| Literature DB >> 35574602 |
Rusha Pal1, Ahmad I M Athamneh2, Riddhi Deshpande3, Jose A R Ramirez4, Kayode T Adu4,5, Pushpanathan Muthuirulan6, Shrikant Pawar7, Manuele Biazzo8, Yiorgos Apidianakis9, Ulrik Kraemer Sundekilde10, Cesar de la Fuente-Nunez11,12,13, Mark G Martens3,14, George P Tegos14, Mohamed N Seleem1,15.
Abstract
Clostridioides difficile infection (CDI) is a life-threatening disease caused by the Gram-positive, opportunistic intestinal pathogen C. difficile. Despite the availability of antimicrobial drugs to treat CDI, such as vancomycin, metronidazole, and fidaxomicin, recurrence of infection remains a significant clinical challenge. The use of live commensal microorganisms, or probiotics, is one of the most investigated non-antibiotic therapeutic options to balance gastrointestinal (GI) microbiota and subsequently tackle dysbiosis. In this review, we will discuss major commensal probiotic strains that have the potential to prevent and/or treat CDI and its recurrence, reassess the efficacy of probiotics supplementation as a CDI intervention, delve into lessons learned from probiotic modulation of the immune system, explore avenues like genome-scale metabolic network reconstructions, genome sequencing, and multi-omics to identify novel strains and understand their functionality, and discuss the current regulatory framework, challenges, and future directions.Entities:
Keywords: C. difficile; Probiotics; discovery informatics; genomic exploration; immunomodulatory; inhibition; metabolomics; multi-omics; regulatory requirements; virulence
Year: 2022 PMID: 35574602 DOI: 10.1080/1040841X.2022.2072705
Source DB: PubMed Journal: Crit Rev Microbiol ISSN: 1040-841X Impact factor: 7.391