Suscetibilidade antimicrobiana de Streptococcus agalactiae isolados de gestantes em um hospital materno infantil de Porto Alegre, Rio Grande do Sul
DOI:
https://doi.org/10.15448/1980-6108.2018.3.30246Palavras-chave:
Streptococcus agalactiae, estreptococos do grupo B, gestantes, antibacterianos, antibioticoprofilaxia, resistência microbiana a medicamentos.Resumo
OBJETIVOS: Caracterizar o perfil de suscetibilidade antimicrobiana de Streptococcus agalactiae isolados de gestantes atendidas em um hospital público.
MÉTODOS: O estudo foi realizado em um hospital materno-infantil público de Porto Alegre, RS, no qual a pesquisa de S. agalactiae em gestantes faz parte da rotina obstétrica. Foram incluídas no estudo as pesquisas por swab anal/vaginal realizadas no período de julho de 2015 a fevereiro de 2016. Os isolados bacterianos foram identificados por testes fenotípicos e foi determinada a suscetibilidade aos antimicrobianos ampicilina, clindamicina, eritromicina e ofloxacino. Foram investigados também os genes de resistência à eritromicina ermB e mefA.
RESULTADOS: No total, 294 coletas foram incluídas e destas, 26 (8%) foram positivas para S. agalactiae. Todos os isolados avaliados foram sensíveis à ampicilina e foram observadas resistências à eritromicina (21,4%), clindamicina (14,3%) e ofloxacino (7,1%), sendo que 66% dos isolados resistentes à eritromicina apresentaram o genótipo mefA.
CONCLUSÕES: Os resultados deste estudo corroboram com o consenso de que em gestantes colonizadas com S. agalactiae é aconselhada a antibioticoprofilaxia intraparto com penicilina G ou ampicilina. A expressiva proporção de isolados resistentes à eritromicina e clindamicina, indicados para a antibioticoprofilaxia intraparto em caso de alergia aos antibióticos beta-lactâmicos, enfatiza a importância da determinação do perfil de suscetibilidade antimicrobiana prévia desses isolados, medida que ainda não faz parte da rotina de exames pré-natais em muitas instituições.
Downloads
Referências
Bolukaoto JY, Monyama CM, Chukwu MO, Lekala SM, Nchabeleng M, Maloba MRB, Mavenyengwa RT, Lebelo SL, Monokoane ST, Tshepuwane C, Moyo SR. Antibiotic resistance of Streptococcus agalactiae isolated from pregnant women in Garankuwa, South Africa. BMC Res Notes. 2015;8:364. https://doi.org/10.1186/s13104-015-1328-0
American College of Obstetricians and Gynecologists. ACOG committee opinion. Prevention of early-onset group B streptococcal disease in newborns. Int J Gynaecol Obstet. 1996;54:197-205. https://doi.org/10.1016/S0020-7292(96)90083-1
Verani JR, Mc gee L, Schrag SJ. Division of Bacterial Diseases, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention (CDC). Prevention of perinatal group B streptococcal disease--revised guidelines from CDC, 2010. MMWR Recomm Rep. 2010; 59(10):1-36.
