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00:17 Okay folks, uh let's go and started. Um Mhm. Yeah.

01:04 . Uh huh. See, so see the schedule. I put the

01:06 up that takes us through the second . Okay, so the next week

01:14 , 10. So week nine spring , no classes, of course.

01:20 so a couple of things to point . So of course I'm starting at

01:25 today. Um the flip class, one of those, you know,

01:31 of questions. The The video for content is up and it's in the

01:39 flipped class folder. So take a at that beforehand. Um it's only

01:46 be the 13th part one material. , so we'll do that next

01:51 It's gonna extend over and I can half a class over two periods.

01:57 , so um so this section, unit is Three chapters, viruses.

02:06 then really 13:14 is metabolism heavy. , so um if you've already looked

02:17 , don't be um Um scared I maybe, I don't know by the

02:23 and 14 material, you'll see probably of pathways in the book. And

02:27 different and time reaction. So you're expected to memorize those things. Um

02:33 definitely look at your lecture notes as going to the book. I take

02:40 material is more, the metabolism is in in stages. The process is

02:46 , like causes slow respirations more like . But was in what comes out

02:49 not all the individual reactions. So , just give you a heads up

02:55 that. Um Okay, so exam will be available on costs of Wednesday

03:02 friday. So do I look at . Um there is no answer key

03:08 everybody has a different combination of questions I'd have to have like 200 different

03:12 keys. Okay so do look through you can't you'll you'll actually right up

03:18 top look at a handful of questions go oh yeah that's what the answer

03:22 . Okay so um but there may some that you are still confusing so

03:28 let me know. Okay um so that but do before you if you

03:34 to meet fine not a problem you to office hours if you want to

03:37 another time because the officer doesn't fit schedule fine too. Um But do

03:44 at the exam first and before we so that you have your best shot

03:50 um you learn more that way I I'm trying to figure out on your

03:54 of course. You know you have options. You have to you don't

03:57 have to look at it again because not, the final exam is not

04:01 in this course. Right? So each exam covers a separate unit.

04:07 um you know you could just not I don't care at all about example

04:11 , I'm just gonna move on. or you know I think it would

04:14 who be to look through the questions . Um And uh hell there could

04:19 a just a flat out mistake I , right? So even for that

04:24 , just just look through it if is an error of course and obviously

04:28 credit for that. So um so about exam, what the exam

04:34 About What I usually get? It's I try to aim for like in

04:38 69, not 69, 68, range right? Somewhere in there And

04:43 range was actually about 15 iron and little bit more than that. So

04:50 individual exams aren't curved, but the grade and the course can possibly be

04:56 . Okay? Um It all depends if the curve benefits, you're not

05:00 curves can go two ways, They can they can lower the letter

05:07 cutoffs, right? Which is what want, right? Rather than a

05:10 and above is a Uh C well it was 60 and a buck

05:16 the C -, right? That's preferable, you know, beneficial curve

05:22 you. But if it takes a to get to 16 minus an 80

05:26 get the c minus and above, you probably don't like that.

05:30 so um I only curve if it you. Okay, So we can

05:34 more about that as we go But uh and I will always gonna

05:40 closer to the end, but for just uh if you didn't mean that

05:46 meet expectations, we think maybe how studied uh if you want advice flash

05:52 on that process. Look at the exam, the first day lecture I

05:59 about 2015 20 minutes. And then talk about how to study. So

06:03 that if necessary but certainly um uh by office hours. Have you

06:10 And we can certainly talk about it . Okay. But uh first thing

06:16 you know once the exam is take a look at it, see

06:20 you got wrong. See if you figure out what the answer is.

06:23 not absolutely let me know, email by. Officers try. Um So

06:31 know, you should have hidden to amnesia, right? Because what you

06:39 well or good or in between on exam one, just you know,

06:44 going to the next thing. Focus exam two. I would recommend that

06:50 you didn't meet expectations, don't do not repeat identically what you did

06:55 study for the first exam, you have to change up the answer.

07:00 you didn't do well in exam one not I'm gonna try even harder.

07:04 . It's not about that. I'm sure you tried hard enough studying

07:08 exam one, but don't try harder a method that got you not very

07:14 results. That's the point. You can try harder fine. But

07:18 you're trying harder with the same it's gonna be the same grade.

07:23 ? Maybe worse. Right? So it up to my advice,

07:28 And uh that's how to change it into what that's what that 20 minutes

07:32 so on. That first day lecture about. Okay. So anyway,

07:37 leave it at that. We have as I said the third time.

07:42 at the exam and it's open. ? See what you missed to see

07:44 you uh if you have questions, me know. All right.

07:48 this week we're back to stuff being again. Right. So we got

07:52 quiz uh this week. Um And then we have smart workers do

08:00 It's the first stuff we're talking mainly about viruses. The part

08:04 Um Let's see. Next monday Alright. So next monday is the

08:11 class. Okay, so that video up. So do take a look

08:14 that. Okay, so main things week. Blackboard please. Smart

08:20 Okay. And looking at exam one it's available. Okay. So um

08:27 chapter six Okay. Is um broken The way I've split it up is

08:36 one described in terms of the viruses somebody could find them. Um What

08:43 some of the features of viruses? How do we classify viruses?

08:48 what are some of the important structural ? And that's part one. Part

08:54 will cover most of that today. two is um the life cycles of

09:00 as you will see. Well, present. Kind of a generic Here's

09:04 viruses, viruses replicate. Um But point out how there will be numerous

09:13 will see of different steps as we through virus cycles next time.

09:20 So it's um discovery of viruses I that we talked about this before.

09:28 So it's all about their discovery is about their size. Okay. Because

09:32 that viruses are on the Lower in of sizes, right? About the

09:39 nm. um .02 microns to about nearly a micron. So these aren't

09:45 you can see with a light Okay. So I have an autopsy

09:52 . Uh they were studying the tobacco will not they didn't know they were

09:57 virus but they were studying the virus caused causes tobacco, tobacco disease and

10:03 plants. Okay. And the what it does is it creates.

