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Maternal immune cell gene expression associates with maternal gut microbiome, milk composition and infant gut microbiome.
Gurung, Manoj; Mulakala, Bharath Kumar; Schlegel, Brent Thomas; Rajasundaram, Dhivyaa; Shankar, Kartik; Bode, Lars; Ruebel, Meghan L; Sims, Clark; Martinez, Audrey; Andres, Aline; Yeruva, Laxmi.
Afiliação
  • Gurung M; Microbiome and Metabolism Research Unit (MMRU), Southeast Area, USDA-ARS, Arkansas Children's Nutrition Center, Little Rock, AR, USA.
  • Mulakala BK; Microbiome and Metabolism Research Unit (MMRU), Southeast Area, USDA-ARS, Arkansas Children's Nutrition Center, Little Rock, AR, USA; Texas A & M, IHA, College Station, TX, USA.
  • Schlegel BT; University of Pittsburgh Medical Center (UPMC), Children's Hospital of Pittsburgh, PA, USA.
  • Rajasundaram D; University of Pittsburgh Medical Center (UPMC), Children's Hospital of Pittsburgh, PA, USA.
  • Shankar K; Department of Pediatrics, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
  • Bode L; Larsson-Rosenquist Foundation Mother-Milk-Infant Center of Research Excellence, University of California San Diego, La Jolla, CA, USA; Department of Pediatrics, University of California San Diego, La Jolla, CA, USA.
  • Ruebel ML; Microbiome and Metabolism Research Unit (MMRU), Southeast Area, USDA-ARS, Arkansas Children's Nutrition Center, Little Rock, AR, USA.
  • Sims C; Department of Pediatrics, University of Arkansas of Medical Sciences, Little Rock, AR, USA.
  • Martinez A; Department of Pediatrics, University of Arkansas of Medical Sciences, Little Rock, AR, USA.
  • Andres A; Department of Pediatrics, University of Arkansas of Medical Sciences, Little Rock, AR, USA.
  • Yeruva L; Microbiome and Metabolism Research Unit (MMRU), Southeast Area, USDA-ARS, Arkansas Children's Nutrition Center, Little Rock, AR, USA. Electronic address: laxmi.yeruva@usda.gov.
Clin Nutr ESPEN ; 63: 903-918, 2024 Oct.
Article em En | MEDLINE | ID: mdl-39209027
ABSTRACT

BACKGROUND:

Pre-pregnancy overweight and obesity promote deleterious health impacts on both mothers during pregnancy and the offspring. Significant changes in the maternal peripheral blood mononuclear cells (PBMCs) gene expression due to obesity are well-known. However, the impact of pre-pregnancy overweight on immune cell gene expression during pregnancy and its association with maternal and infant outcomes is not well explored.

METHODS:

Blood samples were collected from healthy normal weight (NW, pre-pregnancy BMI 18.5-24.9) or overweight (OW, pre-pregnancy BMI 25-29.9) 2nd parity pregnant women at 12, 24 and 36 weeks of pregnancy. PBMCs were isolated from the blood and subjected to mRNA sequencing. Maternal and infant microbiota were analyzed by 16S rRNA gene sequencing. Integrative multi-omics data analysis was performed to evaluate the association of gene expression with maternal diet, gut microbiota, milk composition, and infant gut microbiota.

RESULTS:

Gene expression analysis revealed that 453 genes were differentially expressed in the OW women compared to NW women at 12 weeks of pregnancy, out of which 354 were upregulated and 99 were downregulated. Several up-regulated genes in the OW group were enriched in inflammatory, chemokine-mediated signaling and regulation of interleukin-8 production-related pathways. At 36 weeks of pregnancy healthy eating index score was positively associated with several genes that include, DTD1, ELOC, GALNT8, ITGA6-AS1, KRT17P2, NPW, POT1-AS1 and RPL26. In addition, at 36 weeks of pregnancy, genes involved in adipocyte functions, such as NG2 and SMTNL1, were negatively correlated to human milk 2'FL and total fucosylated oligosaccharides content collected at 1 month postnatally. Furthermore, infant Akkermansia was positively associated with maternal PBMC anti-inflammatory genes that include CPS1 and RAB7B, at 12 and 36 weeks of pregnancy.

CONCLUSIONS:

These findings suggest that prepregnancy overweight impacts the immune cell gene expression profile, particularly at 12 weeks of pregnancy. Furthermore, deciphering the complex association of PBMC's gene expression levels with maternal gut microbiome and milk composition and infant gut microbiome may aid in developing strategies to mitigate obesity-mediated effects.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Microbioma Gastrointestinal / Leite Humano Limite: Adult / Female / Humans / Infant / Newborn / Pregnancy Idioma: En Revista: Clin Nutr ESPEN Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Microbioma Gastrointestinal / Leite Humano Limite: Adult / Female / Humans / Infant / Newborn / Pregnancy Idioma: En Revista: Clin Nutr ESPEN Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos