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Published on: May 30, 2019
Meningococcal and pneumococcal carriage in children with HIV
Neslihan Mete Atasever1, Elif Dede1, Seyhan Yilmaz2
1Department of Child Health and Diseases, Department of Pediatric Infection Diseases, Istanbul University Faculty of Medicine.
Insights
Children living with HIV in Türkiye had low meningococcal and comparable pneumococcal carriage to healthy peers. Vaccination and host immunity influenced serotype distribution, supporting continued immunization strategies for this vulnerable group.
Area of Science:
- Pediatric Infectious Diseases
- Microbiology
- Epidemiology
Background:
- Children living with HIV (CLHIV) face higher risks of invasive meningococcal and pneumococcal diseases, even with treatment and vaccines.
- Limited data exists on nasopharyngeal carriage of these bacteria in CLHIV within Türkiye.
Purpose of the Study:
- To investigate and compare nasopharyngeal carriage rates of Neisseria meningitidis and Streptococcus pneumoniae in CLHIV versus healthy children in Türkiye.
- To identify factors associated with carriage, including vaccination status and time since last vaccination.
Main Methods:
- A multicenter prospective study involving 80 CLHIV and 180 age-matched healthy controls in İstanbul and İzmir.
- Real-time PCR analysis of nasopharyngeal swabs for bacterial detection and molecular methods for serogroup/serotype determination.
- Collection of demographic, clinical, and vaccination data, followed by univariate and multivariate analyses.
Main Results:
- Meningococcal carriage was low in both groups (3.8% CLHIV vs. 8.9% controls), with non-groupable strains found in unvaccinated CLHIV.
- Pneumococcal carriage rates were similar (28.7% CLHIV vs. 23.9% controls).
- Among CLHIV, 65.2% of pneumococcal isolates were PCV13 serotypes; longer time since PCV13 vaccination was associated with lower carriage.
Conclusions:
- CLHIV in Türkiye show low meningococcal and comparable pneumococcal carriage to healthy children.
- Vaccination, particularly PCV13, and host immunity significantly shape pneumococcal serotype distribution.
- Findings underscore the importance of sustained risk-group vaccination, household immunization, and ongoing molecular surveillance for CLHIV prevention strategies.
Background:
Children with HIV (CWH) remain at increased risk for colonization and invasive disease by Neisseria meningitidis and Streptococcus pneumoniae despite antiretroviral therapy (ART) and vaccination. Data on nasopharyngeal carriage in this group are limited in Türkiye.
Methods:
In this multicenter prospective study, nasopharyngeal swabs were obtained from 80 CWH and 180 age-matched healthy controls between July and December 2024 in İstanbul and İzmir. Samples were analyzed by real-time PCR for N. meningitidis and S. pneumoniae , and meningococcal serogroups and pneumococcal serotypes were determined by molecular methods including capsular sequence typing. Demographic, clinical, and vaccination data were collected. Univariate and multivariate analyses assessed factors associated with carriage.
Results:
Meningococcal carriage was detected in 3 of 80 (3.8%) CWH and 16 of 180 (8.9%) controls ( P = 0.15). All meningococcal isolates from CWH were nongroupable and were unvaccinated. Pneumococcal carriage occurred in 23 of 80 (28.7%) CWH and 43 of 180 (23.9%) controls ( P = 0.40). Among CWH isolates, 65.2% were PCV13 serotypes, 26.1% were non-PCV13 serotypes, and 8.7% were nontypeable. Time since the last PCV13 dose was weakly but independently associated with lower pneumococcal carriage [adjusted odds ratio (OR) per month 0.98, 95% confidence interval (CI) 0.97-0.99; P = 0.011], while having vaccinated siblings showed a borderline protective effect.
Conclusion:
In this contemporary cohort from Türkiye, CWH exhibited low meningococcal carriage dominated by nongroupable strains and pneumococcal carriage comparable to healthy children, with a serotype distribution shaped by vaccination and host immunity. These findings support sustained risk-group vaccination, reinforcement of household-level immunization, and continued molecular surveillance to optimize prevention strategies for CWH.
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