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00:05 Okay thank you. Thanks. Hey welcome. Um So um if you

00:43 added the class you'll have access to . Uh It's not my now because

00:51 with yesterday's last date ahead of so if you have it yesterday you

00:55 have blackboard access and not today certainly tomorrow. So that's you do go

01:01 blackboard, check out all this stuff and uh watch three quarter lectures catch

01:09 . Um I just realized I I bring my receiver That captures all your

01:19 information, so we will have a questions today, but I got no

01:23 to receive your prompts, so they count for anything right now.

01:26 so September one, which is the day. They will obviously remember to

01:31 it then, but uh my apologies we'll still do the question will still

01:36 questions which uh I just need to to have that, not forget it

01:41 time. Um So do I do you were here last week and you

01:47 it bigger, I refreshed multiple times the clipper points on blackboards. So

01:57 check if you did use it last to check to make sure you're seeing

02:01 I'm seeing points. Um The other is I'm gonna post, I got

02:06 email from learning the on campus clipper . Uh There was a handful of

02:14 that I remember the email right, were created their account with a personal

02:20 address and that can create problems. ? But that can be fixed but

02:25 have to contact the clicker people and have a contact number for them so

02:31 post on blackboard uh if that's you and they can change the email

02:37 we just can't do that on our here. They do it. So

02:39 that's you they will be able to that, you just need to call

02:43 number okay and I'll post that on work. Um Points. So points

02:50 two points for questions no matter what answer. Two points Okay? Uh

02:55 point for that. By one point just you know using think so but

03:03 the the threshold there is 50%. for example if you have we have

03:09 questions in in on a day and answered four questions you can get four

03:18 to eight points plus one point for it for attendance, they called participation

03:24 what it is called. So total nine points. Okay? So uh

03:31 you answered less than half The answer one of the four questions, you

03:37 get the attendance point. Okay? it's a 50% question, so you

03:40 to answer at least half the questions get the that one point.

03:45 But again for any questions you answer you respond is two points.

03:50 So uh do check blackboard if you the clicker last week, just if

03:56 getting you see your points. Um but we'll start on thursday and if

04:03 do have if you use your clicker and you might not have it registered

04:11 , the points will be there, not a sign to a name,

04:16 once you complete that part of the then there will be assigned to

04:21 So the points will be there again you haven't registered it yet but your

04:25 as soon as you registered then bam assign the points. I don't think

04:30 using a clicker but haven't registered Those points are there, they are

04:34 not time to a name yet so might as well. Um So this

04:42 stuff begins to be some kind of routine now is basically the two bottom

04:49 because so those cover what we just here on the Tuesday and thursday

04:56 Okay 5 to 10 questions summer. okay. Um you have through opens

05:05 you'll have through monday to do it that's monday 59 P. M.

05:12 mastering. So I think pretty much may be a couple of weeks maybe

05:17 but check the schedule that mastering science do each week I think, but

05:25 the schedule is there on blackboard. Take a look but that's the first

05:30 is coming up. Okay. Um questions. Okay so remember that you

05:41 not know when these things do right when you go on the blackboard bam

05:47 schedules are right there in front of for all these things. The syllabus

05:50 the schedules, the reminders, I you twice a week until you do

05:55 . So you literally can't not know is due or coming up. Okay

06:01 I do pay attention to that. so we're going to finish up this

06:08 here today. Okay and uh we're begin with a question but I forgot

06:15 receiver. So we'll kind of do . Yes this way. Alright so

06:20 are meant to be a question that also going to appear at the

06:27 So you kind of get a feel what your answers are now compared to

06:31 they would have been at the Okay so since we can't really do

06:35 let's kind of go through looking for true statement. Okay so a pastor's

06:41 germ theory of communication explains the nature infectious disease problem. Say false say

06:59 . Three you said. Is that ? Come on. Come on.

07:07 cuisine. What does did anybody read ? Okay. Any notes before

07:17 Not good. What does the The germ theory of disease goodness.

07:26 is not gonna be good. All so uh false. What about

07:32 This is that's ecology. 101. probably learned that in grade school,

07:38 speaking you are a producer. What you consider? Absolutely in all senses

07:45 the Lord humans are considering um The . That goes back to last

07:53 Archaea. The simplest of the eukaryotic . Pro okay but not you

08:04 Um Common cold is considered an I. D. Emerging infectious

08:10 Also it's been around for a long . We'll talk about the I.

08:14 . S. At the end. you're the I. D.

