© Distribution of this video is restricted by its owner
Transcript ×
Auto highlight
Font-size
00:05 Testing testing. There we go. . Okay everybody here. Okay.

00:18 so that's a little loud. Um if this is your first day actually

00:29 think last night midnight was the last day to sign up for any course

00:36 the university so um but if you sign up last night uh we don't

00:42 access to bible yet. Um But will you know either later today or

00:49 if you wanted syllabus just email me can send you that but if you

00:54 a little bit you'll have access to board. Um So what else?

01:00 we got the clickers remember uh I I refreshed again right before class so

01:10 you're like a late registering the clickers check now if you want or uh

01:18 after today I'll upload again. Pretty again today the points. And so

01:23 really just to make sure that you're your points that's really what we're doing

01:27 now okay It doesn't count for anything it will count thursday. Okay so

01:34 I'm gonna wipe the slate clean so I'm gonna delete everything uh thursday afternoon

01:40 I upload the points from thursday so now and then make sure you're seeing

01:47 points. If you have any issues to a thicker support. That's all

01:51 information. The syllabus. Okay There's uh go behind the library there's like

01:56 there's only one entrance behind you go to the basement U. H.

02:00 . T. Can help you with as well time. Um Alright so

02:07 week I sent an email yesterday. And that's the kind of emails you'll

02:12 every week actually twice a week Mondays Thursdays I send this out. This

02:17 just just as reminders um of course this stuff is posted on blackboard and

02:23 as well a few days for things whatnot. So um but it doesn't

02:27 just to keep uh inundating you so don't forget. Right? Um So

02:33 be the first weekly quiz will be friday through monday. Right? Those

02:41 things always cover what we talked about previous Tuesday Thursday. Right? But

02:45 will also cover last week so it's chapter one and whatever we cover in

02:51 three on thursday will be the weekly . Okay um remember. Right?

02:58 if if you're in lab if you're lab as well the lab quiz is

03:06 through sunday so don't confuse yourself. ? So thursday through sunday is a

03:12 quiz. If you're in lab friday quiz here. Right? So make

03:17 you've got those two things straight. ? Um and then there's the first

03:22 work it's time to do so uh reminds me so if you did sign

03:28 for a free trial. Okay. work that whenever you started it right

03:36 two weeks it's done. Right? make sure that you know you you

03:43 get the homework that once you get of the trial here that you transition

03:47 the non free period so just be of that. Um Okay, so

03:56 I want to start with was kind just a recap. Ok, what

03:59 talked about last time? Okay. just going here wait, there we

04:10 . Oh, I meant to put in. I had a major

04:17 Alright, this will happen that semester mean I'm getting seen now yet.

04:21 . Uh But I think uh I it was my class because of the

04:28 might have pointed it out. So you see something that's weird. Always

04:31 me out on it. Number I actually had written here in the

04:35 slide, I said marine microbes supplies of years or two. That's

04:41 It's not. It is 50%. . And I completely like I thought

04:46 was zero there I guess, but wasn't. But that is a true

04:51 , right? 50%. Not just factoid. Not that I'm gonna test

04:56 on it, but just to be . Alright. I just wanted to

05:00 that out and while I'm here, other thing is let me go over

05:07 . All right, this is a site. So remember that any any

05:13 you may see. So I come with different ways to present things all

05:18 time. And so I kind of thicker slides will be in here as

05:22 , but if you see something that you wait, I don't have it

05:24 my notes, you'll you'll always have to it where you find it is

05:29 this folder right here. Okay. many unit one folder and a sub

05:34 called quicker question signs and texture So that's where you'll find it.

05:39 , So um now this is this my view, right? You don't

05:43 you won't see. Uh of course see that that's from uh this is

05:51 is not yet reveal yet, but will contain a few other exercise that

05:59 see today. Okay, so always aware of this folder. Right?

06:05 take a look in there to see there's something there's always gonna be clicker

06:10 . That's where they always show But there may be some additional extra

06:13 . So that's where the. so just make a note of

06:16 Um And so of course each unit will have its own similar thing.

06:21 , so that's just something to be of. All Right. Alright,

06:25 enough of that. So let's go to this is for later. Let's

06:29 on to back to here. so uh a little bit of

06:35 right, so we talked about last , kind of the basics of microbiology

06:42 micro right there, microorganisms. Um is an exception to this.

06:48 viruses are the exception uh microbes you know, secular entities after viruses

06:55 self but we call them microbes. You know, they they of course

06:59 reproduce divide. Um They can they evolve and take in food and produce

07:07 . But again remember that viruses got of their own unique thing but we

07:10 consider the microbes. Okay. And we looked at a little bit of

07:14 uh who are the microbes? Right broken down to the different groups.

