Ibemgbo Sylvester Agha, Nyodu Rajni, Chaudhary Sakshi, Verma Dileep Kumar, Dixit Kritika, Nayak Kaustuv, Rani Vandana, Gaind Rajni, Chandele Anmol, Sunil Sujatha
Vector Borne Diseases Group, International Centre for Genetic Engineering and Biotechnology, New Delhi, India.
ICGEB-Emory Vaccine Center, International Centre for Genetic Engineering and Biotechnology, New Delhi, India.
Virus Res. 2022 Oct 15;320:198888. doi: 10.1016/j.virusres.2022.198888. Epub 2022 Aug 14.
With explosive epidemics of chikungunya in India since 2004, chikungunya virus (CHIKV) now co-circulates in geographical areas where Dengue virus (DENV) is already endemic and thus provides opportunity for the same mosquito to be infected with both viruses. Although there are excellent studies that have addressed the clinical of mono and co-infection, we have little to no knowledge on the current viral sequences that pre-dominate co-infections, and the B cell response elicited. In this study, we analyzed febrile patients that were confirmed to have DENV-CHIKV co-infections and asked the following questions: 1) what is the frequency of co-infections found in a single cycle of transmission; 2) what are the viral sequences associated with them; 3) what does the antibody secreting cell / plasmablast response look like in patients that are co-infected with both viruses. We report those co-infections occur at a frequency of 6.7% in the transmission cycle, and while DENV-3 is now frequently detected, we do not see a serotype bias in the patients that are co-infected with ESCA strain of CHIKV. Moreover, the effector B cell response (plasmablasts) observed are specific to both infecting viruses indicating no overt bias. Further studies to associate whether any of these properties have a bearing on clinical disease manifestation will be both timely and important.
自2004年印度爆发基孔肯雅热疫情以来,基孔肯雅病毒(CHIKV)现与登革热病毒(DENV)在登革热病毒已经流行的地理区域共同传播,因此为同一种蚊子感染这两种病毒提供了机会。尽管已有出色的研究探讨了单一感染和共同感染的临床情况,但我们对目前在共同感染中占主导的病毒序列以及引发的B细胞反应知之甚少。在本研究中,我们分析了确诊为DENV-CHIKV共同感染的发热患者,并提出以下问题:1)在单个传播周期中发现的共同感染频率是多少;2)与它们相关的病毒序列是什么;3)同时感染这两种病毒的患者中抗体分泌细胞/浆母细胞反应是什么样的。我们报告在传播周期中共同感染的频率为6.7%,虽然现在经常检测到DENV-3,但在感染CHIKV的ESCA毒株的共同感染患者中我们未发现血清型偏差。此外,观察到的效应B细胞反应(浆母细胞)对两种感染病毒均具有特异性,表明没有明显偏差。进一步研究这些特性是否与临床疾病表现有关将既及时又重要。