Skip to main content
Brazilian Journal of Microbiology logoLink to Brazilian Journal of Microbiology
. 2008 Jun 1;39(2):245–250. doi: 10.1590/S1517-83822008000200009

Antibiotic susceptibility patterns and prevalence of group B Streptococcus isolated from pregnant women in Misiones, Argentina

M Quiroga 1, E Pegels 1, P Oviedo 1, E Pereyra 2, M Vergara 1
PMCID: PMC3768385  PMID: 24031210

Abstract

This study was performed to determine the susceptibility patterns and the colonization rate of Group B Streptococcus (GBS) in a population of pregnant women. From January 2004 to December 2006, vaginal-rectal swabs were obtained from 1105 women attending Dr. Ramón Madariaga Hospital, in Posadas, Misiones, Argentina. The carriage rate of GBS among pregnant women was 7.6%. A total of 62 GBS strains were randomly selected for in vitro susceptibility testing to penicillin G, ampicillin, tetracycline, levofloxacin, gatifloxacin, ciprofloxacin, quinupristin-dalfopristin, linezolid, vancomycin, rifampicin, trimethoprim- sulfametoxazol, nitrofurantoin, gentamicin, clindamycin and erythromycin, and determination of resistance phenotypes. No resistance to penicillin, ampicillin, quinupristin-dalfopristin, linezolid, and vancomycin was found. Of the isolates examined 96.8%, 98.3%, 46.8%, and 29.0% were susceptible to rifampicin, nitrofurantoin, trimethoprim-sulfametoxazol and tetracycline, respectively. Rank order of susceptibility for the quinolones was: gatifloxacin (98.4%) > levofloxacin (93.5%) > ciprofloxacin (64.5%). The rate of resistance to erythromycin (9.7%) was higher than that of other reports from Argentina. High-level resistance to gentamicin was not detected in any of the isolates. Based on our finding of 50% of GBS isolates with MIC to gentamicin equal o lower than 8 μg/ml, a concentration used in one of the selective media recommended for GBS isolation, we suggested, at least in our population, the use of nalidixic acid and colistin in selective media with the aim to improve the sensitivity of screening cultures for GBS carriage in women.

Keywords: Group B Streptococcus, antibiotic susceptibility, prevalence, pregnant women, Argentina

INTRODUCTION

Group B Streptococcus (GBS) is the most common cause of early-onset neonatal sepsis in developed countries (3).

Newborn acquire the organisms intrapartum from their mothers, who are colonized with GBS in the genital tract (41).

Different studies (10) reported that risk-based or screening- based strategies recommended by the Centers for Disease Control and Prevention (CDC) had caused a significant decline in the prevalence of neonatal GBS infections (9,41).

When public health decisions for implementing prevention strategies are needed, a basic point is the knowledge of the prevalence of maternal GBS colonization.

In Argentina, this prevalence varies widely between geographic areas and even between different populations. For instead, it was reported a maternal colonization rate of 1.4% in Cordoba, Argentina (29), 3.2% in Rosario, Argentina (46), or 18.15% in Jose de San Martin Clinical Hospital (22) and 9.39% in Posadas Hospital (17), both of them situated in Buenos Aires, Argentina.

Dr. Ramón Madariaga Hospital is a public institution that serves primarily the uninsured residents of Posadas, the most important city of Misiones, a province situated in the northeaster of Argentina with strong boundaries with Paraguay and Brazil. Although Dr. Ramón Madariaga Hospital accounts for approximately 65% of the city’s births, no data are available about the prevalence of maternal GBS carriers.

Penicillin and ampicillin are the drugs of choice for prevention or treatment of GBS infections, and clindamycin and erythromycin are the recommended alternatives for patients who are allergic to β-lactam agents (41).

Widespread use of these antibiotics in various clinical conditions as well as their accepted efficacy of intrapartum prophylaxis in decreasing early-onset neonatal GBS infections has potentated the emergence of antibiotic resistance (27). Antibiotic resistance amongst GBS is considered an increasing problem so that it was recommended (31) to test the susceptibility of other antibiotics than those recommended as part to established control measures and that could be used as alternative choices for prophylaxis or treatment of GBS infection.

This study was performed to determine the colonization rate of GBS in a population of pregnant patients at Dr. Ramón Madariaga Hospital in Posadas, Misiones and the susceptibility patterns of the isolates to a variety of antibiotics.

