Tm. Morton et al., CHARACTERIZATION OF A CONJUGATIVE STAPHYLOCOCCAL MUPIROCIN RESISTANCEPLASMID, Antimicrobial agents and chemotherapy, 39(6), 1995, pp. 1272-1280
We studied conjugative plasmids encoding high-level mupirocin resistan
ce. These plasmids were found in Staphylococcus aureus isolates from t
wo geographic locations in the United States. Transfer genes on three
mupirocin resistance plasmids with different restriction endonuclease
profiles were indistinguishable by DNA hybridization from those on pG0
1, a conjugative aminoglycoside resistance plasmid representative of s
imilar plasmids that are prevalent in the United States. One mupirocin
resistance plasmid, pG0400 (34 kb), was smaller than pG01 (52 kb) bec
ause of the absence from pG0400 of DNA, found on pG01, that contained
genes encoding resistance to aminoglycosides, trimethoprim, and quater
nary ammonium compounds flanked by directly repeated copies of the ins
ertion sequence (IS)-like element IS431-IS257, The plasmids pG0400 and
pG01 were otherwise indistinguishable except for the presence in pG04
00 of a 4.5-kb HindIII fragment encoding mupirocin resistance. The add
ed mupirocin resistance gene was flanked by two directly repeated copi
es of IS431/257. The nucleotide sequence of DNA contiguous to the outs
ide of the IS elements, as well as those of the elements themselves, w
as identical in both pG01 and pG0400, and there were no target site du
plications flanking either copy of the element. We conclude that the m
upirocin resistance gene was added to an existing conjugative plasmid
in conjunction with the deletion of other resistance genes by recombin
ation at IS elements. The construction of conjugative plasmids carryin
g a mupirocin resistance gene may be a model for the mobility of other
resistance genes newly acquired by staphylococci.