Skip to main page content

• HOME
• Current Issue
• Archive
• Alerts
• About ASM
• Contact us
• Tech Support
• Journals.ASM.org

This Article Abstract Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints and Permissions Copyright Information Books from ASM Press MicrobeWorld Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Gonzalez, J. J. Search for Related Content PubMed PubMed Citation Articles by Gonzalez, J. J.

 Previous Article  |  Next Article 

Antimicrobial Agents and Chemotherapy, June 2005, p. 2525-2527, Vol. 49, No. 6
0066-4804/05/$08.00+0     doi:10.1128/AAC.49.6.2525-2527.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Multicenter Study of the Mechanisms of Resistance and Clonal Relationships of Streptococcus agalactiae Isolates Resistant to Macrolides, Lincosamides, and Ketolides in Spain

J. J. Gonzalez, A. Andreu,^* the Spanish Group for the Study of Perinatal Infection from the Spanish Society for Clinical Microbiology and Infectious Diseases,

Servicio de Microbiologia, Hospital Vall d'Hebron, 08035 Barcelona, Spain

Received 26 November 2004/ Returned for modification 20 December 2004/ Accepted 22 February 2005

Top Abstract Text References

 
Macrolide, lincosamide, and ketolide mechanisms of resistance and clonal relationships were characterized in a collection of 79 resistant group B streptococcus isolates obtained from neonates or pregnant women. The erm(B), erm(TR), and mef(A) genes were present in 62%, 30.4%, and 3.8% of the isolates, respectively. There was considerable clonal diversity among them.

Top Abstract Text References

 
Streptococcus agalactiae (group B streptococcus [GBS]) is the main cause of neonatal sepsis. In Spain, 10% to 18.5% of pregnant women are colonized by GBS in the vagina or lower rectum (3, 8; A. Andreu et al., Abstr. 12th Eur. Congr. Clin. Microbiol. Infect. Dis., Milan, Italy). For prophylactic purposes, colonized women receive penicillin G intrapartum, except for those allergic to penicillin, who receive erythromycin or clindamycin, as recommended by Spanish and U.S. guidelines (16, 17). A recent multicenter study conducted in Spain investigating GBS susceptibility has shown that penicillin, ampicillin, vancomycin, and levofloxacin are always active; however, resistance to erythromycin and azithromycin has risen to 12.45%, resistance to clindamycin has risen to 11.80%, and resistance to telithromycin has risen to 1.80% (9).

Macrolide resistance in streptococci is mainly due to a macrolide-specific efflux mechanism encoded by the mef(A) gene, ribosomal modification by a methylase associated with erm (erythromycin ribosome methylase) genes, and mutations in 23S rRNA and ribosomal proteins L4 and L22 (5, 15, 19, 20). Resistance conferred by Erm methylases can be expressed either constitutively (cMLS_B) or upon induction (iMLS_B). Drug modification by lincosamide nucleotidyltransferases, encoded by the lin(B) genes, which can confer resistance to lincosamides but does not affect macrolides, was first described in Enterococcus faecium (4) and found in Streptococcus agalactiae by Azavedo et al. in 2001 (7).

The aim of this study was to characterize the mechanisms of macrolide, lincosamide, and telithromycin resistance among GBS isolates collected in a multicenter study in Spain and analyze clonal relationships among the resistant isolates.

A total of 79 isolates resistant to macrolides, lincosamides, or telithromycin were studied. The isolates were collected in a multicenter study investigating the antimicrobial susceptibility of 610 GBS isolates from 25 hospitals across Spain (9). Among them, 131 were isolated between 1997 and 2002 from the blood of newborns with early onset GBS disease, and 479 were collected during 2002 from the vagina or rectum of pregnant women. No significant differences were seen between resistant isolates from newborns or pregnant women. The presence of mef(A), erm(B), erm(TR), and lin(B) genes, conferring resistance to macrolides and/or lincosamides, was detected by PCR as previously described (4, 12, 18). The following strains were used as PCR-positive controls: Streptococcus pyogenes containing the mef(A) gene, S. pneumoniae containing erm(TR), S. pneumoniae containing erm(B) (all kindly provided by R. Leclercq), and S. agalactiae containing lin(B) (kindly provided by J. de Azavedo). Pulsed-field gel electrophoresis (PFGE) was performed to analyze chromosomal DNA macrorestriction patterns. DNA was extracted as described by Gordillo et al. (10) and digested with 50 U of SmaI. The percentage of similarity between each banding pattern was determined with Dice's coincidence index, and the distance between clusters was calculated by the unweighted pair-group method with arithmetic averages (UPGMA), using TDI Lane Manager software (TDI, Spain). Statistical assessments were performed with SPSS for Windows (version 10.0). Relationships among clusters and macrolide resistance genes were analyzed using Fisher's exact test. P values of less than 0.05 were considered statistically significant.

