<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>42(3)</volume><submitter>Filippi M</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>With the progression of the Coronavirus disease pandemic, the number of mutations in the viral genome has increased, showing the adaptive evolution of severe acute respiratory syndrome coronavirus 2 in humans and intensification in transmissibility. Long-term infections also allow the development of viral diversity. In this study, we report the case of a child with severe combined immu presenting a prolonged severe acute respiratory syndrome coronavirus 2 infection. We aimed to analyze 3 naso-oropharyngeal swab samples collected between August and December 2021 to describe the amino acid changes present in the sequence reads that may have a role in the emergence of new viral variants.&lt;h4>Methods&lt;/h4>The whole genome from clinical samples was sequenced through high throughput sequencing and analyzed using a workflow to map reads and then find variations/single-nucleotide polymorphisms. In addition, the samples were isolated in cell culture, and a plaque forming units assay was performed, which indicates the presence of viable viral particles.&lt;h4>Results&lt;/h4>The results obtained showed that the virus present in all samples is infectious. Also, there were 20 common mutations among the 3 sequence reads, found in the ORF1ab and ORF10 proteins. As well, a considerable number of uncommon mutations were found.&lt;h4>Conclusions&lt;/h4>In conclusion, we emphasize that genomic surveillance can be a useful tool to assess possible evolution signals in long-term patients.</pubmed_abstract><journal>The Pediatric infectious disease journal</journal><pagination>212-217</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9935232</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Prolonged SARS-CoV-2 Infection and Intra-Patient Viral Evolution in an Immunodeficient Child.</pubmed_title><pmcid>PMC9935232</pmcid><pubmed_authors>Demoliner M</pubmed_authors><pubmed_authors>Fleck JD</pubmed_authors><pubmed_authors>Girardi V</pubmed_authors><pubmed_authors>Filippi M</pubmed_authors><pubmed_authors>Rosado Spilki F</pubmed_authors><pubmed_authors>Motta Rodrigues G</pubmed_authors><pubmed_authors>Frohlich J</pubmed_authors><pubmed_authors>Minuto Paiva R</pubmed_authors><pubmed_authors>Schons Gularte J</pubmed_authors><pubmed_authors>de Abreu Goes Pereira VM</pubmed_authors><pubmed_authors>de-Paris F</pubmed_authors><pubmed_authors>Witt Hansen A</pubmed_authors><pubmed_authors>Soares Falcetta F</pubmed_authors><pubmed_authors>Ribeiro Amorim M</pubmed_authors><pubmed_authors>Machado Arlindo De Mattos E</pubmed_authors><pubmed_authors>Deutschendorf C</pubmed_authors><pubmed_authors>Soares da Silva M</pubmed_authors><pubmed_authors>Proenca Modena JL</pubmed_authors><pubmed_authors>Aparecida Risczik Arruda Correa J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prolonged SARS-CoV-2 Infection and Intra-Patient Viral Evolution in an Immunodeficient Child.</name><description>&lt;h4>Background&lt;/h4>With the progression of the Coronavirus disease pandemic, the number of mutations in the viral genome has increased, showing the adaptive evolution of severe acute respiratory syndrome coronavirus 2 in humans and intensification in transmissibility. Long-term infections also allow the development of viral diversity. In this study, we report the case of a child with severe combined immu presenting a prolonged severe acute respiratory syndrome coronavirus 2 infection. We aimed to analyze 3 naso-oropharyngeal swab samples collected between August and December 2021 to describe the amino acid changes present in the sequence reads that may have a role in the emergence of new viral variants.&lt;h4>Methods&lt;/h4>The whole genome from clinical samples was sequenced through high throughput sequencing and analyzed using a workflow to map reads and then find variations/single-nucleotide polymorphisms. In addition, the samples were isolated in cell culture, and a plaque forming units assay was performed, which indicates the presence of viable viral particles.&lt;h4>Results&lt;/h4>The results obtained showed that the virus present in all samples is infectious. Also, there were 20 common mutations among the 3 sequence reads, found in the ORF1ab and ORF10 proteins. As well, a considerable number of uncommon mutations were found.&lt;h4>Conclusions&lt;/h4>In conclusion, we emphasize that genomic surveillance can be a useful tool to assess possible evolution signals in long-term patients.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2025-04-22T10:16:37.305Z</modification><creation>2025-04-05T23:30:54.246Z</creation></dates><accession>S-EPMC9935232</accession><cross_references><pubmed>36728777</pubmed><doi>10.1097/INF.0000000000003782</doi></cross_references></HashMap>