Associations between helminth infection status and the composition and concentration of fecal bile acids in school-age children in Uganda

N Natasha J. Norton C Chloe M. M. Hand C Candia Rowel M Moses Adriko P Pengfei Cai D Donald P. McManus T Thomas G. Egwang L Lisa A. Reynolds

Abstract

Abstract Over 1 billion people globally are infected with helminths, and understanding the impact of these infections on human health is crucial for further developing effective interventions. We investigated potential associations between helminth infection status and the abundance of fecal bile acids: a group of metabolites known to impact gut physiology and function and have immunomodulatory capabilities. Fecal samples were collected from school-age children in Uganda and used to determine helminth infection status (Kato-Katz technique) and to quantify the fecal bile acid pool (UPLC-MRM/MS). We found that helminth infection status was associated with changes to the fecal bile acid pool and that these differences were dependent on the biological sex of study participants. Females who were coinfected with schistosomes and hookworms had higher levels of unconjugated secondary bile acids than helminth-negative individuals. In males, no significant associations were detected between helminth infection status and levels of unconjugated secondary bile acids, however, there were reduced levels of some species of conjugated primary bile acids in schistosome-infected individuals compared to helminth-negative individuals. Further research into the specific mechanisms underlying these associations and the functional consequences of bile acid perturbations during helminth infection may provide valuable insights into the pathophysiology of helminth infections.

Article Details

Volume / Issue Vol. 15, Issue 1
Published July 15, 2025
ISSN 2045-2322
Publisher Nature Portfolio

Journal Info

Scientific Reports

Nature Portfolio

ISSN: 2045-2322 Open Access Life Sciences

Authors (8)

N

Natasha J. Norton

C

Chloe M. M. Hand

C

Candia Rowel

M

Moses Adriko

P

Pengfei Cai

D

Donald P. McManus

T

Thomas G. Egwang

L

Lisa A. Reynolds