08:17 What's a what's an E. D. Everybody in here should know

08:22 now. Okay. Okay that's an . I. G. Um Handwashing

08:29 soap equal disinfection, sepsis. Okay is handwashing her D. Germany they

08:40 call it okay vaccines work by stimulating body to produce antigens and antibodies not

08:47 . Okay so none of these are . Okay. Alright so we're gonna

08:53 on all of these aspects today as close out Chapter one. So so

09:01 again. So here are some things barnacles, barnacles, barnacle is a

09:11 right there. Hello Chris Station on side of the museum but on the

09:19 of rocks and thinks it's a marine . There's a example of one um

09:26 the middle there is in the middle the this guy here that's a barnacle

09:37 that type. There's also a barnacle goose goose, barnacle and barnacle

09:42 . Okay good veins. But at time uh here are the barnacles here

09:48 they're giving birth to yeast. Okay sounds pretty cool. Um Then you

09:54 uh dust creates please. Money soiling rice. The frogs. You think

10:00 these days. Uh My cell I used to always see lots of

10:04 jump around after a heavy rainfall recipe produce mice. Here's the reference

10:10 This guy actually had a recipe to mice. Okay, place sweaty underwear

10:15 husks a week open jar container, keep it 21 days and bam.

10:20 got mice. Okay, So these describing what, what are these examples

10:29 ? Okay, the example of how natural world actually operates it biogenesis.

10:39 biogenesis. Is it spontaneous combustion spontaneous ? Okay, so it's uh none

10:47 these so spontaneous generation. So, talked about that at the toward the

10:50 last time and the vital force. those people that believed in this concept

11:01 find life from nothing, right? that any kind of organic or even

11:08 material rocks, uh, could give to life under the right conditions.

11:15 what condition was there's got to be President? The violent forces? Air

11:20 , to write about um you have combinations and you know, you can

11:26 have life form. Obviously, we that's insane. We've looked at that

11:31 experiment with uh lies hanging around meat . Right? So they thought the

11:40 that sprang out from the meat from the meat itself, right? The

11:45 generation, of course, was the langley on the meat and laid the

11:50 were the ones producing the maggots. , by this experiment, just you

11:55 error because that's cause uh, air . So air is getting in

12:00 So it fulfills that criteria. But not seeing spontaneous generation. So became

12:09 about this and similar experiments that maybe spontaneous generation doesn't work for complex

12:16 , you know like maggots and mice frogs and things. But then of

12:21 the discovery of microbes gave them gave you know these people another uh venue

12:30 microbes, it can happen with them not with more complex things. And

12:34 that was we saw experiment with right broth and a vessel.

12:42 And boil that broth and it's no in there. People exposed to air

12:50 you actually. Right. So that their argument. There you go.

12:56 can form spontaneously. Uh So it until pasture came in. Okay that

13:03 put that to rest that idea. so he had his hands a lot

13:08 different areas. He trained chemist. he ran into microbiology chemistry knowledge was

13:17 to use because we talked about last with the uh wine production. So

13:25 , you know they're paying one of things wine alright, they are connoisseurs

13:31 wine. And wine production in France of course a big thing and uh

13:37 was an issue with somebody's wine But the taste was totally off.

13:43 so Pastor comes in, looks at process and the big contribution here in

13:49 of microbiology is for the first time show that chemical transformations okay, converting

14:00 , organic materials, chemicals to other can occur due to the action of

14:06 . Okay. And that has implications lots of areas. Okay, because

14:12 also. Yeah, well, I'll to the second. The so the

14:17 equation here is grapes, which which course are carbohydrates and sugar.

14:22 And yeast. The absence of which is what he's studying here is

14:30 . You do this through muscles do when they get fatigued, they will

14:34 produce lactic acid, that's what makes muscles so. Okay. But this

14:40 course is fermentation as well. And uh the key here, he would

14:46 take samples using examples out of the with the microscope and see cells that

14:54 time became more cells. Okay. that cell growth was accompanied by more

15:02 more product in this case ethanol alcohol filmed. Right, So more sells

15:08 alcohol microbes are producing the alcohol uh analysis to prove this microscopy, to

15:16 the member ourselves growing to see if are cells there in the first place

15:21 it was thought before this that this was strictly just chemical, no biology

15:27 at all. Okay. And so off taste of the line often that

15:33 taste is due to contamination bacteria enter process annoyingly. Okay, and created

15:41 bad taste of the wine. And is kind of what led the road

15:44 to not just for wine but other and foods, the pasteurization process.

15:50 ? To minimize mike these microbes uh too spoiled food or drink.

15:58 And so he then studied his further found that there were a number of

16:05 bacteria that could carry on different Right. So I see the acid

16:11 is that irritated. Right. And other many other types of organic

16:16 alcohols and all being alcohol and mostly of short. So smaller organic

16:24 alcohols were produced by bacteria. And can see that there were different

16:29 bacterial types that produce certain types of products. And so he basically cataloged

16:36 this, described it all. This becomes a germ theory. A fermentation

16:40 one. The production of these products do the microbes microbes growing and uh

16:48 of lots of product you can differentiate is producing rich product so forth?

