- Open Access
Enhancing the scalability of Wolbachia-based vector-borne disease management: time and temperature limits for storage and transport of Wolbachia-infected Aedes aegypti eggs for field releases
Parasites & Vectors volume 16, Article number: 108 (2023)
Introgression of the bacterial endosymbiont Wolbachia into Aedes aegypti populations is a biocontrol approach being used to reduce arbovirus transmission. This requires mass release of Wolbachia-infected mosquitoes. While releases have been conducted using a variety of techniques, egg releases, using water-soluble capsules containing mosquito eggs and larval food, offer an attractive method due to its potential to reduce onsite resource requirements. However, optimisation of this approach is required to ensure there is no detrimental impact on mosquito fitness and to promote successful Wolbachia introgression.
We determined the impact of storage time and temperature on wild-type (WT) and Wolbachia-infected (wMel or wAlbB strains) Ae. aegypti eggs. Eggs were stored inside capsules over 8 weeks at 18 °C or 22 °C and hatch rate, emergence rate and Wolbachia density were determined. We next examined egg quality and Wolbachia density after exposing eggs to 4–40 °C to determine how eggs may be impacted if exposed to extreme temperatures during shipment.
Encapsulating eggs for 8 weeks did not negatively impact egg viability or resulting adult emergence and Wolbachia density compared to controls. When eggs were exposed to temperatures within 4–36 °C for 48 h, their viability and resulting adult Wolbachia density were maintained; however, both were significantly reduced when exposed to 40 °C.
We describe the time and temperature limits for maintaining viability of Wolbachia-infected Ae. aegypti eggs when encapsulated or exposed to extreme temperatures. These findings could improve the efficiency of mass releases by providing transport and storage constraints to ensure only high-quality material is utilised during field releases.
Dengue, caused by dengue virus (DENV), is endemic in over 100 countries, with approximately half of the world’s population at risk of infection [1,2,3]. Aedes aegypti is the major vector for DENV as well as Zika virus (ZIKV), chikungunya virus (CHIKV) and yellow fever virus [4, 5]. The prevalence of these viral diseases is continuing to rise because of vector habitat expansion [6, 7] and failure of current prevention strategies such as insecticides .
This has consequently driven the development of several novel biocontrol strategies over the last decade. Population suppression methods involve the release of male insects sterilised by chemical exposure, irradiation or genetic modification [9,10,11,12]. Sterile males then mate with wild females to produce inviable offspring, reducing the population size. Another way to prevent females producing offspring is by releasing incompatible males. This method has been developed through the introduction of the endosymbiotic bacterium Wolbachia into Ae. aegypti. When Ae. aegypti are transinfected with Wolbachia, male sperm are reproductively modified such that when males mate with wild females, their offspring die [13,14,15,16]. All current population suppression technologies involve the continual release of males which reduce the population over time. Alternatively, Wolbachia can be used in a population introgression approach. When Ae. aegypti mosquitoes carry Wolbachia, the transmission potential for viruses such as DENV [14, 17, 18], ZIKV [19, 20], CHIKV [14, 19, 21] and yellow fever virus [21, 22] is reduced. This approach involves the release of both male and female Wolbachia-infected Ae. aegypti. While Wolbachia-uninfected females do not produce viable eggs when mated with Wolbachia-infected males, Wolbachia-infected females can rescue this lethality, providing them a reproductive advantage. Wolbachia is maternally inherited such that, over time, Wolbachia spreads through the population, creating a mosquito population that is refractory to viral transmission. All of these biocontrol methods are dependent on the mass release of mosquitoes that are competitive with natural populations. Therefore, having the tools to implement biocontrol methods that offer a long-term solution, at a scale sufficient to address the significant distribution of mosquito-borne viruses, is of high priority [23,24,25,26,27].
