Benjamin Dupuis
Nicolas Pocquet
Anna-Bella Failloux
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- 1Institut Pasteur, Université Paris Cité, Arboviruses and Insect Vectors, Paris, France
- 2Institut Pasteur de Nouvelle-Calédonie, Unité de Recherche et d'Expertise en Entomologie Médicale (URE-EM), Nouméa, New Caledonia
Mosquito-borne diseases such as chikungunya, dengue, and Zika represent a major burden on global public health. To fight against these arboviruses, vector control strategies are a priority. One existing strategy is based on the use of an endosymbiotic bacterium, Wolbachia, which reduces the transmission of arboviruses by the mosquito Aedes aegypti via a pathogen blocking effect. Wolbachia in Ae. aegypti disrupts several pathways of the host’s metabolism. Trehalose is a carbohydrate circulating mainly in insect hemolymph and plays a role in numerous mechanisms as energy source or stress recovery molecule and in chitin synthesis. This study explores the importance of trehalose in the interactions between Wolbachia and Ae. aegypti, and attempts to understand the pathogen blocking effect.
1 Introduction
Vector-borne diseases exert a significant impact on public health contributing to global morbidity and mortality (Bhatt et al., 2013; LaBeaud et al., 2011). For example, 400 million people are infected by dengue virus (DENV) in the world each year (Bhatt et al., 2013; WHO, 2023a), costing $9 billion (Shepard et al., 2016). Aedes aegypti is a primary vector of several arboviruses including DENV (WHO, 2023b). There is no specific treatment against dengue fever and vector control remains the main strategy to limit its emergence and rapid spread. Among vector control strategies (Achee et al., 2019), insecticide treatments are mainly implemented to interrupt dengue transmission (Van Den Berg et al., 2021). However, control efforts have failed to limit dengue fever epidemics and targeted mosquito populations developed resistance to insecticides (Asgarian et al., 2023), urging the development of alternative vector control strategies. Among them, vector control using Wolbachia pipientis has met with significant success (Hilgenfeld and Vasudevan, 2018).
Wolbachia are Gram-negative bacteria belonging to the Alphaproteobacteria class and the Rickettsiales order. Discovered in 1924 (Hertig and Wolbach, 1924), Wolbachia are obligate intracellular bacteria found in nematodes, insects and other arthropods; 40-60% of insects are infected by Wolbachia (Weinert et al., 2015). These bacteria are vertically transmitted and manipulate their hosts to secure their own transmission to the progeny by: (i) inducing a sex ratio distortion in favor of Wolbachia-infected females via parthenogenesis, feminization, male killing or (ii) sterilizing certain individuals via cytoplasmic incompatibility (Landmann, 2019). These effects are not shared by all Wolbachia strains, e.g. Wolbachia from filarial nematodes. In arthropods, Wolbachia strains manipulate the host reproduction and inhibit the transmission of some pathogens, making them potential candidates for vector control (Gill et al., 2014). In insects, Wolbachia is mainly present in reproductive tissues (ovaries) but also in somatic tissues such as the midgut, fat body, salivary glands and muscles (Mejia et al., 2022; Zouache et al., 2009). The relationship between the host and the endosymbiont can be parasitic, mutualistic or commensal (Newton and Rice, 2020), depending on cellular host conditions and the availability of certain nutrients (Lindsey et al., 2018). In addition, the bacterium modifies the host intracellular environment (Lindsey et al., 2018) affecting the cytoskeleton (microtubule and actin) (Ferree et al., 2005; Sheehan et al., 2016) and also modulates gene expression in the host cell; differential expression of genes related to metabolism (Molloy et al., 2016), immunity (Xi et al., 2008) or synthesis of antioxidant molecules [21, 22]. Additionally, Wolbachia induce oxidative stress (Pan et al., 2012), which indirectly affects host metabolism (Bhardwaj and He, 2020) and immunity (Pan et al., 2012; Zug and Hammerstein, 2015). All these changes induced by Wolbachia affect the replication and transmission of DENV in Ae. aegypti (Reyes et al., 2021; Terradas and McGraw, 2017). This phenomenon is known as pathogen blocking effect or pathogen interference. The exact mechanisms leading to the pathogen-blocking effect are not yet fully elucidated, but they appear to be multifactorial, involving immunity, competition for resources, lipids, and oxidative stress (Reyes et al., 2021; Terradas and McGraw, 2017).
