Epidemiology, laboratory detection, and therapy of penicillin-resistant streptococcal infections

被引:19
作者
Jones, RN
Wilson, WR
机构
[1] Univ Iowa, Coll Med, Dept Pathol, Div Med Microbiol, Iowa City, IA 52242 USA
[2] Mayo Clin & Mayo Grad Sch Med, Rochester, MN 55901 USA
关键词
D O I
10.1016/S0732-8893(98)00039-X
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Streptococci cause a wide range of infections in humans including respiratory tract infections, endocarditis, meningitis, bacteremias, and skin and soft tissue lesions. Mutations in the penicillin binding proteins target sites in these organisms have recently caused resistance to penicillins and cephalosporins. The passage of resistant genetic material from one streptococcal species to another has been recognized as one of the mechanisms by which this resistance has occurred and spread. Such resistance has been a particular problem in Streptococcus pneumoniae and viridans group streptococci with penicillin resistance levels in excess of 25%, now common ir? both groups of organisms worldwide. Fourth-generation cephalosporins, with their enhanced antibacterial activity against Grampositive organisms (cefpirome > cefepime) and their increased stability to the beta-lactamases produced by many bacterial species, offer a new option for the treatment of potentially life-threatening infections such as pneumococcal pneumonia and meningitis with or without bacteremia. Clinical trials are currently in place to evaluate the role of these agents in these, and other, indications of Gram-positive infections. Prior studies of cefpirome therapy for infections caused by Streptococcus spp. were successful, and recent expanded in vitro investi gations profess a future for expanded use of cefpirome to treat infections produced by several Gram-positive species. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:453 / 459
页数:7
相关论文
共 37 条
[1]   IN-VITRO ACTIVITIES OF 22-BETA-LACTAM ANTIBIOTICS AGAINST PENICILLIN-RESISTANT AND PENICILLIN-SUSCEPTIBLE VIRIDANS GROUP STREPTOCOCCI ISOLATED FROM BLOOD [J].
ALCAIDE, F ;
LINARES, J ;
PALLARES, R ;
CARRATALA, J ;
BENITEZ, MA ;
GUDIOL, F ;
MARTIN, R .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (10) :2243-2247
[2]   Antipneumococcal activities of cefpirome and cefotaxime, alone and in combination with vancomycin and teicoplanin, determined by checkerboard and time-kill methods [J].
Bajaksouzian, S ;
Visalli, MA ;
Jacobs, MR ;
Appelbaum, PC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (09) :1973-1976
[3]   Comparative in vitro assessment of sparfloxacin activity and spectrum using results from over 14,000 pathogens isolated at 190 medical centers in the USA [J].
Ballow, CH ;
Jones, RN ;
Johnson, DM ;
Deinhart, JA ;
Schentag, JJ ;
Tritsch, M ;
Ellis, S ;
Burger, J ;
Cole, E ;
Venezia, R ;
George, M ;
Wolf, D ;
Slifkin, M ;
DePalma, J ;
Rudrik, J ;
Sullivan, K ;
Lewis, G ;
Dooley, G ;
Sawicki, R ;
Desiderio, D ;
Louma, R ;
Motyl, M ;
Ruffin, L ;
Torresan, J ;
Dunaway, G ;
Keck, G ;
Truitt, L ;
Brecher, S ;
VanEnk, R ;
Whelen, C ;
Fader, R ;
Whisler, G ;
Jenkins, S ;
Thacker, D ;
DAmato, R ;
Buck, R ;
Buescher, S ;
Lambert, K ;
Tristram, D ;
Kehl, S ;
Lawson, C ;
Washington, J ;
Robertson, K ;
Beall, A ;
Padgett, L ;
Rahman, L ;
Riddle, G ;
DellaLatta, P ;
Marcon, M ;
Northern, I .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1997, 29 (03) :173-186
[4]   GENETICS OF HIGH-LEVEL PENICILLIN RESISTANCE IN CLINICAL ISOLATES OF STREPTOCOCCUS-PNEUMONIAE [J].
BARCUS, VA ;
GHANEKAR, K ;
YEO, M ;
COFFEY, TJ ;
DOWSON, CG .
FEMS MICROBIOLOGY LETTERS, 1995, 126 (03) :299-303
[5]   FAILURE OF TIME-KILL SYNERGY STUDIES USING SUBINHIBITORY ANTIMICROBIAL CONCENTRATIONS TO PREDICT IN-VIVO ANTAGONISM OF CEPHALOSPORIN-RIFAMPIN COMBINATIONS AGAINST STAPHYLOCOCCUS-AUREUS [J].
BRANDT, CM ;
ROUSE, MS ;
TALLAN, BM ;
WILSON, WR ;
STECKELBERG, JM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (09) :2191-2193
[6]   EMERGENCE OF DRUG-RESISTANT PNEUMOCOCCAL INFECTIONS IN THE UNITED-STATES [J].
BREIMAN, RF ;
BUTLER, JC ;
TENOVER, FC ;
ELLIOTT, JA ;
FACKLAM, RR .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1994, 271 (23) :1831-1835
[7]   PROSPECTIVE RANDOMIZED PHASE-II STUDY OF INTRAVENOUS CEFPIROME 1G OR 2G BD IN THE TREATMENT OF HOSPITALIZED-PATIENTS WITH DIFFERENT INFECTIONS [J].
CARBON, C ;
ORTIZ, RG ;
DICTAR, M ;
MORMANDI, JO ;
CLARA, LO ;
GRANINGER, W ;
MITTERMAYER, H ;
KOSMIDIS, J ;
GIAMARELLOU, H ;
VERHOEVEN, H ;
HELLEBRAND, JTH ;
DIJKMAN, GA ;
HUMBERT, G ;
MICOUD, M ;
VEYSSIER, P ;
BAZIN, C ;
LENG, B ;
DUMONT, R ;
VACHON, F ;
PORTER, H ;
SOLLET, JP ;
FROTTIER, J ;
GARRE, M ;
GIBERT, C ;
BERTRAND, A ;
JURIAANS, E ;
VANWYK, J .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1992, 29 :87-94
[8]   RELATEDNESS BETWEEN STREPTOCOCCUS-PNEUMONIAE AND VIRIDANS STREPTOCOCCI - TRANSFER OF PENICILLIN RESISTANCE DETERMINANTS AND IMMUNOLOGICAL SIMILARITIES OF PENICILLIN-BINDING PROTEINS [J].
CHALKLEY, L ;
SCHUSTER, C ;
POTGIETER, E ;
HAKENBECK, R .
FEMS MICROBIOLOGY LETTERS, 1991, 90 (01) :35-42
[9]  
CHERUBIN CE, 1989, REV INFECT DIS, V11, P526
[10]   Emerging resistance to antimicrobial agents in gram-positive bacteria - Enterococci, staphylococci and nonpneumococcal streptococci [J].
Cormican, MG ;
Jones, RN .
DRUGS, 1996, 51 :6-12