Hall J, Adams NH, Bartlett L, Bartlett L, Seale AC, Lamagni T, Bianchi-Jassir F, Lawn JE, Baker CJ, Cutland C, Heath PT, Ip M, Doare KL, Madhi SA, Rubens CE, Saha SK, Schrag S, Meulen AS, Vekemans J, Gravett MG. Maternal Disease With Group B Streptococcus and Serotype Distribution Worldwide: Systematic Review and Meta-analyses. Clinical Infectious Diseases: An Official Publication of the Inf Dis Soc Ame. 2017;65(2):S112-S124. https://doi.org/10.1093/cid/cix660
Costa HPF, Sociedade Brasileira de Pediatria. Prevenção da doença perinatal pelo estreptococo do grupo B. [internet]. Rio de Janeiro; 2011 [acessado em 01 de fevereiro de 2018]. Disponível em: www.sbp.com.br/fileadmin/user_upload/2015/02/SBPEGBCDC2011-2.pdf
Dutra VG, Alves VM, Olendzki AN, Dias CA, de Bastos AF, Santos GO, de Amorin EL, Sousa MÂ, Santos R, Ribeiro PC, Fontes CF, Andrey M, Magalhães K, Araujo AA, Paffadore LF, Marconi C, Murta EF, Fernandes PC Jr, Raddi MS, Marinho PS, Bornia RB, Palmeiro JK, Dalla-Costa LM, Pinto TC, Botelho AC, Teixeira LM, Fracalanzza SE. Streptococcus agalactiae in Brazil: serotype distribution, virulence determinants and antimicrobial susceptibility. BMC Infect Dis. 2014; 14(323):e1-9. https://doi.org/10.1186/1471-2334-14-323
Hays C, Louis M, Plainvert C, Dmytruk N, Touak G, Trieu-Cuot P, Poyart C, Tazi A. Changing epidemiology of group B Streptococcus susceptibility to fluoroquinolones and aminoglycosides in France. Antimicrob Agents Chemother. 2016;60(12):7424-30.
Morozumi M, Wajima T, Takata M, Iwata S, Ubukata K. Molecular characteristics of group B streptococci isolated from adults with invasive infections in Japan. J. Clin. Microbiol. 2016;54(11):2695-700. https://doi.org/10.1128/JCM.01183-16
Clifford V, Heffernan HM, Grimwood K, Garland S, Australasian GBS Resistance Study Group. Variation in erythromycin and clindamycin resistance patterns between New Zealand and Australian group B streptococcus isolates. Aust N Z J Obstet Gynaecol. 2011;51(4):328-32 https://doi.org/10.1111/j.1479-828X.2011.01302.x
Clinical and laboratory standards institute (CLSI). Performance standards for antimicrobial susceptibility testing; twenty-seven informational supplement. CLSI document M100-S27. Wayne, PA: Clinical and Laboratory Standards Institute; 2017.
Mott M, Caierão J, Cunha GR, Perez LRR, Matusiak R, Oliveira KRP, d'Azevedo PA, Dias CAG. Susceptibility profiles and correlation with pneumococcal serotypes soon after implementation of the 10-valent pneumococcal conjugate vaccine in Brazil. Int J Infect Dis. 2014;20:47-51. https://doi.org/10.1016/j.ijid.2013.11.009
Kiss FS, Rossato JS, Graudenz MS, Gutierrez LLP. Prevalência da colonização por Streptococcus agalactiae em uma amostra de mulheres grávidas e não grávidas de Porto Alegre, estado do Rio Grande do Sul. Sci Med. 2013;23(3):169-74.
Carvalho RL, Machado DC, Fiori RM. Colonização de gestantes pelo estreptococo do grupo B: prevalência, fatores associados e cepas virulentas [Internet]. Porto Alegre: Pontifícia Universidade do Rio Grande do Sul; 2009. [acessado em 30 de janeiro de 2018]. Disponível em: http://www.lume.ufrgs.br/bitstream/handle/10183/17768/000722513.pdf?sequence=1
Senger FR, Alves IA, Pellegrini DCP, Prestes DC, Souza EF, Corte ED. Prevalência da colonização por Streptococcus agalactiae em gestantes atendidas na rede pública de saúde de Santo Ângelo – RS. Rev Epi Con Inf. 2016;6(1):e1-5. https://doi.org/10.17058/reci.v6i1.6272
Nunes PR, Oliveira MS. Prevalência de Streptococcus agalactiae em gestantes da Grande Porto Alegre, RS: relato de caso. RBAC. 2015;47(4):178-80.
Linhares JJ, Neto PGC, Vasconcelos JLM, Sairaiva TV, Ribeiro AMF, Siqueira TM, Rocha FR. Prevalência de colonização por Streptococcus agalactiae em gestantes atendidas em maternidade do Ceará, no Brasil, correlacionando com os resultados perinatais. Rev Bras Ginecol Obstet. 2011;33(12):395-400.