Wolbachia strategy is at the base of two distinct and complementary approaches in vector control: (i) incompatible insect technique based on cytoplasmic incompatibility to reduce the size of vector populations and (ii) pathogen-blocking effect to limit the transmission of arboviruses (Caragata et al., 2021). The most commonly Wolbachia strains used for vector control are wMel from Drosophila melanogaster and wAlbB from Aedes albopictus trans-infected in Ae. aegypti (Caragata et al., 2021; Ross, 2021). The pathogen blocking phenotype is Wolbachia strain- and host-dependent (Jiménez et al., 2019); wAlbB enhances, rather than inhibits, West Nile virus infections in Culex tarsalis (Dodson et al., 2014; Glaser and Meola, 2010). The effects produced by Wolbachia are based on a variety of cellular and molecular mechanisms. Indeed, Wolbachia have an effect on the carbohydrate and lipid metabolism and among carbohydrates, trehalose is an essential molecule for growth, fertility, and vitality.
Trehalose (α-D-glucopyranosyl-α-D-glucopyranoside) is a non-reducing disaccharide found in insects (Figure 1A). Present in soluble form at high concentrations (5 to 50mM) in insect hemolymph, its concentration is highly dependent on environmental conditions, nutrition and the insect state of stress (homeostasis disturbance) (Becker et al., 1996; Tamayo et al., 2022; Thompson, 2003). Trehalose participates in several physiological processes such as metabolism, development, chitin synthesis, flight, recovery from stress, and more globally in maintaining homeostasis (Matsuda et al., 2015; Shukla et al., 2015).
Figure 1
Figure 1. Trehalose molecule, synthesis and pathway. (A) Haworth representation of trehalose, a glucose dimer linked by a α,α-1,1 bond. (B) Trehaloneogenesis, the trehalose-forming metabolic pathway. (C) Trehalose involved in trehaloneogenesis and glycolysis. UDP, Uridine diphosphate glucose; iP, inorganic phosphate; TPS, Trehalose 6-phosphate synthase; TPP, Trehalose 6-phosphatase; TREH, Trehalase; GLUT1, Glucose transporter I; HK, Hexokinase; PGM, Phosphoglucomutase; GP, Glycogen phosphorylase; G1P, Glucose 1-phsophate; G6P, glucose 6-phosphate; T6P, trehalose 6-phosphate; HTH, Hypertrehalosemic hormone;TRET1, Trehalose transporter I (Created in https://BioRender.com).
We examine the role of trehalose in interactions between Wolbachia and an arbovirus in Ae. aegypti, and discuss implications of these relationships for the control of mosquito-borne diseases.
2 Trehalose in Aedes aegypti
Trehalose is a molecule synthesized in the fat body through trehaloneogenesis from glucose acquired with food. The trehaloneogenesis pathway diverts one of the intermediates of glycolysis: glucose-6-phosphate (G6P) as substrate for trehalose-6-phosphate synthase (TPS) producing trehalose-6-phosphate (T6P) which is dephosphorylated via trehalose-6-phosphate-phosphatase (TPP) giving trehalose (Figure 1B) (Shukla et al., 2015). Then, this molecule is released in the hemolymph via the trehalose transporters TRET1 (Tamayo et al., 2022) and cleaved into two glucose molecules by trehalases (TREH), which operate in two forms: TREH-1 soluble and TREH-2 anchored in the membrane of all insect cell types (muscle, midgut, salivary glands, fat body) (Tamayo et al., 2022). Finally, glucose molecules produced by cleavage are imported into cells via glucose transporters (GLUT1), initiating multiple metabolic pathways including glycolysis (Figure 1C) (Tamayo et al., 2022). Trehalose can also be imported into various types of cells via TRET1 or through active transporters. Indeed, TRET1 is highly expressed in fat body cells and muscles (Kanamori et al., 2010) while Malpighian tubules possess active transporters for trehalose (Figure 1C) (Kanamori et al., 2010).