To introduce mosquitoes into the wild, eggs, pupae or adult releases have been used. Pupae release devices hold pupae in water and provide protection and sucrose for emerged adults. Release at the pupae stage of life is beneficial because, unlike larvae, pupae do not require food [28, 29]. However, to achieve synchronised development en masse is very difficult as the pupal stage only lasts for approximately 24 h. Adult releases typically involve the packaging of adults in ventilated plastic tubes and manually releasing them from either a slow-moving (30–35 km/h) vehicle or on foot . Aerial release of adults has been investigated in the context of the sterile insect technique, and it involves a specialised release mechanism that stores up to 50,000 mosquitoes, maintains cool temperatures and doses and ejects mosquitoes when prompted [31,32,33]. Aerial releases would greatly reduce operational costs; however, they are not practical in all geographical and social contexts, such as certain climate conditions and informal settlements, meaning ground releases are still of importance. Given that ground release of pupae and adults requires substantial resources to rear and package mosquitoes, egg releases offer an attractive alternative. Release of Wolbachia-infected Ae. aegypti eggs involves the production of eggs at an onsite facility or at a regional hub and shipment to sites where eggs are released into the field in a container of water with sufficient larval food. Egg releases are applicable to any biocontrol methods that do not require sex sorting prior to field release, such as Oxitec’s Friendly™ capsule method, gene drive and other genetically modified mosquito releases [34, 35]. This method has successfully been used to establish Wolbachia in Ae. aegypti populations the field, for example in parts of Queensland, Australia, and Yogyakarta, Indonesia [36,37,38]. However, aliquoting and distributing eggs with larval food while maintaining egg viability is difficult en masse; hence, to improve the egg packaging and delivery method, encapsulation of eggs with larval food in water-soluble capsules has been developed .
Encapsulating eggs with larval food and hatching them with no storage time do not impact hatch rate, emergence rate, adult wing length or Wolbachia density . However, the impact of extended storage time and temperature on encapsulated eggs remains unknown. Studies have shown that when Wolbachia-infected non-encapsulated eggs are stored over extended periods of time, egg viability decreases faster than in Wolbachia-free eggs [40,41,42,43,44,45,46,47,48]. Additionally, both low (< 14 °C) and high (cyclical 22–30 °C) egg storage temperatures have been shown to negatively impact egg viability [48, 49]. Therefore, it is important to determine whether encapsulation further exacerbates this impact and at what temperatures Wolbachia-infected eggs remain viable.
In this study, we investigate whether storage time or temperature impacts fitness measures of encapsulated eggs and whether Wolbachia-infected eggs (wMel and wAlbB—the current strains being utilised in field releases [23, 50]) are impacted differently compared to WT eggs. We then examine the impact of exposure to extreme high and low temperatures on egg viability and Wolbachia density to inform appropriate egg transport and risk management strategies. We report that storing eggs inside of capsules does not negatively impact egg viability, emergence rates or Wolbachia density compared to the control storage method. We show that while egg viability is maintained quite well following exposure to cold temperatures, temperatures > 40 °C can reduce egg viability and Wolbachia density.
Mosquito strains and maintenance
Three Australian mosquito strains were used throughout this study: WT, wMel- and wAlbB-infected Ae. aegypti. The establishment of these colonies has been previously described by Flores et al. . Prior to the start of these experiments, the wMel and wAlbB lines were backcrossed to Australian WT mosquitoes (100% WT males) for an additional three generations to reduce any genetic divergence that may have occurred between the strains. Additionally, partial backcrossing occurred each subsequent generation with 10% of WT males each generation. Experiments took place in the immediate one-eight generations after the completion of full backcrossing. Colonies were maintained under standard laboratory conditions in a climate-controlled insectary at 26 °C, 70% relative humidity (RH) with 12 h:12 h light/dark cycle.
Larval diet was prepared by thoroughly grinding and mixing 35% beef liver powder (Now Foods, USA), 50% tuna meal (Ridley Aqua Feeds, Australia) and 15% brewer’s yeast (Now Foods, USA) together as described by Puggioli et al. . The liquid diet version was prepared by mixing solid components with reverse osmosis (RO) water to form a 7.51% slurry. Food components were stored at 4 °C. In standard rearing conditions to generate eggs for experiments, shrimp wafers (Tetra®, USA) were used and stored at room temperature.