MATERIALS AND METHODS

Bacterial isolates: From January 2004 to December 2006, vaginal-rectal swabs were obtained at 35 to 37 weeks of gestation from 1105 women attending at Dr. Ramón Madariaga Hospital in Posadas; Misiones who agreed to participate in this study.

During the study period, no protocol for prevention of GBS disease, such as routine testing of pregnant women, had been established in the maternity unit of the Hospital.

The samples were collected without speculum. The swabs were placed in Cary-Blair transport media (Difco, Argentina) and transported to the laboratory at room temperature for microbiology analysis. Swabs were inoculated in a selective broth medium, Todd-Hewitt broth supplemented with colistin (10 μg/ml) and nalidixic acid (15 μg/ml) (Laboratorios Britania, Argentina) and incubated at 37°C for 24 hours. The broths were then cultured on 5% sheep’s blood agar plates (Columbia agar base, Laboratorios Britania, Argentina). Culture plates were incubated at 37°C with 5% CO2 for 24 hours. All suspected GBS colonies were sub-cultured and isolated for confirmatory testing. Biochemical standard methods were used to identify GBS (22). GBS identification was completed by group B-specific latex agglutination (Slidex Strepto-Kit, bioMérieux, Marcy l’Etoile, France)

Susceptibility testes: A total of 62 GBS strains were randomly selected for in vitro susceptibility testing. Susceptibility to penicillin G, ampicillin, tetracycline, levofloxacin, gatifloxacin, ciprofloxacin, quinupristin-dalfopristin, linezolid, vancomycin, rifampicin, trimethoprim-sulfametoxazol and nitrofurantoin was tested using microdilution panels (MicroScan, Dade Behring Inc, USA). Susceptibility to clindamycin and erythromycin and determination of resistance phenotypes were performed by the double-disk test on Mueller-Hinton agar (Biokar, France) supplemented with 5% sheep blood (12). Disks of erythromycin (15 μg) and clindamycin (2 μg) were from Laboratorios Britania, Argentina. The different phenotypes of macrolide-lincosamide- streptogramin B (MLSB) resistance were recognized as previously described (43). After 24 h of incubation at 35°C, blunting of the clindamycin inhibition zone proximal to the erythromycin disk was taken to indicate inducible macrolide-lincosamide-streptogramin B (MLSB) resistance. Resistance to clindamycin with no blunting of the clindamycin inhibition zone indicated constitutive resistance. The M phenotype was characterized by susceptibility to clindamycin with no blunting of the inhibition zone around the clindamycin disk. The isolates were considered susceptible or resistant according MIC breakpoints recommended by the Clinical and Laboratory Standards Institute (CLSI) (12). The MIC of gentamicin (Bagó, Argentina) was determined by the agar dilution method according to the guidelines of the CLSI. High-level resistance to gentamicin was defined as a MIC of ≥ 500 μg/ml.

RESULTS

84 of 1105 (7.6%) women tested positive for GBS.

The susceptibilities of the 62 selected isolates to all antibiotics tested except gentamicin are summarized in Table 1. All GBS were susceptible to penicillin G, ampicillin, quinupristin- dalfopristin, linezolid, and vancomycin; and 29.0% were susceptible to tetracycline. 98.3% of the isolates were considered susceptible to nitrofurantoín, 96.8% to rifampicin, and 46.8% to trimethoprim-sulfametoxazol. Rank order of susceptibility for GBS for the quinolones was: gatiloxacin (98.4%) > levofloxacin (93.5%) > ciprofloxacin (64.5%).

Table 1.

Antibiotic susceptibility profiles of group B Streptococcus isolated from pregnant women in Misiones, Argentina.

Antibiotic No. (%) of the isolates with indicated responsea
Susceptible Intermediate Resistant
Penicillin Gb 100 - -
Ampicillinb 100 - -
Clindamycinb 96.7 - 3.3
Erythromycinb 90.2 - 9.8
Vancomycinb 100 - -
Tetracyclineb 71.0 - 29.0
Rifampicinc 96.8 1.6 1.6
Trimethoprim-sulfametoxazolc 46.8 - 53.2
Nitrofurantoínd 98.3 1.6 -
Gatifloxacinb 98.4 - 1.6
Levofloxacinb 93.5 4.8 1.6
Ciprofloxacind 64.5 32.3 3.2
Quinupristin-dalfopristinb 100 - -
Linezolidb 100 - -
a

n= 62;

b

Clinical and Laboratory Standards Institute (CLSI) breakpoint for Streptococcus spp. other than Streptococcus pneumoniae (12);

c

CLSI breakpoint for S. pneumoniae (12);

d

CLSI breakpoint for Enterococcus spp. (12).

