寨卡病毒
病毒学
血清学
表位
病毒
免疫学
生物
医学
抗体
作者
Yiu‐Wing Kam,Juliana Almeida Leite,Siti Naqiah Amrun,Fok‐Moon Lum,Wearn‐Xin Yee,Farhana Abu Bakar,Kai Er Eng,David Chien Lye,Yee‐Sin Leo,Chia-Yin Chong,André Ricardo Ribas Freitas,Guilherme Paier Milanez,José Luiz Proença‐Módena,Laurent Rénia,Fábio Trindade Maranhão Costa,Lisa F. P. Ng,Zika-Unicamp Network,Eliana Amaral,Renato Passini,Helaine Maria Besteti Pires Mayer-Milanez
标识
DOI:10.1093/infdis/jiz092
摘要
BACKGROUND: Zika virus (ZIKV) infections have reemerged as a global health issue due to serious clinical complications. Development of specific serological assays to detect and differentiate ZIKV from other cocirculating flaviviruses for accurate diagnosis remains a challenge. METHODS: We investigated antibody responses in 51 acute ZIKV-infected adult patients from Campinas, Brazil, including 7 pregnant women who later delivered during the study. Using enzyme-linked immunosorbent assays, levels of antibody response were measured and specific epitopes identified. RESULTS: Several antibody-binding hot spots were identified in ZIKV immunogenic antigens, including membrane, envelope (E) and nonstructural protein 1 (NS1). Interestingly, specific epitopes (2 from E and 2 from NS1) strongly recognized by ZIKV-infected patients' antibodies were identified and were not cross-recognized by dengue virus (DENV)-infected patients' antibodies. Corresponding DENV peptides were not strongly recognized by ZIKV-infected patients' antibodies. Notably, ZIKV-infected pregnant women had specific epitope recognition for ZIKV NS1 (amino acid residues 17-34), which could be a potential serological marker for early ZIKV detection. CONCLUSIONS: This study identified 6 linear ZIKV-specific epitopes for early detection of ZIKV infections. We observed differential epitope recognition between ZIKV-infected and DENV-infected patients. This information will be useful for developing diagnostic methods that differentiate between closely related flaviviruses.
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