The presence of both bone sialoprotein-binding protein gene and collagen adhesin gene as a typical virulence trait of the major epidemic cluster in isolates from orthopedic implant infections

被引:50
作者
Campoccia, Davide [1 ]
Speziale, Pietro [2 ]
Ravaioli, Stefano [1 ,3 ]
Cangini, Ilaria [1 ,3 ]
Rindi, Simonetta [2 ]
Pirini, Valter [1 ]
Montanaro, Lucio [1 ,3 ]
Arciola, Carla Renata [1 ,3 ]
机构
[1] Rizzoli Orthopaed Inst, Res Unit Implant Infect, I-40136 Bologna, Italy
[2] Univ Pavia, Dept Biochem, I-27100 Pavia, Italy
[3] Univ Bologna, Dept Expt Pathol, I-40126 Bologna, Italy
关键词
Orthopaedic implant infections; MSCRAMMs; bbp; cna; Staphylococcus aureus; Ribotyping; STAPHYLOCOCCUS-AUREUS STRAINS; PATHOGENESIS; EXPRESSION; CNA; OSTEOMYELITIS; OSTEOPONTIN; RESISTANCE; ARTHRITIS;
D O I
10.1016/j.biomaterials.2009.08.032
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Staphylococcus aureus is a major, highly clonal, pathogen causing implant infections. This study aimed at investigating the diverse distribution of bacterial adhesins in most prevalent S. aureus strain types causing orthopaedic implant infections. 200 S. aureus isolates, categorized into ribogroups by automated ribotyping, i.e. rDNA restriction fragment length polymorphism analysis, were screened for the presence of a panel of adhesins genes. Within the collection of isolates, automated ribotyping detected 98 distinct ribogroups. For many ribogroups, characteristic tandem genes arrangements could be identified. In the predominant S. aureus cluster, enlisting 27 isolates, the bbp gene encoding bone sialoprotein-binding protein appeared a typical virulence trait, found in 93% of the isolates. Conversely, the bbp gene was identified in just 10% of the remaining isolates of the collection. In this cluster, co-presence of bbp with the cna gene encoding collagen adhesin was a pattern consistently observed. These findings indicate a crucial role of both these adhesins, able to bind the most abundant bone proteins, in the pathogenesis of orthopaedic implant infections, there where biomaterials interface bone tissues. This study suggests that specific adhesins may synergistically act in the onset of implant infections and that anti-adhesin strategies should be targeted to adhesins conjointly present. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6621 / 6628
页数:8
相关论文
共 35 条
[1]   Etiology of implant orthopedic infections: A survey on 1027 clinical isolates [J].
Arciola, CR ;
An, YH ;
Campoccia, D ;
Donati, ME ;
Montanaro, L .
INTERNATIONAL JOURNAL OF ARTIFICIAL ORGANS, 2005, 28 (11) :1091-1100
[2]   Prevalence of cna, fnbA and fnbB adhesin genes among Staphylococcus aureus isolates from orthopedic infections associated to different types of implant [J].
Arciola, CR ;
Campoccia, D ;
Gamberini, S ;
Baldassarri, L ;
Montanaro, L .
FEMS MICROBIOLOGY LETTERS, 2005, 246 (01) :81-86
[3]   BONE SIALOPROTEIN (BSP) SECRETION AND OSTEOBLAST DIFFERENTIATION - RELATIONSHIP TO BROMODEOXYURIDINE INCORPORATION, ALKALINE-PHOSPHATASE, AND MATRIX DEPOSITION [J].
BIANCO, P ;
RIMINUCCI, M ;
BONUCCI, E ;
TERMINE, JD ;
ROBEY, PG .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1993, 41 (02) :183-191
[4]   Automated ribotyping of vancomycin-resistant Enterococcus faecium isolates [J].
Brisse, S ;
Fussing, V ;
Ridwan, B ;
Verhoef, J ;
Willems, RJL .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (06) :1977-1984
[5]   Molecular epidemiology of Staphylococcus aureus from implant orthopaedic infections: Ribotypes, agr polymorphism, leukocidal toxins and antibiotic resistance [J].
Campoccia, Davide ;
Baldassarri, Lucilla ;
Pirini, Valter ;
Ravaioli, Stefano ;
Montanaro, Ludo ;
Arciola, Carla R. .
BIOMATERIALS, 2008, 29 (30) :4108-4116
[6]   A novel functional motif of osteopontin for human lymphocyte migration and survival [J].
Cao, Zhiguo ;
Dai, Jianxin ;
Fan, Kexin ;
Wang, Huajing ;
Ji, Guanghui ;
Li, Bohua ;
Zhang, Dapeng ;
Hou, Sheng ;
Qian, Weizhu ;
Zhao, Jian ;
Wang, Hao ;
Guo, Yajun .
MOLECULAR IMMUNOLOGY, 2008, 45 (14) :3683-3692
[7]   Regulation of virulence determinants in vitro and in vivo in Staphylococcus aureus [J].
Cheung, AL ;
Bayer, AS ;
Zhang, GY ;
Gresham, H ;
Xiong, YQ .
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 2004, 40 (01) :1-9
[8]   Clinical and molecular aspects of the pathogenesis of Staphylococcus aureus bone and joint infections [J].
Cunningham, R ;
Cockayne, A ;
Humphreys, H .
JOURNAL OF MEDICAL MICROBIOLOGY, 1996, 44 (03) :157-164
[9]   Staphylococcus aureus collagen adhesin contributes to the pathogenesis of osteomyelitis [J].
Elasri, MO ;
Thomas, JR ;
Skinner, RA ;
Blevins, JS ;
Beenken, KE ;
Nelson, CL ;
Smeltzer, MS .
BONE, 2002, 30 (01) :275-280
[10]   Evolution and pathogenesis of Staphylococcus aureus:: lessons learned from genotyping and comparative genomics [J].
Feng, Ye ;
Chen, Chih-Jung ;
Su, Lin-Hui ;
Hu, Songnian ;
Yu, Jun ;
Chiu, Cheng-Hsun .
FEMS MICROBIOLOGY REVIEWS, 2008, 32 (01) :23-37