Costa NDL, Carvalho M, Pone SM, Júnior SCG. Gestantes colonizadas pelo Streptococcus do grupo B e seus recém-nascidos: análise crítica da conduta adotada no Instituto Fernandes Figueira, Fundação Oswaldo Cruz. Rev Paul Pediatr. 2010;28(2):155-61.
https://doi.org/10.1590/S0103-05822010000200005
Melo SC, Gavena AA, Silva FT, Moreira RC, de Lima Scodro RB, Cardoso RF, Siqueira VL, de Pádua RA, Carvalho MD, Pelloso SM. Performance of hitchens-pike-todd-hewitt medium for group b streptococcus screening in pregnant women. PLOS ONE. 2015;10(4): e0123988. https://doi.org/10.1371/journal.pone.0123988
Kruk CR, Feuerschuette OHM, Silveira SK, Cordazo M, Júniot AT. Epidemiologic profile of Streptococcus agalactiae colonization in pregnant women attending prenatal care in a city of southern of Brazil. Braz J Infect Dis. 2013;17(6): 722-3. https://doi.org/10.1016/j.bjid.2013.07.003
Wollheim C, Sperhacke RD, Fontana SKR, Vanni AC, Kato SK, Araújo PR, Barth AL, Madi JM. Group B Streptococcus detection in pregnant women via culture and PCR methods. Rev Soc Bras Med Trop. 2017;50(2):179-83. https://doi.org/10.1590/0037-8682-0454-2016
Gouvea MIS, Joao EC, Teixeira MLB, Read JS, Fracalanzza SEL, Souza CTV, Souza MJ, Torres Filho HM, Leite CCF. Accuracy of a rapid real-time polymerase chain reaction assay for diagnosis of group B Streptococcus colonization in a cohort of HIV-infected pregnant women. J Matern Fetal Neonatal Med. 2017;30(9):1096-101. https://doi.org/10.1080/14767058.2016.1205021
Freita FTM, Romero GAS. Early-onset neonatal sepsis and the implementation of group B streptococcus prophylaxis in a Brazilian maternity hospital: a descriptive study. Braz J Infect Dis. 2017;21(1):92-7. https://doi.org/10.1016/j.bjid.2016.09.013
Melo SCCS, Costa AB, Silva FTRD, Silva NMMG1 Tashima CM, Cardoso RF, Pádua RAF, Previdelli I, Carvalho MDB, Pelloso SM. Prevalence of Streptococcus agalactiae colonization in pregnant women from the 18th Health Region of Paraná State. Rev Inst Med Trop Sao Paulo. 2018;60:e2. https://doi.org/10.1590/s1678-9946201860002
Otaguiri ES, Morguette AEB, Morey AT, Tavares ER, Kerbauy G, de Almeida Torres RSL, Chaves Júnior M, Tognim MCB, Góes VM, Krieger MA, Perugini MRE, Yamauchi LM, Yamada-Ogatta SF. Development of a melting-curve based multiplex real-time PCR assay for simultaneous detection of Streptococcus agalactiae and genes encoding resistance to macrolides and lincosamides. BMC Pregnancy Childbirth. 2018:18(1):e1-11. https://doi.org/10.1186/s12884-018-1774-5
Silbert S, Rocchetti TT, Gostnell A, Kubasek C, Widen R. Detection of Group B Streptococcus Directly from Collected ESwab Samples by Use of the BD Max GBS Assay. J Clin Microbiol. 2016;54(6):1660-3. https://doi.org/10.1128/JCM.00445-16
Souza VC, Kegele FC, Souza SR, Neves FP, de Paula GR, Barros RR. Antimicrobial susceptibility and genetic diversity of Streptococcus agalactiae recovered from newborns and pregnant women in Brazil. Scand J Infect Dis. 2013;45(10):780-5. https://doi.org/10.3109/00365548.2013.810814
