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Updated: May 16, 2025

Cefoperazone-treated Mouse Model of Clinically-relevant Clostridium difficile Strain R20291
Published on: December 10, 2016
Clostridioides difficile concentration-dependant alterations in gut microbiota of asymptomatic infants
Aleksander Mahnic1,2, Jana Lozar Krivec3,4, Darja Paro-Panjan3,4
1Department for Microbiological Research, National Laboratory of Health, Environment and Food, Maribor, Slovenia. aleksander.mahnic@nlzoh.si.
Insights
Asymptomatic Clostridioides difficile carriage in infants doesn't alter gut microbiota unless pathogen levels are high. Elevated C. difficile indicates dysbiosis, marked by lower diversity and increased Escherichia.
Area of Science:
- Microbiology
- Gastroenterology
- Pediatrics
Background:
- Asymptomatic Clostridioides difficile carriage is common in infants (approx. 40%).
- Infant carriage provides a model to study gut microbiota without disease confounds.
- Antibiotic exposure in infancy is a potential factor influencing C. difficile colonization.
Purpose of the Study:
- To investigate gut microbiome alterations in asymptomatic infants one year after antibiotic treatment.
- To assess the relationship between Clostridioides difficile presence/concentration and gut microbiota structure.
- To identify host-specific factors associated with C. difficile colonization.
Main Methods:
- 16S rRNA amplicon sequencing for bacterial gut community structure.
- Digital PCR for quantifying C. difficile concentration and tcdB gene presence.
- Analysis of extensive metadata alongside microbial data.
Main Results:
- C. difficile detected in 36.8% of infants; tcdB gene in 10.5%.
- Higher C. difficile loads correlated with reduced microbial diversity and increased Escherichia.
- No significant microbiota alterations linked to C. difficile colonization alone or tcdB gene presence.
Conclusions:
- Asymptomatic C. difficile carriage impacts gut microbiota only when pathogen concentration is high.
- Elevated C. difficile proliferation suggests an underlying dysbiotic infant gut microbiota.
- Dysbiosis is characterized by reduced alpha diversity and increased Escherichia abundance.
Background:
Asymptomatic carriage of Clostridioides difficile is highly prevalent in early infancy, affecting approximately 40% of infants. This phenomenon offers a unique opportunity to study its impact on the gut microbiota without the confounding effects of disease. In this study, we analysed C. difficile-associated gut microbiome alterations in 76 asymptomatic infants, one year after receiving antibiotic treatment during early infancy. The presence and concentration of C. difficile were assessed in relation to gut microbiota structure and an extensive set of metadata.
Results:
Bacterial gut community structure was characterized using 16 S rRNA amplicon sequencing, while C. difficile concentration and the presence of the tcdB gene were quantified via digital PCR. C. difficile was detected in 36.8% of infants, with 10.5% testing positive for the tcdB gene. Significant alterations in gut microbiota were observed in relation to C. difficile concentration. Specifically, higher C. difficile loads were associated with reduced microbial diversity, greater deviations from average community structure, and co-occurrence with the genus Escherichia. Conversely, C. difficile colonization alone or the presence of the tcdB gene did not result in significant gut microbiota alterations. Additionally, no host-specific factors were significantly linked to C. difficile prevalence or concentration.
Conclusions:
Asymptomatic carriage of C. difficile in neonates is not associated with significant gut microbiota alterations unless pathogen concentration is considered. Our findings suggest that elevated C. difficile proliferation occurs in dysbiotic infant gut microbiota, characterized by reduced alpha diversity and an increase in Escherichia.
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