| Literature DB >> 30066045 |
Yang Liu1,2, YuLan Sun3,2, Wei Wu1, AQian Li1, XianDa Yang4,2, Shuo Zhang1, Chuan Li1, QiuDong Su1,2, ShaoJian Cai5,2, DaPeng Sun6,2, HaiYang Hu7,2, Zhe Zhang8,2, XiuXu Yang8,2, Idrissa Kamara2,9, Sheku Koroma2,9, Gerald Bangura2,9, Alie Tia2,9, Abdul Kamara9, Matt Lebby9, Brima Kargbo9, Jiandong Li1, Shiwen Wang1, XiaoPing Dong1, YueLong Shu1, WenBo Xu1, George F Gao1,10, GuiZhen Wu1, DeXin Li1, William J Liu11,12, MiFang Liang13.
Abstract
This study aimed to investigate the serological characteristics of Ebola virus (EBOV) infection during the late phase of the Ebola outbreak in Sierra Leone. In total, 877 blood samples from 694 suspected Ebola virus disease (EVD) cases assessed from March to December 2015, were analyzed via real-time reverse transcription polymerase chain reaction (RT-PCR) for viral RNA and enzyme-linked immunosorbent assay (ELISA) and Luminex to detect antibodies against EBOV. Viral load and EBOV-specific IgM/IgG titers displayed a declining trend during March to December 2015. Viral RNA load decreased rapidly at earlier stages after disease onset, while EBOV-specific IgM and IgG still persisted in 58.1% (18/31) and 93.5% (29/31) of the confirmed EVD patients and in 3.8% (25/663) and 17.8% (118/663) of the RNA-negative suspected patients in the later phase, respectively. Dynamic analysis of longitudinally collected samples from eight EVD patients revealed typically reversed trends of declining viral load and increasing IgM and/or IgG titers in response to the EBOV infection. The present results indicate that certain populations of Sierra Leone developed immunity to an EBOV infection in the late phase of the outbreak, providing novel insights into the risk assessment of EBOV infections among human populations.Entities:
Keywords: Ebola virus (EBOV); IgG; IgM; Late phase; Serologic investigation
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Year: 2018 PMID: 30066045 PMCID: PMC6178096 DOI: 10.1007/s12250-018-0044-z
Source DB: PubMed Journal: Virol Sin ISSN: 1995-820X Impact factor: 4.327