Lecture 7 - Bacterial secretion systems Flashcards

1
Q

What is the role of translocation and secretion in bacteria?

A

1/3 of proteins = PM and OM by translocation, external by secretion

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2
Q

How are proteins moved in G+ve vs G-ve bacteria?

A
  • G+ve = translocated across PM thru porous CW or embedded in CW
  • G-ve = translocated across CW or secreted thru OM via 11 systems
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3
Q

What is the Sec system? Which bacteria use it?

A

Major pathway for translocated unfolded proteins across PM in both G+ve and G-ve

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4
Q

What is co-translational translocation in the Sec system?

A

Inserting proteins into PM

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5
Q

Describe the 4 step process of co-translational translocation

A
  1. PM protein’s translation ribosome coupled to translocation by Sec
  2. Signal sequence at N-terminal of 1st protein recog by signal recog particle (SLP)
  3. SRP recruits docking FtsY = delivers protein to SecYEG transmembran channel
  4. Protein escapes by translation into membrane during translocation
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6
Q

What is post translational translocation in the Sec system?

A

Moving unfolded preproteins across PM to periplasm/OM/external

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7
Q

Describe the 5 step process of post-translational translocation

A
  1. Signal peptide at N terminal recog by SecB chaperons
  2. SecB binds signal = delayed folding and delivery to SecA
  3. SecA guides protein to channel then acts as ATPase to translocate preprotein across PM
  4. SecY, SecE and SecG form membrane channel
  5. Signal peptidase removes signal peptide = folding
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8
Q

What is the Tat pathway used for? Which bacteria use it?

A
  • Proteins to be secreted in folded form
  • Both G+ve and G-ve
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9
Q

Compare the Sec-dependent and Sec-independent secretion systems and which types are in each

A
  1. Sec dependent = needs Sec/Tat for transport into periplasm, types 2, 5
  2. Sec independent = doesn’t need Sec/Tat, types 1, 3, 4, 6
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10
Q

Describe how the T2SS works and give example/s of the proteins transported by it

A
  • Pseudopilus in periplasm connects PM proteins to OM channel
  • Piston model = pseudopilus extends/retracts by ATP to push protein thru OM channel
  • AB cholera toxins, proteases, lipases
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11
Q

Describe the process of T5SS and example/s of proteins transported by it

A
  1. N terminal signal peptide of unfolded protein recog by SecB = translocated across PM to periplasm
  2. Unfolded protein autotransported via translocator domain as OM pore and passenger domain to pass thru
  3. Autoproteolytic cleavage to release passenger domain
    Eg. virulence proteins IgA protease of N. gonorrhoeae and Ics of Shigella flexneri
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12
Q

Describe the T1SS and example/s of proteins transported by it

A
  • Bypass Sec and periplasm straight to surface
  • Protein complex = ATP binding cassette (ABC) transported in PM, TolC pore forming in OM, connecting protein
  • Eg. virulence and resistance eg E. coli’s alpha-haemolysin and multidrug efflux
  • G-ve bacteria esp
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13
Q

Describe the T3SS, important bacteria it’s used in, and example/s of proteins transported

A
  • Injectisome needle extends beyond OM to directly inject virulence factors
  • Evolved from flagellar assembly proteins bc base = basal body
  • Eg. E. coli, Salmonella, Shigella, Pseudomonas
  • Toxins, phagocytosis inhibitors, invasins
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14
Q

Describe the T4SS and example/s of proteins transported by it

A
  • 12+ complex forming pilus/tunnel that grows and binds to host integrins = direct transfer
  • Eg. E. coli’s F plasmid
  • Eg. Agrobacterium’s Ti plasmid for oncogenic T-DNA into plants
  • H. pylori’s CagA inflammatory effector
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15
Q

Describe the T6SS and example/s of proteins transported by it

A
  • Related to phage injection system = same phage tail structure of baseplate sheath inner tube, same secretion by contraction, VrgG forming sharp tip
  • Effector proteins assemble and loaded on tip in cytoplasm then contraction and ejection to puncture target cell
  • Eg. E. coli’s T4 lytic phage
  • Eg. peptidoglycan hydrolases in interbacterial warfare
  • V. cholerae’s effectors into macrophages to inactivate actin
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16
Q

What secretion systems are common in G-ve?

A
  • Pilus adhesins for attachment and colonisation
  • Delivery of toxins/effectors to host by secretion systems
17
Q

What is antivirulence and how are secretion systems related to it? What system is currently under study?

A
  • Antivirulence = reduce virulence without antibiotics
  • Block common secretion systems in bacteria eg pilus adhesins and delivery of toxins/effectors
  • T3SS inhibitors identified