For each experiment, mosquitoes were reared for one generation to collect fresh eggs. To do this, eggs were vacuum hatched, and 200 larvae were placed in 3 l RO water and fed daily with liquid larval diet or shrimp wafers. At > 50% pupation, each container was transferred to a 24.5 × 24.5 × 24.5-cm or 20 × 20 × 30-cm cage and adult mosquitoes were provided with a sucrose solution (10% sucrose, 0.4% propionic acid). A blood meal was offered to adult females 5–6 days post emergence via artificial feeders. Human blood was provided by the Australian Red Cross (Supply Agreement 22-05VI-04) or human volunteers (Monash University Human Research Ethics permit 27690). Cups lined with filter paper and half filled with water were provided for oviposition; 96 h after blood feeding, paper substrates with mosquito eggs were dried by pressing between layers of paper towel and cloth for 2 h and then slowly dried over the course of the following day in shallow, paper towel-lined trays and stored at 26 °C and 75 ± 5% RH.
To prepare egg capsules, 150 viable eggs were manually counted and gently brushed from the paper substrate into a size 00 water-soluble hydroxypropyl methylcellulose (HPMC) capsule (The Capsule Guy, Australia) using a small paintbrush. Prior to capsule preparation, hatch rate tests were conducted on eggs from all mosquito lines so that the number of viable eggs per capsule was accurately quantified. Capsules were then topped with 285 mg larval food and 110 mg activated charcoal. Activated charcoal was used as a filler to ensure capsules were completely full. For each experiment, five replicate capsules were prepared for each condition and hatch week. Food-only capsules were prepared and used as larval food for non-encapsulated control groups (i.e. eggs on paper substrate). Control group eggs were prepared by cutting the paper substrate that eggs were laid on into groups of approximately 150 viable eggs.
For all storage conditions, eggs were maintained at 75 ± 5% RH and 22 °C unless specified otherwise. In temperature experiments, eggs contained in capsules or on paper substrate were stored at 18 °C or 22 °C. For extreme temperature experiments, eggs on paper substrate (unencapsulated) were stored at 4 °C, 12 °C, 26 °C, 36 °C or 40 °C. Temperature and humidity were controlled by storing eggs inside a laboratory incubator (Thermoline L + M) with a saturated salt solution and were tracked using hygrochrons (iButton®).
To determine the hatch rate of eggs in capsules or on paper substrate with a food capsule, 150–200 eggs per group were photographed and quantified, using Adobe Photoshop count tool, and submerged in cups with 300 ml RO water. The number of larvae in an individual container was counted 48 h after egg submersion. Larvae were returned to their corresponding containers after counting and allowed to develop to adulthood. Hatch rate was calculated as the percentage of eggs that produced larvae per container.
Emergence rate was determined 14 and 16 days post-hatching and was calculated as the percentage of larvae that emerged as adults per container.
Six days post-emergence, adult females were collected (24–40 females per group) and placed individually into 96-well plates and homogenised in 50 μl squash buffer (10 mM Tris, pH 8.2; 1 mM EDTA; 50 mM NaCl) supplemented with 25 μg/ml proteinase K (Bioline) and a 2-mm glass bead (Pacific Laboratory Products). Samples were clarified by centrifuging for 3 min at 3000 rpm and then incubated in a thermocycler (5 min at 56 °C followed by 5 min at 98 °C). Mosquito homogenates were clarified again by centrifuging at 3000 rpm for 5 min and then supernatants diluted ten-fold using AE buffer (Qiagen). Total relative Wolbachia density was estimated by triplex quantitative polymerase chain reaction (qPCR). qPCR reactions were performed in 10 μl total volume containing 5 μl of 2 × LightCycler 480 Probes Master reaction mix, 2.5 μM primers, 10 μM of each probe (Wolbachia surface protein [wsp], Ribosomal protein S17 [RpS17] and the ankyrin repeat domain-containing protein (DEJ70_01140) in wAlbB [wAlbB141]) and 3 μl diluted (1:10) adult homogenate (see Additional file 1: Table S1 for probe and primer sequences) [53, 54]. Cycling was performed using LightCycler 480 II (Roche) with one cycle at 95 °C for 5 min, followed by 45 amplification cycles of 95 °C for 10 s, 60 °C for 15 s and 72 °C for 1 s. To analyse qPCR data Normalised Expressions (NE) were calculated using the delta Ct method , NE = 2Cq (reference)/2Cq (target), where RpS17 was the reference gene and wsp or wAlbB141 the target gene.
