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Mogili Ramaiah
IARI, Ph.D Scholar
Division of Entomology
New Delhi-110012
Welcome
Term-Paper Presentation
SIGNALING PATHWAYS FOR INSECT
IMMUNE SYSTEM
Contents
 Introduction
 History
 Insect Immune System
 Antimicrobial Peptides
 Signaling pathways activating genes
 Summary
 Conclusion
 References
Introduction
 Animals
 Plants
Introduction
 Greek word “immunis” meaning exempt.
Resistance to infection
 Immunity : The ability of an organism to resist to a
particular infection
 Insects have evolved cellular and molecular defense
mechanisms against infection, these defense mechanisms
called “ IMMUNITY”.
History of Immunology
Louis Maupertuis
(1698-1759)
Experiment :
Paul Ehrlich
(1854-1915)
Proposed : Side chain theory
(antigen-antibody reaction)
Founder of cellular immunology
Noble prize – 1908 (Physiology
and medicine)
Father of natural immunity
Élie Metchnikoff
(1845-1916 )
Discovery of phagocytes( macrophages)
Major defense mechanism in innate immunity
Noble prize in physiology and medicine (1908)
Father of innate immunity
Edward Jenner
(1749-1823)
Pioneer of small pox vaccine
He used it in 1796 in the long title
of his Inquiry into the Variolae
vaccinae known as the Cow Pox
Father of immunology
Rudolf W. Glaser first reported the existence of immunity in the
grasshopper (Glaser, 1918)
Innate immune
response
Adaptive immune
response
Pathogens
 In born
 Present in the body at
all times
 Responds immediately
upon infection
 Responds in the same
way regardless of
infection
 Unable to keep
immunological
memory
Adaptive immunity
 Acquired
 Occurs after the
individual is exposed
to the pathogen
 Slow response
 Responds in a
pathogen and antigen
specific manner
 Keeps immunological
memory for longer
period
Insect immune system
Cellular immune
response
Humoral immune
response
Phagocytosis
Nodulation
Encapsulation
TOLL , IMD, JAK/STAT, JNK
– Production of AMPs
 PRPs – Pattern Recognition proteins
1. PAMPs- Pathogen Associated Molecular Pattern
2. DAMPs- Damage Associated Molecular Pattern
PRRs- Pattern-Recognition Receptors
Membrane-bound PRRs
1.Receptor kinases
2.Toll-like receptors
3. mannose receptor
Cytoplasmic PRRs
1.NOD-like receptors - Nucleiotide oligomerization Domain
(Bacterial)
2. RIG-like receptors – Retinoic acid Inducible gene (Viral)
Antimicrobial Peptides
AMPs are small, 12-50 amino acids, cationic peptides,
which bind anionic bacterial or fungal membranes
leading to disruption and cell death
(Zasloff, 2002; Yount and Yeaman, 2006)
 In spite of great differences in size, amino acid composition and
structure, most of the antimicrobial peptides from insects can be
grouped into one of three categories. The largest category in number
contains
 1.Peptides with intramolecular disulfide bonds forming hairpin-like
beta-sheets or alpha-helical-beta-sheet mixed structures.
 2. Peptides forming amphipathic alpha-helices.
 3.Peptides with an over representation in proline and/or glycine
residues.
 Two types of mode of action:
 1. through peptide-lipid interaction or
 2. through receptor-mediated recognition processes.
Antimicrobial peptides:
Antifungal
Antiparasitic
Antibacterial
Gram positive
Gram negative
Antiviral ? In insect
What do they do?
 Over 150 antimicrobial peptides (AMPs) have been isolated and
characterized in insects.
 Insect AMPs can adopt certain structures or contain unique
sequences and thus can be classified into four groups:
1. α-helical peptides (e.g., cecropin and moricin),
2. Cysteine-rich peptides (e.g., insect defensin and drosomycin),
3. Proline-rich peptides (e.g., apidaecin, drosocin and lebocin), and
4.Glycine-rich proteins (e.g., attacin and gloverin)
(Bulet and Stocklin, 2005; Otvos, 2000).
Cecropins were firstly isolated in H. cecropia after injection with
bacteria (Hultmark et al., 1980; Steiner et al., 1981). These peptides
are produced in response to septic injury by either Gram positive or
Gram negative bacteria and affect on cellular proliferation by
inhibiting the synthesis of proteins of the cell membrane.
Defensins and drosomycin are cysteine-rich peptides. Defensins,
destroy mostly gram-positive bacteria by forming channels in the
plasma membrane which leads to cell lysis, while drosomycin has an
antifungal activity.
Diptericin is an antibacterial peptide that has been found only in
diptera species and is induced upon Gram negative bacteria
infection in a way similar to attacins (Nappi and Ottaviani, 2000).
