p39R861-4, A Type 2 A/C2 Plasmid Carrying a Segment from the A/C1 Plasmid RA1
The largest plasmid in the strain 39R861, which is used as a plasmid size standard, was recovered by conjugation and sequenced to determine its exact size. Plasmid p39R861-4 transferred at high frequency. Although reported to be the A/C 1 plasmid RA1, p39R861-4 is a 155794-bp Type 2 A/C 2 plasmid, i...
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Veröffentlicht in: | Microbial drug resistance (Larchmont, N.Y.) N.Y.), 2015-12, Vol.21 (6), p.571-576 |
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Sprache: | eng |
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Zusammenfassung: | The largest plasmid in the strain 39R861, which is used as a plasmid size standard, was recovered by conjugation and sequenced to determine its exact size. Plasmid p39R861-4 transferred at high frequency. Although reported to be the A/C
1
plasmid RA1, p39R861-4 is a 155794-bp Type 2 A/C
2
plasmid, in which a 39-kb segment, derived from RA1 that includes a relative of the RA1 resistance island, replaces 26.5 kb of the Type 2 backbone. p39R861-4 includes a single copy of IS
10
and two resistance islands with a CR2-
sul2
region in each of them. The 84 kb of backbone between the resistance islands is inverted relative to other known A/C plasmids and this inversion has arisen through recombination between the CR2-
sul2
regions that are inversely oriented. The two resistance islands present before this inversion occurred were one related to but longer than that found in RA1, and one that is a form of the ARI-B island and identical to ARI-B in the A/C
2
plasmid R55. They contain genes conferring resistance to tetracycline (
tetA
(D)), sulfonamides (
sul2
), and florfenicol and chloramphenicol (
floR
). The
tet
(D) determinant is flanked by two IS
26
in a transposon-like structure named Tn
tet
(D). Both resistance islands contain remnants of the two ends of the integrative element GI
sul2
, consistent with the
sul2
gene being mobilized by GI
sul2
rather than by CR2. |
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ISSN: | 1076-6294 1931-8448 |
DOI: | 10.1089/mdr.2015.0133 |