The 79 GBS isolates studied include 76 macrolide- and lincosamide-resistant isolates: 69 displayed a cMLS_B phenotype of resistance, 4 an iMLS_b phenotype, and 3 the efflux pump phenotype. The remaining three isolates were clindamycin resistant but macrolide susceptible. Among the 69 isolates with a cMLS_B phenotype, 11 were telithromycin resistant, with MICs ranging from 4 to >32 mg/liter (see Table 2). The interpretative categories used for each antibiotic followed NCCLS recommendations (13). The MIC breakpoint for telithromycin was taken from Comité de l'Antibiogramme de la Societé Française de Microbiologie recommendations (6).

View this table: [in this window] [in a new window]

TABLE 2. Association between phenotype, genotype, and MICs among 76 GBS isolates resistant to erythromycin and 11 resistant to telithromycina

The distribution of genes encoding macrolide-lincosamide resistance according to phenotype is reported in Table 1. The erm(B) gene was present in 62% of macrolide-resistant isolates, erm(TR) in 30.4%, mef(A) in 3.8%, and lin(B) in 0%. Among GBS isolates with constitutive resistance to MLS_B antibiotics, 71% showed the erm(B) gene and 29% the erm(TR) gene. All four GBS isolates with an inducible resistant phenotype presented the erm(TR) gene. The three isolates with a phenotype typical of efflux pump had the mef(A) gene. Among the 11 telithromycin-resistant isolates, 10 harbored the erm(B) gene and 1 harbored the erm(TR) gene.

View this table: [in this window] [in a new window]

TABLE 1. Correlation between genes for macrolide-lincosamide resistance and phenotype in 79 GBS isolates

Among GBS isolates presenting the cMLS_B resistance phenotype, those associated with erm(B) had MICs of erythromycin identical to those associated with erm(TR) (Table 2). However, isolates with erm(TR) and an inducible phenotype presented lower MICs.

Erythromycin- and lincosamide-resistant GBS isolates showed high clonal diversity. Among the 79 isolates studied, 48 different PFGE patterns were found. Fourteen isolates were repeatedly nontypeable by PFGE, because of incomplete DNA digestion. Four main clusters were defined at 50% homology (CI to CIV): cluster I contained 64.7% of the isolates, CII contained 32.3%, and CIII and CIV contained one isolate each. The CI isolates mainly included those with the erm(B) gene (P = 0.012, ² test), and the CII isolates mainly included those with the erm(TR) gene (P = 0.002, ² test). Resistant isolates causing colonization and sepsis were distributed equally in the different clusters. The three isolates resistant to clindamycin and susceptible to erythromycin and the 11 telithromycin-resistant isolates showed no cluster association.

Our results agree with previous studies conducted in Spain reporting that Erm(B) methylase is the main cause of macrolide resistance in GBS, followed by Erm(TR) (1, 14). This mechanism also predominates in other countries, except in Canada and the United States, where Erm(TR) methylase is the main mechanism (2, 7, 11). In our study, none of the isolates harbored more than one gene for macrolide resistance. However, Betriu et al. (1) found that 26.92% of isolates showed various combinations, mainly erm(B) with erm(A); nonetheless, the origin of the isolates studied was related not only to neonatal sepsis but also to skin and soft tissues, urine, respiratory tract, and others.

The uncommon phenotype of resistance to clindamycin but susceptibility to macrolides has been found by other groups in Spanish isolates (A. B. Campo-Esquisabel, E. Ugalde, A. Portillo, M. A. Martinez-Bernal, and L. Martinez-Martinez, Abstr. 11th Spanish Congr. Clin. Microb. Infect. Dis, abstr. 4, 2004). In 2001, de Azavedo et al. reported a GBS isolate with this type of resistance encoded by the lin(B) gene of Enterococcus faecium, which codes for a lincosamide-inactivating nucleotidyltransferase (7). However, our three resistant isolates did not present the lin(B) gene or the other genes conferring resistance to macrolides and lincosamides.

The presence of the previously unreported 11 (1.4%) telithromycin-resistant GBS isolates implies the need to investigate the mechanism of resistance involved and its dissemination.

 
We are grateful to R. Leclercq for providing Streptococcus pyogenes harboring the mef(A) gene, Streptococcus pneumoniae with erm(TR), and Streptococcus pneumoniae with erm(B) and J. C. S. de Azavedo for Streptococcus agalactiae with lin(B), which were used as control isolates. We wish to thank Guillem Prats, Head of the Microbiology Department of Hospital Vall d'Hebron, for his helpful comments during the writing of the manuscript.

This work was partially supported by the "Red Española de Investigación en Patología Infecciosa" (REIPI-FIS C3/14) and Aventis Pharma, SA.

