<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>104(8)</volume><submitter>Hansen F</submitter><funding>Medical Research Council</funding><funding>Defense Sciences Office, DARPA</funding><funding>Division of Intramural Research, National Institute of Allergy and Infectious Diseases</funding><pubmed_abstract>Distinct cytomegaloviruses (CMVs) are widely distributed across their mammalian hosts in a highly host species-restricted pattern. To date, evidence demonstrating this has been limited largely to PCR-based approaches targeting small, conserved genomic regions, and only a few complete genomes of isolated viruses representing distinct CMV species have been sequenced. We have now combined direct isolation of infectious viruses from tissues with complete genome sequencing to provide a view of CMV diversity in a wild animal population. We targeted Natal multimammate mice (&lt;i>Mastomys natalensis&lt;/i>), which are common in sub-Saharan Africa, are known to carry a variety of zoonotic pathogens, and are regarded as the primary source of Lassa virus (LASV) spillover into humans. Using transformed epi</pubmed_abstract><journal>The Journal of general virology</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10721045</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Isolation and genome sequencing of cytomegaloviruses from Natal multimammate mice (&amp;lt;i&amp;gt;Mastomys natalensis&amp;lt;/i&amp;gt;).</pubmed_title><pmcid>PMC10721045</pmcid><funding_grant_id>MC_UU_00034/5</funding_grant_id><funding_grant_id>D18AC00028</funding_grant_id><funding_grant_id>International Center for Excellence in Research (ICER)</funding_grant_id><funding_grant_id>Intramural Research Program</funding_grant_id><pubmed_authors>Oestereich L</pubmed_authors><pubmed_authors>da Silva Filipe A</pubmed_authors><pubmed_authors>Bane S</pubmed_authors><pubmed_authors>Vucak M</pubmed_authors><pubmed_authors>Nichols J</pubmed_authors><pubmed_authors>Hansen F</pubmed_authors><pubmed_authors>Voigt S</pubmed_authors><pubmed_authors>Ostermann E</pubmed_authors><pubmed_authors>Chan B</pubmed_authors><pubmed_authors>Rosenke K</pubmed_authors><pubmed_authors>Staliunaite L</pubmed_authors><pubmed_authors>Davison AJ</pubmed_authors><pubmed_authors>Sogoba N</pubmed_authors><pubmed_authors>Brune W</pubmed_authors><pubmed_authors>Camiolo S</pubmed_authors><pubmed_authors>Ehlers B</pubmed_authors><pubmed_authors>Jarvis MA</pubmed_authors><pubmed_authors>Streblow DN</pubmed_authors><pubmed_authors>Hughes J</pubmed_authors><pubmed_authors>Redwood AJ</pubmed_authors><pubmed_authors>Feldmann H</pubmed_authors><pubmed_authors>Mauch T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Isolation and genome sequencing of cytomegaloviruses from Natal multimammate mice (&amp;lt;i&amp;gt;Mastomys natalensis&amp;lt;/i&amp;gt;).</name><description>Distinct cytomegaloviruses (CMVs) are widely distributed across their mammalian hosts in a highly host species-restricted pattern. To date, evidence demonstrating this has been limited largely to PCR-based approaches targeting small, conserved genomic regions, and only a few complete genomes of isolated viruses representing distinct CMV species have been sequenced. We have now combined direct isolation of infectious viruses from tissues with complete genome sequencing to provide a view of CMV diversity in a wild animal population. We targeted Natal multimammate mice (&lt;i>Mastomys natalensis&lt;/i>), which are common in sub-Saharan Africa, are known to carry a variety of zoonotic pathogens, and are regarded as the primary source of Lassa virus (LASV) spillover into humans. Using transformed epi</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Aug</publication><modification>2026-05-29T05:46:48.82Z</modification><creation>2025-04-04T18:42:35.206Z</creation></dates><accession>S-EPMC10721045</accession><cross_references><pubmed>37643006</pubmed><doi>10.1099/jgv.0.001873</doi></cross_references></HashMap>