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3 "Siphoviridae"
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Genotyping, Morphology and Molecular Characteristics of a Lytic Phage of Neisseria Strain Obtained from Infected Human Dental Plaque
Ahmed N Aljarbou , Mohamad Aljofan
J. Microbiol. 2014;52(7):609-618.   Published online May 30, 2014
DOI: https://doi.org/10.1007/s12275-014-3380-1
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AbstractAbstract
The lytic bacteriaphage (phage) A2 was isolated from human dental plaques along with its bacterial host. The virus was found to have an icosahedron-shaped head (60±3 nm), a sheathed and rigid long tail (~175 nm) and was categorized into the family Siphoviridae of the order Caudovirales, which are dsDNA viral family, characterised by their ability to infect bacteria and are nonenveloped with a noncontractile tail. The isolated phage contained a linear dsDNA genome having 31,703 base pairs of unique sequence, which were sorted into three contigs and 12 single sequences. A latent period of 25 minutes and burst size of 24±2 particles was determined for the virus. Bioinformatics approaches were used to identify ORFs in the genome. A phylogenetic analysis confirmed the species inter-relationship and its placement in the family.

Citations

Citations to this article as recorded by  
  • The potential for bacteriophages and prophage elements in fighting and preventing the gonorrhea
    Monika Adamczyk-Popławska, Piotr Golec, Andrzej Piekarowicz, Agnieszka Kwiatek
    Critical Reviews in Microbiology.2024; 50(5): 769.     CrossRef
  • Periodontitis: etiology, conventional treatments, and emerging bacteriophage and predatory bacteria therapies
    Anna Łasica, Piotr Golec, Agnieszka Laskus, Magdalena Zalewska, Magdalena Gędaj, Magdalena Popowska
    Frontiers in Microbiology.2024;[Epub]     CrossRef
  • Screening of Anorectal and Oropharyngeal Samples Fails to Detect Bacteriophages Infecting Neisseria gonorrhoeae
    Jolein Gyonne Elise Laumen, Saïd Abdellati, Sheeba Santhini Manoharan-Basil, Christophe Van Dijck, Dorien Van den Bossche, Irith De Baetselier, Tessa de Block, Surbhi Malhotra-Kumar, Patrick Soentjes, Jean-Paul Pirnay, Chris Kenyon, Maia Merabishvili
    Antibiotics.2022; 11(2): 268.     CrossRef
  • A novel phage from periodontal pockets associated with chronic periodontitis
    Yu Zhang, Tong-Ling Shan, Fei Li, Tian Yu, Xi Chen, Xu-Tao Deng, Eric Delwart, Xi-Ping Feng
    Virus Genes.2019; 55(3): 381.     CrossRef
  • Identification of Novel Bacteriophages with Therapeutic Potential That Target Enterococcus faecalis
    M. Al-Zubidi, M. Widziolek, E. K. Court, A. F. Gains, R. E. Smith, K. Ansbro, A. Alrafaie, C. Evans, C. Murdoch, S. Mesnage, C. W. I. Douglas, A. Rawlinson, G. P. Stafford, Marvin Whiteley
    Infection and Immunity.2019;[Epub]     CrossRef
  • Ecology of the Oral Microbiome: Beyond Bacteria
    Jonathon L. Baker, Batbileg Bor, Melissa Agnello, Wenyuan Shi, Xuesong He
    Trends in Microbiology.2017; 25(5): 362.     CrossRef
  • The use of bacteriophages to biocontrol oral biofilms
    Szymon P. Szafrański, Andreas Winkel, Meike Stiesch
    Journal of Biotechnology.2017; 250: 29.     CrossRef
Superinfection Exclusion Reveals Heteroimmunity between Pseudomonas aeruginosa Temperate Phages
In-Young Chung , Hee-Won Bae , Hye-Jung Jang , Bi-o Kim , You-Hee Cho
J. Microbiol. 2014;52(6):515-520.   Published online May 29, 2014
DOI: https://doi.org/10.1007/s12275-014-4012-5
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AbstractAbstract
Temperate siphophages (MP29, MP42, and MP48) were isolated from the culture supernatant of clinical Pseudomonas aeruginosa isolates. The complete nucleotide sequences and annotation of the phage genomes revealed the overall synteny to the known temperate P. aeruginosa phages such as MP22, D3112, and DMS3. Genome-level sequence analysis showed the conservation of both ends of the linear genome and the divergence at the previously identified dissimilarity regions (R1 to R9). Protein sequence alignment of the c repressor (ORF1) of each phage enabled us to divide the six phages into two groups: D3112 group (D3112, MP29, MP42, and MP48) and MP22 group (MP22 and DMS3). Superinfection exclusion was observed between the phages belonging to the same group, which was mediated by the specific interaction between the c repressor and the cognate operator. Based on these, we suggest that the temperate siphophages prevalent in the clinical strains of P. aeruginosa represent at least two distinct heteroimmunity groups.

Citations

Citations to this article as recorded by  
  • Phage against the Machine: The SIE-ence of Superinfection Exclusion
    Michael J. Bucher, Daniel M. Czyż
    Viruses.2024; 16(9): 1348.     CrossRef
  • Transposition Behavior Revealed by High-Resolution Description of Pseudomonas Aeruginosa Saltovirus Integration Sites
    Gilles Vergnaud, Cédric Midoux, Yann Blouin, Maria Bourkaltseva, Victor Krylov, Christine Pourcel
    Viruses.2018; 10(5): 245.     CrossRef
  • Evolutionary Ecology of Prokaryotic Immune Mechanisms
    Stineke van Houte, Angus Buckling, Edze R. Westra
    Microbiology and Molecular Biology Reviews.2016; 80(3): 745.     CrossRef
  • A phage protein that inhibits the bacterial ATPase required for type IV pilus assembly
    In-Young Chung, Hye-Jeong Jang, Hee-Won Bae, You-Hee Cho
    Proceedings of the National Academy of Sciences.2014; 111(31): 11503.     CrossRef
Comparative Genomic Analysis of Bacteriophage EP23 Infecting Shigella sonnei and Escherichia coli
Ho-Won Chang , Kyoung-Ho Kim
J. Microbiol. 2011;49(6):927-934.   Published online December 28, 2011
DOI: https://doi.org/10.1007/s12275-011-1577-0
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AbstractAbstract
Bacteriophage EP23 that infects Escherichia coli and Shigella sonnei was isolated and characterized. The bacteriophage morphology was similar to members of the family Siphoviridae. The 44,077 bp genome was fully sequenced using 454 pyrosequencing. Comparative genomic and phylogenetic analyses showed that EP23 was most closely related to phage SO-1, which infects Sodalis glossinidius and phage SSL-2009a, which infects engineered E. coli. Genomic comparison indicated that EP23 and SO-1 were very similar with each other in terms of gene order and amino acid similarity, even though their hosts were separated in the level of genus. EP23 and SSL-2009a displayed high amino acid similarity between their genes, but there was evidence of several recombination events in SSL-2009a. The results of the comparative genomic analyses further the understanding of the evolution and relationship between EP23 and its bacteriophage relatives.

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