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  4. Circulating androgen regulation by androgen-catabolizing gut bacteria in male mouse gut
 
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Circulating androgen regulation by androgen-catabolizing gut bacteria in male mouse gut

Journal
Gut microbes
Journal Volume
15
Journal Issue
1
Pages
Article number 2183685
Date Issued
2023-02-26
Author(s)
Hsiao, Tsun-Hsien
Chou, Chia-Hong
YI-LUNG CHEN  
Wang, Po-Hsiang
Brandon-Mong, Guo-Jie
TZONG-HUEI LEE  
Wu, Tien-Yu
Li, Po-Ting
Li, Chen-Wei
Lai, Yi-Li
Tseng, Yu-Lin
Shih, Chao-Jen
Chen, Po-Hao
MEI-JOU CHEN  
Chiang, Yin-Ru
DOI
10.1080/19490976.2023.2183685
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/629210
URL
https://api.elsevier.com/content/abstract/scopus_id/85149054404
Abstract
Abnormally high circulating androgen levels have been considered a causative factor for benign prostatic hypertrophy and prostate cancer in men. Recent animal studies on gut microbiome suggested that gut bacteria are involved in sex steroid metabolism; however, the underlying mechanisms and bacterial taxa remain elusive. Denitrifying betaproteobacteria Thauera spp. are metabolically versatile and often distributed in the animal gut. Thauera sp. strain GDN1 is an unusual betaproteobacterium capable of catabolizing androgen under both aerobic and anaerobic conditions. We administered C57BL/6 mice (aged 7 weeks) with strain GDN1 through oral gavage. The strain GDN1 administration caused a minor increase in the relative abundance of Thauera (≤0.1%); however, it has profound effects on the host physiology and gut bacterial community. The results of our ELISA assay and metabolite profile analysis indicated an approximately 50% reduction in serum androgen levels in the strain GDN1-administered male mice. Moreover, androgenic ring-cleaved metabolites were detected in the fecal extracts of the strain GDN1-administered mice. Furthermore, our RT - qPCR results revealed the expression of the androgen catabolism genes in the gut of the strain GDN1-administered mice. We found that the administered strain GDN1 regulated mouse serum androgen levels, possibly because it blocked androgen recycling through enterohepatic circulation. This study discovered that sex steroids serve as a carbon source of gut bacteria; moreover, host circulating androgen levels may be regulated by androgen-catabolizing gut bacteria. Our data thus indicate the possible applicability of androgen-catabolic gut bacteria as potent probiotics in alternative therapy of hyperandrogenism.
Subjects
Androgen; gut microbe; hyperandrogenism; mouse; sex steroids; testosterone catabolism; thauera
SDGs

[SDGs]SDG3

Publisher
Taylor and Francis Ltd.
Type
journal article

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