The following are members of the Spanish Group for the Study of Perinatal Infection: P. Alomar, Hospital Son Dureta, Palma de Mallorca; M. A. Blanco, Hospital Santa Cristina, Madrid; A. Bordes, Hospital Dr. Negrin, Gran Canaria; J. Bosch, Hospital Clínic i Provincial, Barcelona; J. Cacho, Hospital de Getafe, Getafe, Madrid; A. Cid, Hospital da Costa, Burela, Lugo; A. Coira, Hospital Xeral-Calde, Lugo; M. de Cueto, Hospital Virgen Macarena, Sevilla; E. Dopico, Laboratori Clínic l'Hospitalet, l'Hospitalet de Llobregat, Barcelona; J. M. García-Arenzana, Complejo Hospitalario Donosti, Donosti; A. Gil-Setas and A. Mazón, Ambulatorio General Solchaga, Pamplona; C. Gimeno, Hospital Clínico, Valencia; C. Guardia, Laboratori Clínic del Barcelonés Nord i Vallés-CAP Dr. Robert, Badalona, Barcelona; S. Illescas, Hospital Virgen Altagracia, Manzanares, Ciudad Real; T. Juncosa, Hospital Sant Joan de Deu, Esplugues de Llobregat, Barcelona; J. Lite, Hospital Mutua de Terrassa, Terrassa, Barcelona; R. Martinez and B. Orden, Centro Especialidades Argüelles, Madrid; M. P. Perez-Pascual, Hospital Río Ortega, Valladolid; M. Rebollo, Hospital Infanta Cristina, Badajoz; M. de la Rosa, Hospital Virgen de las Nieves, Granada; M. Rodriguez-Mayo, Hospital Arquitecto Marcide, Ferrol; I. Sanfeliu, Coorporació Parc Taulí, Sabadell, Barcelona; F. Sanz, Hospital 12 Octubre, Madrid; P. Villanueva, Ambulatorio Nuestra Señora de Estíbaliz, Vitoria; and L. Viñas, Institut Dexeus, Barcelona.

 
* Corresponding author. Mailing address: Servicio de Microbiología, Hospital Vall d'Hebron, Pg. Vall d'Hebron 119-129, 08035 Barcelona, Spain. Phone: 34-93-274 6867. Fax: 34-93-274 6801. E-mail: anandreu{at}vhebron.net.

Contributing members of the Spanish Group for the Study of Perinatal Infection from the Spanish Society for Clinical Microbiology and Infectious Diseases are listed in Acknowledgments.

Top Abstract Text References

 

