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Welcome to the cannabis data science meetup group. You're in for one of the best treats

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ever today. This may be the best meetup to date. Can't thank you enough for attending

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to make this happen. We've been talking a lot about the top issues for cannabis cultivators

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and one that's come up over and over again is this issue with Popsley in thyroid. Well,

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these awesome scientists at My Florida DNA, a biotech genomics lab in California, Dr.

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Angel Fernandez and Dr. Ajit Anand want to share some of their latest research and they're

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open to field some of the questions we may have because we all come at this group from

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our different perspectives. And so now this is an awesome opportunity for us to actually

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ask and hear from some of the leading scientists in the field to find out what is this issue

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with Popsley in thyroid all about. So let everybody have a chance to chime in and ask

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questions here in a second. But without further ado, Dr. Fernandez or Dr. Anand, would you

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want to take it away and let us know about some of your research?

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Yes. Can you hear us please? Yes? Okay. So thank you very much for having us. As you

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said, we are a molecular biology lab, a genomics lab located in Sacramento in California, just

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in the middle of the most affected region in the world for whole Latin Birolite. Our

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main goal is to offer diagnostic services to farmers and growers. We develop a technology

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that allows us to analyze several thousand samples on a daily basis with an accuracy

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of around 97, 98 percent. We are working actually, we can analyze those plants in a few hours.

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So that is very convenient because the clients, they can get the results basically in two

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days. The process takes longer actually when they see the plants to our lab rather than

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the analysis itself. So for the past year, we have already analyzed around 275,000 samples

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and we are continuously improving our protocol in order to lower the price. We know that

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this is a very big issue in the industry. We know the economical difficulties that our

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clients are suffering. So all the improvements that we are making is basically to lower the

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price so that eventually will be translated in a larger volume of samples that they can

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analyze. So whole Latin Birolite is a Birolite that actually is the equivalent to what happened

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a few years ago with COVID in humans. What we recommend to the clients is to test in

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a regular basis. The plant today might be healthy but tomorrow might be infected without

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showing any visual symptoms. However, the Birolite might be present in their facilities

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and it's very easy to spread to the other plants. So that's why our recommendation

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is to keep testing at least two or three times for the whole cycle of the plant.

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This is phenomenal that you're undertaking this research and testing to help people out.

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I've got a myriad of questions but before I start bombarding questions on you and start

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fielding questions from the audience, Dr. Anand, would you want to maybe tell us a bit

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about your role and maybe what are some of the challenges with testing? You said you're

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doing north of 270,000 lab tests. So that is a well of data right there. So that's a

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thought that comes to mind. So I'll be formalizing my thoughts. But you're welcome to chime in,

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Dr. Anand. And then maybe we can open it up to some questions.

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Sure. Thank you. Thank you all. Good morning, everyone. It's a pleasure to see so many different

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people. I've never met many of you but I know you all are one of the best people who are

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working on cannabis. I entered into the cannabis industry just a couple of years back so I'm

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still learning a lot. For me, when I moved to give you background, I'm a molecular biologist.

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I was one of the leading technologies for the seed companies before I moved into cannabis.

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I was working for the largest seed company, the US. My background is in functional genomics,

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biotechnology, you name it, a lot of things that I've done with microbial engineering

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and so forth and so on. What fascinated me about cannabis and you might ask me this question,

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hey, what are you doing in this crop? Is that the fact that cannabis is growing, it's getting

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a lot of traction and it's one of the 56 largest crop now in the US from the value perspective.

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So there is a lot more to be done. There's a lot of information that's been exchanged

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between the community but we also need a rigorous data-driven science-based approach to resolve

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some of the significant problems that we see. One of the challenges we discuss broadly and

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quite often is the HLVD. To just give you about HLVD, HLVD is half-latent virite. Obviously,

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it's a half virite. To tell you about virite, virite is like naked RNA molecule, one of

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the smallest infectious molecule that primarily only infects plant. That's a good thing about

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it. Many aspects of the half-latent virite, I personally have learned in the last six

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to seven months. We are still trying to figure out, we are learning each and every step through

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the efforts that are put by other organizations like us from the academia. Basically, what

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we are doing is using those learning opportunities to actually support the community with solutions

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that actually create value for the crops. Obviously, everybody talks about economical

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losses and economical losses are not just for cannabis. We have serious issues with

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drought in the Midwest today with all the row crops that you can talk about. There are

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going to be both biotic and abiotic stresses. The biotic are the pathogens and other things

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and abiotic are other stresses which I think we will also have eventually getting into

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cannabis. What I feel is we are just on the tip of the iceberg about when it comes to

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a crop like cannabis. I personally want to use my know-how building those capacities

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in large organizations, bring those intellectual knowledge, bring those experiences to cannabis

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and drive to broaden the knowledge on cannabis and also drive services and solutions that

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actually are attractive and effective to the growers, the breeders and as well as the nurseries

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and cultivators. That is what I am here for. I will talk about the little work we have

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done on HLVD. I wanted to give you about a little background on HLVD. HLVD is very serious

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problem and when you talk about serious problem, I will just put some value. This is all in

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the literature or it has been documented. One of the things is we believe that it is

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90 to 95% of all the cannabis that we grow in California which is the hardwood we are

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sitting is either infected or had been infected in the past. The cost associated with this

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worldwide and it is not a problem in the US a lot. It is a worldwide problem. When it

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comes to the number of strains, in an example that Angel gave about COVID, we have so many

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strains and today a new strain is getting a booster bill for that. The lucky thing about

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this worldwide is the quasi-species of the different types of strains that are infected

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are limited to two and they are very, very small changes. As I said, this is small RNA.

