{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,4]],"date-time":"2026-08-04T17:07:58Z","timestamp":1785863278809,"version":"3.56.0"},"reference-count":15,"publisher":"Oxford University Press (OUP)","issue":"5","license":[{"start":{"date-parts":[[2026,1,9]],"date-time":"2026-01-09T00:00:00Z","timestamp":1767916800000},"content-version":"vor","delay-in-days":1,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"name":"CDC Emerging Infectious Disease Research Core Funds"},{"DOI":"10.13039\/100006229","name":"Oak Ridge Institute for Science and Education","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100006229","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000015","name":"U.S. Department of Energy","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100000015","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100007917","name":"U.S. Department of Agriculture-Agricultural Research Service","doi-asserted-by":"crossref","id":[{"id":"10.13039\/100007917","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/100006225","name":"Oak Ridge Associated Universities","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100006225","id-type":"DOI","asserted-by":"publisher"}]},{"name":"Fred C. Davison Distinguished University Chair"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2026,5,15]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Marburgviruses cause severe hemorrhagic disease in humans, yet characterization of rodent models for pathogenesis and medical countermeasure development remains limited. Here, we investigated clinical course, blood chemistry, viral dissemination, and mucosal viral detection in inbred BALB\/c and outbred CD-1 mice infected with mouse-adapted (MA)-Marburg virus (MARV)\/Angola or MA-Ravn virus (RAVV) to further mouse model development. Regardless of virus or mouse strain, infection resulted in widespread viral dissemination in animals sampled up to 5 days post-infection. However, in animals followed to study end, MA-MARV\/Angola caused severe disease and lethality in both mouse strains, whereas MA-RAVV caused mild or asymptomatic infection.<\/jats:p>","DOI":"10.1093\/infdis\/jiag019","type":"journal-article","created":{"date-parts":[[2026,1,7]],"date-time":"2026-01-07T12:45:23Z","timestamp":1767789923000},"page":"e1267-e1272","source":"Crossref","is-referenced-by-count":1,"title":["Characterization of Mouse-Adapted Marburg and Ravn Viruses in Inbred BALB\/c and Outbred CD-1 Mice"],"prefix":"10.1093","volume":"233","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-1643-7093","authenticated-orcid":false,"given":"Katherine A","family":"Davies","sequence":"first","affiliation":[{"name":"Viral Special Pathogens Branch, Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention , Atlanta, Georgia ,","place":["USA"]},{"name":"United States Department of Agriculture, Zoonotic and Emerging Disease Research Unit, National 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