Autophagy induced by taurolidine protects against polymicrobial sepsis by promoting both host resistance and disease tolerance

Author:

Huang Jie1,Ita Michael2ORCID,Zhou Huiting1ORCID,Zhao He1,Hassan Fara2,Bai Zhenjiang1,O’Leary D. Peter2,Li Yiping1,Redmond H. Paul2,Wang Jiang Huai2,Wang Jian13

Affiliation:

1. Institute of Pediatric Research, Children‘s Hospital of Soochow University, Suzhou 215025, China

2. Department of Academic Surgery, University College Cork, Cork University Hospital, Cork, Ireland

3. Department of Pediatric Surgery, Children’s Hospital of Soochow University, Suzhou 215025, China

Abstract

Significance Disease resistance and tolerance are evolutionarily conserved yet distinct defense strategies that protect the host against microbial infection. Here, we report that taurolidine administered before the start of infection confers protection against polymicrobial sepsis by promoting resistance and tolerance. Notably, taurolidine given after the onset of infection also rescues mice from sepsis-associated lethality by enhancing disease tolerance to organ damage. This protection relies on an intact autophagy pathway, as taurolidine fails to protect autophagy-deficient mice against microbial sepsis. Specifically, taurolidine induces light chain 3-associated phagocytosis, but not xenophagy, in macrophages, resulting in an augmented bactericidal activity with enhanced cellular resistance to infection. These results highlight the importance of autophagy induction for taurolidine-augmented host resistance and disease tolerance and subsequent protection.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Jiangsu Province

Science and Technology of Program of Suzhou

Pediatric Solid Tumor Multidisciplinary Team

Pediatric Precise Surgical Clinical Medical Center of Suzhou

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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