Diet Alters Micronutrient Pathways in the Gut and Placenta that Regulate Fetal Growth and Development in Pregnant Mice

Reprod Sci. 2021 Feb;28(2):447-461. doi: 10.1007/s43032-020-00297-1. Epub 2020 Sep 4.

Abstract

Maternal malnutrition and micronutrient deficiencies can alter fetal development. However, the mechanisms underlying these relationships are poorly understood. We used a systems physiology approach to investigate diet-induced effects on maternal gut microbes and folate/inositol transport in the maternal/fetal gut and placenta. Female mice were fed a control diet (CON) diet, undernourished (UN, restricted by 30% of CON intake) or a high-fat diet (HF, 60% kcals fat) during pregnancy to model normal pregnancy, fetal growth restriction or maternal metabolic dysfunction, respectively. At gestational day 18.5, we assessed circulating folate levels by microbiological assay, relative abundance of gut lactobacilli by G3PhyloChip™, and folate/inositol transporters in placenta and maternal/fetal gut by qPCR/immunohistochemistry. UN and HF-fed mothers had lower plasma folate concentrations vs. CON. Relative abundances of three lactobacilli taxa were higher in HF vs. UN and CON. HF-fed mothers had higher gut proton coupled folate transporter (Pcft) and reduced folate carrier 1 (Rfc1), and lower sodium myo-inositol co-transporter 2 (Smit2), mRNA expression vs. UN and CON. HF placentae had increased folate receptor beta (Frβ) expression vs. UN. mRNA expression of Pcft, folate receptor alpha (Frα), and Smit2 was higher in gut of HF fetuses vs. UN and CON. Transporter protein expression was not different between groups. Maternal malnutrition alters abundance of select gut microbes and folate/inositol transporters, which may influence maternal micronutrient status and delivery to the fetus, impacting pregnancy/fetal outcomes.

Keywords: Folate; Gut; Inositol; Nutrition; Placenta; Pregnancy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animal Feed
  • Animal Nutritional Physiological Phenomena
  • Animals
  • Caloric Restriction
  • Diet*
  • Diet, High-Fat
  • Disease Models, Animal
  • Dysbiosis
  • Energy Intake
  • Female
  • Fetal Development*
  • Fetal Weight
  • Fetus / metabolism*
  • Folic Acid / metabolism
  • Gastrointestinal Microbiome
  • Gastrointestinal Tract / metabolism*
  • Gastrointestinal Tract / microbiology
  • Inositol / metabolism
  • Malnutrition / metabolism*
  • Malnutrition / microbiology
  • Malnutrition / physiopathology
  • Maternal Nutritional Physiological Phenomena
  • Membrane Transport Proteins / genetics
  • Membrane Transport Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Nutritional Status
  • Nutritive Value*
  • Obesity / metabolism*
  • Obesity / microbiology
  • Obesity / physiopathology
  • Placenta / metabolism*
  • Pregnancy

Substances

  • Membrane Transport Proteins
  • Inositol
  • Folic Acid