1
1. Betriu, C., E. Culebras, M. Gomez, I. Rodriguez-Avial, B. A. Sánchez, M. C. Ágreda, and J. J. Picazo. 2003. Erythromycin and clindamycin resistance and telithromycin susceptibility in Streptococcus agalactiae. Antimicrob. Agents Chemother. 47:1112-1114.[Abstract/Free Full Text]
2
2. Biedenbach, D. J., J. M. Stephen, and R. N. Jones. 2003. Antimicrobial susceptibility profile among beta-haemolytic Streptococcus spp. collected in the SENTRY Antimicrobial Surveillance Program—North America, 2001. Diagn. Microbiol. Infect. Dis. 46:291-294.[CrossRef][Medline]
3
3. Bosch, J., A. Palou, L. Serra, E. Alvarez, M. Ricart, R. Ros et al. 1997. Sepsis neonatal precoz por Streptococcus agalactiae: estudio de diez años (1985-1994) y eficacia de la profilaxis intraparto. An. Esp. Pedriar. 46:272-276.
4
4. Bozdogan, B., L. Berrezouga, M.-S. Kuo, D. A. Yurek, K. A. Farley, B. J. Stockman, and R. Leclercq. 1999. A new resistance gene, linB, conferring resistance to lincosamides by nucleotidylation in Enterococcus faecium HM1025. Antimicrob. Agents Chemother. 43:925-929.[Abstract/Free Full Text]
5
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.[Abstract/Free Full Text]
6
6. Comité de l'Antibiogramme de la Société Française de Microbiologie. 2004. 2004 Report of the Comité de l'Antibiogramme de la Societé Française de Microbiologie. Communiqué 2004. Societé Française de Microbiologie, Paris, France.
7
7. De Azavedo, J. C. S., M. McGavin, C. Duncan, D. E. Low, and A. McGeer. 2001. Prevalence and mechanisms of macrolide resistance in invasive and noninvasive group B streptococcus isolates from Ontario, Canada. Antimicrob. Agents Chemother. 45:3504-3508.[Abstract/Free Full Text]
8
8. Gil, E. G., M. C. Rodriguez, R. Bartolomé, B. Berjano, L. Cabero, and A. Andreu. 1999. Evaluation of the Granada agar plate for detection of vaginal and rectal group B streptococci in pregnant women. J. Clin. Microbiol. 37:2648-2651.[Abstract/Free Full Text]
9
9. Gonzalez, J. J., A. Andreu, P. Alomar, M. A. Blanco, A. Bordes, J. Bosch, J. Cacho, A. Cid, A. Coira, M. de Cueto, E. Dopico, J. M. García-Arenzana, A. Gil, A. Mazón, C. Gimeno, C. Guardia, S. Illescas, T. Juncosa, J. Lite, R. Martínez, B. Orden, M. P. Perez, M. Rebollo, M. De La Rosa, M. Rodriguez, I. Sanfeliu, F. Sanz, P. Villanueva, and L. Viñas. 2004. Susceptibility of vertically transmitted group B streptococci to antimicrobial agents. Multicenter study. Enferm. Infecc. Microbiol. Clin. 22:286-291.[CrossRef][Medline]
10
10. Gordillo, M. E., K. V. Singh, C. J. Baker, and B. E. Murray. 1993. Typing of group B streptococci: comparison of pulsed-field gel electrophoresis and conventional electrophoresis. J. Clin. Microbiol. 31:1430-1434.[Abstract/Free Full Text]
11
11. Heelan, J. S., M. E. Hasenbein, and A. J. McAdam. 2004. Resistance of group B streptococcus to selected antibiotics, including erythromycin and clindamycin. J. Clin. Microbiol. 42:1263-1264.[Abstract/Free Full Text]
12
12. Kataja, J., H. Seppala, M. Skurnik, H. Sarkkinen, and P. Huovinen. 1998. Different erythromycin resistance mechanisms in group C and group G streptococci. Antimicrob. Agents Chemother. 42:1493-1494.[Abstract/Free Full Text]
13
13. NCCLS. 2004. Performance standards for antimicrobial susceptibility testing: fourteenth informational supplement. NCCLS document M100-S14. National Committee for Clinical Laboratory Standards, Wayne, Pa.
14
14. Portillo, A., M. J. Gastanares, F. Ruiz-Larrea, and C. Torres. 2003. Clonal diversity among erythromycin-resistant beta-haemolytic Streptococcus isolates in La Rioja, Spain. J. Antimicrob Chemother. 52:485-488.[Abstract/Free Full Text]
15
15. Reinert, R. R., A. Wild, P. Appelbaum, R. Lutticken, M. Y. Cil, and A. Al-Lahham. 2003. Ribosomal mutations conferring resistance to macrolides in Streptococcus pneumoniae clinical strains isolated in Germany. Antimicrob Agents Chemother. 47:2319-2322.[Abstract/Free Full Text]
16
16. Schrag, S., R. Gorwitz, K. Fultz-Butts, and A. Schuchat. 2002. Prevention of perinatal group B streptococcal disease. Revised guidelines from CDC. Morb. Mortal. Wkly. Rep. Recomm. Rep. 51:1-22.
17
17. Spanish Society of Obstetrics and Gynecology, Spanish Society of Neonatology, Spanish Society of Infectious Diseases and Clinical Microbiology, Spanish Society of Chemotherapy, and Spanish Society of Family and Community Medicine. 2003. Prevention of perinatal group B streptococcal disease. Spanish revised guidelines. Enferm. Infecc. Microbiol. Clin. 21:417-423.[CrossRef][Medline]
18
18. Sutcliffe, J., T. Grebe, A. Tait-Kamradt, and L. Wondrack. 1996. Detection of erythromycin-resistant determinants by PCR. Antimicrob. Agents Chemother. 40:2562-2566.[Abstract]
19
19. Weisblum, B. 1998. Macrolide resistance. Drug Resist. Updates 1:29-41.
20
20. Zhong, P., and V. D. Shortridge. 2000. The role of efflux in macrolide resistance. Drug Resist. Updates 3:325-329.[CrossRef][Medline]

---

Antimicrobial Agents and Chemotherapy, June 2005, p. 2525-2527, Vol. 49, No. 6
0066-4804/05/$08.00+0     doi:10.1128/AAC.49.6.2525-2527.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

This article has been cited by other articles:

• Marimon, J. M., Valiente, A., Ercibengoa, M., Garcia-Arenzana, J. M., Perez-Trallero, E. (2005). Erythromycin Resistance and Genetic Elements Carrying Macrolide Efflux Genes in Streptococcus agalactiae. Antimicrob. Agents Chemother. 49: 5069-5074 [Abstract] [Full Text]  

This Article Abstract Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints and Permissions Copyright Information Books from ASM Press MicrobeWorld Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Gonzalez, J. J. Search for Related Content PubMed PubMed Citation Articles by Gonzalez, J. J.