登革病毒(DV)非交叉反应型 Omicron 波 COVID-19 血清增强了 DV3 在体外的感染性。

Supratim Sarker, Chiroshri Dutta, Abinash Mallick, Sayantan Das, Chandrika Das Chowdhury, Abhishek De, Surajit Gorai, Subhajit Biswas
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引用次数: 0

摘要

导言。在印度,随着 Omicron 变种的出现(2021 年至今),SARS-CoV-2 Delta 浪潮(2020-2021 年)逐渐消退。据观察,在登革热大流行的活跃期(2020-2021 年),东南亚的登革热发病率较低。然而,自 2022 年以来,随着 Omicron 波的发展,该地区(包括印度)报告的 3 型登革热(DV3)病例越来越多。在东南亚许多地区登革热发病率整体下降之后,DV3型登革热病例异常激增的原因是什么?因此,我们调查了流行的(Omicron 时代)SARS-CoV-2 血清与不同 DV 血清型的交叉反应现状,并评估了这些血清对细胞培养中 DV 中和的影响。采用侧流免疫测定法检测了 55 份 COVID-19 血清样本(2022 年 1 月至 9 月)和 3 份疫情发生前的存档血清样本,这些样本均来自表面健康的个体。用 Huh7 细胞对 SARS-CoV-2 抗体(Ab)阳性血清进行了 DV1-4 病毒中和试验(VNTs)。对三个存档的 DV 分离物(一个来自 2017 年,两个来自 2021 年)的 DV3 包膜(env)基因进行了 PCR 扩增和测序。SARS-CoV-2抗体阳性样本占血清的74.5%。其中,41.5% 的血清具有 DV 交叉反应性,58.5% 的血清不具有 DV 交叉反应性。根据之前的结果和本研究,DV 交叉反应血清可中和所有 DV 血清型(DV1-4)。无交叉反应的 DV 血清(58.5%)也能交叉中和 DV1、2 和 4,但通过抗体依赖性感染增强作用提高了 DV3 的感染性,这一点从 VNT 中 DV3 滴度明显高于对照血清中的 DV3 滴度可以看出。包括用于 VNT 的分离物 1 在内的三个分离物的 DV3 包膜是相同的。我们的结果表明,SARS-CoV-2 血清的 DV 交叉反应性随着流行率从 Delta 型向 Omicron 型的转变而降低。这些 COVID-19 血清(DV 无交叉反应)可能在 Omicron 波期间导致 DV3 激增方面发挥了重要作用。疑似登革热或 COVID-19 的患者应进行病毒/抗原检测和两种疾病的血清学检测,以明确诊断、预后和疾病管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dengue virus (DV) non-cross-reactive Omicron wave COVID-19 serums enhanced DV3 infectivity in vitro.

Introduction. In India, the SARS-CoV-2 Delta wave (2020-2021) faded away with the advent of the Omicron variants (2021-present). Dengue incidences were observed to be less in Southeast Asia during the active years of the pandemic (2020-2021). However, dengue virus type 3 (DV3) cases were increasingly reported in this region (including India) concurrent with the progression of the Omicron waves since 2022.Hypothesis. What could be the reason(s) behind this unusual DV3 surge after an overall dip in dengue incidences in many parts of Southeast Asia?Aim. We, therefore, investigated the current state of cross-reactivity of prevalent (Omicron era) SARS-CoV-2 serums with different DV serotypes and evaluated the impact of such serums on DV neutralization in cell culture.Methodology. Fifty-five COVID-19 serum samples (January-September 2022) and three pre-pandemic archived serum samples from apparently healthy individuals were tested for DV or SARS-CoV-2 IgM/IgG using the lateral flow immunoassays. DV1-4 virus neutralization tests (VNTs) were done with the SARS-CoV-2 antibody (Ab)-positive serums in Huh7 cells. DV3 envelope (env) gene was PCR amplified and sequenced for three archived DV isolates, one from 2017 and two from 2021.Results. SARS-CoV-2 Ab-positive samples constituted 74.5 % of the serums. Of these, 41.5 % were DV cross-reactive and 58.5 % were not. The DV cross-reactive serums neutralized all DV serotypes (DV1-4), as per previous results and this study. The DV non-cross-reactive serums (58.5 %) also cross-neutralized DV1, 2 and 4 but increased DV3 infectivity by means of antibody-dependent enhancement of infection as evident from significantly higher DV3 titres in VNT compared to control serums. The DV3 envelope was identical among the three isolates, including isolate 1 used in VNTs. Our results suggest that DV cross-reactivity of SARS-CoV-2 serums diminished with the shift from Delta to Omicron prevalence. Such COVID-19 serums (DV non-cross-reactive) might have played a major role in causing DV3 surge during the Omicron waves.Conclusion. Patients suspected of dengue or COVID-19 should be subjected to virus/antigen tests and serological tests for both the diseases for definitive diagnosis, prognosis and disease management.

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