• We are sorry, but NCBI web applications do not support your browser and may not function properly. More information
Logo of aacPermissionsJournals.ASM.orgJournalAAC ArticleJournal InfoAuthorsReviewers
Antimicrob Agents Chemother. Feb 2003; 47(2): 489–493.
PMCID: PMC151724

Macrolide-Resistant Streptococcus pneumoniae and Streptococcus pyogenes in the Pediatric Population in Germany during 2000-2001


In a nationwide study in Germany covering 13 clinical microbiology laboratories, a total of 307 Streptococcus pyogenes (mainly pharyngitis) and 333 Streptococcus pneumoniae (respiratory tract infections) strains were collected from outpatients less than 16 years of age. The MICs of penicillin G, amoxicillin, cefotaxime, erythromycin A, clindamycin, levofloxacin, and telithromycin were determined by the microdilution method. In S. pyogenes isolates, resistance rates were as follows: penicillin, 0%; erythromycin A, 13.7%; and levofloxacin, 0%. Telithromycin showed good activity against S. pyogenes isolates (MIC90 = 0.25 μg/ml; MIC range, 0.016 to 16 μg/ml). Three strains were found to be telithromycin-resistant (MIC ≥ 4 μg/ml). Erythromycin-resistant strains were characterized for the underlying resistance genotype, with 40.5% having the efflux type mef(A), 38.1% having the erm(A), and 9.5% having the erm(B) genotypes. emm typing of macrolide-resistant S. pyogenes isolates showed emm types 4 (45.2%), 77 (26.2%), and 12 (11.9%) to be predominant. In S. pneumoniae, resistance rates were as follows: penicillin intermediate, 7.5%; penicillin resistant, 0%; erythromycin A, 17.4%; and levofloxacin, 0%. Telithromycin was highly active against pneumococcal isolates (MIC90 ≤ 0.016 μg/ml; range, 0.016 to 0.5 μg/ml). The overall resistance profile of streptococcal respiratory tract isolates is still favorable, but macrolide resistance is of growing concern in Germany.

Streptococcus pyogenes is responsible for the majority of cases of pharyngitis in children and adolescents and can also cause severe life-threatening diseases, such as necrotizing fasciitis and toxic shock syndrome (6). Streptococcus pneumoniae continues to be a significant cause of morbidity and mortality in humans and is responsible for respiratory tract infections and otitis media (15).

Macrolide resistance in S. pneumoniae is usually caused by the presence of the erm(B) or mefE [renamed mef(A)] resistance determinants. The erm(B) protein encodes a 23S rRNA methylase, and most pneumococcal strains that harbor the gene are resistant to 14-, 15-, and 16-membered-ring macrolides, lincosamides, and streptogramin B (MLSB phenotype). The mef(A) protein encodes an efflux pump that leads to resistance to only 14- and 15-membered-ring macrolides (24). Other mechanisms of macrolide resistance have only been described in a few clinical isolates of S. pneumoniae, and changes were clustered in a highly conserved sequence of L4 and in the nucleotide residues of domain V of 23S rRNA, which have a key role in macrolide binding (5, 7, 26).

Macrolide resistance has also been increasingly detected in S. pyogenes in Europe and other parts of the world and is mediated by erm(A), mef(A) and, less commonly, by erm(B) mechanisms.

Telithromycin (HMR 3647) is the first of a novel family of antimicrobials, the ketolides, developed specifically for the treatment of community-acquired respiratory tract infections. The ketolides are a new addition to the MLS group of antimicrobials. Ketolides are characterized by a ketone group, which replaces the cladinose sugar at position 3 of the macrolactone ring.

The aims of the present study were (i) to evaluate the prevalence of antibiotic resistance in S. pyogenes and S. pneumoniae isolates in Germany, (ii) to compare the in vitro activity of the new ketolide telithromycin with those of other antibiotics used for the treatment of respiratory tract infections, and (iii) to identify the predominant macrolide resistance mechanisms and macrolide-resistant serotypes and emm types.

