Recent trends in insect gut immunity

The gut is a crucial organ in insect defense against various pathogens and harmful substances in their environment and diet. Distinct insect gut compartments possess unique functionalities contributing to their physiological processes, including immunity. The insect gut’s cellular composition is vital for cellular and humoral immunity. The peritrophic membrane, mucus layer, lumen, microvilli, and various gut cells provide essential support for activating and regulating immune defense mechanisms. These components also secrete molecules and enzymes that are imperative in physiological activities. Additionally, the gut microbiota initiates various signaling pathways and produces vitamins and minerals that help maintain gut homeostasis. Distinct immune signaling pathways are activated within the gut when insects ingest pathogens or hazardous materials. The pathway induced depends on the infection or pathogen type; include immune deficiency (imd), Toll, JAK/STAT, Duox-ROS, and JNK/FOXO regulatory pathways. These pathways produce different antimicrobial peptides (AMPs) and maintain gut homeostasis. Furthermore, various signaling mechanisms within gut cells regulate insect gut recovery following infection. Although some questions regarding insect gut immunity in different species require additional study, this review provides insights into the insect gut’s structure and composition, commensal microorganism roles in Drosophila melanogaster and Tenebrio molitor life cycles, different signaling pathways involved in gut immune systems, and the insect gut post-infection recovery through various signaling mechanisms.


Introduction
Food is vital for life.To thrive in their natural environment and ensure survival, insects must obtain nourishment through various ways such as adaptations, physiological processes, and reproductive activities.Consequently, insects are compelled to gather food from diverse environmental outlets that often harbor harmful microorganisms that can invade the insect's digestive system.Therefore, insect digestive systems must employ expansive defense mechanisms to counteract infection risks or potential harm (1).
The insect gut composition is crucial for orchestrating defense mechanisms.The peritrophic membrane, comprising chitin and protein, collaborates with glycosylated protein-based mucus, intestinal epithelial cells, and intestinal stem cells to establish a robust physical shield against invading pathogenic microorganisms (2).The peritrophic membrane is the foremost defense and a formidable barrier that safeguards the midgut epithelium from abrasive food particles and lethal pathogen incursions (3).The mucosal layer, enriched with mucins, concurrently lubricates the luminal surface and fortifies the epithelium, impeding mechanical damage, pathogens, and toxic molecules (4).Given an insect's diverse dietary repertoire of decaying plants, fungal matter, and pathogenic bacteria, these organisms have evolved an impressive digestive enzyme arsenal for efficient carbohydrate, protein, and lipid processing for complex food sources.Intricate intestinal pH regulation is also pivotal in the initial food digestion stages, with a pH of 5 in the foregut, 7 to 9 in the midgut, and 5 in the hindgut.However, these pH fluctuations physically and chemically affect ingested food material, influencing its overall integrity (1).
In the face of pathogen attacks on host gut epithelial cells are tackled with a pathogen outbreak, cascades of immune responses are triggered, involving the activation of key immune genes.Notably, pattern recognition receptors (PRRs) and antimicrobial peptides (AMPs) are among the immune factors that spring into action.The immune deficiency pathway, orchestrated by the Nuclear Factor-kappaB (NF-kB) transcription factors REL2 and REL2-F, is stimulated, bolstering the host's defense mechanisms (5).Furthermore, the Dualoxidase (Duox) pathway works diligently as another line of defense to maintain gut stability by safeguarding gut mucosa against reactive oxygen species (ROS)-sensitive pathogens (6).Moreover, the intricate protein interplay, including peptidoglycan receptor proteins (PGRPs), serine proteases, serpins, and a range of other molecules, reinforces the immune bolstering process through melanization within the prophenoloxidase (PPO) pathway, which varies in insect species (7).Additionally, the Janus kinase (JAK/STAT) signaling pathway, responsible for regulating cell growth, differentiation, apoptosis, and inflammatory reactions, triggers diverse antimicrobial peptide production, thereby instigating potent intestinal immunity in insects (8).
Various microorganism types have established symbiotic relationships with their hosts throughout evolution, providing extensive support.These microorganisms, commonly known as "commensal/microbiota," are integral for enhancing host fecundity, development, and growth.Specifically, they contribute to food digestion, vitamin production, host gut defense against pathogens, harmful substance detoxification, and stimulating host immune responses (9).Gut microbiota has garnered recognition as a pivotal component for biological control and waste biodegradation while deterring insect-borne disease transmission (9).Furthermore, the gut microbiota provides significant functionalities in synthesizing proteins, catecholamine cross-linkers, and chitin, inducing various immune regulatory pathways to aid recovery from infection (10).The gut microbiota supports host defense by modulating pH and digestive enzyme levels.They actively compete with pathogens for resources, such as living space and nutrients, while producing antimicrobial substances (11).
This review highlights contemporary advancements in understanding the insect gut's immune mechanisms when combating pathogenic threats.Specifically, we delve into the physical, biochemical, and intricate gut immune responses observed in model organisms, such as D. melanogaster and T. molitor, and further insight into post-infection recovery processes.
2 Insect gut structure and function

Foregut
The foregut represents the insect gut threshold, featuring an impermeable cuticle that imparts mechanical and chemical digestion properties facilitated by enzymes secreted from the buccal cavity.This section comprises salivary glands, reservoirs, and stomodeal valves that direct food flow toward the midgut (12).The crop is also integral to this region as it provides initial food storage, while the proventriculus acts as a valve that modifies ingested foodstuff (14).Certain insect species, such as Carpenter bees, symbiotically associate with Lactobacillus and Enterobacteriaceae bacteria predominantly located within the foregut.These microorganisms give support the bees' digestive processes, nutrient delivery, pathogen defense, and immune signaling mechanisms (15).Moreover, the foregut in Bulbitermes spp is a site for xenobiotic degradation and initial metabolic processes (16).In Anopheles culicifacies, the foregut's salivary gland harbors a more diverse symbiotic microorganism array than the midgut and hindgut, responsible for food acquisition, ingestion, and digestion (17).Research on Cephalotes rohweri indicates that the proventriculus valve, positioned between the crop and midgut, filters and effectively prevents pathogenic bacteria and particles larger than 0.2 µm from entering, protecting the host and maintaining host-microbe fidelity (18).Nutrient uptake and digestion are vital physiological processes across various life forms, and the gut-brain axis ensures gut homeostasis by regulating these processes through a neurohumoral communication system.Different neuropeptide classes govern the release of digestive enzymes, muscle activity, and engorgement, with specific neuropeptides presenting dynamic contributions to ecological pest management (19).Notably, Drosophila spp.'s gastric valve and crop function analogously to the stomach.A study investigating Drosophila stomach stem cells unveiled that JAK-STAT signaling regulates stem cell proliferation, Wingless signaling controls selfrenewal, and hedgehog signaling governs cellular differentiation (20).