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It is just like around 256 nucleotides. It is much smaller to what our whole genome is

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or even a plant genome. Just for a comparison, I would say like the virus, if I were to say

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it is a dot, then the viruses are a little point. It is almost 100 times larger than

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a virus. If you look at a spore like a fungal spore, it is around 100x larger than a virus.

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You can see with the naked eye or use a microscope to see a spore, a fungal spore, whether it

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is aspergillus or it is fusarium, but you need very sophisticated electron microscopy

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instruments to see a virus. That is about the virus. The effective loss, the economic

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loss that is caused by the virus is estimated to be 4 billion globally. We are talking about

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a crop which is 5 to 6 billion in the US and we are talking about 4 billion globally analyzed

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large that can happen from a virus like HLVD. You feel like, isn't it silly that this little

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species that cannot even survive by its own is able to now get into a plant, piggyback

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on the plant, use the host machinery and replicate and present the phenotype as a disease. The

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disease often people know in the community is dudding or duds. The dudding and duds disease

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can be easily seen with the stunted growth, the flower quality, the brittleness of the

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plant. Sometimes there is yellowing or darkening of the leaf, but the most common phenotype

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which is very visually noticed is if the disease is expressed, the phenotype is seen, the plant

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will be stunted and duded. We all know that if the plant is stunted and duded or much

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smaller, your yield from that crop is going to be significantly reduced. Another interesting

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aspect about this HLVD is now it doesn't necessarily express every time. We know in plants that

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is genotype dependency and the resistance or tolerance to diseases. Many times the disease

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is not even expressed. You will think about the plant as being growing normal and we have

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a practice of using mother plants and making cuttings and rooting. Unknowingly, without

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knowing that the mother plant is infected, you're making cuttings and then you're basically

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disseminating. Then could there be an environmental effect or could there be another issue with

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another pathogen that the plant starts expressing itself and now you realize, oh my God, I've

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already lost a lot of my plants because now all these plants are infected. This is one

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of the most effective ways of disseminating the disease. Unawareness, unknowingly cutting

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and then putting it to footprint. I want all you folks to understand that that's something

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that we have to proactively think about, especially in cultivation or necessary practice where

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you're using other plants. I would recommend, my best recommendation or medication would

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be is be proactive in testing all the mother plants, making sure that you have done it

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through different growth stages, that you're not missing the opportunity to cut something

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that could have been done much earlier in the beginning. Latency is a good thing I talked

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about where you can't know the disease. The other interesting is the effect on the economical

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value comes from the flowers that you produce. There is very clear documentation that plants

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which are infected may have up to 50% reduction or greater than that in their cannabinoid

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composition. The flowers are actually a little more brittle. They're not compact. If you

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run through a seed, you can see the flow down. I give you a broad perspective and again I

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want to open up with what my thoughts were here so that we can have some good interactive

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session here.

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Phenomenal Dr. Anand. I love it. I love your work. I kind of want to maybe break this down

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into three segments and then we can ask questions about those. Basically, I see this as where

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did the hopslate in viroid originate? How did it take root? Quite literally. That's

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such a problem in the cannabis industry. Then two, I guess focus on what does this actually

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look like? You've already kind of spoken a bit about that. What are the effects of hopslate

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in viroid? How can you potentially spot it, identify it? Then the final thing is the solutions

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which I think is what your company is really working on is the testing. I kind of wanted

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to pick your brain on this and then maybe if anybody else has any questions about the

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origins of hopslate in viroid in the cannabis space. I just was doing a brief poke at the

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research. I'm just going to put them in the chat here so people can look at them just

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for official sources. From what I was reading, and so let me know if this is wrong, it was

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looking like hopslate in viroid was first detected in cannabis maybe around 2017 or

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early 2018. I was basically looking for ground zero. The earliest mention I could find was

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just a case that appeared to be in Oakland in perhaps an indoor grow. Then they mentioned

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another case in 2018 in Santa Barbara. What comes to my mind is what are your best ideas

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or thoughts on how did hopslate in viroid take root in the cannabis industry? What maybe

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made some of the first growers susceptible? Did the fact that cannabis is kind of an illegal

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gray area, did that have any influence? Maybe people weren't following the best procedures

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or maybe it's got something to do with the strains or the cloning. I don't know. What

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are your thoughts? Why did this, maybe the cannabis industry was just right for this,

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but why this particular virus and why do you think it took off like it did? That's my guess.

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My origin question.

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Well, thanks for asking that question. That's a million dollar question. I would say that

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we still are able to, we don't know we have an answer for it. I would just give you the

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pre-historical thing. The pre-historical thing that I want people to remember is it is a

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hop Latin viroid. It was first identified in the 1985-87 time, something around that,

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in hops in Spain. So Northern Spain is where it was first. Now, how did it move? How did

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it reach?

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Let me add, in Spain about 30 years ago, so it's been around for more than 30 years, actually

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almost 40 years. So it was first identified and published in 1987.

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So it would have been there even before that. I'm saying that the fun thing is we have to

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go back and rethink about who, it has been here for almost 40 years, even 50 years. Detections

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were, I mean, again, this is a biological system, which is not like you can do any,

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like indexing or something that pathologists do because the viroid cannot live and needs

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to have a host. So it's probably there for a long time. The other beautiful thing about

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it is it's got a very narrow host. Narrow host where probably it expresses as a phenotype.

