<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Schroeder S</submitter><funding>Bundesministerium für Bildung und Forschung (Federal Ministry of Education and Research)</funding><funding>Bundesministerium für Bildung und Forschung</funding><pagination>5324</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8423819</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(1)</volume><pubmed_abstract>Middle East respiratory syndrome coronavirus (MERS-CoV) is enzootic in dromedary camels across the Middle East and Africa. Virus-induced pneumonia in humans results from animal contact, with a potential for limited onward transmission. Phenotypic changes have been suspected after a novel recombinant clade (lineage 5) caused large nosocomial outbreaks in Saudi Arabia and South Korea in 2016. However, there has been no functional assessment. Here we perform a comprehensive in vitro and ex vivo comparison of viruses from parental and recombinant virus lineages (lineage 3, n = 7; lineage 4, n = 8; lineage 5, n = 9 viruses) from Saudi Arabia, isolated immediately before and after the shift toward lineage 5. Replication of lineage 5 viruses is significantly increased. Transcriptional profiling f</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Functional comparison of MERS-coronavirus lineages reveals increased replicative fitness of the recombinant lineage 5.</pubmed_title><pmcid>PMC8423819</pmcid><funding_grant_id>01KI1723A</funding_grant_id><pubmed_authors>Boulant S</pubmed_authors><pubmed_authors>Eggeling S</pubmed_authors><pubmed_authors>Wolff T</pubmed_authors><pubmed_authors>Hippenstiel S</pubmed_authors><pubmed_authors>Mache C</pubmed_authors><pubmed_authors>Dijkman R</pubmed_authors><pubmed_authors>Thiel V</pubmed_authors><pubmed_authors>Schroeder S</pubmed_authors><pubmed_authors>Kleine-Weber H</pubmed_authors><pubmed_authors>Muth D</pubmed_authors><pubmed_authors>Gultom M</pubmed_authors><pubmed_authors>Pohlmann S</pubmed_authors><pubmed_authors>Muller MA</pubmed_authors><pubmed_authors>Fatykhova D</pubmed_authors><pubmed_authors>Corman VM</pubmed_authors><pubmed_authors>Hocke A</pubmed_authors><pubmed_authors>Drosten C</pubmed_authors><pubmed_authors>Memish ZA</pubmed_authors><pubmed_authors>Stanifer ML</pubmed_authors><pubmed_authors>Richter A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Functional comparison of MERS-coronavirus lineages reveals increased replicative fitness of the recombinant lineage 5.</name><description>Middle East respiratory syndrome coronavirus (MERS-CoV) is enzootic in dromedary camels across the Middle East and Africa. Virus-induced pneumonia in humans results from animal contact, with a potential for limited onward transmission. Phenotypic changes have been suspected after a novel recombinant clade (lineage 5) caused large nosocomial outbreaks in Saudi Arabia and South Korea in 2016. However, there has been no functional assessment. Here we perform a comprehensive in vitro and ex vivo comparison of viruses from parental and recombinant virus lineages (lineage 3, n = 7; lineage 4, n = 8; lineage 5, n = 9 viruses) from Saudi Arabia, isolated immediately before and after the shift toward lineage 5. Replication of lineage 5 viruses is significantly increased. Transcriptional profiling f</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2026-05-09T05:46:36.906Z</modification><creation>2022-02-11T15:00:09.679Z</creation></dates><accession>S-EPMC8423819</accession><cross_references><pubmed>34493730</pubmed><doi>10.1038/s41467-021-25519-1</doi></cross_references></HashMap>