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Published on: July 22, 2012
Rotavirus A Infection Prevalence and Spatio-Temporal Genotype Shift among Under-Five Children in Amhara National
Debasu Damtie1,2,3,4, Aschalew Gelaw1, Yitayih Wondimeneh1
1Department of Medical Microbiology, School of Biomedical and Laboratory Sciences, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia.
Insights
Rotavirus A (RVA) infection remains a significant threat to children in Ethiopia despite vaccination. This study found shifts in RVA genotypes and potential immune escape mechanisms, highlighting the need for ongoing surveillance and vaccine effectiveness research.
Area of Science:
- Virology
- Epidemiology
- Public Health
Background:
- Rotavirus A (RVA) is a leading cause of severe diarrhea and mortality in young children globally and in Ethiopia.
- Despite the introduction of RVA vaccines in Ethiopia in 2013, limited data exist on post-vaccine RVA burden and genotype distribution.
- This study addresses the need for updated information on RVA prevalence and circulating genotypes in Ethiopian children.
Purpose of the Study:
- To assess the prevalence of Rotavirus A (RVA) infection in diarrheic children under five years old in Ethiopia.
- To determine the genotype distribution of circulating RVA strains, including G and P types.
- To analyze the genetic characteristics of RVA strains in relation to vaccine effectiveness.
Main Methods:
- A multi-center, hospital-based cross-sectional study involving 537 diarrheic children under five.
- Rotavirus A detection using one-step reverse-transcriptase polymerase chain reaction (RT-PCR).
- Genotyping via Sanger sequencing of VP7 and VP4 genes, with phylogenetic analysis using MEGA software.
Main Results:
- RVA infection prevalence was 17.5% among diarrheic children.
- The most common G-types were G3 (37%), G12 (28%), and G1 (20%). Predominant P-types were P[8] (51%), P[6] (29%), and P[4] (14%).
- Key G/P combinations included G3P[8] (32.8%) and G12P[6] (28.4%). Ethiopian strains clustered globally, with observed amino acid substitutions in VP4 and VP7 proteins.
Conclusions:
- RVA infection remains prevalent in Ethiopian children despite vaccination efforts.
- A notable shift in circulating genotypes from G1 to G3 and the emergence of unusual combinations like G9P[4] were observed.
- Amino acid substitutions in circulating RVA strains suggest potential for immune escape, warranting further investigation into vaccine effectiveness.
Abstract:
Background: Globally, rotavirus (RV) A (RVA) is the most common cause of severe and sometimes fatal diarrhea in young children. It is also the major cause of acute gastroenteritis among children in Ethiopia. Currently, the WHO has prequalified four RVA vaccines for universal childhood immunization. Ethiopia introduced the monovalent Rotarix vaccine into its national immunization program in 2013. Since then, only a few studies on the burden and genotype distribution of RVA infection post-vaccine introduction have been conducted (mostly at sentinel surveillance sites). Therefore, this study aimed to assess RVA prevalence and genotype distribution among children under five years in Ethiopia (February 2021-December 2022). Methods: This multi-center hospital-based cross-sectional study involved 537 diarrheic children under-five years old. Rotavirus A detection was conducted using a one-step reverse-transcriptase polymerase chain reaction (RT-PCR). Genotyping was conducted by Sanger sequencing of the VP7 (complete) and VP4 (partial) genes. Descriptive analysis and Pearson's chi-squared test were carried out using SPSS version 29. Phylogenetic analysis with 1000 bootstrap replicates was performed using MEGA version 11 software. Statistical significance was set at p < 0.05 for all analyses. Results: The prevalence of RVA infection among diarrheic children was 17.5%. The most prevalent G-types identified were G3 (37%), the previously uncommon G12 (28%), and G1 (20%). The predominant P-types were P[8] (51%), P[6] (29%), and P[4] (14%). The three major G/P combinations observed were G3P[8] (32.8%), G12P[6] (28.4%), and G1P[8] (19.4%). Phylogenetic analysis revealed clustering of Ethiopian strains with the globally reported strains. Many strains exhibited amino acid differences in the VP4 (VP8* domain) and VP7 proteins compared to vaccine strains, potentially affecting virus neutralization. Conclusions: Despite the high RVA vaccination rate, the prevalence of RVA infection remains significant among diarrheic children in Ethiopia. There is an observable shift in circulating RVA genotypes from G1 to G3, alongside the emergence of unusual G/P genotype combinations such as G9P[4]. Many of these circulating RVA strains have shown amino acid substitutions that may allow for neutralization escape. Therefore, further studies are warranted to comprehend the emergence of these unusual RVA strains and the diverse factors influencing the vaccine's diminished effectiveness in developing countries.
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