16:56 produced mixtures. So um uh but , the overriding theme here is converted

17:03 organic material by microbes. Okay. just a chemical or a biological

17:08 And so just do that question in because east um um why beer production

17:15 been going on for centuries before for time. It's like maybe 18 hundreds

17:20 fact. So uh and so these the ones that carry this out where

17:26 come from? Because there was no thing as going to the store and

17:31 yeast off the shelf and dumping it it is what what do you think

17:36 source would be from? What have got? You got one of the

17:42 to make wine for example, anybody any other thought, where would the

17:46 come from? Yes, it's the of the grapes, grapes are on

17:55 , obviously, like they will touch soil, or there's other sources not

17:59 the grapes, but also hands. got beast on your hands like it

18:06 not. Okay, so handling the introduces yeast as well. Okay,

18:13 they weren't wearing gloves have been doing . So uh that's a source source

18:18 these things. And so nowadays we all kinds of yeast strains that are

18:23 for everything, but not then. the conversion of organic material becomes

18:31 microbes, um really becoming a focus idea because the focus in the context

18:41 medical microbiology, infectious disease. What's connection there between this statement at the

18:50 and infectious disease? R r is this thing? This is organic

19:01 Uh it is organic, our bodies organic organic. Um so the not

19:15 disease has has been done by the before. So I thought began that

19:20 organic, these organic bodies can be disease, steak can be attributed to

19:27 micro infected. And by right, that, you know, that idea

19:32 of uh takes hold. And I'm not saying this, this um

19:40 does not explain how infectious organisms No, but just lays an

19:47 oh, microbes can transform organic things other things. Maybe they can transform

19:52 body into a disease? So it's germ theory of disease, that kind

19:56 explains that part, but it kind sets the wheels in motion.

20:01 so kind of back for a second generation. So here is kind of

20:06 he refused this whole process for the part in really just a simple design

20:14 . Nothing complicated, but he fulfills criteria is gonna have their right to

20:21 these spontaneous generation, wackos, gotta have air. And so he

20:27 okay all design flats that has a that's curved, okay, and so

20:35 that collects, so microbes that are the air we're gonna contaminate traveling on

20:41 particles uh and are these kind of ? Okay? And that's how they

20:48 into the material and contaminate? start right. So if you trap

20:53 by gravity then they don't enter, ? So air can get in.

20:59 , But not the best particles Okay. And so this uh then

21:07 that unless you purposefully basically inoculated by the liquid to touch that part,

21:17 now this is essentially the Oculus right and not being to see the collection

21:21 cells that will grow if you allow to go in the broth ok.

21:26 you have growth. Okay? You also do it by just clipping off

21:32 , bring the they're so um so long as you didn't do do either

21:40 these uh to the contaminated, it's and air is getting your right,

21:48 just the air and broth alone don't together to make life. It only

21:55 when you add cells to it. ? And cells in this case from

22:02 travel dust particles a lot. So cells can give rise to new

22:07 Okay. Only life that you live life. And so uh so that

22:12 a key thing that you know that itself from this fourth of course this

22:17 we talked about before you basically And that's why we do the things

22:21 way we do in lab. Um and have been for 100 plus

22:27 when handling bacteria and other microbes. so um if you're studying something you

22:34 want to do something else because in obviously changed the results. I don't

22:40 what's what's going on in that So um so lab lab um uh

22:49 gloves, um a bunch of burning things and loops and tubes containing culture

22:56 um all that for the purpose of out unwanted microbes. Why? Because

23:02 everywhere right there in the air on bench top. So you disinfect your

23:06 top before that where you want your before. So it's it's all for

23:11 purpose. So now the okay, missing a hole on you're missing a

23:25 it. Okay, I'm missing a . Goodness. Okay so imagine.

23:34 . No problem. So we start uh anthrax. Okay, anthrax

23:44 anthrax are due to the bacillus. that's the genus name the city.

23:55 okay so it's a rod shaped cell very long filaments. Okay. Um

24:05 it is the uh we now know course and he just proved this is

24:10 agent that causes anthrax. Okay. so he uh was kind of the

24:18 working as we started. So he he was a country doctor in the

24:24 he see around the rural area there an outbreak of man traction on the

24:29 . And uh he said let me what's going on. So it takes

24:34 samples from infected cows and sees there sees this under the microscope, sees

24:43 in the blood of these disease Now obviously that's not something that seems

24:49 in the blood of a healthy Okay, so kind of around the

24:54 and this is of course we're talking robert. Okay, and so around

25:03 box he kind of had the easy to establish this what's going to be

25:11 the Germ theory of disease. linking a bacteria or other microbes To

25:22 a specific disease and making that link chain of infection. Okay, and

25:31 that, so he comes up with , we'll get more into this,

25:35 is part of Chapter four which comes through the semester, we're gonna revisit

25:41 again. And so we'll go through of the framework. So coach

25:46 right, we're talking about is a a framework for how to for how

25:53 link specific micro disease. Okay, if they process to and then we'll

25:59 into it in detail later, but it's just kind of introduce, you

26:03 who this is and what he's doing initially it's very easy to kind of

26:09 animals. They've got this in their , healthy ones don't. So it's

26:12 kind of easy to make that Okay. Whatever becomes more difficult now

26:18 in having to having the infectious That's not so easy. Right?

