Pregnancy induces transcriptional activation of the peripheral innate immune system and increases oxidative DNA damage among healthy third trimester pregnant women

Abstract

Background: Pregnancy induces physiological adaptations that may involve, or contribute to, alterations in the genomic landscape. Pregnancy also increases the nutritional demand for choline, an essential nutrient that can modulate epigenomic and transcriptomic readouts secondary to its role as a methyl donor. Nevertheless, the interplay between human pregnancy, choline and the human genome is largely unexplored.

Methodology/principal findings: As part of a controlled feeding study, we assessed the influence of pregnancy and choline intake on maternal genomic markers. Healthy third trimester pregnant (n = 26, wk 26-29 gestation) and nonpregnant (n = 21) women were randomized to choline intakes of 480 mg/day, approximating the Adequate Intake level, or 930 mg/day for 12-weeks. Blood leukocytes were acquired at study week 0 and study week 12 for microarray, DNA damage and global DNA/histone methylation measurements. A main effect of pregnancy that was independent of choline intake was detected on several of the maternal leukocyte genomic markers. Compared to nonpregnant women, third trimester pregnant women exhibited higher (P<0.05) transcript abundance of defense response genes associated with the innate immune system including pattern recognition molecules, neutrophil granule proteins and oxidases, complement proteins, cytokines and chemokines. Pregnant women also exhibited higher (P<0.001) levels of DNA damage in blood leukocytes, a genomic marker of oxidative stress. No effect of choline intake was detected on the maternal leukocyte genomic markers with the exception of histone 3 lysine 4 di-methylation which was lower among pregnant women in the 930 versus 480 mg/d choline intake group.

Conclusions: Pregnancy induces transcriptional activation of the peripheral innate immune system and increases oxidative DNA damage among healthy third trimester pregnant women.

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1. Effect of choline intake on peripheral blood leukocyte H3K4me2.

The relative abundance of H3K4me2 at study-end in third trimester pregnant women (right) and nonpregnant women (left) consuming 930 versus 480 mg choline/d. White bar: 480 mg choline/d group, black bar: 930 mg choline/d group. n = 10–13/choline intake and pregnancy status. Values are predicted means ± SEM. Analyzed with general linear models.

Figure 2. Venn diagram of differentially expressed genes by pregnancy.

This figure presents the number of genes differentially expressed in third trimester pregnant versus nonpregnant women at study-baseline (circle on the left) and study-end (circle on the right). The number of genes altered both at study-baseline and study-end are presented in the intersecting area of the two circles. Color scheme: blue represents low expression and yellow represents high expression. n = 12 for pregnant women; n = 10 for nonpregnant women. Analyzed with the LEMMA statistical package.

Figure 3. Hierarchical clustering of differentially expressed immune defense genes (GO: 0006952) in pregnant versus nonpregnant women.

This figure presents the hierarchical clustering of 112 differentially expressed immune defense genes in third trimester women versus nonpregnant women (reference group) at the beginning and end of the controlled feeding study. Color scheme: blue represents low expression and yellow represents high expression. n = 12 for pregnant women; n = 10 for nonpregnant women. Analyzed with Euclidean distances using MultiExperiment Viewer.

Figure 4. Plasma TNFα and IL6 concentrations.

Plasma concentrations of TNFα and IL6 in third trimester pregnant versus nonpregnant women at study-baseline (A) and study-end (B). White bar: nonpregnant women (n = 21); black bar: pregnant women (n = 26). Values are means ± SEM. Analyzed with general linear models.

Figure 5. Peripheral blood leukocyte histone modification marks H3K4me2, H3K9me2 and H3K27me3.

(A) and (C), histone modifications in third trimester pregnant versus nonpregnant women without controlling for percent granulocytes at study-baseline and study-end, respectively; (B) and (D), histone modifications in third trimester pregnant versus nonpregnant women controlling for percent granulocytes at study-baseline or study-end, respectively. White bar: nonpregnant women (n = 21), black bar: pregnant women (n = 26). Data are predicted means ± SEM. Analyzed with general linear models.