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Mobile genetic elements of Fusobacterium nucleatum
1Department of Microbiology, School of Dental Medicine, University of Pennsylvania, Philadelphia 19104-6002, USA.
Plasmid
|January 1, 1995
Summary
Researchers identified small cryptic plasmids and a tetracycline resistance transposon in Fusobacterium nucleatum. These genetic elements could serve as tools for genetic manipulation of this oral bacterium.
Area of Science:
- Microbiology
- Genetics
- Oral Biology
Background:
- Fusobacterium nucleatum is a key gram-negative anaerobic bacterium in human oral flora.
- It significantly impacts oral cavity ecology, particularly in subgingival plaque, due to its adhesive properties.
- Understanding its genetic elements is crucial for developing biotechnological tools.
Purpose of the Study:
- To identify and characterize plasmids and transposons in Fusobacterium nucleatum.
- To explore their potential as tools for genetic manipulation (cloning, transformation, mutagenesis) of oral F. nucleatum isolates.
Main Methods:
- Analysis of laboratory strains for plasmids and transposons.
- Cloning of plasmid species in Escherichia coli for restriction mapping.
- Tetracycline resistance screening.
- Genomic fingerprinting for strain distinctness.
Main Results:
- A homologous family of small cryptic plasmids (6.0–6.6 kb) was identified in 18% of examined strains (n=74).
- Homologous plasmid sequences were found in two of three F. nucleatum subspecies.
- Five strains, belonging to subsp. polymorphum, showed tetracycline resistance due to a TetM determinant within a Tn916-like transposon.
- The transposon and a plasmid co-resided in one strain, with identical transposon hybridization patterns across resistant strains, despite genomic distinctness.
Conclusions:
- Fusobacterium nucleatum harbors cryptic plasmids and a Tn916-like transposon conferring tetracycline resistance.
- These genetic elements, particularly plasmids, show potential for developing genetic tools for F. nucleatum.
- Further research can leverage these findings for genetic engineering of oral bacteria.