2008
DOI: 10.1111/j.1365-2672.2007.03704.x
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Characterization of the rrn operons in the channel catfish pathogen Edwardsiella ictaluri

Abstract: Aims:  To advance diagnostics and phylogenetics of Edwardsiella ictaluri by sequencing and characterizing its rrn operons. Methods and results:  The Edw. ictaluri rrn operons were identified from a 5–7 kbp insert lambda library and from Edw. ictaluri fosmid clones. We present the complete sequences and analysis of all eight Edw. ictaluri rrn operons and unique regions located upstream and downstream. Two rrn operons were located in tandem with 169 bp separating them, which is apparently a conserved feature bet… Show more

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Cited by 8 publications
(11 citation statements)
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References 29 publications
(46 reference statements)
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“…The chromosome is predicted to distinctly harbor 8 rRNA operons, 95 tRNA genes, and 8 stable noncoding RNAs, relatively higher than that of other sequenced enterobacteria (Table S1) and in consistent with the rapid growth of the bacterium [12]. The eight rRNA operons, among which one operon contains a duplication in 5S rRNA gene, are scattered in the circular genome except for two locating in tandem as previously reported [13] (Figure 1). In addition to 77 pseudogenes (including 32 phage and 31 transposase genes), 3,486 coding sequences (CDSs) with an average length of 906 bp were encoded in the chromosome, representing 83.9% of the genome.…”
Section: Resultssupporting
confidence: 78%
“…The chromosome is predicted to distinctly harbor 8 rRNA operons, 95 tRNA genes, and 8 stable noncoding RNAs, relatively higher than that of other sequenced enterobacteria (Table S1) and in consistent with the rapid growth of the bacterium [12]. The eight rRNA operons, among which one operon contains a duplication in 5S rRNA gene, are scattered in the circular genome except for two locating in tandem as previously reported [13] (Figure 1). In addition to 77 pseudogenes (including 32 phage and 31 transposase genes), 3,486 coding sequences (CDSs) with an average length of 906 bp were encoded in the chromosome, representing 83.9% of the genome.…”
Section: Resultssupporting
confidence: 78%
“…The 16S rRNA gene copy numbers for the rest of type strains were determined via pulse-field gel electrophoresis (PFGE) as described by Williams [64].…”
Section: Methodsmentioning
confidence: 99%
“…The DNA sequence flanking each transposon insertion site was identified by single primer PCR and sequencing as described by Karlyshev et al (2000) and modified by Karsi et al (2009). Sequences were identified by BLAST search against the E. ictaluri genome (GenBank #CP001600) (Williams et al, 2008). Predicted protein sequences from the identified E. ictaluri genes were compared to the closest matching protein sequences from the nonredundant protein database at NCBI using the Cluster-V method.…”
Section: Mutant Identificationsmentioning
confidence: 99%