4.8 Review

Phage therapy for Clostridioides difficile infection

期刊

FRONTIERS IN IMMUNOLOGY
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2022.1057892

关键词

Clostridioides difficile; bacteriophage; endolysin; enzyme active domain; cell wall-binding domain; metagenome

资金

  1. Japan Agency for Medical Research and Development (AMED)
  2. JSPS
  3. [22ae0121048h0001]
  4. [22fk0108619h0001]
  5. [22K16329]

向作者/读者索取更多资源

Clostridioides difficile is a bacterium that can be found in the intestinal tract of healthy individuals, but it can also cause infections, particularly hospital-acquired diarrhea following antibiotic treatment. The emergence of highly virulent strains and resistance to antibiotics have led to treatment failures and relapses. Fecal microbiota transplantation (FMT) is considered effective, although safety concerns exist due to antibiotic-resistant bacterial infections. Therefore, the development of specific treatments for C. difficile is urgently needed.
Clostridioides difficile is endemic in the intestinal tract of healthy people. However, it is responsible for many healthcare-associated infections, such as nosocomial diarrhea following antibiotic treatment. Importantly, there have been cases of unsuccessful treatment and relapse related to the emergence of highly virulent strains of C. difficile and resistance to antimicrobial agents. Fecal microbiota transplantation (FMT) is considered an effective therapy for recurrent C. difficile infection. However, its safety is of concern because deaths caused by antibiotic-resistant bacterial infections after FMT were reported. Therefore, the development of effective C. difficile-specific treatments is urgently needed. In this review, we summarize the importance of phage therapy against C. difficile, and describe a novel next-generation phage therapy developed using metagenomic data.

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