2020
DOI: 10.1128/mra.01133-20
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Complete Genome Sequences of Two Vibrio natriegens Bacteriophages

Abstract: Vibrio natriegens, a fast-growing Gram-negative bacterium, is gaining interest as a platform for rapid biotechnology applications and metabolic engineering. Only a few bacteriophages that infect this bacterium have been identified. Here, we describe the isolation and characterization of two V. natriegens bacteriophages isolated from Hatches Creek, Wellfleet, Massachusetts.

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Cited by 3 publications
(2 citation statements)
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“…Interestingly, these bacteriophages give efficacious results in controlling the infections caused by Vibrio , suggesting that phagevB_VpS_PG28 may prove a biological control agent. Complex evolutionary relationships can be predicted between these two phages as both phages were isolated from different territories of the world [ 40 ].…”
Section: Resultsmentioning
confidence: 99%
“…Interestingly, these bacteriophages give efficacious results in controlling the infections caused by Vibrio , suggesting that phagevB_VpS_PG28 may prove a biological control agent. Complex evolutionary relationships can be predicted between these two phages as both phages were isolated from different territories of the world [ 40 ].…”
Section: Resultsmentioning
confidence: 99%
“…The functions of most open reading frames (ORFs) in phage genome sequences in the GenBank database are currently unknown ( 7 ). Limited by gene editing technology and other factors, the genomes of approximately 66 Vibrio phages have been sequenced, but most research on functional genomics has stagnated at homology comparisons, causing studies on the functional genomics of Vibrio phages to lag behind the discovery of new phages and the sequencing of their genomes ( 8 10 ). At present, phage genome editing strategies can be classified into four categories: in vitro oligonucleotide (oligo) splicing, homologous recombination-mediated in vivo PCR DNA fragment splicing, endogenous and exogenous homologous recombination system-mediated editing, and jointly mediated editing by clustered regularly interspaced short palindromic repeat/CRISPR-associated gene (CRISPR–Cas) systems and homologous recombination.…”
Section: Introductionmentioning
confidence: 99%