Week 5 Review Flashcards

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1
Q

What are the different ways of preventing food spoilage? Explain each method.

A

Use osmotic pressure by curing
- Microbes can’t survive in high salinity so foods are preserved with salt, nitrates, nitrites, or sugar

Canning
- The food is blanched or steamed to fill a can easily. This process also lowers the microbial population and destroys enzymes that alter the food. The cans are then filled to the brim, leaving as little space as possible, and then the can is steamed once again to drive out any air spaces. The cans are immediately sealed and sterilized with pressurized steam. The can is cooled and is ready to be packaged.

Aseptic packaging
- Pre-sterilized products are put into packages using an aseptic technique

Irradiation
- Gamma, x-ray, or electron beams are used, to prevent foodborne illnesses, preserve food, control insects, and delay sprouting

Pressure
- Fresh foods and liquid foods are put under very high pressure to prevent spoilage, while also preserving the color and flavor of the food

Fermentation
- Addition of yeast to ferment sugars and produce CO2 and ethanol

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2
Q

What organisms are involved in making each type of cheese?

A

Hard cheeses = produced by lactic acid bacteria
Semisoft cheeses = ripened by penicillium on the surface of the cheese
Blue and Roquefort = produced by penicillium inside the cheese

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3
Q

What organism is used to make alcoholic beverages? What are the fermentation products?

A

Yeast is used to make alcoholic beverages. Yeast ferments sugars and produces CO2

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4
Q

What are the steps in making beer and wine? How are they different (example: substrate)?

A

Beer:
Brewing: malt and hops boiled together for sterilization

Cooling and fermenting: wort (hot mixture) is cooled to 25C, then yeast is added and the mixture is transferred to the fermentation chamber

Priming and bottling: sugars are added before bottling

Aging: yeast will ferment sugars and produce CO2

Wine:
- Grapes are picked and tested, and then crushed and destemmed
- Sulfite is added to kill undesired yeasts and bacteria
- Yeast inoculum is added and fermentation occurs
- The result is pressed to separate solids from wine and the wine is clarified in settling vats, and then filtered
- Wine is aged and then bottled

Differences:
- In beer, you start with hops barley
- Fermenting sugar

  • In wine, you start with grapes
  • Fermenting plant sugar
  • Undergo malolactic fermentation
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5
Q

Why does grape wine-making require malolactic fermentation?

A
  • When the sugars in grapes are used to make products, malic acid is produced which makes the wine taste strongly bitter
  • In malolactic fermentation, lactic acid bacteria is used to convert malic acid into lactic acid (weaker)
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6
Q

Name industrial fermentation products.

A

Vitamins
Amino acids
Steroids
Xanthan
enzymes

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7
Q

How are biomass and bioconversion used for alternative energy sources and for single-cell protein products (SCP)?

A

Biomass, under bioconversion, produces biofuels like methane, ethanol, and hydrogen
- Biofuels are renewable replacement fuels
- Ethanol is in gas (90% gas, 10% ethanol)

Single Cell Protein (SCP) are proteins that are produced by microbes that ferment biomass
- SCP products are used as a substitute for protein-rich food (human food and animal feed)

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8
Q

What are some advantages and disadvantages of SCP?

A

Advantage:
- Rapid growth rates
- Variety of substrates
- Easy manipulation of genetic material
- High protein content
- Low overhead (less land)

Disadvantage:
- High nucleic acid which increases uric acid
- Cell wall indigestible
- Gastrointestinal reactions

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9
Q

What are the steps in the nitrogen cycle?

A

Ammonification
- Bacteria and fungi convert nitrogenous waste into ammonia (NH3)

Nitrification
- Nitrifying soil bacteria converts ammonia (NH3) to nitrites (NO-2) and then to nitrate (NO3-)

Denitrification
- Soil bacteria use nitrate as a terminal electron acceptor in anaerobic respiration and convert it to nitrogen gas (N2), returning to the atmosphere

Nitrogen Fixation
- Take N2 gas from the atmosphere into ammonia NH3 (easily made into macromolecules)

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10
Q

Give examples of bacteria in the nitrogen cycle.

