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Updated: Jul 15, 2026

Experimental Human Pneumococcal Carriage
Published on: February 15, 2013
Longitudinal study on pneumococcal carriage during the first year of life in Bangladesh
Simo M Granat1, Zakaria Mia, Jukka Ollgren
1Department of Vaccines, National Public Health Institute KTL, Helsinki, Finland. Simo.Granat@helsinki.fi
Insights
Pneumococcal carriage develops rapidly in young children in Bangladesh, with specific serogroups dominating. These findings are typical for developing countries and can inform global vaccination strategies.
Area of Science:
- Microbiology
- Epidemiology
- Public Health
Background:
- Pneumococcal conjugate vaccine use highlights the importance of asymptomatic pneumococcal carriage.
- Serotype replacement and herd immunity underscore the need to study pneumococcal carriage dynamics.
Purpose of the Study:
- To describe the development of pneumococcal carriage in a developing country setting.
- To conduct a longitudinal pneumococcal carriage study in Bangladesh.
Main Methods:
- Ninety-nine children and their families in Savar, Bangladesh, were enrolled.
- Nasopharyngeal samples were collected bi-weekly from index children and family members.
- Pneumococci were identified and serotyped from cultured samples.
Main Results:
- High carriage prevalence (40-50%) observed in newborns by 8 weeks.
- Rapid acquisition: 50% of children colonized by 8 weeks.
- Serogroups 6 and 19 predominated in children under 1 year and up to 9 years.
Conclusions:
- Observed pneumococcal carriage features are characteristic of developing countries.
- Longitudinal modeling of carriage data has broad geographic applicability.
- Findings can inform public health interventions and vaccine strategies.
Background:
The strong herd immunity effect and the serotype replacement associated with the use of the pneumococcal conjugate vaccine have highlighted the importance of asymptomatic pneumococcal carriage. To describe the development of pneumoccoccal carriage in a developing country setting we carried out a longitudinal pneumococcal carriage study in Bangladesh.
Methods:
Ninety-nine children, born in Savar, Bangladesh between May 2000 and April 2001, were enrolled in the study with their families. Nasopharyngeal samples were collected at prescheduled 2-4 week intervals from the index children and from their family members. The nasopharyngeal swabs were cultured for pneumococcal growth and pneumococci were identified and serotyped by standard methods.
Results:
We collected 1459 samples (92% of those planned) from the 99 index children and 2865 samples from other family members. The data showed high point prevalences of pneumococcal carriage among newborns (40-50% from 8 weeks of age on), a rapid pneumococcal acquisition with age (50% of the children had been colonized by pneumococci at least once by the age of 8 weeks) and a wide range of different serogroups/types (SGT). SGT 6 and 19 accounted for 35% of the pneumococci isolated from children <1-year-old, followed by SGT 15, 23, and 10 for a total of 56%. The SGT distribution in children up to 9-year-old was similar to that among the <1 year olds, with SGT 6 and 19 predominating. Older children and adults differed from the younger children by not having clearly predominating SGTs.
Conclusions:
The features found in our study are typical of pneumococcal carriage in developing countries. We believe that results from longitudinal modeling of carriage based on these extensive data can have wide geographic application.
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