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Updated: Feb 16, 2026

Development of a Larval Zebrafish Infection Model for Clostridioides difficile
Published on: February 14, 2020
Comparative genome and phenotypic analysis of three Clostridioides difficile strains isolated from a single patient
Uwe Groß1, Elzbieta Brzuszkiewicz2, Katrin Gunka1
1Institute for Medical Microbiology, University Medical Center Göttingen, Göttingen, Germany.
Background:
Clostridioides difficile infections (CDI) have emerged over the past decade causing symptoms that range from mild, antibiotic-associated diarrhea (AAD) to life-threatening toxic megacolon. In this study, we describe a multiple and isochronal (mixed) CDI caused by the isolates DSM 27638, DSM 27639 and DSM 27640 that already initially showed different morphotypes on solid media.
Results:
The three isolates belonging to the ribotypes (RT) 012 (DSM 27639) and 027 (DSM 27638 and DSM 27640) were phenotypically characterized and high quality closed genome sequences were generated. The genomes were compared with seven reference strains including three strains of the RT 027, two of the RT 017, and one of the RT 078 as well as a multi-resistant RT 012 strain. The analysis of horizontal gene transfer events revealed gene acquisition incidents that sort the strains within the time line of the spread of their RTs within Germany. We could show as well that horizontal gene transfer between the members of different RTs occurred within this multiple infection. In addition, acquisition and exchange of virulence-related features including antibiotic resistance genes were observed. Analysis of the two genomes assigned to RT 027 revealed three single nucleotide polymorphisms (SNPs) and apparently a regional genome modification within the flagellar switch that regulates the fli operon.
Conclusion:
Our findings show that (i) evolutionary events based on horizontal gene transfer occur within an ongoing CDI and contribute to the adaptation of the species by the introduction of new genes into the genomes, (ii) within a multiple infection of a single patient the exchange of genetic material was responsible for a much higher genome variation than the observed SNPs.
Insights
Horizontal gene transfer drives Clostridioides difficile infection (CDI) evolution during a single patient infection. This genetic exchange significantly increases genome variation more than single nucleotide polymorphisms (SNPs).
Area of Science:
- Microbiology
- Genomics
- Infectious Diseases
Background:
- Clostridioides difficile infections (CDI) range from mild antibiotic-associated diarrhea to life-threatening conditions.
- This study investigates a unique multiple and isochronal (mixed) CDI case involving three distinct C. difficile isolates.
- The isolates exhibited different morphotypes upon initial observation on solid media.
Purpose of the Study:
- To characterize the genomes of C. difficile isolates from a mixed infection.
- To investigate horizontal gene transfer (HGT) events and their impact on genome variation within an ongoing infection.
- To compare genomic features with reference strains of different ribotypes (RTs).
Main Methods:
- Phenotypic characterization of three C. difficile isolates (DSM 27638, DSM 27639, DSM 27640).
- Generation of high-quality closed genome sequences for the isolates.
- Comparative genomic analysis with seven reference strains, including RT 027, RT 017, and RT 078.
Main Results:
- Isolates belonged to RT 012 (DSM 27639) and RT 027 (DSM 27638, DSM 27640).
- Analysis revealed HGT events, including gene acquisition and exchange between different RTs within the mixed infection.
- Acquisition and exchange of virulence factors, such as antibiotic resistance genes, were observed. RT 027 genomes showed three SNPs and a modification in the flagellar switch.
Conclusions:
- Horizontal gene transfer is an active evolutionary process within ongoing CDI, contributing to species adaptation.
- In a single patient's mixed infection, genetic material exchange between C. difficile strains leads to greater genome variation than SNPs.
- HGT plays a significant role in the adaptation and evolution of C. difficile during infection.
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