Microbiology 2421

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Microbiology 2421

Terry Austin Office MSB 1145

Phone 298-8405

800-460-4636 extension 8405 email – taaustin@templejc.edu

Please log in to D2L

(Desire2Learn) and fill out your profile

(details to follow in a few moments)

WRITE THIS DOWN… https://templejc.desire2learn.com

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D2L with be the primary means of communicating with you as the semester progresses. You will find course files and announcements on this site.

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Lab Supplies List

Microfiber cloth OR lint free cloth (ie flour-sack dish towel) for cleaning slides

** ultra-fine permanent marker (culture labeling) ** alcohol based hand cleaner ** latex ('surgical') gloves ** lab coat or apron

Safety glasses

** Many items may be shared with table partners

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Classroom Performance System

Please obtain your CPS Remote from the TC bookstore before the end of the second week of classes.

This unit will be used to

Take attendance

Review for exams

Take Exams

You will need to go online to activate your CPS remote www.einstruction.com

THIS is also the site where your grades will post automatically after exams.

NOTE – this is NOT part of D2L or

Temple College

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Online Course Environment

Lecture presentations will be made available on the D2L server.

Students are encouraged to go online and print the lecture notes.

Class Online Discussion Forums are for your use to ask questions that might come up during the semester.

https://templejc.desire2learn.com

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Online Presentations

It is strongly suggested that you print the chapter HANDOUT for each chapter. This file contains three slides per page and has note-taking space available. When you print, single sided you should have adequate space available to take notes in class

A printed version of the presentation will save you valuable class time allowing you to be far more efficient in your note taking. Such a printout IS

NOT an adequate substitute for a good set of notes.

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Syllabus Review

Please look at your syllabus as we go over these items

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Chapter 1

The Microbial World &

You

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Microorganisms are ubiquitous

They are present virtually everywhere in the environment, as well as in and on our bodies.

Microorganisms exist in virtually all environmental extremes

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Why study microorganisms?

Microorganisms can be both beneficial and harmful.

Beneficial examples:

 food preservation

Flavor (tangy flavors of yogurt, sour cream, blue cheese)

 food production (vinegar, yogurt, alcohol, sauerkraut…)

 biogeochemical recycling (such as cleanup of oil spills)

 vitamins (enteric bacteria produce some vitamins for you)

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Why study microorganisms?

Microorganisms can be both beneficial and harmful.

Harmful examples:

Disease – microbes make us and our animals sick

 food blights – microbes spoil crops and stored produce

 spoilage – microbes taint stored foods

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History of Microbiology

Origins of Microscopy: Early use of compound (2 lens) microscope

1665 - Robert Hooke (England)

Looking in his microscope at cork, Hooke described "little boxes" or

"cells”

Why is this important?

This was the beginning of the Cell Theory of life… all living things are composed of cells

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1673 - Antoni van Leeuwenhoek

(Holland)

First to observe live microorganisms

Leeuwenhoek called his discoveries "animalcules“ ( tiny animals )

In fact, what Leeuwenhoek observed are now recognized to be… bacteria protozoa

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The Origins of Life?

The next major hurdle for early biologists was

To determine precisely how new living things appeared

One early idea with much support

(now thought rather odd)

flies

Spontaneous Generation ?

During this period (1600’s) there was a common belief that new organisms arose spontaneously from certain substances.

Manure

Mud toads

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Rotting Meat

This view persisted into the 1800’s

maggots

Experimenters begin to examine

Spontaneous Generation

1668 - Francesco Redi (Italy)

(before microscopic observations of Leeuwenhoek),

Redi placed meat in jars some sealed, some jars unsealed.

He showed maggots did not arise “from” decaying meat.

EVIDENCE - No maggots grew on meat which was sealed in jars while they did appear on the meat in open jars

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Problems with this…

Opponents claimed that AIR was necessary for life

 some still believed that simple organisms could arise spontaneously

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Evidence In Support of

Spontaneous Generation

1745 - John Needham (England) boiled meat broths and poured them into covered containers microbes still grew after heated nutrient fluids were poured into covered containers. (He said this was spontaneous)

WHY did bacteria still grow?

The answer will DIRECTLY affect YOU in lab this semester!