10:09 so of course a healthy plant has green leaves, you know, uniform

10:15 . Uh a disease plant from one these viruses has like a splotchy color

10:22 a yellow spots all over it. , Security is a sick plants can

10:28 as well. Um, but so was of course in the early part

10:33 the century, growing tobacco was a it still is but but it was

10:40 important and uh trying to study this was this was during the period of

10:47 knew the coke and the germ theory disease was known and established by this

10:52 . And so of course they well it must be some sort of

10:54 bacterial micro, right? That's causing . And so using, you

11:00 coach postulates, right that only diseased will carry the microbe, right?

11:06 plants do not. If we isolate microbe and applied to the healthy

11:11 healthy plants should come down with Right? We've gone through this

11:16 So, um, so they took plants crunch them up, right?

11:21 like a liquid paste, if you . Then they of course the filters

11:28 available at this time. That would microbes in the bacterial size range.

11:33 so they said, okay, let's that liquidy paste through the filter.

11:38 trap the microbes on top. We'll that stuff to plant a healthy plant

11:43 will find that they come down this and figured out the cost.

11:48 They did that. And it didn't one of the healthy plants. They

11:52 this stuff to ever got sick. only when they looked at the I

11:57 know what properly to do it. they said, well, let's look

11:58 the stuff that comes through the right to infiltrate, that when they

12:03 it to healthy plants, then they this disease. They knew they were

12:08 with something uh, out of their that was really small. And they

12:14 no idea about, Okay. And wasn't really until about 30 years later

12:19 into the micrografx of of that particular that causes this disease. Tobacco mosaic

12:25 . It's only small, end size . Um, it uh, it

12:30 an electron microscope to see it and wasn't developed until a few decades

12:35 And they asked the crystalized it and a picture of it. So,

12:42 , of course viruses um, as talked about before, require folks.

12:48 right. They there's there's no life on this planet that likely doesn't have

12:56 sort of virus that infects. And um, of course, you

13:02 , viruses viruses have been with us for six million years. Right.

13:07 so, uh, they've evolved with . Um, they can effect it

13:12 the longest time. You can always this stuff. There's another dragon.

13:17 there was really no positive benefits of that were spoken. You know,

13:22 I was studying this stuff and even to about maybe 20 years ago,

13:25 years ago. Okay. Uh all new viruses could do was cause

13:30 Okay. But it's come to light they do have important ecologically.

13:35 Even in our own gut, the , the virus isn't there kind of

13:40 populations of microbes in our guts. they do have an influence and

13:46 the because of, you know, microbes are found everywhere. So are

13:50 because they look, they require those that are out there. Okay,

13:56 um, size range I mentioned, talk about at the end likely next

14:07 . Um, what are called giant . So these actually exceed A micron

14:14 a micron 1.5 microns. Um and have a big enough genomes to encode

14:22 certain genes um involved in protein Not the full complement but parts of

14:28 . And so it's believed that maybe giant viruses were once cells that kind

14:33 degenerated maybe into a more Republic Um small viruses. And we talked

14:41 that are RNA viruses like covid and virus. Um it's not that maybe

14:47 small nucleic acid pieces started out as as a genome and science themselves that

14:52 evolved into this form. So there's kinds of speculations of how the virus

14:58 evolved. We see kind of different of viruses this way. Okay.

15:04 now the uh ecology, so just briefly a second ago about you

15:13 that there are positive benefits for Okay, so in controlling populations,

15:19 . So the virus infects a It can potentially kill it eventually.

15:25 in doing so that being that has died as the result of a viral

15:31 becomes detritus. Right? The complete becomes those elements of that entity now

15:39 available to others in the ecosystem. And so the the in aquatic

15:47 they've studied this in marine aquatic studied this, how viruses impacted different

15:53 of um algal populations, Brazilian populations um they don't wipe out the species

16:03 infect. Right? That would be of counterproductive. Um almost completely because

16:11 because the host itself does evolve and can have types that become resistant.

16:18 ? And the virus must have you don't be able to be able

16:20 infect those new uh newly resistant So it's back and forth constantly between

16:28 and them. And um but in so, right. So remember kind

16:32 remember ecology, right? And that that have a single dominant species,

16:42 ? That that is most abundant, ? Because they have a lot of

16:47 in those kinds of ecosystems. For the dominant species kind of overrides

16:53 else and other other species are only smaller proportions and not as diverse.

16:59 , if you can kind of balance out there. All right, then

17:03 can have more diversity. And that's viruses can do in ecosystems is too

17:08 controlling these populations, create more And so this here is a

17:14 So the viral Schunk refers to um see here is that portion that when

17:24 kill their host cells, that material , you know, the composer becomes

17:29 of the material that others can So uh broken down organic matter.

17:35 ? So of course uh others and can can certainly use that. So

17:39 can contribute to that. Okay, whether it's affecting uh on a trophic

17:46 cells or head atrocious. Right. so as a result we create a

17:52 and potentially more diversity in the which is good for everybody.

17:57 Um so we um and this shows again they picture of this process and

18:06 you see in the viral shunt how try this forms organic, that's organic

18:14 is basically just dead organic material Right? And so that can then

18:19 others thriving ecosystem. So things like funding is higher level higher if you

18:25 outs in these ecosystems, uh plenty nutrients and enables them to grow and

18:30 others to grow. Okay, so Alright, so let's look at this

18:37 here. Okay, this we're gonna a little bit about just a basic

18:43 life cycle. Okay. And uh matter how complicated or maybe not so

18:50 viral cycle is there's gonna be some all of them. Okay, this

18:57 kind of hinting at one of those features that are gonna be part of

19:03 viral cycle. Okay. No matter type of virus. So let's see

19:09 we get here. So unless unless process of the viral life cycle occurs

19:16 , it will never reproduce. So of these are part of in viral

19:25 cycle as we'll see. But one them has to curdle for any of

19:29 others. Yeah. Mhm. Okay. Timer's on, while we're

19:51 here thinking about this. Any questions ecology. Thank you. All right

20:08 and down. Mm hmm 543 stragglers in. Mhm. Okay. It's

20:21 108 account. Okay. So if you answered. D um you

20:28 correct. Okay. So it is it all begins or ends really with

20:35 . The virus effect recognizes molecules on periphery of the cell and that's what

20:42 looking for and like a lock and in the lock fits or it doesn't

20:48 the virus effects or it doesn't. . And if d doesn't curl well

20:53 we'll get um replication of host We'll get translation of all proteins.

