| Literature DB >> 29750801 |
Ana Caroline N Botelho1, Juliana G Oliveira1, Andreia P Damasco1, Késia T B Santos1, Ana Flávia M Ferreira1, Gabriel T Rocha1, Penélope S Marinho2, Rita B G Bornia2, Tatiana C A Pinto1, Marco A Américo1, Sergio E L Fracalanzza1, Lúcia M Teixeira1.
Abstract
Group B Streptococcus (GBS) carriage by pregnant women is the primary risk factor for early-onset GBS neonatal sepsis. Intrapartum antibiotic prophylaxis (IAP) can prevent this transmission route, and two main approaches are recommended to base the selection of pregnant women to be submitted to IAP: the risk-based and the culture-based strategies. In Brazil, compliance to such recommendations is poor, and not much is known about GBS carriage. In the present study, 3,647 pregnant women living in Rio de Janeiro State, Brazil, were screened for GBS anogenital colonization, over a period of 8 years (2008-2015). GBS was detected in 956 (26.2%) of them, and presence of vaginal discharge was the only trait associated with a higher risk for GBS colonization. Serotypes Ia (257; 37.3%) and II (137; 19.9%) were the most frequent among 689 (72.1% of the total) GBS isolates evaluated, followed by NT isolates (84; 12.1%), serotype Ib (77; 11.1%), V (63; 9.1%), III (47; 6.8%) and IV (24; 3.5%). Estimated coverage of major serotype-based GBS vaccines currently under clinical trials would vary from 65.2% to 84.3%. All 689 isolates tested were susceptible to ampicillin and vancomycin. Resistance to chloramphenicol, clindamycin, erythromycin, levofloxacin, and tetracycline was observed in 5% (35), 2% (14), 14% (97), 5% (35) and 86% (592) of the isolates, respectively. No significant fluctuations in colonization rates, serotype distribution and antimicrobial susceptibility profiles were observed throughout the period of time investigated. The culture-based approach for IAP recommendation showed to be the best choice for the population investigated when compared to the risk-based, since the first did not increase the number of pregnant women submitted to antibiotic therapy and covered a larger number of women who were actually colonized by GBS. The fact the not all isolates were available for additional characterization, and serotype IX antiserum was not available for testing represent limitations of this study. Nevertheless, to the best of our knowledge, this is the largest investigation on GBS carriage among pregnant women in Brazil up to date, and results are useful for improving GBS prevention and treatment strategies.Entities:
Mesh:
Year: 2018 PMID: 29750801 PMCID: PMC5947911 DOI: 10.1371/journal.pone.0196925
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240
Fig 1Percentages of GBS carriage among 3,647 pregnant women living in Rio de Janeiro, Brazil, over a period of eight years.
The red line indicates relative percentages in each period and the black line represents the tendency line.
Distribution of clinical, social and demographic aspects according to the presence or absence of Streptococcus agalactiae colonization among 3,369 pregnant women enrolled in the present study.
| Aspects evaluated | Number of pregnant women | Number of pregnant women | p-value |
|---|---|---|---|
| Presence of vaginal discharge | |||
| Yes | 358 | 1129 | |
| No | 395 | 1487 | 0.003 |
| Preterm birth | |||
| Yes | 29 | 91 | |
| No | 724 | 2525 | 0.815 |
| Urinary tract infection diagnosed | |||
| Yes | 175 | 604 | |
| No | 578 | 2012 | 0.675 |
| Use of antibiotics during pregnancy | |||
| Yes | 194 | 648 | |
| No | 559 | 1968 | 0.673 |
| Maternal pathology | |||
| Yes | 112 | 419 | |
| No | 641 | 2197 | 0.638 |
| History of previous neonatal death | |||
| Yes | 40 | 86 | |
| No | 713 | 2530 | 0.125 |
| History of neonatal GBS infection | |||
| Yes | 3 | 5 | |
| No | 750 | 2611 | 0.588 |
| Race or skin color | |||
| White | 291 | 1023 | |
| Non-white | 462 | 1593 | 0.057 |
| Marital status | |||
| Married | 223 | 673 | |
| Single | 490 | 1847 | |
| Others | 40 | 96 | 0.299 |
| Level of education | |||
| Elementary School | 247 | 622 | |
| High School | 426 | 1789 | |
| Undergraduation School | 80 | 205 | 0.908 |
| Place of birth | |||
| North region | 5 | 28 | |
| Northeast region | 246 | 613 | |
| Midwest region | 3 | 11 | |
| South region | 2 | 20 | |
| Southeast region | 25 | 79 | |
| Rio de Janeiro | 475 | 1 | |
| Other countries | 2 | 12 | 0.478 |
ap-values < 0.05 were considered statistically significant.
