Assessment of threat of concurrent SARS-CoV-2 and DENV infection in the COVID-19 pandemic in Brazil in 2020: diagnostic and immunological findings

Joyce Carnevale Rodrigues, Débora Familiar-Macedo, Thalia Medeiros, Fabiana Rabe Carvalho, Jorge Reis Almeida, Andrea Alice Silva, Flávia Barreto dos Santos, Luiz José de Souza, Paulo Vieira Damasco, Elzinandes Leal Azeredo, Luzia Maria de-Oliveira-Pinto
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Abstract

Introduction The first peak of COVID-19 in Brazil was between April and May 2020, at a time of the year when outbreaks of other tropical diseases, such as dengue, would be expected. COVID-19 and dengue have similar pathogenesis. In general, both may lead to mild symptoms but may also cause severe and even fatal symptoms, especially in patients with comorbidities and probably in cases of overlapping infections. The general objective of this study was to assess whether, during the 2020 pandemic, there were cases of concomitant infection between SARS-CoV-2 and DENV. Methods For this, we evaluated the specificity and sensitivity of commercial serological anti-SARS-CoV-2 kits using plasma samples from patients with dengue and healthy donors recruited before COVID-19. In the case of confirmed cases of COVID-19/dengue, we evaluated the clinical evolution of these coinfected patients, compared with mono-infected patients; and quantified chemokines CCL2 and CXCL8 by ELISA in COVID-19 patients in order to correlate them with COVID-19/dengue severity and cases. Results and Discussion Our results showed that commercial IgA and IgG anti-SARS-CoV-2 kits presented high sensitivity and specificity. This allowed us to see a low rate of co-detection or coinfection between SARS-CoV-2 and DENV in Rio de Janeiro. Among the 57 COVID-19 patients, anti-DENV IgM was detected in five (8.8%). COVID-19/dengue coinfected patients showed no clinical worsening of COVID-19 and cases in which COVID-19 patients had previous exposure to DENV did not influence the clinical severity of COVID-19. Lastly, CCL2 and CXCL8 appeared to be good markers of COVID-19 severity and did not show increased levels in COVID-19/dengue cases.
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2020年巴西COVID-19大流行中SARS-CoV-2和DENV并发感染的威胁评估:诊断和免疫学结果
巴西COVID-19的第一个高峰是在2020年4月至5月期间,这一时期预计会爆发登革热等其他热带病。COVID-19和登革热的发病机制相似。一般来说,两者都可能导致轻微症状,但也可能导致严重甚至致命的症状,特别是在有合并症的患者和可能重叠感染的病例中。本研究的总体目标是评估在2020年大流行期间,是否存在SARS-CoV-2和DENV合并感染的病例。为此,我们利用登革热患者和COVID-19之前招募的健康供者的血浆样本,评估了商用血清学抗sars - cov -2试剂盒的特异性和敏感性。在确诊的COVID-19/登革热病例中,与单一感染患者相比,我们评估了这些合并感染患者的临床演变;并通过ELISA定量分析COVID-19/登革热患者的趋化因子CCL2和CXCL8,以了解其与COVID-19/登革热严重程度和病例的相关性。结果与讨论本研究结果表明,IgA和IgG抗sars - cov -2试剂盒具有较高的敏感性和特异性。这使我们看到,在巴西里约热内卢,SARS-CoV-2和DENV的共同检测或共同感染率很低。57例新冠肺炎患者中,5例(8.8%)检测到抗denv IgM。COVID-19/登革热共感染患者未出现COVID-19的临床恶化,既往暴露于DENV的病例不影响COVID-19的临床严重程度。最后,CCL2和CXCL8似乎是COVID-19严重程度的良好标志物,并且在COVID-19/登革热病例中未显示出水平升高。
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