Bacteria associated with Crohn’s disease rely on multiple stress responses to survive, multiply, and tolerate antibiotics within white blood cells called macrophages, according to a study published November 14 in the open-access journal
by Olivier Espéli of the College de France and PSL Research University in Paris, France, and colleagues.
Crohn’s disease is a chronic disease that causes inflammation and irritation in the digestive tract. The disease is characterized by an imbalance in the intestinal microbiome. In particular, adherent-invasive Escherichia coli (AIEC) strains have been implicated in the disease. AIEC colonize intestinal cells and survive and replicate within macrophages. In the new study, the researchers demonstrated that the AIEC LF82 strain can switch between replicating and non-growing states within macrophages. This switch can result from a stress response called the stringent response immediately after uptake by macrophages, or at later stages, from DNA damage and a stress response called SOS during replication within macrophages.
First, a stress response called the stringent response halts the replicative cell cycle of AIEC LF82 for a few hours, during which a large number of AIEC LF82 acquire the ability to tolerate antibiotic treatments. Later, when AIEC multiplication restarts, it requires DNA repair, suggesting that AIEC have accumulated DNA damage during the first hours after infection. In this second phase, non-growing bacteria appeared frequently from the population of growing AIEC LF82, raising the proportion of antibiotic-tolerant AIEC LF82 by up to 10% of the population. The results suggest that a reservoir of antibiotic-tolerant, non-growing bacteria could be responsible for long-term survival in the host as well as relapsing infections.
Espéli adds, “Within their macrophage’s niche, Crohn’s disease associated bacteria become tolerant to antibiotics.”
Funding: This work has received support from the program «Investissements d’Avenir » launched by the French Government and implemented by ANR with the references ANR-10-LABX-54 MEMOLIFE (GD and OE) and ANR-11-IDEX-0001-02 PSL* Research University (OE), from the ANR (
) with the reference ANR-18-CE35-0007 (OE) and the support of the association François Aupetit (AFA,
) (OE). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing Interests: I have read the journal’s policy and the authors of this manuscript have the following competing interests: Gaëlle Demarre was employed by Inovarion at the time of the study.
Citation: Demarre G, Prudent V, Schenk H, Rousseau E, Bringer M-A, Barnich N, et al. (2019) The Crohn’s disease-associated Escherichia coli strain LF82 relies on SOS and stringent responses to survive, multiply and tolerate antibiotics within macrophages.
CIRB-Collège de France, CNRS-UMR724, INSERM U1050, PSL Research University, Paris, France
Inovarion, Paris, France
Department of Evolutionary Theory, Max Planck Institute for Evolutionary Biology, Plön, Germany
Institut de Biologie de l’Ecole Normale Supérieure, Département de Biologie, Ecole Normale Supérieure, CNRS, INSERM, PSL Research University, Paris, France
Centre des Sciences du Goût et de l’Alimentation, AgroSup Dijon, CNRS, INRA, Université Bourgogne Franche-Comté, Dijon, France
Microbes, Intestin, Inflammation et Susceptibilité de l’Hôte, UMR Inserm/ Université d’Auvergne U1071, USC INRA 2018, Clermont Ferrand, France
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This part of information is sourced from https://www.eurekalert.org/pub_releases/2019-11/p-hcd111419.php