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Combining multi‐omics analysis to identify host‐targeted targets for the control of Brucella infection

Authors :
Jiuwang Yu
Hongwei Yuan
Jiarong Guo
Zhiheng Dong
Sha Li
Quan Fu
Bilige Aode
Sachula Baoyin
Lidao Bao
Lan Wu
Source :
Microbial Biotechnology, Vol 16, Iss 12, Pp 2345-2366 (2023)
Publication Year :
2023
Publisher :
Wiley, 2023.

Abstract

Abstract Human infections caused by Brucella (called brucellosis) are among the most common zoonoses worldwide with an estimated 500,000 cases each year. Since chronic Brucella infections are extremely difficult to treat, there is an urgent need for more effective therapeutics. As a facultative intracellular bacterium, Brucella is strictly parasitic in the host cell. Here, we performed proteomic and transcriptomic and metabolomic analyses on Brucella infected patients, mice and cells that provided an extensive “map” of physiological changes in brucellosis patients and characterized the metabolic pathways essential to the response to infection, as well as the associated cellular response and molecular mechanisms. This is the first report utilizing multi‐omics analysis to investigate the global response of proteins and metabolites associated with Brucella infection, and the data can provide a comprehensive insight to understand the mechanism of Brucella infection. We demonstrated that Brucella increased nucleotide synthesis in the host, consistent with increased biomass requirement. We also identified IMPDH2, a key regulatory complex that controls nucleotide synthesis during Brucella infection. Pharmacological targeting of IMPDH2, the rate‐limiting enzyme in guanine nucleotide biosynthesis, efficiently inhibits B. abortus growth both in vitro and in vivo. Through screening a library of natural products, we identified oxymatrine, an alkaloid obtained primarily from Sophora roots, is a novel and selective IMPDH2 inhibitor. In further in vitro bacterial inhibition assays, oxymatrine effectively inhibited the growth of B. abortus, which was impaired by exogenous supplementation of guanosine, a salvage pathway of purine nucleotides. This moderately potent, structurally novel compound may provide clues for further design and development of efficient IMPDH2 inhibitors and also demonstrates the potential of natural compounds from plants against Brucella.

Subjects

Subjects :
Biotechnology
TP248.13-248.65

Details

Language :
English
ISSN :
17517915
Volume :
16
Issue :
12
Database :
Directory of Open Access Journals
Journal :
Microbial Biotechnology
Publication Type :
Academic Journal
Accession number :
edsdoj.84a1bd2f60a94168a2910c417c7592c8
Document Type :
article
Full Text :
https://doi.org/10.1111/1751-7915.14307