Midgut
The midgut is a crucial component of the insect's digestive tract that starts from the gastric caeca and serves as a primary site for digestion and nutrient absorption (12).Structurally, the midgut is divided into anterior, median, and posterior regions based on length (21).Comprising a diverse cell array, the midgut epithelium digests and absorbs nutrients and maintains luminal pH levels, endocrine regulation, and epithelial growth in this middle region (22).Within specific regions of this organ, messenger RNA expression governs enzyme secretion tailored for breaking down specific food components, such as proteins, carbohydrates, and lipids.These enzymes, along with the luminal pH, significantly contribute to eradicating pathogenic microorganisms that are ingested with food (22).Moreover, the midgut epithelium employs various secretion methods, including merocrine, apocrine, and micro-apocrine mechanisms.Diverse symbiotic microorganisms reside in the anterior midgut's endoperitrophic space, assisting for digestion, and prompting immune responses (21).Regarding Drosophila, the midgut encompasses 14 distinct subregions that manifest distinct morphological, histological, and genetic properties.Damage to this compartment disrupts gut homeostasis, triggers stem cell proliferation, and stimulates various immune signaling pathways (23).When Nasutitermes takasagoensis digests cellulose, both endogenous endo-b-1,4-glucanase and b-glucosidase genes are uniformly expressed in the midgut, ensuring consistent enzyme production (24).In Locusta migratoria, the lethal giant larvae (Lgl) protein facilitates midgut morphology maintenance and ds-RNAbased insecticide development (25).Throughout Drosophila spp.'s lifespan, numerous regulatory signaling pathways operate within the midgut: the Delta/Notch signaling pathway regulates midgut progenitor cell differentiation, the Wingless and Int-1 (WNT) signaling pathway is responsible for intestinal stem cell (ISC) proliferation and maintenance, the Cytokine/Jak/Stat and Epidermal Growth Factor Receptor (EGFR) signaling pathways govern ISC proliferation, the JNK signaling pathway coordinates stress response and ISC proliferation; the Hippo/Salvador/Warts signaling pathway regulates midgut regeneration; and the cellular redox state influences ISC proliferation (26).

Hindgut
The insect hindgut is structurally divided into the ileum, colon, and rectum, beginning at the pyloric valve after the midgut.Malpighian tubules in this region establish the excretory organs responsible for removing nitrogenous waste as uric acid from the hemolymph.This gut section is entirely covered by epithelial cells, with a muscular layer surrounding the basal membrane.The hindgut sustains greater permeability than the foregut, primarily absorbs nutrients and minerals, and eliminates feces (12).Additionally, the hindgut facilitates salt and amino acid reabsorption to maintain the hemolymph's osmotic balance (27).Prophenoloxidase is a notable melanin production enzyme and serves as an immune response element at wound sites, functioning as the last line of defense against pathogens (26).The hindgut also harbors enteric bacteria, such as Pantoea agglomerans, which induce diverse immune responses (14).

The insect gut's general cellular composition
The insect intestinal system comprises a myriad of cell types, including absorptive enterocytes, secretory enteroendocrine cells, and pluripotent intestinal stem cells.Additionally, muscle cells are situated beneath epithelial cells' basement membranes (Figure 2).A semipermeable non-cellular structure, known as the peritrophic matrix/membrane, is positioned between the lumen and the epithelial layer within the insect gut, protecting enterocytes against abrasive particles and pathogens.Furthermore, a mucus Gut compartments of adult D. melanogaster.The insect intestinal tract can be anatomically divided into three distinct compartments: the foregut, midgut, and hindgut.The foregut encompasses vital structures, such as the mouth, pharynx, esophagus, crop, and proventriculus, with robust cuticles that form a protective barrier against invading pathogens.Moreover, the foregut facilitates enzymatic compound secretions from the buccal cavity and salivary glands.The midgut begins at the gastric caeca and segments into anterior, median, and posterior regions, determined by their respective lengths.This section is notable for its relatively high permeability.The midgut's epithelial lining incorporates diverse cell types with crucial functions, including nutrient digestion and absorption, pH regulation, endocrine modulation, epithelial growth, and safeguarding against pathogenic threats.Lastly, the hindgut starts where the Malpighian tubules and the muscular pyloric sphincter connect, followed by the ileum, colon, and rectum.Distinctive physiological processes in this compartment primarily focus on reabsorbing water, electrolytes, and other beneficial substances from the excreta.This illustration has been adopted from T. H. Napoleao et al (12).layer between the peritrophic matrix and the enterocytes extends throughout the gut (28).Neurons and trachea are intricately integrated into the muscle layer beneath intestinal cells' basement membrane, aiding the insect intestinal system's overall functionality and coordination (1).

Peritrophic membrane
The peritrophic membrane (PM) serves as a protective lining within the insect gut that separates the digestive compartment from the midgut lumen.Its primary functions include luminal surface lubrication to safeguard against food abrasion and pathogen invasion, as well as regulating immune responses.This membrane is composed of chitin fibers cross-linked by chitin-binding PM proteins (PMP); the PM forms a three-dimensional meshwork with water-filled pores.The mucin-like PMPs contain extensively Oglycosylated linker and chitin-binding domains (ChtBD2).In particular, these O-glycans are crucial for lubrication and controlling exclusion (29).Chitin and glycoproteins form the intestinal PM, which activates various regulatory pathways to defend against pathogens and prevent gut tissue damage caused by pore-forming toxins (3).For example, the peritrophic membrane in mosquitos is a vital gut homeostasis regulator and immune response mediator (30).Furthermore, Heme-dependent peroxidase 1 (HPx1) promotes PM assembly and enhances antioxidant capacity while modulating vector competence.The E75 transcription factor induces transcriptional HPx1 activation, and HPx1 knockdown accelerates DUOX-NADPH oxidase's gut reactive oxygen species (ROS) production, thereby enhancing the immunological sensing of microbial infection (31).The peritrophic membrane of insects, exposed mucins and non-mucin protein receptors, functions as a binding site for various insect pathogens, such as Junonia coenia densovirus (JcDV) (32).Different protein classes within the insect PM exhibit distinct activities: Class I PM proteins contribute to PM integrity and function; Class II proteins faintly interact with the PM through adsorption; Class III proteins are released under harsher conditions; and Class IV proteins are covalently linked to other PM proteins or chitin, making their removal challenging (33).Seventeen peritrophic membrane proteins have been identified in the Manduca sexta midgut, and genes encoding peritrophic matrix proteins in Tribolium castaneum are directly associated with insect survival (34).

Mucus layer and mucin
Mucus production is mediated by mucus-forming mucins (Mfmucins).These proteins are glycosylated and form a protective layer on epithelial cells that line the respiratory, digestive, and urogenital tracts in vertebrates.Their primary function is to protect the organ cell lining against infections, dehydration, physical or chemical damage, and other threats while facilitating nutrient flow through the intestinal tract.In particular, studies have evidenced that the mucus layer is involved in Mf-mucins activation (35).While the mucus layer's composition varies by organism, certain molecules remain consistent, particularly proteins extensively modified with N-acetylgalactosamine-based sugars attached to serines or threonines through O-linked glycosylation.Mucin proteins and their constituent O-glycans are fundamental for protecting and maintaining internal epithelial tissue vitality (36).In female insects, mucin proteins are localized in swollen crypts and are associated with symbiotic bacteria that stimulate gut immune responses (37).

