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Human Cytomegalovirus in breast milk is associated with milk composition, the infant gut microbiome, and infant growth

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. Furthe...

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Autores principales: Johnson, Kelsey E., Heisel, Timothy, Fields, David A., Isganaitis, Elvira, Jacobs, Katherine M., Knights, Dan, Lock, Eric F., Rudolph, Michael C., Gale, Cheryl A., Schleiss, Mark R., Albert, Frank W., Demerath, Ellen W., Blekhman, Ran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10370112/
https://www.ncbi.nlm.nih.gov/pubmed/37503212
http://dx.doi.org/10.1101/2023.07.19.549370
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author Johnson, Kelsey E.
Heisel, Timothy
Fields, David A.
Isganaitis, Elvira
Jacobs, Katherine M.
Knights, Dan
Lock, Eric F.
Rudolph, Michael C.
Gale, Cheryl A.
Schleiss, Mark R.
Albert, Frank W.
Demerath, Ellen W.
Blekhman, Ran
author_facet Johnson, Kelsey E.
Heisel, Timothy
Fields, David A.
Isganaitis, Elvira
Jacobs, Katherine M.
Knights, Dan
Lock, Eric F.
Rudolph, Michael C.
Gale, Cheryl A.
Schleiss, Mark R.
Albert, Frank W.
Demerath, Ellen W.
Blekhman, Ran
author_sort Johnson, Kelsey E.
collection PubMed
description 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 a complex relationship between milk CMV, milk kynurenine, and 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.
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spelling pubmed-103701122023-07-27 Human Cytomegalovirus in breast milk is associated with milk composition, the infant gut microbiome, and infant growth Johnson, Kelsey E. Heisel, Timothy Fields, David A. Isganaitis, Elvira Jacobs, Katherine M. Knights, Dan Lock, Eric F. Rudolph, Michael C. Gale, Cheryl A. Schleiss, Mark R. Albert, Frank W. Demerath, Ellen W. Blekhman, Ran bioRxiv Article 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 a complex relationship between milk CMV, milk kynurenine, and 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. Cold Spring Harbor Laboratory 2023-07-19 /pmc/articles/PMC10370112/ /pubmed/37503212 http://dx.doi.org/10.1101/2023.07.19.549370 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Johnson, Kelsey E.
Heisel, Timothy
Fields, David A.
Isganaitis, Elvira
Jacobs, Katherine M.
Knights, Dan
Lock, Eric F.
Rudolph, Michael C.
Gale, Cheryl A.
Schleiss, Mark R.
Albert, Frank W.
Demerath, Ellen W.
Blekhman, Ran
Human Cytomegalovirus in breast milk is associated with milk composition, the infant gut microbiome, and infant growth
title Human Cytomegalovirus in breast milk is associated with milk composition, the infant gut microbiome, and infant growth
title_full Human Cytomegalovirus in breast milk is associated with milk composition, the infant gut microbiome, and infant growth
title_fullStr Human Cytomegalovirus in breast milk is associated with milk composition, the infant gut microbiome, and infant growth
title_full_unstemmed Human Cytomegalovirus in breast milk is associated with milk composition, the infant gut microbiome, and infant growth
title_short Human Cytomegalovirus in breast milk is associated with milk composition, the infant gut microbiome, and infant growth
title_sort human cytomegalovirus in breast milk is associated with milk composition, the infant gut microbiome, and infant growth
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10370112/
https://www.ncbi.nlm.nih.gov/pubmed/37503212
http://dx.doi.org/10.1101/2023.07.19.549370
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