07:22 et cetera. Um a sailor of of course virus. And try and

07:28 a whole different entity. Okay. we'll talk more about that viruses virus

07:34 friends in the next unit. Okay kind of recapping here what we consider

07:40 microbes? Okay so of course the . Right. Some of those two

07:45 of archaea bacteria. Um So we kind of group more or less our

07:55 temperature loving halo files. Um And again viruses are kind of their own

08:03 micro group. Okay you should be with kind of the sizes, you

08:09 uh distinguished group. Right, nanometer of computer viruses? 1 to 10

08:16 , bacteria. Archaea 20 and above . So you should have you know

08:22 basic knowledge of that. Um Of which I'm sure you already know the

08:28 you Cariou um variation. So a word here is really um maybe perspectives

08:41 ? Because I don't want you to this. Okay I'm really I'm merely

08:45 showing you know here are what we microbes but then you have these other

08:52 or this other perspective on microbes. so some can be super science can

09:00 you know a bacterium is of course to the naked eye see themselves.

09:06 if if they happen to grow together a plate and then become invisible,

09:11 itself is not a microbe. It's up of microbe, right? Multi

09:15 micro animals. Right? These are tiny animals, but they are

09:19 multicellular organisms. But um and you know, your your own

09:25 right? Just to make up your or don't don't call those microbes.

09:30 they are of course because they're part a larger entity. Right? They

09:35 can really survive when the parliament So again, don't I don't know

09:43 you think is the right word, just presenting presenting to you some kind

09:46 here's what we know our micro terrorism of other things we see in that

09:51 . Okay. Any questions about So um then we talked a little

10:00 taxonomy anytime. And so um the here is Manera. Right? And

10:09 are the groups that contain your Okay. And so Manera is no

10:17 I don't think people really use that anymore. Right? Because now we've

10:21 uh let me just go over They're here. We've gone into uh

10:29 uh okay, so remember your domains was brought about through discovered through the

10:37 of the 16 S. RNA. ? Um the best way. Maybe

10:44 like a corn ball analogy. remember this this right? All

10:55 Okay. And if you want to a molecule for for comparison right?

11:01 compare among different life forms and related . Right? The analogy maybe if

11:11 want to look at the evolution of right, you probably wouldn't pick the

11:16 , right? Because planes of course transportation. But that's a later evolutionary

11:22 , right? It's characteristic. You look at the way that time transportation

11:31 back in the stone ages, anybody . So we look at the wheels

11:38 can make your way back right, can go back to the stone age

11:41 not beyond very far back in You can see when you can see

11:47 translates involved and go way back using characteristic similarly 16 right? Changed a

11:55 over time. You know without the right? We wouldn't have been around

11:59 make a square one. Right? wouldn't work very well. Right?

12:02 so modifications to the wheel, not for me, but maybe how easily

12:10 can rotate right actions. So don't too deep in the weeds of

12:14 But the point is that enables you go way back in time ships because

12:19 get revolution relationships and the life. it's how we discovered that there are

12:27 groups of and bacteria which is Right? And so um so so

12:35 endosymbiont theory explains, you know how . So we know that for the

12:42 life forms on earth and we'll touch that here at the end today,

12:46 at a little bit about the origins microbes. Okay. And then meta

12:51 . Right? So remember that uh your lab of course certain next week

12:58 this week we saw how liquid um week you're going to do your own

13:06 and do street plates and yourselves uh grow on a plate for you is

13:14 small fraction of what's out there, ? Because we don't know what all

13:18 nutritional departments are. The things that out there. Uh Very complex because

13:24 from your culture by themselves in a out there, they're among Thousands of

13:31 species of microbes and others. And so complex feeding uh cross

13:38 right. one. Uh So we know all the relationships and so we

13:48 factors that enable their growth. So why so many things that were not

13:51 to grow in the lab, but can't use it take a genomic to

13:57 , right? Which is basically just a sample but it's dirt or

14:03 whatever you think of. Then cloning pieces of D. N.

14:11 Using recombinant DNA technology. Okay. we derive a live so a sequence

14:21 sequences of everything that are represented in . Okay, you can use that

14:26 different purposes, whether it's that right? And then you see one

14:30 the types of microbes that are out in that environment, example without having

14:35 culture anything because we have mounds of . Right, mounds of data of

14:42 kinds of things that have been Right, Doing that for decades.