General activity spectra of AMP families
AMP family Acts against
Attacin Anti bacterial (Gram -)
Cecropin Anti bacterial (Gram -)
Defensin Anti bacterial (Gram +)
Diptericin Anti bacterial (Gram -)
Drosomycin Antifungal
Drosocin Antibacterial (Gram -)
Metchnikowin Antifungal
Insect antimicrobial peptides
AMPs
Signaling Pathways:
 The Toll pathway has a dual function, being central in
developmental processes
 Imd functions exclusively in immunity. Both pathways form part
of the humoral immune response that is triggered by the
recognition of microbes and results, via multiphase signal
transduction, in the secretion of antimicrobial peptides and other
microbe-targeting substances.
 Multipurpose pathways JNK and JAK/STAT also contribute to
immunity
 RNA interference is essential to viral defense
The Toll pathway
 Peptidoglycan recognition proteins
(PGRP)
 Spaetzle - processing enzyme (SPE)
and other proteases
 Serine protease Persephone (Psh)
 Myeloid differentiation primary
response 88 (dMyD88), Tube, and
Pelle,
 Cactusis normally bound to the
Nuclear Factor kappa B (NF-κB)
transcription factors Dorsal-related
Immunity Factor (DIF) and Dorsal
kinase
(Stokes et al., 2015
The IMD pathway
 Direct binding between PGRP-LC and
meso-diaminopimelic acid (DAP)-type
PG of Gram-negative bacteria.
 intracellular adaptor protein Immune
deficiency (Imd)
 Drosophila Fas - associated death
domain (dFADD) and the Death related
ced-3/Nedd2-like caspase( DREDD)
 Immune Response Deficient 5 (IRD5)
and Kenny (Key).
(Stokes et al., 2015
JAK/STAT Pathway
 It involves binding of the cytokine
ligand UPD to the transmembrane
receptor DOME, thereby inducing
phosphorylation of DOME by the
receptor-associated JAK tyrosine
kinase HOP.
 This phosphorylation creates a
docking site for inactive
cytoplasmic STAT proteins that in
turn are phosphorylated,
dimerised, and translocated into
the nucleus, where they activate
the transcription of numerous
target genes.
(Stokes et al., 2015
GNBS
In Brief
RNAi gene silencing technology
B2 – FHV(flock house virus)
A1 – CrPV (Cricket Paralysis Virus)
Summary
S.N Component TOLL
Pathway
IMD
Pathway
JAK/STAT
Pathway
1 Signaling molecule
2 Receptor
3 Modulator
4. Cellular activators or
second messengers
5 Transcription factor
6 Cellular effects
7. Example - Pathogens
Conclusion
 Molecular understanding of their mechanism of action is
still lacking.
“If your positivity immune system is low,
Any exposure to a person afflicted negativity can poison your life”
Questions
Why we need to study Immune system of insects?
 Innate Immunity Vs Adaptive Immunity
Important terms AMPs, PRPs, PRRs, JAK/STAT, JNK,
PAMPs, DAMPs etc
Signaling pathways for activating genes


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Molecular mechanism of insect immunity

  • 1.
  • 2.
  • 3. Mogili Ramaiah IARI, Ph.D Scholar Division of Entomology New Delhi-110012 Welcome Term-Paper Presentation SIGNALING PATHWAYS FOR INSECT IMMUNE SYSTEM
  • 4. Contents  Introduction  History  Insect Immune System  Antimicrobial Peptides  Signaling pathways activating genes  Summary  Conclusion  References
  • 6. Introduction  Greek word “immunis” meaning exempt. Resistance to infection  Immunity : The ability of an organism to resist to a particular infection  Insects have evolved cellular and molecular defense mechanisms against infection, these defense mechanisms called “ IMMUNITY”.
  • 7. History of Immunology Louis Maupertuis (1698-1759) Experiment :
  • 8. Paul Ehrlich (1854-1915) Proposed : Side chain theory (antigen-antibody reaction) Founder of cellular immunology Noble prize – 1908 (Physiology and medicine) Father of natural immunity
  • 9. Élie Metchnikoff (1845-1916 ) Discovery of phagocytes( macrophages) Major defense mechanism in innate immunity Noble prize in physiology and medicine (1908) Father of innate immunity
  • 10. Edward Jenner (1749-1823) Pioneer of small pox vaccine He used it in 1796 in the long title of his Inquiry into the Variolae vaccinae known as the Cow Pox Father of immunology Rudolf W. Glaser first reported the existence of immunity in the grasshopper (Glaser, 1918)
  • 12.  In born  Present in the body at all times  Responds immediately upon infection  Responds in the same way regardless of infection  Unable to keep immunological memory Adaptive immunity  Acquired  Occurs after the individual is exposed to the pathogen  Slow response  Responds in a pathogen and antigen specific manner  Keeps immunological memory for longer period
  • 13. Insect immune system Cellular immune response Humoral immune response Phagocytosis Nodulation Encapsulation TOLL , IMD, JAK/STAT, JNK – Production of AMPs
  • 14.  PRPs – Pattern Recognition proteins 1. PAMPs- Pathogen Associated Molecular Pattern 2. DAMPs- Damage Associated Molecular Pattern PRRs- Pattern-Recognition Receptors Membrane-bound PRRs 1.Receptor kinases 2.Toll-like receptors 3. mannose receptor Cytoplasmic PRRs 1.NOD-like receptors - Nucleiotide oligomerization Domain (Bacterial) 2. RIG-like receptors – Retinoic acid Inducible gene (Viral)
  • 15.
