期刊论文详细信息
Virology Journal
Characterization of a ViI-like Phage Specific to Escherichia coli O157:H7
Andrew D Brabban5  Todd Callaway7  Hany Anany1,10  Derek Pickard9  Ana L Toribio9  Hans-Wolfgang Ackermann1  Andre Villegas6  Andrew M Kropinski2  Daniel Bryan5  Anna Castano8  Ayman El-Shibiny3  Bob Blasdel4  Kyobi Skutt-Kakaria5  Elizabeth M Kutter5 
[1] Department of Microbiology, Faculty of Medicine, Laval University, Quebec, QC, Canada;Department of Molecular & Cellular Biology, University of Guelph, ON, Canada;Faculty of Environmental Agricultural Sciences, Suez Canal University, Egypt;Department of Microbiology, The Ohio State University, Columbus, OH;The Evergreen State College, Olympia, WA, USA;Laboratory for Foodborne Zoonoses, Public Health Agency of Canada, Guelph, ON, Canada;USDA Agricultural Station, College Station, TX, USA;Department of Pediatric Neurology, University of Colorado Children's Hospital, Denver, CO;The Wellcome Trust Sanger Institute, Genome Campus, Hinxton, England, UK;Microbiology Department, Ain Shams University, Cairo, Egypt
关键词: T4 core genes;    tail spike;    O157 antigen;    Vi antigen;    bioinformatics;    proteome;    genome;    phage ecology;    phage evolution;    hydroxymethyluracil;    E. coli O157:H7;   
Others  :  1156137
DOI  :  10.1186/1743-422X-8-430
 received in 2011-08-04, accepted in 2011-09-07,  发布年份 2011
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【 摘 要 】

Phage vB_EcoM_CBA120 (CBA120), isolated against Escherichia coli O157:H7 from a cattle feedlot, is morphologically very similar to the classic phage ViI of Salmonella enterica serovar Typhi. Until recently, little was known genetically or physiologically about the ViI-like phages, and none targeting E. coli have been described in the literature. The genome of CBA120 has been fully sequenced and is highly similar to those of both ViI and the Shigella phage AG3. The core set of structural and replication-related proteins of CBA120 are homologous to those from T-even phages, but generally are more closely related to those from T4-like phages of Vibrio, Aeromonas and cyanobacteria than those of the Enterobacteriaceae. The baseplate and method of adhesion to the host are, however, very different from those of either T4 or the cyanophages. None of the outer baseplate proteins are conserved. Instead of T4's long and short tail fibers, CBA120, like ViI, encodes tail spikes related to those normally seen on podoviruses. The 158 kb genome, like that of T4, is circularly permuted and terminally redundant, but unlike T4 CBA120 does not substitute hmdCyt for cytosine in its DNA. However, in contrast to other coliphages, CBA120 and related coliphages we have isolated cannot incorporate 3H-thymidine (3H-dThd) into their DNA. Protein sequence comparisons cluster the putative "thymidylate synthase" of CBA120, ViI and AG3 much more closely with those of Delftia phage φW-14, Bacillus subtilis phage SPO1, and Pseudomonas phage YuA, all known to produce and incorporate hydroxymethyluracil (hmdUra).

【 授权许可】

   
2011 Kutter et al; licensee BioMed Central Ltd.

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