21:02 of Syrians will get maybe this is maybe not all viruses go to the

21:07 but maybe it will. Okay. possibly. Okay. Point is all

21:11 these will occur. And of course will only occur if d occurs

21:17 Okay. And so looking at basic . Okay, so the point here

21:24 that viruses aren't cells as we Okay, so there's a very specific

21:31 . Um a cytoplasmic membrane lipid bi in closing a cytoplasm that may have

21:37 nucleus. If you're you carry out , toyed with their bacterial Procardia type

21:44 . Things like that. They self on their own. They can take

21:48 nutrients and metabolize uh they can So they don't viruses don't have all

21:54 features. Okay. They're certainly not as we know them. But surely

21:59 can evolve. All right. They metabolize like you can't give a virus

22:04 and hope it's going to be you , get energy from it. It

22:07 work that way. Okay. But do have the most basic structure of

22:13 virus. Okay. Is the protein or the capsule that you see here

22:19 and closing a genome. That is the basic structure for every bias.

22:26 . Now, of course there's going be variations of that as we'll

22:29 But at the most basic common structure it captured surrounding genome. Right?

22:34 genome can be D N A R A double stranded single strand different

22:41 The units of the capsule itself are capsule mirror units? Okay, now

22:48 basic uh life cycle will go through as we go through next time you're

22:57 to see different variations of certain Okay, so as mentioned, it

23:03 and ends with recognition. So what's recognizing? Well, it's gonna be

23:07 on the periphery of the cell proteins the surface. Glycoprotein like olympics,

23:13 kinds of molecules. Okay. Um where the virus has evolved to be

23:19 to bind to bind to it and in entry. Okay. Um once

23:26 recognition occurs, okay, it may end up using one or more of

23:32 um components from the host. So asterisk ones. DNA plummer plummer is

23:39 . Okay. Because that depends on viral type that's infected. Right.

23:46 RNA virus for example doesn't need DNA usually there's an exception of that,

23:52 we mentioned, but most do not the because they have an RNA genome

23:58 others that are being a viruses may may not have it some some carrying

24:04 some don't uh Arnie Primaries, some use the host that may have their

24:09 . Okay. But certainly ribosomes Trn nuclear types. They'll all need

24:17 That's all a part of copying viral and making proteins. Okay. But

24:24 , they lack of metabolism in complex . Like we have. Right,

24:29 don't have black calls since they don't so respiration and these kind of

24:33 Okay, so um infection. So recognition. This is a point again

24:40 there can be variation. Right? could be that the capsule with the

24:45 enters itself completely. Right, bacterial , it's only really just the genome

24:52 everything else stays outside. So variations and how it enters it can

24:57 as well. Okay. Um of one of the first steps is to

25:03 copies of the genome. Right. one thing you have to remember is

25:09 we go through different life cycles, might be thinking, well why is

25:12 doing that? And and this is I don't get that. Right.

25:15 I always think of the endgame, . A cell coming in and many

25:21 , right, Being assembled and then . Right. That's that's that's what's

25:28 eventually happen at some point in This represents right many of these which

25:38 lots of proteins. I mean lots our proteins. You gotta assemble

25:41 You gotta put a genome in each of these. Right? So that's

25:48 you have to copy each other. why you have to do translate and

25:53 produce the viral proteins. So everything together. So that takes a lot

25:57 energy. So the whole cell is as a result of that.

26:03 So the consequences can be well, host was going to die,

26:07 and eventually that will happen. But are some cases where the host doesn't

26:11 even though it's infected, right? can be in this state here,

26:18 it integrated into chrome zone. If virus does that Ronald genome does

26:24 then the consequence of the host cell be minimal really. The hotel can

26:30 on its merry way and just keep and functioning. No problem for a

26:35 , eventually that will change. But that is a consequence for some

26:40 Okay, even if they do do , right, they eventually have to

26:45 back into this mode, Right? they ultimately are or they ultimately,

26:53 just get rid of this, make host cell a replication complex a replication

27:02 , basically make that post a replication for themselves at some point, it

27:08 happen immediately almost immediately once they Or it could be it could be

27:12 time down the road. And by , I mean, it could be

27:15 , weeks or months for years. depends on the viral type, but

27:20 that has to happen if they're going perpetuate themselves. Right. And so

27:25 of that of course not just copying genome but transcribing translating gravel genes into

27:32 . Right? That there will be symbol. Right. And so what

27:36 of viral proteins? Well, certainly proteins to make the shell.

27:40 And then there's gonna be other things we'll see. Um then a symbol

27:44 law. Okay. And then uh exit the host and then go on

27:50 infect more hosts. Okay, so couple of things. We're just for

27:56 sake. I'm just showing one virus um there can be more than one

28:02 affecting itself. Um what you see here? Okay. Mhm. In

28:11 of comparing genomes, right. The of this virus that infected, Is

28:18 going to be the same? That's all these progeny viruses, it would

28:24 similar. But viruses do not have they were in the copying genome

28:30 Okay. They're pretty sloppy about Okay. Because they don't have our

28:35 we have all kinds of mechanisms to sure we don't make mistakes. If

28:40 do make mistakes, we can fix . Right. And and we're very

28:44 are our systems are very good at . Okay. Um viruses aren't because

28:49 don't have that kind of apparatus. there will be mistakes made as they

28:54 mistakes equate to mutations. Right. it could be that mutations form are

29:01 too much to even make a viable . So it just goes away.