Trehalose plays a fundamental role in insects due to its versatility in many physiological processes (Thompson, 2003). As the main circulating carbohydrate, it serves not only as an energy source for metabolic activities (Becker et al., 1996; Shukla et al., 2015; Thompson, 2003), but is also involved in energy storage in the form of glycogen (Zeng et al., 2020). Additionally, trehalose acts as a protector against extreme environmental conditions, providing cryoprotection against cold (Huang et al., 2022) and shielding cells from desiccation (Thorat et al., 2012). It is also involved in chitin synthesis (Yang et al., 2024), an essential component of insect exoskeleton, and plays a role in key biological processes such as oogenesis and diapause (Becker et al., 1996; Zeng et al., 2020). Finally, trehalose is crucial for recovery after periods of stress, demonstrating its vital importance for insect survival and adaptation to changing environments (Shukla et al., 2015; Thompson, 2003; Yasugi et al., 2017; Yu et al., 2020).
In insects, trehaloneogenesis is a pathway regulated by hormones (Tellis et al., 2023; Thompson, 2003). Indeed, trehaloneogenesis is activated in fat body cells by hormones secreted from the nervous system (e.g. juvenile hormone analogs, 20-Hydroxyecdysone (20E) and diuretic hormone (DH)) (Shukla et al., 2015; Tellis et al., 2023). Some factors such as exposure to pesticides and temperature shifts, increase trehalase activity while others (hormonal regulation via regulating factors) reduce it (Shukla et al., 2015; Tellis et al., 2023). Thus, trehalose concentration varies throughout insect life. The hypertrehalosemic hormone (HTH) is responsible for regulating trehalose levels in insects (Thompson, 2003). HTH is primarily released in response to increased energy demand or stressful conditions, and it stimulates the release of stored trehalose from tissues to provide an additional energy source for the insect (Thompson, 2003). This helps to maintain trehalose homeostasis and ensures that insects have a readily available energy source when needed (Tellis et al., 2023); HTH is released when insects need additional energy (e.g. for flight) (Thompson, 2003). This stimulates the breakdown of glycogen stored in tissues into glucose (Thompson, 2003). Subsequently, glucose is converted into trehalose, which is released into the hemolymph (Tellis et al., 2023; Thompson, 2003). Additionally, the regulation of trehalose concentration in the hemolymph is ensured by modulating the expression of trehalose transporters, such as TRET1, in the fat body cells (Kanamori et al., 2010; Tamayo et al., 2022).
3 Trehalose as an energy source for Wolbachia in Ae. Aegypti
The presence of Wolbachia disrupts various cellular dynamics of its host. Indeed, Wolbachia can modify the expression of certain host genes (Caragata et al., 2017; Lindsey et al., 2021). Genes involved in membrane transport (glucose transporter, permeases, monocarboxylate or cholesterol transporters) and carbohydrate metabolism are over-expressed, activating the host cell global metabolism (Caragata et al., 2017). Induced changes increase the amount of nutrients imported and metabolic activity, as well as trehalose concentration which depends on iron availability in the organism (Currin-Ross et al., 2021). However, it has been shown that Wolbachia can use trehalose and glycogen reserves, increasing the amount of glucose (Zhang et al., 2021). Wolbachia wMel strain lacks a trehalose-forming pathway, but synthesizes enzymes that can import and use trehalose (Jiménez et al., 2019). Thus, the Wolbachia-infected host may use trehalose to obtain glucose, a main source of energy (Currin-Ross et al., 2021), as well as other nutrients such as glyceraldehyde 3-phosphate (GP3) (Jiménez et al., 2019; Lindsey et al., 2018). The bacterium induces an increased level of glucose (Zhang et al., 2021) and therefore participates in energy metabolism such as glycolysis (Shukla et al., 2015), providing it with essential metabolic intermediates and precursors (G3P) and energy. NADH synthetized could indirectly benefit Wolbachia via the pentose phosphate pathway using G6P as a metabolic precursor.
