chapter 16 Flashcards

1
Q

pathogens

A
  • Microorganisms capable of causing disease (damage to the host)
    • Different species have different virulence properties (ex: streptococcus pneumoniae= highly virulent vs salmonella enterica= moderately virulent)
    • Not all strains of a species have the same ability to cause disease (e.coli)
      A pathogen is usually identified by the set of virulence genes that it carries and expresses
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2
Q

virulence

A
  • Measure of the ability to cause damage to the host, depends on a number of virulence factors
    • Determined by 2 basic features (NOT mutually exclusive):
      1. INVASIVENESS: ability of the microorganism to become established in the host, to overcome the host defense and to spread in the tissues
      TOXIGENICITY: the capacity of the microorgansims to produce substances known as toxin that damage SPECIFIC tissues of the host
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3
Q

invasiveness

A
  • Pathogens use different virulence factors to invade hot tissues:
    1. Adhesins
    2. Capsules
    3. Enzymes that destroy host tissues
    4. Invasins
      Type 3 secretion system (T3SS) and type 4 secretion system (T4SS)
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4
Q

adhesins

A
  • Promote SPECIFIC attachment to the host cell surfaces
    • One adhesin type is usually able to attach to one or a few cell types, determine the site of colonization
    • Afimbrial adhesins: glyco/lipo proteins (not filaments) mediate close attachment
      Fimbriae/pili: polymers, mediate loose attachment
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5
Q

capsule

A
  • Produced by some bacterial pathogens
    • Prevents the pathogens from being destroyed by host immune system (phagocytes)
    • Also mediates attchment to host cells and to other bacteria
    • Essential virulences factor for some bacterial pathogens: streptococcus pneumonia and Haemophilus influenzae
      The capsule is not ONLY a virulence factor (non pathogenic microorgansism may have a capsule too)
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6
Q

invasion: enter hos tissues, multiply , and spread = destruction of host tissues

A
  • Penetration of epidermis: most pathogens use a breach in the skin (wounds, surgery, catheter)
    Penetration of the mucosa: destruction of the single-cell layer or invasion of cells
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7
Q

release of extracelullar enzymes

A
  • Hyaluronidase: degrades hyaluronic acid, a sticky polysaccharide that holds host cells together. Staphylycocci, streptococci, clostridia
    • Collagenase: degrades the protein collagen present in connective tissues (muscle, cartilage). Clostridia
    • Lecithinase: degrades lecithin (phosphatidylcholine) in cell membrane- causes the lysis of red blood cells and destroys tissue cells
      Gas gangrene: clostridium perfringens (stric anaeroe). Infection of a deep wound. Uses lecithinase to lyse host cells, collagenase and hyaluronidase to destroy ECM
    • HEMOLYSIS: some are enzymes (lecithinase, phospholipase) some are cytolisins (pore-forming). Produced by a great variety of bacteria. Cause lysis of red blood cells and a variety of cell types
    • LEUCOCIDIN: causes lysis of leucodytes- white blood cells (WBC)- produced by staphylococci, streptococci and a few Gram-neg
    • PROTEASES: degrade complement proteins and/or antibodies, produced by several bacteria
      COAGULASE: produced by virulent staphylococci; causes insoluble fibrin to be deposited on bacterial cells and cloaks the bacteria from the immune system
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8
Q

invasins

A
  • Surface proteins, or injected proteins, that allow microorganisms to enter cells (invade host cell)
    • Major virulence factor of intracellular pathogens
      Invasion of host cells, including phagocytes, protect the bacterial pathogens against the host immune system; good source of nutrients
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9
Q

growth inside host cells

A
  • Need to modifiy the properties and behaviour of the host cell:
    1. Black phagosome maturation (block digestion)
    2. Increase size of the vacuole
    3. Acquire nutrients
      Block detection of intracellular infection and response (host defense)
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10
Q

type 3 and type 4 secretions systems

A
  • A large number of gram-negative pathogens use T3SS or T4SS
    • T3SS forms a channel through the bacterial cytoplasmic membrane (periplasm), the outer membrane and the host cell membrane so bacterial proteins can be injected into the host cell cytosol
    • Function:
      1. Invasion of host cells
      2. Block phagosome maturation
      3. Take control of host cells
    • T4SS: similar to T3SS but absence of needle-like structure
      Also called injectisomes
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11
Q

