PhagesDB

Last updated
Actinobacteriophage Database
FoundedApril 2010
Location
  • Pittsburgh Bacteriophage Institute at the University of Pittsburgh
Members
20,366 (as of 3/15/2022)
Key people
Dr. Graham Hatfull (HHMI Professor), Dan Russell (Webmaster), Debbie Jacobs-Sera (Phagehunting Program Coordinator), Dr. Welkin H. Pope (Research Assistant Professor), and Dr. Viknesh Sivanathan (HHMI Program Officer)
AffiliationsSEA-PHAGES (Science Education Alliance-Phage Hunters Advancing Genomics and Evolutionary Science)
Website phagesdb.org
Plaque exhibiting bacterial lawn with clearings made by Artharobacter phage GantcherGoblin. GantcherGoblin plaques JW.jpg
Plaque exhibiting bacterial lawn with clearings made by Artharobacter phage GantcherGoblin.

The Actinobacteriophage database, more commonly known as PhagesDB, is an interactive, comprehensive, database-backed website that collects and shares information related to the discovery, characterization and genomics of viruses that typically infect Actinobacterial hosts. It is used to compare these phages and their genomic annotations, allowing the research community to post new findings for analysis. The database provides information on more than 8,000 bacteriophages, as well as over 1,600 fully sequenced phages. [1]

Contents

Design and features

The creation of PhagesDB was carried out using Django, a server hosting environment. [2] PhagesDB has individual entries for each different virus in the database, along with a separate GeneMark page, allowing a user to cross reference the position of genomes to ensure accuracy of data. PhagesDB can be used on its own but is found to be more accurate when used in collaboration with another bio-informatics website like NCBI Blast. [3] The table below indicates the different types (by bacterial host genus) and numbers of phages sequenced:

Phage Types SequencedNumber Sequenced
Actinoplanes1
Arthrobacter240
Brevibacterium2
Corynebacterium12
Gordonia296
Kocuria4
Microbacterium98
Mycobacterium1590
Propionibacterium55
Rhodococcus53
Rothia1
Streptomyces167
Tetrasphaera1
Tsukamurella2

The user can view information on groups of phages in a variety of ways. [4] [5] PhagesDB has amino-acid level details about its phage genomes that are sequenced by integration with Phamerator. [6] [7]

Access and rights to data

Information published in this database can be freely viewed by anyone, and an Application Programming Interface (API) is available. [8] PhagesDB keeps some unpublished data that is not present in any medium, including newly performed genomic sequences. [9]

See also

References and Articles

  1. Russell DA, Hatfull GF, "PhagesDB: the actinobacteriophage database"
  2. "The Web framework for perfectionists with deadlines | Django". www.djangoproject.com. Retrieved 2018-04-11.
  3. Russell, Daniel A.; Hatfull, Graham F. (2017-03-01). "PhagesDB: the actinobacteriophage database". Bioinformatics. 33 (5): 784–786. doi:10.1093/bioinformatics/btw711. ISSN   1367-4803. PMC   5860397 . PMID   28365761.
  4. "The Actinobacteriophage Database". phagesdb.org. Retrieved 2018-04-11.
  5. "The Actinobacteriophage Database | Compare Phages". phagesdb.org. Retrieved 2018-04-11.
  6. "Phamerator". phamerator.org. Retrieved 2018-04-18.
  7. Cresawn, S.G. (2011). "Phamerator: a bioinformatic tool for comparative bacteriophage genomics". BMC Bioinform. 12: 395. doi: 10.1186/1471-2105-12-395 . PMC   3233612 . PMID   21991981.
  8. "Swagger UI". phagesdb.org. Retrieved 2018-04-16.
  9. "The Actinobacteriophage Database | Terms of Use". phagesdb.org. Retrieved 2018-04-16.

Related Research Articles

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<span class="mw-page-title-main">Prophage</span> Bacteriophage genome that is integrated into a bacterial cell

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<i>Escherichia virus T4</i> Species of bacteriophage

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The phi X 174 bacteriophage is a single-stranded DNA (ssDNA) virus that infects Escherichia coli. This virus was isolated in 1935 by Nicolas Bulgakov in Félix d'Hérelle's laboratory at the Pasteur Institute, from samples collected in Paris sewers. Its characterization and the study of its replication mechanism were carried out from the 1950s onwards. It was the first DNA-based genome to be sequenced. This work was completed by Fred Sanger and his team in 1977. In 1962, Walter Fiers and Robert Sinsheimer had already demonstrated the physical, covalently closed circularity of ΦX174 DNA. Nobel prize winner Arthur Kornberg used ΦX174 as a model to first prove that DNA synthesized in a test tube by purified enzymes could produce all the features of a natural virus, ushering in the age of synthetic biology. In 1972–1974, Jerard Hurwitz, Sue Wickner, and Reed Wickner with collaborators identified the genes required to produce the enzymes to catalyze conversion of the single stranded form of the virus to the double stranded replicative form. In 2003, it was reported by Craig Venter's group that the genome of ΦX174 was the first to be completely assembled in vitro from synthesized oligonucleotides. The ΦX174 virus particle has also been successfully assembled in vitro. In 2012, it was shown how its highly overlapping genome can be fully decompressed and still remain functional.

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<span class="mw-page-title-main">CrAssphage</span>

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