26:24 what tuberculosis ends up being. That the next thing he studied. That's

26:29 respiratory disease. It's an organism that it gets in your lungs and kind

26:35 resides there and it can be a disease. But the it's called Mycobacterium

26:43 . This is a very small Okay, um not as prominent as

26:50 this one was okay. And so also not in the blood, it

26:55 in one. So you have to some were called, you know,

26:59 and you can see stuff that occurs of affected people and that's where you

27:05 it. So you have to look the samples. And so a tiny

27:10 can be difficult to find other microbes as well that live there are other

27:15 . And so it proves to So now with this one required developing

27:24 and techniques to culture, right? hadn't been done before. Right?

27:29 we literally use like uh uh, week we saw the Petri dishes

27:35 The solid media. Okay you see um he started with a spiced up

27:43 . So I think I was doing street painting the potato. So later

27:48 , not long after the that was . And so it made it much

27:53 . But nonetheless it's taking samples and putting them on a solid surface to

28:00 able to see them. Okay to able to work with them because although

28:04 can see this under a microscope, all you can do with it.

28:09 just look at Alright get out of environment set up from everything else and

28:16 in pure culture, that's what your is. Okay. And that requires

28:20 sophisticated techniques. They have developed all stuff. Okay. And so um

28:27 let me kind of get rid of real quick. So the and so

28:32 that method which you'll be uh course in lab is central when that

28:40 That was like a huge uh stepping to many areas of microbiology.

28:51 there's lots of sub disciplines and Okay, so now by having a

28:57 to isolate organisms from a patient or environmental sample and then seeing what's out

29:05 . Okay, you can then get multiple types on the plate that you

29:10 in the middle you can pick out ones and then we call subculture to

29:15 plates. So this gives you now to study without. They're both in

29:22 of infectious disease microbial ecology all kinds areas. So that that became when

29:31 happened then microbiology really exploded into all different areas. Because you can study

29:36 types of microbes, granted you couldn't a lot of stuff but certainly a

29:44 of things and it certainly worked Uh So I just bring this up

29:50 with liquid media to show you the the of each type actually different

30:00 Solid media of other types. But can find out once. And so

30:04 a use for these. Right Can with only liquid media alone and nothing

30:12 ? Can you obtain a pure Yes sir. Why not? And

30:27 you because in liquid culture you might different types. Right? There's a

30:34 there's a rod, there's a squiggly . Okay. Can all be in

30:39 . All right. An environmental sample . But you can see that many

30:45 things. You could have got a and see that. But your ability

30:50 work with them and you got to them on solid medium. Right.

30:55 to because now you'll get a workable of the organism on your plate.

31:03 ? You grow up on your plate then transfer and then then you know

31:10 you're here, okay if your culture one type on your plate you can

31:15 use liquid literally is for mass That's what you wanna do. You

31:21 get lots of cells. We need of cells for if you want to

31:25 D. N. A. Sequence if you want to say protein.

31:31 for mass quantities of stuff because um need that in order to get

31:39 there are lots of them to get quantity of materials to work with typically

31:43 . N. A. Or proteins . Right? So so each has

31:47 role. So pure culture can only obtained. Uh So I would begin

31:56 that happened. Very important, the of microbiology and other areas. Um

32:06 we sold coke and others. So establishment of the disease microbes are capable

32:16 certain types capable of causing disease. of course it becomes natural. Well

32:21 do we fight these things? How we get rid of the ad micro

32:26 ? Okay, this is where vaccination in. Uh And these other

32:33 Okay, so smallpox um Very very we'll talk about that scenes later in

32:41 semester and we'll mention variolation, variolation specific to smallpox. Okay, so

32:49 , so there was there's always been smallpox around history. Okay. And

32:55 think some of the 15 hundreds, had the idea during one of these

33:00 where you have smallpox for these bucks okay and those bumps or pustules contain

33:10 violence in life? Live smallpox Okay. And so somebody had the

33:17 . Well says well let me cut of these postures, take some of

33:21 material and cut it into another healthy person. Okay What prompted

33:27 I don't know what they say. so and that mark they make by

33:33 putting the material into the person. the variolation? Okay, so it

33:37 a bump there. You're basically being person my virus. They found that

33:43 good proportion of these people did uh not ever catch smallpox. They were

33:51 . Okay. Unfortunately this vaccination but unfortunately a good portion didn't survive very

34:00 a full blown smallpox virus. So had to be figured out how can

34:06 do this more safely? Okay. rate of people dying, I don't

34:11 . But I think I read somewhere 25 or 30 people that got this

34:15 of variolation died because they got Okay. I mean two thirds

34:19 So that's pretty good. So but , so then uh after that we

34:26 gender and cowpox. Okay. And related to smallpox. Okay pasture.

34:35 expanding this as well, rabies vaccine others. Um And so vaccinations.

