mod 7 Flashcards

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1
Q

Prion

A
  • Non living
  • Defective protein
  • Doesn’t contain DNA/RNA
  • Molecular level low nm
  • Mad-cow disease
  • Creutzfeldt-Jakob disease
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2
Q

Virus

A
  • Non living
  • Non cellular
  • Contains DNA/RNA
  • Requires host to replicate
  • Less then 500 nm
  • COVID-19
  • HIV
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3
Q

Bacteria

A
  • Living
  • Unicellular, prokaryotic
  • Cell Wall
  • Reproduce via binary fission
  • Tuberculosis
  • Salmonella
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4
Q

Protozoan

A
  • Living
  • Eukaryotic Multicellular
  • Complex life style
  • 50-150 micrometers
  • Asexual reproduction
  • Malaria
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5
Q

Fungi

A
  • Living
  • Eukaryotic, some unicellular most multicellular
  • size varies from um to nm
  • Reproduce through spores
  • Athletes foot
    Stem rust
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6
Q

Macroparasite

A
  • Living
  • Eukaryotic multicellular
  • External parasites - ectoparasites
  • Internal parasites - endoparasites
  • mm to metres
  • Tapeworm
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7
Q

Epidemic

A
  • An outbreak of an infectious disease within a defined area or population at the same time. Zaire ebolavirus 2014-2016 in West Africa, transmitted by fruit bats and direct contact.
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8
Q

Pandemic

A

The spread of an infectious disease across a continent or worldwide. COVID-19 2020-2023.

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9
Q

Direct Transmission

A
  • Person to person through exchanges of bodily fluids eg touching, kissing, sexual contact, biting.
  • Droplet spread caused by talking, coughing, sneezing.
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10
Q

Indirect Transmission

A
  • Airborne transmission
  • Contaminated Objects which contains pathogens on its surface
  • Food and drinking water
  • Animal to person contact including scratch or bite from animals
  • Vector borne - spread by blood sucking insects
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11
Q

Robert Koch

A
  • Hypothesised that specific pathogens cause specific disease
  • Experimented the spread of specific pathogen caused diseases through sheep
    Kock postulates
  • Pathogen must be found in all animals suffering from same disease
  • Pathogen must be isolated from a diseased animal and grown in pure culture.
  • Cultured pathogen should cause disease when introduced to healthy animal
  • Pathogen must be re-isolated from the infected animal.
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12
Q

Louis Pasteur

A
  • Disproved spontaneous generation (belief that life spontaneously generated)
    Done via swan-neck experiment, where nutrient broth was placed in a swan neck flask and a broken neck flask exposing broth to the air. After boiling to eliminate pathogens, after a while microbial growth was observed only in the broken neck flask, proving that microbes are airborne.
  • Developed world’s first attenuated vaccine (anthrax)
  • Demonstrated fermentation was caused by living organisms
  • Invented pasteurization
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13
Q

Plant disease example

A
  • Fire blight
  • Destructive plant disease affecting pome fruit worldwide
  • Caused by bacterium Erwinia amylovora, exists in all pome fruit producing countries except Japan and Australia, due to strict quarantine measures.
  • Attacks all parts of pome plants. Infection results in tissue death and bacterial ooze droplets on infected tissue.
  • Transmission via rain, wind, insects and pruning tools.
  • Melbourne’s Royal Botanic Garden’s Outbreak in 1997 causing 20 million dollars lost in revenue, resulting in quarantine measures.
  • Prevention includes on-farm biosecurity and ensuring all staff and visitors participate in hygiene practices.
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14
Q

Animal disease example

A
  • Foot and mouth disease (FMD V)
  • Contagious Viral infection impacting cloven-hoofed animals such as cows.
  • Virus can survive in many environments including live animals, meat and dairy products. Thus it poses great risk to livestock raised in agricultural production. Currently excluded from Australia due to detailed response plans and arrangements, particularly its strict quarantine measures.
  • Causes blisters fevers and blisters in the mouth and hooves of infected animals. While recovery rates are high, infected animals are left weak and debilitated, destroying herds.
  • Potential breakouts of FMD V would cost billions of dollars of agricultural damage in Australia, thus it is imperative that Australia remains FMD V free, by incorporating biosecurity and assuring hygienic practices.
  • 2001 UK outbreak, where importation restrictions caused a 19 billion dollar loss in exportation.
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15
Q

