State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, China; Nanjing Municipal Center for Disease Control and Prevention, Affiliated Nanjing Center for Disease Control and Prevention of Nanjing Medical University, Nanjing, China.
State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, China.
Lancet Planet Health. 2024 Jul;8(7):e463-e475. doi: 10.1016/S2542-5196(24)00119-0.
Nipah virus is a zoonotic paramyxovirus responsible for disease outbreaks with high fatality rates in south and southeast Asia. However, knowledge of the potential geographical extent and risk patterns of the virus is poor. We aimed to establish an integrated spatiotemporal and phylogenetic database of Nipah virus infections in humans and animals across south and southeast Asia.
In this geospatial modelling analysis, we developed an integrated database containing information on the distribution of Nipah virus infections in humans and animals from 1998 to 2021. We conducted phylodynamic analysis to examine the evolution and migration pathways of the virus and meta-analyses to estimate the adjusted case-fatality rate. We used two boosted regression tree models to identify the potential ecological drivers of Nipah virus occurrences in spillover events and endemic areas, and mapped potential risk areas for Nipah virus endemicity.
749 people and eight bat species across nine countries were documented as being infected with Nipah virus. On the basis of 66 complete genomes of the virus, we identified two clades-the Bangladesh clade and the Malaysia clade-with the time of the most recent common ancestor estimated to be 1863. Adjusted case-fatality rates varied widely between countries and were higher for the Bangladesh clade than for the Malaysia clade. Multivariable meta-regression analysis revealed significant relationships between case-fatality rate estimates and viral clade (p=0·0021), source country (p=0·016), proportion of male patients (p=0·036), and travel time to health-care facilities (p=0·036). Temperature-related bioclimate variables and the probability of occurrence of Pteropus medius were important contributors to both the spillover and the endemic infection models.
The suitable niches for Nipah virus are more extensive than previously reported. Future surveillance efforts should focus on high-risk areas informed by updated projections. Specifically, intensifying zoonotic surveillance efforts, enhancing laboratory testing capacity, and implementing public health education in projected high-risk areas where no human cases have been reported to date will be crucial. Additionally, strengthening wildlife surveillance and investigating potential modes of transmission in regions with documented human cases is needed.
The Key Research and Development Program of China.
尼帕病毒是一种人畜共患的副粘病毒,在南亚和东南亚导致了高死亡率的疾病爆发。然而,人们对该病毒的潜在地理范围和风险模式知之甚少。我们旨在建立一个整合的南亚和东南亚人类和动物尼帕病毒感染的时空和系统发育数据库。
在这项地理空间建模分析中,我们开发了一个综合数据库,其中包含了 1998 年至 2021 年期间人类和动物感染尼帕病毒的分布信息。我们进行了系统发育分析,以研究病毒的进化和迁移途径,并进行荟萃分析以估计调整后的病死率。我们使用了两个增强回归树模型来识别溢出事件和流行地区中尼帕病毒发生的潜在生态驱动因素,并绘制了尼帕病毒流行的潜在风险区域。
在九个国家记录了 749 人和 8 种蝙蝠物种感染了尼帕病毒。基于 66 个完整的病毒基因组,我们确定了两个分支——孟加拉分支和马来西亚分支,其最近共同祖先的时间估计为 1863 年。各国之间的调整后病死率差异很大,孟加拉分支的病死率高于马来西亚分支。多变量荟萃回归分析显示,病死率估计与病毒分支(p=0·0021)、来源国(p=0·016)、男性患者比例(p=0·036)和前往医疗机构的旅行时间(p=0·036)之间存在显著关系。与温度相关的生物气候变量和 Pteropus medius 的发生概率是溢出和流行感染模型的重要贡献因素。
尼帕病毒的适宜生态位比以前报道的更广泛。未来的监测工作应集中在有最新预测的高风险地区。具体来说,加强对迄今没有人类病例报告的高风险地区的动物传染病监测工作,提高实验室检测能力,并开展公共卫生教育,将是至关重要的。此外,还需要加强野生动物监测,并调查有记录的人类病例地区的潜在传播模式。
中国的关键研发计划。