Literature DB >> 32422411

Clostridioides difficile proline fermentation in response to commensal clostridia.

Christopher A Lopez1, Tess P McNeely2, Kamila Nurmakova3, William N Beavers4, Eric P Skaar4.   

Abstract

Clostridioides difficile colonizes the intestines of susceptible individuals and releases toxins that mediate disease. To replicate and expand in the intestines, C. difficile ferments proline, and this activity is influenced by the availability of proline and trace nutrients. C. difficile must also compete with the commensal microbiota for these limited nutrients. The specific microbes present in the intestines that may shape the ability of C. difficile to benefit from proline fermentation are unknown. In this study we developed a panel of commensal Clostridia to test the hypothesis that the microbiota influences C. difficile growth through proline fermentation. The experimental panel of Clostridia was composed of murine and human isolates that ranged in their capacity to ferment proline in different media. Competition between wild type C. difficile and a mutant strain unable to ferment proline (prdB:CT) in the presence of these Clostridia revealed that bacteria closely related to Paraclostridium benzoelyticum and Paeniclostridium spp. decreased the benefit to C. difficile provided by proline fermentation. Conversely, Clostridium xylanolyticum drove C. difficile towards an increased reliance on proline fermentation for growth. Overall, the ability of C. difficile to benefit from proline fermentation is contextual and in part dependent on the microbiota.
Copyright © 2020 Elsevier Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2020        PMID: 32422411      PMCID: PMC8025294          DOI: 10.1016/j.anaerobe.2020.102210

Source DB:  PubMed          Journal:  Anaerobe        ISSN: 1075-9964            Impact factor:   3.331


  36 in total

1.  16S ribosomal DNA amplification for phylogenetic study.

Authors:  W G Weisburg; S M Barns; D A Pelletier; D J Lane
Journal:  J Bacteriol       Date:  1991-01       Impact factor: 3.490

2.  Erratum to Paraclostridium benzoelyticum gen. nov. sp. nov., isolated from marine sediment and reclassification of Clostridium bifermentans as Paraclostridium bifermentans comb. nov. Proposal of a new genus Paeniclostridium gen. nov. to accommodate Clostridium sordellii and Clostridium ghonii.

Authors:  T S Sasi Jyothsna; L Tushar; Ch Sasikala; Ch V Ramana
Journal:  Int J Syst Evol Microbiol       Date:  2016-06       Impact factor: 2.747

3.  Thuricin CD, a posttranslationally modified bacteriocin with a narrow spectrum of activity against Clostridium difficile.

Authors:  Mary C Rea; Clarissa S Sit; Evelyn Clayton; Paula M O'Connor; Randy M Whittal; Jing Zheng; John C Vederas; R Paul Ross; Colin Hill
Journal:  Proc Natl Acad Sci U S A       Date:  2010-04-30       Impact factor: 11.205

4.  Antimicrobial activity of lacticin 3,147 against clinical Clostridium difficile strains.

Authors:  Mary C Rea; Evelyn Clayton; Paula M O'Connor; Fergus Shanahan; Barry Kiely; R Paul Ross; Colin Hill
Journal:  J Med Microbiol       Date:  2007-07       Impact factor: 2.472

5.  A defined growth medium for Clostridium difficile.

Authors:  T Karasawa; S Ikoma; K Yamakawa; S Nakamura
Journal:  Microbiology       Date:  1995-02       Impact factor: 2.777

6.  Clostridioides difficile uses amino acids associated with gut microbial dysbiosis in a subset of patients with diarrhea.

Authors:  Eric J Battaglioli; Vanessa L Hale; Jun Chen; Patricio Jeraldo; Coral Ruiz-Mojica; Bradley A Schmidt; Vayu M Rekdal; Lisa M Till; Lutfi Huq; Samuel A Smits; William J Moor; Yava Jones-Hall; Thomas Smyrk; Sahil Khanna; Darrell S Pardi; Madhusudan Grover; Robin Patel; Nicholas Chia; Heidi Nelson; Justin L Sonnenburg; Gianrico Farrugia; Purna C Kashyap
Journal:  Sci Transl Med       Date:  2018-10-24       Impact factor: 17.956

7.  Role of competition for nutrients in suppression of Clostridium difficile by the colonic microflora.

Authors:  K H Wilson; F Perini
Journal:  Infect Immun       Date:  1988-10       Impact factor: 3.441

8.  Functional Intestinal Bile Acid 7α-Dehydroxylation by Clostridium scindens Associated with Protection from Clostridium difficile Infection in a Gnotobiotic Mouse Model.