(Presented in part at the 40th Interscience Conference on Antimicrobial Agents and Chemotherapy, Chicago, Ill. [abstr. C2-693], 2001.)


Consecutive clinical isolates collected between November 2000 and March 2001 from patients with community-acquired respiratory infections (acute pharyngitis caused by S. pyogenes and acute otitis media, acute exacerbations of chronic bronchitis, and pneumonia caused by S. pneumoniae) were collected. Only strains from children less than 16 years of age were included.

Strains were shipped to a central laboratory (National Reference Center for Streptococci, Aachen, Germany), where compliance of the isolates with the criteria for inclusion in the study was checked. Confirmation of the identification of isolates was provided by positive bile solubility and inhibition by optochin for S. pneumoniae. S. pyogenes isolates were identified by their hemolysis on sheep blood agar, Lancefield grouping, by using a commercially available agglutination technique (Slidex, Streptokit; BioMérieux, Marcy l'Etoile, France), and by the pyrrolidonyl-arylamidase test.

MIC testing was performed by using the broth microdilution method as recommended by the National Committee for Clinical Laboratory Standards (NCCLS) (17). Commercially manufactured microtiter plates (Micronaut-S; Merlin Diagnostics, Bornheim, Germany) containing penicillin G, cefotaxime, amoxicillin, erythromycin A, clindamycin, levofloxacin, and telithromycin and cation-adjusted Mueller-Hinton broth (Oxoid, Wesel, Germany), plus 5% lysed horse blood (Oxoid), were used. The final inoculum was 5 × 105 CFU/ml. MICs were determined after incubation at 35°C for 24 h in ambient air. S. pneumoniae ATCC 49619 was used as a control strain. Current NCCLS interpretive criteria were used to define antimicrobial resistance. For telithromycin, breakpoints of ≤1 and ≥4 μg/ml were used for sensitivity and resistance, respectively. Isolates were stored at −70°C on porous beads (Microbank; Mast Diagnostics, Rheinfeld, Germany).

For the detection of erm(B) and mef(A) in pneumococcal strains, we used primers described by Trieu-Cuot et al. (27) and Tait-Kamradt et al. (25). For erm(B) we selected 5′-CGA GTG AAA AAG TAC TCA ACC-3′ (positions 362 to 382) and 5′-GGC GTG TTT CAT TGC TTG ATG-3′ (positions 978 to 958), and for mef(A) we selected 5′-AGT ATC ATT AAT CAC TAG TGC-3′ (positions 57 to 77) and 5′-GTA ATA GAT GCA ATC ACA GC-3′ (positions 551 to 532).

Macrolide-resistant S. pyogenes strains were tested by PCR for the presence of erm(A), erm(B), or mef(A). The following primer pairs were used: 5′-TTA TAA CCG GCA AGG AGA-3′ and 5′-GCT TCA GCA CCT GTC TTA ATT GAT-3′ for erm(A), 5′-AAA (C/T)TG ATT TTT (A/T)GT AAA-3′ and 5′-AGG TAA AGG GCA TTT-3′ for erm(B), and 5′-CTA TGA CAG CCT CAA TGC G-3′ and 5′-ACC GAT TCT ATC AGC AAA G-3′ for mef(A) (4). Nucleotide sequences for 23S rRNA and L4 and L22 ribosomal proteins in Escherichia coli and S. pneumoniae were obtained from the Institute for Genome Research website (http://www.tigr.org/.). Specific oligonucleotide primers were designed from these sequences. Primer sequences and conditions for PCR amplifications were those described by Canu et al. (5). The following primers were used: for rplV (L22), 5′-GCAGACGACAAGAAAACACG-3′ and 5′-GCCGACACGCATACCAATTG-3′; for rplD (L4), (i) 5′-AAAGGTAACGTACCAGGTGC-3′ and 5′-GCGTGGTGGTGGTGTTG-3′ and (ii) 5′-CACGAGTGTCAACTTCAAATAC-3′ and 5′-GAGCGTCTACAGCTACG-3′; for rrl (23S rRNA domain II), 5′-CGGCGAGTTACGATTATGATGC-3′ and 5′-CTCTAATGTCGACGCTAGCC-3′; and for rrl (23S rRNA domain V), (i) 5′-CTGTCTCAACGAGAGACTC-3′ and 5′-CTTAGACTCCTACCTATCC-3′ and (ii) 5′-GTATAAGGGAGCTTGACTG-3′ and 5′-GGGTTTCACACTTAGATG-3′.

