ArticleApplied and environmental microbiology2012
Characterization of the ELPhiS prophage from Salmonella enterica serovar Enteritidis strain LK5.
Article in Applied and environmental microbiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.
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Who cites it
20 citing papers in PubMed, 24 citations in OpenAlex.
- Knowing and Naming: Phage Annotation and Nomenclature for Phage Therapy.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2023Review
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- Computational Prediction of Bacteriophage Host Ranges.Microorganisms · 2022Review
- Genomic and functional characterization of five novel Salmonella-targeting bacteriophages.Virology journal · 2021Article
- Analysis of Yersinia pseudotuberculosis Isolates Recovered from Deceased Mammals of a German Zoo Animal Collection.Journal of clinical microbiology · 2021Article
- Stepwise evolution of Salmonella Typhimurium ST313 causing bloodstream infection in Africa.Nature microbiology · 2021Article
- Review
- Comparative genomics identifies distinct lineages of S. Enteritidis from Queensland, Australia.PloS one · 2018Article
- Complete Genome Sequence of Salmonella enterica Serovar Typhimurium Strain SO3 (Sequence Type 302) Isolated from a Baby with Meningitis in Mexico.Genome announcements · 2016Article
- Complete Genome Sequence of Salmonella enterica Serovar Typhimurium Strain SO2 (Sequence Type 302) Isolated from an Asymptomatic Child in Mexico.Genome announcements · 2016Article
- Computational approaches to predict bacteriophage-host relationships.FEMS microbiology reviews · 2016Review
- Whole genome sequencing provides possible explanations for the difference in phage susceptibility among two Salmonella Typhimurium phage types (DT8 and DT30) associated with a single foodborne outbreak.BMC research notes · 2015Article
- Identification of three extra-chromosomal replicons in Leptospira pathogenic strain and development of new shuttle vectors.BMC genomics · 2015Article
- Genomic Comparison of the Closely-Related Salmonella enterica Serovars Enteritidis, Dublin and Gallinarum.PloS one · 2015Article
- High resolution assembly and characterization of genomes of Canadian isolates of Salmonella Enteritidis.BMC genomics · 2014Article
- Rapid whole-genome sequencing for surveillance of Salmonella enterica serovar enteritidis.Emerging infectious diseases · 2014Article
- Genome Sequence of Salmonella enterica subsp. enterica Strain Durban.Genome announcements · 2014Article
- Microbes, metagenomes and marine mammals: enabling the next generation of scientist to enter the genomic era.BMC genomics · 2013Article
- On the evolutionary history, population genetics and diversity among isolates of Salmonella Enteritidis PFGE pattern JEGX01.0004.PloS one · 2013Article
- PhiSpy: a novel algorithm for finding prophages in bacterial genomes that combines similarity- and composition-based strategies.Nucleic acids research · 2012Article
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Authors and funding
5 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Phages are a primary driving force behind the evolution of bacterial pathogens by transferring a variety of virulence genes into their hosts. Similar to other bacterial genomes, the Salmonella enterica serovar Enteritidis LK5 genome contains several regions that are homologous to phages. Although genomic analysis demonstrated the presence of prophages, it was unable to confirm which phage elements within the genome were viable. Genetic markers were used to tag one of the prophages in the genome to allow monitoring of phage induction. Commonly used laboratory strains of Salmonella were resistant to phage infection, and therefore a rapid screen was developed to identify susceptible hosts. This approach showed that a genetically tagged prophage, ELPhiS (Enteritidis lysogenic phage S), was capable of infecting Salmonella serovars that are diverse in host range and virulence and has the potential to laterally transfer genes between these serovars via lysogenic conversion. The rapid screen approach is adaptable to any system with a large collection of isolates and may be used to test the viability of prophages found by sequencing the genomes of various bacterial pathogens.
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