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Updated: Jan 17, 2026

Generation, Amplification, and Titration of Recombinant Respiratory Syncytial Viruses
Published on: April 4, 2019
Sequence variability of Hungarian RSV G and F proteins between 2017 and 2023: single-center study
Hajnalka Juhász1, Katalin Burián1, Mátyás Bukva2
1Department of Medical Microbiology, Albert Szent-Györgyi Medical and Pharmaceutical Center and Albert Szent Györgyi Medical School, University of Szeged, Szeged, Hungary.
Abstract:
Our study determined the prevalence, types of RSV, and sequence variability of the G and F genes in Hungary between 2017 and 2023. During the study, 1828 respiratory samples were collected from hospitalised pediatric patients. We confirmed the presence of RSV A in 12.74 %, RSV B in 13.85 %, and their simultaneous presence in 0.27 %. The highest RSV positivity was observed in the 2018-2019 season, while the lowest was in the 2017-2018 season. Following the SARS-CoV-2 pandemic, the RSV season has an earlier onset and longer duration than it did previously; however, an earlier onset was already detected in 2018. All RSV A isolates are classified into the A.D., while RSV B into the B.D. clades. The entire ectodomain of G protein showed a high sequence diversity, higher than in the case of B.D. strains. Mutations at position 276, adjacent to the palivizumab binding site of the F protein, could be detected. At the same time, neither K272E/N nor any other mutation is present in the palivizumab binding region in our strains. Several mutations in the nirsevimab binding region could be detected in our strains; however, none of these mutations, which would affect nirsevimab activity, were found in our isolates.
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