29:05 . But the point here is that coming out right, these can slightly

29:11 from each other. But I'm talking clones necessarily coming out. There will

29:16 be variations among the proximity exiting. hope so. Okay. And

29:22 viral types can also sometimes can infect . It's the same cell and that

29:28 create more recombination of genome. Creating more variations. So that's the

29:35 of the virus. Okay. Um I said, we will see variations

29:41 different parts of the steps. But what you're seeing here, it's

29:45 common all viral types and their Um Now one of the things where

29:51 see complicated, more complicated steps maybe a process where you just visually look

29:58 it is animal viruses versus bacterial Now, why would animal viruses be

30:04 complicated? The bacterial are why would be are eukaryotic cells as simple as

30:15 cryonics cells? No, that's the nature of why animal viruses will have

30:21 more second more complex cycles. Because nuclear erotic souls. Their hosts are

30:27 more complicated. So you have some some handle viruses that will go to

30:32 nucleus and do things there are some don't um they'll synthesize proteins in the

30:38 plastic particular and involved in gold et . So things that just because of

30:43 of the eukaryotic host cell is more . So this lifestyle can be a

30:47 more complex. So um so the . So again it's all about for

30:56 the perspective of the virus and it's two. I want to produce

31:08 It's gonna have to infect the Okay. Um And so there's two

31:14 . There's the host range then there's I call maybe call it tissue

31:21 Okay. Or trumpism is the technical tissue specificity. You kind of think

31:29 those are kind of mean the same . So a broader host broad or

31:36 host range refers to how many different can a single virus infected?

31:43 Um rabies virus is the obvious Rabies virus can infect all different types

31:48 mammals. Cast dog, human possums, squirrels, raccoons etcetera.

31:54 many different host types. Okay. A flu virus, cold virus.

32:01 much it's humans. Humans are the post they have. Okay. Um

32:08 so measles and mumps. Another So a narrow host range. So

32:12 means affecting only a small number of . One or one or a few

32:18 of course can be two or Okay. Um Now the tissue specificity

32:26 tissue range if you will. Right that refers to in a single

32:31 So for just looking at humans, we looking at a mass or just

32:37 a whatever spirit animal is. Right is. So just like you have

32:42 single host and we can take a example. Alright, rabies confirmed multiple

32:48 current host range but have a very tissue specificity. Very narrow trope is

32:53 okay rabies viruses only infect nerve That's it. Okay. Um E

33:03 and contract in fact multiple actually has narrow host range as well but has

33:11 broad um tissue specificity. Broad trope um I think it's like multiple cell

33:17 in a single host. That's one the Reasons it's such a deadly

33:22 You require Ebola. You have at about a 50% chance of surviving.

33:28 more upwards of towards 90% chance of . Okay 10% chance of living.

33:35 they can affect the effect cell types can um um make up your blood

33:44 and so if they affect those then blood vessels become leaky. Right?

33:49 dying from Ebola is dying from a where basically fluids are coming out of

33:53 . Right. Not a ah certainly horrific way to die but it's um

34:01 one of the main reasons why it such a high mortality rate number of

34:05 that can affect um Congress with HIV narrow super narrow one cell type,

34:12 ? Certain type of T cells T cells but in in destroying those types

34:18 t helper cells they just shatter the system at that the immune system which

34:22 the ability to produce antibodies and and things. So um even though it

34:27 have a doesn't not have a broad of cell types of effects that when

34:32 doesn't affect the type that's critical to 1's immune system. So um still

34:38 good. Now again let's just to that the target self host virus virus

34:47 cell relationship. Right. Sweeter. know, even even in this state

34:51 , just back up a second in state. They're sitting over here.

34:56 right. It could be a virus uh top of the desk here or

35:02 the door knob over there. Um they can remain viable in that

35:07 . Doesn't mean it's dead. Remember virus can be that occupy that

35:13 non living state. Right. And he can it can remain viable for

35:18 time. It depends on the viral . How typically viruses that are cause

35:25 like HIV papilloma virus, these generally as don't survive as well outside the

35:34 but certainly other types can't. Cold and other types can survive for quite

35:39 time outside of a host. But it all varies. Um the

35:48 Okay so again based structure as you is that capsule surrounding genome. Okay

35:54 we're gonna see some variations to Um one of the things to keep

36:00 mind is the small size of the means it can't contain a bunch of

36:06 . Okay so they're going to actually a small genome. Okay. And

36:11 it becomes important then to keep kind the structure is somewhat simple.

36:18 But then I mean you see and very common for to see this kind

36:22 geometric shape to a viral capsule. . We call these symmetrical types.

36:29 They can be filament tous or helical called or the 20 sided.

36:38 So you see in that type different . Right. So you have different

36:43 see these different color coded components. . Like so and you might think

36:50 , each one must be included for a gene. Alright well no there's

36:56 for this one, there's like three up the outer capsule three proteins.

37:00 it just combines those together to make capsule. Right? So it only

37:05 three genes for those three different capsule . Right. So it kind of

37:09 to maintain efficiency from that aspect because small. Okay and so the um

37:19 so the hepatitis a virus you see is just the protein coat caps,

37:26 surrounding genome. Now a variation of is an enveloped virus. Okay,

37:31 you see the catholic structure here. , in the middle with the black

37:38 , the hexagon with the genome But then you have the envelopes around

37:43 so the envelope has derived from the cell. So as it exits that

37:49 membrane wraps around it. Okay, enveloped viruses. Um I hate to

37:55 absolutes but I'm almost certain only I a viruses have envelopes but through

38:02 no because of the bacterial cell Right. So but certainly and not

38:09 animal viruses do animal viruses can have problem or not. So the ones

38:14 call that lack it are naked Right. So this is a naked

38:18 over here lacking an envelope. And so within the envelope can be

38:27 even though the envelope is host you will have viral proteins as a

38:32 of it. What we call envelope . Right. So these knobby things

38:37 see are are all viral encoded Okay. And we sometimes refer to

38:42 of these as spikes like glycoprotein spikes life for sugar to the protein combinations

38:51 and almost uh in most cases the themselves, they are this prominent like

38:56 see there are involved in attachment to holy recognized host attach and then begin

39:02 life cycle. Okay. Um so virus over here is also one that's

39:09 . Right? There's not an envelope it. Okay. And so the

39:16 viruses envelope, There's many animal viruses are enveloped. The flu virus Covid

39:20 enveloped virus. Um So again, are symmetric viruses. These are all

39:29 the casa. He'd roll type. . Just you see the kind of

39:32 pentagon shaped there. Alright. Um filaments, those viruses uh which are

39:39 symmetrical Ebola is one back of mosaic and you can also wrap the helical

39:48 or the filament this virus in an as you see here. Okay,

39:53 again you see the spikes. All now um a tale virus. This

40:00 a very common structure for a bacterial . They also call these subtext.