POOR TECHNIQUE

Organisms could have fallen in the solutions after boiling & before being transferred into the sealed containers

Organisms might have traveled into the solution from fingers or other contaminated objects

Evidence Against

Spontaneous Generation

1765 - Lazzaro Spallanzani (Italy)

Spalanzani proposed that microorganisms came from air getting into Needham's samples found none in broth after heating in sealed containers

Needham countered by saying…

A ‘vital force’ needed for spontaneous generation was killed by the heating and could not enter the sealed flask

17 let’s leave this argument for now…

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Biogenesis

Life from life…

First major challenge to Spontaneous Generation

1858 - Rudolf Virchow (Germany)

Biogenesis states that

‘All life can arise only from preexisting, living cells’

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Spontaneous Generation Disproved

1861 - Louis Pasteur (France)

Pasteur heated broth in open flasks with s-shaped necks

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FIRST

Broth poured into open neck of flask

THEN neck heated and bent but remains open at tip of neck

FINALLY contents heated to kill organisms

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Pasteur & Others

The discoveries by Pasteur and others lead to the development of aseptic techniques…

… the most important techniques that all microbiologists use methods for preventing contamination by unwanted micro-organisms.

Asceptic Techniques

– Laboratory techniques used to minimize contamination of a sample, culture, work area or individuals.

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Pasteurization

A process developed by Pasteur to kill particular organisms heating which kills pathogens (disease-causing) organisms, but does not damage the food (milk or other).

Classic Pasteurization: Heat to 63 o C for 30 minutes

Modern Pasteurization: Heat to 72 o C for 15 seconds

NOTE: Pasteurization is NOT sterilization

Kills pathogens and most other organisms ( not all organisms killed )

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Further Work of Pasteur

Important business problem:

French businessmen asked Pasteur to help discover why their wine and beer soured. They hoped to prevent spoilage

Common misconception:

• air caused sugars to convert to alcohol

Pasteur discovered instead that yeast are the vital part of this process. Further that bacterial probably caused the spoilage after the process was complete.

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Pasteur continued…

Pasteurization developed in order to save the beer/wine industry!

(and you thought it was to protect your milk…)

This major link between microorganisms and spoiled foods lays the groundwork for the next step of relating diseases to microorganisms

This idea that ‘germs’ or microorganisms might be involved in diseases is referred to as the

Germ Theory of Disease

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Lending Support to Germ Theory

Ignaz Semmelweis (1840's, Hungary)

Joseph Lister (1860, England) don’t shudder when you see these…

Semmelweis showed that simply washing hands by doctors between obstetrical patients reduced the incident of childbirth fever

Lister applied germ theory to other medical procedures, using phenol (an organic acid) to treat wounds (found less incident of infections, many other doctors applied this technique).

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Germ Theory of Disease

Robert Koch (1876, German physician)

First direct proof of bacteria causing disease

What did Koch do???

Linked a bacterium, Bacillus anthracis , to anthrax.

Developed steps to experimentally determine if a microorganism is involved in a disease – Koch’s Postulates

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Koch’s Postulates

1. The same pathogen must be present in every case of the disease

2. The pathogen must be isolated from the diseased host and then grown in pure culture

3. The pathogen from the pure culture must cause the disease when it is inoculated into a healthy, susceptible animal

4. The pathogen must be isolated from the inoculated animal and must be shown to be the original organism.

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Waging war - advances in combating microbial diseases:

VACCINES - 1796 (before Koch) Edward Jenner (British physician)

Developed first vaccine –

Jenner was told by a young milkmaid that she couldn’t get smallpox because she had already been sick from cowpox (milder disease)

He decided to test her tale… collected scrapings from cowpox blisters and inoculated a healthy 8-yr old volunteer with these scrapings.

Scratched arm with contaminated needle. On later exposure to smallpox this volunteer did not contract smallpox

WHY doesn’t this bright milkmaid get credit for her observations?

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Immunology

Jenner’s efforts with smallpox/cowpox inoculations were the:

Origins of immunology – Jenner’s use of body's own defense mechanisms to fight disease

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Antimicrobials & Antibiotics

Paul Ehrlich (Germany), early 1900's. Speculated about a “magic bullet”

"Magic Bullet" - medicine for particular diseases that would ‘hunt/kill’ disease organisms without harming the patient.

Ehrlich tested hundreds of chemical agents before finding Salvarsan

(an arsenic derivative) which was effective against syphilis.

First Modern Antibiotic

Alexander Fleming (Scotland), 1928)

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Fleming tossed out some cultures that were contaminated by mold ...

