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Associations between nasopharyngeal carriage of Group B Streptococcus and other respiratory pathogens during early
Ebenezer Foster-Nyarko1, Brenda Kwambana1, Odutola Aderonke1
1Vaccines and Immunity Theme, Medical Research Council Unit, Banjul, The Gambia.
Insights
Group B Streptococcus (GBS) carriage in Gambian infants is characterized, with serotypes V and II dominating. GBS co-colonization showed associations with Staphylococcus aureus, Streptococcus pneumoniae, and Moraxella catarrhalis.
Area of Science:
- Pediatrics
- Microbiology
- Infectious Diseases
Background:
- Group B Streptococcus (GBS) carriage in West African infants is not well-understood.
- This study investigated GBS co-carriage with other respiratory pathogens in infants in The Gambia.
Purpose of the Study:
- To characterize GBS carriage, serotypes, and antibiotic susceptibility in infants.
- To explore co-carriage patterns of GBS with common respiratory pathogens.
Main Methods:
- 1200 two-month-old infants in The Gambia were assessed.
- Carriage of Beta-haemolytic Streptococci (BHS) groups A-G, Streptococcus pneumoniae, Haemophilus influenzae, Staphylococcus aureus, and Moraxella catarrhalis was evaluated.
Main Results:
- Beta-haemolytic Streptococci prevalence was 20.0%, with GBS being dominant (13.8%), particularly serotypes V and II.
- GBS carriage was associated with Staphylococcus aureus (OR 1.89) and negatively associated with Streptococcus pneumoniae (OR 0.47) and Moraxella catarrhalis (OR 0.61).
- Over 89% of GBS isolates were susceptible to most tested antibiotics, except for tetracycline resistance (89%).
Conclusions:
- This study establishes baseline data for GBS carriage in two-month-old infants in West Africa.
- Serotypes V and II are the dominant GBS serotypes in this region.
- Findings may inform future GBS vaccine development for West Africa.
Background:
In West Africa, the carriage of Group B Streptococcus (GBS), among infants is poorly characterised. We investigated co-carriage of GBS with other respiratory pathogens in the infants' nasopharynx in The Gambia.
Methods:
We assessed the carriage, serotypes and antibiotic susceptibility of Beta-haemolytic Streptococci (BHS) groups A-G; along with the carriage of Streptococcus pneumoniae; Haemophilus influenzae; Staphylococcus aureus and Moraxella catarrhalis in 1200 two-month old infants.
Results:
The BHS prevalence was 20.0 % and GBS dominated (13.8 %), particularly serotypes V and II; serotype V being negatively associated with H. Influenzae carriage (OR 0.41 [95 % CI: 0.18-0.93], p = 0.033). Although co-colonization of GBS and other BHS was not seen, colonization with GBS was positively associated with S. aureus (OR 1.89 [95 % CI: 1.33-2.69], P < 0.001) and negatively associated with S. pneumoniae (OR 0.47 [95 % CI: 0.33-0.67], p < 0.001) and M. catarrhalis (OR 0.61 [95 % CI: 0.40-0.92], p = 0.017). ≥ 89 % of GBS isolates were susceptible to most antibiotics tested, except for tetracycline resistance, which was 89 %.
Conclusion:
This study provides baseline data on the carriage of GBS in two month old infants from West Africa. The dominant serotypes of GBS in this setting are serotypes V and II. This may be important for future GBS vaccine development for the West African sub-region.
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