Data analysis was undertaken using R v 1.4.1717 and visualised using GraphPad Prism v 9.2. Normality was checked using the Shapiro-Wilk test and assumptions using diagnostic plots and residual simulation plots . We performed a generalised linear model (GLM), Kruskal-Wallis H-test or Mann-Whitney U test (non-parametric data) [57,58,59]. Modelling was followed by ANOVAs to compare treatment effect (parametric data) . If significant interactions were identified, we used Tukey’s P-value adjustment method for pairwise comparisons . Two biological replicates were performed for each experiment, and we assessed whether replicate data were significantly different from each other to determine whether replicates were analysed separately or together. Fig. 1 and Additional file 1: Figure S1 and Fig. 2 and Additional file 1: Figure S2 were analysed independently and Figs. 3 and 4 are representative of two independent experiments analysed together including a replicate variable. Statistical outputs are provided in detail in Additional file 2: Dataset S1.
Encapsulating eggs for storage at 22 °C does not exacerbate impacts on egg viability, adult emergence or Wolbachia density compared to controls
To assess the effect of encapsulating eggs on mosquito fitness, we stored WT, wMel- and wAlbB-infected eggs inside capsules. We compared the effect of encapsulation, Wolbachia infection and 8-week storage time on quiescent egg longevity as well as the resulting adult emergence rates and Wolbachia density. When comparing each mosquito line hatched from eggs on paper substrate (control) to encapsulated eggs, hatch rate was not significantly impacted, but was influenced by storage time, with egg viability decreasing over time for all three mosquito lines (ANOVA; hatch rate: encapsulation, F(1,148) = 9.1727, P = 0.7791; hatch rate: storage time, F(1,148) = 31.9372, P < 0.0001****) (Fig. 1a). A repeat experiment showed a small but significant decrease in wMel- and wAlbB-infected egg hatch rate when encapsulated (Additional file 1: Fig. S1a). Promisingly, emergence rates remained high, above an average of 75%, for all groups up to 8 weeks of storage and were not negatively impacted by encapsulation (GLM; P > 0.05 for all comparisons) (Fig. 1b). A repeat experiment showed similar trends, although a significant decrease in emergence at 8 weeks was observed in WT control and wAlbB-infected eggs regardless of encapsulation (Additional file 1: Fig. S1b). When analysing Wolbachia density of emerged adults, it was found that while density changed slightly over time (wAlbB generally increasing and wMel decreasing or remaining consistent) (GLM; Wolbachia density: storage time, P = 0.0076**) encapsulation did not negatively impact Wolbachia density (GLM; Wolbachia density: encapsulation, P = 0.159) (Fig. 1c). The repeat experiment also demonstrated this (Additional file 1: Fig. S1c). Together, these experiments indicate that egg encapsulation does not exacerbate the negative impact of storage time on hatch rate, nor does it negatively impact on adult emergence or Wolbachia density in mosquitoes produced from encapsulated eggs stored for up to 8 weeks.
Encapsulating eggs for storage at 18 °C does not improve egg fitness compared to 22 °C
We next assessed the impact of 18 °C storage temperature on encapsulated egg longevity and adult fitness, as results from Lau et al.  showed that storing Wolbachia-infected eggs at lower temperatures may extend egg longevity. This experiment focused on wMel since this is the Wolbachia strain most widely used in field releases. Initially, we compared hatch rates of eggs from the paper substrate control or capsules stored at each temperature. At 18 °C, encapsulated egg hatch rate was significantly lower than in the controls (Tukey’s multiple comparison; 18 °C, control: capsule, Z = − 3.192 P = 0.0014**), while at 22 °C, the hatch rates of the control and encapsulated eggs were not significantly different to each other (Tukey’s multiple comparison; 22 °C, control: capsule, Z = − 1.118, P = 0.2634) (Fig. 2a). When considering the effect of temperature, hatch rates were slightly higher when stored at 18 °C compared to 22 °C for both control eggs and encapsulated eggs (Tukey’s multiple comparison; control, 18 °C: 22 °C, Z = 3.521 P = 0.0004***; capsule, 18 °C: 22 °C, Z = 2.124, P = 0.0337*). However, this was not found to be a repeatable difference (Additional file 1: Fig. S2). Combined, these results support that encapsulating eggs has no negative impact on egg viability compared to controls and suggest that decreasing storage temperature to 18 °C does not substantially impact egg viability.