Microvilli
Microvilli form the inner intestinal cell surface and are intricately linked to the mucus layer.Microvilli contains jellyassociated enzymes composed of membrane-bound material.The adult insect gut's general cellular composition.Adult insect gastrointestinal tracts comprise various cell types, namely absorptive enterocytes (ECs), secretory enteroendocrine cells (EEs), pluripotent intestinal stem cells (ISCs), and enteroblasts (EBs).These cells are collectively essential for an insect's digestive process.The peritrophic membrane situated between the lumen and epithelial cells is a semipermeable non-cellular structure that serves as a protective barrier, shielding enterocytes from abrasive particles and invading pathogens.Adjacent to the peritrophic membrane lies a mucus layer that further engenders a protective environment for enterocyte cells.Beneath epithelial cells' basement membranes is a muscle cell layer responsible for mechanical movements and contractions in the gut.Positioned underneath the muscle layer, neurons and trachea are present, providing innervation and oxygen supply to the gastrointestinal tract.This illustration has been adopted from T. Kuraishi et al (28).
These enzymes are either bound to the cell membrane or entrapped within the glycocalyx and predicate microvilli formation and structure.The glycocalyx refers to the carbohydrate chain connected to integral proteins and glycolipids on the microvilli.Digestion primarily transpires on the microvilli surface, and insights into microvillar enzymology are invaluable for proteomics studies (38).Moreover, digestive enzymes are synthesized in the rough endoplasmic reticulum, processed in the Golgi complex, and packaged into secretory vesicles.Gut microvillar membranes' physiological operations vary among insect taxa, influencing digestion, absorption, ion homeostasis, signaling, and secretory mechanisms.For instance, hemipteran gut cells manage various secretion types, including exocytic, apocrine, micro-apocrine with budding or pinched-off vesicles, and modified exocytic secretions (39).

Insect gut cells
Enterocytes (ECs), enteroendocrine cells (EEs), ISCs, and enteroblasts (EBs) are the key cellular components involved in regulating the various activities and immune responses within the insect gut.Enterocytes primarily participate in absorption, whereas enteroendocrine cells secrete a diverse array of secretory molecules.ISCs are crucial for intestinal epithelium regeneration influenced by intrinsic factors in addition local and systemic stimuli (40).ISCs continuously generate progenitor cells that differentiate into multiple cell types within the epithelium, thereby maintaining homeostasis (41).Enteroblasts are transient progenitors that differentiate into ECs (42).

Gut microbiota in D. melanogaster
An insect encounters diverse environmental conditions and various foodstuffs harboring assorted microorganisms throughout its life.While most of these microorganisms pass through the insect gut's lumen or interact with the host immune system, certain species are permitted to establish and proliferate within the gut environment called "commensal".These commensal microbes provide metabolic assistance, secondary metabolite production, immune system support, pathogen clearance, gut homeostasis maintenance, intestinal tissue regeneration, and other valuable contributions to the host (43)(44)(45).In Drosophila, the gut microbiota encompasses 5-20 commensal bacteria species, mainly from the Acetobacteraceae and Enterobacteriaceae families or the Lactobacillale order, including Lactobacillus plantarum, L. brevis, Acetobacter p omoru m, Glucon obacter mo rbifer , and Commensalibacter intestine (45).Although gut microbiota compositions vary due to fluctuations in environmental conditions and food availability, numerous studies have consistently identified the following dominant bacterial families in the Drosophila's gut: Acetobacteraceae (55%), Lactobacillaceae (31%), Leuconostocaceae (4%), Enterobacteriaceae (3%), and Enterococceae (2%) (46).Furthermore, ingesting microorganisms, such as Rhodiola crenulate, enhances survival rates and induces antimicrobial peptide gene expressions in D. melanogaster following exposure to pathogens or toxic compounds (47).
Multiple studies have revealed that the gut microbiota influences host immune responses and various physiological activities that include larvae development, nutrient uptake, behavior, and environmental signal responses (48).The gut microbiota produces distinct metabolites sensed by host intestinal receptors, thereby triggering host metabolism (49).Interactions among microbes can influence triglyceride content, highlighting the microbiota's influence on host metabolic processes (50).Notably, Acetobacter persici in the Drosophila gut prompts age-dependent metabolic purine level shifts by activating the innate immune signaling imd pathway in renal tubules (51).Furthermore, selective consumption of dietary components mediated by microbiota can modify the nutritional balance of food and ultimately impact the nutritional status of the host (52).Microbiota-induced signaling and regulatory networks involving genes associated with nutritional traits contribute to the host's nutritional status (53).A substantial larvae accumulation in a specific area can alter food's chemical and bacterial composition, effectuating growth time, pupation height, viability, and body mass alterations without affecting gut microbiota (54).The gut microbial community's composition in insects depends on host-specific factors, with colonization transpiring in specific gut regions (55).Additionally, food sources can influence a microbiome's establishment by reducing predominant member abundance and allowing new microorganisms to colonize (56).Introducing a single microorganism to the D. melanogaster gut can alter the microbial community's symbiotic composition without exhibiting extensive antibacterial activity, potentially influenced by food sources.For example, Rhodiola rosea significantly increases Acetobacter abundance while diminishing Lactobacillales, engendering a symbiotic association (57).
Drosophila spp.exhibits bidirectional signaling through the "microbiota-gut-vagus-brain axis," where gut microbiota can activate host neural circuitry and influence foraging behavior, stress-anxiety responses, and empathy development (58).During undernutrition, specific microbiomes, such as L. plantarum, induce the insulin/IGF-1 signaling (IIS) pathway, regulate glucose import and glycogen synthesis, and increase free amino acid levels by promoting gut peptidase expression via the imd pathway.A genetic L. plantarum screening identified an operon responsible for modifying bacterial cell walls, incorporating D-alanylated teichoic acids, which stimulate host enterocytes to induce gut peptidases (59).The gut microbiota, including Acetobacter spp.and yeast, also modifies host chemosensory responses, feeding preferences, and behavior, depending on the host-microbial history and identity.Different olfactory receptors and pathways are involved in sensing and responding to these changes, known as Olfactory-Guided Microbial Preferences by the host (60).
In addition, the Drosophila gut microbiota manages learning, memory, and sleep homeostasis aspects dependent on the host's genetic background (61).Aggressive behaviors in both male and female Drosophila can be regulated by the microbiome, swaying mate selection during development (62).Interactions between Drosophila and its gut microbiome are foundations for developing new therapeutic drugs and understanding downstream consequences for host health through genome analysis.Notably, these findings have also extended to human precision medicine (63).Various factors influence the interplay between microbiota and their host concerning immune induction.The immune response in D. melanogaster incorporates both humoral and cellular components, including the production of antimicrobial peptides, ROS, reactive chlorine species (RCS), phagocytic cells, and melanization.The gut microbiota directly or indirectly aids in activating the immune response (64,65).Among prevalent D. melanogaster microbiota, Lactobacilli spp.activate the NADPH Oxidases (NOX) pathway in gut tissue, releasing ROS and reducing microbiota overgrowth.Conversely, pathogenic bacteria stimulate ROS and RCS production through the dual oxidase system (Duox), which helps maintain host gut homeostasis (64,65).
Microbiota and pathogens trigger the humoral immune response, inducing the production of antimicrobial peptides through imd and Toll regulatory pathways.These processes are initiated by PRRs in response to conserved microbial-associated molecular patterns (MAMPs) (64,65).PGRPs, such as PGRP-LC, PGRP-LE, PGRP-SD, PGRP-LB, and PGRP-SC, within the IMD signaling cascade also recognize peptidoglycans from the microbiota.Notably, PGRP-LB has been found to protect the host from the harmful peptidoglycan effects on the hemolymph and other organ systems (64,65).The EGFR and JAK-STAT signaling pathways are responsible for gut repair prompted by gut microbiota and pathogens, and the pathway activated depends on the damage sustained.Additionally, histone demethylase KDM5 deficiency begets an overactive IMD response and dysbiosis, whereas L. plantarum normalizes IMD activation and reduces dysbiosis (65).Vibrio cholerae's Type 6 Secretion System (T6SS) and its interaction with Acetobacter pasteurianus microbiota induce the imd pathway in D. melanogaster, triggering immune responses (66).L. plantarum, a gut microbiota, can protect D. melanogaster from common pathogens, such as Pseudomonas aeruginosa and Serratia marcescens, by inducing the host's immune response (56).Moreover, certain yeast commensals in D. melanogaster protect against the pathogenic fungus Aspergillus flavus (67).L. plantarum also mitigates D. melanogaster's susceptibility to the pathogenic fungus Diaporthe FY (68).Furthermore, Erwinia carotovora pathogen infection and commensal microbes can trigger lipid utilization through enterocytes, but with distinct outcomes prevalent upon microbial cues, imd signaling, ROS production, and lipid utilization (64).Cell type-specific responses within the gut can also induce immune responses and are recognized by the gut microbiota.For instance, imd pathway activation in enterocytes invokes an immune response, activation in enteroendocrine cells promotes lipid utilization and improves anabolic growth (64).The microenvironment is also significant in maintaining constitutive immunity and gut microbiota concentration (69).Similarly, antimicrobial peptides and lysozymes, two immune effector families, regulate gut microbiota composition and abundance (70).

