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Risk Factors for Infant Colonization by Hypervirulent CC17 Group B Streptococcus: Toward the Understanding of Late-onset Disease.
Tazi, Asmaa; Plainvert, Céline; Anselem, Olivia; Ballon, Morgane; Marcou, Valérie; Seco, Aurélien; El Alaoui, Fatma; Joubrel, Caroline; El Helali, Najoua; Falloukh, Emile; Frigo, Amandine; Raymond, Josette; Trieu-Cuot, Patrick; Branger, Catherine; Le Monnier, Alban; Azria, Elie; Ancel, Pierre-Yves; Jarreau, Pierre Henri; Mandelbrot, Laurent; Goffinet, François; Poyart, Claire.
Afiliação
  • Tazi A; Department of Bacteriology, University Hospitals Paris Centre-Cochin, French National Center for Streptococci, Assistance Publique - Hôpitaux de Paris (AP-HP).
  • Plainvert C; Département Hospitalo-Universitaire Risks and Pregnancy.
  • Anselem O; Team Barriers and Pathogens of Cochin Institute, Institut National de la Santé et de la Recherche Médicale (INSERM) U1016 - Unité Mixte de Recherche Centre National de la Recherche Scientifique (UMR CNRS) 8104.
  • Ballon M; Paris Descartes University.
  • Marcou V; Department of Bacteriology, University Hospitals Paris Centre-Cochin, French National Center for Streptococci, Assistance Publique - Hôpitaux de Paris (AP-HP).
  • Seco A; Département Hospitalo-Universitaire Risks and Pregnancy.
  • El Alaoui F; Team Barriers and Pathogens of Cochin Institute, Institut National de la Santé et de la Recherche Médicale (INSERM) U1016 - Unité Mixte de Recherche Centre National de la Recherche Scientifique (UMR CNRS) 8104.
  • Joubrel C; Département Hospitalo-Universitaire Risks and Pregnancy.
  • El Helali N; Paris Descartes University.
  • Falloukh E; Department of Obstetrics and Gynecology, Port-Royal Maternity, University Hospitals Paris Centre Cochin Port Royal, AP-HP.
  • Frigo A; Département Hospitalo-Universitaire Risks and Pregnancy.
  • Raymond J; Obstetrical, Perinatal and Pediatric Epidemiology Research Team (Epidémiologie Périnatale, Obstétricale et Pédiatrique), INSERM UMR 1153.
  • Trieu-Cuot P; Département Hospitalo-Universitaire Risks and Pregnancy.
  • Branger C; Paris Descartes University.
  • Le Monnier A; Maternity Unit, Paris Saint Joseph Hospital.
  • Azria E; Département Hospitalo-Universitaire Risks and Pregnancy.
  • Ancel PY; Obstetrical, Perinatal and Pediatric Epidemiology Research Team (Epidémiologie Périnatale, Obstétricale et Pédiatrique), INSERM UMR 1153.
  • Jarreau PH; Department of Microbiology, Louis Mourier Hospital, AP-HP.
  • Mandelbrot L; Department of Bacteriology, University Hospitals Paris Centre-Cochin, French National Center for Streptococci, Assistance Publique - Hôpitaux de Paris (AP-HP).
  • Goffinet F; Département Hospitalo-Universitaire Risks and Pregnancy.
  • Poyart C; Paris Descartes University.
Clin Infect Dis ; 69(10): 1740-1748, 2019 10 30.
Article em En | MEDLINE | ID: mdl-30946447
ABSTRACT

BACKGROUND:

In infants, the mode of acquisition of CC17 group B Streptococcus (GBS), the hypervirulent clone responsible for late-onset disease (LOD), remains elusive.

METHODS:

In a prospective multicenter study in France, we evaluated GBS colonization in mother-baby pairs with 2 months of follow-up between 2012 and 2015. Criteria included positivity for GBS colonization at antenatal screening or at delivery. Maternal vaginal samples and infant oral cavity and stool samples were analyzed at delivery, 21 ± 7 days (D21), and 60 ± 7 days (D60) post-delivery.

RESULTS:

A total of 890 mother-baby pairs were analyzed. GBS colonized 7%, 21%, and 23% of the infants at birth, D21, and D60, respectively, of which 10%, 11%, and 13% were identified as CC17 GBS. Concordance between maternal and infant GBS type was 96%. At D21, the main risk factors for infant colonization by GBS were simultaneous maternal colonization of the vagina (odds ratio [OR], 4.50; 95% confidence interval [CI], 1.69-15.61) and breast milk (OR, 7.93; 95% CI, 3.81-17.14). Importantly, 38% (95% CI, 23%-56%) of infants colonized by CC17 GBS appeared colonized for the first time at D60 vs 18% (95% CI, 14%-24%; P < .049) of infants colonized by non-CC17 GBS. Multivariate analysis showed a higher risk for de novo infant colonization by CC17 at D60 than by other GBS (OR, 2.45; 95% CI, 1.02-5.88).

CONCLUSIONS:

The high incidence of CC17 GBS in LOD is likely due to an enhanced post-delivery mother-to-infant transmission.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções Estreptocócicas / Streptococcus agalactiae / Transmissão Vertical de Doenças Infecciosas Tipo de estudo: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Infant / Male / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Clin Infect Dis Assunto da revista: DOENCAS TRANSMISSIVEIS Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções Estreptocócicas / Streptococcus agalactiae / Transmissão Vertical de Doenças Infecciosas Tipo de estudo: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Infant / Male / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Clin Infect Dis Assunto da revista: DOENCAS TRANSMISSIVEIS Ano de publicação: 2019 Tipo de documento: Article