Dissemination of New Methicillin-Resistant Staphylococcus aureus Clones in the Community
By K. Okuma, K. Iwakawa, J. Turnidge, W. Grubb, J. Bell, F. O'Brien, G. Coombs, J. Pearman, F. Tenover, M. Kapi and 3 more. Journal of Clinical Microbiology, 2002
986 citations recorded by the source corpus.
Subfields: Clinical Biochemistry, Epidemiology, Infectious Diseases
View Paper: https://www.semanticscholar.org/paper/503556e4efe7b5c0ddcab952bf088a466ff280af
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In Clinical Biochemistry
- F. Lowy
- Kunyan Zhang
- E. Stobberingh
- R. H. Deurenberg
- Sahreena S. Lakhundi
- F. Tenover
- Robert S. Daum
- Michael Z. David
In Epidemiology
- F. Tenover
- F. Lowy
- E. Stobberingh
- R. H. Deurenberg
- Robert S. Daum
- Michael Z. David
- Teruyo Ito
- K. Hiramatsu
In Infectious Diseases
- E. Stobberingh
- R. H. Deurenberg
- Kunyan Zhang
- F. Lowy
- Sahreena S. Lakhundi
- Robert S. Daum
- F. Tenover
- Michael Z. David
Citations in the corpus
- Novel Type V Staphylococcal Cassette Chromosome mec Driven by a Novel Cassette Chromosome Recombinase, ccrC (2004, methodology): “Multiple MRSA clones carrying type IV SCCmec were identified in C-MRSA strains from both the United States and Australia by multilocus sequence typing for chromosome genotyping and the PCR technique for SCCmec typing ( 32 ).”
- Pathogenesis of methicillin-resistant Staphylococcus aureus infection. (2008, background): “CA-MRSA strains may also have a growth advantage over HAMRSA strains [27, 76].”
- The molecular evolution of methicillin-resistant Staphylococcus aureus. (2007, methodology): “[39] showed that CA-MRSA strains represent novel acquisitions of SCCmec type IV in the community.”
- Combination of Multiplex PCRs for Staphylococcal Cassette Chromosome mec Type Assignment: Rapid Identification System for mec, ccr, and Major Differences in Junkyard Regions (2006, background): “The results obtained with the M-PCRs were identical to those obtained by traditional methods, which mostly used a set of two primers to identify each gene or different allotypes (7, 10, 18).”
- Emergence of community-associated methicillin-resistant Staphylococcus aureus USA300 genotype as a major cause of health care-associated blood stream infections. (2006, background): “Evidence to support this comes in part from the fact that CA-MRSA PFGE types USA300 and USA400 contain the novel SCCmecIV element, which is considerably smaller than SCCmec elements I, II, and III, which are found in traditional HA-MRSA strains [26].”
- Antimicrobial resistance: the example of Staphylococcus aureus. (2003, background): “It also appears to occur in a more diverse range of MSSA genetic backgrounds, suggesting that it has been heterologously transferred more readily from other staphylococcal species (41).”
- Emergence of Community-Acquired Methicillin-Resistant Staphylococcus aureus USA 300 Clone as the Predominant Cause of Skin and Soft-Tissue Infections (2006, methodology): “For some isolates, we determined SCCmec type by using polymerase chain reaction (PCR)–typing of the mec gene complex as described by Okuma and colleagues (7).”
- Prevalence of Staphylococcus aureus nasal colonization in the United States, 2001-2002. (2006, background): “Valentine leukocidin (PVL); and staphylococcal cassette chromosome mec (SCCmec) type I–IV genes [17, 18].”
- Severe community-onset pneumonia in healthy adults caused by methicillin-resistant Staphylococcus aureus carrying the Panton-Valentine leukocidin genes. (2005, background): “These CO-MRSA strains are globally distributed and clonally disseminated [11, 12].”
- The evolution of Staphylococcus aureus. (2008, methodology): “Furthermore, the larger clonal diversity of CA-MRSA compared to HA-MRSA suggests that more S. aureus lineages have the ability to become CA-MRSA (Enright et al., 2002; Okuma et al., 2002; Feng et al., 2008; Francois et al., 2008).”
- Community-Associated Methicillin-Resistant Staphylococcus aureus: Epidemiology and Clinical Consequences of an Emerging Epidemic (2010, background): “Abundant molecular evidence supports the hypothesis that CA-MRSA clones have arisen in the community by the horizontal transfer of SCCmec elements and PVL genes, molecular features commonly associated with CA-MRSA isolates as well as perhaps other virulence and resistance factors, to the genomes of ”
- Pulsed-Field Gel Electrophoresis Typing of Oxacillin-Resistant Staphylococcus aureus Isolates from the United States: Establishing a National Database (2003, background): “Type I (34 kb) was detected in the first ORSA strain isolated in 1961 in the United Kingdom (strain NCTC 10442) (31); type II (52 kb) was identified in an ORSA strain isolated in 1982 in Japan (strain N315) (30); type III (66 kb) was identified in an MRSA strain isolated in 1985 in New Zealand (stra”
- Practice guidelines for the diagnosis and management of skin and soft-tissue infections. (2005, background): “fluoroquinolones, or rifampin; genotypically, they appear not to be related to local hospital strains and to contain type IV SCCmec cassette not typical of hospital isolates [85, 86].”