emm typing of S. pyogenes isolates was performed according to the method of Podbielski et al. (20). Similarity searching was performed by using the N-terminal hypervariable region of the M gene based on the latest information of the Centers for Disease Control website (http://www.cdc.gov/ncidod/-biotech/strep/strains/emmtypes.html). S. pyogenes CS101 (M type 49) was used as a reference strain. Pneumococcal strains were serotyped by using Neufeld's Quellung reaction, with type and factor sera provided by the Statens Serum Institut, Copenhagen, Denmark. S. pneumoniae ATCC 700669 (serotype 23F), S. pneumoniae ATCC 700670 (serotype 6B), S. pneumoniae ATCC 700671 (serotype 9V), and S. pneumoniae ATCC 700672 (serogroup 14) were used as reference strains.

Multilocus sequence typing was performed according to the method of Enright et al. (8). In brief, internal fragments of the glucose kinase (gki), glutamine transporter protein (gtr), glutamate racemase (murI), DNA mismatch repair protein (mutS), transketolase (recP), xanthine phosphoribosyl transferase (xpt), and acetyl coenzyme A acetyltransferase (yqiL) genes were amplified by PCR by using the following primer pairs: gki-up (5′-GGC ATT GGA ATG GGA TCA CC-3′) and gki-dn (5′-TCT CCT GCT GCT GAC AC-3′), gtr-up (5′-GAG GTT GTG GTG ATT ATT GG-3′) and gtr-dn (5′-GCA AAG CCC ATT TCA TGA GTC-3′), murI-up (5′-TGC TGA CTC AAA ATG TTA AAA TGA TTG-3′) and murI-dn (5′-GAT GAT AAT TCA CCG TTA ATG TCA AAA TAG-3′), mutS-up (5′-GAA GAG TCA TCT AGT TTA GAA TAC GAT-3′) and mutS-dn (5′-AGA GAG TTG TCA CTT GCG CGT TTG ATT GCT-3′), recP-up (5′-GCA AAT TCT GGA CAC CCA GG-3′) and recP-dn (5′-CTT TCA CAA GGA TAT GTT GCC-3′), xpt-up (5′-TTA CTT GAA GAA CGC ATC TTA-3′) and xpt-dn (5′-ATG AGG TCA CTT CAA TGC CC-3′), and yqiL-up (5′-TGC AAC AGT ATG GAC TGA CCA GAG AAC AAG ATG C-3′) and yqiL-dn (5′-CAA GGT CTC GTG AAA CCG CTA AAG CCT GAG-3′). For each locus, every different sequence was assigned a distinct allele number, and each isolate was defined by a series of seven integers (the allelic profile) corresponding to the alleles at the seven loci, in the order (alphabetical) of gki, gtr, murI, mutS, recP, xpt, and yqiL. Isolates with an identical allelic profile were assigned to the same sequence type (ST).


In all, 640 isolates comprising 307 S. pyogenes and 333 S. pneumoniae isolates were collected by 13 centers. Pneumococcal strains were isolated from the following sources: nasopharynx (n = 184 [55.3%]), ear swabs (n = 87 [26.1%]), eye swabs (n = 40 [12.0%]), sputum (n = 5 [1.5%]), paracentesis (n = 8 [2.4%]), and other sources (n = 9 [2.7%]). S. pyogenes isolates were mainly isolated from the throat (n = 222 [72.3%]), 46 (15.0%) strains were isolated from other respiratory sources, and 39 (12.7%) strains were isolated from wound infections.

Pneumococci were predominantly isolated from infants and young children ≤5 years of age (n = 221, 66.4% of cases), followed by the children in the 5- to 10-year age group (n = 90, 27.0% of cases). S. pyogenes infections were mainly seen among children 5 to 10 years of age (n = 255, 46.6% of cases).

