Tonto Prince Baffour, Sy Mouhamad, Ndiaye Ibrahima Mbaye, Toure Mariama, Gaye Amy, Aidara Mariama, Mbaye Amadou Moctar, Dia Abdoulaye Kane, Diallo Mamadou Alpha, Gomis Jules Francois, Yade Mamadou Samb, Diedhiou Younous, Dieye Baba, Diongue Khadim, Seck Mame Cheikh, Badiane Aida S, Herrera Bobby Brooke, Ndiaye Daouda
Rutgers Global Health Institute, Rutgers University, New Brunswick, New Jersey, USA.
Department of Medicine, Division of Allergy, Immunology, and Infectious Diseases and Child Health Institute of New Jersey, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA.
J Med Virol. 2025 Mar;97(3):e70282. doi: 10.1002/jmv.70282.
Arthritogenic alphaviruses such as chikungunya (CHIKV) and o'nyong-nyong (ONNV) viruses have shown capacity to cause widespread epidemics, with recurrent and sporadic outbreaks occurring throughout sub-Saharan Africa. We analyzed the seroprevalence for CHIKV and ONNV in 470 non-febrile subjects from three regions in Senegal (Sindia, 2018; Thies, 2018; and Kedougou, 2022/2023) using retrospective samples. We assessed the presence of anti-CHIKV IgG and neutralizing antibody titers against CHIKV and ONNV via enzyme-linked immunosorbent assay (ELISA) and microneutralization tests, respectively, and determined risk factors of CHIKV and ONNV exposure by binary logistic regression. The overall alphavirus seroprevalence based on an anti-CHIKV virus like particle (VLP) IgG ELISA was 38.5%, with rates varying geographically: Kedougou (48.6%), Thies (31.9%), and Sindia (14.9%). Neutralizing antibody titers revealed CHIKV and ONNV seroprevalence rates of 7.4% and 9.8%, respectively, with significant variations by region and age group. Cross-reactivity analysis showed that 82.9% of CHIKV cases exhibited a neutralizing response to ONNV, while 71.7% of ONNV cases cross-neutralized CHIKV. Residents of Thies had significantly higher odds of CHIKV infection (aOR, 3.147; 95% CI: 1.164-8.510) while ONNV infection was more likely in Kedougou (aOR, 3.888; 95% CI: 1.319-11.466). Furthermore, older age (> 40 years) was a significant risk factor both CHIKV (aOR, 2.094; 95% CI: 0.846-5.185) and ONNV infection (aOR, 2.745; 95% CI: 1.212-6.216). Our study confirms the co-circulation of CHIKV and ONNV in Senegal, highlighting their geographic and demographic distribution. These findings underscore the need for continued surveillance, alphavirus testing, and tailored public health strategies to mitigate their impact in Senegal.
基孔肯雅病毒(CHIKV)和奥尼昂-尼昂病毒(ONNV)等致关节炎甲病毒已显示出引发广泛疫情的能力,在撒哈拉以南非洲地区反复出现散发性疫情。我们使用回顾性样本分析了来自塞内加尔三个地区(辛迪亚,2018年;捷斯,2018年;凯杜古,2022/2023年)的470名无发热症状受试者的CHIKV和ONNV血清阳性率。我们分别通过酶联免疫吸附测定(ELISA)和微量中和试验评估抗CHIKV IgG的存在以及针对CHIKV和ONNV的中和抗体滴度,并通过二元逻辑回归确定CHIKV和ONNV暴露的危险因素。基于抗CHIKV病毒样颗粒(VLP)IgG ELISA的总体甲病毒血清阳性率为38.5%,不同地区有所差异:凯杜古(48.6%)、捷斯(31.9%)和辛迪亚(14.9%)。中和抗体滴度显示CHIKV和ONNV的血清阳性率分别为7.4%和9.8%,在不同地区和年龄组存在显著差异。交叉反应分析表明,82.9%的CHIKV病例对ONNV呈现中和反应,而71.7%的ONNV病例交叉中和CHIKV。捷斯的居民感染CHIKV的几率显著更高(调整后比值比,aOR,3.147;95%置信区间:1.164 - 8.510),而凯杜古居民感染ONNV的可能性更大(aOR,3.888;95%置信区间:1.319 - 11.466)。此外,年龄较大(> 40岁)是CHIKV(aOR,2.094;95%置信区间:0.846 - 5.185)和ONNV感染(aOR,2.745;95%置信区间:1.212 - 6.216)的重要危险因素。我们的研究证实了CHIKV和ONNV在塞内加尔共同传播,突出了它们的地理和人口分布情况。这些发现强调了持续监测、甲病毒检测以及制定针对性公共卫生策略以减轻其在塞内加尔影响的必要性。