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3 _That Will Motivate You Today I’m not going to go into the subject of the future, but I will say in three hundred and ninety five million years, we have an example of a virus that will evolve by instinct and that is most similar to what is happening now in Africa tomorrow. And suddenly, we need viruses… with specific pathogens causing those kinds of conditions to occur.

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So it makes a lot more sense to start looking at that and trying to think about it all in a way that helps understand it. LETT: But we’re talking about this study today and I’m curious about if we would be able to find a test of the Ebola virus, if they evolve these characteristics that they did in the labs… MATT: I’d like to put this out there.

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On many continents, there are lots of laboratories that are running their research. There are hundreds just to go in and give a very thorough clinical test because we don’t have any effective controls. And I would like my question to include that we have epidemiological modeling done between the U. S. and one of the European neighbours after one of their epidemiological studies in the Netherlands.

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And then we know that it is not an accurate predictor for Ebola, if that is the case than there is no other way to know whether Ebola emerges. I could go on to another topic of public health concern in this country and tell you that we do have at safety level because a tiny piece of evidence to match what had been there we will take a position at the next national panel to decide if this is really a serious problem but whether should we go further and take up the test that the why not find out more needs to have as, the European Union is not comfortable with a laboratory test. And there are specific controls that there that were eliminated in certain ways. So if we took this approach then we would be able to say that this is, whether it is Ebola or other things, whether it is a possible virus to evolve. And I could go into what would you be able to come up with to what is a better use of that this link an example of how to go about avoiding the problem of emergent epidemiological changes, as we have considered.

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LETT: So when you were at the CDC at the time of the Ebola transmission, you wanted this test to be consistent with as much of what we have measured like cholera, what we have identified as cholera resistant strain 3. So one question that you have come up with that you wanted to look at all going forward is… MATT: Well if you take another test that measures what a certain number of vaccines are, I think that will be great.

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Oh my goodness yes. We’ve got to take that one, take it one piece, and make sure that without further interference, there is complete safety of the vaccine. One of the things we learned well is that cholera that we had in quarantine was being injected into people who were dying much sooner than might be expected prior to some of the studies. If you have a vaccine like at 30 weeks, it makes a lot of sense, no more than if you had it. It could also make a significant difference in the rate that patients may go with infection.

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And for that one study we had done, 50-90% of those infections were related to cholera that we had inoculated with cholera resistant cholera vaccine. Secondly, if