Among pneumococcal strains, 92.5% of isolates were found to be susceptible to penicillin G (MIC ≤ 0.06 μg/ml) and 7.5% were found to be penicillin intermediate (MIC = 0.1 to 1 μg/ml). Isolates highly resistant to penicillin G (MIC ≥ 2 μg/ml) were not detected. Totals of 58 (17.4%) and 29 (8.7%) strains were resistant to erythromycin A and clindamycin, respectively. Amoxicillin (MIC50 ≤ 0.016 μg/ml; MIC90 = 0.03 μg/ml; all strains were susceptible) and cefotaxime (MIC50 ≤ 0.016 μg/ml; MIC90 < 0.03 μg/ml; 1.5% intermediate) showed good activity against penicillin-susceptible and penicillin-intermediate isolates. All strains were levofloxacin and telithromycin susceptible.

S. pyogenes strains were susceptible to β-lactams. Resistance to erythromycin A was detected in 42 (13.7%) strains. All strains were levofloxacin susceptible, and three strains were resistant to telithromycin.

Erythromycin-resistant strains (n = 100 [58 S. pneumoniae and 42 S. pyogenes]) were analyzed for the underlying resistance determinants. A total of 29 (50%) of the pneumococcal strains showed the erm(B) type of resistance, and 29 (50%) showed the mef(A) type of resistance.

S. pyogenes strains belonged to the following resistance genotypes: mef(A) (n = 22, 42.5%), erm(A) (n = 16, 38.0%), and erm(B) (n = 4, 9.5%).

The antimicrobial susceptibility results for macrolide-resistant strains are presented in Table Table1.1. Mef(A)-positive pneumococcal strains showed slightly elevated telithromycin MICs (MIC90 0.25 μg/ml). All erythromycin-resistant pneumococcal strains [erm(B) and mef(A)-positive strains] remained telithromycin susceptible. Clindamycin was only active against mef(A)-positive strains. Erythromycin-resistant pneumococcal strains showed reduced sensitivity to β-lactams. Penicillin G-intermediate strains were more often found among erm(B)-positive strains (31%) compared to mef(A)-positive strains (10.3%) (Table (Table11).

Antimicrobial susceptibility of macrolide-resistant S. pneumoniae and S. pyogenes isolates with different resistance genotypes

All erm(A)- and 88.2% of mef(A)-positive erythromycin-resistant S. pyogenes remained telithromycin susceptible. All (n = 4) erm(B)-positive S. pyogenes strains were telithromycin intermediate (n = 1) or resistant (n = 3).

The three telithromycin-resistant strains were screened for mutations in 23S rRNA and ribosomal proteins L4 and L22. Since better discrimination between mutated alleles was obtained for denatured DNA fragments between 150 and 500 bp, portions of the rrl gene (domains II and V of 23S rRNA), the entire rplV gene and two overlapping fragments of the L4 gene (rplD) were amplified. The three fragments amplified from rrl, two for domain V and one for domain II, included bases critical for erythromycin resistance: G2057, A2058, A2062, G2505, C2611, and A752 (5). All three strains showed the wild type for L4, L22, and the erm gene, but a new mutation in the 23S rRNA was detected (T2166C). In addition, all strains showed an identical MLS type (ST 52) and emm type (emm 28), indicating the clonal relatedness of the strains. Strains were isolated in different federal states in Germany (Table (Table22).

Characteristics of three telithromycin-resistant S. pyogenes strainsa

Erythromycin-resistant pneumococcal strains were serotyped; serotypes 14 (n = 13, 22.4%), 19F (n = 11, 19.0%), 19A (n = 8, 13.8%), and 23F (n = 7, 12.1%) were predominant. Most erythromycin-resistant serotype 14 (10 of 13 strains) and 23F (6 of 7 strains) strains were mef(A) positive, whereas the MLSB type of resistance was mainly seen among serogroup 19 (18 of 19 strains).

emm typing of erythromycin-resistant S. pyogenes isolates (n = 42) showed that strains of emm type 4 (n = 19, 45.2%) and 77 (n = 11, 26.2%) accounted primarily for macrolide resistance, whereas emm type 12 (n = 5, 11.9%) and emm type 28 (n = 4, 9.5%) were only rarely represented among resistant isolates.

