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   <subfield code="a">Comprehensive mapping infection-enhancing epitopes of dengue pr protein using polyclonal antibody against prM</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Yayan Luo, Xiaolan Guo, Huijun Yan, Danyun Fang, Gucheng Zeng, Junmei Zhou, Lifang Jiang]</subfield>
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   <subfield code="a">Dengue vaccine development is considered a global public health priority, but the antibody-dependent enhancement (ADE) issues have critically restricted vaccine development. Recent findings have demonstrated that pre-membrane (prM) protein was involved in dengue virus (DENV) infection enhancement. Although the importance of prM antibodies have been well characterized, only a few epitopes in DENV prM protein have ever been identified. In this study, we screened five potential linear epitopes located at positions pr1 (1-16aa), pr3 (13-28aa), pr4 (19-34aa), pr9 (49-64aa), and pr10 (55-70aa) in pr protein using peptide scanning and comprehensive bioinformatics analysis. Then, we found that only pr4 (19-34aa) could elicit high-titer antibodies in Balb/c mice, and this epitope could react with sera from DENV2-infected patients, suggesting that specific antibodies against epitope peptide pr4 were elicited in both DENV-infected mice and human. In addition, our data demonstrated that anti-pr4 sera showed limited neutralizing activity but significant ADE activity toward standard DENV serotypes and imDENV. Hence, it seems responsible to hypothesize that anti-pr4 serum was infection-enhancing antibody and pr4 was infection-enhancing epitope. In conclusion, we characterized a novel infection-enhancing epitope on dengue pr protein, a finding that may provide new insight into the pathogenesis of DENV infection and contribute to dengue vaccine design.</subfield>
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   <subfield code="a">The Author(s), 2015</subfield>
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   <subfield code="a">Dengue virus</subfield>
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   <subfield code="a">Synthetic peptides</subfield>
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   <subfield code="a">Antibody-dependent enhancement</subfield>
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   <subfield code="u">Guangzhou Brain Hospital (Guangzhou Huiai hospital, the affiliated hospital of Guangzhou Medical University), 510370, Guanghzou, China</subfield>
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   <subfield code="a">Guo</subfield>
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   <subfield code="u">Key Laboratory for Tropic Diseases Control, Ministry of Education of China, Department of Microbiology, Zhongshan School of Medicine, Sun Yat-sen University, 510080, Guangzhou, China</subfield>
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   <subfield code="a">Yan</subfield>
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   <subfield code="u">Key Laboratory for Tropic Diseases Control, Ministry of Education of China, Department of Microbiology, Zhongshan School of Medicine, Sun Yat-sen University, 510080, Guangzhou, China</subfield>
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   <subfield code="a">Fang</subfield>
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   <subfield code="u">Key Laboratory for Tropic Diseases Control, Ministry of Education of China, Department of Microbiology, Zhongshan School of Medicine, Sun Yat-sen University, 510080, Guangzhou, China</subfield>
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   <subfield code="a">Zeng</subfield>
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   <subfield code="u">Key Laboratory for Tropic Diseases Control, Ministry of Education of China, Department of Microbiology, Zhongshan School of Medicine, Sun Yat-sen University, 510080, Guangzhou, China</subfield>
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   <subfield code="a">Zhou</subfield>
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   <subfield code="u">Key Laboratory for Tropic Diseases Control, Ministry of Education of China, Department of Microbiology, Zhongshan School of Medicine, Sun Yat-sen University, 510080, Guangzhou, China</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
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