# Prevalence and molecular epidemiology of rotavirus gastroenteritis among children in Nairobi’s urban informal settlements following introduction of the Rotavac® vaccine

**Authors:** Winfred Mbithi, Ernest A. Wandera, Anthony K. Nyamache, Daniel Hungerford, Amos Njuguna, Michael Mugo, Aoko Johnpaul Ogutha, Christine Kioko, Darius Ideke, Carlene Sang, James Nyangao, Phelgona Otieno, Fredrick Were, Khuzwayo C. Jere, Nigel A. Cunliffe, Samuel Kariuki, Cecilia Mbae

PMC · DOI: 10.1186/s41182-026-00917-7 · 2026-02-06

## TL;DR

This study examines the impact of the Rotavac® vaccine on rotavirus gastroenteritis in Nairobi's urban informal settlements, finding it to be effective despite the presence of diverse and emerging strains.

## Contribution

The study provides new evidence on Rotavac® vaccine effectiveness and strain diversity in Nairobi's urban informal settlements following vaccine introduction.

## Key findings

- Rotavirus was detected in 19.5% of stool samples, with the highest detection in children aged 12–23 months.
- Rotavac® vaccine effectiveness was estimated at 74.1%, with vaccinated children showing significantly lower rotavirus prevalence.
- Emerging rotavirus strains, including equine-like strains, were identified, highlighting the need for ongoing surveillance.

## Abstract

Rotavirus is the leading cause of acute gastroenteritis among children under five years of age globally. In Kenya, rotavirus vaccination was introduced in 2014 using Rotarix® (G1P[8]), with a subsequent national transition to Rotavac® (G9P[11]) vaccine, in 2023. Evidence on post-introduction rotavirus disease burden, strain diversity, and Rotavac® vaccine effectiveness in Kenya remains limited. This study assessed the burden of rotavirus gastroenteritis and vaccine effectiveness of the rotavirus vaccine among children under five years of age in Nairobi’s urban slums, after the rollout of the Rotavac® vaccine.

In this cross-sectional surveillance study, 353 stool samples were collected from children under five years of age presenting with acute gastroenteritis at selected health facilities in Mukuru informal settlement, Nairobi, between October 2023 and November 2024. The samples were analyzed using TaqMan array card PCR and multiplexed semi-nested RT-PCR. Vaccine effectiveness for overall rotavirus vaccination and Rotavac® specifically was estimated using a post-hoc test-negative case–control analysis.

Rotavirus was detected in 19.5% (69/353; 95% CI 15.5–24.1%) of the samples. The highest detection occurred among children aged 12–23 months at 24.4% (30/123; 95% CI 17.1–33.0%), with significant differences across age groups (p = 0.023). Rotavirus prevalence was significantly lower among vaccinated children 18.4% (60/327; 95% CI 14.3–23.0%), compared with unvaccinated children 34.6% (9/26; 95% CI 17.2–55.7%) (p = 0.044). The predominant strain was G2P[4] (29.0%; 20/69), which also dominated among the vaccinated children (31.7%; 19/60), while G12P[6] was most frequent among unvaccinated children (33.3%; 3/9). Newly detected strains included G2P[8] and G12P[8], and two equine-like strains (G3P[8]eG3 and G2G3P[4]P[8]eG3). Short electropherotypes predominated. First-dose vaccine coverage was 92.6% (327/353) while the last-dose coverage was 76.2% (269/353). Estimated Rotavac® vaccine effectiveness was 74.1% (95% CI 16.3–92.0%), and overall rotavirus vaccine effectiveness was 57.6% (95% CI 18.1–99.8%).

Rotavirus remains a significant cause of gastroenteritis among children in Nairobi’s urban informal settlements. The circulation of diverse and emerging strains underscores the need for continued molecular surveillance to monitor vaccine performance and guide future immunization strategies.

## Linked entities

- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** acute gastroenteritis (MESH:D005759), rotavirus disease (MESH:D012400)
- **Chemicals:** Rotavac (-)
- **Species:** Rotavirus (genus) [taxon 10912], Equus caballus (domestic horse, species) [taxon 9796]
- **Mutations:** G12P

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12961793/full.md

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Source: https://tomesphere.com/paper/PMC12961793