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Bacterial Artificial Chromosomes: A Functional Genomics Tool for the Study of Positive-strand RNA Viruses
Published on: December 29, 2015
Complete genome sequence of Cronobacter sakazakii bacteriophage vB_CsaM_GAP161
Reza Abbasifar1, Andrew M Kropinski, Parviz M Sabour
1Canadian Research Institute for Food Safety, University of Guelph, Guelph, Ontario, Canada.
Abstract:
Cronobacter sakazakii is an opportunistic pathogen that causes infant meningitis and is often associated with milk-based infant formula. We have fully sequenced the genome of a newly isolated lytic C. sakazakii myovirus, vB_CsaM_GAP161, briefly named GAP161. It consists of 178,193 bp and has a G+C content of 44.5%. A total of 277 genes, including 275 open reading frames and two tRNA-encoding genes, were identified. This phage is closely related to coliphages RB16 and RB43 and Klebsiella pneumoniae phage KP15.
Insights
We sequenced the genome of the Cronobacter sakazakii myovirus GAP161, a bacteriophage potentially useful for combating this pathogen. This research provides genomic insights into a phage targeting a bacterium linked to infant meningitis.
Area of Science:
- Microbiology
- Genomics
- Virology
Background:
- Cronobacter sakazakii is an opportunistic pathogen linked to infant meningitis, often associated with milk-based infant formula.
- Bacteriophages (phages) are viruses that infect bacteria and are being explored as therapeutic agents.
Purpose of the Study:
- To fully sequence the genome of a newly isolated lytic Cronobacter sakazakii myovirus, named vB_CsaM_GAP161 (GAP161).
- To provide genomic data for understanding phage-CRISPR interactions and potential phage therapy applications against Cronobacter sakazakii.
Main Methods:
- Whole-genome sequencing of the isolated bacteriophage GAP161.
- Bioinformatic analysis to identify genes, open reading frames (ORFs), and tRNA-encoding genes.
- Comparative genomics to determine phylogenetic relationships with other known phages.
Main Results:
- The complete genome of the C. sakazakii myovirus GAP161 was sequenced, measuring 178,193 base pairs with a G+C content of 44.5%.
- A total of 277 genes were identified, including 275 open reading frames and two tRNA-encoding genes.
- Phage GAP161 was found to be closely related to coliphages RB16 and RB43, and Klebsiella pneumoniae phage KP15.
Conclusions:
- The genomic characterization of C. sakazakii phage GAP161 provides a foundation for further research into its biological properties.
- This phage represents a potential candidate for phage therapy strategies aimed at controlling Cronobacter sakazakii infections, particularly in vulnerable infant populations.
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