Affiliation:
1. School of Biological Sciences, University of Sydney, Sydney, New South Wales 2006, Australia,1 and
2. Microbiology Unit, Department of Biochemistry, University of Oxford, Oxford OX1 3QU, United Kingdom2
Abstract
ABSTRACT
Based on structural and functional properties, three groups of large staphylococcal multiresistance plasmids have been recognized, viz., the pSK1 family, pSK41-like conjugative plasmids, and β-lactamase–heavy-metal resistance plasmids. Here we describe an analysis of the replication functions of a representative of each of these plasmid groups. The replication initiation genes from the
Staphylococcus aureus
plasmids pSK1, pSK41, and pI9789::Tn
552
were found to be related to each other and to the
Staphylococcus xylosus
plasmid pSX267 and are also related to
rep
genes of several plasmids from other gram-positive genera. Nucleotide sequence similarity between pSK1 and pI9789::Tn
552
extended beyond their
rep
genes, encompassing upstream divergently transcribed genes,
orf245
and
orf256
, respectively. Our analyses revealed that genes encoding proteins related to the deduced
orf245
product are variously represented, in several types of organization, on plasmids possessing six seemingly evolutionarily distinct types of replication initiation genes and including both theta-mode and rolling-circle replicons. Construction of minireplicons and subsequent functional analysis demonstrated that
orf245
is required for the segregational stability of the pSK1 replicon. In contrast, no gene equivalent to
orf245
is evident on the conjugative plasmid pSK41, and a minireplicon encoding only the pSK41
rep
gene was found to exhibit a segregational stability approaching that of the parent plasmid. Significantly, the results described establish that many of the large multiresistance plasmids that have been identified in clinical staphylococci, which were formerly presumed to be unrelated, actually utilize an evolutionarily related theta-mode replication system.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
69 articles.
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