34:40 sure we all know by now. , is due to stimulating the immune

34:47 . Okay. Doing so by introducing the agent infectious agent into the

34:55 Okay. And um that of course to production of antibodies. Okay.

35:05 the thing that induces that on bacterium virus or protozoan or fungus, whatever

35:13 infectious agent is, they have particular on their services. Alright. Could

35:20 a simple wall, could be in spike spiky things on on on the

35:27 . Right. It could be a yellow that's flopping around right. Um

35:32 could be uh anything that's kind of the periphery is what can potentially be

35:37 as an anti engine. Right? gin and engines can stimulate the body

35:43 produce antibodies. Okay, so the interaction, right let's say we'll go

35:51 this better semester. But the engine body reaction in a nutshell basically leads

35:58 elimination of of the agent. Okay and you're consistent has memory that can

36:08 these these infections and so if it again down the road then your body

36:13 respond fairly quickly. Okay. So key though is the attenuation. So

36:21 attenuate something means you're limiting it, inactivating it. Your it's not as

36:30 as it once was. Right? in you're in different ways to do

36:34 . You can use temperature elevated temperature inactivate certain chemicals to do this just

36:41 . Okay, what you're trying to is to um uh have a form

36:48 the infectious agent that will not cause but will give an immune response.

36:53 that's the whole idea and it's a position way to do this.

37:00 But one of the, one of best ways though is to have what's

37:06 a hole. So this is our virus let's say. Okay and so

37:15 we can activate but it's still capable activate this virus but it's still capable

37:26 reproducing. that's ideal? You can , can't cause disease. Okay so

37:35 there's ways to do that. Okay that kind of virus is one of

37:39 really strong meeting because it gets into because replicates your body continually sees it

37:47 time it sees it can strengthen the system response. Okay, so that's

37:51 we call a live continuing back Right again, we're gonna go into

37:59 details on this later. But just now I just wanted to point that

38:03 what we call a live attenuated So it's as close as you can

38:08 to the real thing but it doesn't disease. So there's different ways to

38:17 this. Okay and use part of but the main thing is engines stimulate

38:26 immune system and that's the whole crux this thing. Okay so the question

38:33 is generous cowpox vaccine. So why cowpox effective as a vaccine even though

38:43 did not contain smallpox, do you ? Exactly exactly. Just what we

38:52 um cross reaction. Okay so engines you can have um anybody can produce

39:03 and another man is very very similar will react with that as well.

39:08 so the same reason that that's why effective vaccine obviously now it's a small

39:16 vaccine but back then that was a kind of innovative discover. So um

39:25 so anybody can just all about binding each other specificity and that um so

39:37 uh is there any questions? So is one of my pet peeves.

39:45 is why I bring up this So they think you know what's gonna

39:48 to this person is gonna get a ? Okay so let me clarify

39:55 Obviously don't have A. B. . Or D. Okay. Which

40:01 below is correct. A. C. Or D. So the

40:04 there lies my arm before I received vaccination, is that correct?

40:10 Yeah there's disaffected my before I so are correct. Both are correct.

40:23 would be the correct term? It's this or that it's Auntie sepsis.

40:36 ? The nurse applied antiseptic my arm I see the vaccination. Okay so

40:43 people just use that terminal time. this of course is outside the context

40:49 sterilization that that person can have Okay sterilization microbiology microbiological speaking means you

40:59 have something, There is no viruses or present. All all gone

41:08 gone from a sterilized object. Um of course that's why he didn't

41:15 that to the arm. And you have any skin cells there. Uh

41:20 infection versus antiseptics. This infection is the getting rid of microbes strong inanimate

41:30 , objects. Right? Door bench, top wall. Okay that's

41:36 disinfection. So for that reason disinfectants be much stronger in terms of harshness

41:44 I think of bleach bleach versus isopropyl I create on your skin. Of

41:50 you can't put bleach if you want , but it's a good idea.

41:54 drink bleach. Like somebody once you have to get rid of

41:59 Okay, um doesn't work. So so Hannah sepsis is our formulations that

42:05 made for for skin for tissues. that takes us into an antiseptics and

42:14 in terms of this historical perspective. um so some advice and lister,

42:21 similar advice um A he makes it hand washing as a way to reduce

42:31 . Um You work in a Uh So there were 22 parts of

42:38 hospital. Both were for uh for were pregnant mothers gave birth maternity.

