Volume 27, Number 9—September 2021
CME ACTIVITY - Research
Maternal Carriage in Late-Onset Group B Streptococcus Disease, Italy
Table 1
Characteristic | LOD cases in preterm neonates, n = 18† | LOD cases in full-term neonates, n = 80 | p value | Total, N = 98 |
---|---|---|---|---|
Median birthweight, g (IQR) | 1,285 (987–1,800) | 3,185 (2,898–3,518) | NA | 3,110 (2,570–3,425) |
Gestational age at delivery, wks, median (IQR) | 31.0 (27.0–33.0) | 39.0 (38.0–40.0) | NA | 39 (38–40) |
Vaginal delivery | 4 (22.2) | 56 (70.0) | <0.01 | 60 (61.2) |
Planned caesarean section | 8 (44.4) | 18 (22.5) | 0.11 | 26 (26.5) |
IAP exposure‡ | 9 (50.0) | 29 (36.3) | 0.42 | 38 (38.8) |
Age at onset, median, d (IQR) | 33 (26–45) | 27 (15–43) | 0.08 | 29 (16–43) |
Mechanical ventilation | 7 (38.9) | 4 (5.0) | <0.01 | 11 (11.2) |
Focal infection§ | 0 | 6 (7.5) | 0.51 | 6 (6.1) |
Meningitis with or without sepsis¶ | 8 (57.1) | 32 (56.1) | 0.82 | 40 (56.3·) |
Brain lesions at discharge from hospital# | 7 (38.9) | 15 (18.8) | 0.12 | 22 (22.4) |
Death | 1 (5.6) | 1 (1.3) | 0.81 | 2 (1.0) |
*Values are no. (%) except as indicated. GBS, group B streptococcus; IAP, intrapartum antibiotic prophylaxis; IQR, interquartile range; LOD, late-onset disease; NA, not applicable. †14 were early to moderate and 4 were late preterm neonates. ‡IAP was adequate (ampicillin, penicillin, or cefazolin given >4 h before delivery) in 3/9 (33.3%) cases in preterm neonates and in 17/29 (58.6%) cases in full-term neonates. §GBS-positive blood culture result associated with focal signs outside the respiratory tract (cellulitis, arthritis, parotiditis, others) (10). ¶Percentage and significance were calculated based on findings from lumbar puncture (in preterm neonates, 14 cases; in full-term neonates, 57 cases). Meningitis was culture-proven in 36/40 cases. #Brain lesions were confirmed through ultrasound, magnetic resonance study, or both.
References
- Madrid L, Seale AC, Kohli-Lynch M, Edmond KM, Lawn JE, Heath PT, et al.; Infant GBS Disease Investigator Group. Infant group B streptococcal disease incidence and serotypes worldwide: systematic review and meta-analyses. Clin Infect Dis. 2017;65(suppl_2):S160–72. DOIPubMedGoogle Scholar
- Puopolo KM, Lynfield R, Cummings JJ; COMMITTEE ON FETUS AND NEWBORN; COMMITTEE ON INFECTIOUS DISEASES. Committee on Infectious Diseases. Management of infants at risk for group B streptococcal disease. Pediatrics. 2019;144:
e20191881 . DOIPubMedGoogle Scholar - Nanduri SA, Petit S, Smelser C, Apostol M, Alden NB, Harrison LH, et al. Epidemiology of invasive early-onset and late-onset group B streptococcal disease in the United States, 2006 to 2015: multistate laboratory and population-based surveillance. JAMA Pediatr. 2019;173:224–33. DOIPubMedGoogle Scholar
- Seale AC, Bianchi-Jassir F, Russell NJ, Kohli-Lynch M, Tann CJ, Hall J, et al. Estimates of the burden of group B streptococcal disease worldwide for pregnant women, stillbirths, and children. Clin Infect Dis. 2017;65(suppl_2):S200–19. DOIPubMedGoogle Scholar