Malaria Adaptation

A
  • Caused by 4 parasitic protozoan species of Plasmodium, where Plasmodium Falciparum is the main contribution to mortality.
  • At each life stage of the plasmodium species, different antigen molecules are produced preventing host from launching immune response
  • When inside red blood cells, Plasmodium produce adhesion proteins which surface on the red blood cell, interfering with the movement through capillaries, thus facilitating reproduction and survival of the parasite.
  • Before the adaptive immune system can respond to foreign adhesion proteins, plasmodium alters adhesion proteins on RBC, protecting them against immune system
  • While in human liver cells, Plasmodium kills cells, causing separation between surrounding cells, emerging gaps through which parasites move to infect other liver cells. Parasites also accumulate calcium ions from liver cells, used to block presentation of antigens, thus avoiding immune system.
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16
Q

HIV Adaptation

A
  • Virus infection that attacks lymphocytes to deteriorate immune response, which can lead to AIDS.
  • High replication rate and antigen proteins on virus surface mutate rapidly, avoiding adaptive immune system.
  • Virus covered in glycans, a carbohydrate that assists in avoiding detection.
  • Interferon is a protein produced by WBCs in response to viral infections, essential in communication between T and B lymphocytes. HIV blocks interferon signaling.
17
Q

Response of plants to fungal pathogen

A

Phytophthora Cinnamomi is a soil borne pathogen which affects the Australian plant Eucalyptus Marginata. P Cinnamomi affects the roots and stems of susceptible plants, causing root rot and preventing the absorption of nutrients. E Marginata uses its cell wall and secretion of antimicrobial chemicals to prevent infection. Cell walls contain cellulose and lignin which act as a physical barrier against the pathogen. Cellulosic material which thickens the wall in response to the pathogen restricts access to the under layer of the plant. The secretion of an oil contains antimicrobial properties which inhibit the spread of P.Cinnamomi through the plant tissue.

18
Q

Physical barriers in first line of defence

A
  • First line of defence known as the primary immune response is composed of a range of physical and chemical barriers which are non specific and prevent pathogen entry
    -Skin is composed of upper thin epidermis, middle dermis containing hair follicles, sweat and sebaceous glands, and nerves. Then there is the hypodermis, the bottom fatty layer containing blood and lymph vessels.
  • Epidermis cells contain keratin which bind the cellular matrix, making it impenetrable for pathogens.
  • Dead epidermal cells are constantly shedded and replaced, removing microbes present on the surface.
  • Sebaceous and sweat glands produce sebum and sweat, producing an acidic and salty environment.
19
Q

Innate immune system outline

A
  • Non specific resistance
  • 1st and 2nd line of defence
  • Phagocytes, inflammation, natural killer cells (NK) and Mast cell production of histamines.
20
Q

Adaptive system outline

A
  • Third line of defence that involves 2 broad groups of lymphocytes
  • B cells produced in bone marrow and responsible for antibody-mediated immunity
  • T cells produced in bone marrow but mature in thymus and are responsible for cell mediated immunity.
  • B and T cells can be in three stages: naive cells mature within tissue but have not been exposed to antigens, effector cells have encountered a specific antigen and have become active in the removal, and memory cells which continue to circulate once the pathogen has been eliminated.
21
Q

Mast cells (Innate)

A
  • release histamines in damaged tissue which increases the permeability of blood vessels allowing for phagocytes to quickly transfer between blood vessels to reach responsible pathogens.
22
Q

Inflammation response (Innate)

A
  • occurs at site of infection
  • mast cells become activated once pattern recognition receptors (PRRs) detect pathogen associated molecular patterns on pathogen surface
  • Mobile phagocytes are attracted to site of infection as mast cells and macrophages release cytokines
  • Blood vessels at infected areas supplied with extra blood, making area swollen and increasing temperature in an attempt to eliminate pathogens.
23
Q

