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PAIDB V2.0: Exploration and Analysis of Pathogenicity and Resistance Islands

Overview
Specialty Biochemistry
Date 2014 Oct 23
PMID 25336619
Citations 70
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Abstract

Pathogenicity is a complex multifactorial process confounded by the concerted activity of genetic regions associated with virulence and/or resistance determinants. Pathogenicity islands (PAIs) and resistance islands (REIs) are key to the evolution of pathogens and appear to play complimentary roles in the process of bacterial infection. While PAIs promote disease development, REIs give a fitness advantage to the host against multiple antimicrobial agents. The Pathogenicity Island Database (PAIDB, http://www.paidb.re.kr) has been the only database dedicated to providing comprehensive information on all reported PAIs and candidate PAIs in prokaryotic genomes. In this study, we present PAIDB v2.0, whose functionality is extended to incorporate REIs. PAIDB v2.0 contains 223 types of PAIs with 1331 accessions, and 88 types of REIs with 108 accessions. With an improved detection scheme, 2673 prokaryotic genomes were analyzed to locate candidate PAIs and REIs. With additional quantitative and qualitative advancements in database content and detection accuracy, PAIDB will continue to facilitate pathogenomic studies of both pathogenic and non-pathogenic organisms.

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References
1.
McArthur A, Waglechner N, Nizam F, Yan A, Azad M, Baylay A . The comprehensive antibiotic resistance database. Antimicrob Agents Chemother. 2013; 57(7):3348-57. PMC: 3697360. DOI: 10.1128/AAC.00419-13. View

2.
Hsiao W, Wan I, Jones S, Brinkman F . IslandPath: aiding detection of genomic islands in prokaryotes. Bioinformatics. 2003; 19(3):418-20. DOI: 10.1093/bioinformatics/btg004. View

3.
Miriagou V, Carattoli A, Fanning S . Antimicrobial resistance islands: resistance gene clusters in Salmonella chromosome and plasmids. Microbes Infect. 2006; 8(7):1923-30. DOI: 10.1016/j.micinf.2005.12.027. View

4.
Yoon S, Reiss D, Bare J, Tenenbaum D, Pan M, Slagel J . Parallel evolution of transcriptome architecture during genome reorganization. Genome Res. 2011; 21(11):1892-904. PMC: 3205574. DOI: 10.1101/gr.122218.111. View

5.
Boyd D, Peters G, Cloeckaert A, Boumedine K, Chaslus-Dancla E, Imberechts H . Complete nucleotide sequence of a 43-kilobase genomic island associated with the multidrug resistance region of Salmonella enterica serovar Typhimurium DT104 and its identification in phage type DT120 and serovar Agona. J Bacteriol. 2001; 183(19):5725-32. PMC: 95465. DOI: 10.1128/JB.183.19.5725-5732.2001. View