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Whole genome sequencing identifies an allele responsible for clear vs. turbid plaque morphology in a Mycobacteriophage

BACKGROUND: Whole genome sequencing promises to revolutionize our ability to link genotypic and phenotypic variation in a wide range of model and non-model species. RESULTS: Here we describe the isolation and characterization of a novel mycobacteriophage named BGlluviae that grows on Mycobacterium s...

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Detalles Bibliográficos
Autores principales: Gudlavalleti, Bhavani S., Phung, Trong, Barton, Charles L., Becker, Allysson, Graul, Brittany L., Griffin, Jarod T., Hays, Connor J., Horn, Bailey, Liang, David R., Rutledge, Lauren M., Szalanczy, Alexandria M., Gaffney, Bobby L., King, Rodney A., Rinehart, Claire A., Staples, Amanda K., Stewart, Alexander A., Nydam, Marie L., O’Quin, Kelly E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7282100/
https://www.ncbi.nlm.nih.gov/pubmed/32513117
http://dx.doi.org/10.1186/s12866-020-01833-4
Descripción
Sumario:BACKGROUND: Whole genome sequencing promises to revolutionize our ability to link genotypic and phenotypic variation in a wide range of model and non-model species. RESULTS: Here we describe the isolation and characterization of a novel mycobacteriophage named BGlluviae that grows on Mycobacterium smegmatis mc(2)155. BGlluviae normally produces turbid plaques but a spontaneous clear plaque was also recovered. The genomic DNA from pure populations of the BGlluviae phage and the clear plaque mutant were sequenced. A single substitution, at amino acid 54 (I to T), in the immunity repressor protein resulted in a clear plaque phenotype. CONCLUSIONS: This substitution is predicted to be located at the subunit interaction interface of the repressor protein, and thus prevents the establishment of lysogeny.