Literature DB >> 26169276

Fecal Microbiota Transplantation Eliminates Clostridium difficile in a Murine Model of Relapsing Disease.

Anna M Seekatz1, Casey M Theriot2, Caitlyn T Molloy1, Katherine L Wozniak1, Ingrid L Bergin3, Vincent B Young4.   

Abstract

Recurrent Clostridium difficile infection (CDI) is of particular concern among health care-associated infections. The role of the microbiota in disease recovery is apparent given the success of fecal microbiota transplantation (FMT) for recurrent CDI. Here, we present a murine model of CDI relapse to further define the microbiota recovery following FMT. Cefoperazone-treated mice were infected with C. difficile 630 spores and treated with vancomycin after development of clinical disease. Vancomycin treatment suppressed both C. difficile colonization and cytotoxin titers. However, C. difficile counts increased within 7 days of completing treatment, accompanied by relapse of clinical signs. The administration of FMT immediately after vancomycin cleared C. difficile and decreased cytotoxicity within 1 week. The effects of FMT on the gut microbiota community were detectable in recipients 1-day posttransplant. Conversely, mice not treated with FMT remained persistently colonized with high levels of C. difficile, and the gut microbiota in these mice persisted at low diversity. These results suggest that full recovery of colonization resistance against C. difficile requires the restoration of a specific community structure.
Copyright © 2015, American Society for Microbiology. All Rights Reserved.

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Year:  2015        PMID: 26169276      PMCID: PMC4567621          DOI: 10.1128/IAI.00459-15

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  32 in total

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3.  Decreased diversity of the fecal Microbiome in recurrent Clostridium difficile-associated diarrhea.

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Journal:  Appl Environ Microbiol       Date:  2009-10-02       Impact factor: 4.792

5.  Antibiotic treatment of clostridium difficile carrier mice triggers a supershedder state, spore-mediated transmission, and severe disease in immunocompromised hosts.

Authors:  Trevor D Lawley; Simon Clare; Alan W Walker; David Goulding; Richard A Stabler; Nicholas Croucher; Piero Mastroeni; Paul Scott; Claire Raisen; Lynda Mottram; Neil F Fairweather; Brendan W Wren; Julian Parkhill; Gordon Dougan
Journal:  Infect Immun       Date:  2009-06-29       Impact factor: 3.441

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Authors:  D van der Waaij
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  64 in total

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3.  Effects of intrauterine contraception on the vaginal microbiota.

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4.  A human gut ecosystem protects against C. difficile disease by targeting TcdA.

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Journal:  J Gastroenterol       Date:  2016-06-21       Impact factor: 7.527

5.  The gut microbiome composition associates with bipolar disorder and illness severity.

Authors:  Simon J Evans; Christine M Bassis; Robert Hein; Shervin Assari; Stephanie A Flowers; Marisa B Kelly; Vince B Young; Vicky E Ellingrod; Melvin G McInnis
Journal:  J Psychiatr Res       Date:  2016-12-10       Impact factor: 4.791

6.  Freeze-dried fecal samples are biologically active after long-lasting storage and suited to fecal microbiota transplantation in a preclinical murine model of Clostridioides difficile infection.

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7.  Outbreaks of Typhlocolitis Caused by Hypervirulent Group ST1 Clostridioides difficile in Highly Immunocompromised Strains of Mice.

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Review 8.  Control of Clostridium difficile Infection by Defined Microbial Communities.

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Journal:  Microbiol Spectr       Date:  2017-09

9.  Modified Mouse Model of Clostridioides difficile Infection as a Platform for Probiotic Efficacy Studies.

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10.  Increased Relative Abundance of Klebsiella pneumoniae Carbapenemase-producing Klebsiella pneumoniae Within the Gut Microbiota Is Associated With Risk of Bloodstream Infection in Long-term Acute Care Hospital Patients.

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Journal:  Clin Infect Dis       Date:  2019-05-30       Impact factor: 9.079

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