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Islands of non-essential genes, including a DNA translocation operon, in the genome of bacteriophage 0305ϕ8-36

We investigate genes of lytic, Bacillus thuringiensis bacteriophage 0305ϕ8-36 that are non-essential for laboratory propagation, but might have a function in the wild. We isolate deletion mutants to identify these genes. The non-permutation of the genome (218.948 Kb, with a 6.479 Kb terminal repeat...

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Autores principales: Pathria, Saurav, Rolando, Mandy, Lieman, Karen, Hayes, Shirley, Hardies, Stephen, Serwer, Philip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3357382/
https://www.ncbi.nlm.nih.gov/pubmed/22666654
http://dx.doi.org/10.4161/bact.19546
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author Pathria, Saurav
Rolando, Mandy
Lieman, Karen
Hayes, Shirley
Hardies, Stephen
Serwer, Philip
author_facet Pathria, Saurav
Rolando, Mandy
Lieman, Karen
Hayes, Shirley
Hardies, Stephen
Serwer, Philip
author_sort Pathria, Saurav
collection PubMed
description We investigate genes of lytic, Bacillus thuringiensis bacteriophage 0305ϕ8-36 that are non-essential for laboratory propagation, but might have a function in the wild. We isolate deletion mutants to identify these genes. The non-permutation of the genome (218.948 Kb, with a 6.479 Kb terminal repeat and 247 identified orfs) simplifies isolation of deletion mutants. We find two islands of non-essential genes. The first island (3.01% of the genomic DNA) has an informatically identified DNA translocation operon. Deletion causes no detectable growth defect during propagation in a dilute agarose overlay. Identification of the DNA translocation operon begins with a DNA relaxase and continues with a translocase and membrane-binding anchor proteins. The relaxase is in a family, first identified here, with homologs in other bacteriophages. The second deleted island (3.71% of the genome) has genes for two metallo-protein chaperonins and two tRNAs. Deletion causes a significant growth defect. In addition, (1) we find by “in situ” (in-plaque) single-particle fluorescence microscopy that adsorption to the host occurs at the tip of the 486 nm long tail, (2) we develop a procedure of 0305ϕ8-36 purification that does not cause tail contraction, and (3) we then find by electron microscopy that 0305ϕ8-36 undergoes tail tip-tail tip dimerization that potentially blocks adsorption to host cells, presumably with effectiveness that increases as the bacteriophage particle concentration increases. These observations provide an explanation of the previous observation that 0305ϕ8-36 does not lyse liquid cultures, even though 0305ϕ8-36 is genomically lytic.
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spelling pubmed-33573822012-06-04 Islands of non-essential genes, including a DNA translocation operon, in the genome of bacteriophage 0305ϕ8-36 Pathria, Saurav Rolando, Mandy Lieman, Karen Hayes, Shirley Hardies, Stephen Serwer, Philip Bacteriophage Research Paper We investigate genes of lytic, Bacillus thuringiensis bacteriophage 0305ϕ8-36 that are non-essential for laboratory propagation, but might have a function in the wild. We isolate deletion mutants to identify these genes. The non-permutation of the genome (218.948 Kb, with a 6.479 Kb terminal repeat and 247 identified orfs) simplifies isolation of deletion mutants. We find two islands of non-essential genes. The first island (3.01% of the genomic DNA) has an informatically identified DNA translocation operon. Deletion causes no detectable growth defect during propagation in a dilute agarose overlay. Identification of the DNA translocation operon begins with a DNA relaxase and continues with a translocase and membrane-binding anchor proteins. The relaxase is in a family, first identified here, with homologs in other bacteriophages. The second deleted island (3.71% of the genome) has genes for two metallo-protein chaperonins and two tRNAs. Deletion causes a significant growth defect. In addition, (1) we find by “in situ” (in-plaque) single-particle fluorescence microscopy that adsorption to the host occurs at the tip of the 486 nm long tail, (2) we develop a procedure of 0305ϕ8-36 purification that does not cause tail contraction, and (3) we then find by electron microscopy that 0305ϕ8-36 undergoes tail tip-tail tip dimerization that potentially blocks adsorption to host cells, presumably with effectiveness that increases as the bacteriophage particle concentration increases. These observations provide an explanation of the previous observation that 0305ϕ8-36 does not lyse liquid cultures, even though 0305ϕ8-36 is genomically lytic. Landes Bioscience 2012-01-01 /pmc/articles/PMC3357382/ /pubmed/22666654 http://dx.doi.org/10.4161/bact.19546 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Research Paper
Pathria, Saurav
Rolando, Mandy
Lieman, Karen
Hayes, Shirley
Hardies, Stephen
Serwer, Philip
Islands of non-essential genes, including a DNA translocation operon, in the genome of bacteriophage 0305ϕ8-36
title Islands of non-essential genes, including a DNA translocation operon, in the genome of bacteriophage 0305ϕ8-36
title_full Islands of non-essential genes, including a DNA translocation operon, in the genome of bacteriophage 0305ϕ8-36
title_fullStr Islands of non-essential genes, including a DNA translocation operon, in the genome of bacteriophage 0305ϕ8-36
title_full_unstemmed Islands of non-essential genes, including a DNA translocation operon, in the genome of bacteriophage 0305ϕ8-36
title_short Islands of non-essential genes, including a DNA translocation operon, in the genome of bacteriophage 0305ϕ8-36
title_sort islands of non-essential genes, including a dna translocation operon, in the genome of bacteriophage 0305ϕ8-36
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3357382/
https://www.ncbi.nlm.nih.gov/pubmed/22666654
http://dx.doi.org/10.4161/bact.19546
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