Authors:  Nicolas Studer; Lyne Desharnais; Markus Beutler; Sandrine Brugiroux; Miguel A Terrazos; Laure Menin; Christian M Schürch; Kathy D McCoy; Sarah A Kuehne; Nigel P Minton; Bärbel Stecher; Rizlan Bernier-Latmani; Siegfried Hapfelmeier
Journal:  Front Cell Infect Microbiol       Date:  2016-12-20       Impact factor: 5.293

9.  Clostridium difficile Alters the Structure and Metabolism of Distinct Cecal Microbiomes during Initial Infection To Promote Sustained Colonization.

Authors:  Matthew L Jenior; Jhansi L Leslie; Vincent B Young; Patrick D Schloss
Journal:  mSphere       Date:  2018-06-27       Impact factor: 4.389

10.  Comparative genome and phenotypic analysis of Clostridium difficile 027 strains provides insight into the evolution of a hypervirulent bacterium.

Authors:  Richard A Stabler; Miao He; Lisa Dawson; Melissa Martin; Esmeralda Valiente; Craig Corton; Trevor D Lawley; Mohammed Sebaihia; Michael A Quail; Graham Rose; Dale N Gerding; Maryse Gibert; Michel R Popoff; Julian Parkhill; Gordon Dougan; Brendan W Wren
Journal:  Genome Biol       Date:  2009-09-25       Impact factor: 13.583

View more
  7 in total

1.  d-Proline Reductase Underlies Proline-Dependent Growth of Clostridioides difficile.

Authors:  Michael A Johnstone; William T Self
Journal:  J Bacteriol       Date:  2022-07-13       Impact factor: 3.476

Review 2.  Contribution of Inhibitory Metabolites and Competition for Nutrients to Colonization Resistance against Clostridioides difficile by Commensal Clostridium.

Authors:  Amber D Reed; Casey M Theriot
Journal:  Microorganisms       Date:  2021-02-12

3.  The development of live biotherapeutics against Clostridioides difficile infection towards reconstituting gut microbiota.

Authors:  Yongrong Zhang; Ashley Saint Fleur; Hanping Feng
Journal:  Gut Microbes       Date:  2022 Jan-Dec

4.  The Stickland Reaction Precursor trans-4-Hydroxy-l-Proline Differentially Impacts the Metabolism of Clostridioides difficile and Commensal Clostridia.

Authors:  A D Reed; J R Fletcher; Y Y Huang; R Thanissery; A J Rivera; R J Parsons; A K Stewart; D J Kountz; A Shen; E P Balskus; C M Theriot
Journal:  mSphere       Date:  2022-03-30       Impact factor: 5.029

5.  Gut associated metabolites and their roles in Clostridioides difficile pathogenesis.

Authors:  Andrea Martinez Aguirre; Joseph A Sorg
Journal:  Gut Microbes       Date:  2022 Jan-Dec

6.  Intestinal Inflammation and Altered Gut Microbiota Associated with Inflammatory Bowel Disease Render Mice Susceptible to Clostridioides difficile Colonization and Infection.

Authors:  Lisa Abernathy-Close; Madeline R Barron; James M George; Michael G Dieterle; Kimberly C Vendrov; Ingrid L Bergin; Vincent B Young
Journal:  mBio       Date:  2021-06-15       Impact factor: 7.867

Review 7.  Microbial adaptation to the healthy and inflamed gut environments.

Authors:  Yijie Guo; Sho Kitamoto; Nobuhiko Kamada
Journal:  Gut Microbes       Date:  2020-11-09
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.