14:46 huge database of information that we can . Okay. That's how we can

14:53 identify something that maybe we can't culture proven to be a very um let's

15:02 . So any questions. Probably five . Oh, so, so um

15:18 . So we're gonna today we're gonna a little bit about um your medical

15:24 , uh ecology. Okay, and we get to the ecology

15:31 I'm gonna tie that in with I in this course schedule, the

15:41 our metabolism crazy like that report. so only and I'm doing it in

15:48 context of microbial ecology. Because as get to travel for Rose to get

15:55 to cover metabolism, these kind of things, um you need to

16:02 Okay, so when we get we'll go through it. Okay,

16:08 let's look at this question. This a question. Okay. And I

16:12 this every once in a while. call it like a before and

16:15 Okay, now, and I'll probably take a picture of the data and

16:23 we're gonna see the question toward the . Right? And we're gonna see

16:28 many changes you're gonna change your All right, everybody gets it

16:32 So, as with all these questions you see collecting questions you are uh

16:42 collaborate and he has better than All right, that's fine. So

16:48 fact encourage, right, we're not as your neighbor, they have an

16:53 . Okay, So, um and remember these don't count for anything until

17:01 . Okay, we're gonna put the on it, yep, that one's

17:11 . Okay. Mhm. So as looking at the question, remember spontaneous

17:30 of life from non life. And um as was mentioned after fast

17:41 a few people. Well, how life begin? Wasn't that spontaneous

17:48 Yeah, we have a different name it that we'll discuss that more toward

17:54 end. Okay, Alright, so gonna let it go to one

18:06 Oops, dammit. She's my Okay. Oh, let's see

18:17 Got it. Alright, so onward go. Okay, so pasture.

18:25 the pasture. I don't suppose anybody organic chemistry. Get Yeah. Remember

18:33 extra auditory laboratory molecules concept. I either. So that 40 years

18:42 But um anyway, I was pastor was the one that uh discovered that

18:49 , so he was the 1st 10 , but then he wore a much

18:53 hats. Microbiologist, certainly. Um and so um and of course in

19:05 this argument of spontaneous generation, he himself as well. Okay. And

19:09 we're gonna come back to that first of the big things he does here

19:17 this uh so chemical processes, He's a chemist. He's, you

19:22 , lots of chemists, you obviously you have a very active and

19:26 make products. Right. And so is all thought to be strictly just

19:30 what we call a biotic processes, biotic means something that occurs without

19:35 Okay, So in chemical processes were to be just that eight by from

19:42 product. But there's no other living involved in that. Okay, of

19:48 , that's that's what he discovered among things. Okay. And so he

19:53 in at the request of the french and the french love anything. They

20:00 wine, uh wine. And so was there were problems with production with

20:12 like vinegar or or similar types of taste, not good. Okay,

20:19 he was probably figure out what's going and this is how we discovered

20:23 Okay, so fermentation is basically the basic sense of metabolism without air.

20:32 . Alright. Anaerobic. Okay. so um so the basic equation of

20:39 is grapes. Right. And Right? And let it sit.

20:44 ? And that sitting part sit for while, it will produce ethanol.

20:50 . And so, um and of other chemicals that give wine taste.

20:57 . And so no thoughts strictly thinking is a biotic, no living things

21:01 . Right. Of course, pasture otherwise. Right. Because it's actually

21:06 . He looked under the microscope followed process and saw the company growth of

21:12 . So growing as possible. Making and more product. Right. Thus

21:18 conclusion is cells are what are generating ? The product is a biological metabolism

21:26 on here. Okay, it's a process that their current here.

21:30 so um attributable to East. the question is where these come from

21:39 and water and suddenly your wine, the East at this way for thousands

21:49 years. Right. But it was or pyramid yeasts are where anybody's guess

21:57 we have a few choices here. . Where on the there on the

22:05 . Right. So um or whether hops to make beer, you can

22:11 microbes that are on the actual fruits whatever you're using it for me.

22:16 , And that's the source. Nowadays, of course we have.

22:20 said all kinds of yeast strains and special yeast strains for wine and beer

22:26 , but this is where they Okay, so um but alright,

22:32 if everything goes right, you only this process going on when you have

22:37 microbes introduced, then you can have products for reform. And this is

22:42 you have on right. And so those of you that you too you

22:51 to drink. Okay, assume. if you go order wine in a

22:56 and the guy brings up the bottle he pours a little bit for you

22:59 have a taste, right? That's see it off. So,

23:08 that's what I said. But um , so uh so this comes from

23:16 , of course, right contamination and know, um heat things to eliminate

23:27 what microbes and these kind of especially in milk production. But um

23:33 you know, basically the takeaway here , you know, clean up the

23:36 and how you're doing this to eliminate . Okay, so this out of

23:42 comes a german theory of fermentation um basically says um these these transformations are

23:52 through through so that your micro um the the production of the products

24:02 accompanied by increase in cell numbers. . Which which you can draw the

24:08 ? Okay, microbes are growing and Medtronics. Okay. And that he

24:13 even um microbes that fermented. This fermentation we're talking about. They could

24:19 different products, not just to see gas, it but things like formic

24:22 , appropriate manic acid, uh mute ethanol, different typically short organic alcohols

24:31 uh assets. Okay, and oftentimes one could be that specific for one

24:41 one and product and he could, figured that out. Okay, so

24:46 running theme here is what's in the . Right, So conversion of organic

24:51 by. Okay, so kind of that in the back of your head

24:58 a couple of slides, we will that idea. Okay, so back

25:03 spontaneous generation, so we looked at at the end last time to say

25:13 microbes can only come from so that this kind of experience, of course

25:22 step one is to uh take your . Ok, and these days it

25:29 have been literally like a soup beef or something like that. So they

25:34 to sterilize it, Kill anything that's there and then the 22 um the

25:43 and the variable so the cooling it then leaving the flask open.

