Literature DB >> 29208562

Microbiologic factors affecting Clostridium difficile recurrence.

C H Chilton1, D S Pickering1, J Freeman2.   

Abstract

BACKGROUND: Recurrent Clostridium difficile infection (rCDI) places a huge economic and practical burden on healthcare facilities. Furthermore, rCDI may affect quality of life, leaving patients in an rCDI cycle and dependant on antibiotic therapy. AIMS: To discuss the importance of microbiologic factors in the development of rCDI. SOURCES: Literature was drawn from a search of PubMed from 2000 onwards with the search term 'recurrent Clostridium difficile infection' and further references cited within these articles. CONTENT: Meta-analyses and systematic reviews have shown that CDI and rCDI risk factors are similar. Development of rCDI is attendant on many factors, including immune status or function, comorbidities and concomitant treatments. Studies suggest that poor bacterial diversity is correlated with clinical rCDI. Narrow-spectrum gut microflora-sparing antimicrobials (e.g. surotomycin, cadazolid, ridinilazole) are in development for CDI treatment, while microbiota therapeutics (faecal microbiota transplantation, nontoxigenic C. difficile, stool substitutes) are increasingly being explored. rCDI can only occur when viable C. difficile spores are present, either within the gut lumen after infection or when reacquired from the environment. C. difficile spore germination can be influenced by gut environmental factors resulting from dysbiosis, and spore outgrowth may be affected stage by some antimicrobials (e.g. fidaxomicin, ramoplanin, oritavancin). IMPLICATIONS: rCDI is a significant challenge for healthcare professionals, requiring a multifaceted approach; optimized infection control to minimize reinfection; C. difficile-targeted antibiotics to minimize dysbiosis; and gut microflora restoration to promote colonization resistance. These elements should be informed by our understanding of the microbiologic factors involved in both C. difficile itself and the gut microbiome.
Copyright © 2017 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Antimicrobial persistence; Clostridium difficile; Intestinal microbiota; Recurrence; Spores

Mesh:

Substances:

Year:  2017        PMID: 29208562     DOI: 10.1016/j.cmi.2017.11.017

Source DB:  PubMed          Journal:  Clin Microbiol Infect        ISSN: 1198-743X            Impact factor:   8.067


  16 in total

1.  Engineering probiotics to inhibit Clostridioides difficile infection by dynamic regulation of intestinal metabolism.

Authors:  Elvin Koh; In Young Hwang; Hui Ling Lee; Ryan De Sotto; Jonathan Wei Jie Lee; Yung Seng Lee; John C March; Matthew Wook Chang
Journal:  Nat Commun       Date:  2022-07-04       Impact factor: 17.694

2.  The early stage peptidoglycan biosynthesis Mur enzymes are antibacterial and antisporulation drug targets for recurrent Clostridioides difficile infection.

Authors:  Madhab Sapkota; Ravi K R Marreddy; Xiaoqian Wu; Manish Kumar; Julian G Hurdle
Journal:  Anaerobe       Date:  2019-11-21       Impact factor: 3.331

3.  Microbiota restoration reduces antibiotic-resistant bacteria gut colonization in patients with recurrent Clostridioides difficile infection from the open-label PUNCH CD study.

Authors:  Amy Langdon; Drew J Schwartz; Christopher Bulow; Xiaoqing Sun; Tiffany Hink; Kimberly A Reske; Courtney Jones; Carey-Ann D Burnham; Erik R Dubberke; Gautam Dantas
Journal:  Genome Med       Date:  2021-02-16       Impact factor: 11.117

Review 4.  Fecal microbiota transplantation for recurrent Clostridioides difficile, safety, and pitfalls.

Authors:  Avnish Sandhu; Teena Chopra
Journal:  Therap Adv Gastroenterol       Date:  2021-12-23       Impact factor: 4.409

5.  Ethical Implications of the Fecal Microbiota Transplantation: Disclosure of a False-Positive HIV Test.

Authors:  Caitlyn Hollingshead; Jacob Ciricillo; Joel Kammeyer
Journal:  Case Rep Infect Dis       Date:  2021-12-06

6.  The Fatty Acid Synthesis Protein Enoyl-ACP Reductase II (FabK) is a Target for Narrow-Spectrum Antibacterials for Clostridium difficile Infection.

Authors:  Ravi K R Marreddy; Xiaoqian Wu; Madhab Sapkota; Allan M Prior; Jesse A Jones; Dianqing Sun; Kirk E Hevener; Julian G Hurdle
Journal:  ACS Infect Dis       Date:  2018-12-13       Impact factor: 5.084

Review 7.  Application of Microbiome Management in Therapy for Clostridioides difficile Infections: From Fecal Microbiota Transplantation to Probiotics to Microbiota-Preserving Antimicrobial Agents.

Authors:  Chun-Wei Chiu; Pei-Jane Tsai; Ching-Chi Lee; Wen-Chien Ko; Yuan-Pin Hung
Journal:  Pathogens       Date:  2021-05-24

8.  High Abundance of Proteobacteria in Ileo-Anal Pouch Anastomosis and Increased Abundance of Fusobacteria Associated with Increased Pouch Inflammation.

Authors:  Andreas Munk Petersen; Hengameh Chloé Mirsepasi-Lauridsen; Marianne K Vester-Andersen; Nikolaj Sørensen; Karen Angeliki Krogfelt; Flemming Bendtsen
Journal:  Antibiotics (Basel)       Date:  2020-05-08

9.  What's a Biofilm?-How the Choice of the Biofilm Model Impacts the Protein Inventory of Clostridioides difficile.

Authors:  Madita Brauer; Christian Lassek; Christian Hinze; Juliane Hoyer; Dörte Becher; Dieter Jahn; Susanne Sievers; Katharina Riedel
Journal:  Front Microbiol       Date:  2021-06-10       Impact factor: 5.640

Review 10.  Anti-virulence strategies for Clostridioides difficile infection: advances and roadblocks.

Authors:  David Stewart; Farhan Anwar; Gayatri Vedantam
Journal:  Gut Microbes       Date:  2020-11-09
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