Of the 62 isolates, 2 (3.2%) were resistant to clindamycin and 6 (9.7%) were resistant to erythromycin. Among the erythromycin-resistant isolates, 2 expressed the inducible macrolide-lincosamide-streptogramin B (MLSB) resistance phenotype, 2 the constitutive MLSB resistance phenotype and 2 the M resistance phenotype.

The gentamicin MIC ranged from 2 to 256 μg/ml, MIC90 = 64 μg/ml and MIC50= 8 μg/ml. High-level resistance to gentamicin was not detected in any of the isolates.

DISCUSSION

GBS is an important cause of infection in pregnant women and their newborns in many countries, but there are still few data available from Latin America (13,15,45,48). Maternal GBS colonization continues to be the most important risk factor for developing disease in the newborn (6). Implementation of rational GBS disease prevention protocols must be preceded by collection of data at the community level, due to variations in maternal GBS colonization in different populations (50).

The prevalence of maternal colonization by GBS depends on the culture methods, including the number and type of sites cultured and type of medium used, time of pregnancy, race, origin, age, parity and social-economic level (26). In Argentina the prevalence of GBS in pregnant women varies from 1 to 19% (2,8,14,17,22,29,34,36,46).

The carriage rate of GBS among pregnant women in the present study was 7.6%. Due to the differences of the population size and socio-economic status in each study, it is difficult to determine if the difference on GBS colonization rates between the Argentinean study groups are due to genetic differences between the populations or the uneven geographic distribution of GBS.

In this study neither penicillin-resistant nor intermediately penicillin-susceptible GBS strains were found as it was reported by different authors (1,27,44).

At least in our population, penicillin or ampicillin remain the drugs of choice for intrapartum antibiotic prophylaxis for GBS colonization in pregnant women.

Penicillin is also the preferred choice for the treatment of infections caused by GBS. However, in vitro studies indicate that the rate of killing of GBS by these antibiotics is relatively slow compared with other streptococcal pathogens and have led some authors to recommend dual therapy using a penicillin plus gentamicin for severe GBS-associated infection (31). This approach requires the pathogen to be susceptible to both penicillin and aminoglycoside antibiotics. High-level resistance to aminoglycoside indicates that the isolate will not be affected synergistically by the combination of both antimicrobial agents. None of the strains tested in this study showed high-level resistance to gentamicin.

Erythromycin and clindamycin are the drugs of choice for women with serious penicillin allergy who are colonized with GBS (11). An increase in resistance of GBS to erythromycin has been reported (5,18,25,32).

In our strains we found that 3.2 and 9.7% of the isolates were resistant to clindamycin and erythromycin, respectively. This rate of resistance to erythromycin was higher than that of other reports from Argentina like those of Lopardo et al. (5.2%) (33), Pérez et al. (6.0%)(39), Di Bartolomeo et al. (1.74%) (17), García et al. (2.1%) (22), and Mollerach et al. (2.4%) (37), similar to that reported by Lermontov Borges et al. (9.4%) in Brazil (30), but lower than reports from other countries (16, 19, 27).

Resistance to erythromycin and clindamycin is caused by 2 main mechanisms in Streptococcus spp.: target site methylation of the 23S ribosomal component of the large (50S) ribosomal subunit and an active efflux pump. The methylases can be expressed constitutively or they can be inducible. This mechanism renders the bacteria resistant to most macrolide, lincosamide and streptogramin B compounds (MLSB phenotype). When the resistance mechanism due to active efflux is present, streptococci are resistant to macrolides, but susceptible to lincosamides and streptogramin B (M phenotype) (18).

M and MLSB resistance phenotypes were observed in two and four erythromycin -resistant isolates, respectively. Other authors have highlighted the prevalence of MLSB resistance phenotype over M phenotype in GBS (1,16,38,40).

