Human cytomegalovirus in breast milk is associated with milk composition and the infant gut microbiome and growth.
Kelsey E JohnsonNelmary Hernandez-AlvaradoMark BlackstadTimothy HeiselMattea AllertDavid A FieldsElvira IsganaitisKatherine M JacobsDan KnightsEric F LockMichael C RudolphCheryl A GaleMark R SchleissFrank W AlbertEllen W DemerathRan BlekhmanPublished in: Nature communications (2024)
Human cytomegalovirus (CMV) is a highly prevalent herpesvirus that is often transmitted to the neonate via breast milk. Postnatal CMV transmission can have negative health consequences for preterm and immunocompromised infants, but any effects on healthy term infants are thought to be benign. Furthermore, the impact of CMV on the composition of the hundreds of bioactive factors in human milk has not been tested. Here, we utilize a cohort of exclusively breastfeeding full-term mother-infant pairs to test for differences in the milk transcriptome and metabolome associated with CMV, and the impact of CMV in breast milk on the infant gut microbiome and infant growth. We find upregulation of the indoleamine 2,3-dioxygenase (IDO) tryptophan-to-kynurenine metabolic pathway in CMV+ milk samples, and that CMV+ milk is associated with decreased Bifidobacterium in the infant gut. Our data indicate two opposing CMV-associated effects on infant growth; with kynurenine positively correlated, and CMV viral load negatively correlated, with infant weight-for-length at 1 month of age. These results suggest CMV transmission, CMV-related changes in milk composition, or both may be modulators of full-term infant development.
Keyphrases
- preterm infants
- human milk
- low birth weight
- public health
- gestational age
- gene expression
- physical activity
- small molecule
- cell proliferation
- intensive care unit
- mental health
- electronic health record
- induced pluripotent stem cells
- epstein barr virus
- climate change
- single cell
- acute respiratory distress syndrome
- long non coding rna
- diffuse large b cell lymphoma
- rna seq
- extracorporeal membrane oxygenation
- mechanical ventilation
- drug induced
- tissue engineering