42:46 One maternity ward was handled by like and 2nd year medical residents. The

42:53 ones are had by midwives. Ones had by midwives hand a very

42:59 incidence of what's called child bed fever to pregnant mothers affection, bacterial infection

43:07 and mother often dies as a result so much higher in the area where

43:14 1st and 2nd year residents were It turns out the first secondary residents

43:23 go to the maternity ward after they done their kind of medical training

43:27 Right? So they often come out a of a, you know in

43:31 school, one works on cadavers, ? As part of the learning anatomy

43:37 and whatnot. And so they would out of the room full of blood

43:41 guts and everything else and say, , okay, so obviously not

43:47 And so midwives and much more in and they were very painless and really

43:55 and wash their hands and stuff. so some white sees this and

43:59 okay, you wash your hands and simple act, you know, dramatically

44:04 um this mortality rate of this disease to this day in the hospital

44:12 Um you know, it's still a uh where people acquire infections in

44:23 They went in there to either get arthroscopic procedure or this surgery or that

44:29 whatever. And they're while they're they get infectious disease, hospital acquired

44:34 . Right? And so that comes mishandling of medical implements, mishandling of

44:43 , you know, changing bedding and for patients and not really loves these

44:46 of things. And the number one to do is wash hands all over

44:51 place in hospitals. And uh very that simple thing to reduce infection Transmission

44:59 disease. Uh Lister was one that similar ways antiseptics and lister disinfectants.

45:09 he introduced the use of medical disinfecting uh capitalism and so forth.

45:18 , so that of course directly reduced infections. Okay, then finally,

45:25 to show you two pictures here. don't. All right, let's go

45:30 you a couple of points on We'll talk about this later. But

45:34 me just show you now it's gonna you understand. Okay, so here's

45:41 pro cario factory first. Let me show you this. Um So up

45:48 this is uh the discovery of So Fleming in his penicillin mod that

45:56 to drop on. So this is a plate. It's a street plate

46:00 of bacteria. Yeah here's where a dropped on it and you can see

46:05 an area where the cells won't bacterial cells will grow. But as

46:13 get closer to the stopped growing. it was included something and they're being

46:19 by the mold diffusing into the honor inhibiting growth. That was concluded that

46:25 may be onto something antimicrobial agents. of course that's concealing. And since

46:31 time we've developed discovered and developed but having common they typically target one type

46:41 process of molecules in a set very art is cell wall synthesis. As

46:47 will learn next time. And then week about structures and and so the

46:54 walls one common to many bacteria. uh are all synthesis. Um uh

47:10 is another target. Uh protein synthesis tetracycline. You may have heard of

47:18 protein synthesis some aspect of it uh . So he's targeted typically individual

47:27 And that's the thing about now Okay because if the bacteria becomes resistant

47:36 these things of course have to acquire change right enable them to survive the

47:46 okay so if you have a bacterium has say if anybody affects cell

47:55 Well if it makes one change it often times just counteract that and change

48:03 requires one mutation. Okay and knowing fast bacteria grow and have a little

48:08 higher mutation rate, it's certainly Okay contrast that is something like a

48:18 . It's actually hard to kind of because this has lots of targets.

48:24 can dissolve the membrane, you can can inhibit proteins that you can have

48:28 of different targets and very very hard . So they accumulate enough mutations to

48:36 every possible effect. So so that why for that reason it's very hard

48:43 really become resistant to the disinfectant or . But for antibiotics it is a

48:51 easier. Okay and of course we're fighting antibiotic resistant bacteria. Multi

48:57 Right? So it's a constant battle all they have to do is acquire

49:02 change. Maybe that enables them to a modular breaks down. That's what

49:10 penicillin can do. Um or they whatever the antibiotic target itself. Just

49:16 one little change and maybe they can't with it anymore. Or have a

49:21 protein that becomes modified to pump So it doesn't take a lot to

49:27 resistant. But what you have to of course to enable this to enable

49:35 that they have the presence of the there have that. That's why it's

49:44 not good to prescribe broad spectrum antibiotics kill everything kind of the shotgun

49:50 that's what kind of contribute to these . And uh so being smart

49:55 um using antibiotics with the whole you know, stop uh we have

50:04 . Okay. We'll talk about this more detail later, but it's obviously

50:09 real problem. Okay, so the part of this is um look a

50:17 bit about ecology. Okay. But want to bring up a couple of

50:23 because in about a week and a , um we're gonna start on

50:32 That is a subject that, although going to try to make it as

50:39 as palatable as possible. Okay, couple basic um concepts to understand.

50:49 , and that's the purpose of these couple of slides. Okay, so

50:54 are your basic, basic ecosystem So remember that the trophic food change

51:01 levels. Right? And so producers in what category? So you are

51:12 producer? Okay. So you would um Which one of these?

51:21 well you're gonna introduce her. We're . I'm sorry. Which one You're

51:30 ? You're a consumer. What the ? That's what I'm trying to

51:35 Our producers. Head of trucks and , herbivores, nope, nope.

51:43 . Okay, so as basic as sounds haircut and trust me, I

51:49 people mistake this all the time. not sure what it is.

51:55 you're what you watch, that's all . Um and so this kind of

52:12 us to this question. Okay, leads us into. So if you

52:20 at this. So ski, Okay slide is a call him the one

52:29 the founders of soil microbiology. Gonna soil anthropology about that. Well it

52:38 out you find different types of metabolisms there than than our types of

52:45 Okay so this is the type of called enrichment media. And we'll learn

52:53 this in public enrichment media. You formulate the components you you make a

53:02 components that growth certain type of bacteria you want to start over others.