- Berardi A, Rossi C, Creti R, China M, Gherardi G, Venturelli C, et al. Group B streptococcal colonization in 160 mother-baby pairs: a prospective cohort study. J Pediatr. 2013;163:1099–104.e1. DOIPubMedGoogle Scholar
- Tazi A, Plainvert C, Anselem O, Ballon M, Marcou V, Seco A, et al. Risk factors for infant colonization by hypervirulent CC17 group B Streptococcus: toward the understanding of late-onset disease. Clin Infect Dis. 2019;69:1740–8. DOIPubMedGoogle Scholar
- Manning SD, Lewis MA, Springman AC, Lehotzky E, Whittam TS, Davies HD. Genotypic diversity and serotype distribution of group B streptococcus isolated from women before and after delivery. Clin Infect Dis. 2008;46:1829–37. DOIPubMedGoogle Scholar
- Lin FY, Weisman LE, Troendle J, Adams K. Prematurity is the major risk factor for late-onset group B streptococcus disease. J Infect Dis. 2003;188:267–71. DOIPubMedGoogle Scholar
- Joubrel C, Tazi A, Six A, Dmytruk N, Touak G, Bidet P, et al. Group B streptococcus neonatal invasive infections, France 2007-2012. Clin Microbiol Infect. 2015;21:910–6. DOIPubMedGoogle Scholar
- Berardi A, Rossi C, Lugli L, Creti R, Bacchi Reggiani ML, Lanari M, et al.; GBS Prevention Working Group, Emilia-Romagna. Group B streptococcus late-onset disease: 2003-2010. Pediatrics. 2013;131:e361–8. DOIPubMedGoogle Scholar
- Verani JR, McGee 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(RR-10):1–36.PubMedGoogle Scholar
- Le Doare K, Kampmann B. Breast milk and Group B streptococcal infection: vector of transmission or vehicle for protection? Vaccine. 2014;32:3128–32. DOIPubMedGoogle Scholar
- Filleron A, Lombard F, Jacquot A, Jumas-Bilak E, Rodière M, Cambonie G, et al. Group B streptococci in milk and late neonatal infections: an analysis of cases in the literature. Arch Dis Child Fetal Neonatal Ed. 2014;99:F41–7. DOIPubMedGoogle Scholar
- Zimmermann P, Gwee A, Curtis N. The controversial role of breast milk in GBS late-onset disease. J Infect. 2017;74(Suppl 1):S34–40. DOIPubMedGoogle Scholar
- Le Doare K, Kampmann B, Vekemans J, Heath PT, Goldblatt D, Nahm MH, et al. Serocorrelates of protection against infant group B streptococcus disease. Lancet Infect Dis. 2019;19:e162–71. DOIPubMedGoogle Scholar
- Imperi M, Pataracchia M, Alfarone G, Baldassarri L, Orefici G, Creti R. A multiplex PCR assay for the direct identification of the capsular type (Ia to IX) of Streptococcus agalactiae. J Microbiol Methods. 2010;80:212–4. DOIPubMedGoogle Scholar
- Creti R, Fabretti F, Orefici G, von Hunolstein C. Multiplex PCR assay for direct identification of group B streptococcal alpha-protein-like protein genes. J Clin Microbiol. 2004;42:1326–9. DOIPubMedGoogle Scholar
- Imperi M, Gherardi G, Berardi A, Baldassarri L, Pataracchia M, Dicuonzo G, et al. Invasive neonatal GBS infections from an area-based surveillance study in Italy. Clin Microbiol Infect. 2011;17:1834–9. DOIPubMedGoogle Scholar
- Creti R, Imperi M, Berardi A, Pataracchia M, Recchia S, Alfarone G, et al.; Italian Neonatal GBS Infections Working Group. Neonatal group B Streptococcus infections. Pediatr Infect Dis J. 2017;36:256–62. DOIPubMedGoogle Scholar