Most (16 of 19 strains) of the emm type 4 and all of the emm type 12 erythromycin-resistant S. pyogenes strains were mef(A) positive. All emm type 77 strains were erm(A)/erm(TR) positive; all telithromycin-nonsusceptible erm(B) strains (n = 4) were emm type 28. All strains were from different geographic regions of Germany.


The worldwide increase in antibiotic resistance in these species has become a serious infectious disease problem within the last 20 years. Prior to the early 1990s, penicillin resistance remained uncommon among clinical isolates of S. pneumoniae in Germany despite the emergence of this problem in many parts of Europe, e.g., Hungary, Spain, and France (2). In contrast, decreased susceptibility to macrolides in S. pyogenes and to β-lactams and macrolides in S. pneumoniae has only recently been reported in Germany (4, 21, 23) and is comparable to resistance rates reported from The Netherlands (10) and Northern European countries (18). Highly penicillin-resistant strains are extremely rare in Germany, as documented by this and other studies. As in many other countries, macrolide resistance in pneumococci has overcome the level of β-lactam resistance in Germany, and rates are still increasing in both S. pneumoniae and S. pyogenes (21, 23, 28).

The rate of erythromycin A resistance in pneumococci documented by the present study (17.4%) is significantly higher than those reported earlier by our working group. A study on pneumococcal respiratory tract infections of strains collected in Germany between 1998 and 1999 covered 358 infections of children <5 years of age; the rate of clarithromycin resistance was 9.2%. The latter and the present studies both used the same laboratory network, and the data should therefore be comparable. Thus, it is alarming to note that the rate of macrolide resistance in pneumococcal respiratory tract isolates in children has nearly doubled within the last 2 years (23).

In addition, a similar increase to even higher levels of macrolide resistance has been reported for pneumococcal invasive disease in both children and adults in Germany (21, 28).

It is noteworthy that there is a parallel macrolide resistance profile in S. pyogenes and S. pneumoniae in children in Germany. In the present study a rate of 13.7% of macrolide resistance was documented in S. pyogenes strains.

In a study by Adam et al. performed between December 1995 and May 1998 in children, macrolide resistance was documented for 6.0% of all S. pyogenes strains tested (n = 4.698) (1). Brandt et al. recently reported macrolide resistance to be present in 17 of 216 (7.9%) S. pyogenes strains isolated from throat infections in the Aachen region of Germany between January 1997 and July 1997 (4). Again, these data suggest that, as for pneumococci, the frequency of macrolide resistance is increasing in Germany.

Methylation of a ribosomal target and active efflux of erythromycin A are the two most important factors involved in the resistance of streptococci to macrolides. Among macrolide-resistant pneumococci in Germany, efflux and MLSB strains are equally distributed, as documented here. Similar data have recently been reported from Canada and the United States, where ~50% of macrolide-resistant S. pneumoniae harbor mef(A) (11, 13). In contrast, in many European countries, such as France and Spain, the spread of macrolide resistance among pneumococci is mainly due to erm(B)-positive strains (9, 19).

Other newer macrolides such as clarithromycin, azithromycin, and roxithromycin are incapable of overcoming MLSB resistance (22). In the present study, the new ketolide telithromycin demonstrated excellent activity against pneumococcal strains, including macrolide-resistant isolates, thus confirming recently published data (16, 22).

In addition, our study showed that there is a clear correlation between genotype profile and phenotype susceptibility patterns in S. pyogenes: erm(A) strains showed high-level resistance to erythromycin and susceptibility to telithromycin; all those highly resistant to macrolides and intermediate or resistant to telithromycin had the erm(B), as recently described by Bemer-Melchior et al. (3) and by Javala et al. (12).

