Comparative genomic and phenomic analysis of Clostridium difficile and Clostridium sordellii, two related pathogens with differing host tissue preference.
Open accessAbstract
BACKGROUND: Clostridium difficile and C. sordellii are two anaerobic, spore forming, gram positive pathogens with a broad host range and the ability to cause lethal infections. Despite strong similarities between the two Clostridial strains, differences in their host tissue preference place C. difficile infections in the gastrointestinal tract and C. sordellii infections in soft tissues. RESULTS: In this study, to improve our understanding of C. sordellii and C. difficile virulence and pathogenesis, we have performed a comparative genomic and phenomic analysis of the two. The global phenomes of C. difficile and C. sordellii were compared using Biolog Phenotype microarrays. When compared to C. difficile, C. sordellii was found to better utilize more complex sources of carbon and nitrogen, including peptides. Phenotype microarray comparison also revealed that C. sordellii was better able to grow in acidic pH conditions. Using next generation sequencing technology, we determined the draft genome of C. sordellii strain 8483 and performed comparative genome analysis with C. difficile and other Clostridial genomes. Comparative genome analysis revealed the presence of several enzymes, including the urease gene cluster, specific to the C. sordellii genome that confer the ability of expanded peptide utilization and survival in acidic pH. CONCLUSIONS: The identified phenotypes of C. sordellii might be important in causing wound and vaginal infections respectively. Proteins involved in the metabolic differences between C. sordellii and C. difficile should be targets for further studies aimed at understanding C. difficile and C. sordellii infection site specificity and pathogenesis.
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The chemical similarity between C. difficile toxin A and P. sordellii hemorrhagic toxin has been identified and immunological cross-reactivity recognized, with both species 71% homologous at the genomic level.
“The chemical similarity between C. difficile toxin A and P. sordellii hemorrhagic toxin has been identified and immunological cross-reactivity recognized, with both species 71% homologous at the genomic level (Martinez and Wilkins, 1988;Scaria et al., 2015).”
From Novel Lethal Clostridial Infection in Florida Manatees (Trichechus manatus latirostris): Cause of the 2013 Unusual Mortality Event in the Indian River Lagoon (2022) · cites this paper as Scaria et al., 2015
The Background reports immunological cross-reactivity between toxins of C. difficile and C. sordellii. The Results and discussion section on gene repertoire comparison reports homologous toxin proteins, including a C. sordellii hemorrhagic toxin, but does not establish the claimed chemical similarity between the specific toxins or state that the species are 71% homologous at the genomic level. Page numbers are unavailable in our copy. (LLM, conf=0.87)
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Clostridium difficile infection: new developments in epidemiology and pathogenesis
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High-throughput generation, optimization and analysis of genome-scale metabolic models
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Cited by
Sorted by citations
Landsberg, J. H., Tabuchi, M., Rotstein, D. S., Subramaniam, K., Rodrigues, T. C. S., Waltzek, T. B., Stacy, N. I., Wilson, P. W., Kiryu, Y., Uzal, F. A., et al. (2022) · Frontiers in Marine Science · doi:10.3389/fmars.2022.841857 · Cited by 20 · see citing works
- Authors
- Scaria, J., Suzuki, H., Ptak, C. P., Chen, J.-W., Zhu, Y., Guo, X.-K., & Chang, Y.-F.
- Affiliations
- South Dakota State University (US)
- Yamaguchi University (JP)
- Cornell University (US)
- Shanghai Jiao Tong University (CN)
- Corresponding author
- Chang, Yung-Fu
- Venue
- BMC Genomics
- Published
- 2015-06-10
- Volume
- 16
- Issue
- 1
- Pages
- 448-448
- ISSN
- 1471-2164 (ISSN-L)
- PMC
- PMC4462011
- OpenAlex
- W1560169010
- Cited by
- 26
- References
- 2
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 2 · 2023: 2 · 2022: 5 · 2021: 3 · 2020: 1 · 2019: 4 · 2018: 1 · 2017: 3 · 2016: 3
- FWCI
- 1.82
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- BMC Genomics (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- U.S. Department of Health and Human Services
- U.S. Department of Agriculture
- National Institutes of Health (n01ai30054-10-0-2)
- National Institute of Allergy and Infectious Diseases (N01 AI030054, N01AI30054)
- Topics
- Health Sciences › Medicine › Infectious Diseases › Clostridium difficile and Clostridium perfringens research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Bacterial Identification and Susceptibility Testing
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Keywords
- Clostridium difficile, Clostridium sordellii, comparative genomics, phenotypic profiling, peptide utilization, acid resistance, urease gene cluster, draft genome sequence, wound infection, vaginal infection, pathogenesis, virulence
- MeSH terms
- Hydrogen-Ion Concentration, Phenotype, Phylogeny, Clostridioides difficile, Genome, Bacterial, Sequence Analysis, DNA, Genomics, Clostridium sordellii, Paraclostridium sordellii, Host Specificity, High-Throughput Nucleotide Sequencing
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