Larvae were then reared to adulthood and emergence and Wolbachia density were assessed. Notably, we observed a reduction in emergence following 8 weeks of storage, which was not seen in Fig. 1b, but was observed in a repeat experiment (Additional file 1: Fig. S1b), perhaps due to batch variation in egg and food quality. Post hoc analysis revealed that the reduction in adult emergence observed over time was most significant for control eggs stored at 22 °C, but was not influenced by encapsulation or storage temperature (GLM; emergence: encapsulation, P = 0.6574; emergence: temperature, P = 0.2738) (Fig. 2b). Overall, emergence rate was not affected by egg encapsulation or storage at 18 °C compared to 22 °C. Adult Wolbachia density, while variable between groups, showed no clear trends of change with extended egg storage time (Fig. 2c). Most notably, no loss of Wolbachia was observed in any group (a critical concern for maintaining maternal transmission of Wolbachia in field releases), and encapsulation was not a source of variance for Wolbachia density (Kruskal-Wallis H-test; Wolbachia density: encapsulation, H = 1.164, P = 0.2806).
Storage of Ae. aegypti eggs at 40 °C for 48 h induces lethality and Wolbachia loss
Mosquito eggs are transported from production facilities to release sites via air freight when local release sites do not have the capacity for large-scale production. When transporting eggs, ambient temperatures can reach extreme highs and lows, potentially impacting egg viability and Wolbachia density. Therefore, understanding the temperature range through which eggs remain viable, and Wolbachia is not negatively affected, is critical to ensure high quality control. To test this, we stored eggs on paper substrate at temperatures ranging from 4–40 °C and hatched after 8 or 48 h storage to assess egg viability. Low temperatures (4 °C and 12 °C) did not negatively impact egg viability of WT (Tukey’s multiple comparison, 0 h: 48 h; 12 °C, Z = − 2.051, P = 0.1002; 4 °C, Z = − 1.638, P = 0.2295), wMel-infected (Tukey’s multiple comparison, 0 h: 48 h; 12 °C, Z = − 0.443, P = 0.8976; 4 °C, Z = 0.071, P = 0.9973) or wAlbB-infected eggs (Tukey’s multiple comparison, 0 h: 48 h; 12 °C, Z = − 0.299, P = 0.9519; 4 °C, Z = − 1.5 P = 0.2909) (Fig. 3a). Larvae were then reared at 26 °C and adults were sampled to measure Wolbachia density. wMel density was negatively impacted by low temperatures (Kruskal-Wallis H-test; wMel Wolbachia density: storage temperature, H = 17.614, P = 0.0002*** whereas wAlbB was not negatively impacted, but instead showed a slight increase in density (Kruskal-Wallis H-test; wAlbB Wolbachia density: storage temperature, H = 7.7577, P = 0.0208*) (Fig. 3d–e). There were two instances (out of 160 samples) of wMel loss occurring when eggs were stored at 4 °C (Fig. 3d).
Next, we stored eggs at high temperatures of 36 °C and 40 °C. WT and wMel-infected egg viability was maintained when eggs were exposed to 36 °C, while wAlbB-infected egg viability decreased slightly. All three lines had significantly decreased viability when stored at 40 °C for 48 h (Tukey’s pairwise comparison, 40 °C, 0 h: 48 h; WT, Z = − 7.36, P < 0.0001****; wMel, Z = − 9.894, P < 0.0001****; wAlbB, Z = − 3.876, P = 0.0003***) (Fig. 4a–c). However, wAlbB-infected egg viability was inconsistent across replicate experiments. Both experimental replicates indicated a significant decrease in viability stored at 36 °C after 48 h, while in one experimental repeat, 40 °C had no significant impact on egg viability. Little to no impact was seen on Wolbachia density in adults that emerged from eggs stored at 36 °C (Wilcoxon signed-rank test, 36 °C Wolbachia density, 8 h: 48 h; wMel, Z = − 3.0538, P = 0.0023**; wAlbB, Z = − 1.4402, P = 0.1498) (Fig. 4d). However, density was significantly decreased when eggs were stored at 40 °C for 48 h, where near complete Wolbachia loss was observed in the majority of both wMel- and wAlbB-infected adults (Wilcoxon signed rank test, 40 °C Wolbachia density, 8 h: 48 h; wMel, Z = − 8.2106, P < 0.0001****; wAlbB, Z = − 8.2106, P < 0.0001****) (Fig. 4e). These data demonstrate that if eggs are exposed to temperatures of 40 °C or above for 48 h they should be discarded as viability will be significantly decreased and adults that do emerge are unlikely to be Wolbachia-infected.