40:05 call these complex viruses because there are combination of different parts. You see

40:09 capture the capital structure here. All . But then we see a bunch

40:14 other stuff. Right? That's typically they refer to as a complex

40:19 Um The addition of these other parts kind of look weird in the

40:23 But that's really all a part of ability to attach to a cell to

40:28 fibers here, tail fibers. And part here called a shaft or sheath

40:38 actually compressible. It will actually compress top of the cell much like a

40:43 . And that genome then is shot which is sitting in the captured up

40:49 cut into the cell. And so bacterial viruses has mentioned they um it's

40:55 the genome that goes inside the Everything else stays outside. So when

40:59 see one of these particles okay without genome because it's just infected cell,

41:06 called it a ghost because it's just a protein shell. But there's no

41:10 genome in there because it's been inserted the host. Um Now asymmetrical

41:19 So you might look at that and , well that's not asymmetrical. It's

41:22 . Okay. And it's uh they're and so cold viruses like this.

41:29 covid virus is like this. The virus is like this um the it's

41:38 of a blobby oblong type shape. not a perfect sphere. Okay which

41:42 why it's a symmetrical can be kind um uh oblong kind of oval

41:49 Kind of you know amorphous blob in cases they kind of changes shape that

41:55 . Um And so the other thing this is a distinction is you don't

42:01 see the um these the genome itself be surrounded by curry with protein.

42:11 it's a nuclear nuclear proteins can just to the genome and coated. Okay

42:19 that's one way to protect it. but then it does have the

42:25 Okay it does have envelope protein sticking of it. So um the flu

42:31 , it's the don't worry about this we'll talk about it later. But

42:36 uh this part the H. And . Right here flu viruses having

42:42 And N. Numbers. Alright. one N. One H. Two

42:45 . One. What have you? refers to these two components of the

42:50 virus envelope proteins. The gluten is one that allows it to catch the

42:57 one allows us to use it the um the uh Tamiflu which you may

43:04 familiar with. Maybe you've taken it actually interferes with this component here so

43:11 can't exit the cell. Okay so so again so the there's so much

43:21 viruses. Um Even though the man around remember their parents just have a

43:25 about blobby form I think before we to questions any question about structure.

43:33 exactly about uh because it's not you you can't draw a line bisected and

43:43 halves because it kind of blobby It has it's not completely symmetrical the

43:50 itself or is it? Yes it's shape itself. Yeah. Uh Yeah

44:03 to the to the genome directly by to the genome. So it'll coat

44:08 whole length of the genome and so it's undergoing through life cycle it'll it'll

44:15 the genome. I believe that those will kind of come off that you

44:21 well it's copy then go back on bind to it. Not all not

44:29 viruses are like that but you will something like a flu virus. And

44:34 is the same way as those um I call proteins actually sometimes they're called

44:40 capsule proteins because there binding to the but but it's not a feature of

44:49 viral type but some have it that . Okay bring into question. Look

44:56 these questions. This is um this goes to you know particularly RNA viruses

45:02 we can apprehend heads around DNA viruses how the last several worked better because

45:10 like us they have a DNA Right So we're used to D.

45:13 . A RNA protein. Okay but viruses can have depending on the type

45:21 definitely be very different from that. and as we flip through RNA virus

45:28 cycles. It's me back up. the it's the RNA virus types that

45:34 to confuse people. Okay, so is a good this will show you

45:42 the first atomic beef. Sure. , mm hmm. Yeah.

46:38 Seconds. Okay. Here we Yes, it is only above.

46:54 . So as we'll see next time sure. Um, we can have

47:03 new viruses and so designation of plus minus. Alright. Plus minus

47:12 Okay. Or you can have You can have one that's called plus

47:16 . All right. And so the minus distinction. Okay, So here

47:22 let's just say this is um frankly you can be DNA DNA can

47:31 DNA RNA. Okay. Or it be RNA RNA. Mhm. And

47:43 all three combinations are possible. And I'm gonna bring this up because when

47:48 see what plus RNA virus, a or new virus. Okay. What

47:52 that mean? It really just goes to the clinic acid base pairing terminology

48:01 rules. Right? If you have and regardless forget create virus don't you

48:07 . But when you're talking about nucleic , whether it's DNA DNA DNA RNA

48:11 RNA, they each have that plus relationship to each other. Right?

48:17 if we have, let's just hey, you G C.

48:22 Well what is the complimentary form? ? From the U. A.

48:30 . G. Right? And this be the plus and that will be

48:34 mightiest. The point is they're not complementary complementary form to the A.

48:41 is not a UGC. It just work that way. It's not because

48:46 a virus it's just because that's the gas and rules. Okay. And

48:51 the plus strand those referred to as containing the coding information. Right?

48:59 can um it's RNA. The plus is the one that can be

49:06 Right? So that is one that be used for translation plus R.

49:12 . A. Okay. The minus . And the other thing is and

49:18 you're copying a plus strand let's say make it let's say these strands open

49:24 . Okay let me have a G. C. Okay.

49:31 C. G. Right so we a restaurant so that's opened up right

49:37 we're gonna copy it. Right. the copy for that going to be

49:41 minus or plus strand? Yes. It's gonna be -1 and this one

49:45 going to be a plus strand. . Just the way it works.