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It doesn't mean that we know that we today understand is it only those three hosts or

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is it actually present in other plant species but does not have a disease, right? It doesn't

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express the disease.

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So the hosts are like a couple of different hop varieties. Then there is this stinking

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needle and now we have cannabis, obviously. Now, how did it move from Spain to California

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or it was already present in Europe? People went unnoticed and it was just that we happened

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to start noticing a plant phenotype in the maybe the late 2017s. I know the first report

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was something around 2018, 2019, where two groups simultaneously came and reported it.

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But it must have been here. Somebody really paid attention and then tried to identify

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what's that hop, right? Hemp and hop are closely related if you look at that too. Now, one

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of the most likely, again, I'm not an epidemiologist, I'm not a plant pathologist, so don't take

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my word with like, it's a grain of salt, let's say. It's likely it got cross-infected. And

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somehow the population moved here. And that's why we say US has a very strong quarantine

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when you bring seeds or plants, anything from foreign countries. This is exactly a great

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example of something that probably got in a ship, got an airplane and reached here.

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Now that is my understanding, but I again want to make sure that people understand I'm

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giving a hypothesis. I don't have any supporting data or something to prove that's the only

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possible way it reached. It could have also come with seed because now we have heard about

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even seed can transmit it and that's more of a latest knowledge. So I would open it

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up for people to figure out what exactly happened, but we know that we started seeing this disease

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in the cultivation parts of California, in the Santa Barbara area, and eventually now

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all of California probably has it in the early 20, 70s and 80s, I mean, 2018 to be more precise.

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May I cut in for a sec? This is John Abrams. So I became familiar with this in 2016 with

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my work in Humboldt. The name associated with this was Rick Crumb. There was a report, in

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fact, I think we presented in 2017 at MJ Biz on what this viroid was. We didn't know it

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was a viroid at that time. We were calling it PCIA, putative cannabis infectious agent,

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and then we were going to try and identify what it was molecularly. We left that to others

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and the story is as you said. The index strain, as we remember in Humboldt in about this time,

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was GG4 or Gorilla Glue. And so it was intriguing and of course Humboldt cultivation being what

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it is, this is kind of how it spread. So anyways, I would call your attention to presentations

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at the MJ Biz Science Symposium and I think it's 2017, but it reflects the story starting

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in 2016.

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Thank you, John. That's a good thing that you brought to me again. As in the beginning,

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I said, I'm learning a lot of things about this viroid.

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May I ask another more broad question regarding your discussion of its etiology coming out

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of Northern Spain? And I guess that's a cannabis, not a hemp derivative, but a cannabis derivative

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report. My thinking is that this has been circulating a lot longer. There were reports

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of hemp diebacks in the literature. What I particularly remember is at the time of the

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Soviet invasion of Hungary in 1956, there was a report strangely of hemp was a major

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cultivar in Hungary during that time and it took a beating. Same thing in Serbia, if I

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remember correctly. So my major question is if this has been circulating for a lot longer,

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I'm wondering if the current hemp strains, there were a number of classic hemp cultivars,

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they have some endogenous resistance that is worth understanding or looking at.

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Okay, John, I completely agree with you. When you mentioned about the inherent genotype

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specific resistance or genotype specific exclusion, not expressing the phenotype, that's not only

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unique for this. I think the whole world understands how wild germ plasms and germ plasms have

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helped to identify and breed for those resistance in other crops. So it may be a great opportunity

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for us to go and see if we can actually systematically do this study and identify the cultivars.

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I would more or less say, I don't like to say resistance or tolerance more or less.

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Identify those in genetics or germ plasms, which are actually much more tolerant to this

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HLVD and then incorporate that into our breeding programs. We can then mechanistically identify

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if there is a specific gene or specific QTL or a specific mechanism, which could be an

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RNA silencing mechanism that allows that particular plant to overcome the disease or doesn't

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allow the viral to amplify or increase the titer that results in a disease.

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Sorry, John. So what is clear is that more research is needed and also even to find out

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the origin. What we are saying is that what has been documented is that in Spain in 1987

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was identified in hop. But I'm pretty sure I agree with you. Probably 30, 40 years, even

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before that was already in Russia, in Serbia, in East European countries and even in Asia.

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So for that, I mean, there are today we have molecular tools that we can use to identify

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the real origin and even to retrieve to know the exact date or year or, you know, a presumptive

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year of the spread and origin of this. But the problem that we are facing in cannabis,

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all of us, is that we are less than 20 organizations worldwide, including public and private organizations

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doing research. This is a very novel topic. And when we compare the research done cannabis

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versus the rest of the crops, tomatoes, soybeans, almonds, whatever, for similar pathogens or

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any other trade, obviously they are 50 years ahead of us in research. So what he was mentioning

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about the germoplasm, wild species, wild ecotypes, that is extremely important to analyze those

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genetics and trying to breathe them or incorporate the genes into the domesticated or the standard

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cannabis that we are using today.

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I just wanted to add to the comment is that the fact that we haven't got as much excitement

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for cannabis across the public institutions, so because of the current regulatory regimes,

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it hasn't really attracted our universities to do as simple fundamental basic research

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that happens with most of the other crops. And lack of that has also limited our expansion

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in the industry as well, because now industries are working with limited amount of funds.

