Skip to content

Biosecurity Interventions

📋Page Status
Page Type:ResponseStyle Guide →Intervention/response page
Quality:55 (Adequate)
Importance:72.5 (High)
Last edited:2026-02-05 (1 day ago)

A common misconception—articulated by figures like Ramez Naam—is that the EA/x-risk community’s biosecurity work consists primarily of restricting what LLMs can say about biology. In reality, AI capability restrictions represent just one of at least six major intervention categories, and likely not the one receiving the most investment. The portfolio spans DNA synthesis screening, pathogen-agnostic surveillance, medical countermeasures, AI capability evaluations, physical environmental defenses, and governance reform.

This page maps the full landscape of biosecurity interventions relevant to AI-enabled biological risks, organized by Kevin Esvelt’s Delay, Detect, Defend framework—the dominant conceptual model in this space.

DimensionAssessmentEvidence
Total EA Biosecurity Funding$230M+ from Open Philanthropy alone140+ grants across Biosecurity & Pandemic Preparedness fund1
Intervention Categories6+ distinct categoriesDNA screening, surveillance, countermeasures, AI evals, physical defenses, governance
% That Is “LLM Restrictions”Small minorityMost funding goes to detection infrastructure, screening technology, and countermeasures
Government AdoptionGrowingCDC Biothreat Radar ($52M proposed FY2026); OSTP synthesis screening framework; military ANTI-DOTE program
Key FrameworkDelay / Detect / DefendSecureBio’s organizing model, widely adopted
Biggest GapMedical countermeasuresResilience-based approaches like broad-spectrum antivirals remain underfunded relative to need

Loading diagram...
InterventionKey ActorsEA/x-Risk Adjacent?Funding Scale
DNA Synthesis ScreeningSecureDNA, IBBIS/NTI, IGSCYes (SecureDNA founded by Esvelt)$10M+
Metagenomic SurveillanceSecureBio/NAO, CDC NWSSYes (NAO is SecureBio project)$10M+; $52M proposed government
AI Bio-Capability EvaluationsSecureBio (VCT), Anthropic, OpenAI, RANDMixed (SecureBio is EA; labs are industry)Embedded in lab budgets
Medical CountermeasuresRed Queen Bio, BARDA, platform vaccine developersPartially (Red Queen Bio funded by OpenAI)$15M seed; billions in government
Far-UVC & Physical DefensesBlueprint Biosecurity, Columbia University, UshioYes (Blueprint is EA-funded)$1M+ in EA grants
AI Capability RestrictionsAnthropic (ASL-3), OpenAI (preparedness), Google DeepMindIndustry-led with EA influenceEmbedded in lab operations
Biosecurity GovernanceNTI Bio, CSIS, Council on Strategic Risks, Johns Hopkins CHSMixed$7.8M+ from Open Philanthropy to NTI

Delay: Slowing Dangerous Capability Proliferation

Section titled “Delay: Slowing Dangerous Capability Proliferation”

DNA synthesis screening is arguably the most concrete, technically mature biosecurity intervention. The goal: prevent anyone from ordering synthetic DNA that could be used to reconstruct dangerous pathogens.

Key initiatives:

  • SecureDNA — A Swiss nonprofit foundation co-founded by Kevin Esvelt, providing free, privacy-preserving screening software to DNA synthesis providers. Uses cryptographic protocols so that neither the order contents nor the hazard database are revealed during screening. Can detect hazardous sequences down to 30 base pairs—already exceeding the OSTP framework’s 2026 requirement of 50bp screening.2

  • IBBIS (International Biosecurity and Biosafety Initiative for Science) — Launched by NTI in 2024, headquartered in Geneva, led by Piers Millett (former Deputy Head of the BWC Implementation Support Unit). Develops the Common Mechanism for international DNA synthesis screening.3

  • OSTP Synthesis Screening Framework — The Biden administration’s April 2024 framework requiring federally funded researchers to procure synthetic nucleic acids only from screened providers. Implementation began April 2025 (200nt minimum), with 50nt minimum from October 2026. The Trump administration’s May 2025 Executive Order directed revision of the framework but maintained its core screening requirements.4

Critical gap: A January 2026 Nature Communications paper by Edison, Toner, and Esvelt demonstrated that unregulated DNA fragments can be assembled to bypass synthesis screening entirely—they acquired fragments sufficient to reconstruct the 1918 influenza virus from dozens of providers. The paper argues fragments must be regulated as select agents.5

This is the intervention Ramez Naam and others often assume constitutes the entirety of EA biosecurity work. In practice, it’s one piece of a much larger portfolio:

  • Anthropic’s ASL-3: Activated for Claude Opus 4 specifically due to CBRN capability concerns. Involves increased internal security (preventing model theft) and deployment restrictions limiting misuse for weapons development.6
  • OpenAI’s Preparedness Framework: GPT-5 and ChatGPT Agent deployed with “High capability” safeguards after evaluations couldn’t rule out meaningful assistance to novice bioweapon actors.7
  • Google DeepMind: Gemini 2.5 Deep Think deployed with additional mitigations after CBRN knowledge assessments.7
  • Open-source gap: DeepSeek described as “worst tested” for biosafety by Dario Amodei (2025), with minimal content filtering for dangerous biological information.8
  • Biological Weapons Convention (BWC): The primary international treaty, though lacking a verification protocol. EA-adjacent organizations (NTI Bio, Council on Strategic Risks) actively push for strengthening.9
  • CSIS 2025 Report: Found current measures “ill-equipped” for AI-enabled bioterrorism threats.10
  • Dual-use research oversight: Ongoing debates about gain-of-function research moratorium and DURC policies.