49:52 And so they have that relationship to other and so now the minus

49:56 Alright my strand. All right. be copied into A plus. Right

50:03 so that's actually what um that is the minus RNA virus. Right when

50:10 copies its genome that copies a Right and that's that's actually an

50:15 R. N. A. It be translated into proteins. Okay so

50:19 template that is can be directly translated A plus Arnie the template that can

50:24 copied into a translatable M. Is a minus party. Okay.

50:31 synthesis. Okay. That's the realm the retrovirus. Okay. Also an

50:41 virus. Okay. But it turns into a deal turns the okay so

50:51 different. All right. And so there's a reason it does that okay

50:58 retroviruses have the ability to what's the of making it into an art into

51:04 . D. N. A. do that? Yeah. Uh Not

51:13 because when it goes into um not because it will ah but I don't

51:22 the answer if I'd say it but get to the second anybody else.

51:29 . Now it kind of has to with the life cycle of the virus

51:32 a retrovirus. Let me remember what might recall the retrovirus what this mod

51:39 . Mhm. Um There are certain I mentioned we had a picture of

51:44 life cycle. Certain viruses can integrate a whole genome. So record viruses

51:52 what that's what they do. So they're an RNA virus they can't integrate

51:56 host chromosome unless they turn it into . Right There's the forms of

52:00 N. A. So you have integrate has to be set in the

52:04 material. So a retrovirus will will RNA. It's RNA genome into

52:10 N. A. And then they integrate into the host and they will

52:13 so retroviruses that do that can integrate the host chromosome and be there for

52:19 and years. Um Bless you. then um while in that state,

52:27 In the integrated state, they can express jeans. They can then initiate

52:33 lifecycle replication. Right? So we'll about that next time. But but

52:39 it's a unique type and it's not retrovirus there. Um There are

52:43 N. A viruses that do that well. Herpes virus uh if you

52:49 had like a type that gives you fever blister and it breaks out All

52:54 . That's actually the herpes virus that's into the chromosome to sell under stress

53:00 is when it, you know, out. It will come out of

53:02 come out of the chromosome begin And that's that reaction you get from

53:08 fever blister. The papilloma virus that cause cervical cancer. It's one of

53:14 pipes. So uh so there's like said, they're varies there's some viruses

53:19 that's what they do. They integrate the host chromosome. There's bacterial

53:23 What does that do that as Okay, so all different types of

53:28 . Okay. Um and so we really um this is one of the

53:36 things that people stumble over. It plus minus. And mm hmm.

53:41 does it do this? And not ? So one of the things you

53:43 to remember is is always what's the game for the virus is to make

53:48 of viral progeny. And then that's to exit the host and infect

53:53 Okay. So if step one is that process to make copy genomes,

53:59 ? Because we've got to put genomes all our assembly wired captives.

54:04 Well that means you have to copy or you have to copy that.

54:10 . What happened? Right. And you copy right, like I showed

54:16 , you copy a plus into a . If you're minus. Do you

54:20 if you copied into a plus? . That's why it happens.

54:26 And this will be this certainly is gonna be the last time I mentioned

54:29 . Right. But I figured that's kind of planted in your head now

54:33 we get there it won't be so , confusing. Hopefully. Okay,

54:40 , uh, let's look at I put this in just for yeah,

54:45 as a I know we're all sick coronavirus but you hear this, you

54:52 throw a rock at the picture if want. Um, uh,

54:57 so RNA virus. Okay. And , there's a table at the end

55:03 by no means memorize table that has the viral types and all the

55:08 Don't you memorize it? I put in there just to show really how

55:15 the viruses of group. There are many that us humans have interactions with

55:21 original are in a category. not just coronavirus, but the flu

55:26 cold virus, rabies virus, west virus which is endemic in this part

55:31 the States. Um lots of measles mumps, so many that are in

55:36 are in a category. Um This one of those plus. Right.

55:41 I mean it's genome can be can as a template to be for translation

55:49 . Um it has the spike proteins course. That's what the vaccine is

55:54 those um antibodies form will bind uh these spike proteins. Okay, of

56:04 , in doing so minimizes the chances greatly lessens the effect that they don't

56:09 host sex. Okay. Um it a genome you see here that is

56:17 . Right? So you see really lack of a of a one of

56:25 geometric caps. It's right. You really see that here in the

56:30 Right. It's because it's been replaced the capsule proteins binding to the

56:36 That's what you see here. Kind of that reddish copper ish

56:41 Those are those are called nuclear protein coding the genome. Right.

56:46 it kind of takes the place of , you know, for more general

56:52 of the capital we've seen. So proteins themselves, the capital proteins themselves

56:56 directly coat gene. Okay. Um so the so and again, don't

57:06 not gonna test you on this, just just if you don't know already

57:10 lineage of COVID are from 2000 to was the SARS a sudden acute respiratory

57:19 that actually was just confined, I it was Hong kong and didn't really

57:23 beyond That area to become a Um it subsided. And then just

57:31 years later it emerged that the Middle variety, again, it was pretty

57:38 just confined to that area. And third variation is third time's a

57:44 No intended. Uh that one obviously contained. Right, We can speculate

57:49 all the reasons for that. But that but they do share a

57:56 for sure in structure. They're all new viruses, coronaviruses, similarity and

58:02 oh, so much similarity, proteins things. So um so it's uh

58:09 and so one of the factors that to why it can cause this is

58:15 so for the delta variant, recall that had more severe symptoms. That's

58:23 the omicron we have now um as , in terms of the number of

58:30 uh if you're going to code it is the time to get it to

58:33 because it's not not near as severe what uh this form was. But

58:40 and part of it is the types cells, the solar cells in

58:47 that's a particular type of receptor found those cells and the covid virus actually

58:52 to that. So your LDL ourselves obviously in the if you don't recall

58:57 LBO lie right, a little small shapes, you know that we were

59:05 bronchial tubes all terminate, you know that's where the oxygen exchange occurs right