25:49 Or sealing it. Okay? It sealed. Never had growth. If

25:54 expose the air you had growth. he had the idea that okay,

25:58 stuff in the air that's falling into , that's causing growth. It's not

26:02 . Okay, of course, that's what those people said, they

26:05 Yeah, this this is a spontaneous . Okay, life coming from non

26:11 . Right? When it was there was no rush. Uh doesn't

26:17 follow the principles you have to have right yet. That final force air

26:26 convinced and ingeniously, just through the design of his flask right, creates

26:32 situation where air can come in. that's the films, the criteria for

26:39 spontaneous generation. People we have air , but the way he designed the

26:47 opening of the flask, right? the swan that flask traps microbes by

26:53 . So air contaminants typically are hitching ride on particles and their pet dander

27:03 particles, etc. Right? So you have to wait for gravity to

27:07 of trap them, which this does you are allowing Aaron, but you

27:12 get contamination of the liquid medium. so you only ever saw growth if

27:17 get the faster touched that the contaminants are in that crack in the neck

27:23 you or you simply just snap off neck, right? Break it and

27:28 it to air. Then you get and so he can see under the

27:33 that uh these contaminants from coming you originally from the air but but he

27:39 the criteria right? So this remained and it was exposed to air.

27:44 so basically life can only come from existing life right now. Yes life

27:53 on this earth obviously by you know being not about that at the end

28:01 aside from that event right, everything his form today is come from pre

28:07 life. Okay. And so um so subsequently you know if you look

28:13 just what is in the air and samples from a tabletop bench top and

28:18 and see that micro was basically Right? In terms of what he

28:23 doing, right? Air or surrounding that these things are everywhere. Okay

28:29 in lab this week, if you're lab you're finding that out if you

28:33 a set of plates where you can air um so and you'll see micro

28:42 gonna pop up right on tomorrow or whatever day lab. So that's why

28:49 have to work with, you have do so in a way that you

28:56 introduce unwanted microbes that's what aseptic technique . So next week. Okay,

29:07 eliminate anyone microbes because we know that . Right. So um and so

29:15 course these when these techniques were developed with gross medium and we'll talk about

29:22 in a second. So, um Tyndall was a guy who repeated

29:32 but significantly there were times when he textures. Okay. But sometimes did

29:42 growth in the classics even after Okay, so basically he's the discoverer

29:48 in those four forming that 30. talk about those guys a few

29:53 But in those performers are existence various , temperature radiation ph Okay. It's

30:04 why we have to use an autoclave sterilize things to kill in those performers

30:10 most other non in those performers are much killed in the first minute or

30:16 of an artifact treatment. But you to be more persistent to kill in

30:20 performers because we're so resistant. And when he found out he had to

30:27 , right. So here's a typical those performing bacteria. Okay, so

30:32 white uh if you will, that's what we call it. Don't worry

30:40 for I think it is. But so these are completely sports here.

30:48 on the set. These are completely cells right here, a vegetative

30:55 simply just a functioning reproducing cell Call it the normal selling.

31:01 Um and so this is a cell here that's in the process of

31:07 Okay. And this is one that , has formed it. Okay,

31:11 you have like three different types typically , so do um sorry um cycles

31:22 so as you boil it. Any of these forms you see?

31:30 uh of of these forms right my pen's not working now. Hold

31:37 . Okay. Any of these forms vegetative types. Those are the ones

31:43 to being killed. These types are these are kind of somewhat in the

31:51 . Okay, Depending on how far they are in their sport formation.

31:54 . But these are resistant. And so as you boil it and

32:00 the vegetative types of rest, when it comes back down and then

32:05 end of sport type, some of with Germany Germany needed to make to

32:11 into uh Find one. Here we . You turn into one of these

32:20 that to a vegetative type when you a seed pour water and so is

32:33 . So what you do is as alternate and everything is killed.

32:46 So that's what you found out you to do it again. This

32:50 this is why we have we have lot of these things, right?

32:55 there's as you learn a few there's two major groups with was the

33:05 that botulism. Right? These are those performing types. Okay. But

33:16 is there's not really too many bad now except for and racks aside from

33:24 , most of those are just kind benign soil bugs. But anyway,

33:28 any questions about that. So um I said, we'll get more nuts

33:35 bolts and those performers later. But okay so so back to this idea

33:43 pasture and in um microbes are responsible converting organic material to end products.