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And obviously we have to do things that we can educate the community also, but at the

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same time provide a way of generating revenue for the organization to survive. So we can

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use many of the other crop models, as I was saying, the amount of work that I was doing

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in the raw crops to sort of streamline the science-based research on cannabis, but we

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have to take a village to do it together. It may not be a single institution that can

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be able to achieve those things. But understanding how this wire art originated, how it spread,

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I think again, going back to those wild germ plasma, if they are still maintained, somebody

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has seed, we may be able to really go back and figure it out because of the modern genomic

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tools. And this is a small wire art like 256 nucleotides. We can do a million of those

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seeds being sequenced for this just in a day. That's the power we have to do, the tools

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we have to do.

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I may just chime in with the thought because that snippet of information that John said,

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that this may have been prevalent in gorilla glue. That may kind of tie a lot together

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and piggyback on some of your work over at MyFloridna. Because what I'm thinking now,

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especially since you're saying that this virus may have been around for 40 plus years, is

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there was sort of a fun article that came out recently that was saying that they're

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finding these ancient viruses that are getting thawed out in the permafrost. And so what

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comes to my mind is probably these viruses in hemp have kind of been co-evolving just

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for probably a long time.

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Let me finish this and then I'll let you chime in Dr. Anand. And then so for whatever

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reason, probably because cannabis has been pretty underground in the United States, my

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guess is cultivators have had to rely a lot on clones. And then we've discussed in the

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past somebody discovered this one variety, gorilla glue, and for a number of reasons

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it's just become insanely popular. We were seeing that it's by and for the top selling

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strain in Washington state. And then that's not even including all the different varieties

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it's been mixed with. So it could just be that this one variety was selected. Unfortunately,

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that one variety was super susceptible to the virus and then it's just been cloned and

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spread. And then this kind of piggybacks on the question in the comments is, you know,

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are clones really being tested? So those are more thoughts rather than questions.

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But I think maybe you had something to chime in with Dr. Anand.

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I wanted to go back to what you said. You know, it may have been, but the answer is

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it is been there over 40 years because we know the earliest documentation is 1987. So

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we had just shot a 14 years today. And when a disease is discovered, it's only when somebody

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really noticed and this emphasis wants to know exactly is going. So which tells you

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it could have been there even earlier than that. It's only the diagnostics and our capability

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of being able to identify this came with the sophistication of instruments that we had

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by then. So again, think about looking for a 256 nucleotide virus. I'm thinking about

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my 1987, I'm still in school probably. I was doing much more laborious way of detecting

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a DNA when I came to school in the 1990s. But our detection capabilities may not have

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been that. So again, we might have used classical processes for identifying these diseases at

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that point, you know, by cross-infecting and there are ways that people do that.

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So the second comment of whether the virus has been sort of emerging. The point I mentioned

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is even though the virus has been collected 50 or 60 different strains have been identified.

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The thing is they all seem to have are very stable. We're not seeing very quasi species

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of RNA, which is third in other virus that also has infecting plants and PSL, it is one

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of the more PSS TV is one of the most extensively studied. That's a good news. The good news

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is most of the virus that are infecting are still belonging to the two class that I said

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can one and can two. And they're infected. And whether they're infected, they're present

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in the US and they also present globally. And the third question or comment that was

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about clones, I think that is imperative. That is what I think is an important thing.

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Testing where you get the clones, who provides the clone, I think is the best step. So I

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would say that, you know, to be able to do that early enough is the best mode of preventing

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the disease proactively testing clones before they are grown and multiple stages. Like even

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when you get a clone, don't just wait for the first few leaves and test it because our

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study tells it pretty clearly that if you wait a little longer, you do it every weekly

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or bi weekly. Even if the virus is at low titles, they're going to increase over a period

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of a couple of weeks and which would have been not detected. Now would have identified

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as an infected plant. So having something would I call it. Yeah. I have something called

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an SOP of pest management practices, a cultivation management practice will help us avoid the

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virus load. And again, Angel, please go ahead. Yes. Because I read a question in the chat

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asking if the, all the clones sold in California are being tested for first for HLV. Well,

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so this is one of our recommendation that even a grower buys for tissue culture labs,

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the clones and even if those tissue culture they have tested, they had done the test,

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the testing for HLV at that earliest stage, they might be negative. Then two, two, three

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weeks later, the vital load can increase, right? And become positive the plant. So our

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recommendation to the growers is just randomly select a few plants to make sure that everything

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is clean and the infectational level is 0%. I mean, based on statistics and based on the

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numbers of plants that they will get from the, from the tissue culture or their nurseries.

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And to make an analogy of that is again, I go back to the COVID era where we all have

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tested on weekly, monthly basis to make sure that the population, the amount of infection

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that we have in the population is reduced. So I think this is exactly Angel, what is

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it is that you have to have a routine testing plan and we are here to help it. We have solutions

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that we want to provide on site so that you are capable of making all those decisions

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and necessarily as supporting you. So this is similar to a problem in straight

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out mammalian cell biotechnology that has been solved, I would say years ago, when you're

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propagating transfected or recombinant mammalian cells for blockbuster biologic drugs worldwide,

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you have to make sure that your endogenous retroviruses and all that are not brought

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forward into your culture systems. So it is very standard to create master cell banks

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and working cell banks that go through elaborate characterization to make sure it's clean and

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free of infectious agents and virus. This is standard practice in the biotechnology

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industry and there are organizations that are very good at running these tests. My view

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is we have to do the same thing in cannabis if we want to go forward with this. And it

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comes to the major question of creating master cell banks of, I've always been a fan of protoplasts

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to do this. The technology is not there yet, but you would have a well characterized protoplast

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master cell bank and then you would come out of that and use best practices to keep this

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down. The paradigm is in biotech, in mammalian scale up cell culture biotech. I think we

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have to do the same thing here. John, I totally agree with your comment and

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thanks for putting it. I think this is what we normally say seed banks when it comes to

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plant germplasm and we have seed banks like the UC Davis has seed banks for hemp. There

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is a seed bank for hemp in I think University of Washington. Yeah, in Cornell I met also

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another gentleman in one of the conferences that they have also started going and collecting

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seeds from different places. Yeah, you're right John.

