question
How do bacteria evade the innate immune system?
answer
Intracellular residence
- invasins
- protection from innate immune system
- not 100% fool proof (cytotoxic T cells)
- ex. Mycobacterium tuberculosis in macrophage
- have ability to prevent lysosome and phagosome from fusing or stop pH from dropping
Bacterial capsule (polysaccharide layer)
- prevents membrane attack complex (MAC) in complement cascade
- prevent antimicrobials from accessing cell
- prevent antigens from being detected
- tested by Griffith's classic experiment (smooth vs. rough strains) with transformation (when organism takes up DNA from surrounding environment and express it)
Modifying surface structures
- LPS (lipopolysaccharide) on surface of Gram - bacteria
- can modify phosphate groups in inner core into other groups that isn't so negatively charged to repel positively charged antimicrobials
- change composition of antigens in O antigen
- invasins
- protection from innate immune system
- not 100% fool proof (cytotoxic T cells)
- ex. Mycobacterium tuberculosis in macrophage
- have ability to prevent lysosome and phagosome from fusing or stop pH from dropping
Bacterial capsule (polysaccharide layer)
- prevents membrane attack complex (MAC) in complement cascade
- prevent antimicrobials from accessing cell
- prevent antigens from being detected
- tested by Griffith's classic experiment (smooth vs. rough strains) with transformation (when organism takes up DNA from surrounding environment and express it)
Modifying surface structures
- LPS (lipopolysaccharide) on surface of Gram - bacteria
- can modify phosphate groups in inner core into other groups that isn't so negatively charged to repel positively charged antimicrobials
- change composition of antigens in O antigen
question
How do A-B subunit toxins work, and what are some examples?
answer
- responsible for millions of deaths every year
- two subunits (A and B)
- B recognizes host cell and binds to receptor on host cell to gain entry into cell
- A does the damage/toxic activity
- ADP-Ribosylation (toxin adds ADP-ribose to part of genome)
- gene carried by virus (can cause bacteria w/out toxin gene to get it)
Examples:
- Diphtheria toxin produced by Corynebacterium diphtheriae (toxin adds ADP-ribose onto TEF (translation elongation factor) which leads to shut down of translation in cell = no more protein = cell death)
- Cholera toxin produced by Vibrio cholerae (kills by dehydration by diarrhea) (toxin adds ADP-ribose to G protein = causes non-homeostasis draws water out into intestine w/ ions via chloride channels = diarrhea = death)
- Tetanus toxin produced by Clostridium tetani (toxin targets neurons, spastic paralysis) (one of the most toxic)
- Botulinum toxin produced by Clostridium botulinum (flaccid paralysis) (one of the most toxic)
- two subunits (A and B)
- B recognizes host cell and binds to receptor on host cell to gain entry into cell
- A does the damage/toxic activity
- ADP-Ribosylation (toxin adds ADP-ribose to part of genome)
- gene carried by virus (can cause bacteria w/out toxin gene to get it)
Examples:
- Diphtheria toxin produced by Corynebacterium diphtheriae (toxin adds ADP-ribose onto TEF (translation elongation factor) which leads to shut down of translation in cell = no more protein = cell death)
- Cholera toxin produced by Vibrio cholerae (kills by dehydration by diarrhea) (toxin adds ADP-ribose to G protein = causes non-homeostasis draws water out into intestine w/ ions via chloride channels = diarrhea = death)
- Tetanus toxin produced by Clostridium tetani (toxin targets neurons, spastic paralysis) (one of the most toxic)
- Botulinum toxin produced by Clostridium botulinum (flaccid paralysis) (one of the most toxic)
question
How does hemolysin benefit bacteria? How do we use it to our advantage?
What is hemolysin, how does it help bacterial pathogens, and how can we use it to identify organisms?
What is hemolysin, how does it help bacterial pathogens, and how can we use it to identify organisms?
answer
- hemolysin disrupts cell membrane of RBC (causes RBCs to lyse open) (inserts barrel end into cell membrane to create pore)
- bacteria uses the iron in hemoglobin
- can streak bacteria on blood agar and see hemolysis (alpha, beta, gamma) to identify organisms
- bacteria uses the iron in hemoglobin
- can streak bacteria on blood agar and see hemolysis (alpha, beta, gamma) to identify organisms
question
What is endotoxin and how does it cause the clinical sign associated with endotoxic shock?
answer
- LPS (lipopolysaccharide)
- Gram neg. bacteria
- on outer membrane
- Lipid A in membrane (anchor) (similar b/w species) (conserved)
- core (linker region) (some diversity b/w strains) (fairly conserved)
- O antigen (long chain that varies) (different carbohydrates that link in different ways) (very diverse)
- induce inflammation and fever as an immune response
- Reaction to endotoxins can lead to anaphylactic shock and death
- sepsis
- Gram neg. bacteria
- on outer membrane
- Lipid A in membrane (anchor) (similar b/w species) (conserved)
- core (linker region) (some diversity b/w strains) (fairly conserved)
- O antigen (long chain that varies) (different carbohydrates that link in different ways) (very diverse)
- induce inflammation and fever as an immune response
- Reaction to endotoxins can lead to anaphylactic shock and death
- sepsis
question
What is the difference between an intoxication disease and an infection?
answer
intoxication illness = when you consume toxic material but not live organisms themselves (ex. foodborne intoxication: bacteria killed by cooking/heat but toxins not inactivated)
infection = consuming organisms that cause the illness
infection = consuming organisms that cause the illness
question
What is the difference between active and passive immunization?
answer
Active
- deliver actual etiologic agent (or part of it) to host and they build their own immune response to it (prevention)
- Pro = activate memory cells/long lasting immunity
- Con = takes several weeks to become immune
Passive
- deliver antibodies to host
- Pro: immediate immune response
- Con: immune system (yours) doesn't have memory for future infections (no lasting immunity)
- ex. breastfeeding, convalescent plasma (CCP)
- deliver actual etiologic agent (or part of it) to host and they build their own immune response to it (prevention)
- Pro = activate memory cells/long lasting immunity
- Con = takes several weeks to become immune
Passive
- deliver antibodies to host
- Pro: immediate immune response
- Con: immune system (yours) doesn't have memory for future infections (no lasting immunity)
- ex. breastfeeding, convalescent plasma (CCP)
question
What is the difference between an inactivated vaccine and an attenuated vaccine?
answer
Inactivated
- killed organism
- can't cause infection
- Pro: no risk of infection
- Con: not as strong immune response
Attenuated
- modified live organism
- can cause mild disease/infection
- miss the things that make them bad (lose abilities to replicate in human cells)
- better immunity and long lasting
- ex. Tuberculosis; BCG = cow version
- killed organism
- can't cause infection
- Pro: no risk of infection
- Con: not as strong immune response
Attenuated
- modified live organism
- can cause mild disease/infection
- miss the things that make them bad (lose abilities to replicate in human cells)
- better immunity and long lasting
- ex. Tuberculosis; BCG = cow version