33:57 the idea becomes, well, others these human bodies of ours, these

34:06 organic material material. But um particularly here me at least so maybe disease

34:25 they're transforming the organic beings into Eye disease state. Okay, so

34:33 that's the idea of okay maybe I'm saying is the one that is not

34:38 one that figured out just disease Right? That right? That was

34:43 idea going around, right? So of uh within study and that's what

34:52 study. And so this chain of attributing a profession disease to a specific

34:59 okay. And so right out of box, he he struck pretty

35:07 Okay. But that I mean I take a lot to establish that uh

35:13 he looked at Angela is a disease his time uh he got the country

35:22 a country doctor and so he saw of cattle coming down with this and

35:25 he lived. And so he saw the disease blood the microscope and bam

35:34 saw uh so obviously you look at blood sample you shouldn't have seen.

35:47 . And so obviously signals a septicemia call it a reflection of the

35:52 So and so he saw that And okay, so that became kind

35:59 pretty easy to make the connection. , now get a little more difficult

36:04 you look at tuberculosis. Okay. so the this required a second.

36:15 he couldn't. So it's very disease disease of the lungs. And people

36:22 tuberculosis had a hacking, hacking persistent cough and congestion. So he would

36:30 at uh samples of like flan of and it's kind of hard to find

36:38 right? Because the organism is rather . Okay. You can see in

36:47 context of uh bacteria maybe there it be difficult to not as easy as

36:56 , you see. Oh yeah, definitely bacteria in there. So that's

37:00 it required isolation isolation. And uh is the development now of all these

37:07 techniques that you're learning in lab next . Um street play um technique types

37:16 , right? Um and that that's was developed. So he could isolate

37:22 tuberculosis organism. Okay. And so the of course this it's almost like

37:30 rules, Not surprisingly from this point which is like 1867 from that point

37:38 for like the next 30 years, call the golden because now you have

37:42 vehicle to isolate my and study. this had applications all over us,

37:50 ? When you were a microbial Ecologist immunology or whatever. Now you have

37:56 method to isolate grow stuff and that that's why I feel this exploded after

38:04 time. And so um the and as I'm sure you know right.

38:10 you take a sample the there's and are um um different forms of

38:18 right? Basically just a supplying the elements you need to grow. But

38:24 can put it in different forms. can be a liquid solid, different

38:32 for different types. Um I'm not go into all the uses but the

38:37 basic right liquid in place. That's you use in lab liquid cultures and

38:41 cultures. And so um labor cultures used in Monitoring growth because a culture

38:52 in the liquid. Um this appears much clear, but as right.

39:00 we can measure that. So you measure growth using liquid. Uh and

39:06 you can even grow grow and that's about 50 mils you can grow again

39:17 , you know here in 50 m gallons. You want volumes of

39:24 Okay, that's the utility of liquid . Solid media will always be a

39:31 of getting into your culture. But absolutely not. Because that's that's

39:42 allows you to visualize the bacterial types you see in the plate here.

39:50 What's there? What's in what's in liquid? Okay. Yes, you

39:56 look into the microscope a solid surface mean, okay, different colony

40:13 And that's how you can then do manipulations came up your culture. So

40:18 know it seems all very amazing, ? But these are things that are

40:22 to this day. Um Even even the advances of meta genomics, you

40:27 do this stuff. Okay. Um okay. Any questions at that

40:35 Okay. Alright. So here's the . This is not this is not

40:40 this is not the same one from that was coming later. This is

40:44 different one. Okay. So which A. D. E. Is

40:51 is consistent with coach postulates. So take a read. All right

41:06 I'll give you a hint. A not So it's one of the one

41:17 the above Ron. Give you some . Remember two heads may be better

41:57 one collaborate. Forgive me. let's count down from four if you're

42:17 sure. So we're here to figure the dramatic pause. Okay um if

42:29 answered, if you answered, you are correct. Okay. So

42:39 that is one of the a healthy uh with disease causing symptoms of that

42:49 . So A B. C. D. He thought it was really

43:00 1 to 1 relationship. One One disease. Okay. Um He

43:06 not aware because what what what is . So that's the um he wasn't

43:21 of that. He didn't think that people would have could carry infectious organism

43:24 not have disease. But that's certainly case many of our infectious diseases are

43:30 that uh, occurred because a healthy carrying a source is president,

43:42 uh, measles and mumps, lots different infectious diseases are humans. That's