Lymph system (Innate)

A
  • bacteria and other microbes are picked up in lymphatic fluid and trapped inside lymph nodes, where they can be attacked and destroyed by phagocytes.
24
Q

Complement system (Innate)

A
  • Includes group of over 50 proteins which activate when encountering pathogen
  • Triggers cascade that coats pathogen in complement proteins, enhancing the binding of antibodies to pathogen and cells
  • System also increases inflammation
25
Q

Cell death to seal off pathogen (Innate)

A
  • Infected cells or macrophages that have engulfed a pathogen undergo apoptosis - results in both cell and pathogen death.
26
Q

Natural killer cells (innate)

A
  • Cytotoxic
  • Small granules in their cytoplasm which contain special proteins (perforin and proteases) that are released in close proximity to a cell ‘‘tagged’ for killing.
  • Do not require prior activation and serve to contain viral infections while adaptive immune response generates antigen-specific cytotoxic T cells
27
Q

B cells and antibody mediated immunity

A
  • Each naive B cell contains B cell receptor (BCR)
  • B cell activation requires presentation of the antigen by the T helper cell
  • Results in B cell differentiation into memory B cells or plasma cells which act as antibody factories
  • Antibodies bind with antigens to form a antibody-antigen complex, causing them to clump together and making them more recognizable to macrophages
  • Memory B cells accumulate in spleen and lymph system.
28
Q

Antibody structure

A
  • Each antibody consists of 4 polypeptides - 2 heavy chains and 2 light chains joined to form a Y molecule
  • Heavy chain and lower end of light chain are the constant portion and don’t change.
29
Q

Antibody function

A
  • neutralization - antibodies bind to antigen molecules on surface of pathogen
  • agglutination - antibodies bind to antigens on the surface of host cells and form antibody-antigen complexes which activate phagocytes and the complement cascade leading to destruction of the cell and pathogens (apoptosis).
30
Q

Types of T cells

A
  • All contain T cell receptor (CD3) which is the binding site for antigen presented cells (APC) via major histocompatibility complex molecules
  • Killer T cells attack and destroy foreign cells, infected host cells and abnormal ‘self’ cells including tumor cells
  • Helper T cells become activated by antigen presenting cells and they stimulate the cloning of specific B and T cells by the secretion of interleukins
  • Memory T cells - remain in the body and reactivate quickly when reexposed to pathogen
  • suppressor T cells stops immune response when antigen is destroyed
31
Q

Procedures to stop disease spread

A
  • hygiene practices: personal hygiene, communal hygiene, food hygiene
  • quarantine: inspection, regulation, restriction of movement, enforced destruction of diseased organisms
  • Vaccination: Active immunity contains a live attenuated or inactivated version of pathogen leading to production of memory cells, or passive immunity which involves injection of antibodies into an individual providing immediate protection, but no memory cells.
  • Public health campaigns: grim reaper 1987 commercial, slip, slap slop.
  • Pesticides: chemicals used to prevent spread of infectious animal and plant pathogens and insect vectors, such as mosquito vectors.
  • Genetic engineering: modification of an organism’s genome via insertion of a transgene. Male Aedes Aegypti mosquitoes (Zika virus). Offspring of modified males and wild females can’t survive to adulthood due to unnatural food source.
32
Q

Antibiotics

A
  • Drugs used to fight BACTERIAL infections. Alexander Fleming discovered Penicillin in 1928.
  • Bactericidal antibiotics directly kill bacteria by interfering with function of cell wall, such as penicillin.
  • Bacteriostatic antibiotics stop bacteria from multiplying by interfering with DNA replication or other metabolic processes
  • Advantages: saved over 200 million lives, crucial pharmaceutical in the field of medicine
  • Disadvantages: Limited to bacterial infections, and side effects such as nausea and diarrhea may occur, and misuse and overuse has catalyzed bacterial resistance.