TY - JOUR
T1 - Epidemiology of Group B Streptococcus
T2 - Maternal Colonization and Infant Disease in Kampala, Uganda
AU - PROGRESS Study Group
AU - Kyohere, Mary
AU - Davies, Hannah Georgia
AU - Karampatsas, Konstantinos
AU - Cantrell, Liberty
AU - Musoke, Philippa
AU - Nakimuli, Annettee
AU - Tusubira, Valerie
AU - Nsimire, Juliet Sendagala
AU - Jamrozy, Dorota
AU - Khan, Uzma Basit
AU - Bentley, Stephen D.
AU - Spiller, Owen B.
AU - Farley, Caitlin
AU - Hall, Tom
AU - Daniel, Olwenn
AU - Beach, Simon
AU - Andrews, Nick
AU - Schrag, Stephanie J.
AU - Cutland, Clare L.
AU - Gorringe, Andrew
AU - Leung, Stephanie
AU - Taylor, Stephen
AU - Heath, Paul T.
AU - Cose, Stephen
AU - Baker, Carol
AU - Voysey, Merryn
AU - Le Doare, Kirsty
AU - Sekikubo, Musa
AU - Djennad, Abdelmajid
AU - Nyamaizi, Agnes
AU - Ssali, Agnes
AU - Amone, Alexander
AU - Wamawobe, Amusa
AU - Nanyunja, Carol
AU - Najuka, Christine
AU - Komugisha, Cleophas
AU - Sseremba, Christine
AU - Nakibuuka, Lydia
AU - Kibirige, Daniel
AU - Shelley, Dan R.
AU - Portal, Edward A.R.
AU - Duckworth, Ellie
AU - Karafillakis, Emilie
AU - O'hara, Geraldine
AU - Matovu, Godfrey
AU - Seeley, Janet
AU - Peacock, Joseph
AU - Cowie, Katie
AU - Hookham, Lauren
AU - Chalker, Vicki
N1 - Publisher Copyright:
© 2025 The Author(s). Published by Oxford University Press on behalf of Infectious Diseases Society of America.
PY - 2025/4/1
Y1 - 2025/4/1
N2 - Background: Child survival rates have improved globally, but neonatal mortality due to infections, such as group B Streptococcus (GBS), remains a significant concern. The global burden of GBS-related morbidity and mortality is substantial. However, data from low and middle-income countries are lacking. Vaccination during pregnancy could be a feasible strategy to address GBS-related disease burden. Methods: We assessed maternal rectovaginal GBS colonization and neonatal disease rates in a prospective cohort of 6062 women-infant pairs. Surveillance for invasive infant disease occurred in parallel at 2 Kampala hospital sites. In a nested case-control study, we identified infants <90 days of age with invasive GBS disease (iGBS) (n = 24) and healthy infants born to mothers colonized with GBS (n = 72). We measured serotype-specific anticapsular immunoglobulin G (IgG) in cord blood/infant sera using a validated multiplex Luminex assay. Results: We found a high incidence of iGBS (1.0 per 1000 live births) within the first 90 days of life across the surveillance sites, associated with a high case fatality rate (18.2%). Maternal GBS colonization prevalence was consistent with other studies in the region (14.7% [95% confidence interval, 13.7%-15.6%]). IgG geometric mean concentrations were lower in cases than controls for serotypes Ia (0.005 vs 0.12 μg/mL; P =. 05) and III (0.011 vs 0.036 μg/mL; P =. 07) and in an aggregate analysis of all serotypes (0.014 vs 0.05 μg/mL; P =. 02). Conclusions: We found that GBS is an important cause of neonatal and young infant disease in Uganda and confirmed that maternally derived antibodies were lower in early-onset GBS cases than in healthy exposed controls.
AB - Background: Child survival rates have improved globally, but neonatal mortality due to infections, such as group B Streptococcus (GBS), remains a significant concern. The global burden of GBS-related morbidity and mortality is substantial. However, data from low and middle-income countries are lacking. Vaccination during pregnancy could be a feasible strategy to address GBS-related disease burden. Methods: We assessed maternal rectovaginal GBS colonization and neonatal disease rates in a prospective cohort of 6062 women-infant pairs. Surveillance for invasive infant disease occurred in parallel at 2 Kampala hospital sites. In a nested case-control study, we identified infants <90 days of age with invasive GBS disease (iGBS) (n = 24) and healthy infants born to mothers colonized with GBS (n = 72). We measured serotype-specific anticapsular immunoglobulin G (IgG) in cord blood/infant sera using a validated multiplex Luminex assay. Results: We found a high incidence of iGBS (1.0 per 1000 live births) within the first 90 days of life across the surveillance sites, associated with a high case fatality rate (18.2%). Maternal GBS colonization prevalence was consistent with other studies in the region (14.7% [95% confidence interval, 13.7%-15.6%]). IgG geometric mean concentrations were lower in cases than controls for serotypes Ia (0.005 vs 0.12 μg/mL; P =. 05) and III (0.011 vs 0.036 μg/mL; P =. 07) and in an aggregate analysis of all serotypes (0.014 vs 0.05 μg/mL; P =. 02). Conclusions: We found that GBS is an important cause of neonatal and young infant disease in Uganda and confirmed that maternally derived antibodies were lower in early-onset GBS cases than in healthy exposed controls.
KW - anticapsular antibody
KW - correlate of protection
KW - group B Streptococcus
KW - invasive disease
KW - risk reduction
UR - http://www.scopus.com/inward/record.url?scp=105002439830&partnerID=8YFLogxK
U2 - 10.1093/ofid/ofaf167
DO - 10.1093/ofid/ofaf167
M3 - Article
AN - SCOPUS:105002439830
SN - 2328-8957
VL - 12
JO - Open Forum Infectious Diseases
JF - Open Forum Infectious Diseases
IS - 4
M1 - ofaf167
ER -