Staphylococcus aureus accessory gene regulator (agr) group II:: Is there a relationship to the development of intermediate-level glycopeptide resistance?

被引:158
作者
Sakoulas, G
Eliopoulos, GM
Moellering, RC
Novick, RP
Venkataraman, L
Wennersten, C
DeGirolami, PC
Schwaber, MJ
Gold, HS
机构
[1] Beth Israel Deaconess Med Ctr, Dept Med, Div Lab & Transfus Med, Boston, MA 02215 USA
[2] Beth Israel Deaconess Med Ctr, Dept Pathol, Boston, MA 02215 USA
[3] Harvard Med Sch, Boston, MA USA
[4] Skirball Inst Biomol Med, New York, NY USA
[5] NYU, Sch Med, New York, NY USA
关键词
D O I
10.1086/368128
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We previously determined that all 6 Staphylococcus aureus strains with confirmed intermediate-level resistance to glycopeptides (glycopeptide intermediate S. aureus [GISA]) from the United States that we tested belonged to accessory gene regulator (agr) group II. In the present study, we found that 56% of surveyed bloodstream methicillin-resistant S. aureus isolates (n=148) at our hospital were agr group II, whereas only 24% of methicillin-susceptible S. aureus isolates (n=33) were agr group II (P=.001). Population analysis of genetically engineered agr-null and parent wild-type strains of groups I, II, and IV revealed that, when agr function is lost, the agr group II knockout S. aureus was most likely to develop glycopeptide heteroresistance after growth in 1 mug/mL but not 16 mug/mL vancomycin. This strain was unique in showing decreased autolysis after growth in these conditions. This study suggests that some S. aureus strains have an intrinsic survival advantage under a glycopeptide selective pressure, which is possibly related to reduced autolysis after exposure to subinhibitory concentrations of glycopeptide.
引用
收藏
页码:929 / 938
页数:10
相关论文
共 49 条
[31]   Genetic variation among hospital isolates of methicillin-sensitive Staphylococcus aureus:: Evidence for horizontal transfer of virulence genes [J].
Moore, PCL ;
Lindsay, JA .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (08) :2760-2767
[32]  
NAIMI TS, 2002, 10 INT S STAPH STAPH, P19
[33]  
*NAT COMM CLIN LAB, 2000, METH DIL ANT SUSC TE, P7
[34]  
Novick RP, 2000, GRAM-POSITIVE PATHOGENS, P392
[35]   SYNTHESIS OF STAPHYLOCOCCAL VIRULENCE FACTORS IS CONTROLLED BY A REGULATORY RNA MOLECULE [J].
NOVICK, RP ;
ROSS, HF ;
PROJAN, SJ ;
KORNBLUM, J ;
KREISWIRTH, B ;
MOGHAZEH, S .
EMBO JOURNAL, 1993, 12 (10) :3967-3975
[36]   The evolution of pandemic clones of methicillin-resistant Staphylococcus aureus:: Identification of two ancestral genetic backgrounds and the associated mec elements [J].
Oliveira, DC ;
Tomasz, A ;
de Lencastre, H .
MICROBIAL DRUG RESISTANCE-MECHANISMS EPIDEMIOLOGY AND DISEASE, 2001, 7 (04) :349-361
[37]   TRENDS IN ANTIMICROBIAL UTILIZATION AT A TERTIARY TEACHING HOSPITAL DURING A 15-YEAR PERIOD (1978-1992) [J].
PALLARES, R ;
DICK, R ;
WENZEL, RP ;
ADAMS, JR ;
NETTLEMAN, MD .
INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 1993, 14 (07) :376-382
[38]  
PEARMAN JW, 2002, 10 INT S STAPH STAPH, P18
[39]  
RENZONI A, 2002, 42 INT C ANT AG CHEM, P71
[40]   Accessory gene regulator (agr) locus in geographically diverse Staphylococcus aureus isolates with reduced susceptibility to vancomycin [J].
Sakoulas, G ;
Eliopoulos, GM ;
Moellering, RC ;
Wennersten, C ;
Venkataraman, L ;
Novick, RP ;
Gold, HS .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (05) :1492-1502