Lytton Simon D, Yeasmin Mahmuda, Ghosh Asish Kumar, Bulbul Md Rakibul Hassan, Molla Md Maruf Ahmed, Herr Martha, Duchmann Helmut, Sharif Md Mohiuddin, Nafisa Tasnim, Amin Md Robed, Hosen Nur, Rahman Md Tanvir, Islam Sumaiya, Islam Alimul, Shamsuzzaman Abul Khair Mohammad
SeraDiaLogistics, 81545 Munich, Germany.
National Institute of Laboratory Medicine and Referral Center, Sher E-Bangla Nagar, Dhaka 1207, Bangladesh.
Pathogens. 2021 May 22;10(6):637. doi: 10.3390/pathogens10060637.
The assessment of antibody responses to severe acute respiratory syndrome coronavirus-2 is potentially confounded by exposures to flaviviruses. The aims of the present research were to determine whether anti-dengue antibodies affect the viral load and the detection of anti-coronavirus nucleocapsid (N)-protein antibodies in coronavirus infectious disease 2019 (COVID-19) in Bangladesh.
Viral RNA was evaluated in swab specimens from 115 COVID-19 patients by real-time reverse transcription polymerase chain reaction (rT-PCR). The anti-N-protein antibodies, anti-dengue virus E-protein antibodies and the dengue non-structural protein-1 were determined in serum from 115 COVID-19 patients, 30 acute dengue fever pre-COVID-19 pandemic and nine normal controls by ELISA.
The concentrations of viral RNA in the nasopharyngeal; Ct median (95% CI); 22 (21.9-23.3) was significantly higher than viral RNA concentrations in oropharyngeal swabs; and 29 (27-30.5) < 0.0001. Viral RNA concentrations were not correlated with-dengue IgG levels. The anti-nucleocapsid antibodies were IgA 27% positive and IgG 35% positive at days 1 to 8 post-onset of COVID-19 symptoms versus IgA 0% and IgG 0% in dengue patients, < 0.0001. The levels of anti- nucleocapsid IgA or IgG versus the levels of anti-dengue IgM or IgG revealed no significant correlations.
Viral RNA and anti-nucleocapsid antibodies were detected in COVID-19 patients from dengue-endemic regions of Bangladesh, independently of the dengue IgG levels.
对严重急性呼吸综合征冠状病毒2的抗体反应评估可能因接触黄病毒而受到干扰。本研究的目的是确定抗登革热抗体是否会影响孟加拉国2019冠状病毒病(COVID-19)患者的病毒载量以及抗冠状病毒核衣壳(N)蛋白抗体的检测。
通过实时逆转录聚合酶链反应(rT-PCR)对115例COVID-19患者的拭子样本中的病毒RNA进行评估。通过酶联免疫吸附测定法(ELISA)对115例COVID-19患者、30例COVID-19大流行前的急性登革热患者和9例正常对照者的血清中的抗N蛋白抗体、抗登革热病毒E蛋白抗体和登革热非结构蛋白-1进行检测。
鼻咽部病毒RNA浓度;Ct中位数(95%置信区间);22(21.9 - 23.3)显著高于口咽拭子中的病毒RNA浓度;以及29(27 - 30.5)< 0.0001。病毒RNA浓度与登革热IgG水平无关。COVID-19症状发作后第1至8天,抗核衣壳抗体IgA阳性率为27%,IgG阳性率为35%,而登革热患者中IgA和IgG均为0%,< 0.0001。抗核衣壳IgA或IgG水平与抗登革热IgM或IgG水平之间无显著相关性。
在孟加拉国登革热流行地区的COVID-19患者中检测到病毒RNA和抗核衣壳抗体,与登革热IgG水平无关。