Related Experiment Video
Updated: Oct 21, 2025

Experimental Human Pneumococcal Carriage
Published on: February 15, 2013
Pneumococcal Carriage in Burkina Faso After 13-Valent Pneumococcal Conjugate Vaccine Introduction: Results From 2
Lassané Kaboré1,2, Tolulope Adebanjo3, Berthe Marie Njanpop-Lafourcade1
1Agence de Médecine Préventive, Ouagadougou, Burkina Faso.
Background:
Burkina Faso, a country in Africa's meningitis belt, introduced 13-valent pneumococcal conjugate vaccine (PCV13) in October 2013, with 3 primary doses given at 8, 12 and 16 weeks of age. To assess whether the new PCV13 program controlled pneumococcal carriage, we evaluated overall and serotype-specific colonization among children and adults during the first 3 years after introduction.
Methods:
We conducted 2 population-based, cross-sectional, age-stratified surveys in 2015 and 2017 in the city of Bobo-Dioulasso. We used standardized questionnaires to collect sociodemographic, epidemiologic, and vaccination data. Consenting eligible participants provided nasopharyngeal (all ages) and oropharyngeal (≥5 years only) swab specimens. Swab specimens were plated onto blood agar either directly (2015) or after broth enrichment (2017). Pneumococci were serotyped by conventional multiplex polymerase chain reaction. We assessed vaccine effect by comparing the proportion of vaccine-type (VT) carriage among colonized individuals from a published baseline survey (2008) with each post-PCV survey.
Results:
We recruited 992 (2015) and 1005 (2017) participants. Among children aged <5 years, 42.8% (2015) and 74.0% (2017) received ≥2 PCV13 doses. Among pneumococcal carriers aged <1 year, VT carriage declined from 55.8% in 2008 to 36.9% in 2017 (difference, 18.9%; 95% confidence interval, 1.9%-35.9%; P = .03); among carriers aged 1-4 years, VT carriage declined from 55.3% to 31.8% (difference, 23.5%; 6.8%-40.2%; P = .004); and among participants aged ≥5 years, no significant change was observed.
Conclusion:
Within 3 years of PCV13 implementation in Burkina Faso, we documented substantial reductions in the percentage of pneumococcal carriers with a VT among children aged <5 years, but not among persons aged ≥5 years. More time, a change in the PCV13 schedule, or both, may be needed to better control pneumococcal carriage in this setting.
Insights
The 13-valent pneumococcal conjugate vaccine (PCV13) significantly reduced pneumococcal carriage in young children in Burkina Faso within three years. However, older individuals did not show a similar reduction in vaccine-type pneumococcal carriage.
Area of Science:
- Public Health
- Vaccinology
- Epidemiology
Background:
- Burkina Faso, located in Africa's meningitis belt, introduced the 13-valent pneumococcal conjugate vaccine (PCV13) in October 2013.
- The vaccine was administered in a schedule of three primary doses at 8, 12, and 16 weeks of age.
Purpose of the Study:
- To evaluate the impact of the PCV13 program on pneumococcal carriage in Burkina Faso.
- To assess both overall and serotype-specific pneumococcal colonization in children and adults in the first three years post-introduction.
Main Methods:
- Two population-based, cross-sectional, age-stratified surveys were conducted in Bobo-Dioulasso in 2015 and 2017.
- Nasopharyngeal and oropharyngeal swabs were collected, and pneumococci were serotyped using multiplex polymerase chain reaction.
- Vaccine effects were assessed by comparing vaccine-type (VT) carriage proportions from post-PCV surveys to a 2008 baseline survey.
Main Results:
- Among children under 5 years old, vaccine-type pneumococcal carriage declined significantly from 55.8% in 2008 to 36.9% in 2017 among carriers under 1 year, and from 55.3% to 31.8% among carriers aged 1-4 years.
- In participants aged 5 years and older, no significant change in vaccine-type pneumococcal carriage was observed.
- Vaccination coverage with at least two PCV13 doses among children under 5 years increased from 42.8% in 2015 to 74.0% in 2017.
Conclusions:
- Within three years of PCV13 introduction in Burkina Faso, substantial reductions in vaccine-type pneumococcal carriage were observed in children under 5 years.
- No significant reduction in vaccine-type pneumococcal carriage was observed in individuals aged 5 years and older.
- Further time, adjustments to the PCV13 schedule, or both may be necessary to effectively control pneumococcal carriage in the entire population.
More Related Videos
Related Concept Videos
Pneumonia I: Introduction
Risk Factors
Various factors influence the likelihood of developing pneumonia. Age plays a crucial role, with infants, children under two, and individuals over 65 at increased risk due to their...
Pulmonary Tuberculosis IV
Several diagnostic approaches are used to detect TB. The conventional method is the Tuberculin Skin Test (TST), also known as the Mantoux test. However, this method has...
Pulmonary Tuberculosis V
Latent tuberculosis infection occurs when TB bacteria are present in a person's body, but are not causing illness or symptoms. It is not contagious, and preventive treatment is crucial to avoid the...
Pulmonary Tuberculosis I
Causative Organism
The primary infectious agent causing tuberculosis is Mycobacterium tuberculosis, a slow-growing, acid-fast, aerobic rod that exhibits sensitivity to heat and ultraviolet light. Instances of Mycobacterium bovis and Mycobacterium avium contributing to the development of TB infection are rare.
Mode of...
Pulmonary Tuberculosis II
Here is a detailed explanation of its pathophysiology:
Transmission: The process begins when a person inhales droplet nuclei containing M. tuberculosis. These are typically released into the air when an individual with pulmonary or...
Pulmonary Tuberculosis III
The first classification is based on the development of the disease, and it includes the following categories:

