David Robertson (@equal_ibrium) header
David Robertson (@equal_ibrium) profile picture

Historian of science/medicine. Intrigued and appalled by the response to covid-19. Retweets ≠ endorsements. Opinions my own.

Suisse
Joined April 2017
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Since COVID China has strengthened its biosafety with 2020 Biosafety Law & 2025 National Health Commission’s regulation. But persistent concerns over transparency, & the rapid expansion of laboratory capacity offset these gains. So biosafety risks persist sites.google.com/view/ibca-i…
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"[M]ore labs and more work with dangerous pathogens also means more opportunity for something to go wrong....Equipment fails. Samples are mishandled. Procedures are breached. Humans tire." "We know this because it has happened before." unherd.com/2026/10/the-lesso…
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Russia says lab worker didn’t die of plague. WHO, U.S. experts want to know what killed her. healthbeat.org/2026/10/06/ru…
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Healthbeat found a D.N. Shipilova listed as a co-author of plague bacteria research by scientists from the Irkutsk institute that was presented earlier this year. The study examined the antibiotic susceptibility of Yersinia pestis strains.
Russia says lab worker didn’t die of plague. WHO, U.S. experts want to know what killed her. healthbeat.org/2026/10/06/ru…
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"In the six years since the Covid-19 outbreak, the world has been building even more bioresearch facilities...[M]eanwhile oversight of the science and the security measures at those facilities is struggling to keep up." vox.com/health/505366/russia…
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1/6 During his guest intramuros NIH lecture today (6 Oct 2026), Andersen repeated the false claims of Worobey et al and Pekar et al, which have not survived post-publication peer-review. Slides and analysis follow 👇🏻 @NIHDirector_Jay @bgurley @mbw61567742 @nizzaneela #DRASTIC
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🚨FAUCI DIARY UPDATE🚨 Today, Senator Paul released the 203 missing diary pages from 2015–2019. paul.senate.gov/readingroom/
🚨FAUCI DIARY UPDATE🚨 Based on the diary page numbers of the prior releases, there appeared to be a 206-page gap between the material released on July 25 and July 27. Today, Senator Paul released 3 pages from this gap, leaving 203 pages in that sequence still unaccounted for. ** September 28th release ** Section Label: EXCERPT FROM FAUCI’S NOTES PDF pages: 2–4 Diary pages: 499–501 Dates: March 3, 2016 – March 10, 2016 ** July 27th release ** Section Label: HISTORICAL RECORD OF HIV/AIDS PDF pages: 3–465 Diary pages: 1–463 Dates: April 11, 2001 – July 8, 2015 Note that this section states that the written record “will start today (April 11, 2001)” but includes descriptions of earlier events, including March 2 and April 3–10, 2001. ** July 25th release ** Section Label: None (Part 1 is not explicitly labeled) PDF pages: 2–270 Diary pages: 670–938 Dates: Dec. 30, 2019 – Aug. 4, 2020 Section Label: Historical Record of A. S. Fauci – Part 2 PDF pages: 271–583 Diary pages: 1–313 Dates: Aug. 5, 2020 – Jan. 9, 2021 Section Label: Historical Record of A. S. Fauci – Part 3 PDF pages: 584–720 No visible diary page numbers Dates: Jan. 10, 2021 – June 16, 2021 Section Label: Historical Record of A. S. Fauci – Part 4 PDF pages: 721–1141 No visible diary page numbers Dates: May 1, 2021 – Dec. 17, 2022 Note: Parts 3 and 4 overlap: Part 3 runs through June 16, 2021, while Part 4 begins on May 1, 2021. @gdemaneuf - please let me know if there's anything I should add or correct in this summary
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Last year, as part of a comprehensive review of NIH’s intramural policies, I announced that NIH was adopting an updated agency-wide framework to embed principles of academic freedom within our Intramural Research Program. This framework recognizes that intramural researchers must be free to share their scientific viewpoints and to communicate their scientific findings through manuscripts, presentations, media interviews, and so on. This includes hosting outside lecturers for events focused on their scientific work. Today, NIH reaffirms this commitment to academic freedom as members of the intramural research community host Kristian G. Andersen, MPhil, PhD, as a guest lecturer. Dr. Andersen is a co-author of a March 2020 paper published in Nature Medicine titled “The proximal origin of SARS-CoV-2.” The paper’s authors assert: “Our analyses clearly show that SARS-CoV-2 is not a laboratory construct or a purposefully manipulated virus.” They further write that “we do not believe that any type of laboratory-based scenario is plausible.” The paper was cited extensively by members of the media, social media companies, and government officials to refute or suppress lab-origin hypotheses and to discredit anyone who publicly dissented from the dominant natural-origins narrative. As then-NIH Director Dr. Francis Collins wrote, “this study leaves little room to refute a natural origin for COVID-19.” Yet before and after the paper’s publication, Dr. Andersen himself expressed substantially more uncertainty. In January, he wrote in an email that some features of the virus “(potentially) look engineered.” One month after the paper’s publication, he wrote privately that he was not fully convinced that every lab-based scenario could be ruled out. In January 2025, the Central Intelligence Agency released the results of an assessment conducted during the Biden administration that found a “research-related origin” of SARS-CoV-2 was “more likely than a natural origin,” while assessing both theories as plausible. Given the evidence I’ve seen, I think the preponderance of evidence supports the theory that the virus leaked from a lab. I am keenly aware that no hypothesis about the origins of SARS-CoV-2 has been conclusively proven. When it comes to open scientific questions like this, our ability to pursue truth depends on our freedom to explore various hypotheses, weigh all available evidence, and deliberate openly. This freedom was denied to many scientists during the pandemic. 𝗜 𝗮𝗺 𝗽𝗹𝗲𝗮𝘀𝗲𝗱 𝘁𝗵𝗮𝘁 𝗮𝗹𝗹 𝗡𝗜𝗛 𝘀𝗰𝗶𝗲𝗻𝘁𝗶𝘀𝘁𝘀 𝗮𝗻𝗱 𝘁𝗵𝗲𝗶𝗿 𝗴𝘂𝗲𝘀𝘁𝘀—𝗻𝗼 𝗺𝗮𝘁𝘁𝗲𝗿 𝘄𝗵𝗮𝘁 𝘁𝗵𝗲𝘆 𝘁𝗵𝗶𝗻𝗸 𝗮𝗯𝗼𝘂𝘁 𝘁𝗵𝗲 𝗼𝗿𝗶𝗴𝗶𝗻𝘀 𝗼𝗳 𝗦𝗔𝗥𝗦-𝗖𝗼𝗩-𝟮—𝗲𝗻𝗷𝗼𝘆 𝗶𝘁 𝗻𝗼𝘄.
