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Clonal Distribution of Bone Sialoprotein-binding Protein Gene Among Staphylococcus Aureus Isolates Associated with Bloodstream Infections

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Publisher Springer
Specialty Microbiology
Date 2014 May 16
PMID 24827510
Citations 8
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Abstract

Staphylococcus aureus is a leading cause of bloodstream infections (BSI) and diseases that may be caused by hematogenous spread. The staphylococcal adhesin, for which the association with the infections emerging as a complication of septicemia has been well documented, is a bone sialoprotein-binding protein (Bbp). The aim of the study was to assess the prevalence of a bbp gene in S. aureus bloodstream isolates associated with BSI and to investigate to what degree the distribution of this gene is linked to the clonality of the population. Spa typing, used in order to explore the genetic population structure of the isolates, yielded 29 types. Six spa clusters and seven singletons were identified. The most frequent was spa clonal complex CC021 associated with MLST CC30 (38%). The bbp gene was found in 47% of isolates. Almost all isolates (95%) clustered in spa clonal complex CC021 were positive for this gene. All isolates carrying the bbp gene were sensitive to methicillin, and if clustered in the spa CC021, belonged to agr group III. Our study shows that Bbp is not strictly associated with BSI. However, one may conclude that for clonally related S. aureus strains most commonly causing BSI, the risk of Bbp-mediated complications of septicemia is expected to be higher than for other strains.

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References
1.
Lina G, Piemont Y, Bes M, Peter M, Gauduchon V, Vandenesch F . Involvement of Panton-Valentine leukocidin-producing Staphylococcus aureus in primary skin infections and pneumonia. Clin Infect Dis. 1999; 29(5):1128-32. DOI: 10.1086/313461. View

2.
Grundmann H, Aanensen D, van den Wijngaard C, Spratt B, Harmsen D, Friedrich A . Geographic distribution of Staphylococcus aureus causing invasive infections in Europe: a molecular-epidemiological analysis. PLoS Med. 2010; 7(1):e1000215. PMC: 2796391. DOI: 10.1371/journal.pmed.1000215. View

3.
Berendt T, Byren I . Bone and joint infection. Clin Med (Lond). 2005; 4(6):510-8. PMC: 4951986. DOI: 10.7861/clinmedicine.4-6-510. View

4.
Cunningham R, Cockayne A, Humphreys H . Clinical and molecular aspects of the pathogenesis of Staphylococcus aureus bone and joint infections. J Med Microbiol. 1996; 44(3):157-64. DOI: 10.1099/00222615-44-3-157. View

5.
Wisniewska K, Szewczyk A, Piechowicz L, Bronk M, Samet A, Swiec K . The use of spa and phage typing for characterization of clinical isolates of methicillin-resistant Staphylococcus aureus in the University Clinical Center in Gdańsk, Poland. Folia Microbiol (Praha). 2012; 57(3):243-9. PMC: 3345334. DOI: 10.1007/s12223-012-0148-z. View