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But I think it has to be beyond seeds. I think you actually have to go to tissue culture

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based cell banking in this case because I think it's difficult. How do you screen seeds

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effectively? It's a destructive analysis. Once you've taken a seed and tried to analyze

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it for viroid presence, it's not a seed anymore. True.

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What I'm saying is getting the quality seeds and then maintaining it. You can germinate

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seeds and then test it and then as well as get more seeds. Obviously, you're not talking

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about 50 seeds being saved. That's one viable. Now the reason I think that's a viable process

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because it's been already known and documented for other crops. Protoplast on the other hand

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is very difficult in crops. Regenerating plants from protoplast is not easy.

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Yeah, no, I agree. But I think that if I were to push where the tech needs to go, I think

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that needs better development. Yeah. And the other thing about protoplast is

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also when you do long-term cultures with protoplast, you also can introduce variation. So there

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is another way of looking at this is taking these shoots or the nodal tips.

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And that is to make synthetic seeds or doing cryopreservation, which has again been done

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with the plant germ blossoms. So there are multitudes of approach. I mean, I just wanted

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to know. But again, as I told you, there needs to be an institutional commitment to do these

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things to support. I mean, a private institution cannot do it.

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And it comes to my mind and I wouldn't be doing justice if I didn't ask it. So I've

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studied economics. And so what always comes to my mind is cost. And so that's kind of

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what keeps coming back to mind is you say, oh, test every clone and test them frequently.

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And so that seems like that may be a high cost. And then what John's describing with

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the tissue culture, if I'm getting that right. So that sounds even more costly. And I think

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that may be a problem, right, is a lot of the growers are as far as agriculture goes,

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they're small scale farmers, right? These are as far as right there is some really large

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agriculture plots out there. So these are kind of small, small scale agriculture. And

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so maybe people are just, they're maybe hoping their plants don't have the virus, because

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right, it appears that you find out pretty late, the effects if you don't test for it.

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So maybe everything looks like it's going along well. And then their flowers, like you

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said, they get dusted. And then, you know, they're maybe just trying to salvage it at

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that point. So I guess my question is, you know, if somebody's trying to be super cost

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effective, you know, is it worth waiting a little while into the vegetative stage to

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test because maybe the virus is spread a bit more? Or are you running a risk of spreading

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it to your other plants at that point? Like, what are your thoughts for somebody who, I

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mean, just imagine this really small scale cultivator who's really trying to be budget

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conscious? No, would you still recommend they test and then you know, at what stage I think?

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And then every and then another idea is every clone? Or could you potentially, you know,

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get away with doing like a random sample of clones? If that's a worthwhile question.

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There are several options and obviously depending on the size of the cultivator, the budget,

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one strategy that they can do is they can pull one leaf from several plants all together

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in one chip. And then we do the analysis for that pool. That is a way to save money. The

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only problem is that if one plant or the pool becomes positive, you will have to go back

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and analyze individually which plant is the positive one. I mean, in an ideal scenario,

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obviously is to test every single plant, but the reality is that no one, even large corporations,

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they can do that, right? So frequency is very important. I think my personal recommendation

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as a scientist is even for those growers with very limited budget is to test less plants,

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but more frequently rather than waiting 10, 12 weeks and at the end decide to analyze

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20 plants or 50 plants because the infectation level might be high, the spread, the disease

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can be already spread. So it's better to analyze less plants, but at an earlier stage. And

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the pooling strategy is neither a bad idea. What do you think, Ajit?

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I mean, I agree with you, like, you know, it is not possible for a small scale grower

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to do every plant. So in our study, at least we are showing that we can do it as early

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as like five, six weeks. This is five, six weeks after cutting from another plant, which

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basically if you take three weeks for rooting and you're talking about one or two weeks

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before the leaves are emerging that you're actually testing it and you can test that.

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So whatever best fits for a small grower is what I think our recommendation is, whether

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it's pooling, three dimensional pooling, making rows and columns and randomly random block

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design is what the other way, but do frequently check because the, this culprit is going to

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be latter. This guy will not, I don't want to be gender biased, but this is not going

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to express. And sometimes we are cheated by the virus. And it's so be proactive in preventing

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it out of your control. And the only way to do is to know if you by chance have a plant

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that you've infected. Because then all other things that the way it's spreading in the

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facility is all through your mechanical cutting, your tools, the SAP, you know, it seems like

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what I've heard from one of the strongest pathologists is well known, even rubbing this

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wire art on the leaf doesn't allow it to infect. So it's mostly coming from the SAP, wherever

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you're going or it's spreading through water because roots are growing. So again, Angela's

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correct. You know, be proactive and find out what best fits your budget and is your best

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solution.

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Can I ask, given that you've done very large scale testing, does your database include

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any information about the plant samples coming in as like strain names or anything like that

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beyond that? The reason I'm asking this question is I'm wondering if you were to look globally

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at your large data sets now, are there potential hints in the data for strain names that are

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underrepresented and can be somewhat defined therefore as having some degree of resistance?

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I realize there's all sorts of confounding issues in bringing that forward. But as a

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matter of fact, do you record from your sample submitters the name of the strain?