  • 16. Antimicrobial Peptides AMPs are small, 12-50 amino acids, cationic peptides, which bind anionic bacterial or fungal membranes leading to disruption and cell death (Zasloff, 2002; Yount and Yeaman, 2006)
  • 17.  In spite of great differences in size, amino acid composition and structure, most of the antimicrobial peptides from insects can be grouped into one of three categories. The largest category in number contains  1.Peptides with intramolecular disulfide bonds forming hairpin-like beta-sheets or alpha-helical-beta-sheet mixed structures.  2. Peptides forming amphipathic alpha-helices.  3.Peptides with an over representation in proline and/or glycine residues.  Two types of mode of action:  1. through peptide-lipid interaction or  2. through receptor-mediated recognition processes.
  • 19.  Over 150 antimicrobial peptides (AMPs) have been isolated and characterized in insects.  Insect AMPs can adopt certain structures or contain unique sequences and thus can be classified into four groups: 1. α-helical peptides (e.g., cecropin and moricin), 2. Cysteine-rich peptides (e.g., insect defensin and drosomycin), 3. Proline-rich peptides (e.g., apidaecin, drosocin and lebocin), and 4.Glycine-rich proteins (e.g., attacin and gloverin) (Bulet and Stocklin, 2005; Otvos, 2000).
  • 20. Cecropins were firstly isolated in H. cecropia after injection with bacteria (Hultmark et al., 1980; Steiner et al., 1981). These peptides are produced in response to septic injury by either Gram positive or Gram negative bacteria and affect on cellular proliferation by inhibiting the synthesis of proteins of the cell membrane. Defensins and drosomycin are cysteine-rich peptides. Defensins, destroy mostly gram-positive bacteria by forming channels in the plasma membrane which leads to cell lysis, while drosomycin has an antifungal activity. Diptericin is an antibacterial peptide that has been found only in diptera species and is induced upon Gram negative bacteria infection in a way similar to attacins (Nappi and Ottaviani, 2000).
  • 21. General activity spectra of AMP families AMP family Acts against Attacin Anti bacterial (Gram -) Cecropin Anti bacterial (Gram -) Defensin Anti bacterial (Gram +) Diptericin Anti bacterial (Gram -) Drosomycin Antifungal Drosocin Antibacterial (Gram -) Metchnikowin Antifungal
  • 24. Signaling Pathways:  The Toll pathway has a dual function, being central in developmental processes  Imd functions exclusively in immunity. Both pathways form part of the humoral immune response that is triggered by the recognition of microbes and results, via multiphase signal transduction, in the secretion of antimicrobial peptides and other microbe-targeting substances.  Multipurpose pathways JNK and JAK/STAT also contribute to immunity  RNA interference is essential to viral defense
  • 25. The Toll pathway  Peptidoglycan recognition proteins (PGRP)  Spaetzle - processing enzyme (SPE) and other proteases  Serine protease Persephone (Psh)  Myeloid differentiation primary response 88 (dMyD88), Tube, and Pelle,  Cactusis normally bound to the Nuclear Factor kappa B (NF-κB) transcription factors Dorsal-related Immunity Factor (DIF) and Dorsal kinase (Stokes et al., 2015
  • 26. The IMD pathway  Direct binding between PGRP-LC and meso-diaminopimelic acid (DAP)-type PG of Gram-negative bacteria.  intracellular adaptor protein Immune deficiency (Imd)  Drosophila Fas - associated death domain (dFADD) and the Death related ced-3/Nedd2-like caspase( DREDD)  Immune Response Deficient 5 (IRD5) and Kenny (Key). (Stokes et al., 2015
  • 27. JAK/STAT Pathway  It involves binding of the cytokine ligand UPD to the transmembrane receptor DOME, thereby inducing phosphorylation of DOME by the receptor-associated JAK tyrosine kinase HOP.  This phosphorylation creates a docking site for inactive cytoplasmic STAT proteins that in turn are phosphorylated, dimerised, and translocated into the nucleus, where they activate the transcription of numerous target genes. (Stokes et al., 2015
  • 29. RNAi gene silencing technology B2 – FHV(flock house virus) A1 – CrPV (Cricket Paralysis Virus)
  • 30.
  • 31. Summary S.N Component TOLL Pathway IMD Pathway JAK/STAT Pathway 1 Signaling molecule 2 Receptor 3 Modulator 4. Cellular activators or second messengers 5 Transcription factor 6 Cellular effects 7. Example - Pathogens
  • 32. Conclusion  Molecular understanding of their mechanism of action is still lacking.
  • 33. “If your positivity immune system is low, Any exposure to a person afflicted negativity can poison your life”
  • 34.
  • 35. Questions Why we need to study Immune system of insects?  Innate Immunity Vs Adaptive Immunity Important terms AMPs, PRPs, PRRs, JAK/STAT, JNK, PAMPs, DAMPs etc Signaling pathways for activating genes 