toxigenicity

A
  • Many pathogens are able to produce toxins that cause damage to the cells. Extracellular enzymes that cause damage are toxins
    • Toxin production is not always necessary for an organism to be highly virulent. Damage can be caused by the host’s own immune system or be a result of the large numbers of pathogens present
    • Bacterial pathogens are associated with 2 distinct categories of diseases:
      1. INFECTIOUS DISEASES (pneumonia, meningitis, syphilis): result from the pathogen’s growth
      2. INTOXICATIONS (food poisoning): result from the presence of a specific toxin
    • Toxins are divided in 2 categories:
      1. EXOTOXINS (exo=external): secreted into the surrounding as the bacterial pathogen grows
      ENDOTOXINS (endo=internal): part of the bacterial pathogens
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12
Q

exotoxins

A
  • Soluble, secreted or released when the organism is lysed, usually proteins, usually heat-labile (destroyed by heat)
    • Highly immunogenix (antibody response inactivates exotoxins)
    • Extremely potent, amongst the most lethal substances known
    • Categorized by their target:
      1. Neurtoxins (nerve tissue): 1 mg of C. botulinum neurotoxin is sufficient to kill 10^6 guinea pig. 1 pund is enough to kill the entire human population
      2. Enterotoxins (GI tract)
      3. Nephrotoxins (kidney)
      4. Hepatotoxins (liver)
      5. Cardiotoxins (heart)
    • Extracellular enzymes (hyalurodinase collagenase
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13
Q

AB toxins

A
  • Modify host cells
    • Composed of 2 subunits:
      1. Enzymatic subunit (A)
      2. Binding/cell entry (B)
    • Subunit A modifies a target inside the host cell leading to damage to the host ex: ADP-ribosyltransferase
    • Subunit B binds to specific cell receptors providing tissue/cell type specificity
      Ex: diphteria toxin
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14
Q

AB toxin: botulinum toxin

A
  • Colstridium botulinum
    • Neutrotoxin:
      1. Block acetylchone release in neuromuscular junction
      ** it will inhibit the contraction of the muscles
      2. Flaccid paralysis
    • Affects humans, cattle, horses, duck..
    • BOTOX:
      1. Reduces wrinkles/frown
      2. Muscle spasms
      Hyperhydrosis (excessive sweating)
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15
Q

AB toxin: tetanus toxin

A
  • Clostridium tetanii, found in soil (spore)
    • Bacteria is able to infect deep puncture wounds and produces the toxin TeNT. The toxin diffuses away, enters the blood stream and acts on neurons
    • Causes spastic paralysis: bowed spines, clenched arm and leg muscles, and locked jaws
    • it will inhibit the release of glycine which allows the relaxation of muscle by stopping acetycholine
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16
Q

AB5 toxin: cholera toxin

A
  • Infection by Vibrio cholerae is characterized by severe diarrhea, massive loss of fluid from the intestinal tract
    B: bind to intestinal cells
    A: activates adenylate cyclase, produce cAMP
    • Steps:
      1. Activation of epithelial adenylate cyclase by cholera toxin
      2. NA+ movement blocked, net Cl- movement to lumen
      Massive water movement to the lumen; cholera symptoms
17
Q

endotoxins

A
  • Endo= internal: part of the bacterial pathogen
    • Lipid A of LPS from Gram-negative bacterial pathogens. Released during multiplication or lysis of bacterial cells
    • HEAT STABLE; cannot be inactivated
    • Weakly immunogenic (no antibosy are produced against LPS)
    • Very EFFECTIVE ACTIVATOR OF THE IMMUNE SYSTEM, produce general systemic effects: fever (pyrogenic), shock, weakness, inflammation, diarrhea; SEPTIC SHOCK
      Important cause of symptoms in all gram-negative bacterial infections (salmonella, e.coli)
18
Q

vaccine against toxins

A
  • Endotoxins are highly antigenic: stimulates the host defense systems to produce antibodies that can neutralize the toxin
    • Vaccines against exotoxins:
      1. A toxin is toxic, it cannot be used as it is
      2. Toxins are first inactivated by heat or formaldehyde = toxoids
      3. Toxoids are no longer toxic, byt still antigenic (induce antibody response)
      4. Ex: vaccines against the diphteria toxin (DTaP)
      Endotoxins cannot be inactivated by heat or formaldehyde and cannot be convert to a toxoid: no vaccines against endotoxins