15.3/17.4/15.4 Flashcards

1
Q

What are adhesins?

A

Proteins that aid in attachment to host cell receptors

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2
Q

Where are adhesins most commonly found?

A

Fimbriae or pili

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3
Q

T/F Adhesins can be universally used and don’t have specificity

A

F

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4
Q

What is it called when bacteria is in blood?

A

-bacteremia

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5
Q

What is it called when viruses are in the blood?

A

vieremia

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6
Q

What is it called when toxins are in the blood?

A

toxemia

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7
Q

What is it called when bacteria is present and multiplying in the blood?

A

Septicemia

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8
Q

What are extracellular enzymes used to host tissues called?

A

Exoenzymes

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9
Q

What exoenzymes degrade hyaluronic acid that cements cells together to promote spreading through tissues? Example: Hyaluronidase S in S. aureus

A

Glycohydrolases

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10
Q

What exoenzymes degrade DNA released by dying cells (bacteria and host cells) that can trap the bacteria, thus promoting spread? Example: DNAse produced by S. aureus

A

Nucleases

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11
Q

What exoenzymes degrade the phospholipid bilayer of host cells causing cellular lysis, and degrade the membrane of phagosomes to enable escape into the cytoplasm?

A

Phospholipases

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12
Q

What exoenzymes degrades collagen in connective tissue to promote spread?

A

Proteases

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13
Q

What are biological poisons that assist in ability to invade and cause tissue damage?

A

Toxins

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14
Q

What category of toxin can be defined as lipopolysaccharides that triggers host inflammatory responses; can cause sever fever and shock?

A

Endotoxins

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15
Q

What type of toxin can be defined as proteins mostly produced by Gram (+); targets receptors on specific cells

A

Exotoxins

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16
Q

What uses blood cells of a horseshoe crab mixed with a patient’s serum; observed chromogenically or by coagulation? What does it detect?

A

Limulus amebocyte lysate (LAL) Test; endotoxin

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17
Q

What uses antibodies to detect endoxins?

A

ELISA - enzyme-linked immunosorbent assay

18
Q

What is intracellular targeting?

A

a category of exotoxin with A and B regions for activity and binding

19
Q

What is called when the subcategory of exotoxins are phospholipases that degrade bilayer membrane

A

Membrane-disrupting

20
Q

What can Hemolysins and Leukocidins do and what are they?

A

Membrane-disrupting exotoxins that can target RBC, WBC, and other cells

21
Q

What triggers the excessive production of cytokines by immune cells? What are examples of this?

A

Superantigen; S. aureus and Toxic Shock Syndrome

22
Q

What are these examples of:
- Capsules that enlarge bacterial cells so phagocytes cannot engulf pathogens
- Proteases digest host antibody molecules

A

Host evasion

23
Q

What is antigenic variation?

A

Alteration of cell surface to hide from immune cell recognition

24
Q

What is antigenic drift and shift a virulence of?

A

A virulence factor for viruses

25
Q

What virulence in viruses are point mutations causing slight changes in spike proteins (H and N)?

A

Antigenic drift

26
Q

What virulence in virus are major changes in spike proteins due to gen reassortment?

A

Antigenic shift

27
Q

What virulence properties do bacteria and viruses have in common?

A

Adhesins and antigenic variation

28
Q

What virulence properties do Fungi and Bacteria have?

A

Adhesins, exoenzymes, and toxins

29
Q

What are produced by Claviceps purpurea and Aspergillus spp. that contaminate grains and other staple crops

A

Mycotoxins

30
Q

What virulence properties do Protozoans and Bacteria have in common?

A

Adhesins, toxins, antigenic variation, etc.

31
Q

Which virulence factor is this?
- Plasmodium Falciparum quickly changes adhesive protein for RBCs to avoid immune recognition; causes chronicity in malaria patients

A

Antigenic variation

32
Q

What is Glycan gimmickry and what uses this type of method?

A

mimic host cells to evade the immune system; host evasion that helminths use

33
Q

How is diapedesis intitiated?

A

Complement factor 5a and cytokines

34
Q

What is the process of leukocytes passing through capillary walls to tissues?

A

Diapedesis/extravasation

35
Q

What is the process of flattening out and squeezing through cellular junction after “rolling adhesion”?

A

Transendothelial migration

36
Q

What does PAMPS represent?

A

Pathogen-associated molecular patterns; for auto recognition

37
Q

What can peptidoglycan, LPS, Flagellin, Microbial DNA/RNA, and lipopeptides be examples of?

A

PAMPs

38
Q

What are the structures that allow phagocytic cells to detect PAMPs?

A

Pattern recognition receptors (PRRs)

39
Q

What binds to PAMPs and communicates with phagocyte nuclease to elicit a response?

A

Toll-like receptor (TLRs)

40
Q

What can PRRs on macrophages also respond to?

A

Chemical distress signals from damaged or stressed cells; inflammatory response

41
Q

What happens when PAMP is recognized

A

Phagocyte activates genes for phagocytosis, cell proliferation, interferon production, and/or cytokines

42
Q

Order the phagocytosis stages in the right order?

A
  • Expulsion of debris
  • Formation of phagosome
  • Formation of phagolysosome and pathogen particle degradation
  • Pathogen engulfment (phagocytosis)