- Springman AC, Lacher DW, Waymire EA, Wengert SL, Singh P, Zadoks RN, et al. Pilus distribution among lineages of group b streptococcus: an evolutionary and clinical perspective. BMC Microbiol. 2014;14:159. DOIPubMedGoogle Scholar
- Berardi A, Baroni L, Bacchi Reggiani ML, Ambretti S, Biasucci G, Bolognesi S, et al.; GBS Prevention Working Group Emilia-Romagna. The burden of early-onset sepsis in Emilia-Romagna (Italy): a 4-year, population-based study. J Matern Fetal Neonatal Med. 2016;29:3126–31. DOIPubMedGoogle Scholar
- Berardi A, Rossi C, Bacchi Reggiani ML, Bastelli A, Capretti MG, Chiossi C, et al. An area-based study on intrapartum antibiotic prophylaxis for preventing group B streptococcus early-onset disease: advances and limitations. J Matern Fetal Neonatal Med. 2017;30:1739–44. DOIPubMedGoogle Scholar
- Khatami A, Randis TM, Tavares L, Gegick M, Suzman E, Ratner AJ. Vaginal co-colonization with multiple Group B Streptococcus serotypes. Vaccine. 2019;37:409–11. DOIPubMedGoogle Scholar
- Carreras-Abad C, Cochet M, Hall T, Ramkhelawon L, Khalil A, Peregrine E, et al. Developing a serocorrelate of protection against invasive group B streptococcus disease in pregnant women: a feasibility study. Health Technol Assess. 2019;23:1–40. DOIPubMedGoogle Scholar
- Ratner AJ. Enhanced postnatal acquisition of hypervirulent group B Streptococcus. Clin Infect Dis. 2019;69:1749–51. DOIPubMedGoogle Scholar
- Tazi A, Disson O, Bellais S, Bouaboud A, Dmytruk N, Dramsi S, et al. The surface protein HvgA mediates group B streptococcus hypervirulence and meningeal tropism in neonates. J Exp Med. 2010;207:2313–22. DOIPubMedGoogle Scholar
- Campisi E, Rosini R, Ji W, Guidotti S, Rojas-López M, Geng G, et al. Genomic analysis reveals multi-drug resistance clusters in group B Streptococcus CC17 hypervirulent isolates causing neonatal invasive disease in southern mainland China. Front Microbiol. 2016;7:1265. DOIPubMedGoogle Scholar
- Martins ER, Pedroso-Roussado C, Melo-Cristino J, Ramirez M; Portuguese Group for the Study of Streptococcal Infections. Streptococcus agalactiae causing neonatal infections in Portugal (2005–2015): diversification and emergence of a CC17/PI-2b multidrug resistant sublineage. Front Microbiol. 2017;8:499. DOIPubMedGoogle Scholar
- Teatero S, Ramoutar E, McGeer A, Li A, Melano RG, Wasserscheid J, et al. Clonal Complex 17 Group B Streptococcus strains causing invasive disease in neonates and adults originate from the same genetic pool. Sci Rep. 2016;6:20047. DOIPubMedGoogle Scholar
- Perez PF, Doré J, Leclerc M, Levenez F, Benyacoub J, Serrant P, et al. Bacterial imprinting of the neonatal immune system: lessons from maternal cells? Pediatrics. 2007;119:e724–32. DOIPubMedGoogle Scholar
- Le Doare K, Bellis K, Faal A, Birt J, Munblit D, Humphries H, et al. SIgA, TGF-β1, IL-10, and TNFα in colostrum are associated with infant group B Streptococcus colonization. Front Immunol. 2017;8:1269–79. DOIPubMedGoogle Scholar
- Dangor Z, Khan M, Kwatra G, Izu A, Nakwa F, Ramdin T, et al. The association between breast milk group B streptococcal capsular antibody levels and late-onset disease in young infants. Clin Infect Dis. 2020;70:1110–4.PubMedGoogle Scholar