The DOI matches its Crossref record; 42 of the 42 references it cites were found in a registry or an index.
The Evolution of Pandemic Clones of Methicillin-Resistant Staphylococcus aureus : Identification of Two Ancestral Genetic Backgrounds and the Associated mec Elements
Abstract
Previous surveillance studies carried out by our laboratories, primarily in Southern and Eastern Europe, Latin America, and the United States, have characterized 3,067 methicillin-resistant Staphylococcus aureus (MRSA) hospital isolates by a combination of molecular typing methods. Nearly 70% of these isolates could be classified into five clonal types showing extensive geographic spread. Representative isolates of these clonal types were now reexamined for their genetic relatedness by multilocus sequence typing (MLST) and by sequencing the polymorphic region of protein A ( spaA typing), and also for the type of the Staphylococcal Chromosomal Cassette (SCC mec ) resident in the bacteria. Three of the previously classified clonal types (Iberian, Brazilian, and Hungarian clones) shared a common or closely related genetic background A, which was the same as the background of the earliest European isolates of MRSA from England and Denmark. The Pediatric and New York/Japan clones belonged to a completely different genetic background B. The three recently described SCC mec types were specifically associated with different pandemic clones: types I and III with isolates of genetic background A and type II with isolates of genetic background B. A novel SCC mec related to type I, called SCC mec type IV, was identified in some MRSA strains belonging to genetic background A as well as B. Structural variations in SCC mec types I and III were also observed. The data allow tentative identification of an evolutionary pathway for the emergence of pandemic MRSA clones and also provide evidence for the multiple, yet restricted, numbers of acquisition of the mec element by S. aureus .
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“Fourteen major types of SCCmec have been described and sequenced, and within the major types are several subtypes [26,27,28,29,30,31,32].”
From Molecular Mechanisms of Drug Resistance in Staphylococcus aureus (2022) · cites this paper as [30]
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1 retracted
A Link Between Virulence and Ecological Abundance in Natural Populations of Staphylococcus aureus
Day, N., Moore, C. E., Enright, M. C., Berendt, A. R., Smith, J. M., Murphy, M. F., Peacock, S. J., Spratt, B. G., & Feil, E. J. (2001) · Science · doi:10.1126/science.1056495 · Cited by 108
RetractedMaiden, M. C. J., Bygraves, J. A., Feil, E., Morelli, G., Russell, J. E., Urwin, R., Zhang, Q., Zhou, J., Zurth, K., Caugant, D. A., et al. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.6.3140 · Cited by 3,833
Enright, M. C., Day, N. P. J., Davies, C. E., Peacock, S. J., & Spratt, B. G. (2000) · Journal of Clinical Microbiology · doi:10.1128/jcm.38.3.1008-1015.2000 · Cited by 3,063
Whole genome sequencing of meticillin-resistant Staphylococcus aureus
Kuroda, M., Ohta, T., Uchiyama, I., Baba, T., Yuzawa, H., Kobayashi, I., Cui, L., Oguchi, A., Aoki, K.-I., Nagai, Y., et al. (2001) · The Lancet · doi:10.1016/s0140-6736(00)04403-2 · Cited by 1,961
The evolutionary history of methicillin-resistant Staphylococcus aureus (MRSA)
Enright, M. C., Robinson, D. A., Randle, G., Feil, E. J., Grundmann, H., & Spratt, B. G. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.122108599 · Cited by 1,588
Enright, M. C., & Spratt, B. G. (1998) · Microbiology · doi:10.1099/00221287-144-11-3049 · Cited by 1,074
Katayama, Y., Ito, T., & Hiramatsu, K. (2000) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.44.6.1549-1555.2000 · Cited by 1,038
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Cited by
Waves of resistance: Staphylococcus aureus in the antibiotic era
Chambers, H. F., & DeLeo, F. R. (2009) · Nature Reviews Microbiology · doi:10.1038/nrmicro2200 · Cited by 2,718
Vandenesch, F., Naimi, T., Enright, M. C., Lina, G., Nimmo, G. R., Heffernan, H., Liassine, N., Bes, M., Greenland, T., Reverdy, M.-E., et al. (2003) · Emerging Infectious Diseases · doi:10.3201/eid0908.030089 · Cited by 1,727
Methicillin-Resistant Staphylococcus aureus: Molecular Characterization, Evolution, and Epidemiology
Lakhundi, S., & Zhang, K. (2018) · Clinical Microbiology Reviews · doi:10.1128/cmr.00020-18 · Cited by 1,637
Antimicrobial resistance: the example of Staphylococcus aureus
Lowy, F. D. (2003) · Journal of Clinical Investigation · doi:10.1172/jci18535 · Cited by 1,445
Zhang, K., McClure, J.-A., Elsayed, S., Louie, T., & Conly, J. M. (2005) · Journal of Clinical Microbiology · doi:10.1128/jcm.43.10.5026-5033.2005 · Cited by 1,037
Metadata
- Authors
- Oliveira, D. C., Tomasz, A., & de Lencastre, H.
- Venue
- Microbial Drug Resistance
- Publisher
- SAGE Publications
- Published
- 2001-12
- Volume
- 7
- Issue
- 4
- Pages
- 349-361
- ISSN
- 1076-6294 (ISSN-L)
- 1931-8448
- OpenAlex
- W2134366416
- Cited by
- 301
- References
- 42
- FWCI
- 10.95
- Type
- journal article
- Language
- en
- Open access
- closed
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- Oliveira, D. C., Tomasz, A., & de Lencastre, H. (2001). The Evolution of Pandemic Clones of Methicillin-Resistant Staphylococcus aureus : Identification of Two Ancestral Genetic Backgrounds and the Associated mec Elements. Microbial Drug Resistance. https://doi.org/10.1089/10766290152773365
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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