2011
DOI: 10.1016/j.virusres.2010.11.012
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The genome sequence and proteome of bacteriophage ΦCPV1 virulent for Clostridium perfringens

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Cited by 27 publications
(23 citation statements)
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“…Five ORFs were identified as structural protein genes, encoding products for the major capsid (ORF-10), tail (ORF-13), connector (ORF-16), collar (ORF-17) and pre-neck appendage (ORF-21) proteins. All putative structural proteins had highest similarity with Clostridium phage UCPV1 [7], ranging from 51.0 to 62.8% amino acid similarity. The pre-neck appendage proteins of UCP24R and UCPV1 have low global alignment similarity to their closest BLASTp hit (Bacillus phage GA-1, accession NP_073695, 28.1%), but they share a common protein domain architecture (Pfam domain PF12708) with the pre-neck appendages of six other podoviruses, including Bacillus phage U29.…”
mentioning
confidence: 99%
“…Five ORFs were identified as structural protein genes, encoding products for the major capsid (ORF-10), tail (ORF-13), connector (ORF-16), collar (ORF-17) and pre-neck appendage (ORF-21) proteins. All putative structural proteins had highest similarity with Clostridium phage UCPV1 [7], ranging from 51.0 to 62.8% amino acid similarity. The pre-neck appendage proteins of UCP24R and UCPV1 have low global alignment similarity to their closest BLASTp hit (Bacillus phage GA-1, accession NP_073695, 28.1%), but they share a common protein domain architecture (Pfam domain PF12708) with the pre-neck appendages of six other podoviruses, including Bacillus phage U29.…”
mentioning
confidence: 99%
“…A virulent short-tailed bacteriophage ΦCPV1 was isolated in the Russian Federation utilizing C. perfringens as the host and was classified in the family Podoviridae (Volozhantsev et al, 2011). The purified virus had an icosahedral head and collar of approximately 42 and 23 nm in diameter, respectively, with a structurally complex tail of 37 nm lengthwise and a basal plate of 30 nm (Figure 1C).…”
Section: Resultsmentioning
confidence: 99%
“…Additionally, the viruses were purified by isopycnic centrifugation and analyzed by SDS-PAGE followed by mass spectrometry of the proteins. Subsequent identification of the phage genomic open reading frame ( ORF ) descriptive bacteriophage structure and identification of potential lytic proteins was completed by full-genome nucleotide sequencing, genome annotations, and BLAST analyses as described in detail by the investigators (Seal et al, 2011; Oakley et al, 2011; Volozhantsev et al, 2011, 2012; Morales et al, 2012). Recombinant proteins were produced by cloning bacteriophage genes encoding putative lysins such as N -acetylmuramoyl-l-alanine amidases and expression in E. coli (Simmons et al, 2010, 2012).…”
Section: Methodsmentioning
confidence: 99%
“…5). Host specificity has routinely been observed relative to the bacteriophages isolated from various C. perfringens isolates that is most likely due to evolution of the receptor and anti-receptor molecules Volozhantsev et al, 2011;Oakley et al, 2011). Therefore, selection of appropriate 'bacteriophage cocktails' may not necessarily be effective against many of the various bacterial isolates that exist in the environment and cause disease.…”
Section: Discussionmentioning
confidence: 99%
“…The major tail protein represented approximately 12.7% of the total protein, with an apparent size of 27 kDa while a minor structural protein composing 2.1% of the virion protein was reported with a predicted size of 55.1kD. More recently the proteins of virulent bacteriophages infecting C. perfringens have been described in detail Volozhantsev et al, 2011). From the siphoviruses , four principle virion protein regions were identified (Fig.…”
Section: Characteristics Of Clostridium Perfringens Bacteriophage Andmentioning
confidence: 99%