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1/14 🚨 A lab worker at the Irkutsk Anti-Plague Research Institute (Иркутский противочумный институт) has reportedly died of a suspected dangerous infection. Nearly 200 contacts watched. Rospotrebnadzor (Роспотребнадзор) chief Anna Popova (Анна Попова) is on site. 🧵👇🏻
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Good take.
In this era of artificial intelligence, it is becoming urgent to distinguish human art from what machines produce. There is an ontological difference, even before an aesthetic one, between art and what a machine can generate through statistical calculation based on millions of images created by others. Algorithms lack the spark of humanity. For this reason, the Church wishes to renew an alliance with artists and cultural institutions to safeguard our humanity.
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Dr. Peter Jahrling, @NIAIDFunding Chief Scientist, compared Gain of Function work on pandemic pathogens to "looking for a gas leak with a lighted match". archive.is/v7usJ#selection-8… h/t @R_H_Ebright
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David Robertson retweeted
I think one reason I don't believe claims that it's reasonably likely that AI "ends humanity" is that it must be 100x more likely at least that it kills, like, 1000 people first, and in that case there there would presumably be a major realignment.
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*** Happening Today at 3:00 PM *** "Scientific Responsibility in Research on Dangerous Pathogens" Waksman Institute, Rutgers University Speakers - Simon Wain-Hobson, @R_H_Ebright, and Neil Harrison waksman.rutgers.edu/event/sc…
🚨Inaugural event - September 11, 2026🚨 🦠Scientific Responsibility in Research on Dangerous Pathogens🦠 Friday, September 11 at 3:00 PM in the Waksman Institute Auditorium at @RutgersU The event will open with virtual welcome remarks from Rutgers President William F. Tate IV and feature: Simon Wain-Hobson (Professor Emeritus, Institut Pasteur) @R_H_Ebright (Professor, Rutgers University) Neil L. Harrison (Professor, Columbia University) The discussion will examine dangerous gain-of-function research, the governance and oversight of high-risk pathogen research, and the ongoing debate over the origin of COVID-19.
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Via my ongoing litigation, I just received some 400 pages of heavily redacted Energy Department records on the origin of Covid. Part 1: documentcloud.org/documents/…
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From 2005: "More than 700 scientists sent a petition…to…NIH protesting…the shift of tens of millions of dollars in…research money since 2001 away from pathogens that cause major…health problems to obscure germs the government fears might be used in a bioterrorist attack."
"Newly disclosed documents reveal that Fauci's National Institute of Allergy and Infectious Diseases (NIAID) had a formal institutional partnership with the CIA, one that provided cover for the agency's biological-threat research." pjmedia.com/matt-margolis/20…
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“The Fed needs clear market signals, as unfiltered as possible.” -Kevin Warsh, while Scott Bessent is running around doing Treasury interventions
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"A deeper reckoning, moreover, may shed light on the creepy, long-running nexus between biological research and America’s national-security state. [...] At least one US intelligence agency — the CIA — has already concluded that the novel coronavirus ... unherd.com/2026/08/the-great…
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🧵“let’s be blunt… [it’s] a bloody good document” On the latest episode of "In Defense of Virology," Simon Wain-Hobson and I discuss why the new US policy on regulation of dangerous gain-of-function research is a major step in the right direction. (1/n)
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An exciting grant from 2018 also offers insights into how coronaviruses can acquire cleavage motifs for the cellular protease furin!
An exciting new preprint offers insights into how SARS-CoV-2 and other coronaviruses can acquire cleavage motifs for the cellular protease furin. A thread on the importance of the furin motif in the SARS-CoV-2 spike and its possible origins.🧵 To infect a cell, coronaviruses must first get inside. The spike protein handles this, with help from the host cell. Spike binds receptors on the cell surface. After activation by cellular proteases, it drives fusion of the viral and cellular membranes, allowing delivery of the viral genome into the cell. This step is essential for infection. For SARS-CoV-2, spike activation involves two key cleavages. Furin cleaves at the S1/S2 site during virus production. A second cleavage by TMPRSS2 at S2′ then occurs during entry into human respiratory cells. The furin cleavage motif matters: disrupting it reduces infection of human respiratory cells and attenuates SARS-CoV-2 in animal models. The closest known relatives of SARS-CoV-2 (sarbecoviruses) come from bats, consistent with an evolutionary ancestry in bat coronaviruses. Yet none of the known closely related bat sarbecoviruses has a furin cleavage motif at S1/S2. This absence has featured prominently in discussions of SARS-CoV-2’s origin, including claims that the site might have been acquired through laboratory manipulation. Let’s examine whether furin cleavage motifs are generally advantageous for sarbecoviruses and how they can be acquired.
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