53:11 . Very common. And that's what . Okay and do it. So

53:16 found these unusual metabolic types. Okay what's what's over here? Okay What

53:27 grow on this of a three You said B. That's correct.

53:37 little tropes. Okay so little tropes unusual type like they never heard of

53:42 things. Okay but they are their is really critical okay in the environment

53:51 to us and others what they do they use something as one example

53:57 Two S. Okay they can use like ammonium. Okay they can use

54:06 iron. Okay. Um and other other types of organic. Okay remember

54:22 has what in it? Yes. . Carbon. Okay is there something

54:30 from those ingredients on the left? how does it how how these how

54:37 folks get their car C. U C. 02. Okay.

54:47 there carbon? Okay remember carbon based forms, base base because our main

54:58 are made a part D. A. Carbohydrates, lipids, proteins

55:05 all have a base structure of carbon they have different tabs to it to

55:10 to make each of these types of . So carbon based carbon based life

55:15 . Okay so everything's gonna have carbon that's really what what this here is

55:25 about autotrophs. Right? What is carbon source that differentiates? What type

55:33 are completely complex organic material like us leave your hair? You C.

55:42 then you're okay. And that's We consume these complex organic materials and

55:50 off the 02. Use that use to make complex materials like starch,

55:59 , store starch, things like And so we can uh you can

56:06 can differentiate and again we'll get into in Chapter five. But whereas hetero

56:14 a carbon source not the energy, photo life energy, chemo, chemical

56:21 . Right? Um We can we add those terms like photo et

56:28 Right? But now it's really you basically it sounds okay because when you

56:40 microbiology perspective will change what you have provide to grow these types.

56:49 And so in terms of the ecosystems uh so any ecosystem because it's ecology

56:58 on one, right, what's the abundant kind of reform and ecosystem

57:04 plants and terrestrial ecosystem allergy freshwater Okay, there are the producers,

57:15 going to use the organic materials that consumers, you know different levels typically

57:25 you have carnivores that rewards and so and so forth. You have palm

57:29 . Right? That's what we are . And so but but ultimately what

57:40 is both forms consumers and producers end becoming compost of the speed decomposition is

57:48 to occur. You're gonna die. compose. So um the composition provides

57:58 right, breaks down organic material and provides that a source for us.

58:04 so when we look at this basic , breaking down better Gangotri at what

58:11 our microbes Presidency of producers, So where do they fit in?

58:23 all three of their producers or They're decomposing. Right. Um So

58:29 that's that's the diversity of bacteria are . They lots different lifestyle so they

58:36 them all. You find types that in all levels. Okay. And

58:41 it's it's their activity here. And do not don't memorize this triangle over

58:48 . Okay. But that that nitrogen nitrogen cycle critical for life because not

58:57 do they do microbes especially bacteria cycle different elements. Right? Here is

59:03 cycling of nitrogen. Right? They also cycle carbon phosphorus sulfur. These

59:09 especially N. S. And Especially NNp. Right. Those minerals

59:16 critical for producers. Right? Planks are great, right?

59:21 02 of water, they're good to but they can't make their own nitrogen

59:26 phosphorous, right? You know a growing crocs right? When they have

59:32 have phosphorus to promote. So um they're not provided to it artificially is

59:41 natural cycle phosphorus cycle driven by bacteria provide so. Supercritical. Okay.

59:50 of course if plants aren't happy environments plants are happy ultimately would not happen

59:57 because we need to eat the plants or we eat the things that eat

60:01 plants. Right? So were affected affected by it as well. So

60:07 I just threw in. So we've talking about little troughs right? This

60:12 where they fit in in this part the cycle. So they use things

60:18 ammonia and that's their that's their That's how they get energy but they

60:26 C. 02. That's the nature check and so yeah this this is

60:34 of illustrate you know what we've done microbes how we use them to benefit

60:42 . And so they kind of high processes. One that typically use microbe

60:48 some sort to get rid of the soil or other toxic chemicals many bacterial

60:56 can use can eat things like uh chemicals and things and get rid of

61:03 environment. Wastewater crete in the process all familiar with. Um not only

61:09 technology. Right? That's right this drinking water um bacteria that break down

61:16 material in wastewater can provide clean Um the common DNA technology biotechnology.

61:26 so this has led to. So know common technology relies on producing basically

61:36 What's the utility of that? Well the source D. N.

