Development of giant bacteriophage ÏKZ is independent of the host transcription apparatus.
J Virol
; 88(18): 10501-10, 2014 Sep.
Article
em En
| MEDLINE
| ID: mdl-24965474
ABSTRACT
UNLABELLED Pseudomonas aeruginosa bacteriophage ÏKZ is the type representative of the giant phage genus, which is characterized by unusually large virions and genomes. By unraveling the transcriptional map of the â¼ 280-kb ÏKZ genome to single-nucleotide resolution, we combine 369 ÏKZ genes into 134 operons. Early transcription is initiated from highly conserved AT-rich promoters distributed across the ÏKZ genome and located on the same strand of the genome. Early transcription does not require phage or host protein synthesis. Transcription of middle and late genes is dependent on protein synthesis and mediated by poorly conserved middle and late promoters. Unique to ÏKZ is its ability to complete its infection in the absence of bacterial RNA polymerase (RNAP) enzyme activity. We propose that transcription of the ÏKZ genome is performed by the consecutive action of two ÏKZ-encoded, noncanonical multisubunit RNAPs, one of which is packed within the virion, another being the product of early genes. This unique, rifampin-resistant transcriptional machinery is conserved within the diverse giant phage genus. IMPORTANCE The data presented in this paper offer, for the first time, insight into the complex transcriptional scheme of giant bacteriophages. We show that Pseudomonas aeruginosa giant phage ÏKZ is able to infect and lyse its host cell and produce phage progeny in the absence of functional bacterial transcriptional machinery. This unique property can be attributed to two phage-encoded putative RNAP enzymes, which contain very distant homologues of bacterial ß and ß'-like RNAP subunits.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Pseudomonas aeruginosa
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Proteínas de Bactérias
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Bacteriófagos
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RNA Polimerases Dirigidas por DNA
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Regulação Viral da Expressão Gênica
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Fagos de Pseudomonas
Idioma:
En
Revista:
J Virol
Ano de publicação:
2014
Tipo de documento:
Article
País de afiliação:
Bélgica