging of a zebrafish larva reveals... view more 

Credit: Caitlin Murdoch (2019)

A host protein called Serum Amyloid A (Saa) is a major factor mediating the effects of the microbiota on the function of immune cells called neutrophils, according to a study published March 7 in the open-access journal PLOS Pathogens by John Rawls of Duke University School of Medicine, and colleagues.

Experiments in zebrafish showed that Saa produced by the intestine in response to the microbiota serves as a signal to neutrophils to restrict aberrant activation, decreasing inflammation and bacterial killing potential while simultaneously enhancing their ability to migrate to wounds.

The intestine is colonized by complex microbial communities called the microbiota, which impact diverse aspects of host physiology, including the development and function of the immune system. The microbiota strongly impacts the activity of innate immune cells called neutrophils, which are essential for host defense against infection, but the underlying mechanisms remain poorly understood. Caitlin Murdoch, a graduate student in Dr. Rawls' lab suspected that the effects of the microbiota on immunity could be mediated by Saa. This host protein is produced by the intestine and liver in response to the microbiota, but until now, its functions in living organisms were elusive.

Using normal and mutant zebrafish, the researchers demonstrate that Saa promotes the recruitment of neutrophils to sites of injury, yet restricts the clearance of pathogenic bacterial infection. Analysis of isolated neutrophils revealed that Saa reduces the bactericidal activity of these cells and their expression of pro-inflammatory genes. These effects depend on microbiota colonization, suggesting that this protein mediates the microbiota's effects on host immunity. Collectively, these data establish that Saa induced by the microbiota in the intestine signals to neutrophils, tuning the extent to which they may be activated by other microbes or respond to injury. Because antibiotic treatment results in reduced intestinal Saa in mice, the authors suggest that antibiotic treatment could be associated with Saa-mediated aberrations in neutrophil function. They speculate that secondary infections that can occur following antibiotic use could be due in part to concomitant alterations in the production of this protein.

The authors add, "Our study demonstrates that a host protein made in the intestine following exposure to the microbiota affects innate immune cell populations, both in the gut and other tissues. Microbially responsive secretion of host factors from the intestine can therefore serve as a molecular rheostat which controls the development and function of the host innate immune system."

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Research Article

Funding: This work was supported by NIH grant P01-DK094779 to JFR; AI130236 to DMT; and NSF grant DGE-1644868 to CCM. The Zeiss Z.1 Lightsheet microscope was supported by NIH S10 1S10OD020010-1A1. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing Interests: The authors have declared that no competing interests exist.

Citation: Murdoch CC, Espenschied ST, Matty MA, Mueller O, Tobin DM, Rawls JF (2019) Intestinal serum amyloid a suppresses systemic neutrophil activation and bactericidal activity in response to microbiota colonization. PLoS Pathog 15(3): e1007381. https://doi.org/10.1371/journal.ppat.1007381

Author Affiliations:

Department of Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, North Carolina, United States of America

Department of Immunology, Duke University School of Medicine, Durham, North Carolina, United States of America

Department of Medicine, Duke University School of Medicine, Durham, North Carolina, United States of America

In your coverage please use this URL to provide access to the freely available paper: http://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1007381

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