61:42 Can be many different things. The Covid vaccine that was rolled out

61:49 is a product of the common Um You can have the gene itself

61:57 be an antigen, right? A agent of some sort and you can

62:05 a growing up and that can be a vaccine of some sort. Okay

62:14 that's just one example. So we this technology for all areas stuff you

62:21 you wouldn't believe okay the enzymes that putting laundry detergents right? It would

62:27 wrong to using this technology. So it's everywhere. You you wouldn't think

62:35 something you would think but it's uh been going on for half a

62:40 Okay uh so that kind of comes biotechnology, biotechnology basically uh it's taking

62:48 biological process which can be whole cell . It can be a reaction in

62:56 self it can be a protein other from that cell. But those entities

63:04 used to make things that we want need. Right different applications applications across

63:11 areas whether it's pharmaceutical, medical uh industry. Levi Strauss uses bacteria to

63:21 their their die for their genes. um So many areas. Okay.

63:28 a lot of benefit to us agriculturally well. Okay So um so I'm

63:37 of closed down chapter one with talking little about you know they have this

63:42 on this course. certainly the second for medical medical event. And we've

63:50 mentioned about the microbiome and how um know microbiome we possess members our own

64:00 . And so they obviously must have kind of a benefit. And so

64:03 see that in different types of symbiotic and so I won't go through more

64:10 detail later. But you know, the most part they fall into two

64:16 , commence elastic or mutually stick. . And mutual is um I think

64:22 of that is both benefit we benefit that. So production of vitamins,

64:30 of bacteria. They produce very intensive that we don't produce. They break

64:38 certain food materials, we can't break um They boost the immune system.

64:44 they have that's certainly an individualistic for because they always have a home,

64:49 food. They provide these services to . But many are also commenced

64:55 So they don't have or harm. course they do. Right. So

65:02 most fall into those two categories. . And so there's always some types

65:07 transients. So you're born. It boring microbiome. Okay. You heard

65:13 you get it from your mother basically you're the birth canal. Okay.

65:19 then it changes over time you begin eat food of course inhale microbes and

65:25 but it can change that kind of down the base microbiome like your first

65:32 years of life but then it can you can change periodically if you're on

65:39 antibiotics having to go through some kind chemotherapy treatment that can change temporarily your

65:47 . Um uh even geographic you can somewhere prepare the time and just being

65:54 that environment can suddenly change your So point being is that you

65:59 parts of your body can change here there over time. But it's with

66:06 , it's there. It's it's a thing. Okay. And uh but

66:11 are types within your microbiome that can on you on occasion. Okay,

66:18 infectious disease of course it's all about types. Okay, producing uh there's

66:25 there's a process they go through the has to uh there's a sore

66:32 Okay then has to go from that to you. Okay, transmission then

66:40 if it does get to you then to overcome a number of obstacles right

66:45 then set in multiply policies. So it's not easy, there's obstacles

66:51 the way. Okay. But so know, is the infectious agent part

66:57 your microbiome. That's what we call pathogens. So opportunistic types are normally

67:06 of your microbiome. Um but conditions change that they become infectious. Very

67:14 category or things like a staph Okay, staff or mucous membranes.

67:21 skin inhabitants. But if you provide access to a part of your body

67:28 have and they can cause a problem you don't clean it very well,

67:33 can get in there and cause an maybe or holding nothing more but usually

67:39 opportunistic types. So they normally don't problems, but you know, if

67:44 gain in creating a part of your by accident or by a wound or

67:49 you're on antibiotics and the resistance is that can happen to you. Now

67:55 with a primary pathogen. That's what Stafford oftentimes an opportunistic pathogen. But

68:06 persons if you have that, you have that accent. Is is this

68:11 is not part of your normal Okay. So if you've got that

68:15 required mechanism motive transmission and it's there cause problems just like you had

68:25 Right? That's not a opportunity. a primary, it's a professional disease

68:33 if you will. Okay. And course, you know, in terms

68:37 your Whether one or the other you can okay. Um and you

68:50 how simple they are. What's the of your immune system? Right.

68:54 what is, what is the package ? What is it, what

68:58 what's with it, you know, many numbers are affecting you? Um

69:03 it uh what are the various factors something will happen a lot because those

69:09 the are the features that possessed by pathogen that enables to cause disease.

69:16 could be a number of different Okay. And how dangerous uh an

69:22 agent is relates to what are factors many Okay uh there could be things

69:33 can be toxins, that can be general factor. So it all depends

69:39 the type of agent and uh and know, bring those factors combined with

69:46 york immune immune system, health all together to determine whether you come down

69:52 . Okay, so these are things talk about as we go through the

69:58 . Okay, So any questions. . Uh good question. So uh

70:16 the question was about our current make us has the diversity of our

70:23 mind, I guess more successful. tend to think yes, because they

70:27 to be more of a bubble we want to expose ourselves to. I

70:32 I see my step daughter was there kind of feeling in the bubble and

70:38 and stuff. Right? I'm a believer in expose yourself that not always

70:47 . I know you jump in a either. Okay, But don't,

70:52 know, it's okay to interact with environment and I think that a lot

70:56 truth in what you say, so be a I guess what I'm

71:00 Okay, but don't go to the either. Right, Any other Alright

71:06 , we just got one more, we'll save that for next time

71:09 So uh thank you and see you

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