The Nucleic Acid Observatory (NAO), operated by SecureBio under Jeff Kaufman’s leadership, represents perhaps the most distinctive EA contribution to biosecurity—and one that has nothing to do with LLM restrictions.

How it works: Unlike traditional PCR-based surveillance (which can only detect known pathogens), the NAO performs untargeted metagenomic sequencing of wastewater—sequencing all genetic material in a sample. This means it can detect completely novel, engineered, or unknown pathogens, including those specifically designed to evade traditional surveillance.11

Three detection modes:

  1. Known pathogen alerts — Automated matching against pathogen databases
  2. Genetic engineering detection — “Chimera detection” pipeline flags signs of engineering
  3. Growth-based anomaly detection — Identifies any organism undergoing exponential growth, even if never seen before

Current scale (as of November 2025):

  • 31 sampling sites across 19 US cities
  • ≈60 billion read pairs sequenced weekly
  • Demonstrated detections: measles in Kauai County wastewater, West Nile Virus in Missouri12

Government adoption: The President’s FY2026 Budget proposes $52 million for Biothreat Radar, a national pathogen detection system at CDC drawing directly on NAO’s pilot findings. Designed to detect novel pathogens before 12 in 100,000 Americans are infected.13

Military adoption: Through the ANTI-DOTE program (Defense Innovation Unit), the NAO performs metagenomic sequencing at 5 US military facilities in the Indo-Pacific region.14

Evaluating whether AI systems can meaningfully assist bioweapon development:

  • Virology Capabilities Test (VCT): Developed by SecureBio, CAIS, and MIT. 322 multimodal questions testing practical virology laboratory knowledge. Key finding: leading AI models outperform the vast majority of practicing virologists sampled. Now adopted by major AI labs for pre-deployment testing.15
  • RAND Red-Team Study (2024): 12 teams of 3 people given 80 hours over 7 weeks to plan biological attacks with/without LLM access. Found no statistically significant difference in plan viability—but this was with 2024-era models.16
  • OpenAI 100-Person Study: 50 biology PhDs + 50 students, assessed across 5 stages (ideation, acquisition, magnification, formulation, release). Found GPT-4 provided “at most a mild uplift.”17
  • FRI Expert Survey: Forecasting Research Institute survey estimated AI capabilities matching expert virologists would increase annual epidemic probability from 0.3% to 1.5% (5x increase).18

This is the category Ramez Naam specifically highlighted as more promising than restriction-based approaches—and EA/x-risk organizations are working on it.

  • Red Queen Bio — Spun out of HelixNano (clinical-stage mRNA therapeutics), raised a $15M seed round led by OpenAI in 2025. Core thesis: “defensive co-scaling”—coupling defensive compute and funding to the same forces driving the AI capability race. Works with frontier labs to map AI-enabled biothreats and pre-build medical countermeasures.19
  • Platform vaccine technologies — mRNA platforms (demonstrated during COVID-19) enable rapid design of vaccines against novel pathogens within days of sequencing. The Coalition for Epidemic Preparedness Innovations (CEPI) has invested over $1.5B in pandemic preparedness vaccines, including its 100 Days Mission to compress vaccine development timelines.
  • Broad-spectrum antivirals — Still underdeveloped relative to need. Could provide pathogen-agnostic treatment.

Blueprint Biosecurity, an EA-funded organization, has made far-UVC technology a centerpiece of their work:

  • Far-UVC light (222nm) can inactivate 99.8% of airborne pathogens in occupied spaces while remaining safe for human exposure—the light is absorbed by dead skin cells before reaching living tissue.20
  • Columbia University research (David Brenner) demonstrated effectiveness; technology licensed to Ushio Inc. (Care222 product line).21
  • Blueprint’s EXHALE Program: ≈$1M in grants to evaluate far-UVC against real human-generated respiratory aerosols (Emory, Virginia Tech, University of Nebraska). Results expected mid-2026.22
  • Blueprint’s Project AIR: Launched to address three bottlenecks—global health agency endorsements, real-world implementation guidance, and multinational funding.22
  • Key limitation: No binding regulatory standards exist worldwide for safe far-UVC dosage as of 2025.23