New macrolide resistance genotypes (L4, L22, and 23S rRNA) and mutations others than mef(A) and erm(B) were not observed in the present collection of pneumococcal strains. The three telithromycin-resistant S. pyogenes strains showed wild type for L4, L22, and the erm gene, but a new mutation in the 23S rRNA was detected. The role of this mutation needs to be determined by further transformation experiments. In addition, it is a striking finding of the present study that all telithromycin resistant erm(B) S. pyogenes strains belonged to a single emm type (emm 28) and MLS type (ST 52), indicating the likelihood of clonal relatedness of strains.

The mef(A) gene was not found in erm-positive strains, contrary to observations in a recent study from Finland (14).

In summary, the present study demonstrated the dramatic increase of macrolide resistance in S. pneumoniae and S. pyogenes strains in Germany. Telithromycin showed excellent activity against macrolide-resistant S. pneumoniae possessing the mef(A) or erm(B) genotype and against S. pyogenes possessing the mef(A) and erm(A) genotype. In view of their excellent activity against macrolide-resistant strains, ketolides may be an attractive alternative for the treatment of respiratory tract infections caused by these important pathogens.


S. pyogenes reference strains were kindly provided by Helena Seppälä, Turku, Finland [strain A200, erm(A)/erm(TR) positive]; Aftab Jasir, Lund, Sweden [strains 544 and 517R, erm(B)]; and Joyce Sutcliffe, Groton, Conn. [strain O2C1064, mef(A)-positive]. We thank Nelli Neuberger and Claudia Cremer for excellent technical assistance.

We thank Susanne Reinert (SR Medical Communications GmbH) for organizing and monitoring the study.

We thank the following persons and institutions for their cooperation and for providing isolates: B. Wille, Institut für Krankenhaushygiene und Infektionskontrolle, Giessen, Germany; G. Schonard, Laborarztpraxis, Bad Hersfeld, Germany; U. Grimmer, Laborarztpraxis, Chemnitz, Germany; M. Seewald, Institut für Medizin Diagnostik, Berlin, Germany; R. Pfüller, Medizinisch-Diagnistische Institute, Berlin, Germany; J. Ungeheuer, Labor Frohreich und Partner, Hamburg, Germany; J. Enzenhauer, Osnabrück, Germany; Untersuchungsamt, Hanover, Germany; A. Krenz-Weinreich, Plön, Germany; E. Kühnen, Trier, Germany; H. G. Enders, Stuttgart, Germany; U. Walter, Wülfrath, Germany; J. Lenzen, Bonn, Germany; M. Jacobs, Mikrobiologisches Labor, Dillingen, Germany; W. Dirr, Augsburg, Germany; H. Hofmeister, Weiden, Germany; J. Matthes, Neuötting, Germany; F. Pranada, Gemeinschaftspraxis für Labormedizin, Dortmund, Germany; N. Schöngen, Gemeinschafts Praxis für Labormedizin, Leverkusen, Germany; and B. Hövener, Aachen, Germany.


