Insect Defences 2 Flashcards

1
Q

What does insect immune response consist of?

A

cellular and humoral elements

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2
Q

Cellular + humoral defences respond to…

A

…similar cues, e.g. components of pathogen surface molecules (sugars, lipopolysaccharides, proteins)

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3
Q

cellular defences mediated by…

A

… haemocytes

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4
Q

humoral defences mediated by…

A

…array of non-cellular mechanisms

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5
Q

name of the structures that the immune system is designed to recognise?

A

pathogen-associated molecular patterns (PAMPs)

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6
Q

insects and mammals have evolved…

A

…pattern-recognition receptors (PRRs) that bind conserved PAMPs

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7
Q

what are PRRs?

A

glycoproteins found at surface of variety of defence cells

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8
Q

gram -ve cell wall

A

consists of a single layer of peptidoglycan and has a layer of outer-membrane consisting of lipopolysaccharide, membrane proteins and porins

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9
Q

gram +ve cell wall

A

Gram-positive bacteria are surrounded by many layers of peptidoglycan (PG), which form a protective shell that is 30–100 nm thick (Silhavy et al. 2010).

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10
Q

PRRs recognise + bind…

A

…PAMPs - microbial molecular components NOT part of eukaryotes

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11
Q

What immune responses can be triggered by the recognition of PAMPs by different PRRs (esp toll and toll-like receptors)

A

phagocytosis

nodule formation

encapsulation

melanisation

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12
Q

cellular immune response

A
  • haemocytes play crucial role in wound healing + protection against infection throughout life of insect
  • secretion of compounds, e.g. phenoloxidase (contributes to humoral immunity)
  • direct involvement via cellular immunity
  • remove small particles by phagocytosis - microbes delivered to lysosomes + destroyed
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13
Q

cellular immune responses include…

A

phagocytosis

encapsulation

nodule formation

wound healing

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14
Q

Humoral immune response
Melanisation

A
  • Phenoloxidase (PO) = highly reactive + enzyme responsible for melanin synthesis
  • toxic quinone intermediates + reactive oxygen + nitrogen spp produced during melanin formation
  • mechanical injuries/presence of pathogens = melanin deposition around damaged tissue, isolating + preventing development of pathogen
  • POs also important for pigmentation + sclerotisation of many tissues
  • PO inactive form = proPO + stored in circulating haemocytes
  • released in response to wounding or microbial products
  • activated by limited proteolysis through action of specific serine protease
  • PO activation + melanisation also play key role in coagulation of haemolymph = clot formation
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15
Q

Toxic intermediates + reactive oxygen/nitrogen species

A
  • activation of proPO system = rapidly triggered upon pathogen invasion or injury to cuticle
  • during proPO activation, reactive oxygen and nitrogen intermediates (e.g. peroxides) made
  • cause oxidative damage to pathogens directly or indirectly
  • melanin + intermediates in its synthesis = toxic
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16
Q

Anti-microbial peptides (AMPs)

A

Cationic peptides < 100 aa residues (15-50)

Amphipathic structure = charged + hydrophobic areas

generate pore in membrane, or penetrate, bind + disrupt intracellular target

synthesised in fat body or in gut cells in response to infection + released into haemolymph

17
Q

Anti-microbial peptides

A

transcription acitvated:
via IMD (immune deficiency) signalling pathways in response to Gram- bacteria binding to receptors = peptidoglycan recognition proteins (PGRPs) (a type of PRR) on surface of insect cells
- via Toll signalling pathway activated by Gram + bacteria and fungi

18
Q

AMP specificity

A
  • Defensins (4 kD) Lyse bacterial cells by formation of membrane channels - occur across animal kingdom
  • Cecropins (3-4 kD) act like detergents, killing many, not all, bacteria - Gram +ve and -ve bacteria - creates membrane changes - various insects
  • Attacins (22-28 kD) narrower range - Gram -ve bacteria. prevent bacterial cell division by inhibiting biosynthesis of outer membrane proteins - various insects
  • Diptericin (8.6 kD) - active only against limited range of Gram-ve bacteria - seems to function by disrupting cytoplasmic membrane of growing bacteria