Mueller Siguna
Independent Transdisciplinary Researcher, Kaernten, Austria.
Front Bioeng Biotechnol. 2023 Aug 4;11:1209054. doi: 10.3389/fbioe.2023.1209054. eCollection 2023.
The urgent need for improved policy, regulation, and oversight of research with potential pandemic pathogens (PPPs) has been widely acknowledged. A 2022 article in Frontiers in Virology raises questions, reporting on a 100% sequence homology between the SARS-CoV-2 furin cleavage site (FCS) and the negative strand of a 2017 patented sequence. Even though Ambati and collaborators suspect a possible inadvertent or intentional cause leading to the FCS insert, the related underpinnings have not been studied from the perspective of potential biorisk policy gaps. A commentary on their article contests the low coincidence likelihood that was calculated by Ambati et al., arguing that the sequence match could have been a chance occurrence alone. Additionally, it has been suggested that the odds of the recombination event may be low. These considerations seem to have put many speculations related to any implied viral beginnings, notably from a research setting likely outside the Wuhan Institute of Virology, to rest. However, potential implications for future disasters in terms of biosafety and biosecurity have not been addressed. To demonstrate the of the Ambati et al. postulate, a theoretical framework is developed that substantially extends the research orientations implicated by these authors and the related patent. It is argued that specific experimental conditions, in combination, could significantly increase the implied recombination profile between coronaviruses and synthetic RNAs. Consequently, this article scrutinizes these largely unrecognized vulnerabilities to discuss implications across the spectrum of the biological risk landscape, with special attention to a potential "crime harvest." Focusing on insufficiently understood features of interaction between the natural and man-made world, vulnerabilities related to contaminants, camouflaging, and various misuse potentials fostered by the digitization and computerization of synthetic biology, it highlights novel biorisk gaps not covered by existing PPP policy. Even though this work does not aim to provide proof of the viral origin, it will make the point that, in theory, a convergence of under-appreciated lab experiments and technologies could have led to the SARS-CoV-2 FCS insert, which analogously could be exploited by various threat actors for the clandestine genesis of similar or even worse pathogens.
人们普遍认识到,迫切需要改进对具有潜在大流行病原体(PPP)研究的政策、监管和监督。《病毒学前沿》2022年的一篇文章提出了一些问题,报道了严重急性呼吸综合征冠状病毒2(SARS-CoV-2)弗林蛋白酶切割位点(FCS)与2017年一项专利序列的负链之间存在100%的序列同源性。尽管安巴蒂及其合作者怀疑可能存在导致FCS插入的无意或有意原因,但尚未从潜在生物风险政策差距的角度研究相关的潜在因素。对他们文章的一篇评论对安巴蒂等人计算出的低巧合可能性提出质疑,认为序列匹配可能只是偶然发生。此外,有人认为重组事件的几率可能很低。这些考虑似乎使许多与任何隐含的病毒起源相关的猜测,尤其是来自可能不在武汉病毒研究所的研究机构的猜测平息了。然而,在生物安全和生物安保方面对未来灾难的潜在影响尚未得到解决。为了证明安巴蒂等人假设的合理性,本文构建了一个理论框架,该框架大大扩展了这些作者和相关专利所涉及的研究方向。本文认为,特定的实验条件相结合,可能会显著增加冠状病毒与合成RNA之间隐含的重组情况。因此,本文仔细研究了这些在很大程度上未被认识到的漏洞,以讨论整个生物风险领域的影响,特别关注潜在的“犯罪成果”。本文关注自然与人为世界相互作用中尚未得到充分理解的特征、与污染物相关的漏洞、伪装以及合成生物学数字化和计算机化所带来的各种滥用可能性,强调了现有PPP政策未涵盖的新的生物风险差距。尽管这项工作并非旨在提供病毒起源的证据,但它将表明,从理论上讲,未得到充分重视的实验室实验和技术的结合可能导致了SARS-CoV-2 FCS插入,类似地,各种威胁行为者可能利用这一点秘密制造类似甚至更危险的病原体。