Emergence of the M phenotype of erythromycin-resistant Pneumococci in South Africa

被引:34
作者
Widdowson, CA [1 ]
Klugman, KP [1 ]
机构
[1] S African Inst Med Res, Dept Clin Microbiol & Infect Dis, ZA-2000 Johannesburg, South Africa
关键词
D O I
10.3201/eid0402.980216
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Erythromycin-resistant pneumococci have been isolated in South Africa since 1978; however, from 1987 to 1996, resistance to macrolides was only detected in 270 (2.7%) of 9,868 blood or cerebrospinal fluid (CSF) pneumococcal isolates, most of which were obtained from the public sector. In South Africa, macrolide use in the public sector is estimated at 56% of that in the private sector. Most erythromycin-resistant strains (89%) exhibited resistance to erythromycin and clindamycin (macrolide-lincosamide-streptogramin in B phenotype). In the United States, most erythromycin-resistant pneumococci exhibit the newly described M phenotype (resistance to erythromycin alone), associated with the mefE gene. The M phenotype in South Africa increased significantly in the last 10 years, from 1 of 5,115 to 28 of 4,735 of blood and CSF isolates received from 1987 to 1991 compared with 1992 to 1996 (p = 5x10(-7)). These data suggest that, although macrolide resistance in pneumococci remains low in the public sector, the mefE gene is rapidly emerging in South Africa.
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页码:277 / 281
页数:5
相关论文
共 28 条
[1]  
Aszkenasy O M, 1995, Commun Dis Rep CDR Rev, V5, pR45
[2]   IN-VITRO ACTIVITIES OF A STREPTOGRAMIN (RP59500), 3 MACROLIDES, AND AN AZALIDE AGAINST 4 RESPIRATORY-TRACT PATHOGENS [J].
BARRY, AL ;
FUCHS, PC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (01) :238-240
[3]   FAILURE OF PRISTINAMYCIN TREATMENT IN A CASE OF PNEUMOCOCCAL PNEUMONIA [J].
BURUCOA, C ;
PASDELOUP, T ;
CHAPON, C ;
FAUCHERE, JL ;
ROBERT, R .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1995, 14 (04) :341-342
[4]   The continued emergence of drug-resistant Streptococcus pneumoniae in the United States: An update from the centers for disease control and prevention's pneumococcal sentinel surveillance system [J].
Butler, JC ;
Hofmann, J ;
Cetron, MS ;
Elliott, JA ;
Facklam, RR ;
Breiman, RF ;
Camp, C ;
Charache, P ;
Dern, R ;
Jackson, M ;
Hadley, WK ;
HoppeBauer, J ;
Jacobs, MR ;
Schreiber, J ;
Boxerbaum, B ;
Menuey, BC ;
Tyler, PG ;
Monahan, J ;
Moore, H ;
Siegel, JD ;
Sherer, D ;
Rogers, P ;
Welch, D ;
Fine, D ;
Radike, J ;
Fiore, A ;
Alexander, M ;
Deaver, K .
JOURNAL OF INFECTIOUS DISEASES, 1996, 174 (05) :986-993
[5]  
DIXON JMS, 1967, LANCET, V1, P573
[6]   Antimicrobial resistance of Streptococcus pneumoniae recovered from outpatients in the United States during the winter months of 1994 to 1995: Results of a 30-center national surveillance study [J].
Doern, GV ;
Brueggemann, A ;
Holley, HP ;
Rauch, AM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (05) :1208-1213
[7]   Susceptibilities of 228 penicillin- and erythromycin-susceptible and -resistant pneumococci to RU 64004, a new ketolide, compared with susceptibilities to 16 other agents [J].
Ednie, LM ;
Spangler, SK ;
Jacobs, MR ;
Appelbaum, PC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (05) :1033-1036
[8]   SUBSTRATE-BINDING AND ANTIBIOTIC-BINDING SITES AT PEPTIDYL-TRANSFERASE CENTRE OF ESCHERICHIA-COLI RIBOSOMES [J].
FERNANDEZMUNOZ, R ;
MONRO, RE ;
TORRESPI.R ;
VAZQUEZ, D .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1971, 23 (01) :185-+
[9]   FAILURE OF CHLORAMPHENICOL THERAPY IN PENICILLIN-RESISTANT PNEUMOCOCCAL MENINGITIS [J].
FRIEDLAND, IR ;
KLUGMAN, KP .
LANCET, 1992, 339 (8790) :405-408