43:49 we called reservoir source of it. ? So it could be a healthy

43:53 as a source and other people get . Um, the uh, let's

43:59 about the rest of these in the of his postulates. Okay. So

44:03 one, just because you have to , we have like um boy,

44:10 plus years of knowledge since devices So naturally we're going to know a

44:17 more things that he did. But it doesn't mean that he came

44:21 with you just throw out it's still the CDC Center for Disease Control uses

44:26 framework. But we're now aware of of the anomalies, some of the

44:33 that may occur. Okay. but his work still holds. We

44:38 know I have more information. So essentially what he did was

44:42 looking at the tuberculosis was using animal is critical to any kind of

44:49 We do this. And of course only saw the disease and healthy in

44:56 individuals. Animals, not in healthy . Okay. And he could isolate

45:02 infectious agent from the and we now , of course you can't isolate everything

45:07 . We still haven't isolated the syphilis we know about that for a long

45:13 . Right? We have yet to able to cultivate it in the

45:17 Okay. Uh he was fortunate that was able to do all this just

45:21 locked in and he was able to for, right? But of course

45:26 we know that it's not always so . Okay. Um and so I

45:31 in the culture and pure culture and putting in a healthy susceptible,

45:38 And that animal comes down in terms the same disease. Okay. So

45:44 in this is the re isolation. ? So you're you're you're really isolating

45:49 organism each time. So that's very . So let me corroborate something.

45:57 ? Repeated, repeat the results. powerful information that leads you to believe

46:04 this is because of agent of this . Right? So like I

46:08 we have exceptions to this, For variations of this asymptomatic carriers?

46:14 It's not always when disease. One , for example, qualifying number of

46:20 things that can be bacterial and viral be uh fungal, I think maybe

46:27 a couple of instances of that. it's not always uh one disease.

46:32 pattern. It could be multiple Um One pathogen. One disease.

46:39 you can have um for example. Right. It also causes different types

46:50 skin infections. You heard of the flesh eating disease, Right? Causes

46:57 can cause a number of skin infection . It can cause rheumatic fever.

47:03 can cause scarlet fever, different Okay. So it's not always a

47:09 relationship with these things. Okay. we mentioned culture building that everything is

47:15 culture. Like you can't isolate the . So viruses, right? Those

47:20 uh have not yet been discovered uh microscope to see it. Right?

47:30 you have to use you can't you to have uh that really complicated

47:37 So, um but again despite the variations, you know, you still

47:44 framework is still something you stick But you know, what can there

47:49 be differences as you go through the . Um Any questions about that?

47:56 . Yeah. Yeah. I think was probably the thinking at the

48:04 Yeah, of course it became qualified , but when he was first working

48:08 that, that was the assumption that the time 1-1 relationship because it was

48:14 of a difference, right? We really know a lot of sex organs

48:17 that time. So as we learn and more after that we can see

48:22 , you know, multiple things that the disease and so forth.

48:26 Alright. Um okay, so fighting . So immunization, vaccination. Um

48:36 first, it used to be um vaccination came into play um early on

48:43 like the term very lazy only refers smallpox and that's a basic, taking

48:52 some kind of nice and cut uh smallpox forms forms a rash and pustules

48:59 the skin and there's an accurate virus these in these pustules. You take

49:03 material and you would cut it into healthy personal skin but it would make

49:10 abuse the disease most. Sometimes they because you're giving personal full blown small

49:17 . Right? So in some cases die probably uh 10 15% of

49:25 Right? But but if they smallpox they survived it and they were

49:35 Okay. Of course. Now we things more safely. Okay. And

49:42 and to do it more safely means attenuate, right to attenuate is still

49:49 the new response. But we've inactivated . You can do it through temperature

49:55 activation, inactivate the virus or But the goal there in continuation is

50:04 um keep the I think we all the pathway of immunization at least the

50:10 . Right. So you have a enters your body and the entities

50:17 That your body looks for antigens, ? Antigens on the virus or bacterium

50:21 what have you. You form antibodies . Okay. And we'll talk about

50:27 later in the semester because it's it's more to it than just this.

50:32 I'm just kind of giving you the right now. But antibody and you

50:37 um antibodies to engine could be anything for a virus, bacteria. That's

50:44 on the surface because that's what your sees as what's on the surface of

50:48 virus or bacteria. Alright. Uh are things like or or viral coating

50:56 out, right? These are potential And that's what you form in the

50:59 response to? So what you wanna continuation is to limit or inactivate the

51:07 or bacteria. So it can't cause in you but still retains the ability

51:13 to stimulate the immune system. So the Covid vaccine does the same

51:19 . Okay, engineer a little But we'll talk about vaccines and things

51:24 . But that's kind of the central here is have the antigens intact,

51:30 ? The immune system, but not to cause disease. Right. That's

51:34 that's what we do when we Um And so so Jenner and his

51:41 he had a safer alternative, smallpox was cowpox, very similar disease um

51:51 cows. It only produces like these on his on his others females.

51:57 But he found when he injected cowpox it resulted in immunity to smallpox as

52:04 . What's the in terms of that financial curry anyway. Well, guess

52:17 that's what we call uh in geological cross reactivity. Okay, So if

52:24 engines are similar cowpox and smallpox, ? And you get a reaction.