Metcalf BJ, Chochua S, Gertz RE Jr, Hawkins PA, Ricaldi J, Li Z, Walker H, Tran T, Rivers J, Mathis S, Jackson D, Glennen A, Lynfield R, McGee L, Beall B. Active Bacterial Core surveillance team. Short-read whole genome sequencing for determination of antimicrobial resistance mechanisms and capsular serotypes of current invasive Streptococcus agalactiae recovered in the USA. Clin Microbiol Infect. 2017;23(8):574.e7-574.e14. https://doi.org/10.1016/j.cmi.2017.02.021
Sigaúque B, Kobayashi M, Vubil D, Nhacolo A, Chaúque A, Moaine B, Massora S, Mandomando I, Nhampossa T, Bassat Q, Pimenta F, Menéndez C, Carvalho MDG, Macete E, Schrag SJ. Invasive bacterial disease trends and characterization of group B streptococcal isolates among young infants in southern Mozambique, 2001–2015. PLoS One. 2018;13(1):e0191193. https://doi.org/10.1371/journal.pone.0191193
Piccinelli G, Carlentini G, Gargiulo F, Caruso A, De Francesco MA. Analysis of Point Mutations in the pbp2x, pbp2b, and pbp1a Genes of Streptococcus agalactiae and Their Relation with a Reduced Susceptibility to Cephalosporins. Microb Drug Resist. 2017;23(8):1019-24. https://doi.org/10.1089/mdr.2017.0013
Crespo-Ortiz MP, Casta-eda-Ramirez CR, Recalde-Bola-os M, Vélez-Londo-o JD. Emerging trends in invasive and noninvasive isolates of Streptococcus agalactiae in a Latin American hospital: a 17-year study. BMC Infect Dis. 2014;14:428. http://doi.org/10.1186/1471-2334-14-428
Goossens H. Antibiotic consumption and link to resistance. Clin Microbiol Infect. 2009;15(3):12-5. https://doi.org/10.1111/j.1469-0691.2009.02725.x
García-Rey C, Martín-Herrero JE, Baquero F. Antibiotic consumption and generation of resistance in Streptococcus pneumoniae: the paradoxical impact of quinolones in a complex selective landscape. Clin Microbiol Infect. 2006;12(3):55-66. https://doi.org/10.1111/j.1469-0691.2006.01397.x
Barros RR, Souza AF, Oliveira Luiz FB. Polyclonal spread of Streptococcus agalactiae resistant to clindamycin among pregnant women in Brazil. J Antimicrob Chemother. 2016:71(7):2054-6. https://doi.org/10.1093/jac/dkw085
Hawkins PA, Law CS, Metcalf BJ, Chochua S, Jackson DM, Westblade LF, Jerris R, Beall BW, McGee L. Cross-resistance to lincosamides, streptogramins A and pleuromutilins in Streptococcus agalactiae isolates from the USA. J Antimicrob Chemother. 2017;72(7):1886-92. https://doi.org/10.1093/jac/dkx077
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 Chemothe. 2003;47(11):3605-9. https://doi.org/10.1128/AAC.47.11.3605-3609.2003
Piccinelli G, Gargiulo F, Corbellini S, Ravizzol, G, Bonfanti C, Caruso A, De francesco MA. Emergence of the first levofloxacin-resistant strains of Streptococcus agalactiae isolated in Italy. Antimicrob Agents Chemother. 2015;59(4):2466-9. https://doi.org/10.1128/AAC.05127-14
Barros RR, Kegele FC, Paula GR, Brito MA, Duarte RS. Molecular characterization of the first fluoroquinolone resistant strains of Streptococcus agalactiae isolated in Brazil. Braz J Infect Dis. 2012;16(5):476-8. https://doi.org/10.1016/j.bjid.2012.05.003
Downloads
Publicado
Como Citar
Edição
Seção
Licença
Copyright (c) 2018 Scientia Medica
Este trabalho está licenciado sob uma licença Creative Commons Attribution 4.0 International License.