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So let me take this one, Ajit. So we don't have a database for HLV. What we developed

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last year is myflora cloud. Okay. And this is a platform where the clients, they get

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access to all the data, their data, all the statistics and so on. Obviously we cannot

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to share that information publicly because that belongs to the clients and we don't even

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know the name of the strain. Some clients, they want for their own record and for their

400
00:48:00,440 --> 00:48:09,520
own statistics, they want to add the name of the cultivars so like that they can check

401
00:48:09,520 --> 00:48:17,600
or they can retrieve the information month by month based on cultivar or year by year

402
00:48:17,600 --> 00:48:21,880
or whatever information they want to add. But there are many other clients that they

403
00:48:21,880 --> 00:48:29,360
just number the plants. So if they send us 500 plants, they number one to 500 and we

404
00:48:29,360 --> 00:48:37,480
don't know that information. But again, this is not a, this is a platform like AT&T or

405
00:48:37,480 --> 00:48:46,040
T-Mobile that you as a user, you get in and then you can check the bill from last month,

406
00:48:46,040 --> 00:48:55,360
how much energy you have spent. But it's not available for the public in general.

407
00:48:55,360 --> 00:49:04,560
What about the concept of incentivizing your submitters to provide more information to

408
00:49:04,560 --> 00:49:13,520
help understand whether there are more resistant strains? We believe there are. We also believe

409
00:49:13,520 --> 00:49:20,400
that there may be epigenetic stress factors that drive towards this and we may be in a

410
00:49:20,400 --> 00:49:29,760
position to determine at a cultivation level if you're running stress cultivation or whatever.

411
00:49:29,760 --> 00:49:36,200
Interestingly anecdotally, we were on a call last week with some Mendo-Sino area growers

412
00:49:36,200 --> 00:49:43,160
and there's the topic came up that is this prevalent in higher mercine strains which

413
00:49:43,160 --> 00:49:50,480
would fit with our models of mercine gross and moto being a stress factor indicator in

414
00:49:50,480 --> 00:49:57,160
cannabis. So I would encourage you, maybe there's you dropped your rates or something

415
00:49:57,160 --> 00:50:03,480
like that if the submitter provides more information and you start to build your data set that

416
00:50:03,480 --> 00:50:09,360
way. So what I would do instead is probably to

417
00:50:09,360 --> 00:50:19,000
create like a consortium including association of growers from different locations, different

418
00:50:19,000 --> 00:50:28,520
states where everybody submit samples and my Florida DNA will take the responsibility

419
00:50:28,520 --> 00:50:36,840
of doing the genetic analysis for free and then what we can do is to write a scientific

420
00:50:36,840 --> 00:50:48,160
article, a scientific manuscript and make it available for the community as a whole.

421
00:50:48,160 --> 00:51:01,080
But we wouldn't be able to use our clients' data and make them public or make a scientific

422
00:51:01,080 --> 00:51:09,480
analysis. So basically we are super happy to do this kind of analysis but good from

423
00:51:09,480 --> 00:51:19,200
scratch where we sit down, we set the foundation of the analysis, what information we want

424
00:51:19,200 --> 00:51:25,200
to get from there, what information the community really needs and my Florida DNA would take

425
00:51:25,200 --> 00:51:33,400
the leadership and would do the genetic analysis again for that consortium free of charge and

426
00:51:33,400 --> 00:51:47,040
then with the condition of making the data public. We are a group of scientists, we are

427
00:51:47,040 --> 00:51:54,000
coming from academic institutions. This is the first time that we decided, we have decided

428
00:51:54,000 --> 00:52:07,800
to put all of our knowledge in a private company so our mind is very academic oriented and

429
00:52:07,800 --> 00:52:13,880
that's why we published this recent publication which is the largest analysis done so far

430
00:52:13,880 --> 00:52:22,720
for HLE because we want to show to the public the technologies and get data from there.

431
00:52:22,720 --> 00:52:31,040
We should then talk further because with the connections that we are developing in Mendocino

432
00:52:31,040 --> 00:52:37,720
Cannabis Alliance as one and the Humboldt County Growers Association which represents

433
00:52:37,720 --> 00:52:46,400
a lot of farms, those would be two key stakeholders if you will and they are certainly all aware

434
00:52:46,400 --> 00:52:51,360
of this so we should talk further about how to move this along.

435
00:52:51,360 --> 00:52:54,400
We are happy to do that.

436
00:52:54,400 --> 00:53:02,400
I thought it was a good idea because the data science meet up after all and so it was kind

437
00:53:02,400 --> 00:53:10,480
of in line with a thought I had that maybe you may ask people if they want to opt in,

438
00:53:10,480 --> 00:53:15,160
that's kind of in line with John's comment in that you've got this sort of gold mine

439
00:53:15,160 --> 00:53:22,600
here and if you just sort of ask people for various data points, sort of who knows what

440
00:53:22,600 --> 00:53:26,200
you may find, right?

441
00:53:26,200 --> 00:53:31,920
How many weeks of vegetation was this plant in, what strain, if they're willing to share

442
00:53:31,920 --> 00:53:35,160
their location, so on and so forth.

443
00:53:35,160 --> 00:53:41,120
A couple of people I think had wanted to ask questions and I apologize to them for not

444
00:53:41,120 --> 00:53:49,680
getting around to it but Candice, Larissa, Blue or anybody, you're welcome to chime in

445
00:53:49,680 --> 00:53:53,320
down with any questions you may have.

446
00:53:53,320 --> 00:54:01,280
So my apologies I didn't get to everybody's questions but I was thinking that the conversation

447
00:54:01,280 --> 00:54:08,240
was going well since we finally got to sort of the data side.