How the X-Risk Approach Differs from Traditional Biosecurity

Section titled “How the X-Risk Approach Differs from Traditional Biosecurity”
DimensionTraditional Public HealthEA/X-Risk Approach
Detection methodPCR targeting known pathogensUntargeted metagenomic sequencing
Threat modelNatural disease outbreaksNatural pandemics AND deliberate/engineered threats
Design prioritySensitivity for known targetsDetection of completely novel threats
Scale of ambitionMonitor known diseasesEarly warning for civilization-threatening pandemics
ScreeningVoluntary industry guidelinesCryptographic screening infrastructure (SecureDNA)
CountermeasuresReactive (design after pathogen identified)Proactive (pre-build against AI-mapped threats)

OrganizationFocusEA-Adjacent?Key Funding
SecureBioDelay/Detect/Defend framework; NAO; AI evalsYes$9.4M+ from Open Philanthropy
SecureDNADNA synthesis screening technologyYes (Esvelt co-founder)Swiss foundation
IBBISInternational screening standardsPartially (NTI-launched)Open Philanthropy via NTI
Blueprint BiosecurityFar-UVC technology deploymentYes$900K from Open Philanthropy (2024)
Red Queen BioAI-driven medical countermeasuresPartially (OpenAI-funded)$15M seed (OpenAI-led)
NTI BioBiosecurity governance, BWCPartially$7.8M from Open Philanthropy
Council on Strategic RisksNational security biosecurity policyNo (traditional national security)Various
CSISPolicy research on AI-bio threatsNoVarious
Johns Hopkins CHSBiosecurity policy and analysisNoVarious
Centre for Long-Term ResilienceUK biosecurity policyYesEA-funded

Open Philanthropy (renamed Coefficient Giving in November 2025) is the dominant funder. Key biosecurity grants:

RecipientAmountPurpose
SecureBio$4,000,000General biosecurity research (3 years)
SecureBio (NAO)$3,430,000Nucleic Acid Observatory program
SecureBio$1,420,937Biosecurity research (3 years)
SecureBio$570,000Pathogen Early Warning Project
NTI Biosecurity$7,831,500Global catastrophic biological risk reduction (3 years)
Blueprint Biosecurity$900,000General support (2024)

Other EA-aligned funders include the Musk Foundation (NAO sensitivity research), Longview Philanthropy (>$50M directed in 2025 across x-risk areas), Founders Pledge (recommends SecureBio and IBBIS), and Survival and Flourishing Fund.


A key tension in biosecurity strategy—highlighted by Ramez Naam—is whether to prioritize restricting dangerous capabilities (limiting what AI models can say, restricting DNA synthesis) or building resilience (making it so that even if someone creates a pathogen, we can detect and respond fast enough to prevent catastrophe).

The EA/x-risk community’s actual position is: both are necessary, and the portfolio reflects this. The Delay/Detect/Defend framework explicitly incorporates both restriction (Delay) and resilience (Detect + Defend). The field generally agrees that:

  1. Restrictions buy time but are insufficient alone—information wants to be free, and restrictions become harder as capabilities proliferate (especially via open-source models)
  2. Resilience is the long-term solution but isn’t ready yet—metagenomic surveillance, far-UVC, and platform vaccines are still scaling
  3. The transition period is the most dangerous — we need restrictions now while building resilience infrastructure for the future

This is substantively different from the perception that EA biosecurity work is “only about limiting what LLMs can do.”

Key Questions (5)
  • How much of total EA biosecurity funding goes to resilience/defense vs. restriction/delay interventions?
  • Will DNA synthesis screening remain effective as benchtop synthesizers proliferate?
  • Can metagenomic surveillance scale fast enough to detect engineered pathogens with long incubation periods?
  • Is the 'defense favored' assumption correct long-term, or will offense always have an advantage in biology?
  • How much does open-source AI (e.g., DeepSeek) undermine restriction-based approaches?

  1. Coefficient Giving — Biosecurity & Pandemic Preparedness Fund

  2. SecureDNA platform; Security analysis

  3. IBBIS Common Mechanism; NTI announcement

  4. OSTP Framework; NIH implementation

  5. Edison, Toner & Esvelt 2026, Nature Communications

  6. 2026 International AI Safety Report

  7. 2026 International AI Safety Report 2

  8. Bioweapons page analysis of open-source risks
  9. NTI Bio BWC work

  10. CSIS 2025 report

  11. NAO methodology; P2RA study in The Lancet Microbe

  12. NAO Updates November 2025

  13. Biothreat Radar proposal

  14. PHC Global ANTI-DOTE program

  15. VCT paper; SecureBio announcement

  16. RAND 2024 study

  17. OpenAI biological threat study

  18. FRI AI-enabled biorisk survey

  19. Red Queen Bio; OpenAI $15M seed

  20. Far-UVC efficacy - Scientific Reports

  21. Columbia University far-UVC research

  22. Blueprint Biosecurity far-UVC program; EXHALE; Project AIR 2

  23. Far-UVC regulatory status