59:09 the line. And so certainly if cells are binding there, you're gonna

59:16 what's called an inflammatory response. your immune system will react. But

59:21 of the process is, you the fluid build up occurs in the

59:26 because of this effect and the inflammation um that you know, you

59:33 where are the symptoms like shortness of and uh it can lead to a

59:38 viral pneumonia. Okay. And obviously people died from this. And so

59:46 , the desert formulas of course, the delta variety, which of course

59:51 been now replaced by the omicron um doesn't have the severe effects like this

59:57 presume because the changes that occurred mutations these particular spike proteins such that maybe

60:05 doesn't bind as tightly or or maybe maybe doesn't reach down into the well

60:11 of our cells may be more upper track. Um so whatever the

60:17 it doesn't produce the same bad effects um anyway, okay, the

60:27 viral genomes. Okay, so um mentioned boxes small, nothing big genome

60:35 average size. It's probably in the base pair range. So here we

60:42 the zika virus which made notoriety maybe three or four years ago I

60:50 I think the first cases in South um affecting infants. Um, the

60:58 plus RNA virus it so some of kind of and I certainly don't,

61:04 don't have to memorize the specific viral that are synthesized but just to show

61:10 , okay, what are the types things the virus culture? Well,

61:13 proteins for sure. Okay. It have some other components that are involved

61:19 entry or exit of the cell, involved in the life cycle process.

61:25 very common for viral genes to be . They at different times. What

61:31 call early in late genes are very common to speak of viral genes

61:37 are turned on the beginning of the cycle and then turned off and then

61:41 that come later. And so we that initial parts of a viral infection

61:45 we'll get into the cell and the genome later parts of the infection are

61:50 and then exit. So there's going be different components needed at different times

61:54 that reason. Um The flu farmers bringing up again only for the fact

62:01 it's kind of unusual form of the . It's what we call segmented.

62:07 you see there's basically eight different segments . It's not one continuous chromosome.

62:15 so what that means is opportunities. for much more recombination occurring multiple viruses

62:23 a cell, Those segments can interact recombine with each other creating different

62:29 And so if you follow the lineage the flu virus, you're originated in

62:36 aquatic uh aquatic birds, ducks, , these kinds of things, wild

62:42 and then migrated into domestic birds, and so forth. Um And then

62:49 into swine. So in the re along the way it performs that eventually

62:56 humans. Okay. And you can at a flu virus genome and here

63:03 has been color coded. So you see the the lineage of yellow

63:08 avian or bird segments read I assume probably the swine segments, the green

63:17 the human form. So combinations and uh flu virus is constantly changing.

63:23 know, flu shot one year will work the next you constantly to get

63:27 flu shot. Um uh and so know, that's that's the nature of

63:33 flu virus, fortunately it doesn't have the level of mortality rate that the

63:42 the delta variant of Covid had. I think flu viruses like maybe .01%

63:48 . I think that delta variant was maybe 1% mortality doesn't seem like a

63:53 . But you know, when you talking about the population around the

63:58 it does become a lot. Um so hopefully we're gonna be in

64:02 state where with the omicron network it'll be around, it's like going

64:12 , but at least be manageable low like we can control and not cause

64:18 the stuff that has caused with So um any questions. Yeah.

64:29 . Actually I'm gonna do it again a 2nd 7 years. Hold on

64:32 I'm gonna end actually kind of with of that. And then it will

64:35 on next, you'll be sick of by the time this week is over

64:39 other. But yeah, I will into plus minus again shortly. So

64:45 talk just a bit about. So one viral roids and pry ons.

64:53 , um number one they're they're well forgot I had it written up here

64:59 . There are not viruses. You might say that virus like

65:04 because they require a host but they have the viral structure. I don't

65:08 a capsule. They don't have all other features. Okay, so a

65:14 basically is really only a concern. I can't say that because we depend

65:21 course many fruits and vegetables, that's of what the thyroids infected. So

65:25 were affected by that since we eat things. Okay. But in terms

65:29 directly affected, there's no virus the diseases or infections of humans as

65:35 as I know, it's strictly plants among plants, vegetables and groups seem

65:43 be the main one targets uh think version is the one that's been most

65:49 . But you know, in a aren't a it's basically infectious RNA with

65:55 , that's all it is. And uh we all know Arnie's not

66:01 stranded like DNA but RNA can fold . Right, so it's all complementary

66:06 parents. And so it can fold and that secondary structure we call it

66:11 important to its viability. Its That's right. RDS can have catalytic

66:18 . Okay, These are relatively You can see they're just under under

66:25 nucleotides long. But remember that RNA RNA can be have enzyme activity.

66:32 the RNA that makes up the small of the Viber zone is the one

66:36 forms the peptide bond. Right? they can have that. But the

66:40 implants is typically gene expression. I the virus itself can interact with proteins

66:47 it can interfere with the expression of . Okay, that's basically what they

66:53 . Okay, um now the Okay, so whereas viral roids are

67:00 RNA molecules and that's it. Nothing more to them. And they do

67:04 to host our memories to replicate But the Priam's now are just proteins

67:11 themselves. Right. So prions um infectious proteins. There's no gas id

67:18 nuclear gastric component. There's you it's just a protein. It folded

67:23 . Right? And that structure is for its function. And so these

67:28 um I think first discovered in sheep is a disease and sheep, it's

67:37 neurological condition. It's the name, the legacy clinical name spongiform encephalopathy encephalopathy

67:48 of describes kind of what it really. Um So in a affected

67:56 it will pry on protein. So is a normal form that's present in

68:01 and in other animals. Okay, has a function. We don't really

68:05 what the function is. So the prion protein, as weird as it

68:11 . I've seen that there may be role in copper copper metabolism. It

68:16 been confirmed. But I see that lot in terms of potential functions of

68:21 normal form it's found um a lot neurons. Okay. I think the

68:28 membranes I believe. And so um the normal form is of course benign

68:36 cause disease. That's when it becomes admiral form. You see there on

68:40 right, that form is the one informed they form aggregates together. They

68:45 of clump together. Okay. And disease which is called Creutzfeldt Jacob

68:52 So apparently in each animal type it its own name. Okay. It's

68:57 being goats. Um Creutzfeldt jakob in , I mean scrapie in sheep,

69:03 don't even know that but that's that's because it um And so the the

69:11 of these animal forms leads to uh generation death of the neuron eventually it's

