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

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...

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Autores principales: Yu, Jiuwang, Yuan, Hongwei, Guo, Jiarong, Dong, Zhiheng, Li, Sha, Fu, Quan, Aode, Bilige, Baoyin, Sachula, Bao, Lidao, Wu, Lan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686141/
https://www.ncbi.nlm.nih.gov/pubmed/37882474
http://dx.doi.org/10.1111/1751-7915.14307
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author Yu, Jiuwang
Yuan, Hongwei
Guo, Jiarong
Dong, Zhiheng
Li, Sha
Fu, Quan
Aode, Bilige
Baoyin, Sachula
Bao, Lidao
Wu, Lan
author_facet Yu, Jiuwang
Yuan, Hongwei
Guo, Jiarong
Dong, Zhiheng
Li, Sha
Fu, Quan
Aode, Bilige
Baoyin, Sachula
Bao, Lidao
Wu, Lan
author_sort Yu, Jiuwang
collection PubMed
description 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.
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spelling pubmed-106861412023-11-30 Combining multi‐omics analysis to identify host‐targeted targets for the control of Brucella infection Yu, Jiuwang Yuan, Hongwei Guo, Jiarong Dong, Zhiheng Li, Sha Fu, Quan Aode, Bilige Baoyin, Sachula Bao, Lidao Wu, Lan Microb Biotechnol Regular Issue 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. John Wiley and Sons Inc. 2023-10-26 /pmc/articles/PMC10686141/ /pubmed/37882474 http://dx.doi.org/10.1111/1751-7915.14307 Text en © 2023 The Authors. Microbial Biotechnology published by Applied Microbiology International and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Regular Issue
Yu, Jiuwang
Yuan, Hongwei
Guo, Jiarong
Dong, Zhiheng
Li, Sha
Fu, Quan
Aode, Bilige
Baoyin, Sachula
Bao, Lidao
Wu, Lan
Combining multi‐omics analysis to identify host‐targeted targets for the control of Brucella infection
title Combining multi‐omics analysis to identify host‐targeted targets for the control of Brucella infection
title_full Combining multi‐omics analysis to identify host‐targeted targets for the control of Brucella infection
title_fullStr Combining multi‐omics analysis to identify host‐targeted targets for the control of Brucella infection
title_full_unstemmed Combining multi‐omics analysis to identify host‐targeted targets for the control of Brucella infection
title_short Combining multi‐omics analysis to identify host‐targeted targets for the control of Brucella infection
title_sort combining multi‐omics analysis to identify host‐targeted targets for the control of brucella infection
topic Regular Issue
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686141/
https://www.ncbi.nlm.nih.gov/pubmed/37882474
http://dx.doi.org/10.1111/1751-7915.14307
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