泰国尼帕病毒二十年的一次卫生监测。

Supaporn Wacharapluesadee, Siriporn Ghai, Prateep Duengkae, Pattarapol Manee-Orn, Weerapong Thanapongtharm, Abhinbhen W Saraya, Sangchai Yingsakmongkon, Yutthana Joyjinda, Sanipa Suradhat, Weenassarin Ampoot, Bundit Nuansrichay, Thongchai Kaewpom, Rachod Tantilertcharoen, Apaporn Rodpan, Kachen Wongsathapornchai, Teerada Ponpinit, Rome Buathong, Saowalak Bunprakob, Sudarat Damrongwatanapokin, Chanida Ruchiseesarod, Sininat Petcharat, Wantanee Kalpravidh, Kevin J Olival, Martha M Stokes, Thiravat Hemachudha
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引用次数: 7

摘要

背景:尼帕病毒(NiV)感染可引起脑炎,死亡率> 75%,由于其大流行的潜力,使其成为世卫组织优先考虑的病原体。在马来西亚、印度、孟加拉国和菲律宾南部都发生了新冠肺炎疫情。新冠病毒在狐蝠属的果蝠中自然传播,在东南亚和南亚广泛发现。在泰国的果蝠中发现了马来西亚和孟加拉国的NiV菌株。本研究总结了泰国20年来对新冠病毒的预防性One Health监测,包括对蝙蝠、感染新冠病毒的蝙蝠居住的栖息地附近的人和猪进行三角监测。方法:自2001年以来,定期从泰国最大的莱雷疟原虫栖息地春武里省Wat Luang村和其他省份的蝙蝠、猪和健康人类志愿者身上采集样本并检测NiV。还对2001年至2012年脑炎患者存档的脑脊液标本进行了NiV检测。采用巢式逆转录聚合酶链反应(RT-PCR)检测NiV RNA。采用酶联免疫吸附法或多重微球免疫分析法检测NiV抗体。结果:2002 - 2020年,RT-PCR每年在果蝠中检测到NiV RNA(主要为孟加拉国株)。2017年从蝙蝠尿液中直接测序的NiV全基因组序列与2004年孟加拉国患者的NiV同源性为99.17%。迄今为止,未在健康志愿者、脑炎患者或猪中发现niv特异性IgG抗体或RNA。在收集样本的过程中,100名社区成员接受了如何与蝙蝠安全生活的培训。结论:来自泰国蝙蝠和孟加拉国患者的新冠病毒基因组具有高度同一性,这凸显了新冠病毒在泰国爆发的潜力。将新冠病毒跨部门监测结果传达给国家当局和村民,从而采取预防控制措施,加强对已知新冠病毒感染栖息地附近的猪和人的监测,并在社区一级提高警惕并减少危险行为。这种积极主动的“同一个健康”监测方法是一个成功的故事;加强人类、动物和野生动物部门之间的合作对于预防人畜共患疾病暴发至关重要。
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Two decades of one health surveillance of Nipah virus in Thailand.

Background: Nipah virus (NiV) infection causes encephalitis and has > 75% mortality rate, making it a WHO priority pathogen due to its pandemic potential. There have been NiV outbreak(s) in Malaysia, India, Bangladesh, and southern Philippines. NiV naturally circulates among fruit bats of the genus Pteropus and has been detected widely across Southeast and South Asia. Both Malaysian and Bangladeshi NiV strains have been found in fruit bats in Thailand. This study summarizes 20 years of pre-emptive One Health surveillance of NiV in Thailand, including triangulated surveillance of bats, and humans and pigs in the vicinity of roosts inhabited by NiV-infected bats.

Methods: Samples were collected periodically and tested for NiV from bats, pigs and healthy human volunteers from Wat Luang village, Chonburi province, home to the biggest P. lylei roosts in Thailand, and other provinces since 2001. Archived cerebrospinal fluid specimens from encephalitis patients between 2001 and 2012 were also tested for NiV. NiV RNA was detected using nested reverse transcription polymerase chain reaction (RT-PCR). NiV antibodies were detected using enzyme-linked immunosorbent assay or multiplex microsphere immunoassay.

Results: NiV RNA (mainly Bangladesh strain) was detected every year in fruit bats by RT-PCR from 2002 to 2020. The whole genome sequence of NiV directly sequenced from bat urine in 2017 shared 99.17% identity to NiV from a Bangladeshi patient in 2004. No NiV-specific IgG antibodies or RNA have been found in healthy volunteers, encephalitis patients, or pigs to date. During the sample collection trips, 100 community members were trained on how to live safely with bats.

Conclusions: High identity shared between the NiV genome from Thai bats and the Bangladeshi patient highlights the outbreak potential of NiV in Thailand. Results from NiV cross-sectoral surveillance were conveyed to national authorities and villagers which led to preventive control measures, increased surveillance of pigs and humans in vicinity of known NiV-infected roosts, and increased vigilance and reduced risk behaviors at the community level. This proactive One Health approach to NiV surveillance is a success story; that increased collaboration between the human, animal, and wildlife sectors is imperative to staying ahead of a zoonotic disease outbreak.

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