Department of Pathobiological Sciences, University of Wisconsin School of Veterinary Medicine, Madison, WI, USA.
Department of Paediatrics, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Sci Rep. 2024 May 7;14(1):10431. doi: 10.1038/s41598-024-61236-7.
Reverse zoonotic respiratory diseases threaten great apes across Sub-Saharan Africa. Studies of wild chimpanzees have identified the causative agents of most respiratory disease outbreaks as "common cold" paediatric human pathogens, but reverse zoonotic transmission pathways have remained unclear. Between May 2019 and August 2021, we conducted a prospective cohort study of 234 children aged 3-11 years in communities bordering Kibale National Park, Uganda, and 30 adults who were forest workers and regularly entered the park. We collected 2047 respiratory symptoms surveys to quantify clinical severity and simultaneously collected 1989 nasopharyngeal swabs approximately monthly for multiplex viral diagnostics. Throughout the course of the study, we also collected 445 faecal samples from 55 wild chimpanzees living nearby in Kibale in social groups that have experienced repeated, and sometimes lethal, epidemics of human-origin respiratory viral disease. We characterized respiratory pathogens in each cohort and examined statistical associations between PCR positivity for detected pathogens and potential risk factors. Children exhibited high incidence rates of respiratory infections, whereas incidence rates in adults were far lower. COVID-19 lockdown in 2020-2021 significantly decreased respiratory disease incidence in both people and chimpanzees. Human respiratory infections peaked in June and September, corresponding to when children returned to school. Rhinovirus, which caused a 2013 outbreak that killed 10% of chimpanzees in a Kibale community, was the most prevalent human pathogen throughout the study and the only pathogen present at each monthly sampling, even during COVID-19 lockdown. Rhinovirus was also most likely to be carried asymptomatically by adults. Although we did not detect human respiratory pathogens in the chimpanzees during the cohort study, we detected human metapneumovirus in two chimpanzees from a February 2023 outbreak that were genetically similar to viruses detected in study participants in 2019. Our data suggest that respiratory pathogens circulate in children and that adults become asymptomatically infected during high-transmission times of year. These asymptomatic adults may then unknowingly carry the pathogens into forest and infect chimpanzees. This conclusion, in turn, implies that intervention strategies based on respiratory symptoms in adults are unlikely to be effective for reducing reverse zoonotic transmission of respiratory viruses to chimpanzees.
逆转人畜共患呼吸道疾病威胁着撒哈拉以南非洲的大型猿类。对野生黑猩猩的研究已经确定了大多数呼吸道疾病爆发的病原体是“普通感冒”儿科人类病原体,但逆转人畜共患传播途径仍不清楚。在 2019 年 5 月至 2021 年 8 月期间,我们对乌干达基巴莱国家公园附近的 234 名 3-11 岁的儿童和 30 名经常进入公园的森林工人进行了前瞻性队列研究。我们收集了 2047 份呼吸道症状调查,以量化临床严重程度,同时每月大约收集 1989 份鼻咽拭子进行多重病毒诊断。在整个研究过程中,我们还从附近基巴莱的 55 个社会群体中收集了 445 份野生黑猩猩的粪便样本,这些社会群体经历了反复的、有时是致命的人类起源呼吸道病毒疾病的流行。我们对每个队列中的呼吸道病原体进行了特征描述,并检查了检测到的病原体的 PCR 阳性率与潜在危险因素之间的统计学关联。儿童表现出高发病率的呼吸道感染,而成年人的发病率则低得多。2020-2021 年的 COVID-19 封锁显著降低了人和黑猩猩的呼吸道疾病发病率。人类呼吸道感染在 6 月和 9 月达到高峰,当时儿童回到学校。鼻病毒是导致 2013 年基巴莱社区 10%黑猩猩死亡的爆发的罪魁祸首,它是整个研究中最常见的人类病原体,也是每个月采样时唯一存在的病原体,甚至在 COVID-19 封锁期间也是如此。鼻病毒也最有可能由成年人无症状携带。虽然我们在队列研究中没有在黑猩猩身上检测到人类呼吸道病原体,但我们在 2023 年 2 月的一次爆发中检测到了两只黑猩猩携带人类偏肺病毒,它们与 2019 年研究参与者检测到的病毒在基因上相似。我们的数据表明,呼吸道病原体在儿童中传播,成年人在一年中高传播时期会无症状感染。这些无症状成年人可能会无意中将病原体带入森林并感染黑猩猩。这一结论反过来又意味着,基于成年人呼吸道症状的干预策略不太可能有效减少呼吸道病毒向黑猩猩的逆转人畜共患传播。