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Culturing and Maintaining Clostridium difficile in an Anaerobic Environment
Published on: September 14, 2013
Enterococcus faecalis Isolated From Infant Feces Inhibits Toxigenic Clostridioides (Clostridium) difficile
Chonticha Romyasamit1, Anucha Thatrimontrichai2, Aratee Aroonkesorn3
1Department of Biomedical Sciences, Faculty of Medicine, Prince of Songkla University, Songkhla, Thailand.
Insights
Six safe Enterococcus faecalis strains isolated from infant feces show potent anti-Clostridioides difficile activity. These potential probiotics inhibit C. difficile spore germination and protect colon cells from infection, offering a novel treatment strategy.
Area of Science:
- Microbiology
- Probiotics
- Gastroenterology
Background:
- Clostridioides difficile infection (CDI) is a leading cause of hospital-acquired diarrhea.
- Probiotics, particularly lactic acid bacteria, are explored as alternative treatments for CDI.
- Enterococci are being investigated for their potential probiotic properties against CDI.
Purpose of the Study:
- To identify novel probiotic Enterococcus strains effective against C. difficile.
- To evaluate the protective effects of these strains on colon adenocarcinoma (HT-29) cells.
- To assess the safety and probiotic characteristics of isolated Enterococcus strains.
Main Methods:
- Nine Enterococcus strains from infant feces were identified as E. faecalis.
- Probiotic properties evaluated: simulated gastrointestinal survival, cell adhesion, safety (virulence genes, antibiotic resistance, Galleria mellonella infection model).
- Anti-C. difficile activity assessed: agar well-diffusion, spore germination/sporulation inhibition, and protection of HT-29 cells via immunofluorescence assay.
Main Results:
- All nine E. faecalis strains demonstrated tolerance to simulated gastrointestinal conditions and enhanced HT-29 cell adhesion.
- Six strains were deemed safe, lacking virulence phenotypes or transferable antibiotic resistance genes, and did not infect G. mellonella.
- These six safe strains significantly inhibited C. difficile spore germination and sporulation, with E. faecalis PK 1302 showing maximal effect.
- Cell-free supernatants from E. faecalis strains reduced C. difficile-induced cytopathic effects on HT-29 cells, preserving cell structure and tight junctions.
Conclusions:
- Six E. faecalis isolates exhibit significant anti-C. difficile activity and protective effects on colon cells.
- These E. faecalis strains are promising candidates for probiotic development.
- Potential applications include preventing C. difficile colonization and treating C. difficile infection.
Abstract:
Clostridioides (Clostridium) difficile infection is implicated as a major cause of antibiotic-associated diarrhea in hospitals worldwide. Probiotics, especially lactic acid bacteria, are the most frequently used alternative treatment. This study aims to identify potential probiotic enterococci strains that act against C. difficile strains and exert a protective effect on colon adenocarcinoma cells (HT-29 cells). To this end, nine Enterococcus strains isolated from the feces of breast-fed infants were investigated. They were identified as E. faecalis by 16s rRNA sequencing and MALDI-TOF. The probiotic properties including their viabilities in simulated gastrointestinal condition, cell adhesion ability, and their safety were evaluated. All strains exhibited more tolerance toward both pepsin and bile salts and adhered more tightly to HT-29 cells compared with the reference probiotic strain Lactobacillus plantarum ATCC 14917. Polymerase chain reaction (PCR) results exhibited that six of nine strains carried at least one virulence determinant gene; however, none exhibited virulence phenotypes or carried transferable antibiotic resistance genes. These strains did not infect Galleria mellonella when compared to pathogenic E. faecalis strain (p < 0.05). Moreover, their antibacterial activities against C. difficile were examined using agar well-diffusion, spore production, and germination tests. The six safe strains inhibited spore germination (100 - 98.20% ± 2.17%) and sporulation, particularly in C. difficile ATCC 630 treated with E. faecalis PK 1302. Furthermore, immunofluorescence assay showed that the cytopathic effects of C. difficile of HT-29 cells were reduced by the treatment with the cell-free supernatant of E. faecalis strains. These strains prevented rounding of HT-29 cells and preserved the F-actin microstructure and tight junctions between adjacent cells, which indicated their ability to reduce the clostridial cytopathic effects. Thus, the study identified six E. faecalis isolates that have anti-C. difficile activity. These could be promising probiotics with potential applications in the prevention of C. difficile colonization and treatment of C. difficile infection.
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