To date, Wolbachia has been successfully established in Ae. aegypti populations in cities across the globe to protect 10 million people from mosquito-borne diseases . This remains a small proportion of the world’s population at risk of dengue, estimated to be 2.92–3.97 billion people . As programmes such as those implementing Wolbachia introgression, gene drive or genetic modification, scale-up and work in new regions, they require a cost reductive and resource efficient method for mass mosquito releases. Release of mosquitoes at the egg stage is attractive as they can be produced off site and then shipped to release areas, removing the need for local mosquito-rearing facilities. Furthermore, they can be used to encourage community engagement by involving residents in the rear and release process . This method overcomes financial and regulatory hurdles associated with establishing on-site facilities; however, maintaining egg quality and Wolbachia infection is essential for successful deployment . Thus, egg and food capsules offer an opportunity to improve the scalability of egg releases. Our study tested the long-term storage of eggs inside of capsules as a method that could aid the mass distribution of eggs.
Promisingly, we found that encapsulating eggs has no negative impact on viability of WT, wMel- or wAlbB-infected eggs. Over time, egg viability dropped in Wolbachia-infected and uninfected lines; however, encapsulation did not exacerbate this loss. There is extensive literature evidencing that Wolbachia-infected eggs lose viability faster than WT [40,41,42,43,44,45,46,47,48]. While it is still not clear why this occurs, it is important to know that encapsulation does not further impact egg viability over time. Emergence rate and adult Wolbachia density were also unaffected by encapsulation or storage time. Overall, regardless of Wolbachia infection status, encapsulated eggs were not more susceptible to reduced fitness.
Next, we tested whether reducing the storage temperature to 18 °C could improve encapsulated egg viability and adult fitness compared to 22 °C. While this is lower than the defined ideal range for WT Aedes eggs storage of between 20–26 °C and 70–85% RH from one study , others have shown that lower egg storage temperatures can extend egg longevity when compared with higher temperatures [48, 64]. We found that the viability of eggs infected with wMel was not impacted by reducing storage temperature to 18 °C. The negative impact of egg storage increased with time, particularly in eggs stored at 22 °C, but this was irrespective of encapsulation. Consequentially, emergence rates were also reduced over time potentially due to an overabundance of food which can lead to poor water conditions unsuitable for aquatic mosquito health . Wolbachia density was unaffected by encapsulation and time. While the impacts of 18 °C storage on egg viability were somewhat inconsistent here, future work could be done to determine whether an ideal temperature can be established for Wolbachia-infected Ae. aegypti egg longevity. Overall, encapsulating eggs and storing at 18–22 °C did not negatively impact mosquito fitness measures.