Wolbachia also affects host hormone regulation. Indeed, this bacterium impacts the regulation of its host’s insulin/IGF-like signaling pathways (Ikeya et al., 2009). The insulin/IGF pathway, in turn, is known to affect trehalose carbohydrate storage in insects (Bobrovskikh and Gruntenko, 2023; Broughton et al., 2005). Furthermore, it has been shown that the level of juvenile hormone (JH) is elevated in Wolbachia-infected Drosophila melanogaster males (Zhang et al., 2021). This hormone is known to regulate trehalose synthesis (Xu et al., 2013). Finally, Wolbachia-induced oxidative stress (Pan et al., 2012) leads to a hormonal response with synthesis of hormones belonging to the adipokinetic hormones (AKH) family (Chaitanya et al., 2016); this hormone also plays a role in increasing the amount of trehalose, using glycogen reserves for energy purposes (Huang et al., 2012; Lu et al., 2019). The increased amount of energy produced would compensate for losses of resources diverted by Wolbachia. Glycolysis is an essential component of intracellular bacteria-host interactions; it was shown that pyruvate maintains the symbiotic relationship (Melnikow et al., 2013; Voronin et al., 2019, 2016). In addition, in immune cells, sugar metabolism (from trehalose and glucose), particularly the pentose phosphate pathway (PPP cycle), is crucial not only for fighting and regulating infections but also for protecting the host from the effects of its own immune response and for ensuring the fitness (Kazek et al., 2024). This phenomenon could be accentuated with DENV infection. Indeed, competition for resources and energy becomes critical, and trehalose regulation may help in host cell survival.
4 Trehalose as a key molecule in the regulation of oxidative stress
As previously mentioned, Wolbachia induces oxidative stress, resulting in increased concentrations of reactive oxygen species (ROS) (H2O2, O2•, OH•) (Pan et al., 2012). Oxidative stress is unsustainable for the cell if prolonged, as ROS induce lipid peroxidation, damage to genetic material or apoptosis (Kodrík et al., 2015; Martemucci et al., 2022). To preserve cell integrity, it is vital to counterbalance this oxidative stress with antioxidant mechanisms (Felton and Summers, 1995). These can be antioxidant enzymes such as Glutathione S-transferase (GST), or antioxidant molecules such as glutathione, ascorbic acid, uric acid and carbohydrates (Felton and Summers, 1995), which are ubiquitous in insect tissues (fat bodies, midgut, Malpighian tubes) (Felton and Duffey, 1992). Antioxidant molecules trap molecules responsible for oxidative stress (Felton and Summers, 1995). As trehalose is a carbohydrate, it could be a key molecule in the regulation of Wolbachia-induced oxidative stress in Ae. aegypti. Indeed, trehalose can scavenge free radicals, thus acting as an antioxidant, at least in insect hemolymph (Felton and Summers, 1995). Thus, oxidative stress can be attenuated by regulating trehalose metabolism (Peng et al., 2024; Thorat et al., 2016). Similarly, trehalose intake reduces the amount of oxidizing molecules, giving it at least an antioxidant effect (Peng et al., 2024). The increase in trehalose seems to be involved in regulating redox balance (Thorat et al., 2016). Furthermore, trehalose is also involved in redox balance in many other organisms (antioxidant molecule), as in yeast, certain bacteria, mammals and plants (Benaroudj et al., 2001; Luo et al., 2008; Reyes-DelaTorre et al., 2012; Zhang et al., 2023), trehalose accumulation during cellular stress such as oxidative stress may reduce free radical damage via mechanisms that remain unclear (Benaroudj et al., 2001; Reyes-DelaTorre et al., 2012). We therefore suggest a similar accumulation mechanism in Ae. aegypti, participating in the regulation of oxidative stress, as Wolbachia does (Pan et al., 2012).
