Molecular characterization of VP6 and NSP4 genes of unusual G and P Rotavirus group A isolated from children with acute gastroenteritis

Author:

Dellis Charilaos1,Tatsi Elizabeth Barbara1ORCID,Koukou Dimitra-Maria1,Filippatos Filippos1,Vetouli Evangelia2,Michos Athanasios1,Syriopoulou Vasiliki1

Affiliation:

1. National and Kapodistrian University of Athens School of Health Sciences: Ethniko kai Kapodistriako Panepistemio Athenon

2. Department of Microbiology, "P. & A. Kyriakou" Children's Hospital

Abstract

Abstract Group A Rotavirus (RVA), which causes acute gastroenteritis (AGE) in children worldwide, is categorized mainly based on VP7 (genotype G) and VP4 (genotype P) genes. Genotypes that circulate at < 1% are considered unusual. Important genes are also VP6 (genotype I) and NSP4 (genotype E). VP6 establishes the group and affects immunogenicity, while NSP4, as enterotoxin, is responsible for the clinical symptoms. Aim of this study was to genotype and molecularly characterize the VP6 and NSP4 genes of unusual RVA. Unusual RVA strains extracted from fecal samples of children ≤ 16 years with AGE, were genotyped in VP6 and NSP4 genes with Sanger sequencing. Phylogenetics was performed using MEGA 11. In a 15-year period (2007–2021), 54.8% (34/62) of unusual RVA were successfully I and E genotyped. Three different I and E genotypes were identified; I2 (73.5%, 25/34) and E2 (35.3%, 12/34) were the commonest. E3 genotype was detected from 2017 onwards. The uncommon combination of I2-E3 was found in 26.5%(9/34) of the strains and G3-P[9]-I2-E3 was the most frequent G-P-I-E combination (20.6%,7/34). Statistical analysis showed that children infected with E2 strains had a higher relative frequency of dehydration(50%) compared to those with E3 genotype(p = 0.019). Multiple substitutions were detected in both genes, but their functional effect remains unknown. The results of this study highlight the genetic diversity of RVA strains but should be interpreted with caution as they are not based on whole genome sequencing. Continuous surveillance of the RVA based on the whole genome will provide a better knowledge of its evolution.

Publisher

Research Square Platform LLC

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