448
00:54:08,240 --> 00:54:11,160
We are happy to come back another time.

449
00:54:11,160 --> 00:54:19,040
I know this is a very hot topic and it takes time so we will be happy to come back next

450
00:54:19,040 --> 00:54:24,480
week or in a few weeks and resume the conversation if we don't have enough time today.

451
00:54:24,480 --> 00:54:25,480
It's okay.

452
00:54:25,480 --> 00:54:30,520
Well I'll reach out to everyone who attended and see if they do have any questions that

453
00:54:30,520 --> 00:54:34,120
they may want to ask you in a future week.

454
00:54:34,120 --> 00:54:39,320
Real quick, welcome to the group Trevor, we're just sort of wrapping up our talks on Hopsley

455
00:54:39,320 --> 00:54:40,800
and Viroid.

456
00:54:40,800 --> 00:54:45,040
If you have any questions, now is the perfect time.

457
00:54:45,040 --> 00:54:55,360
No questions, I just kind of wanted to pop in and just kind of get a feel for the space

458
00:54:55,360 --> 00:54:58,880
and say this is my first time in the space.

459
00:54:58,880 --> 00:55:06,280
Yeah, I think I came a little late, I had a work meeting.

460
00:55:06,280 --> 00:55:12,840
We can kind of move to the third part which is basically okay we've discussed the origins

461
00:55:12,840 --> 00:55:18,600
of Hopsley and Viroid, now we've discussed what it looks like in the industry and now

462
00:55:18,600 --> 00:55:21,400
we've been brainstorming solutions.

463
00:55:21,400 --> 00:55:27,720
So I guess I'll let Dr. Fernandez and Dr. Enand, I'll let you two have the sort of the final

464
00:55:27,720 --> 00:55:35,840
words here, but you know what do you see as a future for cannabis cultivators and you

465
00:55:35,840 --> 00:55:43,360
know how can they you know overcome this obstacle to keep delivering top-notch cannabis flowery

466
00:55:43,360 --> 00:55:44,360
to people.

467
00:55:44,360 --> 00:55:48,800
So what are your thoughts?

468
00:55:48,800 --> 00:55:50,920
Let me jump in Angel if you don't mind.

469
00:55:50,920 --> 00:55:58,600
I think as we were saying our first and foremost recommendation know the plant you have and

470
00:55:58,600 --> 00:56:05,000
when I say that know what the material is and there is where again some of our technologies

471
00:56:05,000 --> 00:56:09,440
will come which means you know we have DNA fingerprinting which can be another conversation

472
00:56:09,440 --> 00:56:10,440
that we can use.

473
00:56:10,440 --> 00:56:15,560
What is the genetics that you have in your grow area, whether the plant is infected or

474
00:56:15,560 --> 00:56:24,200
non-infected, what is the source of the material, that information is very important to both

475
00:56:24,200 --> 00:56:28,960
the grower and as a scientific community for us so that we can look at the progression

476
00:56:28,960 --> 00:56:31,120
of that.

477
00:56:31,120 --> 00:56:37,160
We like this idea of a consortium where the consortium of growers, cultivators and the

478
00:56:37,160 --> 00:56:48,320
nursery can come together and use our sophisticated tools which allow us to be able to understand

479
00:56:48,320 --> 00:56:56,160
what's the issue, what the constraints are and can we recommend some germplasm of genetics

480
00:56:56,160 --> 00:56:57,160
that is superior.

481
00:56:57,160 --> 00:57:03,640
That's a learning that is going to mutually help each other.

482
00:57:03,640 --> 00:57:10,440
I recommend also to work with us on some of the tools that we have developed which is

483
00:57:10,440 --> 00:57:16,640
very high throughput, very reliable, very sensitive and as well as affordable.

484
00:57:16,640 --> 00:57:22,240
You can do that either by sending it to us or we can provide you also possibly on-site

485
00:57:22,240 --> 00:57:31,680
solutions but diagnosis is the best way to prevent the disease so do that proactively.

486
00:57:31,680 --> 00:57:37,960
Now the whole suite of things that opens up with this is when we have more system-extremely

487
00:57:37,960 --> 00:57:42,320
study that goes on with cannabis, we could unravel many things including what John was

488
00:57:42,320 --> 00:57:47,320
saying, maybe there are genotypes which are varieties which are resistance and then looking

489
00:57:47,320 --> 00:57:49,800
for using that for resistance breeding.

490
00:57:49,800 --> 00:57:54,840
That makes me more of understanding how this virus presents itself.

491
00:57:54,840 --> 00:58:01,200
So what our team can do is only do the diagnostic but we need the phenotypic data as well from

492
00:58:01,200 --> 00:58:03,400
the other end.

493
00:58:03,400 --> 00:58:09,000
We have done experiments, we have done huge scale testing with people or growers where

494
00:58:09,000 --> 00:58:15,720
they have had 30-40% of infection down to like 3-5% infection today which basically

495
00:58:15,720 --> 00:58:21,160
says that and historically that tells you that if you have a good practice of managing

496
00:58:21,160 --> 00:58:27,160
this disease you will figure out how to control the disease in your growing.

497
00:58:27,160 --> 00:58:32,720
And there is a lot more scope to understand if there is a host mechanism, is a gene to

498
00:58:32,720 --> 00:58:38,200
gene interaction, is this is the resistant pathway but this will take a lot more dedicated

499
00:58:38,200 --> 00:58:43,480
work and we need public institutions to jump into it.