Our study suggests that erythromycin and clindamycin resistance varied among geographic regions of Argentina. So that, for women who are allergic to penicillin the selection of an alternative prophylactic antibiotic should be guided by the antibiotic resistance patterns in each region. The rate of erythromycin resistance in GBS strongly supports the current CDC recommendation that antibiotic susceptibility testing should be performed if erythromycin or clindamycin therapy is needed to prevent neonatal GBS infection (25).

In agreement with other published studies all isolates tested in this study were susceptible to vancomycin (4,38,44), quinupristin-dalfopristin and linezolid (19,49).

We detected high percentages of tetracycline-resistant GBS. Our results were similar to those reported in Argentina (33) and those recorded in several studies performed in other countries (20,35,47).

Resistance to quinolones has only recently been described for GBS (28). In our study we identified 1.6 and 6.5% of the isolates resistant to gatifloxacin and levofloxacin, respectively. As it was reported (23), gatifloxacin appeared to be more active than levofloxacin against GBS. As observed with pneumococci (21), our results find ciprofloxacin to be less active than the newer quinolones.

No resistance to nitrofurantoin was found in the GBS isolates tested by Simoes et al. (44). In this study, the susceptibility rate of nitrofurantoin was 98.3%. We agree with these authors that nitrofurantoin could be a good option for the treatment of both asymptomatic and symptomatic bacteriuria caused by GBS.

Of interest is our finding of 50% of GBS isolates with MIC to gentamicin equal o lower than 8 μg/ml in light of a controversy which has existed concerning the use of gentamicin (8 μg/ml) in selective broth medium (7). At least in our population, our finding supports the position of García et al. (22) who recommended the use of nalidixic acid and colistin in selective media with the aim to improve the sensitivity of screening cultures for GBS carriage in women.

With more widespread use of antibiotics, selection of antibiotic-resistant GBS may occur. If resistance continues to be identified and increasing, surveillance of antibiotic resistance patterns among several antimicrobial classes will be important in determining optimal prophylaxis and treatment of GBS infections.

RESUMO

Sensibilidade a antibióticos e prevalência de Streptococcus do grupo B em mulheres grávidas em Missiones, Argentina

Esse estudo objetivou determinar os padrões de sensibilidade a antibióticos e as taxas de colonização de Streptococcus do grupo B (GBS) em uma população de mulheres grávidas. Entre janeiro de 2004 e dezembro de 2006, foram obtidos swabs vaginais-retais de 1105 mulheres no Hospital Dr. Ramon Madariaga, em Posadas, Missiones, Argentina. A positividade para GBS nas mulheres grávidas foi 7,6%. Um total de 62 cepas de GBS foi selecionado ao acaso para testes in vitro de sensibilidade a penicilina G, ampicilina, tetraciclina, levofloxacina, gatifloxacina, ciprofloxacina, quinupristina- dalfopristina, linezolida, vancomicina, rifampicina, trimetoprim- sulfametoxazol, nitrofurantoína, gentamicina, clindamicina e eritromicina, e determinação dos fenótipos de resistência. Nao foi encontrada resistência à penicilina, ampicilina, quinupristina- dalfopristina, linezolida e vancomicina. Entre as cepas, 96,8%, 98,3%, 46,8% e 29,0% foram sensíveis à rifampicina, nitrofurantoína, trimetoprim-sulfametoxazol e tetraciclina, respectivamente. Para as quinolonas, a ordem de sensibilidade foi: gatifloxacina (98,4%) > levofloxacina (93,8%) > ciprofloxacina (64,5%). A taxa de resistência à eritromicina (9,7%) foi superior a de outros relatos na Argentina. Nenhuma das cepas apresentou alto nível de resistência à gentamicina. Devido a 50% das cepas de GBS terem apresentado MIC para gentamicina igual ou inferior a 8 mg/ml, correspondente à concentrado usada em um dos meios seletivos recomendados para GBS, sugeriu-se ao menos em nossa população, o emprego de ácido nalidíxico e colistina em meios seletivos para melhorar a sensibilidade da triagem de culturas para GBS em mulheres grávidas.

Palavras-chave: Streptococcus do grupo B, sensibilidade a an­tibióticos, prevenção, mulheres grávidas, Argentina.

