Shuo Jia1, Xinning Huang1, Hua Li1, Dianzhong Zheng1, Li Wang1, Xinyuan Qiao1, Yanping Jiang1, Wen Cui1, Lijie Tang1,2, Yijing Li1,2, Yigang Xu3,4. 1. Heilongjiang Key Laboratory for Animal Disease Control and Pharmaceutical Development, College of Veterinary Medicine, Northeast Agricultural University, Harbin, People's Republic of China. 2. Northeast Science Inspection Station, Key Laboratory of Animal Pathogen Biology of Ministry of Agriculture of China, Harbin, People's Republic of China. 3. Heilongjiang Key Laboratory for Animal Disease Control and Pharmaceutical Development, College of Veterinary Medicine, Northeast Agricultural University, Harbin, People's Republic of China. yigangxu_china@sohu.com. 4. Northeast Science Inspection Station, Key Laboratory of Animal Pathogen Biology of Ministry of Agriculture of China, Harbin, People's Republic of China. yigangxu_china@sohu.com.
Correction to: Microb Cell Fact (2020) 19:186 10.1186/s12934-020-01449-3
Unfortunately, in the original publication [1] of the article, an error was found in Fig. 1b and Fig. 4b. In Fig. 1b, the background noises of images in panel anti-E2 and panel anti-ctxB were modified. Although the modification does not change the conclusions of the Western blotting experiment (anti-E2 and anti-ctxB), the authors had reperformed the experiment again and reassembled Fig. 1b with the new results. In Fig. 4b, the image of the panel pPG-E2-ctxB/Lc W 56 was one of the results of the pPG-E2/Lc W 56 group, which was mistaken by the students and should be corrected.The corrected Figs. 1 and 4 are provided in this correction.
Fig. 1
Construction of the recombinant Lactobacillus strains and identification of the proteins of interest expressed by the recombinant Lactobacillus strains. a Schematic illustration of the construction of the recombinant pPG-E2 and pPG-E2-ctxB plasmids. b Identification of the proteins of interest expressed by the recombinant strains pPG-E2/Lc W56 and pPG-E2-ctxB/Lc W56 using Western blot with mouse anti-E2 or anti-ctxB mAb, respectively. c Identification of the E2 protein expressed by pPG-E2/Lc W56 by IFA. d Identification of the fusion protein E2-ctxB expressed by pPG-E2-ctxB/Lc W56 by IFA
Fig. 4
Detection of T lymphocytes expressing Bcl-6 in the PPs of the mice in each group on day 7 after oral vaccination by IHC assay (a) and fluorescence IHC assay (b)
Construction of the recombinant Lactobacillus strains and identification of the proteins of interest expressed by the recombinant Lactobacillus strains. a Schematic illustration of the construction of the recombinant pPG-E2 and pPG-E2-ctxB plasmids. b Identification of the proteins of interest expressed by the recombinant strains pPG-E2/Lc W56 and pPG-E2-ctxB/Lc W56 using Western blot with mouse anti-E2 or anti-ctxB mAb, respectively. c Identification of the E2 protein expressed by pPG-E2/Lc W56 by IFA. d Identification of the fusion protein E2-ctxB expressed by pPG-E2-ctxB/Lc W56 by IFADetection of T lymphocytes expressing Bcl-6 in the PPs of the mice in each group on day 7 after oral vaccination by IHC assay (a) and fluorescence IHC assay (b)