Transient and Prolonged Response of Chicken Cecum Mucosa to Colonization with Different Gut Microbiota

PLoS One. 2016 Sep 29;11(9):e0163932. doi: 10.1371/journal.pone.0163932. eCollection 2016.

Abstract

In this study we determined protein and gene expression in the caeca of newly hatched chickens inoculated with cecal contents sourced from hens of different ages. Over 250 proteins exhibited modified expression levels in response to microbiota inoculation. The most significant inductions were observed for ISG12-2, OASL, ES1, LYG2, DMBT1-L, CDD, ANGPTL6, B2M, CUZD1, IgM and Ig lambda chain. Of these, ISG12-2, ES1 and both immunoglobulins were expressed at lower levels in germ-free chickens compared to conventional chickens. In contrast, CELA2A, BRT-2, ALDH1A1, ADH1C, AKR1B1L, HEXB, ALDH2, ALDOB, CALB1 and TTR were expressed at lower levels following inoculation of microbiota. When chicks were given microbiota preparations from different age donors, the recipients mounted differential responses to the inoculation which also differed from the response profile in naturally colonised birds. For example, B2M, CUZD1 and CELA2A responded differently to the inoculation with microbiota of 4- or 40-week-old hens. The increased or decreased gene expression could be recorded 6 weeks after the inoculation of newly hatched chickens. To characterise the proteins that may directly interact with the microbiota we characterised chicken proteins that co-purified with the microbiota and identified a range of host proteins including CDD, ANGPTL6, DMBT1-L, MEP1A and Ig lambda. We propose that induction of ISG12-2 results in reduced apoptosis of host cells exposed to the colonizing commensal microbiota and that CDD, ANGPTL6, DMBT1-L, MEP1A and Ig lambda reduce contact of luminal microbiota with the gut epithelium thereby reducing the inflammatory response.

Grants and funding

This work was supported by Grantova Agentura Ceske Republiky, project number 15-11688S, recipient Ivan Rychlik Ministry of Education of the Czech Republic, project number CZ.1.05/2.1.00/01.0006–ED0006/01/01, recipient Ivan Rychlik. Ministry of Education of the Czech Republic, project number CZ.1.07/2.3.00/30.0064, recipient Ivan Rychlik. BBSRC, project number BB/K004468/1, recipient Adrian L. Smith. DEFRA, project number OD0221, recipient Adrian L. Smith. Part of salary of Ivan Rychlik was paid by the project 15-11688S provided by Grantova Agentura Ceske Republiky. The rest of income of Ivan Rychlik was paid by institutional funding of permanent staff of the Veterinary Research Institute Brno, Czech Republic, and this was not directly associated with the work reported in this manuscript. All the funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.