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The Immune System of Triatomines

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Triatominae - The Biology of Chagas Disease Vectors

Part of the book series: Entomology in Focus ((ENFO,volume 5))

Abstract

All insects rely on an innate immune system to eliminate potentially lethal parasites and pathogens. In kissing bugs, this immune system comprises a plethora of elements that first recognize parasites and pathogens as non-self, followed by a multi-faceted response to eliminate them. There is an intriguing molecular interplay between kissing bugs and pathogens; the insects wish to eliminate pathogens while not eliminating the obligate intestinal microbial symbionts on which they depend for survival. Beneficial bacteria and the human parasite Trypanosoma cruzi survive in the lumen of the intestinal tract but are eliminated if they enter the hemocoel. The closely related parasite, Trypanosoma rangeli, however, survives in the hemocoel and later establishes in the salivary glands. Our understanding of triatomine-pathogen interactions has expanded dramatically due to the availability of new molecular and genetic tools that allow us to understand the expression and function of immune molecules, and the mechanisms by which they function. The immune system in triatomines has three main components: physical barriers, cellular responses (phagocytosis, nodulation, and encapsulation), and humoral factors (antimicrobial peptides, lectins, reactive oxygen and nitrogen species, and the phenoloxidase cascade). Here, we describe the current knowledge and adaptations of the innate immune system of triatomines, how it interacts with pathogens and parasites, and the challenges we face in studying these interactions.

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Abbreviations

AA:

Arachidonic acid

AMG:

Anterior midgut

AMP:

Antimicrobial peptides

CLR:

C-type lectin

DAMP:

Damage-associated molecular patterns

DTU:

Discrete typing units

DUOX:

Dual oxidase

ERK:

Extracellular signal-regulated kinase

GI:

Gastrointestinal

GIPL:

Glycoinositolphospholipid

GNBP:

Gram-negative binding proteins

Gr−:

Gram-negative bacteria

Gr+:

Gram-positive bacteria

IMD:

Immune deficiency pathway or protein

JAK/STAT:

Janus kinase/signal transducer and activator of transcription

JNK:

Jun N-terminal kinase

LOX:

Lipoxygenase

LPS:

Lipopolysaccharides

NADPH:

Nicotinamide adenine dinucleotide phosphate

NO:

Nitric oxide

NOS:

Nitric oxide synthase

NOX:

NADPH oxidase

OUT:

Operational taxonomic units

PAF:

Platelet activating factor biosynthetic pathway

PAMP:

Pathogen associated molecular patterns

PGRP:

Peptidoglycan recognition receptors

PLA2:

Phospholipase A2

PMG:

Posterior midgut

PMM:

Perimicrovillar membrane

PO:

Phenoloxidase

PPO:

Prophenoloxidase

PRR:

Pattern recognition receptors

Pvr:

Platelet-derived growth factor and vascular endothelial growth factor-receptor related

Pxt:

Peroxinectin

RNS:

Reactive nitrogen species

TNF:

Tumor necrosis factor

TOR:

Target of rapamycin

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Correspondence to Carl Lowenberger .

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Salcedo-Porras, N., Lowenberger, C. (2021). The Immune System of Triatomines. In: Guarneri, A., Lorenzo, M. (eds) Triatominae - The Biology of Chagas Disease Vectors . Entomology in Focus, vol 5. Springer, Cham. https://doi.org/10.1007/978-3-030-64548-9_14

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