Baric Transcribed Interview (Redacted) — page 83
of 155 pages
← p.82 p.84 → · this page in the original PDF · package
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have a furin cleavage site, you could drop in a cleavage
site, using that clone. So technically, it could be
engineered, and it should be discussed.
MS. SALAZAR: Do you have any reason to believe that
they don't have that capability?
DR. BARIC: There is no evidence that they had a
molecular clone of that virus. They only had one molecular
clone. They weren't very good at reverse genetics. And
the molecular clone they had WIV1. And WIV1, they would
take spike genes of other sarbecos and drop it into that
clone because they had a difficult time making more clones.
The problem with coronavirus is part of the genome sequence
is really toxic in bacteria, so you have to come up with
ways around that.
And so best example of this is a virus emerged in
southern China called SADS coronavirus, 2016 or so. It
caused 100 percent or 99 percent mortality in piglets.
It's related to a virus called HKU2. They were trying to
make a molecular clone for that virus for three or four
years. We started around 2019, made a clone, published it
before them.
MS. SALAZAR: And why were they trying to do that?
DR. BARIC: I mean, they had a virus that caused 99
percent mortality in piglets that could destroy their swine
industry, so obviously it was important for them to develop
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Records on this page
| Record | Date | Type | Pages |
|---|---|---|---|
| baric_ti:utt:00740 | 2026-04-10 | transcript segment | 82–83 |
| baric_ti:utt:00741 | 2026-04-10 | transcript segment | 83 |
| baric_ti:utt:00742 | 2026-04-10 | transcript segment | 83 |
| baric_ti:utt:00743 | 2026-04-10 | transcript segment | 83 |
| baric_ti:utt:00744 | 2026-04-10 | transcript segment | 83–84 |