Gut microbiota in T. molitor
Like Drosophila, commensal microorganisms in T. molitor also affect gut immune responses and various physiological activities.
The surrounding environment is a substantial source of diverse beneficial and pathogenic microorganisms.Different microorganism types could enter the T. molitor gut and establish themselves as symbionts or pathogens.Symbiotic microorganisms contribute to numerous physiological activities and environmentally friendly actions, such as detoxification in phytophagous insects, lignocellulose degradation in xylophagous insects, and antimicrobial compound production to protect against pathogens (71).
Experimental data has revealed that T. molitor harbors Bacillus, Lactococcus, Weissella, Escherichia, and Clostridiaceae spp. in an open environment but is dominated by Enterococcus spp.and some unclassified Enterobacteriaceae in a closed ecosystem.
Microorganisms in the open environment actively contribute to host metabolism and immune activity, whereas the closed ecosystem offers the opportunity to select probiotic strains for improving growth efficiency (72).Another study on the gut of T. molitor identified fermentative bacteria, such as Weissella and Lactococcus spp.; proteolytic bacteria responsible for protein degradation, like Rahnella and Cronobacter spp.; and other microbiota groups, including Lactobacillus, Bacillus, Spiroplasma, Clostridium, Enterobacter, and Pantoea found in different concentrations across gut regions, with the hindgut containing the most diversity (73).Moreover, the gut microbiota in T. molitor was revealed to have significant plasticity in response to environmental factors, particularly soil.The composition of microbiota can rapidly fluctuate from one commensal group to another based on alterations in soil composition (74).
T. molitor and its gut microbiota degrade polystyrene (PS), polyvinyl chloride (PVC), polyethylene (PE), acrylonitrile butadiene styrene (ABS), polyurethane (PU), bio-based crosslinked polymers, and other plastic polymers (75).Research findings have identified eight specific microorganisms responsible for polystyrene biodegradation in T. molitor: Citrobacter freundii, Klebsiella aerogenes, S. marcescens, Stenotrophomonas maltophilia, Bacillus thuringiensis, P. aeruginosa, Enterococcus faecalis, and Enterobacter asburiae.It has been studied that T. molitor gut secretory factors and gut microbiota contribute to plastic degradation.Emulsifying factors with 30-100 kDa molecular weights were found in the T. molitor gut.In contrast, gut microbiome-produced secretory factors with molecular weights below 30 kDa were responsible for degrading plastic molecules (76).In addition, T. molitor's gut microenvironments may be plays a crucial for plastic biodegradation.Therefore, combining T. molitor, specific gut microbiota, and an artificial microenvironment's design will be a promising chamber for effective plastic degradation (76,77).
Moreover, studies have demonstrated that although polystyrene provides some nutrients to T. molitor, but polystyrene has negative impacts on growth and development (78).T. molitor cannot survive on a diet consisting solely of plastic; additional essential nutrients are required (79).For example, different food supplements, such as bran with a 7:1 (w/w) plastic ratio, can promote T. molitor growth (80).Another study revealed that for polystyrene degradation, Erwinia olea, Lactococcus lactis, and Lactococcus garviae were the dominant microbiota in the gut of T. molitor (81).Similarly, for polyurethane degradation by T. molitor's different gut microbiota, such as Paraclostridium, Chryseobacterium, Kosakonia, and Pseudomonas, were found to be responsible.During the degradation process, they can degrade the polymer by 35% within 17 days, but it experiences a weight loss of 14% (82).On the other hand, T. molitor's gut microbiota breakdown long-chain and branched polymers by diffusing extracellular depolymerase, producing shorter chains containing 16 carbon atoms.The microbiota utilizes fatty acid degradation pathways to generate intermediate products during plastic degradation, while T. molitor acts as a downstream decomposer (79).Additionally, T. molitor's gut microbiota can create cracks and holes in plastic sheets, form biofilms, and utilize them as a carbon source for growth (83).Furthermore, plastic molecular weight critically affects biodegradation.Plastic with low, medium, high, and ultra-high molecular weights can significantly influence metabolic pathways, induce intestinal dysbiosis, and alter gut microbiome composition (81,84).Generally, T. molitor employs an extensive depolymerization process for plastic biodegradation, although the depolymerization of ultra-high molecular weight plastics is limited (84).
In addition, for plastic degradation, the gut microbiota involves the secretion of siderophores such as enterobactin and yersiniabactin, enzymes, and specific enzymatic genes such as undecaprenyl-phosphate galactose phosphotransferase [EC:2.7.8.6].Furthermore, the supernatant of intestinal content acts as a surfactant, enhancing the hydrophilicity of plastic and providing physical support for the gut microbiomes (77).A fascinating discovery revealed that Enterobacter hormaechei LG3 produces a biofilm on the plastic's surface for degradation under anaerobic conditions.In this study, researchers identified degradative enzyme-expressing genes of the peroxidase family, including tpx, ahpC, and bcp (85).Another study demonstrated that phosphatases, esterases, leucine arylamidase, ß-galactosidase, ß-glucuronidase, a-glucosidase, ß-glucosidase, chitinase, amannosidase, a-fucosidase, and numerous other enzymes are involved in plastic degradation.Furthermore, the study suggested that enzymatic activity plays a more substantial role in plastic biodegradation than gut microbiota (86).
Moreover, to the environmental considerations regarding plastic degradation, T. molitor holds promise and has been approved by the European Union as a protein source to meet global food demand.Recent efforts have focused on enhancing T. molitor's nutritional value by incorporating probiotic strains, such as Pediococcus pentosacceus KVL-B19-01 and Enterococcus faecium 669, as commensal gut bacteria.These strains contribute as gut microbiota and promote host growth and development.Moreover, they protect against entomopathogenic fungi, such as Metarhizium brunneum (87).P. pentosaceus significantly protects T. molitor from six different insect pathogenic strains, including B. thuringiensis and species of Serratia and Pseudomonas bacteria (88).Another research study demonstrated that introducing Lactobacillus and Bifidobacterium strains, such as Lactobacillus casei 01 and Bifidobacterium animalis ssp.lactis Bb1 into the T. molitor gut, optimized them as gut microbiota without adversely affecting the host.In addition, these introduced strains can produce short-chain fatty acids (SCFA) and lactate (89).
J. Poveda et al. investigated T. molitor frass' potentiality, including gut microbiota, as a biofertilizer and verified that it can enhance plant growth, even under stressful conditions (90).Conversely, parasitic symbionts hinder T. molitor mass production, as these symbionts can transfer to humans when T. molitor is used as a food source (91).When parasites are introduced into the insect gut microbiota, they stimulate the innate immune system through nonspecific cellular constituents known as hemocyte.Hemocytes respond to infectious agents by activating the phenoloxidase enzymatic cascade, ultimately producing specific antimicrobial peptides.However, parasites can alter the gut microbiota due to their transient nature, and in some cases, the host gut microbiota participates in establishing these parasites (92).Furthermore, T. molitor gut microbiota assists in detoxifying toxic food-derived compounds, such as plant-derived glucoside salicin.In summary, T. molitor's immune mechanisms and gut microbiota are strikingly adaptable as vital host defense components (93).