5 Trehalose in Ae. aegypti - Wolbachia interactions
Interactions between Wolbachia and Ae. aegypti can take various forms and lead to different effects: metabolic (Lindsey et al., 2018; Ponton et al., 2015; Reyes et al., 2021), immune (Caragata et al., 2017; McGraw, 2004; Souza-Neto et al., 2009; Ye et al., 2013) or others (Lindsey et al., 2018). All together they impact DENV replication, leading to a pathogen-blocking effect (Reyes et al., 2021; Terradas and McGraw, 2017). Exchanges and interactions between Wolbachia and its mosquito host take place via diverse detection and signaling processes (Lindsey, 2020). In addition, Wolbachia interacts with its host’s RNA (Terradas et al., 2017); the miRNA (micro) pathway participates in “pathogen-blocking” effect by wMelPop strain in Ae. aegypti (Hedges et al., 2008). Inhibition of certain miRNAs leads to a decrease in Wolbachia density, suggesting that the endosymbiont facilitates its maintenance in the host by manipulating host gene expression via miRNAs (Zhang et al., 2013), as piRNAs (Mayoral et al., 2014). piRNAs are important in cell signaling and host immune responses. Nevertheless, the nature of all the interactions between Wolbachia and its host is not fully understood.
5.1 Trehalose as potential glycolipid
Trehalose may play a role in these interactions. This molecule has been shown to be crucial in interactions between the bean bug and a Gram-negative symbiont bacterium (Lee et al., 2023). The same role can be suggested in the relationship between Ae. aegypti and Wolbachia. Indeed, the trehalose imported by the cell carrying Wolbachia could directly serve the endosymbiont itself. It is believed that Wolbachia do not have their own trehaloneogenesis pathway (Jiménez et al., 2019). However, the Wolbachia wMel strain possesses a PEP (phosphoenolpyruvate) system for trehalose transport within the bacterium (Jiménez et al., 2019), as well as a trehalose 6-phosphate-specific phosphohydrolase, resulting in trehalose production (Jiménez et al., 2019). A portion of the trehalose could be used for the synthesis of trehalose-forming glycolipids, as it is the case in other types of intracellular bacteria (Asselineau and Asselineau, 1978; Reinink et al., 2019). A hypothesis here is that these glycolipids could play a role in the Wolbachia-induced pathogen-blocking effect in Ae. aegypti. Indeed, these molecules are reported as having immunostimulant properties (Asselineau and Asselineau, 1978; Vanaporn and Titball, 2020) and can be brought into contact with the host through as yet unknown mechanisms, supporting the immune system priming hypothesis in pathogen blocking effect.
5.2 Trehalose as an autophagy inducer
Autophagy is a self-degradative process pivotal for re-equilibrating energy sources at critical times in development and response to stress (Jo et al., 2021; Li et al., 2022; Tracy and Baehrecke, 2013). Autophagy is a highly conserved intracellular mechanism in eukaryotes (Glick et al., 2010; Kuo et al., 2018). Although the mechanism remains universal, some proteins involved in this process are different in insects (Brackney, 2017; Jain et al., 2015; Kuo et al., 2018). Autophagy is an important process involved in interactions between Wolbachia and Ae. aegypti. Host autophagy directly affects Wolbachia density (Deehan et al., 2021), but also Wolbachia infection (Hargitai et al., 2022). Autophagy could also indirectly allow Wolbachia colonization in Ae. aegypti, since this mechanism regulates oxidative stress (Chaitanya et al., 2016; Wu et al., 2009), avoiding apoptosis. Activation of autophagy can also eliminate pathogens such as arboviruses (Jo et al., 2021; Mahanta et al., 2023; Wu et al., 2009), since arboviruses also influence autophagy in infected cells (Barletta et al., 2016; Echavarria-Consuegra et al., 2019; Heaton and Randall, 2011). Trehalose has been shown to induce and regulate autophagy in many organisms, with mechanisms that need to be determined. This molecule induces autophagy leading to various effects in human cells: an antiviral effect (Belzile et al., 2016), an antioxidant effect (Honma et al., 2018; Mizunoe et al., 2018), an induction of apoptosis in the cell (Darabi et al., 2018) or a renewal effect of intracellular components (Xu et al., 2019). Trehalose-inducing autophagy effect is also described in plants (Williams et al., 2015). It is conceivable that the highly conserved process of autophagy could also be induced by trehalose in insect cells and participates in interactions between Wolbachia and Ae. aegypti.