References

  • 1.Aitmhand R., Moustaoui N., Belabbes H., Elmdaghri N., Benbachir M. Serotypes and antimicrobial susceptibility of group B streptococcus isolated from neonates in Casablanca. Scand. J. Infect. Dis. 2000;32(3):339–340. doi: 10.1080/00365540050166108. [DOI] [PubMed] [Google Scholar]
  • 2.Alaniz A.D., D’Agata J.M., Floridia R.A., Lara C.S., Melian M.V., Rodríguez B.L., Ruiz B.B. Prevalência de colonización por Streptococcus agalactiae en una población de mujeres embarazadas del Hospital Dr. Guillermo Rawson. Acta Bioquím. Clin. Latinoam. 2005;2:54. Suplemento. [Google Scholar]
  • 3.American Academy of Pediatrics and Committee on Fetus and Newborn Revised guidelines for prevention of early-onset group B streptococcal (GBS) infection. Pediatrics. 1997;99:489–496. doi: 10.1542/peds.99.3.489. [DOI] [PubMed] [Google Scholar]
  • 4.Andrews J.I., Diekema D.J., Hunter S.K., Rhomberg P.R., Pfaller M.A., Jones R.N., Doern GV. Group B streptococci causing neonatal bloodstream infection: antimicrobial susceptibility and serotyping results from SENTRY centers in the Western Hemisphere. Am. J. Obstet. Gynecol. 2000;183(4):859–862. doi: 10.1067/mob.2000.108839. [DOI] [PubMed] [Google Scholar]
  • 5.Aracil B., Minambres M., Oteo J., De La Rosa M., Gomez-Garces J.L., Alos A.J. Susceptibility of strains of Streptococcus agalactiae to macrolides and lincosamides, phenotype patterns and resistance genes. Clin. Microbiol. Infect. 2002;8(11):745–748. doi: 10.1046/j.1469-0691.2002.00450.x. [DOI] [PubMed] [Google Scholar]
  • 6.Baker C.J., Edwards M.S. Group B streptococcal infections (Chapter 26) In: Remington J.S., Klein J.O., editors. Infectious diseases of the fetus and newborn infant. 5th Edition. Philadelphia, USA: W.B. Saunders Co; 2001. pp. 1091–1156. [Google Scholar]
  • 7.Berkowitz K., Regan J.A., Greenberg E. Antibiotic resistance patterns of Group B streptococci in pregnant women. J. Clin. Microbiol. 1990;28(1):5–7. doi: 10.1128/jcm.28.1.5-7.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Catan M.A., Caraballo T., Chianea E., Baldarene C., García C., Escalante I. Argentina: XVII Congreso Latinoamericano de Microbiología, Buenos Aires; 2004. Aislamientos bacterianos en pacientes embarazadas con 35 a 37 semanas de gestación; p. E-266. [Google Scholar]
  • 9.Centers for Disease Control and Prevention Prevention of perinatal group B streptococcal disease: a public health perspective. MMWR. 1996;45(RR-7):1–24. [PubMed] [Google Scholar]
  • 10.Centers for Disease Control and Prevention Decreasing incidence of perinatal group B streptococcal disease-United States, 1993-1995. MMWR. 1997;46(21):473–477. [PubMed] [Google Scholar]
  • 11.Centers for Disease Control and Prevention Prevention of perinatal group B streptococcal disease. MMWR. 2002;51:1–22. [Google Scholar]
  • 12.Clinical and Laboratory Standards Institute . Wayne, PA: M100-S16; 2006. Performance standards for antimicrobial susceptibility testing; sixteenth informational supplement. [Google Scholar]
  • 13.Collins T.S., Calderon M., Gilman R.H., Vivar A., Charache P. Group B streptococcal colonization in a developing country: its association with sexually transmitted disease and socioeconomic factors. Am. J. Trop. Med. Hyg. 1998;59(4):633–636. doi: 10.4269/ajtmh.1998.59.633. [DOI] [PubMed] [Google Scholar]
  • 14.Cotaimich H.O., Belbruno G., Torresi E., Nitardi J., Corte M., Vilches G. Argentina: Buenos Aires; 2004. Prevalência de portación de Estreptococo beta- hemolítico del grupo B en gestantes de la ciudad de Río Tercero, Córdoba. XVII Congreso Latinoamericano de Microbiología; p. E-265. [Google Scholar]
