<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhou X</submitter><funding>the National Key R&amp;D Program of Guangzhou</funding><funding>Xinjiang Key Laboratory of Animal Infectious Diseases</funding><funding>Key Laboratory of Livestock Disease Prevention of Guangdong Province</funding><funding>Guangdong Academy of Agricultural Sciences (Jinying's light talent project)</funding><funding>the Department of Agriculture and Rural Affairs of Guangdong Province</funding><pagination>1790</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11200575</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(12)</volume><pubmed_abstract>Rotavirus is a major causative agent of diarrhoea in children, infants, and young animals around the world. The associated zoonotic risk necessitates the serious consideration of the complete genetic information of rotavirus. A segmented genome makes rotavirus prone to rearrangement and the formation of a new viral strain. Monitoring the molecular epidemiology of rotavirus is essential for its prevention and control. The quantitative RT-PCR targeting the NSP5 gene was used to detect rotavirus group A (RVA) in pig faecal samples, and two pairs of universal primers and protocols were used for amplifying the G and P genotype. The genotyping and phylogenetic analysis of 11 genes were performed by RT-PCR and a basic bioinformatics method. A unique G4P[6] rotavirus strain, designated S2CF (RVA/Pig-tc/CHN/S2CF/2023/G4P[6]), was identified in one faecal sample from a piglet with severe diarrhoea in Guangdong, China. Whole genome sequencing and analysis suggested that the 11 segments of the S2CF strain showed a unique Wa-like genotype constellation and a typical porcine RVA genomic configuration of G4-P[6]-I1-R1-C1-M1-A8-N1-T1-E1-H1. Notably, 4 of the 11 gene segments (VP4, VP6, VP2, and NSP5) clustered consistently with human-like RVAs, suggesting independent human-to-porcine interspecies transmission. Moreover, a unique 344-nt duplicated sequence was identified for the first time in the untranslated region of NSP5. This study further reveals the genetic diversity and potential inter-species transmission of porcine rotavirus.</pubmed_abstract><journal>Animals : an open access journal from MDPI</journal><pubmed_title>Emergence of a Novel G4P[6] Porcine Rotavirus with Unique Sequence Duplication in NSP5 Gene in China.</pubmed_title><pmcid>PMC11200575</pmcid><funding_grant_id>2023B1212060040</funding_grant_id><funding_grant_id>R2023PY-JG019</funding_grant_id><funding_grant_id>2022SDZG02</funding_grant_id><funding_grant_id>202206010192</funding_grant_id><funding_grant_id>2023KLA003</funding_grant_id><pubmed_authors>Mi X</pubmed_authors><pubmed_authors>Xiao G</pubmed_authors><pubmed_authors>Jia H</pubmed_authors><pubmed_authors>Liu B</pubmed_authors><pubmed_authors>Hou X</pubmed_authors><pubmed_authors>Wei J</pubmed_authors><pubmed_authors>Zhai SL</pubmed_authors><pubmed_authors>Zhou X</pubmed_authors><pubmed_authors>Guo Q</pubmed_authors><pubmed_authors>Wei Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Emergence of a Novel G4P[6] Porcine Rotavirus with Unique Sequence Duplication in NSP5 Gene in China.</name><description>Rotavirus is a major causative agent of diarrhoea in children, infants, and young animals around the world. The associated zoonotic risk necessitates the serious consideration of the complete genetic information of rotavirus. A segmented genome makes rotavirus prone to rearrangement and the formation of a new viral strain. Monitoring the molecular epidemiology of rotavirus is essential for its prevention and control. The quantitative RT-PCR targeting the NSP5 gene was used to detect rotavirus group A (RVA) in pig faecal samples, and two pairs of universal primers and protocols were used for amplifying the G and P genotype. The genotyping and phylogenetic analysis of 11 genes were performed by RT-PCR and a basic bioinformatics method. A unique G4P[6] rotavirus strain, designated S2CF (RVA/Pig-tc/CHN/S2CF/2023/G4P[6]), was identified in one faecal sample from a piglet with severe diarrhoea in Guangdong, China. Whole genome sequencing and analysis suggested that the 11 segments of the S2CF strain showed a unique Wa-like genotype constellation and a typical porcine RVA genomic configuration of G4-P[6]-I1-R1-C1-M1-A8-N1-T1-E1-H1. Notably, 4 of the 11 gene segments (VP4, VP6, VP2, and NSP5) clustered consistently with human-like RVAs, suggesting independent human-to-porcine interspecies transmission. Moreover, a unique 344-nt duplicated sequence was identified for the first time in the untranslated region of NSP5. This study further reveals the genetic diversity and potential inter-species transmission of porcine rotavirus.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jun</publication><modification>2026-05-23T03:21:27.921Z</modification><creation>2026-05-23T03:08:18.585Z</creation></dates><accession>S-EPMC11200575</accession><cross_references><pubmed>38929409</pubmed><doi>10.3390/ani14121790</doi></cross_references></HashMap>