Comparative genomic analysis of bacteriophages specific to the channel catfish pathogen Edwardsiella ictaluri
被引:27
|
作者:
Carrias, Abel
论文数: 0引用数: 0
h-index: 0
机构:
Auburn Univ, Dept Fisheries & Allied Aquaculture, Auburn, AL 36849 USAAuburn Univ, Dept Biol Sci, Auburn, AL 36849 USA
Carrias, Abel
[5
]
Welch, Timothy J.
论文数: 0引用数: 0
h-index: 0
机构:
ARS, Natl Ctr Cool & Cold Water Aquaculture, USDA, Kearneysville, WV 25430 USAAuburn Univ, Dept Biol Sci, Auburn, AL 36849 USA
Welch, Timothy J.
[4
]
Waldbieser, Geoffrey C.
论文数: 0引用数: 0
h-index: 0
机构:
ARS, USDA, Catfish Genet Res Unit, Thad Cochran Natl Warm Water Aquaculture Ctr, Stoneville, MS USAAuburn Univ, Dept Biol Sci, Auburn, AL 36849 USA
Waldbieser, Geoffrey C.
[3
]
Mead, David A.
论文数: 0引用数: 0
h-index: 0
机构:
Lucigen Corp, Middleton, WI USAAuburn Univ, Dept Biol Sci, Auburn, AL 36849 USA
Mead, David A.
[2
]
Terhune, Jeffery S.
论文数: 0引用数: 0
h-index: 0
机构:
Auburn Univ, Dept Fisheries & Allied Aquaculture, Auburn, AL 36849 USAAuburn Univ, Dept Biol Sci, Auburn, AL 36849 USA
Terhune, Jeffery S.
[5
]
Liles, Mark R.
论文数: 0引用数: 0
h-index: 0
机构:
Auburn Univ, Dept Biol Sci, Auburn, AL 36849 USAAuburn Univ, Dept Biol Sci, Auburn, AL 36849 USA
Liles, Mark R.
[1
]
机构:
[1] Auburn Univ, Dept Biol Sci, Auburn, AL 36849 USA
[2] Lucigen Corp, Middleton, WI USA
[3] ARS, USDA, Catfish Genet Res Unit, Thad Cochran Natl Warm Water Aquaculture Ctr, Stoneville, MS USA
[4] ARS, Natl Ctr Cool & Cold Water Aquaculture, USDA, Kearneysville, WV 25430 USA
[5] Auburn Univ, Dept Fisheries & Allied Aquaculture, Auburn, AL 36849 USA
Background: The bacterial pathogen Edwardsiella ictaluri is a primary cause of mortality in channel catfish raised commercially in aquaculture farms. Additional treatment and diagnostic regimes are needed for this enteric pathogen, motivating the discovery and characterization of bacteriophages specific to E. ictaluri. Results: The genomes of three Edwardsiella ictaluri- specific bacteriophages isolated from geographically distant aquaculture ponds, at different times, were sequenced and analyzed. The genomes for phages eiAU, eiDWF, and eiMSLS are 42.80 kbp, 42.12 kbp, and 42.69 kbp, respectively, and are greater than 95% identical to each other at the nucleotide level. Nucleotide differences were mostly observed in non-coding regions and in structural proteins, with significant variability in the sequences of putative tail fiber proteins. The genome organization of these phages exhibit a pattern shared by other Siphoviridae. Conclusions: These E. ictaluri-specific phage genomes reveal considerable conservation of genomic architecture and sequence identity, even with considerable temporal and spatial divergence in their isolation. Their genomic homogeneity is similarly observed among E. ictaluri bacterial isolates. The genomic analysis of these phages supports the conclusion that these are virulent phages, lacking the capacity for lysogeny or expression of virulence genes. This study contributes to our knowledge of phage genomic diversity and facilitates studies on the diagnostic and therapeutic applications of these phages.