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OspA
outer surface protein in lyme bacteria. Present inside tick when temperature is low (25 C) It helps the bacteria adhere to the stomach of the tick. Decreases when temperature of tick increases
OspC
Outer surface protein of lyme bacteria. Is only present when the temperature is that of mammals (37 C). So when the tick bites the animal, OspC production increases. This allows the bacteria to move from the stomach to the salivary glands of the tick.
VlsE
A surface lipoprotein that has antigenic variation which allows the surface of the bacteria to change during the process of infection.
Antigenic variation
VlsE has silent cassette genes in front of it that it uses to incorporate into its surface protein to provide a plethora of different antigens in order to avoid detection by the immune system
Gram Negative Quorum Sensing
LasI produce Acylhomoserine lactone (Quorum sensing molecule) which is permeable to cell membranes, then activates LasR which binds to DNA.
Gram positive quorum sensing
Use small peptides as their quorum sensing signal. Peptides are not cell permeable and interact with a cell surface receptor/sensor kinase in order to enter the cell.
Type III effector proteins
1) ExoU
2) ExoS
3) ExoT
4) ExoY
ExoT
Prevents phagocytosis by
1) Targeting Rho and inactivates it thro hydrolysis of GTP (GAP activity)
2) Targeting Crk and ADP-ribosylating it. (inhibits Crks protein-protein interaction)
ExoS
prevents phagocytosis by
1) Targeting Rho and inactivating it thro GAP activity
2) *Targets ERM and ADP ribosylation blocks its normal phosphorylation capability
Similiarities between ExoT and ExoS
They both have Rho GAP activity, and ADP-ribosylation activity. They both have 2 targets and 2 mechanisms that inhibit phagocytosis.
ExoU
Used to break host cells membranes. Phospholipase A2: enzyme that targets phospholipids breaks esterbond at the 2 position of phospholipids and releases a arachidonic fatty acid , which feeds into eicosanoid synthesis (inflammation).
Exotoxin A
enters host cell and targets EF2 and ADP-ribosylates an amino acid on it, to render it non functioning and stop protein synthesis.
Type IV pili
Allow bacteria to adhere to host cell
Type II secretion
Secrete pili and toxins. The synthesis/elongation of pili in the periplasm/middle membrane pushes the toxin out of the cell.
L. monocytogenes properties
Gram positive rod shaped bacteria that uses host actin for mobility and can withstand a large range of temps. It escapes into the cytoplasm of host cells and spreads to adjacent cells.
Internalin A ( InlA )
Cell surface protein that binds to E-cadherin host receptor, which is in tight junctions. This cell surface protein helps with endocytosis of bacteria.
Internalin B (InlB)
Cell surface protein that binds to host Met receptor, and uses Clathrin mediated endocytosis to be engulfed.
Listerolicen O (LLO)
Pore forming Toxin that allows the bacteria to escape the endosome and enter the cytoplasm. It is activated by a cholesterol membrane and low pH.
Phospholipase C (PLC)
contributes to the breakdown of the endosome
ActA
Recruits ARP2/3 and increases its activity which is to recruit Monomeric Actin to it and uses them to make polymerized actin. This is done to propel the bacteria forward.
Efferocytosis and Listeria monocytogenes
Listeria uses the hosts efferocytosis ability to promote cell to cell transfer. They damage the cell cytoskeleton which produces Phosphatidylserine on the cell surface which is recognized by macrophages Tim4 receptors to engulf the injured cell. Listeria then infects that macrophage in the same way
Zoonose
Disease that can be transmitted from animals to humans
What kind of bacterial shape is Borrelia burgdorferi?
Spirochetes
Borrelia burgdorferi's genome is mainly (circular/linear)
Linear. This is unique to Borrelia
Lipoproteins
Proteins that are secreted into the periplasm via the SEC pathway. In the periplasm, they are modified with a lipid and can be docked into the cytoplasmic or outer membrane
What is unique about Borrelia's lipoproteins?
Mainly surface-exposed.
What is an important signal for the changing expression of Borrelia's lipoproteins?
Temperature:
OspC is synthesized at 37C
OspC is not synthesized at 24C
Which of the following temperatures is OspC synthesized? 37C or 24C
37C- within the mammal
Variable major protein (VlsE)
Has the potential for antigenic variation by recombination of normally silent alleles allowing for distinct forms of VlsE protein to be expressed
Phase variation
Simplest form of antigenic variation
Doesn't involve genetic mutation
Simply turning a gene on, or turning a gene off
How to calculate phenotypes of phase variation
# of phenotypes= 2^N
Where N is number of independently regulated genes
Serotype
Bacteria that are antigenically similar
Mosaic effect
Borrelia burgdorfi can express many distinct antigens at one time
Where are the combined (variable) regions present in the Borrelia glycolipid
The "cone" top
Antibodies are most likely directed to this site
OspA is present when the Borrelia is in (tick/mammal)
Tick
OspC is present when the Borrelia is in (tick/mammal)
Mammal
VlsE is present when the Borrelia is in (tick/mammal)
Mammal
Of the following, which is most necessary for Borrelia infection and why: OspA, OspC or VlsE
OspC
Pseudomonas aeruginosa
Gram negative
Found in soil
Resistant to most antibiotics
Lots of virulence factors (LPS, TIIISS, Exotoxin A, Biofilm formation)
Steps of biofilm formation
Attachment
Growth
Dispersal
Acyl-homoserine lactones
Used by gram negative bacteria for quorum sensng
Genes required for growth of biofilm:
LasR response regulator
LasI
LasI
Required for synthesis of a mature biofilm
Makes acylhomoserine lactone.
Takes an acyl chain from an acyl carrier protein and uses S-adenosyl-methionine
T/F: All bacteria have a form of LasI
True
DeltaLasI Borrealis mutant characteristic:
Able to adhere to surfaces but unable to form the architecture of a mature biofilm
Alginate
Coating that surrounds pseudomonas when it is in the CF lungs to mask it from host immune system.
arr
Aminoglycoside resistance regulator
Is a phosphodiesterase that cleaves a small molecule called cyclic-di-GMP
In the pond environment, there is (high/low) c-di-GMP.
In the human environment, there is (high/low) c-di-GMP
High=biofilms
Low
c-di-GMP effector functions
Motility
Virulence
Sessility and biofilm formation
Cell cycle progression
Pseudomonas' Type III secretion system secretes:
ExoU
ExoT
ExoS
ExoY
Which Pseudomonas effector molecule disrupts tight junctions
ExoS
Which Pseudomonas effector molecule enhances eicosanoid synthesis
ExoU
Which Pseudomonas effector molecule functions in the same way as Anthrax?
ExoY
Pseudomonas' Type II secretion system secretes:
Phospholipase C
Exotoxin A
Chitin-binding protein
Elastase
Lipase
When Psuedomonas recognizes an HSL, transcribes two proteins for virulence:
LasA= Protease
LasB= Elastase
Brominated furinone
Has no effect on survival of biofilms, simply makes them vulnerable to antibiotics
Tobramycin
Increases biofilm formation
What type of antibiotics INCREASES biofilm formation
Aminoglycosides