Staff Publications

Staff Publications

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    'Staff publications' is the digital repository of Wageningen University & Research

    'Staff publications' contains references to publications authored by Wageningen University staff from 1976 onward.

    Publications authored by the staff of the Research Institutes are available from 1995 onwards.

    Full text documents are added when available. The database is updated daily and currently holds about 240,000 items, of which 72,000 in open access.

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Record number 562733
Title Low doses of diarrhoeagenic E. coli induce enhanced monocyte and mDC responses, and prevent against re-infection in a human challenge model
Author(s) Porbahaie, Mojtaba; Belt, Maartje van den; Ulfman, L.H.; Ruijschop, R.; Lucas-van de Bos, Elly; Lenz, Stefanie; Alen-Boerrigter, Ingrid van; Teodorowicz, M.; Savelkoul, H.F.J.; Neerven, R.J.J. van
Source In: WIAS Annual Conference 2020 WIAS - p. 32 - 32.
Department(s) Cell Biology and Immunology
WIAS
Publication type Abstract in scientific journal or proceedings
Publication year 2020
Abstract A human challenge model was developed to study nutritional interventions to prevent infection with diarrhoeagenic Escherichia coli, one of the major and most common causes of diarrhea. Challenges with high doses of E. coli was shown to prevent clinical symptoms upon re-infection. Here we aimed to study if a low dose primary E. coli challenge induced only partial protection against re-infection. Thirty healthy male volunteers were selected,randomized, and orally exposed to increasing concentrations of E. coli strain E1392/75-2A(10e6, 10e7, 10e8, 10e9, and 10e10 CFU). Clinical symptoms of gastrointestinal discomfort were recorded, and stool and blood samples were collected. These were analyzed for immunological responses, stool characteristics, and inflammatory markers. After primary infection,E. coli-specific serum IgG(CFA/II) titers increased in a dose-dependent manner.Three weeks later, all volunteers were re-infected with a high E. coli dose(10e10 CFU). Surprisingly,all primary E. coli doses protected largely against clinical symptoms upon re-infection,with no significant dose-dependency. The only significant dose-dependent effect was a stronger increase in %fecal wet weight after E. coli re-infection in the subjects that received a lower dose at primary infection. Additionally, in vitro stimulation with E. coli resulted in increased numbers of IL-6+/TNF-a+ monocytes and mDC compared to before the primary infection, but this was not dose-dependent. In conclusion, E. coli infection with as few as 10e6 bacteria largely protected against re-infection. Although a dose-dependent increase of the IgG response to E. coli was observed after primary infection, and adose-dependent decrease in the change in %fecal wet weight, the IgG response did not directly correlate with clinical protection at secondary infection. The enhanced mDC and monocyte response after primary infection, even though not dependent on E. coli dose, indicates that E. coli infection induces innate memory to bacterial infection.
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