A

Ammonification = many
Nitrification = nitrosomonas, nitrobacter
Denitrification = bacillus, pseudomonas
N2 Fixation = axobacter, cyanobacteria, purple and green bacteria

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11
Q

What are the steps involved in typical wastewater treatment?

A

Flushed toilet water goes into waste water tanks, and go through a filter called a bar screen that removes large debris from the water

Then at the sedimentation tank, solids settle to the bottom as sludge

The sludge goes to a sludge digester that gets rid of odors and harmful organisms, and then transported to solid disposal where solids are sent to a landfill or used as fertilizer

At the sedimentation tank, water goes to secondary aeration that provides oxygen for microorganisms, then goes to secondary clarifier where microorganisms decompose organic material and absorb nutrients

The liquid goes to a disinfection tank, killing remaining harmful bacteria, and then is discharged into waterways

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12
Q

What is the difference between etiology and pathogenesis?

A

Etiology = the cause of disease
Pathogenesis= the “course” of the disease

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13
Q

How are infection and disease-related?

A

Infection= the invasion and growth of pathogens in the body
Disease= the actual damage or improper functioning of tissues

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14
Q

Name locations in the host where abundant microflora can be found.

A

Upper respiratory tract (nose, throat)
Eyes
Mouth
Skin
Gastrointestinal tract
Outer genitourinary (lower urethra in both sexes)

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15
Q

Which locations have no normal microbiota?

A

Lower respiratory tract
Peritoneal cavity
Muscles
Circulatory system
Central nervous system

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16
Q

How does competitive exclusion/ microbial metabolism affect the growth of pathogens? How does it protect against infection?

A

Competitive exclusion/microbial antagonism: normal microbiota compete with pathogenic microorganisms, so slows/prevent pathogenic growth

Protect by:
- Competing for nutrients
- Producing harmful substances
- pH and available oxygen

17
Q

What are the different types of symbiosis? Give examples of each type.

A

Commensalism: one organism benefits, the other is unaffected
- Corynebacteria surface of the eye

Mutualism: both organisms benefit
- E. coli produces vitamin K; large intestines provide nutrients for E. coli

Parasitism: one organism benefits at the expense of another
- Salmonella typhi causes typhoid fever

18
Q

Under what conditions do normal microbiota cause disease?

A

Organisms can obtain access through broken skin or mucous membranes

The host is weakened (therapy for cancer, transplants)

Damage to normal microbiota by antimicrobial drugs may lead to secondary infections

19
Q

What do Koch’s Postulates establish? What are the steps in Koch’s Postulates? What are some exceptions to Koch’s Postulates?

A

Koch’s Postulates establish microorganisms cause specific diseases.

Steps:
- The same microorganism is present in every case
- Microorganisms isolated from the host and grown in pure culture
- Microorganism from pure culture causes disease in “healthy” animals
- Pathogen isolated from “healthy” animal = original microorganism

Exceptions:
- The disease may be caused by a number of different microbes
- Some pathogens cause several disease conditions
- Some pathogens only cause disease in certain organisms

20
Q

How is a disease diagnosed?

A

Look at:
Signs and symptoms the patient is showing
Communicability of microorganism
Host’s conditions
Pattern of disease
Frequency disease
severity/duration of disease

21
Q

What is the difference between signs and symptoms?

A

Signs = objective changes that can be observed or measured
Symptoms = subjective changes noticed only by the host

22
Q

What is the difference between communicable and noncommunicable diseases?

A

Communicable = transmitted from infected to susceptible host
- Contagious disease: easily spread

Non-communicable = not usually transmitted
- Some microorganisms that grow outside the body
- Weakened host

23
Q

What is the difference between incidence and prevalence?

A

Incidence = number of new cases (risk)
Prevalence = total number affected in a population (how widespread)

24
Q

What are the different types of infection? Give examples.

