Recurrent infection progressively disables host protection against intestinal inflammation

Author:

Yang Won Ho123ORCID,Heithoff Douglas M.13ORCID,Aziz Peter V.123ORCID,Sperandio Markus4ORCID,Nizet Victor5ORCID,Mahan Michael J.13,Marth Jamey D.123ORCID

Affiliation:

1. Center for Nanomedicine, University of California, Santa Barbara, Santa Barbara, CA 93106, USA.

2. Sanford Burnham Prebys Medical Discovery Institute, University of California, Santa Barbara, Santa Barbara, CA 93106, USA.

3. Department of Molecular, Cellular, and Developmental Biology, University of California, Santa Barbara, Santa Barbara, CA 93106, USA.

4. Walter-Brendel-Centre for Experimental Medicine, Ludwig-Maximilians-University, Munich, Germany.

5. Department of Pediatrics and Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, La Jolla, CA 92093, USA.

Abstract

Minor infections cause big problems Pathogenic infection has been implicated in the chronic inflammation seen in inflammatory bowel diseases (IBDs) such as ulcerative colitis and Crohn's disease. Yang et al. show that recurrent, low-level, and fully resolving Salmonella enterica Typhimurium (ST) infections can precipitate severe colonic inflammation in mice. ST-induced TLR4 activation resulted in increased neuraminidase 3 (Neu3) production and activity in the duodenum. This led to intestinal alkaline phosphatase (IAP) desialylation and degradation. IAP deficiency caused a marked increase in commensal bacteria-generated lipopolysaccharide-phosphate in the colon, provoking inflammation. Treatment with calf IAP or the antiviral drug zanamivir (which inhibits Neu3 activity) prevented this inflammatory cascade. This pathway may serve as an effective target for future human IBD therapies. Science , this issue p. eaao5610

Funder

National Institutes of Health

German Research Foundation

Wille Family Foundation

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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