69:19 very slow progressing disease. Right? not doesn't happen overnight accumulation of damage

69:26 neurons myth. And then when a uh dies. Okay, degenerates,

69:33 left with basically uh an open spot the brain tissue. Okay. And

69:38 these but they are sometimes called Um But basically the brain tissue becomes

69:45 of holes where the neurons used to and that gives the the that tissue

69:51 spongy consistency, hence the name So you get you get that kind

69:56 form to it. Of course you imagine the effects of that uh severe

70:01 impairment and motor lack of motor skills whatnot. Right? So but again

70:06 slow progressing disease. Um and so quote air quotes replication, it's really

70:15 binding. So so a misfolded form to a normal form and that in

70:23 creates the abnormal form. So it like a chain reaction occurring again gradually

70:28 time, where then it becomes more more full of these prion proteins.

70:35 . Uh Apparently I guess because the it folds up, it can be

70:40 resistant to chemical treatments. Uh Physical . High heat. Okay. The

70:47 way you catch this is eating the of an infected animal. But even

70:53 the number of cases of mad cow in the United States is like infinity

70:58 , right? You're not that's something not gonna die of. Just put

71:01 that way. Um But you in in the rare case you do

71:08 eat meat of a suspected animal, basically beat the heck out of

71:13 Okay, no, rare steak would super well done. Okay. But

71:18 then I probably wouldn't want to eat anyway, but all because of the

71:21 of the protein to these conditions. And so this little graphic here just

71:27 kind of there's kind of shows the forming where the neurons used to

71:32 Um And then uh kind of a or just showing red shows the accumulation

71:40 the abnormal forms coming together. Um in the neuron will will degenerate,

71:47 function. Yes, this aggregation Okay. Um there's no other kind

71:54 prion human prion disease I'm aware of than this. Okay. There there

71:59 is some evidence that aside from acquiring , you're eating infected meat. Is

72:06 there may be a genetic component, I'm not sure how well established that

72:12 . Then maybe you can share it then the leo for this misfolded

72:17 There is some evidence to suggest Um Anyway, so that's so prions

72:24 viruses, infectious RNA is infectious Okay. And no really no other

72:30 components to either of those things. , um let's look at this

72:36 Okay, what do you think about ? Any questions about thyroid problems?

72:48 , he said it just takes a like I said, it's still progressing

72:53 humans. It takes a while to if I assume it probably can mimic

72:59 dementia. I would think that those of things would creep in as your

73:03 slowly degraded. Um But yeah, it's it's slow progressing. So those

73:08 kind of the kind of things. see. Maybe motor function begins to

73:12 after the bad things. Yeah, not aware that they're there is.

73:20 don't think there is any kind of for that, I think to be

73:24 , I'm not really sure how far are actually working on that because it's

73:28 rare to get it. But I'm aware that there is any kind of

73:32 for it. Okay. Timer Oops. Sorry, mm hmm.

74:10 . Any strangling and jump in hurry . Okay. Which could not be

74:17 as the cartridge. You're right. gonna be can't ferment, right?

74:21 not gonna be like an e coli it's gonna ferment the sugar or

74:24 Okay. But certainly the other the are possible things you can use to

74:30 viruses. Okay. Kind of the is um the Baltimore classification which basically

74:40 what's what's the genome type and what's route to get to the M.

74:47 form where you can then translate into proteins? Okay, D.

74:52 A viruses that's fairly easy for us wrap our heads around because that's how

74:57 do DNA RNA protein. Okay. now the RNA viruses mentioned earlier can

75:04 a little trickier than the one thing have. Right, this is absolutely

75:08 viral enzyme. Is this an independent april embrace? Okay. We

75:15 What kind of memories do we We have a D. N.

75:20 dependent much different. We only produce S molecules from DNA templates.

75:29 That's not what an RNA virus It copies its art and you know

75:34 to make another RNA is a copy that. Right. And that's what

75:38 RNA dependent RNA polymerase does. So we would you carry those?

75:43 don't have that enzyme. It's a enzyme. Okay. And so um

75:49 the plus on a virus. The that directly is a template.

75:55 ? It's it is an M. . You can make proteins from that

75:59 proteins from that. Uh In the course the double strand has both

76:04 Plus and a minus. So you directly uh copy the the translate to

76:09 stream. The plus single strand of . Um is one that ah can

76:18 copied into a minus and then copied a plus. Okay, he could

76:25 form right here could serve right directly a as a template. Okay.

76:33 protein senses but it becomes a numbers . Right? Remember they always from

76:38 enemy. They make lots of You need lots of protein. So

76:42 one genome coming in isn't gonna really enough to make a lot of protein

76:46 quickly. So let's let's make more of that N. R.

76:51 The only way to do that is go through this intermediate. Okay,

76:56 , it's not because it's a It's because it's a nucleic acid base

77:00 rules. That's all it is. . So if you wanna make lots

77:04 copies of this then we have to lots of copies of the miners.

77:10 to make probably the plus room. , so the plus minus again is

77:17 um the relationship between the two nuclear acids, right? It could be

77:21 . N. A. D. . A. On your right.

77:25 just one of those the plus train carrying that coding information. Okay.

77:30 other one is the anti sense we it. Okay. And you can

77:34 the minus anti sense and copied into plus sense of strength. It's what

77:39 do when we're when we're carrying out translation, right? We're taking a

77:47 minus DNA strand and popping into a RNA strand. And that's the

77:52 R. A. That goes to right. So that's what we do

77:56 ? The virus is not doing anything . It's just following those base pairing

78:01 . Okay. So as mentioned right? The the the minus RNA

78:08 be copied into A plus and then retrovirus into D. N.

78:15 Questions. I'm gonna go over it . And you have to start next

78:18 . But you can hold on I go to lab those things that many

78:23 you do. Um But for some you do but so I don't want

78:29 hold you up. But we will we'll begin next lecture with this as

78:33 . So plus minus think about Okay. Yeah mm

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