1. Adam, D., H. Scholz, and M. Helmerking. 2000. Short-course antibiotic treatment of 4782 culture-proven cases of group A streptococcal tonsillopharyngitis and incidence of poststreptococcal sequelae. J. Infect. Dis. 182:509-516. [PubMed]
2. Baquero, F. 1995. Pneumococcal resistance to beta-lactam antibiotics: a global geographic overview. Microb. Drug Resist. 1:115-120. [PubMed]
3. Bemer-Melchior, P., M. E. Juvin, S. Tassin, A. Bryskier, G. C. Schito, and H. B. Drugeon. 2000. In vitro activity of the new ketolide telithromycin compared with those of macrolides against Streptococcus pyogenes: influences of resistance mechanisms and methodological factors. Antimicrob. Agents Chemother. 44:2999-3002. [PMC free article] [PubMed]
4. Brandt, C. M., M. Honscha, N. D. Truong, R. Holland, B. Hovener, A. Bryskier, R. Lütticken, and R. R. Reinert. 2001. Macrolide resistance in Streptococcus pyogenes isolates from throat infections in the region of Aachen, Germany. Microb. Drug Resist. 7:165-170. [PubMed]
5. Canu, A., B. Malbruny, M. Coquemont, T. A. Davies, P. C. Appelbaum, and R. Leclercq. 2002. Diversity of ribosomal mutations conferring resistance to macrolides, clindamycin, streptogramin, and telithromycin in Streptococcus pneumoniae. Antimicrob. Agents Chemother. 46:125-131. [PMC free article] [PubMed]
6. Cunningham, M. W. 2000. Pathogenesis of group A streptococcal infections. Clin. Microbiol. Rev. 13:470-511. [PMC free article] [PubMed]
7. Depardieu, F., and P. Courvalin. 2001. Mutation in 23S rRNA responsible for resistance to 16-membered macrolides and streptogramins in Streptococcus pneumoniae. Antimicrob. Agents Chemother. 45:319-323. [PMC free article] [PubMed]
8. Enright, M. C., B. G. Spratt, A. Kalia, J. H. Cross, and D. E. Bessen. 2001. Multilocus sequence typing of Streptococcus pyogenes and the relationships between emm type and clone. Infect. Immun. 69:2416-2427. [PMC free article] [PubMed]
9. Fitoussi, F., C. Doit, P. Geslin, N. Brahimi, and E. Bingen. 2001. Mechanisms of macrolide resistance in clinical pneumococcal isolates in France. Antimicrob. Agents Chemother. 45:636-638. [PMC free article] [PubMed]
10. Hermans, P. W. M., M. Sluijter, K. Elzenaar, A. van Veen, J. Schonkeren, F. Nooren, W. van Leeuwen, A. de Neeling, B. van Klingeren, H. Verbrugh, and R. de Groot. 1997. Penicillin-resistant Streptococcus pneumoniae in the Netherlands: results of a 1-year molecular epidemiologic survey. J. Infect. Dis. 175:1413-1422. [PubMed]
11. Hoban, D. J., A. K. Wierzbowski, K. Nichol, and G. G. Zhanel. 2001. Macrolide-resistant Streptococcus pneumoniae in Canada during 1998-1999: prevalence of mef(A) and erm(B) and susceptibilities to ketolides. Antimicrob. Agents Chemother. 45:2147-2150. [PMC free article] [PubMed]
12. Jalava, J., J. Kataja, H. Seppala, and P. Huovinen. 2001. In vitro activities of the novel ketolide telithromycin (HMR 3647) against erythromycin-resistant Streptococcus species. Antimicrob. Agents Chemother. 45:789-793. [PMC free article] [PubMed]
13. Johnston, N. J., J. C. De Azavedo, J. D. Kellner, and D. E. Low. 1998. Prevalence and characterization of the mechanisms of macrolide, lincosamide, and streptogramin resistance in isolates of Streptococcus pneumoniae. Antimicrob. Agents Chemother. 42:2425-2426. [PMC free article] [PubMed]
14. Kataja, J., P. Huovinen, M. Skurnik, H. Seppala, et al. 1999. Erythromycin resistance genes in group A streptococci in Finland. Antimicrob. Agents Chemother. 43:48-52. [PMC free article] [PubMed]
15. Musher, D. M. 1992. Infections caused by Streptococcus pneumoniae: clinical spectrum, pathogenesis, immunity, and treatment. Clin. Infect. Dis. 14:801-807. [PubMed]