bp-value refers to the comparison between white and black ethnicities only, since only three pregnant women were of other ethnicities.
cSoutheast region except Rio de Janeiro State, which is shown separately.
dOther countries included Angola, Argentina, Australia, Bolivia, Chile, China, Colombia, Cuba, France, Paraguay, Peru, Senegal and Uruguay. GBS-positive pregnant women comprised one from Chile and one from China.
Number of Streptococcus agalactiae isolates analyzed according to the period of time included in the study.
| Period of time | Total number of GBS isolates | Number (%) of GBS isolates submitted to serotyping and antimicrobial susceptibility testing |
|---|---|---|
| 2008–2009 | 363 | 240 (66.1%) |
| 2010–2011 | 277 | 138 (49.8%) |
| 2012–2013 | 194 | 194 (100%) |
| 2014–2015 | 122 | 117 (95.9%) |
| 2008–2015 | 956 | 689 (72.1%) |
Fig 2Distribution of serotypes among 689 Streptococcus agalactiae isolates recovered from colonized pregnant women living in Rio de Janeiro, Brazil, according to the period of time investigated.
Fig 3Distribution of antimicrobial resistant profiles among 689 Streptococcus agalactiae isolates recovered from colonized pregnant women living in Rio de Janeiro, Brazil, according to the period of time investigated.
Chl-R, Chloramphenicol-resistant isolates; Cli-R, Clindamycin-resistant isolates; Ery-R, Erythromycin-resistant isolates; Lev-R, Levofloxacin-resistant isolates; Tet-R, Tetracycline-resistant isolates.
Antimicrobial susceptibility profiles among 689 Streptococcus agalactiae isolates recovered from colonized pregnant women in Rio de Janeiro, Brazil.
| Antimicrobial susceptibility profile | Number (%) of isolates | Serotype (Number of isolates) | Phenotype | ||||
|---|---|---|---|---|---|---|---|
| Chl | Cli | Ery | Lev | Tet | |||
| S | S | S | S | R | 495 (71.8%) | Ia (220); Ib (54); II (78); III (30); IV (24); V (55), NT (34) | ----- |
| S | S | R | S | R | 48 (7%) | Ia (8); Ib (9); II (6) III (11), NT (5) | M (39) |
| Ia (7); V (2) | iMLSB (9) | ||||||
| S | S | S | S | S | 97 (14.1%) | Ia (15); Ib (8); II (46), NT (28) | ---- |
| S | R | R | S | R | 14 (2.1%) | II (5); III (6); V (3) | cMLSB (14) |
| R | S | R | R | R | 35 (5%) | Ia (7), Ib (6), II (2), V (3), NT (17) | M (35) |
aChl, chloramphenicol; Cli, clindamycin; Ery, erythromycin; Lev, levofloxacin; Tet, tetracycline.
bPhenotype of resistance to macrolides, lincosamines and streptogramin B: M, resistance to macrolides; CMLSB, constitutive resistance to macrolides, lincosamines and streptogramin B; iMLSB, induced resistance to macrolides, lincosamines and streptogramin B.