Schistosomiasis Induces Persistent DNA Methylation and Tuberculosis-specific Immune Changes

Author:

DiNardo Andrew R.,Nishiguchi Tomoki,Mace Emily M.,Rajapakshe Kimal,Mtetwa Godwin,Kay Alexander,Maphalala Gugu,Secor W. Evan,Mejia Rojelio,Orange Jordan S.,Coarfa Cristian,Bhalla Kapil N.,Graviss Edward A,Mandalakas Anna M.,Makedonas George

Abstract

AbstractEpigenetic mechanisms, like DNA methylation, determine immune cell phenotype. To understand the epigenetic alterations induced by helminth co-infections, we evaluated the longitudinal effect of ascariasis and schistosomiasis infection on CD4+ T cell DNA methylation and the downstream tuberculosis (TB)-specific and BCG-induced immune phenotype. All experiments were performed on human primary immune cells from a longitudinal cohort of recently TB-exposed children. Compared to age-matched uninfected controls, children with active Schistosoma haematobium and Ascaris lumbricoides infection had 751 differentially DNA methylated genes with 72% hyper-methylated. Gene ontology pathway analysis identified inhibition of IFN-γ signaling, cellular proliferation, and the Th1 pathway. Targeted RT-PCR after methyl-specific endonuclease digestion confirmed DNA hyper-methylation of the transcription factors BATF3, ID2, STAT5A, IRF5, PPARg, RUNX2, IRF4 and NFATC1 and cytokines or cytokine receptors IFNGR1, TNFS11, RELT (TNF receptor), IL12RB2 and IL12B (p< 0.001; Sidak-Bonferroni). Functional blockage of the IFN-γ signaling pathway was confirmed with helminth-infected individuals having decreased up-regulation of IFN-γ-inducible genes (Mann-Whitney p < 0.05). Hypo-methylation of the IL-4 pathway and DNA hyper-methylation of the Th1 pathway was confirmed by antigen-specific multidimensional flow cytometry demonstrating decreased TB-specific IFN-γ and TNF and increased IL-4 production by CD4+ T cells (Wilcoxon signed rank P <0.05). In S.haematobium infected individuals, these DNA methylation and immune phenotypic changes persisted at least six months after successful deworming. This work demonstrates that helminth infection induces DNA methylation and immune perturbations that inhibit TB-specific immune control and that the duration of these changes are helminth-specific.

Publisher

Cold Spring Harbor Laboratory

Reference68 articles.

1. Trained immunity: A smart way to enhance innate immune defence;Mol Immunol,2015

2. Bacille Calmette-Guerin induces NOD2-dependent nonspecific protection from reinfection via epigenetic reprogramming of monocytes;Proceedings of the National Academy of Sciences of the United States of America,2012

3. Regulation of the transcriptional program by DNA methylation during human alphabeta T-cell development;Nucleic Acids Res,2015

4. Transcriptional and epigenetic control of T helper cell specification: molecular mechanisms underlying commitment and plasticity;Annu Rev Immunol,2012

5. An epigenetic silencing pathway controlling T helper 2 cell lineage commitment;Nature,2012

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