TLR sensing of bacterial spore-associated RNA triggers host immune responses with detrimental effects

Author:

Choo Min-Kyung1ORCID,Sano Yasuyo1,Kim Changhoon2ORCID,Yasuda Kei3ORCID,Li Xiao-Dong4ORCID,Lin Xin5ORCID,Stenzel-Poore Mary6,Alexopoulou Lena7ORCID,Ghosh Sankar8ORCID,Latz Eicke9ORCID,Rifkin Ian R.3ORCID,Chen Zhijian J.4,Stewart George C.10ORCID,Chong Hyonyong2,Park Jin Mo1ORCID

Affiliation:

1. Cutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA 02129

2. Macrogen Inc., Seoul 08511, Republic of Korea

3. Renal Section, Department of Medicine, Boston University School of Medicine, Boston, MA 02118

4. Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390

5. Department of Molecular and Cellular Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030

6. Department of Molecular Microbiology and Immunology, Oregon Health and Science University, Portland, OR 97239

7. Centre d'Immunologie de Marseille-Luminy, Aix-Marseille Université, UM2, 13288 Marseille, France

8. Department of Microbiology and Immunology, College of Physicians and Surgeons, Columbia University, New York, NY 10032

9. Institute of Innate Immunity, University Hospital, University of Bonn, 53127 Bonn, Germany

10. Department of Veterinary Pathobiology and Bond Life Science Center, University of Missouri, Columbia, MO 65211

Abstract

The spores of pathogenic bacteria are involved in host entry and the initial encounter with the host immune system. How bacterial spores interact with host immunity, however, remains poorly understood. Here, we show that the spores of Bacillus anthracis (BA), the etiologic agent of anthrax, possess an intrinsic ability to induce host immune responses. This immunostimulatory activity is attributable to high amounts of RNA present in the spore surface layer. RNA-sensing TLRs, TLR7, and TLR13 in mice and their human counterparts, are responsible for detecting and triggering the host cell response to BA spores, whereas TLR2 mediates the sensing of vegetative BA. BA spores, but not vegetative BA, induce type I IFN (IFN-I) production. Although TLR signaling in itself affords protection against BA, spore RNA–induced IFN-I signaling is disruptive to BA clearance. Our study suggests a role for bacterial spore–associated RNA in microbial pathogenesis and illustrates a little known aspect of interactions between the host and spore-forming bacteria.

Funder

National Institutes of Health

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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