Biosecurity Program, The Kirby Institute, UNSW Medicine, University of New South Wales, Sydney 2052, Australia.
College of Health Solutions and College of Public Service and Community Solutions, Arizona State University, Phoenix, AZ 85287.
Mil Med. 2020 Aug 14;185(7-8):e952-e957. doi: 10.1093/milmed/usaa084.
Smallpox, caused by variola virus, was eradicated in 1980, but remains a category A bioterrorism agent. A decade ago, smallpox ranked second after anthrax in a multifactorial risk priority scoring analysis of category A bioterrorism agents. However, advances in genetic engineering and synthetic biology, including published methods for synthesizing an Orthopoxvirus, require the assumptions of this scoring for smallpox and other category A agents to be reviewed.
The risk priority framework was reviewed and revised to account for the capability for creation of synthetic or engineered smallpox and other category A agents.
The absolute score for all agents increased because of gene editing and synthetic biology capability, which was not present when the framework was developed more than a decade ago, although new treatments revised scores downward for smallpox, Ebola, and botulism. In the original framework, smallpox scored 0 for global availability, given the high security around known seed stocks of variola in two laboratories in the United States and Russia. Now, smallpox can be created using synthetic biology, raising the score for this criterion to 2. Other agents too, such as Ebola, score higher for availability, based on synthetic biology capability. When advances in synthetic biology and genetic engineering are considered, smallpox and anthrax are now equally ranked the highest category A bioterrorism agents for planning and preparedness.
Revision of a risk priority framework for category A bioterrorism agents shows that smallpox should be elevated in priority for preparedness planning, and that gene editing and synthetic biology raises the overall risk for all agents. The ranking of categories A, B, and C agents should also be revisited, as there is an endless possibility of engineered threats that may be more severe than any agent on the category A list.
天花是由天花病毒引起的,于 1980 年被根除,但仍然是 A 类生物恐怖主义制剂。十年前,在对 A 类生物恐怖主义制剂进行的多因素风险优先排序分析中,天花仅次于炭疽,排名第二。然而,遗传工程和合成生物学的进步,包括已发表的合成正痘病毒的方法,要求重新审查对天花和其他 A 类制剂进行评分的假设。
审查和修订了风险优先框架,以考虑合成或工程化天花和其他 A 类制剂的创建能力。
由于基因编辑和合成生物学能力的存在,所有制剂的绝对得分都有所增加,而在十多年前制定该框架时,这些能力并不存在,尽管新的治疗方法使天花、埃博拉和肉毒杆菌的得分有所下降。在原来的框架中,由于在美国和俄罗斯的两个实验室中,天花病毒的高安全性,天花在全球的供应情况得分为 0。现在,天花可以通过合成生物学来制造,从而使该标准的分数提高到 2。其他制剂,如埃博拉,也因合成生物学能力而在供应方面获得更高的分数。考虑到合成生物学和基因工程的进步,天花和炭疽现在在规划和准备方面被列为同等最高的 A 类生物恐怖主义制剂。
对 A 类生物恐怖主义制剂风险优先排序框架的修订表明,天花应在准备计划中提高优先级,基因编辑和合成生物学提高了所有制剂的总体风险。A、B 和 C 类制剂的排名也应重新考虑,因为可能存在比 A 类名单上任何制剂都更严重的工程化威胁。