Correction to: Establishment of Murine Infection Models with Biological Clones of Dengue Viruses Derived from A Single C
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CORRECTION
Correction to: Establishment of Murine Infection Models with Biological Clones of Dengue Viruses Derived from A Single Clinical Viral Isolate Zhihang Zheng1,2,3 • Min Li1 • Zhihua Liu1,2,3 • Xia Jin1,3
•
Jin Sun1
Ó Wuhan Institute of Virology, CAS 2020
Correction to: Virologica Sinica https://doi.org/10.1007/s12250-020-00229-y During the layout of the article, the square brackets in the legends were mistakenly shifted in every subfigure. The corrected figure is shown below (Fig. 3).
The original article can be found online at https:// doi.org/10.1007/s12250-020-00229-y. & Jin Sun [email protected] & Xia Jin [email protected] 1
CAS Key Laboratory of Molecular Virology and Immunology, Institut Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai 200031, China
2
Chinese Academy of Sciences, University of Chinese Academy of Sciences, Beijing 100049, China
3
Shanghai Public Health Clinical Center, Fudan University, Shanghai 201508, China
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Virologica Sinica
Fig. 3 Weight loss and survival curve of AG6 mice after infection with DENV-2 8H2-7-LP and DENV-2 1D4-5-SP. AG6 mice between 6–8 weeks old were infected with two viral variants and the parental isolate through s.c. injection. Three different dose of viruses, 103 PFU (A, D; n = 3), 104 PFU (B, E; n = 3), and 105 PFU (C, F; LP and SP n = 4, Parental n = 3), were inoculated into mice. Mice injected with
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PBS were included within each panel for control (CT, n = 6). Weight change was recorded and presented as a ratio to the initial weight on day 0. Moribund mice with weight loss over 20% were euthanatized and recorded as death. Two-way ANOVA was used in statistical analysis of differences among groups, *P \ 0.05, **P \ 0.01, ***P \ 0.001,****P \ 0.0001, n.s., not significant.
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