Molecular fingerprinting of Staphylococcus aureus isolated from patients with osteomyelitis in Argentina and clonal distribution of the cap5(8) genes and of other selected virulence genes
The molecular fingerprinting of a collection of 94 Staphylococcus aureus isolates from patients with osteomyelitis in Argentina was performed. Twenty-three SmaI pulsed-field gel electrophoresis (PFGE) types and 37 spa types were identified. The isolates were assigned to 23 sequence types (STs). The...
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Veröffentlicht in: | European journal of clinical microbiology & infectious diseases 2012-10, Vol.31 (10), p.2559-2566 |
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Zusammenfassung: | The molecular fingerprinting of a collection of 94
Staphylococcus aureus
isolates from patients with osteomyelitis in Argentina was performed. Twenty-three SmaI pulsed-field gel electrophoresis (PFGE) types and 37
spa
types were identified. The isolates were assigned to 23 sequence types (STs). The proportion of methicillin-resistant
S. aureus
(MRSA) isolates was significantly higher among
cap5 S. aureus
(35/61) compared with
cap8 S. aureus
(8/33) isolates (
p
= 0.0025). Twenty-four of the 94 isolates carried the
lukS
-PV/
lukF
-PV genes, which were significantly associated to
cap5
[(23/38) compared with
cap8 S. aureus
isolates (1/32) (
p
= 0.0001)]. Forty of the 94 isolates carried genes of the
egc
locus (
seg/sei
). The distribution of
seg/sei
genes among isolates was related to certain clones. Isolates of the four
agr
types were found in the
S. aureus
collection. Whereas
agr
I isolates were evenly distributed among
cap5
and
cap8 S. aureus
isolates (32/61 and 14/33, respectively), the
agr
II group was composed of 29
cap5 S. aureus
isolates and agr III was composed of 16
cap8 S. aureus
isolates. Two clones originally associated to animals (ST 188, 7 isolates and ST 1796, 5 isolates) were associated with chronic osteomyelitis and lack of capsular polysaccharide (CP) production. Loss of CP production remains the single factor among those investigated that is associated with chronic osteomyelitis. |
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ISSN: | 0934-9723 1435-4373 |
DOI: | 10.1007/s10096-012-1596-8 |