Journal of Bacteriology, September 1998, p. 4886-4892, Vol. 180, No. 18
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Department of Microbiology1 and Laboratory of Bacterial Drug Resistance,2 Gunma University School of Medicine, Maebashi, Gunma, Japan
Received 11 May 1998/Accepted 21 July 1998
Plasmid pMG1 (65.1 kb) was isolated from a gentamicin-resistant
Enterococcus faecium clinical isolate and was found to
encode gentamicin resistance. EcoRI restriction of pMG1
produced five fragments, A through E, with molecular sizes of 50.2, 11.5, 2.0, 0.7, and 0.7 kb, respectively. The clockwise order of the
fragments was ACDEB. pMG1 transferred at high frequency to
Enterococcus strains in broth mating. pMG1 transferred
between Enterococcus faecalis strains, between
E. faecium strains, and between E. faecium and
E. faecalis strains at a frequency of approximately
10
4 per donor cell after 3 h of mating. The pMG1
transfers were not induced by the exposure of the donor cell to culture
filtrates of plasmid-free E. faecalis FA2-2 or an E. faecium strain. Mating aggregates were not observed by
the naked eye during broth mating. Small mating aggregates of several
cells in the broth matings were observed by microscopy, while no
aggregates of donor cells which had been exposed to a culture filtrate
of E. faecalis FA2-2 or an E. faecium strain
were observed, even by microscopy. pMG1 DNA did not show any homology
in Southern hybridization with that of the pheromone-responsive
plasmids and broad-host-range plasmids pAM
1 and pIP501. These
results indicate that there is another efficient transfer system in the
conjugative plasmids of Enterococcus and that this system
is different from the pheromone-induced transfer system of E. faecalis plasmids.
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