When taking out the garbage later, taking a second look noticed a clear around the mold where no bacteria were growing.

he had accidentally discovered a mold which inhibited bacterial growth

Mold was Penicillium notatum

– A.F. named the compound

Penicillin

Serendipity = the faculty or phenomenon of finding valuable or agreeable things not sought for.

Virology

1892, Dmitri Iwanowski speculated about tobacco mosaic virus.

Attempted to isolate the agent responsible for this economically disastrous plant disease

Tried to isolate by using filtration (common technique at the time)

He reported that the factor causing the disease was so small that it was not filtered out by filters small enough to stop all known bacteria .

‘this is something smaller than any know bacterium

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IMPORTANT: He did NOT understand the organism as a virus as we now understand the concept

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Next Major Steps In Virology

1935, Wendel Stanley crystallized TMV – in doing so, he showed that it was something different than cellular life.

1940's - electron microscope allowed direct visualization of virus particles. These things looked like nothing we had seen before!

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Naming and Classification

Our system of naming = Binomial nomenclature

Binomial bi = two & nomial = names TWO NAMES

1735, Carolus Lennaeus: Names usually based on Latin and consists of: Genus species

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Classification

Kingdom

Phylum

Class

Order

Family

Genus

Species

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Classification

5 Kingdoms: as defined by Whittaker

Monera - archae (‘blue-green bacteria’) and true bacteria

Protista – protozoans ( Paramecium , Amoeba etc.)

Fungi – fungi and molds

Plantae - plants

Animalia - animals

Classification

3 Domains: 1978, Carl Woese

(Domain = a level of classification above Kingdoms)

Archaea – ancient ‘bacteria-like’ organisms (more on this subject in a moment)

Eubacteria

– ‘true bacteria’

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Eukarya

– organisms whose cells have a nucleus

(the previous two DO NOT have nuclei)

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Two Main Groups of

Microorganisms

The difference? Some have a nucleus, some don’t

Prokaryotes

– HAVE NO NUCLEUS

Examples = Bacteria and Archaea

Eukaryotes

– DNA enclosed in membrane called the nucleus.

Examples = Fungi, Protozoa, Algae, Multicellular animal parasites

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Microorganisms include:

Bacteria

•single celled

•no nucleus,

•cell walls contain peptidoglycan (structural molecule of sugar & amino acid combination)

•Reproduce by binary fission

•Some derive nutrients from organic materials, which can come from living or dead organisms.

•Some make food via photosynthesis

•Some can use inorganic compounds as a food source

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Microorganisms include:

Archae Similar to bacterial (no nucleus).

Cell walls lack peptidoglycan .

Often found in extreme environments (Great Salt Lake, Dead Sea, hot springs, thermal vents)

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Three major groups of Archae

methanogens – produce methane as a waste product

-gen = ‘producing’ extreme halophiles

– thrive in high salt environments

-phile

= ‘loving’ extreme thermophiles

– thrive in hot waters

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Fungi

Fungi– are eukaryotes. HAVE NUCLEI..

Unicellular or multicellular

Cell wall of chitin.

Reproduce sexually or asexually (eg. budding)

Yeast is a unicellular fungi larger than bacteria.

Other fungi include molds which form visible mycelia. Obtain nutrients from organic material in their environment.

Protozoa

Protozoa – unicellular, eukaryotic microbes. Remember, eukaryote means that these HAVE a nucleus.

Includes organisms like Amoeba , Paramecium etc.

Reproduce sexually or asexually, many shapes, some are parasites, derive nutrients from environment.

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Many are mobile moving by flagella , cilia , or pseudopods (flowing),

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Algae

Algae – photosynthetic eukaryotes many have cell wall made of cellulose (like plants) present in soil, water (fresh & salt)..

Unicellular or multicelluar/colonial

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Multicellular Animal Parasites

These are not strictly microorganisms, but are medically important

‘small things’ so they will be mentioned in this class.

Includes flatworms and roundworms

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Viruses

Viruses are vastly different from other life forms. They are NOT cellular life forms

Contain a core of nucleic acid (RNA or DNA) genetic material. This core is often surrounded by protein coat.

Viruses can not reproduce on their own. They must use the cellular machinery of other organisms to reproduce.

All viruses are obligate intracellular parasites

& can’t reproduce outside host cells

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Prions

Infections protein particles

These odd agents have only been partially understood in the past decade.

Responsible for such diseases as: (nine identified)

Mad-Cow Disease

Creutchfeld-Jakob

Spongiform Encephalopathys

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