6 Conclusion and discussion
Trehalose is an essential disaccharide for insects. Its role in maintaining metabolism in the presence of Wolbachia, in stress recovery, as an antioxidant and potentially as an inducer of autophagy and priming of the immune system through glycolipid synthesis, makes it a key molecule to understand the Ae. aegypti - Wolbachia - arbovirus relationship (Figure 2).
Figure 2
Figure 2. The role of trehalose in interactions between Wolbachia and Aedes aegypti. The green circles with a W represent Wolbachia bacteria. TREH, Trehalase; GLUT1, Glucose transporter; TRET, Trehalose transporter; Tnut, Transporter of nutrients; G6P, glucose 6-phosphate; G3P, Glycéraldéhyde-3-phosphate; JH, Juvenile hormone; AKH, Adipokinetic hormones; miRNA, microRNA. (Created in https://BioRender.com).
Despite the knowledge recently acquired on the interactions between Wolbachia and Ae. aegypti, many questions remain unresolved. Future research avenues are proposed, including experimental studies to elucidate the precise role of trehalose in Wolbachia colonization and pathogen blocking effect. The potential role of trehalose in autophagy induction should be addressed by experimentally testing if trehalose supplementation leads to autophagic structure formation. Similarly, the presence of trehalose forming lipids should be confirmed.
It has been shown that inactivation of TRET decreases significantly trehalose concentration in the hemolymph of Anopheles gambiae, responding differently to various stresses including infection with Plasmodium falciparum; low levels of circulating trehalose significantly reduced parasite infection, suggesting that trehalose plays a role in the sporogonic development of the parasite (Liu et al., 2013). These results could inspire further studies on arboviral infections, by carrying out inactivation or RNAi studies targeting trehaloneogenesis proteins to find out whether viral replication and vectorial competence of Ae. aegypti are affected.
Finally, the additional knowledge gained could contribute to a better understanding of the pathogen blocking effect, enabling the conception of transgenic mosquito lines devoid of Wolbachia but having kept the pathogen-blocking effect. In addition, this knowledge will help in designing new-generation insecticides targeting trehaloneogenesis proteins, as is currently being done (García and Argüelles, 2021; Matassini et al., 2020).
Author contributions
BD: Writing – original draft. NP: Writing – review & editing. A-BF: Writing – review & editing.
Funding
The author(s) declare that financial support was received for the research and/or publication of this article. This study was supported by the Institut Pasteur (Project Explore) and the Laboratoire d’Excellence “Integrative Biology of Emerging Infectious Diseases” (grant n°ANR-10-LABX-62-IBEID). BD received a doctoral fellowship from ANRS-MIE (ArboFrance). The funders had no role in study design, data collection and interpretation, or decision to submit the work for publication.
Acknowledgments
We thank Christian Mitri, Marie Vazeille, Lazare Brézillon-Dubus, Adrien Blisnick, and Marine Viglietta for their comments, and Patricia Smiley for editing the manuscript.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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The author(s) declare that no Generative AI was used in the creation of this manuscript.
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Keywords: trehalose, Wolbachia, pathogen-blocking effect, Aedes aegypti, antioxidant, autophagy
Citation: Dupuis B, Pocquet N and Failloux A-B (2025) Understanding the role of trehalose in interactions between Wolbachia and Aedes aegypti. Front. Cell. Infect. Microbiol. 15:1547873. doi: 10.3389/fcimb.2025.1547873
Received: 18 December 2024; Accepted: 04 March 2025;
Published: 18 March 2025.
Edited by:
Shengzhang Dong, Johns Hopkins University, United StatesReviewed by:
Amit Sinha, New England Biolabs, United StatesChinmay V. Tikhe, Johns Hopkins University, United States
Copyright © 2025 Dupuis, Pocquet and Failloux. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Anna-Bella Failloux, YW5uYS1iZWxsYS5mYWlsbG91eEBwYXN0ZXVyLmZy