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Volume 20, Number 2—February 2014
Research

Novel Paramyxovirus Associated with Severe Acute Febrile Disease, South Sudan and Uganda, 2012

César G. Albariño, Michael Foltzer, Jonathan S. Towner, Lory A. Rowe, Shelley Campbell, Carlos M. Jaramillo, Brian H. Bird, DeeAnn M. Reeder, Megan E. Vodzak, Paul Rota, Maureen G. Metcalfe, Christina F. Spiropoulou, Barbara Knust, Joel P. Vincent, Michael A. Frace, Stuart T. Nichol, Pierre E. Rollin, and Ute StröherComments to Author 
Author affiliations: Centers for Disease Control and Prevention, Atlanta, Georgia, USA (C.G. Albariño, J.S. Towner, L.A. Rowe, S. Campbell, B.H. Bird, P. Rota, M.G. Metcalfe, C.F. Spiropoulou, B. Knust, J.P. Vincent, M.A. Frace, S.T. Nichol, P.E. Rollin, U. Ströher); Geisinger Medical Center, Danville, Pennsylvania, USA (M. Foltzer, C.M. Jaramillo); Bucknell University, Lewisburg, Pennsylvania, USA (D.M. Reeder, M.E. Vodzak)

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Figure 3

A) Virus isolation confirmed by reverse transcription PCR. SosV was isolated after intracranial and intraperitoneal inoculation into 2-day-old suckling mice. A specific reverse transcription PCR designed to amplify 2,188 bp of the SosV genome was performed by using RNA from brains (Br), liver (Lv), and spleen (Sp) of the euthanized animals. Viral RNA was found only in the brain, not in liver or spleen. B) Propagation of SosV in cell culture. Homogenized tissues (brain, liver, and spleen) were us

Figure 3. A) Virus isolation confirmed by reverse transcription PCRSosV was isolated after intracranial and intraperitoneal inoculation into 2-day-old suckling miceA specific reverse transcription PCR designed to amplify 2,188 bp of the SosV genome was performed by using RNA from brains (Br), liver (Lv), and spleen (Sp) of the euthanized animalsViral RNA was found only in the brain, not in liver or spleenB) Propagation of SosV in cell cultureHomogenized tissues (brain, liver, and spleen) were used to infect H292 cellsFixed monolayers were stained with convalescent-phase serum from the patient and anti-human AlexaFluor 488 antibody (Invitrogen, Grand Island, NY, USA)C) Sosuga virus particleVirus morphologic appearance was examined by taking supernatants from infected Vero-E6 cells, clarifying by slow-speed centrifugation, and depositing on grids for negative staining and examination by transmission electron microscopyPleomorphic virions can be observedNeg.ctrl, negative control; Se, serum; SosV, Sosuga virus.

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Page created: January 15, 2014
Page updated: January 15, 2014
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