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Proteus mirabilis converting phage 5006Mpa has an oversized genome
The Journal of General Virology
|November 1, 1981
Summary
Proteus mirabilis phage 5006Mpa carries an ampicillin resistance gene via insertion of transposon Tn1. This genetic insertion results in a larger phage genome but does not eliminate essential wild-type genes.
Area of Science:
- Microbiology
- Genetics
- Molecular Biology
Background:
- Proteus mirabilis phage 5006M is a known bacterial virus.
- Phage 5006Mpa is a variant of phage 5006M, exhibiting ampicillin resistance.
- Transposon Tn1 is a mobile genetic element conferring antibiotic resistance.
Purpose of the Study:
- To characterize the genetic basis of ampicillin resistance in Proteus mirabilis phage 5006Mpa.
- To determine the location and size of the genetic insertion responsible for ampicillin resistance.
- To assess the impact of the insertion on the overall phage genome structure.
Main Methods:
- Comparative genome analysis of phage 5006M and 5006Mpa.
- Identification and mapping of the ampicillin resistance marker.
- Genome size determination.
Main Results:
- The ampicillin resistance of phage 5006Mpa is attributed to the insertion of transposon Tn1.
- This insertion constitutes approximately 9.8% of the phage genome.
- The modified phage 5006Mpa genome is approximately 5% larger than the wild-type phage 5006M genome.
- No loss of wild-type genetic material was observed in the phage population.
Conclusions:
- Proteus mirabilis phage 5006Mpa harbors an ampicillin resistance gene via Tn1 insertion.
- The genetic modification leads to a larger phage genome without compromising essential wild-type genetic information.
- This finding contributes to understanding phage evolution and antibiotic resistance mechanisms.