<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(9)</volume><submitter>Kikuti M</submitter><pubmed_abstract>Describing PRRSV whole-genome viral diversity data over time within the host and within-farm is crucial for a better understanding of viral evolution and its implications. A cohort study was conducted at one naïve farrow-to-wean farm reporting a PRRSV outbreak. All piglets 3-5 days of age (DOA) born to mass-exposed sows through live virus inoculation with the recently introduced wild-type virus two weeks prior were sampled and followed up at 17-19 DOA. Samples from 127 piglets were individually tested for PRRSV by RT-PCR and 100 sequences were generated using Oxford Nanopore Technologies chemistry. Female piglets had significantly higher median Ct values than males (15.5 vs. 13.7, Kruskal-Wallis &lt;i>p&lt;/i> &lt; 0.001) at 3-5 DOA. A 52.8% mortality between sampling points was found, and the odds of dying by 17-19 DOA decreased with every one unit increase in Ct values at 3-5 DOA (OR = 0.76, 95% CI 0.61-0.94, &lt;i>p&lt;/i> = 0.01). Although the within-pig percent nucleotide identity was overall high (99.7%) between 3-5 DOA and 17-19 DOA samples, ORFs 4 and 5a showed much lower identities (97.26% and 98.53%, respectively). When looking solely at ORF5, 62% of the sequences were identical to the 3-5 DOA consensus. Ten and eight regions showed increased nucleotide and amino acid genetic diversity, respectively, all found throughout ORFs 2a/2b, 4, 5a/5, 6, and 7.</pubmed_abstract><journal>Viruses</journal><pagination>1837</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10535563</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Porcine Reproductive and Respiratory Syndrome (PRRSV2) Viral Diversity within a Farrow-to-Wean Farm Cohort Study.</pubmed_title><pmcid>PMC10535563</pmcid><pubmed_authors>Kiehne R</pubmed_authors><pubmed_authors>Pamornchainavakul N</pubmed_authors><pubmed_authors>Yang M</pubmed_authors><pubmed_authors>Kikuti M</pubmed_authors><pubmed_authors>Vilalta C</pubmed_authors><pubmed_authors>Paploski IAD</pubmed_authors><pubmed_authors>Kevill J</pubmed_authors><pubmed_authors>Corzo CA</pubmed_authors><pubmed_authors>VanderWaal K</pubmed_authors><pubmed_authors>Schroeder D</pubmed_authors><pubmed_authors>Lenskaia T</pubmed_authors><pubmed_authors>Odogwu NM</pubmed_authors><pubmed_authors>Sanhueza J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Porcine Reproductive and Respiratory Syndrome (PRRSV2) Viral Diversity within a Farrow-to-Wean Farm Cohort Study.</name><description>Describing PRRSV whole-genome viral diversity data over time within the host and within-farm is crucial for a better understanding of viral evolution and its implications. A cohort study was conducted at one naïve farrow-to-wean farm reporting a PRRSV outbreak. All piglets 3-5 days of age (DOA) born to mass-exposed sows through live virus inoculation with the recently introduced wild-type virus two weeks prior were sampled and followed up at 17-19 DOA. Samples from 127 piglets were individually tested for PRRSV by RT-PCR and 100 sequences were generated using Oxford Nanopore Technologies chemistry. Female piglets had significantly higher median Ct values than males (15.5 vs. 13.7, Kruskal-Wallis &lt;i>p&lt;/i> &lt; 0.001) at 3-5 DOA. A 52.8% mortality between sampling points was found, and the odds of dying by 17-19 DOA decreased with every one unit increase in Ct values at 3-5 DOA (OR = 0.76, 95% CI 0.61-0.94, &lt;i>p&lt;/i> = 0.01). Although the within-pig percent nucleotide identity was overall high (99.7%) between 3-5 DOA and 17-19 DOA samples, ORFs 4 and 5a showed much lower identities (97.26% and 98.53%, respectively). When looking solely at ORF5, 62% of the sequences were identical to the 3-5 DOA consensus. Ten and eight regions showed increased nucleotide and amino acid genetic diversity, respectively, all found throughout ORFs 2a/2b, 4, 5a/5, 6, and 7.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Aug</publication><modification>2024-11-06T00:24:54.046Z</modification><creation>2024-11-06T00:24:54.046Z</creation></dates><accession>S-EPMC10535563</accession><cross_references><pubmed>37766244</pubmed><doi>10.3390/v15091837</doi></cross_references></HashMap>