A

Severity of duration:
Acute infection: develops rapidly but lasts only a short time
- Common cold

Chronic infections: slower but continue to reoccur over extended periods
- tuberculosis

Latent infections: the causative agent may remain inactive for some time but becomes active
- Shingles by varicella virus

Host environment:
Localized infection: microorganism confined to a particular tissue
- abscesses

Systemic (generalized) infection: microorganism carried by the circulatory system to different tissues
- measles

25
Q

What is sepsis and what are the types of sepsis?

A

Sepsis: a toxic inflammatory condition caused by microbes (mainly bacteria and toxins) spreading from a certain tissue

Bacteremia: the presence of bacteria in the blood

Fungemia: the presence of fungi in the blood

Viremia: the presence of a virus in the blood

Toxemia: the presence of toxins made by microorganisms in the blood

26
Q

What is the difference between pathogenicity and virulence?

A

Pathogenicity = ability to cause a disease by overcoming host defense
Virulence = degree of pathogenicity

27
Q

How is virulence measured?

A

Estimated through experimental studies of the lethal dose
- LD50: least lethal dose that kills 50% of the animals in the test group

28
Q

What are the portals of entry?

A

Mucous membranes:
- Gastrointestinal tract
- Respiratory tract
- Genitourinary tract
- Conjunctiva

Skin: parenteral access when mucous membrane or skin are penetrated or injured

29
Q

In what ways do pathogens damage the host? Give examples.

A

COVID-19 upregulates cytokines (cell messengers that activate/suppress certain cells)
- IL-1B induces other cells to make cytokines that attract other immune cells
- Some patients have cytokine storm (inflammatory response)

Siderophores: take iron from the host’s iron-transporting proteins, forming a siderophore-iron complex
- Iron is needed for bacterial growth but low free iron concentration
- Bacterial receptors bind to the siderophore-iron complex and uptake iron

Toxins: poisonous substances produced by microorganisms that can inhibit host cell function or kill the host

30
Q

What are the two main types of toxins? Be able to compare and contrast each.

A

Exotoxins (Gram +)
- Immediately released into the surrounding environment
- Proteins made by pathogenic bacteria and secreted during the log phase
- A-B toxins, membrane-disruptive toxins, and superantigens

Endotoxins (Gram -)
- It is not released until the bacteria is killed by the immune system.
- lipopolysaccharide (LPS) found on the outer membrane of gram negatives released when bacteria die
- Cause pyrogenic response (fever)
- Release TNF (tumor necrosis factor)
- Binds to cells and alters metabolism
- damages blood capillaries, leads to loss of fluids, and decreases blood pressure

31
Q

Describe the groups of exotoxins

A

Grouped by action:
A-B Toxins: A does the damage, B is recognition to enter the cell
Bacteria release toxin
- Toxin enters the cell by endocytosis
- A subunit dissociates from B
- A subunit moved to the cytoplasm
- Toxic action of A initiates cellular changes

Membrane-disruptive toxins: lyse host cells by disrupting plasma membrane
Include:
Leukocidins: kill leukocytes by forming protein channels and preventing phagocytosis by macrophages
Hemolysins: kill erythrocytes
Ex: staphylococcus and streptococci

Superantigens
- Antigens (bacterial proteins) that provoke a very intense immune response
- Non-specifically cause proliferation of T cells
- T cells stimulate the release of excess cytokines (regulate an immune response)
- Cytokines enter the bloodstream and cause a massive inflammatory response, sepsis shock, death
Ex: toxic shock syndrome, food poisoning

32
Q

Give examples of exotoxins

A

Diphtheria toxin (Corynebacterium diphtheria): A-B toxin that interferes with protein synthesis

Cholera toxin (Vibrio cholerae): A-B toxin causes cells to secrete fluids and electrolytes (ions that maintain osmotic balance)

Botulinum toxin and tetanospasmin (clostridium): A-B neurotoxins