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1.
Viruses ; 10(8)2018 07 26.
Article in English | MEDLINE | ID: mdl-30050020

ABSTRACT

Pectobacterium atrosepticum is a phytopathogen of economic importance as it is the causative agent of potato blackleg and soft rot. Here we describe the Pectobacterium phage vB_PatP_CB5 (abbreviated as CB5), which specifically infects the bacterium. The bacteriophage is characterized in detail and TEM micrographs indicate that it belongs to the Podoviridae family. CB5 shares significant pairwise nucleotide identity (≥80%) with P. atrosepticum phages φM1, Peat1, and PP90 and also shares common genome organization. Phylograms constructed using conserved proteins and whole-genome comparison-based amino acid sequences show that these phages form a distinct clade within the Autographivirinae. They also possess conserved RNA polymerase recognition and specificity loop sequences. Their lysis cassette resembles that of KP34virus, containing in sequential order a U-spanin, a holin, and a signal⁻arrest⁻release (SAR) endolysin. However, they share low pairwise nucleotide identity with the type phage of the KP34virus genus, Klebsiella phage KP34. In addition, phage KP34 does not possess several conserved proteins associated with these P. atrosepticum phages. As such, we propose the allocation of phages CB5, Peat1, φM1, and PP90 to a separate new genus designated Phimunavirus.


Subject(s)
Genome, Viral , Pectobacterium/virology , Phylogeny , Podoviridae/classification , DNA, Viral/genetics , Microscopy, Electron, Transmission , Podoviridae/isolation & purification , Podoviridae/ultrastructure , Sequence Analysis, DNA , Solanum tuberosum/microbiology
2.
Virology ; 443(2): 187-96, 2013 Sep 01.
Article in English | MEDLINE | ID: mdl-23755967

ABSTRACT

Phage therapy has a long tradition in Eastern Europe, where preparations are comprised of complex phage cocktails whose compositions have not been described. We investigated the composition of a phage cocktail from the Russian pharmaceutical company Microgen targeting Escherichia coli/Proteus infections. Electron microscopy identified six phage types, with numerically T7-like phages dominating over T4-like phages. A metagenomic approach using taxonomical classification, reference mapping and de novo assembly identified 18 distinct phage types, including 7 genera of Podoviridae, 2 established and 2 proposed genera of Myoviridae, and 2 genera of Siphoviridae. De novo assembly yielded 7 contigs greater than 30 kb, including a 147-kb Myovirus genome and a 42-kb genome of a potentially new phage. Bioinformatic analysis did not reveal undesired genes and a small human volunteer trial did not associate adverse effects with oral phage exposure.


Subject(s)
Bacteriophages , Biological Therapy/adverse effects , Biological Therapy/methods , Escherichia coli Infections/therapy , Metagenomics/methods , Proteus Infections/therapy , Administration, Oral , Bacteriophages/classification , Bacteriophages/genetics , Bacteriophages/ultrastructure , Gram-Negative Bacteria/classification , Gram-Negative Bacteria/virology , Humans , Microscopy, Electron, Transmission , Myoviridae/classification , Myoviridae/genetics , Myoviridae/ultrastructure , Podoviridae/classification , Podoviridae/genetics , Podoviridae/ultrastructure , Russia , Siphoviridae/classification , Siphoviridae/genetics , Siphoviridae/ultrastructure , Treatment Outcome
3.
Curr Microbiol ; 61(4): 315-21, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20204638

ABSTRACT

Four phages infectious to Mesorhizobium strains were identified in soil samples taken from local Robinia pseudoacacia stands. Based on their polyhedral heads and short noncontractile tails, three of the phages, Mlo30, Mam12, and Mam20, were assigned to group C of Bradley's classification, the Podoviridae family, while phage Mlo1, with its elongated hexagonal head and a long flexible tail represented subgroup B2 bacteriophages, the Siphoviridae family. The phages were homogeneous in respect of their virulence, as they only lysed Mesorhizobium strains, but did not affect strains of Rhizobium or Bradyrhizobium. On the basis of one-step growth experiments, the average virus yield was calculated as approximately 10-25 phage particles for phages Mlo30, Mam12 and Mam20, and as many as 100-120 for phage Mlo1. The rate of phage adsorption to heat-treated cells showed differences in the nature of their receptors, which seemed to be thermal sensitive, thermal resistant, or a combination of the two. Only the receptor for phage Mlo30 was likely to be an LPS molecule, which was supported by a neutralization test. The smooth LPS with O-antigenic chains of the phage-sensitive M. loti strain completely reduced the bactericidal activity of virions at a concentration of 1 µg/ml. The molecular weights of phage DNAs estimated from restriction endonuclease cleavage patterns were in the range from approximately 39 kb for group C phages to approximately 80 kb for B2.


Subject(s)
Alphaproteobacteria/virology , Bacteriophages/physiology , Bacteriophages/ultrastructure , DNA, Viral/analysis , Rhizosphere , Robinia/microbiology , Adsorption , Alphaproteobacteria/physiology , Bacteriophages/classification , Bacteriophages/isolation & purification , Bradyrhizobium/physiology , Bradyrhizobium/virology , Cloning, Molecular , Microscopy, Electron , Nitrogen Fixation , Podoviridae/classification , Podoviridae/isolation & purification , Podoviridae/physiology , Podoviridae/ultrastructure , Rhizobium/physiology , Rhizobium/virology , Siphoviridae/classification , Siphoviridae/isolation & purification , Siphoviridae/physiology , Siphoviridae/ultrastructure , Soil , Soil Microbiology , Symbiosis , Virion/ultrastructure , Virus Attachment
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