  • 15.De Lourdes Collado M., Kretschmer R.R., Becker I., Guzmán A., Gallardo L., Lepe C.M. Colonization of Mexican pregnant women with group B Streptococcus. J. Infect. Dis. 1981;143(1):134. doi: 10.1093/infdis/143.1.134. (letter) [DOI] [PubMed] [Google Scholar]
  • 16.De Mouy D., Cavallo J.D., Leclercq R., Fabre R., the AFORCOPI-BIO Network. Antibiotic susceptibility and mechanisms of erythromycin resistance in clinical isolates of Streptococcus agalactiae: French multicenter study. Antimicrob. Agents Chemother. 2001;45:2400–2402. doi: 10.1128/AAC.45.8.2400-2402.2001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Di Bartolomeo S., Gentile M., Priore G., Valle S., Di Bella A. Streptococcus agalactiae in pregnant women. Prevalence at the Posadas Hospital. Rev. Argent. Microbiol. 2005;37(3):142–144. [PubMed] [Google Scholar]
  • 18.DiPersio L.P, DiPersio J.R. High rates of erythromycin and clindamycin resistance among OBGYN isolates of group B Streptococcus. Diagn. Microbiol. Infect. Dis. 2006;54(1):79–82. doi: 10.1016/j.diagmicrobio.2005.07.003. [DOI] [PubMed] [Google Scholar]
  • 19.Fluegge K., Supper S., Siedler A., Berner R. Antibiotic susceptibility in neonatal invasive isolates of Streptococcus agalactiae in a 2-year Nationwide Surveillance Study in Germany. Antimicrob. Agents Chemother. 2004;48(11):4444–4446. doi: 10.1128/AAC.48.11.4444-4446.2004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Fujita K., Murono K., Sakata H., Yoshioka H. Susceptibility of group B streptococci to 30 antibiotics including new cephalosporins. Acta Paediatr. Jpn. 1985;27:247–252. [Google Scholar]
  • 21.Fung-Tomc J., Minassian B., Kolek B., Washo T., Huczko E., Bonner D. In vitro antibacterial spectrum of a new broad- spectrum 8-methoxy fluoroquinolone, gatifloxacin. J. Antimicrob. Chemother. 2000;45(4):437–446. doi: 10.1093/jac/45.4.437. [DOI] [PubMed] [Google Scholar]
  • 22.Garcia S.D., Eiseth M.C., Lazzo M.J., Copolillo E., Barata A.D., de Torres R., Vay C.A., Famiglietti A.M. Group B Streptococcus carriers among pregnant women. Rev. Argent. Microbiol. 2003;35(4):183–187. [PubMed] [Google Scholar]
  • 23.Gordon K.A., Beach M.L., Biedenbach D.J., Jones R.N., Rhomberg PR., Mutnick AH. Antimicrobial susceptibility patterns of beta-hemolytic and viridans group streptococci: report from the SENTRY Antimicrobial Surveillance Program (1997-2000) Diagn. Microbiol. Infect. Dis. 2002;43(2):157–162. doi: 10.1016/s0732-8893(02)00374-7. [DOI] [PubMed] [Google Scholar]
  • 24.Gray B.M., Pass M.A., Dillon H.C. Laboratory and field evaluation of selective media for isolation of group B streptococci. J. Clin. Microbiol. 1979;9:466–470. doi: 10.1128/jcm.9.4.466-470.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Heelan J.S., Hasenbein M.E., McAdam A.J. Resistance of Group B Streptococcus to selected antibiotics, including erythromycin and clindamycin. J. Clin. Microbiol. 2004;42(3):1263–1264. doi: 10.1128/JCM.42.3.1263-1264.2004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Hickman M.E., Rench M.A., Ferrieri P., Baker C.J. Changing Epidemiology of Group B Streptococcal Colonization. Pediatrics. 1999;104(2):203–209. doi: 10.1542/peds.104.2.203. [DOI] [PubMed] [Google Scholar]
