Microbiome-derived bile acid signatures in early life and their association with islet autoimmunity
Lamichhane, Santosh; Dickens, Alex M.; Buchacher, Tanja; Lou, Tianai; Charron-Lamoureux, Vincent; Kattelus, Roosa; Karmacharya, Pragya; da Silva, Lucas Pinto; Kråkström, Matilda; Rasool, Omid; Sen, Partho; Walker, Corinn; Patan, Abubaker; Gentry, Emily C.; Zuffa, Simone; Arzoomand, Aron; Lakshmikanth, Tadepally; Mikeš, Jaromir; Mebrahtu, Aman; Vatanen, Tommi; Raffatellu, Manuela; Zengler, Karsten; Hyötyläinen, Tuulia; Xavier, Ramnik J.; Brodin, Petter; Lahesmaa, Riitta; Dorrestein, Pieter C.; Knip, Mikael; Orešič, Matej (2025-12)
Lamichhane, Santosh
Dickens, Alex M.
Buchacher, Tanja
Lou, Tianai
Charron-Lamoureux, Vincent
Kattelus, Roosa
Karmacharya, Pragya
da Silva, Lucas Pinto
Kråkström, Matilda
Rasool, Omid
Sen, Partho
Walker, Corinn
Patan, Abubaker
Gentry, Emily C.
Zuffa, Simone
Arzoomand, Aron
Lakshmikanth, Tadepally
Mikeš, Jaromir
Mebrahtu, Aman
Vatanen, Tommi
Raffatellu, Manuela
Zengler, Karsten
Hyötyläinen, Tuulia
Xavier, Ramnik J.
Brodin, Petter
Lahesmaa, Riitta
Dorrestein, Pieter C.
Knip, Mikael
Orešič, Matej
12 / 2025
Nature Communications
38
Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:tuni-202601131351
https://urn.fi/URN:NBN:fi:tuni-202601131351
Kuvaus
Peer reviewed
Tiivistelmä
Emerging studies reveal that gut microbes can conjugate diverse amino acids to bile acids, known as microbially conjugated bile acids. However, their regulation and health effects remain unclear. Here, we analyzed early-life microbially conjugated bile acid patterns and their link to islet autoimmunity. We quantified 110 microbial bile acids in 303 stool samples collected longitudinally (3–36 months) from children who developed one or more islet autoantibodies and controls who remained autoantibody-negative. We identified distinct age-dependent trajectories of these bile acid amidates and correlated them with gut microbiome composition. We found that altered levels of ursodeoxycholic and deoxycholic acid conjugates were linked to islet autoimmunity as well as modulated monocyte activation in response to immunostimulatory lipopolysaccharide and Th17/Treg cell balance. These findings suggest that microbially conjugated bile acids influence immune development and type 1 diabetes risk.
Kokoelmat
- TUNICRIS-julkaisut [23862]
