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. 2018 Apr 19;8:6488. doi: 10.1038/s41598-018-24845-7

Author Correction: Duck plague virus Glycoprotein J is functional but slightly impaired in viral replication and cell-to-cell spread

Yu You 1,2,3,#, Tian Liu 1,2,3,#, Mingshu Wang 1,2,3,#, Anchun Cheng 1,2,3,, Renyong Jia 1,2,3, Qiao Yang 1,2,3, Ying Wu 1,2,3, Dekang Zhu 2,3, Shun Chen 1,2,3, Mafeng Liu 1,2,3, XinXin Zhao 1,2,3, Shaqiu Zhang 1,2,3, Yunya Liu 1,2,3, Yanling Yu 1,2,3, Ling Zhang 1,2,3
PMCID: PMC5906648  PMID: 29670204

Correction to: Scientific Reports 10.1038/s41598-018-22447-x, published online 06 March 2018

In Figure 3B, the upper and the lower immunofluorescence images are the same. The correct Figure 3 appears below as Figure 1.

Figure 1.

Figure 1

Rescue mutant viruses and Identification of gJ expression. (A) Purification and enrichment of mutant viruses. Purification and enrichment of mutant viruses were obtained by the three times passage after transfection. (B) Immunofluorescence detection of gJ expression. DEF cells were infected at 1000 TCID50, and gJ expression was detected by indirect immunofluorescence at 36 hpi. Rabbit anti-gJ were used as primary antibody, and goat anti-rabbit IgG TRITC were used as secondary antibody. (C) Anti-gJ monoclonal antibody (MAb) was used to detect gJ via western immunoblot analysis. DPV CHv-BAC-ΔgJ infected DEF cells were detected as parental virus.


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