Evolution of IS 26 -bounded pseudo-compound transposons carrying the tet (C) tetracycline resistance determinant
Plasmid, ISSN: 0147-619X, Vol: 112, Page: 102541
2020
- 8Citations
- 5Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations8
- Citation Indexes8
- CrossRef2
- Captures5
- Readers5
Article Description
A large plasmid, pCERC14, found in an antibiotic resistant commensal Escherichia coli isolate recovered from a healthy adult was sequenced. pCERC14 was 162,926 bp and carried FII-18 and FIB-1 replicons and an F-like transfer region as well as several virulence determinants, some of which are involved in the uptake of iron which would be advantageous for the commensal lifestyle. The plasmid backbone is interrupted in 11 places by complete IS (IS 1 (4 copies), IS 2 (2), IS 629 (2) and single IS 100, IS 186, ISEc33) and in three places by partial IS copies. The antibiotic resistance genes were found in two IS 26 -bounded pseudo-compound transposons (PCT). One contained a remnant of a class 1 integron that includes a dfrA5 gene cassette and the sul1 gene conferring resistance to trimethoprim and sulphonamides, respectively. The second, named PTn tet (C)-var, contained a 4828 bp DNA segment that includes the tet (C) tetracycline resistance determinant. As tet (C) is relatively rare in E. coli and other Gram-negative bacterial isolates, the structure and evolution of tet (C)-containing PCT in available sequences was examined. The largest identified was PTn tet (C), a close relative of PTn tet (C)-var, and a potential progenitor for these PCT. Most PCT shared one internal boundary with PTn tet (C) but the length of the central tet (C)-containing segment was shorter due to IS 26 -mediated deletions. The most abundant variant form, previously named Tn 6309, was widely distributed and, in a derivative of it, most of the tetA (C) gene has been replaced by the tetA (A) gene presumably by homologous recombination.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0147619X20300536; http://dx.doi.org/10.1016/j.plasmid.2020.102541; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85091663472&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/32979461; https://linkinghub.elsevier.com/retrieve/pii/S0147619X20300536; https://dx.doi.org/10.1016/j.plasmid.2020.102541
Elsevier BV
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