  • 27.Hsueh PR., Teng L.J., Lee L.N., Ho S.W., Yang P.C., Luh K.T. High incidence of erythromycin resistance among clinical isolates of Streptococcus agalactiae in Taiwan. Antimicrob. Agents Chemother. 2001;45(11):3205–3208. doi: 10.1128/AAC.45.11.3205-3208.2001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Kawamura Y., Fujiwara H., Mishima N., Tanaka Y., Tanimoto A., Ikawa S., Itoh Y., Ezaki T. First Streptococcus agalactiae isolates highly resistant to quinolones, with point mutations in gyrA and parC. Antimicrob. Agents Chemother. 2003;47(11):3605–3609. doi: 10.1128/AAC.47.11.3605-3609.2003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Larcher J.S., Capellino F., De Giusto R., Travella C., Balagione F.G., Kreiker G., Cardona H.P, Zarate A., Vilaro M., Hernández D., Ruiz Orrico G. Group B streptococcus colonization during pregnancy and prevention of early onset of disease. Medicina. 2005;65(3):201–206. (Buenos Aires) [PubMed] [Google Scholar]
  • 30.Lermontov Borges I., Cerqueira d’Oliveira R.E., Dias de Castro A.C., Bona de Mondito S.S. Streptococcus agalactiae in pregnant women: prevalence of colonization and antimicrobial susceptibility evaluation. Rev. Bras. Ginecol. Obstet. 2005;27(10):575–579. [Google Scholar]
  • 31.Liddy H., Holliman R. Group B Streptococcus highly resistant to gentamicin. J. Antimicrob. Chemother. 2002;50(1):142–143. doi: 10.1093/jac/dkf090. [DOI] [PubMed] [Google Scholar]
  • 32.Lin F.Y., Azimi PH., Weisman L.E., Philips J.B., Regan J., Clark P, Rhoads G.G, Clemens J., Troendle J., Pratt E., Brenner R.A., Gill V. Antibiotic susceptibility profiles for Group B streptococci isolated from neonates, 1995-1998. Clin. Infect. Dis. 2000;31(1):76–79. doi: 10.1086/313936. [DOI] [PubMed] [Google Scholar]
  • 33.Lopardo H.A., Vidal P., Jeric P., Centron D., Paganini H., Facklam R.R., The Argentinian Streptococcus Study Group. Elliott J. Six-Month multicenter study on invasive infections due to Group B streptococci in Argentina. J. Clin. Microbiol. 2003;41(10):4688–4694. doi: 10.1128/JCM.41.10.4688-4694.2003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Marramá M., de Olivera A., Ferreira Y., Botiglieri M. Argentina: Buenos Aires; 2004. Prevalência de portación de Estreptococo ß hemolítico grupo “B” (EGB) en una clínica de la ciudad de Córdoba. XVII Congreso Latinoamericano de Microbiología; p. E-263. [Google Scholar]
  • 35.Melin P, Rodríguez-Cuns G., Fernández W.V., De Mol P. Antimicrobial susceptibility of Streptococcus agalactiae isolated from patients in Belgium, 1989-1991 and 1996-1999. In: Martin R., Tagg J.R., editors. Streptococci and streptococcal diseases: entering the new millennium. Proceedings of the XIV Lancefield International Symposium on Streptococci and Streptococcal Diseases. New Zealand: Securacopy, Auckland; 2000. pp. 305–309. [Google Scholar]
  • 36.Mendosa M.A., Morano S., Nardin M.E., Roldán L., Ahumada C., Mendez E. Argentina: Buenos Aires; 2004. Estreptococo grupo B: prevalencia de portación en embarazadas de dos centros de salud de Santa Fe. XVII Congreso Latinoamericano de Microbiología; p. E-264. [Google Scholar]
  • 37.Mollerach A., Mendez E., Massa R., Di Conza J. Streptococcus agalactiae isolated in Santa Fe, Argentina: antibiotic susceptibility and erythromycin-clindamycin resistance mechanisms. Enferm. Infecc. Microbiol. Clin. 2007;25(1):67–68. doi: 10.1016/s0213-005x(07)74230-1. [DOI] [PubMed] [Google Scholar]
  • 38.Pearlman M., Pierson C.L., Faix R.G. Frequent resistance of clinical group B streptococci isolates to clindamycin and erythromycin. Obstet. Gynecol. 1998;92:258–261. doi: 10.1016/s0029-7844(98)00155-0. [DOI] [PubMed] [Google Scholar]
