Prevalence of Naopharyngeal Carriage in Children in the Community

Streptococcus pneumoniae bacteria (pneumococcus) is a major cause of disease and disability worldwide, and is vaccine-preventable. In 2015, the Ministry of Health of Nepal began providing a 10-valent pneumococcal conjugate vaccine to infants (PCV10) as the vaccine was introduced into its routine infant immunization schedule.

Estimating the impact of PCV on transmission in the community

The pneumococcus is a bacterium that is often found in the nasopharynx (i.e., the back part of the nasal cavity) of children and adults without causing disease or symptoms. Pneumococcal disease occurs when the bacteria move from this harmless location—nasopharyngeal carriage—to other more vulnerable parts of the body, including the lungs (pneumonia) or more invasive locations such as the blood (bacteremia and sepsis) or the membranes that surround and protect the brain (meningitis).

Those who carry pneumococcus in their nasopharynx - regardless of whether they are sick or not - can spread the bacterium to others. For this reason, preventing carriage in a child provides protection to other members of the household including siblings and grandparents, who are at higher risk of developing pneumococcal disease than those in the general community; this type of vaccine effect is often called “indirect protection”.

More than 90 distinct pneumococcal serotypes have been identified throughout the world, with a small number of these serotypes accounting for most disease in infants. The vaccine Nepali children receive, PCV10, protects against 10 pneumococcal serotypes. The COCA study is measuring whether these pneumococcal serotypes are less likely to circulate in Nepal following the introduction of PCV10, as an indicator of the vaccine's effectiveness. The study is also measuring:

  • The amount of pneumococcal DNA present in the nasopharynx (i.e. carriage density) of each child surveyed,
  • How many different serotypes each child is carrying in the nasopharynx as children are likely to be carrying more than one type,
  • Whether serotypes absent from the vaccine are more likely to circulate after vaccine introduction, and
  • Whether there are differences in carriage trends in rural versus urban households.

Since 2015, we have measured carriage in thousands of healthy children up to five years of age from an urban setting in Kathmandu and a rural setting in Okhaldhunga.

Preliminary results: Declines in vaccine-type carriage

Preliminary results suggest that the vaccine is working to reduce vaccine-type carriage. The proportion of children carrying the type of pneumococcal bacteria included in the vaccine decreased by 66% in the first two years of vaccine use, from 28% to 10%. This indicates that PCV10 is likely having an important impact on the health of young children in Nepal.

Fig. 1 In an urban setting, the proportion of children carrying vaccine-type pneumococcal bacteria has declined since the introduction of PCV10

21% 17% 14% 11% 8%
PCV10 serotypes: 1, 4, 5, 6B, 7F, 9V, 14, 18C, 19F, 23F; PCV13 additional serotypes: 3, 6A, 19A. Ages ranged from 6 months to five years. 2018 data do not include samples from December.

Fig. 2 In a rural setting, the proportion of children carrying vaccine-type pneumococcal bacteria has declined since the introduction of PCV10

29% 10% 8%
PCV10 serotypes: 1, 4, 5, 6B, 7F, 9V, 14, 18C, 19F, 23F; PCV13 additional serotypes: 3, 6A, 19A. Ages ranged from 6 months to 2 years. Children in the rural site were not sampled as much, therefore data from all years are not available. December 2018 data were not included.

Carriage trends in rural versus urban households

Nasopharyngeal swabs were collected from healthy children in urban (Kathmandu valley; age 6-59 months) and rural (Okhaldhunga, age 6-23 months) Nepal in 2018 and 2019, and were cultured at Patan Hospital. The number of children aged less than 15 years in the household of swabbed children was compared to nasopharyngeal carriage prevalence.

Results showed that in the urban area, carriage prevalence was 67.9%(668/983), 74.8%(533/713), 81.6%(111/136) and 84.1%(37/44), respectively, for households with 0,1,2 and ≥3 other children (p<0.001). In the rural area, prevalence was 89.4% (219/245), 95.2%(220/231), 90.4%(75/83) and 91.6%(33/36), respectively, for households with 0,1,2 and ≥3 other children (p=0.121).

Fig. 3 Carriage prevalence in households with 0,1,2 and ≥3 children (Urban vs Rural)

67.9%,74.8%,81.6%,84.1% 89.4%,95.2%,90.4%,91.6% Carriage Prevalence Region 0 1 2 >3

Prevalence of pneumococcal nasopharyngeal carriage increased with presence of other children within the household, presumably due to increased transmission, in the urban setting, where carriage was lower. There was no association in rural setting, where prevalence was higher, possibly due to different socioeconomics and mixing patterns of children in rural Nepal.

Impact of PCV10 on Younger Children

In the urban sites, researchers are assessing the impact of PCV10 on infants between 0-8 weeks of age, who are too young to be immunized. The results may indicate whether PCV10 offers indirect protection by preventing carriage (and associated transmission) even in children who do not directly receive the vaccine.

Preliminary findings show a statistically significant decrease in the proportion of children too young to be immunized carrying the types of pneumococcal bacteria contained in PCV10 (from 5.2% in 2014 to 2.3% in 2017). In 2019, we will assess if this decline continues.

Does an accelerated vaccination schedule affect carriage?

Researchers did not find evidence of a difference in carriage prevalence after immunization between to the two different vaccine schedules (6+10 vs 6+14).

Read more about the accelerated schedule.

Analysis of this study is ongoing. For more information, contact our study coordinator.

Published Results

See site
Communications Resource, News
Rose Weeks
June 23, 2020
See site
See site
Meeru Gurung, Merryn Voysey, Stephen Thorson et al.
June 18, 2020
See site
See site
Ganesh Prasad Sah, Meeru Gurung, Merryn Voysey et al.
June 18, 2020
See site
See site
Animesh Khulal, Meeru Gurung, Sanjeev Man Bijukchhe et al.
June 17, 2020
See site
See site
Poster
Meeru Gurung, Rama Kandasamy, Stephen Thorson, et al.
June 2016
See site
See site
Poster
Rama Kandasamy, Rebecca Gladstone, Shrijana Strestha, et al.
June 2016
See site
See site
Poster
Raju Pandit, Stephen Thorson, Meeru Gurung, et al.
April 2018
See site
See site
Poster
Pratistha Maskey, Meeru Gurung, Stephen Thorson, et al.
April 2018
See site

This website uses cookies to improve your experience, as described in our privacy policy.
Click “accept” to consent to use of cookies and similar technologies while on our site.