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Genome-wide Gene Deletions in Streptococcus sanguinis by High Throughput PCR
Published on: November 23, 2012
Genome analysis of an inducible prophage and prophage remnants integrated in the Streptococcus pyogenes strain SF370
Carlos Canchaya1, Frank Desiere, W Michael McShan
1Nestlé Research Center, Nestec Ltd. Vers-chez-les-Blanc, CH Lausanne 26, Switzerland.
Abstract:
The mitomycin C inducible prophage SF370.1 from the highly pathogenic M1 serotype Streptococcus pyogenes isolate SF370 showed a 41-kb-long genome whose genetic organization resembled that of SF11-like pac-site Siphoviridae. Its closest relative was prophage NIH1.1 from an M3 serotype S. pyogenes strain, followed by S. pneumoniae phage MM1 and Lactobacillus phage phig1e, Listeria phage A118, and Bacillus phage SPP1 in a gradient of relatedness. Sequence similarity with the previously described prophages SF370.2 and SF370.3 from the same polylysogenic SF370 strain were mainly limited to the tail fiber genes. As in these two other prophages, SF370.1 encoded likely lysogenic conversion genes between the phage lysin and the right attachment site. The genes encoded the pyrogenic exotoxin C of S. pyogenes and a protein sharing sequence similarity with both DNases and mitogenic factors. The screening of the SF370 genome revealed further prophage-like elements. A 13-kb-long phage remnant SF370.4 encoded lysogeny and DNA replication genes. A closely related prophage remnant was identified in S. pyogenes strain Manfredo at a corresponding genome position. The two prophages differed by internal indels and gene replacements. Four phage-like integrases were detected; three were still accompanied by likely repressor genes. All prophage elements were integrated into coding sequences. The phage sequences complemented the coding sequences in all cases. The DNA repair genes mutL and mutS were separated by the prophage remnant SF370.4; prophage SF370.1 and S. pneumoniae phage MM1 integrated into homologous chromosomal locations. The prophage sequences were interpreted with a hypothesis that predicts elements of cooperation and an arms race between phage and host genomes.
Insights
This study characterizes Streptococcus pyogenes prophage SF370.1, revealing its genetic makeup and relationship to other phages. It highlights phage-host interactions, suggesting cooperation and an evolutionary arms race.
Area of Science:
- Microbiology
- Virology
- Genomics
Background:
- Streptococcus pyogenes is a significant human pathogen.
- Bacteriophages (phages) can integrate into bacterial genomes as prophages.
- Understanding prophage genomes is crucial for deciphering phage-host interactions and bacterial evolution.
Purpose of the Study:
- To characterize the mitomycin C inducible prophage SF370.1 from a highly pathogenic Streptococcus pyogenes strain.
- To investigate the genetic organization and evolutionary relationships of SF370.1 with other known phages.
- To identify and analyze other prophage-like elements within the S. pyogenes SF370 genome.
Main Methods:
- Genome sequencing and analysis of prophage SF370.1.
- Comparative genomics to determine relatedness to other Siphoviridae phages.
- Bioinformatic screening of the S. pyogenes SF370 genome for additional prophage elements.
- Analysis of integration sites and genetic context of prophages.
Main Results:
- Prophage SF370.1 possesses a 41-kb genome with genetic organization similar to SF11-like pac-site Siphoviridae.
- SF370.1 is most closely related to prophage NIH1.1 and shows decreasing relatedness to other bacterial and archaeal phages.
- The study identified additional prophage remnants (e.g., SF370.4) and phage-like integrases within the S. pyogenes SF370 genome.
- Prophage elements were found integrated into coding sequences, including DNA repair genes, and encoded virulence factors like pyrogenic exotoxin C.
Conclusions:
- Prophage SF370.1 encodes lysogenic conversion genes, including pyrogenic exotoxin C, contributing to S. pyogenes pathogenicity.
- The integration of prophages into host genomes can lead to significant genomic alterations and influence bacterial evolution.
- The findings support a hypothesis of ongoing cooperation and evolutionary "arms race" between phage and host genomes.
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