Phenotypic and Genotypic Characteristics of Persistent Methicillin-Resistant Staphylococcus aureus Bacteremia In Vitro and in an Experimental Endocarditis Model

被引:99
作者
Xiong, Yan Q. [1 ,2 ]
Fowler, Vance G., Jr. [4 ]
Yeaman, Michael R. [2 ]
Perdreau-Remington, Francoise [3 ]
Kreiswirth, Barry N. [5 ,6 ]
Bayer, Arnold S. [2 ]
机构
[1] Harbor UCLA, Med Ctr, Dept Med, Div Infect Dis,Los Angeles Biomed Res Inst, Torrance, CA 90502 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA
[3] Univ Calif San Francisco, Dept Med, Div Infect Dis, San Francisco, CA USA
[4] Duke Univ, Med Ctr, Div Infect Dis, Durham, NC USA
[5] Publ Hlth Res Inst, Newark, NJ USA
[6] Univ Med & Dent New Jersey, Newark, NJ 07103 USA
基金
美国国家卫生研究院;
关键词
PLATELET MICROBICIDAL PROTEIN; EXPERIMENTAL INFECTIVE ENDOCARDITIS; VIRULENCE; MEMBRANE; OUTCOMES; BINDING; AGR; SUSCEPTIBILITY; DISSEMINATION; PATHOGENESIS;
D O I
10.1086/595738
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Persistent MRSA bacteremia (PB) represents an important subset of Staphylococcus aureus infections and correlates with poor clinical outcomes. Methods. We profiled relevant in vitro phenotypic and genotypic characteristics of MRSA isolates from 39 persons with bacteremia ( 21 had PB and 18 had resolving bacteremia [RB]). We also compared the intrinsic virulence and responsiveness to vancomycin of selected PB and RB strains in an experimental endocarditis model (IE). Results. PB and RB isolates differed significantly with regard to several in vitro characteristics that are believed to impact endovascular infections. PB isolates exhibited significantly more resistance to the cationic defensin hNP-1, enhanced membrane fluidity, and substantially greater adhesion to fibronectin, fibrinogen, and endothelial cells. Genotypically, PB isolates had higher frequency of SCCmec II, CC30, and spa 16; and higher rates of agr type III, cap8, tst-1, and cna carriage. Finally, a prototypic PB strain was more resistant to vancomycin treatment in the infective endocarditis model than a RB comparator strain, despite equivalent virulence profiles. Conclusions. Our findings indicate that PB isolates may have specific virulence signatures that distinguish them from RB isolates. These data suggest that methods might be developed to identify patients at higher risk for PB in real-time, thereby optimizing the effectiveness of anti-MRSA therapeutic strategies.
引用
收藏
页码:201 / 208
页数:8
相关论文
共 34 条
[1]   Impact of the high-affinity proline permease gene (putP) on the virulence of Staphylococcus aureus in experimental endocarditis [J].
Bayer, AS ;
Coulter, SN ;
Stover, CK ;
Schwan, WR .
INFECTION AND IMMUNITY, 1999, 67 (02) :740-744
[2]   In vitro resistance of Staphylococcus aureus to thrombin-induced platelet microbicidal protein is associated with alterations in cytoplasmic membrane fluidity [J].
Bayer, AS ;
Prasad, R ;
Chandra, J ;
Koul, A ;
Smriti, M ;
Varma, A ;
Skurray, RA ;
Firth, N ;
Brown, MH ;
Koo, SP ;
Yeaman, MR .
INFECTION AND IMMUNITY, 2000, 68 (06) :3548-3553
[3]   Clinical features associated with bacteremia due to heterogeneous vancomycin-intermediate Staphylococcus aureus [J].
Charles, PGP ;
Ward, PB ;
Johnson, PDR ;
Howden, BP ;
Grayson, ML .
CLINICAL INFECTIOUS DISEASES, 2004, 38 (03) :448-451
[4]   Influence of in vitro susceptibility phenotype against thrombin-induced platelet microbicidal protein on treatment and prophylaxis outcomes of experimental Staphylococcus aureus endocarditis [J].
Dhawan, VK ;
Yeaman, MR ;
Bayer, AS .
JOURNAL OF INFECTIOUS DISEASES, 1999, 180 (05) :1561-1568
[5]   In vitro resistance to thrombin-induced platelet microbicidal protein is associated with enhanced progression and hematogenous dissemination in experimental Staphylococcus aureus infective endocarditis [J].
Dhawan, VK ;
Bayer, AS ;
Yeaman, MR .
INFECTION AND IMMUNITY, 1998, 66 (07) :3476-3479
[6]   Phenotypic resistance to thrombin-induced platelet microbicidal protein in vitro is correlated with enhanced virulence in experimental endocarditis due to Staphylococcus aureus [J].
Dhawan, VK ;
Yeaman, MR ;
Cheung, AL ;
Kim, E ;
Sullam, PM ;
Bayer, AS .
INFECTION AND IMMUNITY, 1997, 65 (08) :3293-3299
[7]   Roles of 34 virulence genes in the evolution of hospital- and community-associated strains of methicillin-resistant Staphylococcus aureus [J].
Diep, BA ;
Carleton, HA ;
Chang, RF ;
Sensabaugh, GF ;
Perdreau-Remington, F .
JOURNAL OF INFECTIOUS DISEASES, 2006, 193 (11) :1495-1503
[8]   Risk of endocarditis among patients with prosthetic valves and Staphylococcus aureus bacteremia [J].
El-Ahdab, F ;
Benjamin, DK ;
Wang, A ;
Cabell, CH ;
Chu, VH ;
Stryjewski, ME ;
Corey, GR ;
Sexton, DJ ;
Reller, LB ;
Fowler, VG .
AMERICAN JOURNAL OF MEDICINE, 2005, 118 (03) :225-229
[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]   Contribution of clumping factor B to pathogenesis of experimental endocarditis due to Staphylococcus aureus [J].
Entenza, JM ;
Foster, TJ ;
Eidhin, DN ;
Vaudaux, P ;
Francioli, P ;
Moreillon, P .
INFECTION AND IMMUNITY, 2000, 68 (09) :5443-5446