52:31 ? So safer alternative. So the are very similar to what smallpox

52:37 And so you produce kind of antibodies will react also to smallpox, that's

52:43 that's a good choice because it's gonna obviously much safer for the person getting

52:46 vaccine? Um Alright. So look this question while you're answering. Are

52:59 any questions so far? Yeah. , activity needs. So they have

53:09 they had very similar and so their responds similarly to so Yeah.

53:25 I put this one in because this one of my pet peeves.

53:31 And you'll see what that is here a second. Okay. So we're

53:37 have this done arm there we get shot. Okay. Let's count down

54:04 six. Let's speak now. Alright. Um Who answered C.

54:23 in cat? A lot of All right. Said see why do

54:29 say? See what's the corrector? quite you know, correct anybody know

54:44 right. But what's the firm anti ? So, I didn't sterilize

54:52 If you sterilize it, then person would have the arm. Right?

54:57 you put that or? Right. Disinfected. No disinfection is um reserved

55:07 inanimate objects, bench tops, uh floor, maybe more harsher chemicals can

55:15 used because of that. So, acceptance of the terms. So if

55:18 have your isopropyl alcohol in the employment or any kind of chemical that you

55:24 tissue, tissue and sepsis. So tattoo is really the the misuse of

55:31 term sterilization. It's not always right . You know, you didn't um

55:43 if you sterilize something, whatever you , there is no virus etc.

55:51 you sterilized, right? And you're not doing that when you're rubbing your

55:56 . Okay, so we're talking about control of microbes in Chapter five I

56:04 . Okay. So uh speaking of disinfectants, uh his story is work

56:18 the doctor from the hospital. Uh noticed that in the maternity ward there

56:24 a ward, pregnant mothers and also separate one that pregnant women would work

56:31 midwives write another section where uh the medical students, right? But the

56:40 that would check on the pregnant women help them to their birth. And

56:45 often they would come out of because have different rotations in different parts of

56:51 curriculum. And so they often come of the room, right? Full

56:56 blood and everything else without seeming or of blood and blood and guts and

57:04 else, right? And of course was very much higher instance of what's

57:09 child bed fever. Right? So infects uh affects the mother,

57:15 It's actually a streptococcus infection. But comes from certainly from unsanitary um

57:24 Okay? And the midwives are much , right? They knew what was

57:29 on. So they didn't clean their and everything before any kind of touching

57:33 woman and checking the baby in the much lower. So someone's goes,

57:39 , let's wash hands. Not washing . The instances of it's still the

57:45 one thing you do in the You constantly are on the hospital.

57:50 wash your hands, wash your That is the number one thing that

57:53 transmission of diseases in the hospital. , from patient to patient. So

57:58 still to this day washing your Okay? But that's an acceptance that

58:04 tissue Lester disaffected like surgical instruments and using various chemicals for disinfection. So

58:11 of these practices of course lower levels infectious disease. Um So antibiotics,

58:17 course, we know about antibiotics and Fleming discovered. Um and so of

58:24 we're certainly well aware. Don't only these images in there just to give

58:29 a visual. We'll go through the of resistance, but for now don't

58:33 about it. But broad aware different that bacteria resistance. Um multi drug

58:41 types. There's uh we're constantly looking antibiotics or chemically modifying the ones we

58:50 to kind of tweet them and maybe them less resistant. So it's certainly

58:57 because they evolve them and then we to kind of active. Okay,

59:03 , okay, now the last bit this is focused on. Um so

59:18 introduction because again, certainly too heavy that we learned a couple of basics

59:29 first. Hopefully that'll help. So, so question. Hey,

59:34 trophy wife uses inorganic materials for Okay, um Okay, so here

59:43 a sample growth meeting. Okay, we've got to s for energy.

59:51 had some essential minerals right? To adequate oxygen. Um Right temperature.

60:08 , so the question is, what ? This is even a clicker

60:14 So sorry, nothing to choose Okay. All right. So what

60:21 do it need? What else does need is yeah. Okay, water

60:32 say okay, water. Okay, . Anything else? What car?

60:40 ? Okay, so carbon. So if we know that, how

60:50 you suppose this guy? Yes, but for you say it would be

61:03 like this. Okay. Or this glucose. Yeah, the C.

61:24 . Right? Um so trucks are we call the type of your familiarity

61:33 patrols. I'm gonna guess this Probably plants, plants uh, photosynthetic

61:41 . Right? These are autotrophs, ? They use fixed C.