D. melanogaster's and T. molitor's gut immune response
Diverse immune signaling pathways are intricately involved in mediating the gut immune response in D. melanogaster and T. molitor.These pathways are triggered by various signaling molecules released by pathogens and are sometimes associated with commensal microorganisms.The specific immune signaling pathways activated upon gut infection depend on the infecting microorganism's nature and composition.The following sections explore the immune signaling pathways crucial for maintaining gut homeostasis and defense mechanisms.

Imd signaling pathway in D. melanogaster
Peptidoglycan, a bacterial cell wall component derived from Gram-negative bacteria and Gram-positive bacilli, recognition mediates the immune response of gut cells in D. melanogaster.The peptidoglycan structure consists of 1,4-linked Nacetylglucosamine and N-acetylmuramic acid cross-linked sugar chains, four amino acids, and meso-diaminopimelic acid, forming what is known as DAP-type peptidoglycan.The detection of this peptidoglycan by Drosophila gut cells relies on the presence of PGRPs.Notably, the genes responsible for encoding PGRP are categorized by their transcript lengths.Upon DAP-type peptidoglycan binding, PGRP-LC and PGRP-LE transmembrane receptors activate the imd pathway (Figure 3).This binding event generates a signaling complex involving IMD, Dredd, and fasassociated protein and the death domain (FADD), subsequently translocating to the plasma membrane.Dredd is activated through K63-ubiquitination mediated by the E3-ligase inhibitor of apoptosis 2 (IAP2).Dredd cleaves IMD at its N-terminus, revealing an IAP2binding motif and facilitating its interaction with IAP2's BIR domain.As a result, the TAK1/TAB2 complex is recruited to the signaling complex.TAK1 then functions as a MAPKKK kinase and Imd pathway in D. melanogaster and T. molitor.(A) The immune deficiency (imd) pathway in the Drosophila midgut concurrently initiates in the proventriculus, anterior, median, and posterior regions.All receptors in these regions are essential for imd pathway activation.Peptidoglycan (PGN) recognition proteins (PGRP)-LEs and PGRP-LCs within the insect gut identify the polymeric and monomeric diaminopimelic acid (DAP) type PGN derived from gram-negative bacteria and gram-positive bacilli.These recognition signals are then translocated to the imd pathway within the cytoplasm.The intracellular domain of PGRP-LCs is subsequently activated and recruit IMD and, form a complex with the fas-associated protein and the death domain (dFADD).This complex facilitates cleaving phosphorylated Relish, a protein with an N-terminal Rel DNA-binding domain and inhibitory ankyrin (ANK) repeats.The Relish domain is translocated to the nucleus, where it binds to NF-kB-response elements and begins transcribing genes encoding antimicrobial peptides.Meanwhile, the inhibitory Relish domain remains in the cytoplasm.Relish phosphorylation is mediated by a kB kinase (IKK) complex inhibitor, comprising immune responses deficient 5 (Ird5) and Kenny.This complex is activated by the mitogen-activated protein (MAP) kinase transforming growth factor (TGF)-b activated kinase1 (dTAK1), operating in an IMD and FADD-dependent manner.(B) The imd pathway activates in response to Gram-negative bacteria and Gram-positive bacilli infection in T. molitor's gut.Signal transduction within gut cells hypothetically incorporates imd pathway activation, which comprises a death domain that facilitates TmFADD (TAK1 activator) and TmDredd (a caspase) recruitment.The activated TmTAK1, a protein kinase, then phosphorylates Relish through TmIKK-b, -g, and -ϵ.This phosphorylation event translocates the Rel domain into the nucleus, initiating antimicrobial peptide gene transcription.This illustration has been adopted from M. A. M. Kojour et al and Y. Lu et al (94, 95).
The predominant intracellular receptor for monomeric peptidoglycan (PGN) in the Drosophila midgut is PGRP-LE.Conversely, in the proventriculus and hindgut, PGRP-LC binds to PGRP-LE in the ventriculus, facilitating the identification of monomeric and polymeric PGN structures.Commensal bacteria commonly present in the Drosophila gut, such as Acetobacter and Lactobacilli spp., harbor DAP-type PGNs.These bacteria maintain basal imd pathway activation and contribute to gut homeostasis (96).A comprehensive investigation concluded that the imd pathway is pivotal in governing antimicrobial peptide production and preserving barrier integrity within the gut.Remarkably, the coordinated imd and JNK signaling activities have been implicated in gut cell shedding regulation and controlled transcription factor GATAe expression, effectively controlling pathogen infections (98).Intriguingly, another experimental study revealed that microbial metabolic signals, specifically the short-chain fatty acid acetate, can induce imd pathway activation in enteroendocrine cells.This activation subsequently triggers endocrine peptide Tachykinin (Tk) upregulation, promoting larval development by influencing lipid metabolism and insulin signaling (99).
The imd pathway is a crucial immune signaling pathway in D. melanogaster, strictly regulated by various factors.Negative regulators, such as Pirk and PGRP-LB, balance bacterial infection and gut microbiota tolerance, while PGRP-LE acts as a sensor (100).In investigating the response to killed bacteria in Drosophila, specifically Escherichia coli and Staphylococcus aureus, genderspecific variations were observed due to differential receptor, signaling molecule, and protein expressions (101).Several common pathogenic microbes inhabit Drosophila's intestinal tract, including Pseudomonas entomophila, Vibrio cholerae, Candida albicans, Enterococcus faecalis, and Staphylococcus xylosus.Certain pathogens, like S. marcescens and P. aeruginosa, can breach the intestinal barrier and activate the imd pathway (102, 103).While gram-positive bacteria generally activate the Toll pathway, a study demonstrated that the imd pathway and ROS partake in clearing ingested S. aureus, highlighting their versatile roles in insect gut immune defense (104).Microbial metabolites, such as acetate, can stimulate the imd pathway in anterior midgut enteroendocrine cells, producing antimicrobial peptides to protect against pathogens (105).In addition, Histone acetyltransferase Tip60 is an essential regulator in downregulating the imd signaling pathway by blocking dietary acetate and other acetyl-CoA sources, thereby blocking the pathway and fine-tuning gut immunity (106).On the other hand, the commensal gut microbiota can induce necrosis, activate the imd pathway, and alter bacterial populations, impacting D. melanogaster's lifespan (107).Furthermore, the imd pathway and mustard mutants suppress V. cholerae infection and cholera toxins by inducing intestinal stem cell proliferation.This protective mechanism facilitates epithelial regeneration, protecting against pathogenic invasion (108).The imd signaling pathway is also vital for maintaining gut microbiota lysozyme concentrations, further contributing to gut homeostasis (70).The basic similarities and differences of imd and Toll signaling pathways in D. melanogaster and T. molitor have mentioned below in consideration of recognition receptor, adapter molecule, regulatory molecule, transcription factor and proteolytic cascades (Table 1).Experimental studies reveal that gut and Malpighian tubules of D. melanogaster are not directly related to the expression of genes related Toll signaling pathway.However, in consideration of T. molitor the gut immune response is stimulated by the Toll and imd immune signaling pathways (Table 2).The imd is the major regulatory pathway for gut and Malpighian tubules in D. melanogaster.

