Erratum to: Preliminary characterization of Tasmanian aquareovirus (TSRV) isolates

Erratum to: Preliminary characterization of Tasmanian aquareovirus (TSRV) isolates Arch Virol (2017) 162:635 DOI 10.1007/s00705-017-3238-z ERRATUM Erratum to: Preliminary characterization of Tasmanian aquareovirus (TSRV) isolates 1,4 2 3 3 • • • • Sandra C. Zainathan Jeremy Carson Mark St. J. Crane Lynette M. Williams 3 3 3 3 • • • • John Hoad Nicholas J. G. Moody Nicholas Gudkovs Andrew Leis 3 3 3 1 • • • Sandra Crameri Alex D. Hyatt John Young Barbara F. Nowak Published online: 4 February 2017 Springer-Verlag Wien 2017 Erratum to: Arch Virol in Spurr’s epoxy resin. Ultrathin sections were double- DOI 10.1007/s00705-016-3132-0 stained in uranyl acetate and lead citrate and examined on a Philips CM120 transmission electron microscope at The published article contains incomplete author listing. 120 kV.’’ The correct details got updated here. Instead, the existing procedure for negative staining In addition, the original publication contains some should be followed by: redundant Materials and Methods that do not affect the Stained, air-dried virions were examined using a JEOL outcomes of the study. The following paragraph concern- (Japan) JEM-1400 transmission electron microscope ing thin section EM is not relevant to the published equipped with a high-contrast polepiece and LaB cathode, manuscript and should be disregarded: and operated at an accelerating voltage of 120 kV. ‘‘Thin section EM was used to examine the infected Micrographs were recorded on an Ultrascan (Gatan, cells, which were pelleted by centrifugation (20009g for Pleasanton, CA) 2K x 2K charge-coupled device (CCD) 5 min), fixed (2.5% glutaraldehyde in Sorensen’s phos- camera. phate buffer [300 mOsm/kg, pH 7.2 for 40 min], rinsed in Acknowledgements This work was performed at an buffer and post-fixed with 1% (w/v) osmium tetroxide NCRIS funded facility. The authors also acknowledge the 0.1 M cacodylate buffer (1 h) and rinsed with milli-Q facilities, and the scientific and technical assistance, of the water (3 9 5 min). The cells were dehydrated through Australian Microscopy & Microanalysis Research Facility graded ethanol (70 to 100%) and infiltrated and embedded at CSIRO. The online version of the original article can be found under doi:10.1007/s00705-016-3132-0. & Sandra C. Zainathan sandra@umt.edu.my National Centre for Marine Conservation and Resource Sustainability, University of Tasmania, Launceston, TAS 7248, Australia Department of Primary Industries, Park, Water and Environment, Launceston, TAS 7248, Australia CSIRO Australian Animal Health Laboratory (AAHL), Geelong, VIC 3220, Australia Present Address: School of Fisheries Science and Aquaculture, University Malaysia Terengganu, Terengganu, Malaysia http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Archives of Virology Springer Journals
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Publisher
Springer Journals
Copyright
Copyright © 2017 by Springer-Verlag Wien
Subject
Biomedicine; Virology; Medical Microbiology; Infectious Diseases
ISSN
0304-8608
eISSN
1432-8798
D.O.I.
10.1007/s00705-017-3238-z
Publisher site
See Article on Publisher Site

Abstract

Arch Virol (2017) 162:635 DOI 10.1007/s00705-017-3238-z ERRATUM Erratum to: Preliminary characterization of Tasmanian aquareovirus (TSRV) isolates 1,4 2 3 3 • • • • Sandra C. Zainathan Jeremy Carson Mark St. J. Crane Lynette M. Williams 3 3 3 3 • • • • John Hoad Nicholas J. G. Moody Nicholas Gudkovs Andrew Leis 3 3 3 1 • • • Sandra Crameri Alex D. Hyatt John Young Barbara F. Nowak Published online: 4 February 2017 Springer-Verlag Wien 2017 Erratum to: Arch Virol in Spurr’s epoxy resin. Ultrathin sections were double- DOI 10.1007/s00705-016-3132-0 stained in uranyl acetate and lead citrate and examined on a Philips CM120 transmission electron microscope at The published article contains incomplete author listing. 120 kV.’’ The correct details got updated here. Instead, the existing procedure for negative staining In addition, the original publication contains some should be followed by: redundant Materials and Methods that do not affect the Stained, air-dried virions were examined using a JEOL outcomes of the study. The following paragraph concern- (Japan) JEM-1400 transmission electron microscope ing thin section EM is not relevant to the published equipped with a high-contrast polepiece and LaB cathode, manuscript and should be disregarded: and operated at an accelerating voltage of 120 kV. ‘‘Thin section EM was used to examine the infected Micrographs were recorded on an Ultrascan (Gatan, cells, which were pelleted by centrifugation (20009g for Pleasanton, CA) 2K x 2K charge-coupled device (CCD) 5 min), fixed (2.5% glutaraldehyde in Sorensen’s phos- camera. phate buffer [300 mOsm/kg, pH 7.2 for 40 min], rinsed in Acknowledgements This work was performed at an buffer and post-fixed with 1% (w/v) osmium tetroxide NCRIS funded facility. The authors also acknowledge the 0.1 M cacodylate buffer (1 h) and rinsed with milli-Q facilities, and the scientific and technical assistance, of the water (3 9 5 min). The cells were dehydrated through Australian Microscopy & Microanalysis Research Facility graded ethanol (70 to 100%) and infiltrated and embedded at CSIRO. The online version of the original article can be found under doi:10.1007/s00705-016-3132-0. & Sandra C. Zainathan sandra@umt.edu.my National Centre for Marine Conservation and Resource Sustainability, University of Tasmania, Launceston, TAS 7248, Australia Department of Primary Industries, Park, Water and Environment, Launceston, TAS 7248, Australia CSIRO Australian Animal Health Laboratory (AAHL), Geelong, VIC 3220, Australia Present Address: School of Fisheries Science and Aquaculture, University Malaysia Terengganu, Terengganu, Malaysia

Journal

Archives of VirologySpringer Journals

Published: Feb 4, 2017

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