61:43 Right? But there are bacterial Right? Uh So uh so the

61:54 is, right, everything on planet needs this. Right? So remember

62:02 H O N. P. Right? Essential elements for life and

62:15 . Because all of our biomolecules have as a framework, right? A

62:25 skeleton of some sort. Right? we add phosphate to it to make

62:33 . Uh you know, the point so Right. But it just so

62:46 that some can use what we call more complex forms like this. They

62:52 have the more simplified forms. So , because you can't you can take

62:58 and break it down to something And that's what you do. You

63:05 , I want to use a C . You can't break down C

63:09 You can only build it up six 02. You're making you're making things

63:16 this, you're going this way. , If you're not a trophy,

63:21 taking C. 02 as a building to make these more complex Or if

63:25 are a hetero trough, which you are, you're going that way.

63:31 breaking that down just to feel your . That's what that calls us

63:36 The respiration is all about. So cycle between each other. Okay,

63:44 now, uh this is a So producers. Right. So,

63:53 , you have etcetera. So producers but Sheriff give you a hint.

64:20 are not carnivores. Probably that Right. Okay. Let's count this

64:32 . 4321. Yes. Autotrophs. . Right. The autotrophs are the

64:41 really for any ecosystem. Right. the most of any ecosystem plants?

64:46 . Ecosystems allergy santa bacteria. So producers produce right 60 oh to

64:54 organic molecules that different levels of consumers on. Right. And so among

65:03 , corner wars are different types of . Okay. The composers are kind

65:08 their own category. But let's kind bring this back. He's the one

65:14 discovered these unusual inorganic materials. Little means like to as a carbon.

65:34 , so hence the term with a and chemo. Autotrophs in attainable.

65:40 , so, um, and so the term, you'll see the next

65:46 is this term redox. Right? , reduction reactions. Right,

65:53 Right. That's oxidized are complex. sources that uh a little trophy would

66:05 these materials and get energy from Okay. And for or indeed any

66:13 was like for or The energy they from oxidizing these kinds of inorganic materials

66:23 goes to fixing c. 0. five minutes 222 is a very energy

66:37 process. Um Okay, so the fundamental types, right? I know

66:54 speak from 18 years of teaching us lot of especially we start combining that

67:06 fundamental idea of life needs carbon. sometimes to see, oh to form

67:14 sometimes we make more complex form. You know both seo two and glucose

67:21 both organic carbon. Right? It's more simpler form and break it

67:27 So kind of certainly those things sink . Okay. Um We did chapter

67:35 growth certainly will get the next unit that these things like give go to

67:45 um the composition very important process, ? Um producer become So composers are

67:59 eat right? Eat that organic Okay. And so that activity is

68:05 that really brings the different points of and makes them available to others for

68:12 to use keeps the whole ecosystem going . So in in these different levels

68:19 here here here, where are Oh yeah my first the producers and

68:32 consumers, those decomposes during all levels over the place. Okay. Um

68:38 why they're so important for us our . Um So this geochemical cycling is

68:44 we talked about when we were saying decomposition about my criminal activities can bring

68:51 the breakdown and the release of these that are in your life and make

68:56 more available. So that's what this cycling is about. Is making these

69:01 of nitrogen no C. H. . M. P. S.

69:04 everything needs to make them available. and so we'll talk about nitrogen cycle

69:10 in more detail later but it is of those critical um functions for.

69:16 heavy. It's basically all bacteria that all sides of the triangle.

69:21 And it's what life relies because I before um plants allergy your photo as

69:30 as they are is giving some light water. They can't make essential elements

69:36 nitrogen and phosphorus. Right. Which ? So they rely rely on this

69:41 cycle. They rely on on this Okay on this process to provide them

69:48 forms that's what plants primarily reliable. use things like this but then to

69:54 it into the atmosphere. Okay that's process. We got to get it

69:59 the ecosystem. There's bacteria that do super perfect. Right then of course

70:04 others that other activities that release So d identification puts it back into

70:09 atmosphere so it's constantly so and again sides all sides bacteria drip during my

70:17 types of bacteria. Okay I just one is the third trophy, anybody

70:23 a guess. A. B. C. C. Is correct that

70:31 trophy is this is C. I'm , it's not C. B.

70:36 has to call me out on that . This that's little trophy.

70:41 we're taking energetic material, ammonium, energy from it. Okay, that's

70:51 little trophy. Okay. Um Endo symbiosis. Okay, so your

71:01 with your microchip? That's so kind notch symbiosis because intimate, intimate

71:15 right? You certainly have somebody else your micro right there in your gut

71:19 on your skin. They're all over . Okay, just like cow

71:26 different microbes uh digesting its new about . Uh This this right here is

71:34 , this is primarily responsible for this , the fixation. So different types

71:45 association with plants. There's bacterial plant is very very important. Okay and

71:53 um so lastly, Okay well you what let's this is we only got

72:03 two things to go. Let's just that we only got two more things

72:07 cover. So we'll do that next folks, so that you get the

72:11 truck through this truck, through this , bad weather, um See you

72:17 on third.

-
+