Imd signaling pathway T. molitor
The imd pathway in T. molitor is activated upon the recognition of pathogens by PRRs, such as PGRP-LC or PGRP LE.An intracellular signal is transmitted to the adaptor protein IMD.The IMD forms a signal complex with dFADD, K63, and caspase DREDD which induces IMD cleavage (Figure 3).Then, the K63polyubiquitin molecule activates TAK1 and TAB2's ubiquitinbinding domain.Relish phosphorylation and the subsequent translocation, which produce antimicrobial peptides for pathogen clearance, depend on the Imd signaling upstream receptors; PGRP LE/LC, relevant adaptor molecules; FADD, DREDD, TAB2, TAK1, and the IKK complex comprising TmIKK-and (94).Moreover, IKK/NEMO as a non-catalytic regulatory subunit is pivotal in the NF-ĸB pathway signaling (136).

JAK/STAT signaling pathway in D. melanogaster
When D. melanogaster ingests gram-negative bacteria, the imd signaling pathway activates, producing various antimicrobial peptides.The JAK/STAT signaling pathway synthesizes antibacterial and Drosomycin-like peptides with antifungal properties, specifically within D. melanogaster's anterior midgut (142,143).Scientific investigations have demonstrated that the JAK/STAT, JNK, and DUOX pathways contribute to epithelial renewal through cell proliferation, ensuring gut homeostasis when faced with pathogenic infections.The JAK/STAT signaling pathway's activation is facilitated by hop Tum-l or upd-3 expressions, encouraging gut renewal during infection, and may also be involved in non-infectious stages (143).
The JAK-STAT pathway, consisting of hopscotch/hop (JAK) and Stat92E (STAT transcription factor), in D. melanogaster responds to IL-3, IL-5, and IFN-g hematopoietic cytokines and growth factors including granulocyte-macrophage colony-stimulating factor (GM-CSF), erythropoietin (EPO), growth hormone (GH), and prolactin.JAK activates when cytokines bind to their respective receptors, leading to receptor dimerization and subsequent association with the receptor's cytoplasmic tail (Figure 4).Consequently, JAKs undergo phosphorylation at tyrosine residues, which serve as docking sites for STAT molecules (Stat92E)'s Src homology 2 (SH2) domains.Simultaneously, STAT is phosphorylated at tyrosine (Tyr-704) by JAKs, enabling STAT dimer formation and translocation into the nucleus.Subsequently, the STAT dimers bind to specific genes with the TTCCCGGAA binding sequence (108).Notably, a scientific study highlights the JAK-STAT pathway's prominence in controlling intestinal stem cell differentiation, gut immunity, tissue regeneration, cell fate determination, and overall cell homeostasis in D. melanogaster.Additionally, D. melanogaster enteroendocrine cells secrete assorted neuropeptides responsible for regulating gut physiology and promoting growth (145).
Drosophila gut cells' intricacy includes the ability to discern commensal bacteria from their pathogenic counterparts by detecting uracil's metabolic signature and secretion from pathogens during the stationary growth phase.Intriguingly, diverse phenotypic activities manifest among genetically similar strains of Drosophila gut epithelia.For example, while the Lactobacillus brevis strain EW exhibits colitogenic behavior, another L. brevis strain is a harmonious commensal bacterium.Uracil, notably integral to this intricate system, induces gut epithelium cell renewal through the DUOX signaling pathway and activates the JAK-STAT pathway via cytokine Unpaired-3 expression, orchestrating gut homeostasis (148).Uracil is formidably intricate, as it activates the Hedgehog (Hh) signaling pathway and spurs the cell adhesion molecule Cadherin 99C (Cad99C) into action.The resulting endosome formations are pivotal for activating PLCß/PKC/Ca2 + -dependent DUOX machinery (149,150).Furthermore, studies have unveiled the complex dance between lipogenesis induction, DUOX activity blockade, and ATG1-dependent lipophagy-induced lipolysis, a process indispensable for DUOX activation.TRAF3-AMPK/WTS-ATG1 pathway components deftly modulate infection-induced lipolysis, diminishing DUOX activation and any lingering D. melanogaster gut infections (151).Amidst intricacies, the Mesh protein regulates DUOX expression and gut bacteria proliferation by forming an Arrestin-mediated MAPK JNK/ ERK phosphorylation cascade (152).In the grand tapestry of gut biology, DUOX-dependent reactive oxygen species are invaluable as they dictate the delicate balance between gut cell repair, pathogenic bacteria eradication, and host survival during infection (153).

JNK/FOXO signaling pathway in D. melanogaster
Within the realm of cellular intricacies, the c-Jun N-terminal kinases, esteemed members of the mitogen-activated protein kinase family, stand as guardians of tissue homeostasis, diligently overseeing gut functionality, cell damage repair, the delicate dance between cell survival and death, the orchestrated responses to DNA damage, and regulate inflammatory cytokines.While JNK1, JNK2, and JNK3 genes are responsible for JNK protein production in most organisms, a solitary   Duox-ROS defense mechanisms in D. melanogaster.The immune response in the insect gut produces reactive oxygen species.Similar to the IMD pathway, ROS is activated under basal conditions in response to gut microbiota and ingested microorganisms.However, this response is significantly amplified upon microbial infection.Microbially derived uracil triggers the activation of the adaptor molecules guanine-nucleotide-binding protein q subunit-a (Gaq) and phospholipase Cb (PLCb).These molecules stimulate inositol-3-phosphate synthesis, releasing intracellular calcium and transcribing Duox, the gene responsible for encoding oxidase enzymes.Duox transcription can also be induced by the p38 mitogen-activated protein kinase pathway and transcription factor Atf2.Under basal conditions, the activity of the Duox pathway is tightly regulated.The transcription of Duox is downregulated by MAPK phosphatase 3 (Mkp3), which is induced by PLCb and Calcineurin B (CanB) in the absence of microbial infections.The specific activities of G protein-coupled receptors (GPCRs) in this pathway remain to be determined and require further investigation.This illustration has been adopted from N. Buchon et al (146).basket (bsk)-encoded JNK gene and the two Hemipterous (hep) and DJun/DFos JNK kinases activate this multifaceted pathway in D. melanogaster.When the JNK signaling pathway diverges from the imd pathway, a distinct cascade at the dTAK1 stage begins (Figure 6).Traversing D. melanogaster's embryonic stage, the JNK pathway relies on the slipper (slpr) for activation, setting transcription factors AP-1 into motion while simultaneously stimulating the Forkhead Box O transcription factor FOXO, thus maintaining gut homeostasis (155).
Inquiries into dietary influences have revealed that high-sugar edibles incite gut stem cell differentiation, showcasing the JNK pathway's complexity and prominence (156).Another study unveiled that activating the JNK/FOXO pathway stimulates dPrxV, essential for the subsequent pathogenic onslaught within D. melanogaster's gut (157).

