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Gut Microbiota-Gut Metabolites and Infection: Approaching Sustainable Solutions for Therapy.

作者信息

Gurung Bijay, Stricklin Maranda, Wang Shaohua

机构信息

Department of Biomedical Sciences, Ohio University Heritage College of Osteopathic Medicine, Ohio University, Athens, OH 45701, USA.

Infectious and Tropical Disease Institute, Ohio University, Athens, OH 45701, USA.

出版信息

Metabolites. 2024 Jan 22;14(1):74. doi: 10.3390/metabo14010074.


DOI:10.3390/metabo14010074
PMID:38276309
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10819375/
Abstract

() infection (CDI) is the most common hospital-acquired infection. With the combination of a high rate of antibiotic resistance and recurrence, it has proven to be a debilitating public health threat. Current treatments for CDI include antibiotics and fecal microbiota transplantation, which contribute to recurrent CDIs and potential risks. Therefore, there is an ongoing need to develop new preventative treatment strategies for CDI. Notably, gut microbiota dysbiosis is the primary risk factor for CDI and provides a promising target for developing novel CDI therapy approaches. Along with gut microbiota dysbiosis, a reduction in important gut metabolites like secondary bile acids and short-chain fatty acids (SCFAs) were also seen in patients suffering from CDI. In this review study, we investigated the roles and mechanisms of gut microbiota and gut microbiota-derived gut metabolites, especially secondary bile acids and SCFAs in CDI pathogenesis. Moreover, specific signatures of gut microbiota and gut metabolites, as well as different factors that can modulate the gut microbiota, were also discussed, indicating that gut microbiota modulators like probiotics and prebiotics can be a potential therapeutic strategy for CDI as they can help restore gut microbiota and produce gut metabolites necessary for a healthy gut. The understanding of the associations between gut microbiota-gut metabolites and CDI will allow for developing precise and sustainable approaches, distinct from antibiotics and fecal transplant, for mitigating CDI and other gut microbiota dysbiosis-related diseases.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bda6/10819375/cc49d79ac093/metabolites-14-00074-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bda6/10819375/cc49d79ac093/metabolites-14-00074-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bda6/10819375/cc49d79ac093/metabolites-14-00074-g001.jpg

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[5]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Effects of Synbiotic , , and Prebiotics on the Growth Stimulation of Beneficial Gut Microbiota.

Foods. 2023-10-20

[2]
Microbiome profile and calprotectin levels as markers of risk of recurrent infection.

Front Cell Infect Microbiol. 2023

[3]
Probiotic supplementation during antibiotic treatment is unjustified in maintaining the gut microbiome diversity: a systematic review and meta-analysis.

BMC Med. 2023-7-19

[4]
Short-Chain Fatty-Acid-Producing Bacteria: Key Components of the Human Gut Microbiota.

Nutrients. 2023-5-6

[5]
Butyrate Protects against Clostridium difficile Infection by Regulating Bile Acid Metabolism.

Microbiol Spectr. 2023-8-17

[6]
Characterization of the gut microbiome of patients with infection, patients with non- diarrhea, and -colonized patients.

Front Cell Infect Microbiol. 2023

[7]
, a New "Superbug".

Microorganisms. 2023-3-26

[8]
Gut microbiome and mycobiome in inflammatory bowel disease patients with infection.

Front Cell Infect Microbiol. 2023

[9]
Butyrate Differentiates Permissiveness to Clostridioides difficile Infection and Influences Growth of Diverse C. difficile Isolates.

Infect Immun. 2023-2-16

[10]
Characterization of Short Chain Fatty Acids Produced by Selected Potential Probiotic Strains.

Biomolecules. 2022-12-7

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