Untargeted Metabolomic Analysis of Lactation-Stage-Matched Human and Bovine Milk Samples at 2 Weeks Postnatal
Authors:
- Dominick J. LemasDominick J. Lemas
- Xinsong DuXinsong Du
- Bethany Dado-SennBethany Dado-Senn
- Ke XuKXKe Xu
- Amanda DobrowolskiADAmanda Dobrowolski
- Marina MagalhãesMMMarina Magalhães
- Juan J. Aristizabal-HenaoJAJuan J. Aristizabal-Henao
- Bridget E. YoungBYBridget E. Young
- Magda FrancoisMFMagda Francois
- Lindsay A. ThompsonLTLindsay A. Thompson
- Leslie A. ParkerLPLeslie A. Parker
- Josef NeuJNJosef Neu
Open Access
Abstract
Epidemiological data demonstrate that bovine whole milk is often substituted for human milk during the first 12 months of life and may be associated with adverse infant outcomes. The objective of this study is to interrogate the human and bovine milk metabolome at 2 weeks of life to identify unique metabolites that may impact infant health outcomes. Human milk (n = 10) was collected at 2 weeks postpartum from normal-weight mothers (pre-pregnant BMI < 25 kg/m2) that vaginally delivered term infants and were exclusively breastfeeding their infant for at least 2 months. Similarly, bovine milk (n = 10) was collected 2 weeks postpartum from normal-weight primiparous Holstein dairy cows. Untargeted data were acquired on all milk samples using high-resolution liquid chromatography–high-resolution tandem mass spectrometry (HR LC-MS/MS). MS data pre-processing from feature calling to metabolite annotation was performed using MS-DIAL and MS-FLO. Our results revealed that more than 80% of the milk metabolome is shared between human and bovine milk samples during early lactation. Unbiased analysis of identified metabolites revealed that nearly 80% of milk metabolites may contribute to microbial metabolism and microbe–host interactions. Collectively, these results highlight untargeted metabolomics as a potential strategy to identify unique and shared metabolites in bovine and human milk that may relate to and impact infant health outcomes.Keywords
Funding Information
- National Institute of Diabetes and Digestive and Kidney Diseases (K01DK115632, UL1TR001427)
- National Center for Advancing Translational Sciences (K01DK115632, UL1TR001427)
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