Evidence map›Paper›PMID 40475255›Full record

ArticleiScience2025

Urine metabolomic analyses reveal metabolite disruptions in steroid hormone biosynthesis in monkeypox.

Xiaofeng Yang, Huiqin Yang, Chudan Liang, Fei Tang, Zhenyu Long, Linjin Fan, Yulong Wang, Zequn Wang, Mou Zeng, Weifang Kang and 10 more

Abstract read
In one paragraph

Article in iScience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

20 authors.

Xiaofeng YangZhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Huiqin YangGuangzhou Key Laboratory of Clinical Pathogen Research for Emerging and Major Infectious Diseases, Institute of Infectious Diseases, Guangzhou Eighth People's Hospital, Guangzhou Medical University, Guangzhou, Guangdong, China.
Chudan LiangZhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Fei TangZhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Zhenyu LongGuangzhou Key Laboratory of Clinical Pathogen Research for Emerging and Major Infectious Diseases, Institute of Infectious Diseases, Guangzhou Eighth People's Hospital, Guangzhou Medical University, Guangzhou, Guangdong, China.
Linjin FanSchool of Public Health (Shenzhen), Sun Yat-sen University, Shenzhen 518107, China.
Yulong WangZhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Zequn WangZhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Mou ZengGuangzhou Key Laboratory of Clinical Pathogen Research for Emerging and Major Infectious Diseases, Institute of Infectious Diseases, Guangzhou Eighth People's Hospital, Guangzhou Medical University, Guangzhou, Guangdong, China.
Weifang KangZhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Pengfei YeZhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Wendi ShiZhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Yuandong ZhouZhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Jingyan LinZhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Hongxin HuangZhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Huijun YanZhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Jian WangGuangzhou Key Laboratory of Clinical Pathogen Research for Emerging and Major Infectious Diseases, Institute of Infectious Diseases, Guangzhou Eighth People's Hospital, Guangzhou Medical University, Guangzhou, Guangdong, China.
Linghua LiGuangzhou Key Laboratory of Clinical Pathogen Research for Emerging and Major Infectious Diseases, Institute of Infectious Diseases, Guangzhou Eighth People's Hospital, Guangzhou Medical University, Guangzhou, Guangdong, China.
Jun QianZhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Linna LiuGuangzhou Key Laboratory of Clinical Pathogen Research for Emerging and Major Infectious Diseases, Institute of Infectious Diseases, Guangzhou Eighth People's Hospital, Guangzhou Medical University, Guangzhou, Guangdong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monkeypox virus (MPXV) poses a global health threat. Viral infection can alter host metabolic homeostasis, while its changes may influence disease severity and progression. The relationship between MPXV and metabolites has not been reported. we employed metabolomics to characterize the mpox specific metabolic features by comparing changes in urinary metabolites from patients with MPXV infection, HIV infection, and HIV-MPXV co-infection. The metabolic changes caused by MPXV were mainly concentrated in amino acid and hormone metabolism. Further analysis showed that 5'-dihydroadenosine and uric acid can serve as potential molecular markers for MPXV and HIV-MPXV co-infected patients, respectively. Confirmed by targeted metabolomics and ELISA methods, MPXV infection caused severe disorders in the metabolic pathways of steroid hormones such as testosterone and progesterone in humans. Our findings identify dysregulated metabolism as an underpinning of MPXV pathogenicity, and increasing the anti-inflammatory capacity of patients may play a role to some extent against mpox.

Indexed as

MetabolomicsVirology

Identifiers

PMID40475255
PMCPMC12140030

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