ArticlePloS one2008
Secondary chromosomal attachment site and tandem integration of the mobilizable Salmonella genomic island 1.
Article in PloS one, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.
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Who cites it
18 citing papers in PubMed.
- Investigation of class 1 integrons and virulence genes in the emergent Salmonella serovar Infantis in Turkey.International microbiology : the official journal of the Spanish Society for Microbiology · 2022Article
- Overview ofFrontiers in microbiology · 2022Article
- Genomic islands targeting dusA in Vibrio species are distantly related to Salmonella Genomic Island 1 and mobilizable by IncC conjugative plasmids.PLoS genetics · 2021Article
- "Does the Salmonella Genomic Island 1 (SGI1) confer invasiveness properties to human isolates?"BMC infectious diseases · 2017Article
- Review
- The master regulator of IncA/C plasmids is recognized by the Salmonella Genomic island SGI1 as a signal for excision and conjugal transfer.Nucleic acids research · 2015Article
- Early strains of multidrug-resistant Salmonella enterica serovar Kentucky sequence type 198 from Southeast Asia harbor Salmonella genomic island 1-J variants with a novel insertion sequence.Antimicrobial agents and chemotherapy · 2012Article
- High-density transcriptional initiation signals underline genomic islands in bacteria.PloS one · 2012Article
- Article
- Promoter strength driving TetR determines the regulatory properties of Tet-controlled expression systems.PloS one · 2012Article
- Junker: an intergenic explorer for bacterial genomes.Genomics, proteomics & bioinformatics · 2011Article
- Antimicrobial resistance and virulence determinants in European Salmonella genomic island 1-positive Salmonella enterica isolates from different origins.Applied and environmental microbiology · 2011Article
- The Salmonella genomic island 1 is specifically mobilized in trans by the IncA/C multidrug resistance plasmid family.PloS one · 2010Article
- Units of plasticity in bacterial genomes: new insight from the comparative genomics of two bacteria interacting with invertebrates, Photorhabdus and Xenorhabdus.BMC genomics · 2010Article
- Novel IS711-specific chromosomal locations useful for identification and classification of marine mammal Brucella strains.Journal of clinical microbiology · 2010Article
- Spontaneous excision of the Salmonella enterica serovar Enteritidis-specific defective prophage-like element phiSE14.Journal of bacteriology · 2010Article
- Truncated tni module adjacent to the complex integron of salmonella genomic island 1 in Salmonella enterica serovar Virchow.Antimicrobial agents and chemotherapy · 2009Article
- Article
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundThe Salmonella genomic island 1 is an integrative mobilizable element (IME) originally identified in epidemic multidrug-resistant Salmonella enterica serovar Typhimurium (S. Typhimurium) DT104. SGI1 contains a complex integron, which confers various multidrug resistance phenotypes due to its genetic plasticity. Previous studies have shown that SGI1 integrates site-specifically into the S. enterica, Escherichia coli, or Proteus mirabilis chromosome at the 3' end of thdF gene (attB site). METHODOLOGY/PRINCIPAL
findingsHere, we report the transfer of SGI1 to a Delta thdF mutant of S. Typhimurium LT2. In the absence of thdF, the frequency of transconjugant formation was reduced by around thirty times of magnitude. Through DNA sequencing SGI1 was shown to integrate specifically into a secondary attachment site (2(nd)attB), which is located in the intergenic region between the chromosomal sodB and purR genes. At this 2(nd)attB site, we found that a significant fraction of SGI1 transconjugants (43% of wild type and 100% of Delta thdF mutant) contained tandem SGI1 arrays. Moreover, in wild type S. Typhimurium LT2 transconjugants, SGI1 integrated into both attachment sites, i.e., thdF and sodB-purR. The formation of SGI1 tandem arrays occurred in both specific attB sites. There was heterogeneity in the size of the SGI1 tandem arrays detected in single transconjugant colonies. Some arrays consisted as far as six SGI1s arranged in tandem. These tandem arrays were shown to persist during serial passages with or without antibiotic selection pressure. CONCLUSIONS/SIGNIFICANCE: The ability of integration into two distinct chromosomal sites and tandem array formation of SGI1 could contribute to its spread and persistence. The existence of a secondary attachment site in the Salmonella chromosome has potential implications for the mobility of SGI1, which may integrate in other attachment sites of other bacterial pathogens that do not possess the 1(st) or 2(nd) specific SGI1 attB sites of Salmonella.
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