Other signaling pathways in D. melanogaster
Safeguarding against viral invasion in D. melanogaster's gut epithelia is entrusted to the ERK signaling pathway.This intricate defense mechanism unfolds through two signals.First, the peptidoglycan recognition secretion factor Pvf2 emanates from the gut microbiota A. pomorum.The virus sets off a signaling cascade, triggering kinase Cdk9 release, which is indispensable for Pvf2 production (158).Further revelations have verified that the p38 pathway-mediated heat-shock factor is pivotal for safeguarding the gut against pathogenic assault by managing the JNK pathway (159).

T. molitor's gut immune response
The pathways in T. molitor's gut immune response are each directed by a diverse array of signaling molecules released by the gut and its commensal inhabitants.These immune signaling pathways vary by the specific invading microorganisms, unveiling a fascinating interplay between host and pathogen.

Toll signaling pathway
The Toll signaling pathway begins when GNBP3 recognizes fungal ß-glucan and Lys-type PGN, namely PGRP-SA and GNBP1, JNK pathway in D. melanogaster.The JNK pathway branches off from the Immune deficiency pathway at dTAK1, comprising the single gene basket (bsk) and two JNK kinases, Hemipterous (hep) and DJun/DFos.A broad range of intrinsic and extrinsic factors can activate this pathway.For example, the slipper (slpr) triggers JNK activation during embryonic dorsal closure, prompting various tissue-and context-specific cellular responses.The JNK signaling pathway is pivotal for regulating and promoting several crucial physiological processes that influence gut immunity and homeostasis, including antimicrobial responses regulated by the transcription factor Relish.This process also involves cytoprotection, which induces protective gene expressions, such as hsp68, gstD1, fer1HCH, and mtnA, in response to oxidative damage.Furthermore, the JNK pathway influences metabolism and controls inflammation-induced apoptosis, wound healing, and cell proliferation, which are regulated by Upd3.Negative JNK pathway regulation occurs through Puckered (Puc) and Pvr activity.This illustration has been adopted from G. Tafesh-Edwards and I. Eleftherianos et al (154).
from gram-positive bacteria.These extracellular PRRs activate a serine cascade, culminating in extracellular cytokine Spätzle induction and its binding with the Toll receptor ligand.Within this intricate network, the trimeric complex formed by adaptor protein MyD88, Tube, and the kinase Pelle invoke a series of phosphorylation events.Pelle phosphorylates Cactus, an inhibitory protein.Meanwhile, the transcription factors Dorsal and Dorsal-related immunity factor (Dif) within the cytoplasm traverse into the nucleus, where they generate an array of antimicrobial peptides (Figure 7) (161).Remarkably, the Toll signaling pathway's activation is not initiated through direct contact with the microorganisms but rather upon detecting the cytokine-like polypeptide Spätzle, evidencing Semmelweis and Osiris genes' influence in gram-positive-dependent Toll activation (94).
Regarding T. molitor's gut immunity, TmPGRP-SA mRNA levels are upregulated in response to E. coli and C. albicans invasion.This upregulation triggers antimicrobial peptide transcription, including TmTenecin-2, -4; TmDefensin-2; TmColeoptericin-1, -2; and TmAttacin-1a, 1b, and -2 (139).The cystine knot protein TmSpzlike is expressed upon E. coli invasion, generating numerous AMPs to protect the gut epithelia (162).Through a study on Coleoptericin gene expression in T. molitor's gut immunity among E. coli, S. aureus, and C. albicans; it was discovered that the infection of E. coli tantalized the genes TmCole B and TmCole C of Coleoptericin, while fungi did not share the same allure (163).In addition, TmToll-2 expression was elevated in young larvae gut after E. coli, S. aureus, and C. albicans invasion (164).C. albicans infection in young T. molitor larvae induced TmToll-3 within the gut; however, AMP gene transcription factors were downregulated by E. coli infection (165).The potent production and proliferation of specialized daughter from intestinal stem cells are crucial in gut cell self-renewal following infection (136).ISC proliferation generates two distinct daughter cell types: ISC with self-renewal capacity and enteroblast cells capable of differentiating into enterocytes or enteroendocrine cells.Controlling ISC proliferation is paramount during gut epithelial damage from pathogens or toxic substances.Rapid ISC proliferation excessively accumulates cells, exhibiting pathogenic behavior.Conversely, if ISC proliferation is slowed, damaged cells cannot be adequately replaced, resulting in compromised gut integrity and ultimately leading to the demise of the host (166).
Moreover, a multitude of signaling pathways, namely JNK, JAK/Stat, Hippo, EGFR, Wg, Hh, and Dpp/BMP, are intricately involved in the complex process of gut recovery in insect (136).The regulatory molecule Myc influences downstream events within the Wingless, EGFR, Jak-Stat, and Hippo pathways, effectively proliferating intestinal stem cells (Figure 8).Conversely, in conditions of cellular stress within enterocytes the Upd3 ligands of the Jak-Stat pathway exhibit the ability to activate the JNK pathway, whereas the Keren ligands of the EGFR pathway can induce the activation of the Hippo pathway.When enteroblasts are stressed, Upd2 ligand production activates the Hedgehog pathway, and EBs activate Wingless ligands to stimulate the JNK pathway.
Consequently, every cell within the gut possesses the remarkable capacity to regulate ISC proliferation; thus, each type is crucial in restorative processes following gut infection (166).
Nonetheless, researchers are actively investigating the interplay between intestinal renewal and immune pathways.While the imd pathway does not directly induce intestinal stem cell division, it does modulate commensal microorganisms within the gut to ensure homeostasis (168).Conversely, reactive oxygen species molecules, including SDS, DSS, and bleomycin, can stimulate ISC proliferation through the DUOX pathway.Similarly, ROS molecules can activate the Jak-Stat pathway by inducing redox-sensitive protein tyrosine phosphatases, the JNK pathway through thioredoxin, and the Wnt pathway via nucleoredoxin (166).One scientific study demonstrated that translational blockage triggered by P. entomophila infection subsequently released pore-forming toxins, and the host response producing reactive oxygen species can hinder immune response and impair gut repair.This impairment transpires through GCN2 kinase activation and rapamycin pathway inhibition (169).In response to apoptosis, pathogenic infections, and JNK-mediated stress signaling, enterocytes produce various cytokines, such as Upd, Upd2, and Upd3.These cytokines activate Jak/Stat signaling in ISC, promoting their proliferation and stimulating Delta/Notch signaling to facilitate gut tissue repair (170).In addition, the epidermal growth factor receptor (EGFR) pathway is initiated by Spitz, Keren, and Vein EGF Frontiers in Immunology frontiersin.orgligands.Combined with the JAK/STAT pathway, this effectively triggers intestinal stem cell proliferation, facilitating proper infected gut tissue renewal from pathogen-induced damage Another investigation uncovered EGFR/MAPK pathway induction by the Insulin/Pi3K/TOR signaling cascade, serving as a crucial mechanism for gut renewal under stressful conditions by promoting the growth of EBs and ECs.The E2f1 transcription factor is essential for this induction; the Ras/Raf signaling pathway actively upregulates E2f1 levels and ensures proper transcriptional induction and fine-tuning of the EGFR/RAS/MAPK pathway activity, ultimately driving efficient gut regeneration (172).Moreover, during pathogenic infections within the gut, the YKi pro-growth transcription factor activates the Hippo pathway, influencing ISC differentiation and contributing to gut defense and repair (173).In a comprehensive gene expression study, 1833 genes were identified as responsible for ISC expression, 233 genes governed enterocyte function, 433 genes regulated enteroendocrine cell activity, and 2646 genes influenced Enteroblast behavior.Either directly or indirectly, these genes are vital for intricate gut tissue damage repair (174).

