Literature DB >> 35770172

Battling Enteropathogenic Clostridia: Phage Therapy for Clostridioides difficile and Clostridium perfringens.

Jennifer Venhorst1, Jos M B M van der Vossen2, Valeria Agamennone2.   

Abstract

The pathogenic Clostridioides difficile and Clostridium perfringens are responsible for many health care-associated infections as well as systemic and enteric diseases. Therefore, they represent a major health threat to both humans and animals. Concerns regarding increasing antibiotic resistance (related to C. difficile and C. perfringens) have caused a surge in the pursual of novel strategies that effectively combat pathogenic infections, including those caused by both pathogenic species. The ban on antibiotic growth promoters in the poultry industry has added to the urgency of finding novel antimicrobial therapeutics for C. perfringens. These efforts have resulted in various therapeutics, of which bacteriophages (in short, phages) show much promise, as evidenced by the Eliava Phage Therapy Center in Tbilisi, Georgia (https://eptc.ge/). Bacteriophages are a type of virus that infect bacteria. In this review, the (clinical) impact of clostridium infections in intestinal diseases is recapitulated, followed by an analysis of the current knowledge and applicability of bacteriophages and phage-derived endolysins in this disease indication. Limitations of phage and phage endolysin therapy were identified and require considerations. These include phage stability in the gastrointestinal tract, influence on gut microbiota structure/function, phage resistance development, limited host range for specific pathogenic strains, phage involvement in horizontal gene transfer, and-for phage endolysins-endolysin resistance, -safety, and -immunogenicity. Methods to optimize features of these therapeutic modalities, such as mutagenesis and fusion proteins, are also addressed. The future success of phage and endolysin therapies require reliable clinical trial data for phage(-derived) products. Meanwhile, additional research efforts are essential to expand the potential of exploiting phages and their endolysins for mitigating the severe diseases caused by C. difficile and C. perfringens.
Copyright © 2022 Venhorst, van der Vossen and Agamennone.

Entities:  

Keywords:  Clostridioides difficile; Clostridium perfringens; endolysin; enteropathogen; phage (bacteriophage); phage therapy

Year:  2022        PMID: 35770172      PMCID: PMC9234517          DOI: 10.3389/fmicb.2022.891790

Source DB:  PubMed          Journal:  Front Microbiol        ISSN: 1664-302X            Impact factor:   6.064


  144 in total

1.  Synergistic lethal effect of a combination of phage lytic enzymes with different activities on penicillin-sensitive and -resistant Streptococcus pneumoniae strains.

Authors:  J M Loeffler; V A Fischetti
Journal:  Antimicrob Agents Chemother       Date:  2003-01       Impact factor: 5.191

2.  Isolation and characterization of temperate bacteriophages of Clostridium difficile.

Authors:  Shan Goh; Thomas V Riley; Barbara J Chang
Journal:  Appl Environ Microbiol       Date:  2005-02       Impact factor: 4.792

3.  Bacteriophage mediated control of necrotic enteritis caused by C. perfringens in broiler chickens.

Authors:  Reham A Hosny; Ahmed F Gaber; Hend K Sorour
Journal:  Vet Res Commun       Date:  2021-09-13       Impact factor: 2.459

4.  Evaluation of bacteriophage therapy to control Clostridium difficile and toxin production in an in vitro human colon model system.

Authors:  Emma Meader; Melinda J Mayer; Dietmar Steverding; Simon R Carding; Arjan Narbad
Journal:  Anaerobe       Date:  2013-05-17       Impact factor: 3.331

5.  Metagenome Data on Intestinal Phage-Bacteria Associations Aids the Development of Phage Therapy against Pathobionts.

Authors:  Kosuke Fujimoto; Yasumasa Kimura; Masaki Shimohigoshi; Takeshi Satoh; Shintaro Sato; Georg Tremmel; Miho Uematsu; Yunosuke Kawaguchi; Yuki Usui; Yoshiko Nakano; Tetsuya Hayashi; Koji Kashima; Yoshikazu Yuki; Kiyoshi Yamaguchi; Yoichi Furukawa; Masanori Kakuta; Yutaka Akiyama; Rui Yamaguchi; Sheila E Crowe; Peter B Ernst; Satoru Miyano; Hiroshi Kiyono; Seiya Imoto; Satoshi Uematsu
Journal:  Cell Host Microbe       Date:  2020-07-10       Impact factor: 21.023

6.  Bacteriophages are more virulent to bacteria with human cells than they are in bacterial culture; insights from HT-29 cells.

Authors:  Jinyu Shan; Ananthi Ramachandran; Anisha M Thanki; Fatima B I Vukusic; Jakub Barylski; Martha R J Clokie
Journal:  Sci Rep       Date:  2018-03-23       Impact factor: 4.379

7.  Dietary trehalose enhances virulence of epidemic Clostridium difficile.

Authors:  J Collins; C Robinson; H Danhof; C W Knetsch; H C van Leeuwen; T D Lawley; J M Auchtung; R A Britton
Journal:  Nature       Date:  2018-01-03       Impact factor: 49.962

8.  Capsular Polysaccharide Is a Receptor of a Clostridium perfringens Bacteriophage CPS1.

Authors:  Eunsu Ha; Jihwan Chun; Minsik Kim; Sangryeol Ryu
Journal:  Viruses       Date:  2019-10-31       Impact factor: 5.048

Review 9.  An update on the human and animal enteric pathogen Clostridium perfringens.

Authors:  Raymond Kiu; Lindsay J Hall
Journal:  Emerg Microbes Infect       Date:  2018-08-06       Impact factor: 7.163

10.  A Novel Bacteriophage Lysin-Human Defensin Fusion Protein Is Effective in Treatment of Clostridioides difficile Infection in Mice.

Authors:  Zhong Peng; Shaohui Wang; Mussie Gide; Duolong Zhu; Hiran Malinda Lamabadu Warnakulasuriya Patabendige; Chunhui Li; Jianfeng Cai; Xingmin Sun
Journal:  Front Microbiol       Date:  2019-01-11       Impact factor: 5.640

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