16. Nagai, K., P. C. Appelbaum, T. A. Davies, L. M. Kelly, D. B. Hoellman, A. T. Andrasevic, L. Drukalska, W. Hryniewicz, M. R. Jacobs, J. Kolman, J. Miciuleviciene, M. Pana, L. Setchanova, M. K. Thege, H. Hupkova, J. Trupl, and P. Urbaskova. 2002. Susceptibilities to telithromycin and six other agents and prevalence of macrolide resistance due to L4 ribosomal protein mutation among 992 pneumococci from 10 Central and Eastern European countries. Antimicrob. Agents Chemother. 46:371-377. [PMC free article] [PubMed]
17. National Committee for Clinical Laboratory Standards. 2000. Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically (M7-A4). Approved standard M100-S8, 4th ed. National Committee for Clinical Laboratory Standards, Wayne, Pa.
18. Nielsen, S. V., and J. Henrichsen. 1996. Incidence of invasive pneumococcal disease and distribution of capsular types of pneumococci in Denmark, 1989-94. Epidemiol. Infect. 117:411-416. [PMC free article] [PubMed]
19. Perez-Trallero, E., C. Fernandez-Mazarrasa, C. Garcia-Rey, E. Bouza, L. Aguilar, J. Garcia-de-Lomas, and F. Baquero. 2001. Antimicrobial susceptibilities of 1,684 Streptococcus pneumoniae and 2,039 Streptococcus pyogenes isolates and their ecological relationships: results of a 1-year (1998-1999) multicenter surveillance study in Spain. Antimicrob. Agents Chemother. 45:3334-3340. [PMC free article] [PubMed]
20. Podbielski, A., B. Melzer, and R. Lutticken. 1991. Application of the polymerase chain reaction to study the M protein(-like) gene family in beta-hemolytic streptococci. Med. Microbiol. Immunol. 180:213-227. [PubMed]
21. Reinert, R. R., A. Al-Lahham, M. Lemperle, C. Tenholte, C. Briefs, S. Haupts, H. H. Gerards, and R. Lütticken. 2002. Emergence of macrolide and penicillin resistance among invasive pneumococcal isolates in Germany. J. Antimicrob. Chemother. 49:61-68. [PubMed]
22. Reinert, R. R., A. Bryskier, and R. Lütticken. 1998. In vitro activities of the new ketolide antibiotics HMR 3004 and HMR 3647 against Streptococcus pneumoniae in Germany. Antimicrob. Agents Chemother. 42:1509-1511. [PMC free article] [PubMed]
23. Reinert, R. R., S. Simic, A. Al-Lahham, S. Reinert, M. Lemperle, and R. Lütticken. 2001. Antimicrobial resistance of Streptococcus pneumoniae recovered from outpatients with respiratory tract infections in Germany from 1998 to 1999: results of a national surveillance study. J. Clin. Microbiol. 39:1187-1189. [PMC free article] [PubMed]
24. Sutcliffe, J., A. Tait Kamradt, and L. Wondrack. 1996. Streptococcus pneumoniae and Streptococcus pyogenes resistant to macrolides but sensitive to clindamycin: a common resistance pattern mediated by an efflux system. Antimicrob. Agents Chemother. 40:1817-1824. [PMC free article] [PubMed]
25. Tait-Kamradt, A., J. Clancy, M. Cronan, F. Dib-Hajj, L. Wondrack, W. Yuan, and J. Sutcliffe. 1997. MefE is necessary for the erythromycin-resistant M phenotype in Streptococcus pneumoniae. Antimicrob. Agents Chemother. 41:2251-2255. [PMC free article] [PubMed]
26. Tait-Kamradt, A., T. Davies, M. Cronan, M. R. Jacobs, P. C. Appelbaum, and J. Sutcliffe. 2000. Mutations in 23S rRNA and ribosomal protein L4 account for resistance in pneumococcal strains selected in vitro by macrolide passage. Antimicrob. Agents Chemother. 44:2118-2125. [PMC free article] [PubMed]
27. Trieu-Cuot, P., C. Poyart-Salmeron, C. Carlier, and P. Courvalin. 1990. Nucleotide sequence of the erythromycin resistance gene of the conjugative transposon Tn1545. Nucleic Acids Research 18:3660.. [PMC free article] [PubMed]
28. von Kries, R., A. Siedler, H. J. Schmitt, and R. R. Reinert. 2000. Proportion of invasive pneumococcal infections in German children preventable by pneumococcal conjugate vaccines. Clin. Infect. Dis. 31:482-487. [PubMed]

Articles from Antimicrobial Agents and Chemotherapy are provided here courtesy of American Society for Microbiology (ASM)
PubReader format: click here to try


Related citations in PubMed

See reviews...See all...

Cited by other articles in PMC

See all...


Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...