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Mycoplasma arthritidis bacteriophage MAV1 prophage integration, deletions, and strain-related polymorphisms
L R Washburn1, E J Miller, S Mukherjee
1Division of Basic Biomedical Sciences, University of South Dakota School of Medicine, 414 E. Clark Street, Vermillion, SD 57069-2390, USA. lwashbur@usd.edu
Abstract:
Temperate bacteriophage MAV1 is found in certain highly virulent strains of Mycoplasma arthritidis. Integration sites, portions of the right and left prophage ends, and flanking DNA from eight prophages in seven M. arthritidis strains were characterized in this study. attb and attp sites conformed for the most part to the consensus sequence TATTTTT, although minor polymorphisms were noted. Prophages were integrated into similar sites in four strains, suggesting that these strains may have had a common ancestor. Two strains had three prophage copies each, and integration sites were identical. Two strains had two copies each. One of these shared two of the integration sites occupied in the three-copy strains, while the other shared one of these sites and harbored a second prophage in a unique site. Integration sites in the two strains with one prophage each were unique. Four MAV1 copies contained extensive substitutions within a region encoding a putative structural protein and the putative repressor protein. A 3-kb fragment was deleted from the right side of two of these copies. It is proposed that polymorphisms within MAV1 prophage integration sites and within the prophages themselves may help to identify phylogenetic relationships among virulent M. arthritidis strains.
Insights
The MAV1 bacteriophage integrates into virulent Mycoplasma arthritidis strains at specific DNA sites. Variations in these integration sites and the phage DNA itself may reveal evolutionary links between different M. arthritidis strains.
Area of Science:
- Microbiology
- Virology
- Genetics
Background:
- Mycoplasma arthritidis is a bacterium that can cause severe infections.
- The temperate bacteriophage MAV1 is found in some virulent M. arthritidis strains.
- Understanding phage-host interactions is crucial for studying bacterial virulence.
Purpose of the Study:
- To characterize the integration sites of the MAV1 bacteriophage in M. arthritidis.
- To investigate potential correlations between MAV1 prophage characteristics and M. arthritidis strain phylogeny.
- To identify genetic variations within MAV1 prophages in different strains.
Main Methods:
- DNA sequencing of prophage ends and flanking regions from eight MAV1 prophages in seven M. arthritidis strains.
- Analysis of att sites and prophage integration site sequences.
- Comparison of MAV1 prophage sequences for structural variations and deletions.
Main Results:
- MAV1 att sites largely matched the consensus sequence TATTTTT, with minor polymorphisms observed.
- Identical integration sites were found in strains with multiple prophage copies, suggesting common ancestry.
- Four MAV1 copies exhibited significant substitutions in genes for structural and repressor proteins, with two also showing a 3-kb deletion.
- Unique integration sites were identified in strains with single prophage copies.
Conclusions:
- MAV1 integration site polymorphisms can be used to trace phylogenetic relationships among virulent M. arthritidis strains.
- Variations within the MAV1 prophage genome, including gene substitutions and deletions, provide further markers for strain differentiation.
- This study highlights the utility of bacteriophage genetics in understanding bacterial evolution and virulence.
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