Potential Associations between Hematogenous Complications and Bacterial Genotype in Staphylococcus aureus Infection
VG Fowler Jr, CL Nelson, LM McIntyre… - The Journal of …, 2007 - academic.oup.com
VG Fowler Jr, CL Nelson, LM McIntyre, BN Kreiswirth, A Monk, GL Archer, J Federspiel…
The Journal of infectious diseases, 2007•academic.oup.comBackground. The impact of bacterial clonality on infections caused by Staphylococcus
aureus is unclear. Methods. Three hundred seventy-nine S. aureus isolates (125 methicillin-
resistant S. aureus [MRSA] and 254 methicillin-susceptible S. aureus [MSSA]) were
genotyped by spa typing and multilocus sequence typing. For MRSA isolates, the
staphylococcal chromosomal cassette mec (SCC mec) element was also typed. Three
clinical categories were identified: nasal carriage only (n= 118), uncomplicated infection (n …
aureus is unclear. Methods. Three hundred seventy-nine S. aureus isolates (125 methicillin-
resistant S. aureus [MRSA] and 254 methicillin-susceptible S. aureus [MSSA]) were
genotyped by spa typing and multilocus sequence typing. For MRSA isolates, the
staphylococcal chromosomal cassette mec (SCC mec) element was also typed. Three
clinical categories were identified: nasal carriage only (n= 118), uncomplicated infection (n …
Abstract
Background. The impact of bacterial clonality on infections caused by Staphylococcus aureus is unclear.
Methods. Three hundred seventy-nine S. aureus isolates (125 methicillin-resistant S. aureus [MRSA] and 254 methicillin-susceptible S. aureus [MSSA]) were genotyped by spa typing and multilocus sequence typing. For MRSA isolates, the staphylococcal chromosomal cassette mec (SCCmec) element was also typed. Three clinical categories were identified: nasal carriage only (n = 118), uncomplicated infection (n = 104), and bacteremia with hematogenous complications (n = 157).
Results. By use of eBURST, 18 clonal complexes (CCs) were found in 371 isolates. Eight CCs accounted for 89%of isolates and occurred in all clinical categories. CC5 (P = .0025) and CC30 (P = .0308) exhibited a significant trend toward more frequent hematogenous complications. Isolates within spa types 2 and 16 showed the same significant trend and grouped within CC5 and CC30, respectively. SCCmec II isolates also showed the same significant trend compared with SCCmec IV; 96% were CC5 or CC30.
Conclusions. Although most S. aureus genotypes exhibited the capacity to cause invasive disease, strains within CC5 and CC30 exhibited a significant trend toward increasing levels of hematogenous complications. Isolates within these CCs were also implicated by use of spa and SCCmec typing. The genetic determinants underlying these findings remain to be demonstrated.
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