Conclusions and prospects
Despite these insights and explanations, numerous questions pertaining to insect gut immunity defense mechanisms of gut immunity in insects remain unanswered.Notably, inquiries arise regarding the mechanisms by which the immune system controls the composition and abundance of gut microorganisms.Additionally, the intricate relationship between gut microbiota and host behavior and physiological activities warrants further exploration.Furthermore, elucidating the precise mechanisms underlying gut microbiota dysbiosis remains a critical area of investigation.The differential activation of the Toll pathway in gut immunity between D. melanogaster and T. molitor raises intriguing questions, necessitating an examination of the underlying reasons for this discrepancy study.Moreover, unraveling the exact mechanisms that trigger the activation of intestinal renewal pathways in T. molitor presents an intriguing avenue for future research.Furthermore, understanding the intricate mechanisms underlying gut immunity during both pathogenic and non-pathogenic viral infections in T. molitor is of paramount importance.Exploration of the stages of infection, the duration required for gut tissue recovery following pathogen incorporation, and the precise pathogenic dose or number of infectious doses required for infection in D. melanogaster and T. molitor are crucial aspects that demand further investigation.
In the context of considering the utilization of T. molitor as a viable food source for human consumption, it is important to investigate the intricate interplay between the pathogens harbored within the T. molitor gut and the commensal microorganisms residing within the human intestinal ecosystem.A critical inquiry arises as to whether the commensal microorganisms present in T. molitor confer any advantageous attributes upon their introduction into the human intestinal milieu.Furthermore, during gut infections, T. molitor elicits the production of antimicrobial peptides as a defense mechanism against invading pathogens.An intriguing avenue for exploration emerges regarding the potential implications of these AMPs on human intestinal immunity.Could these AMPs be harnessed as a means to fortify human immune responses, potentially through targeted injections or other innovative modalities?Moreover, as T. molitor is ingested as a food source, various metabolites derived from diverse metabolic pathways are generated.It is imperative to ascertain the potential repercussions of these intermediate products on the integrity and functionality of the human intestinal tract.Meticulous investigations encompassing these concerns are promising for unraveling the intricacies underlying insect gut immune defense.Furthermore, such endeavors bear the potential for far-reaching applications spanning a vast array of disciplines.

FIGURE 4 JAK
FIGURE 4JAK/STAT pathway in D. melanogaster.The JAK/STAT pathway is activated upon pathogen invasion and produces antimicrobial peptides in the midgut, including antifungal Drosomycin-like peptides.This pathway is also vital for cell proliferation.Tissue damage prompted by pathogenic infection induces upd3 cytokine expression.Upon upd3 cytokine binding, the dimerized domeless receptors Hopscotch (Hop)/JAK activate, and Hopscotch phosphorylates itself and specific tyrosine residues on the receptors in cytoplasmic regions.These phosphorylated tyrosine residues serve as Stat92E binding sites, a transcription factor component of the STAT family.Hopscotch further phosphorylates Stat92E at tyrosine residues, promoting its dimerization and subsequent translocation into the nucleus.Once in the nucleus, Stat92E binds to the promoter regions of its target genes.The JAK/STAT signaling pathway also upregulates Socs36E gene expression This illustration has been adopted from C. Kietz and A. Meinander et al (144).

FIGURE 7
FIGURE 7Toll signaling pathway in T. molitor.Circulating pathogen recognition receptor GNBP3 recognizes the fungal cell walls' b-1,3 glucan component and activates the Toll pathway in T. molitor.Simultaneously, GNBP1 and the peptidoglycan recognition proteins PGRP-SA and PGRP-SD recognize Gram-positive bacteria's lyse-type peptidoglycan (PGN).In Tm, PGN/b-1,3-glucan exposure binds Lys-type PGN to TmPGRP-SA, thereby recruiting TmGNBP1 and Tm modular serine protease (MSP) zymogen.In the presence of calcium ions (Ca2 + ), the PGN/TmPGRP-SA/TmGNBP1 complex induces the activation of the TmMSP zymogen, resulting in the activation of TmMSP.This initiates a proteolytic cascade involving three serine proteases: MSP, Spz processing enzyme (SPE), and SPE-activating enzyme (SAE).The activated SPE cleaves pro-Spz, leading to the generation of processed Spz.A specific three-serpin complex (SPN40, 55, and 48) combines with serine proteases to prevent pro-Spz processing and phenoloxidase-mediated melanin synthesis.Next, downstream signaling through the Toll pathway is activated when mature Spz binds to its receptor, triggering the TmMyD88, TmTube, TmPelle, TmPellino, and TmTumor necrosis factor receptor-associated factor (TRAF) association in the cytosol.TmCactin binds to Cactus, resulting in the release of Dorsal-related immunity factor (Dif) and Dorsal from Cactus.This process translocates Dif and Dorsal into the nucleus, where they promote antimicrobial peptide gene transcription.This illustration has been adopted from M. A. M. Kojour et al and K.Ryu et al (94,160).

FIGURE 8
FIGURE 8 Insect gut renewal through different signaling pathways during infection in D. melanogaster.Various signaling pathways have been recently identified as regulators for intestinal stem cell proliferation.Jak/Stat, EGFR, Hippo, JNK, or Wingless pathway activation in ISCs alone can induce ISC proliferation.The transcription factor Myc functions as a downstream effector shared by Jak/Stat, EGFR, Hippo, and Wingless pathways in promoting ISC proliferation.Additionally, proper insulin receptor signaling in ISCs is necessary for its proliferation.In response to cellular stress, Enterocytes exhibit changes in gene expression regulated by the JNK and Hippo pathways, resulting in the induction of Jak/Stat pathway ligands, particularly Upd3, and EGFR pathway ligands, particularly Keren.Ligands of the EGFR pathway namely Vein and Spitz are expressed in visceral muscles and progenitors, respectively.Under stressed conditions, Enteroblasts produce Upd2 through activation of the Hedgehog pathway.EBs also express the Wingless ligand, regulated by the JNK pathway.The activity of the Hippo pathway in ISCs may be modulated by the intercellular interaction between two atypical cadherins: Fat in ISCs and Dachsous in ECs.Collectively, the diverse cellular components within the gut epithelium possess the ability to regulate ISC proliferation, functioning as intricate sensors that respond to environmental damage and initiate the gut renewal program.This illustration has been adopted from J.-H. Lee et al (167).

TABLE 1
Basic similarities and differences of imd and Toll signaling pathway in D. melanogaster and T. molitor.

TABLE 2
Tissue specific gene expression of imd and Toll pathway in D. melanogaster and T. molitor.