Genetic Characterization of Archived Bunyaviruses and their Potential for Emergence in Australia
Bixing Huang, Cadhla Firth, Daniel Watterson, Richard Allcock, Agathe M.G. Colmant, Jody Hobson-Peters, Peter D. Kirkland, Glen Hewitson, Jamie McMahon, Sonja Hall-Mendelin, Andrew F. van den Hurk, and David Warrilow
Author affiliations: Author affiliations: Queensland Health Forensic and Scientific Services, Brisbane, Queensland, Australia (B. Huang, G. Hewitson, J. McMahon, S. Hall-Mendelin, A.F. van den Hurk, D. Warrilow); Commonwealth Scientific and Industrial Research Organisation, Geelong, Victoria, Australia (C. Firth); The University of Queensland, St. Lucia, Queensland, Australia (D. Watterson, A.M.G. Colmant, J. Hobson-Peters); University of Western Australia, Nedlands, Western Australia, Australia (R. Allcock); QEII Medical Centre, Nedlands (R. Allcock); Elizabeth Macarthur Agriculture Institute, Menangle, New South Wales, Australia (P. Kirkland)
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Figure 2
Figure 2. Sequences of Salt Ash (SASHV) and Murrumbidgee virus (MURBV) in archived stocks of Gan Gan (GGV) and Trubanaman viruses, respectively, from Australia. Archived material that was designated GGV (upper panel) and Trubanaman (lower panel) virus was extracted. This material was used in an assay designed to detect the small (S), medium (M), and large (L) segments of SASHV and MURBV viruses as indicated below the panels. Lane M, 100-bp ladder (Promega Corporation, Madison, WI, USA); lanes 1–3, GGV sample 1; lanes 4–6, GGV sample 2; lanes 7–9, MURBV sample 1; lanes 10–12, MURBV sample 2.
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