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Stephen M. Kwong

Researcher at University of Sydney

Publications -  31
Citations -  1944

Stephen M. Kwong is an academic researcher from University of Sydney. The author has contributed to research in topics: Plasmid & Mobile genetic elements. The author has an hindex of 19, co-authored 28 publications receiving 1266 citations. Previous affiliations of Stephen M. Kwong include University of Texas MD Anderson Cancer Center & National University of Singapore.

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Journal ArticleDOI

Mobile Genetic Elements Associated with Antimicrobial Resistance

TL;DR: The characteristics of the major types of mobile genetic elements involved in acquisition and spread of antibiotic resistance in both Gram-negative and Gram-positive bacteria are outlined, focusing on the so-called ESKAPEE group of organisms, which have become the most problematic hospital pathogens.
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An updated view of plasmid conjugation and mobilization in Staphylococcus.

TL;DR: It is suggested that a greater research focus on the molecular biology of conjugation is essential if the accretion and dissemination of antimicrobial-resistance genes in the human and animal pathogen Staphylococcus aureus is to be recognized from increasingly in silico analyses.
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The RepA_N replicons of Gram-positive bacteria: a family of broadly distributed but narrow host range plasmids.

TL;DR: Comparison of stability determinants associated with the RepA_N replicons suggests that they have a modular evolution as has been observed in other plasmid families.
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Staphylococcus aureus multiresistance plasmid pSK41: analysis of the replication region, initiator protein binding and antisense RNA regulation.

TL;DR: The replication region of pSK41 encodes a protein product, Rep, which was shown to be essential for replication; mutations that truncated Rep could be complemented in trans and transcriptional start points for both RNAI and the rep‐mRNA were defined.
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Molecular basis of antibiotic multiresistance transfer in Staphylococcus aureus

TL;DR: The structural basis for antibiotic multiresistance acquisition by S. aureus is revealed and novel strategies for therapeutic intervention are suggested, including DNA minor groove-targeted polyamide that inhibits NES with low micromolar efficacy.