  • 39.Pérez J., Limansky A., Toresani I., Ebner G, Di Bartolomeo S., de Inocente I., Pretto G, Salazar N., Laferrara M., Bottiglieri M., Ballester D., Morales M., Rivera L., Cacace M.L., Castro H., Roldán L., Notario R., Borda N., Cera G., Spoletti M.J., Gregorini E., Sutich E.G. Distribution of capsular types and antimicrobial susceptibility of Streptococcus agalactiae causing infections in Argentina. Rev. Argent. Microbiol. 2004;36(2):63–67. [PubMed] [Google Scholar]
  • 40.Portillo A., Lantero M., Olarte I., Ruiz-Larrea F., Torres C. MLS resistance phenotypes and mechanisms in ß-hemolytic group B, C and G Streptococcus isolates in La Rioja, Spain. J. Antimicrob. Chemother. 2001;47:115–116. doi: 10.1093/jac/47.1.115. [DOI] [PubMed] [Google Scholar]
  • 41.Schrag S., Gorwitz R., Fultz-Butts K., Schuchat A. Prevention of perinatal group B streptococcal disease: revised guidelines from CDC. MMWR. 2002;51:1–22. (RR11) [PubMed] [Google Scholar]
  • 42.Schuchat A. Epidemiology of group B streptococcal disease in the United States: shifting paradigms. Clin. Microbiol. Rev. 1998;11(3):497–513. doi: 10.1128/cmr.11.3.497. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Seppala H., Skurnik M., Soini H., Roberts M.C., Huovinen P. A novel erythromycin resistance methylase gene (ermTR) in Streptococcus pyogenes. Antimicrob. Agents Chemother. 1998;42(2):257–262. doi: 10.1128/aac.42.2.257. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Simoes J.A., Aroutcheva A.A., Heimler I., Faro S. Antibiotic resistance patterns of group B streptococcal clinical isolates. Infect. Dis. Obstet. Gynecol. 2004;12(1):1–8. doi: 10.1080/10647440410001722269. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Solorzano-Santos F., Echaniz-Aviles G, Conde-Glez C.J., Calderon- Jaimes E., Arredondo-Garcia J.L., Beltran-Zuniga M. Cervicovaginal infection with group B streptococci among pregnant Mexican women. J. Infect. Dis. 1989;159(5):1003. doi: 10.1093/infdis/159.5.1003. (letter) [DOI] [PubMed] [Google Scholar]
  • 46.Toresani I., Limansky A., Bogado I., Guardati M.C., Viale A., Sutich E.G. Phenotypic and genotypic study of Streptococcus agalactiae in vagina of pregnant women in Argentina. Medicina (Buenos Aires) 2001;61(3):295–300. [PubMed] [Google Scholar]
  • 47.Traub W.H., Leonhard B. Comparative susceptibility of clinical group A, B, C, F, and G β-hemolytic streptococcal isolates to 24 antimicrobial drugs. Chemotherapy. 1997;43:10–20. doi: 10.1159/000239529. [DOI] [PubMed] [Google Scholar]
  • 48.Trujillo H. Group B streptococcal colonization in Medellin, Colombia. Pediatr. Infect. Dis. J. 1990;9(3):224–225. doi: 10.1097/00006454-199003000-00023. (letter) [DOI] [PubMed] [Google Scholar]
  • 49.Tubau F., Fernandez-Roblas R., Linares J., Martin R., Soriano F. In vitro activity of linezolid and 11 other antimicrobials against 566 clinical isolates and comparison between NCCLS microdilution and Etest methods. J. Antimicrob. Chemother. 2001;47:675–680. doi: 10.1093/jac/47.5.675. [DOI] [PubMed] [Google Scholar]
  • 50.Whitney C.G., Daly S., Limpongsanurak S., Festin M.R., Thinn K.K., Chipato T., Lumbiganon P., Sauvarin J., Andrews W., Tolosa J.E., Global Network For Perinatal And Reproductive Health The international infections in pregnancy study: group B streptococcal colonization in pregnant women. J. Matern. Fetal Neonatal Med. 2004;15(4):267–274. doi: 10.1080/14767050410001668617. [DOI] [PubMed] [Google Scholar]

Articles from Brazilian Journal of Microbiology are provided here courtesy of Brazilian Society of Microbiology

RESOURCES