500
00:58:43,480 --> 00:58:48,520
We as a private organization do not have a grow facility.

501
00:58:48,520 --> 00:58:52,960
All that we can do is, yeah we can support some tissue culture work, we can get rid of

502
00:58:52,960 --> 00:58:57,440
some of the virus, but that's a limitation of what we can do.

503
00:58:57,440 --> 00:59:02,600
Indra, please jump in if you have any other thoughts.

504
00:59:02,600 --> 00:59:20,920
Yes, my main recommendation is obviously encourage growers to test before getting a surprise.

505
00:59:20,920 --> 00:59:32,200
There are, we start seeing many reports stating that the quality of cannabidiol, its concentration

506
00:59:32,200 --> 00:59:40,600
and so on is significantly decreasing.

507
00:59:40,600 --> 00:59:48,880
It's true that we have had many clients that started with levels even above 50% and right

508
00:59:48,880 --> 00:59:59,480
now are around 5%, 6% of the overall infectational level of the facilities and that is thanks

509
00:59:59,480 --> 01:00:01,680
to the testing.

510
01:00:01,680 --> 01:00:03,760
There is not a secret for that.

511
01:00:03,760 --> 01:00:10,120
We understand that the small growers they might have a very limited budget but there

512
01:00:10,120 --> 01:00:18,380
are always solutions by for example by pulling plants, 5, 7 plants in one tube.

513
01:00:18,380 --> 01:00:25,600
That is, you can get information for a very small amount of dollars.

514
01:00:25,600 --> 01:00:34,280
We will be glad to create a consortium and help the industry moving forward with this

515
01:00:34,280 --> 01:00:40,320
problem that is affecting actually the whole community.

516
01:00:40,320 --> 01:00:41,600
Well thank you for your work.

517
01:00:41,600 --> 01:00:47,680
I would just like to end with this in that we always come across these big problems,

518
01:00:47,680 --> 01:00:54,520
these big issues but there is always a little ray of light and the one here is the virus

519
01:00:54,520 --> 01:01:01,520
itself for now it looks like it's remaining pretty constant so that's good.

520
01:01:01,520 --> 01:01:08,560
I have a lot of faith in all of the brilliant innovators and entrepreneurs out there and

521
01:01:08,560 --> 01:01:17,960
that's what's kind of so cool about this is that one person's problem is an opportunity

522
01:01:17,960 --> 01:01:20,280
for an entrepreneur.

523
01:01:20,280 --> 01:01:27,240
So for example my Florida DNA, so we've got cultivators with 50% detection rates and if

524
01:01:27,240 --> 01:01:35,400
you can lower your 50% detection rate to 5% all of a sudden that unmanageable problem

525
01:01:35,400 --> 01:01:41,360
can now be managed and as I was saying in the hemp fields you may never fully eradicate

526
01:01:41,360 --> 01:01:42,360
it right.

527
01:01:42,360 --> 01:01:50,520
There was curly top virus and there was just a small percentage of plants that get affected

528
01:01:50,520 --> 01:01:54,160
by it but overall the hemp field can power through.

529
01:01:54,160 --> 01:01:59,400
So if you can get your cultivation down to maybe a 5% detection rate then hopefully you

530
01:01:59,400 --> 01:02:02,920
can kind of power through that and overcome.

531
01:02:02,920 --> 01:02:10,360
So we'd just like to say as always the future is bright and a big thank you to Dr. Fernandez

532
01:02:10,360 --> 01:02:17,600
and Dr. Anand at my Florida DNA for coming and teaching us a thing or two about hopsley

533
01:02:17,600 --> 01:02:22,480
and viroid and giving us a little bit of hope for the future.

534
01:02:22,480 --> 01:02:23,480
So thank you both.

535
01:02:23,480 --> 01:02:31,800
Sure thank you very much for having us and feel free to contact us anytime with questions

536
01:02:31,800 --> 01:02:38,720
so all the audience can get answered to that.

537
01:02:38,720 --> 01:02:40,000
Thank you from my end too.

538
01:02:40,000 --> 01:02:44,480
Thank you for making the time for us to come and present and I want to thank the community.

539
01:02:44,480 --> 01:02:48,400
What we are doing is because of the community participation and we are here today because

540
01:02:48,400 --> 01:02:53,200
we are able to learn and also at the same time provide solutions.

541
01:02:53,200 --> 01:02:54,280
Thank you.

542
01:02:54,280 --> 01:02:56,240
Thank you very much for your presentation.

543
01:02:56,240 --> 01:02:57,240
Very very interesting.

544
01:02:57,240 --> 01:02:58,240
Good morning.

545
01:02:58,240 --> 01:03:03,640
And thank you all to all the members of the Cannabis Data Science Meetup.

546
01:03:03,640 --> 01:03:08,600
This meetup wouldn't happen without all of you fine folks, all of your brilliant ideas,

547
01:03:08,600 --> 01:03:10,480
your thoughts, your ideas, your questions.

548
01:03:10,480 --> 01:03:13,680
You're the people making this happen at the end of the day.

549
01:03:13,680 --> 01:03:15,260
So thank you.

550
01:03:15,260 --> 01:03:17,760
Thank you for making the meetup happen.

551
01:03:17,760 --> 01:03:24,480
Hopefully we can move the cannabis space forward at least by a molecule or today at least by

552
01:03:24,480 --> 01:03:25,600
a virus.

553
01:03:25,600 --> 01:03:30,960
So slowly but surely I think we're making progress.

554
01:03:30,960 --> 01:03:59,520
Thank you.