In field application of egg releases, the World Mosquito Program uses air freight to deliver eggs to release sites that cannot support mass production on site, which leaves eggs vulnerable to exposure to extreme temperatures. Currently, shipments aim to maintain temperatures between 15–25 °C. However, data loggers transported with the eggs indicate that temperatures can reach outside of this range, especially when being shipped to remote locations with shipment times of up to 5 days . Gaining a detailed understanding of what conditions egg viability and Wolbachia density are vulnerable to will inform project sites of the potential impact on egg quality if egg stocks are exposed to extreme temperatures. We measured the impact of short-term (48-h) exposure of eggs to 4–40 °C on egg viability and resulting adult Wolbachia density. At 4 °C and 8 °C, egg viability and wAlbB density were unaffected. wMel density decreased at 4 °C, but there were only two cases of Wolbachia loss out of the 160 samples tested. Previous studies have also demonstrated that Ae. aegypti eggs are tolerant to low temperatures, maintaining high viability when laid and stored at 16 °C [49, 67]. At high temperatures, egg viability and Wolbachia density were unaffected by exposure to 36 °C, but were significantly negatively affected when stored at 40 °C for 48 h. Loss of Wolbachia from egg stocks is detrimental because these eggs are no longer usable for Wolbachia introgression releases. In fact, releasing Wolbachia-free females would increase potential viral vectors within a population. All three lines behaved similarly, with the exception of wAlbB in one experimental repeat, which maintained viability at 40 °C despite reduced viability at 36 °C. Given the inconsistency of these results, it is unclear whether wAlbB eggs perform better at this higher temperature. wAlbB has been found to be relatively stable at high temperatures (26–37 °C) compared to wMel [47, 68,69,70]. Ross et al.  found that while wAlbB was more temperature tolerant, egg viability decreased at a similar rate to wMel-infected eggs when exposed to cycling temperatures for 1 week that reach a maximum of 38 °C or above. Adult wMel density decreased after maximum egg storage temperatures of 36 °C, while wAlbB was maintained under all temperatures (egg viability was lost before a decrease in wAlbB was observed) . Our data suggest that wAlbB is susceptible to drop out at acute high temperatures. Although wAlbB is more temperature tolerant, Lau et al. , showed that if eggs are stored at high temperatures (22–30 °C) for longer than 6 weeks, fertility of wAlbB-infected females derived from the eggs significantly decreases, while wMel and WT fertility remains stable. In this study we did not observe a significant negative fitness effect of wAlbB. However, as our methods did not assess fertility, our results may underestimate the impacts of wAlbB on Ae. aegypti. Given this, care must be taken not to expose eggs to high temperatures when storing for long periods of time. While eggs were not encapsulated in these experiments, it is likely similar temperature limits would apply but further testing is required in case temperatures within capsules differ from ambient. These results provide insight into the impact of extreme temperature exposure on Wolbachia-infected Ae. aegypti eggs to ensure resources are not wasted on inviable egg stocks.
In summary, our work has shown that encapsulating eggs with larval food and storing over an 8-week period does not negatively impact egg viability or resulting adult emergence and Wolbachia density compared to the control egg storage method. In addition, we established that egg viability and adult Wolbachia density are maintained well when exposed to 4–36 °C for 48 h, but both are significantly reduced when eggs are stored at 40 °C for > 8 h. Mass insect release biocontrol methods rely on the maintenance of insect fitness with Wolbachia introgression methods additionally requiring high Wolbachia infection prevalence. Capsule-based egg releases improve the ease and scale at which eggs and larval food can be consistently aliquoted and transported to the field. Compared to pupae or adult releases, capsules also provide a substantial logistical benefit for mass insect releases due to the reduced on-site resource requirements. Overall, this work improves our understanding of the factors that influence Ae. aegypti fitness and provides evidence for an improved egg release method that could aid large-scale application of Wolbachia introgression.
Availability of data and materials
All data are provided within the text and Additional files.
- Ae :
- wsp :
Wolbachia surface protein
- RpS17 :
Ribosomal surface protein S17
Generalised linear model
Brady OJ, Gething PW, Bhatt S, Messina JP, Brownstein JS, Hoen AG, et al. Refining the global spatial limits of dengue virus transmission by evidence-based consensus. PLoS Negl Trop Dis. 2012;6:e1760.
da Oliveira LNS, Itria A, Lima EC. Cost of illness and program of dengue: a systematic review. PLoS One. 2019. https://doi.org/10.1371/journal.pone.0211401.
Messina JP, Brady OJ, Golding N, Kraemer MUG, Wint GRW, Ray SE, et al. The current and future global distribution and population at risk of dengue. Nat Microbiol. 2019;4:1508–15.
Martina BE, Barzon L, Pijlman GP, de la Fuente J, Rizzoli A, Wammes LJ, et al. Human to human transmission of arthropod-borne pathogens. Curr Opin Virol. 2017;22:13–21.
Souza-Neto JA, Powell JR, Bonizzoni M. Aedes aegypti vector competence studies: a review. Infect Genet Evol. 2019;67:191–209.
Messina JP, Brady OJ, Pigott DM, Golding N, Kraemer MUG, Scott TW, et al. The many projected futures of dengue. Nat Rev Microbiol. 2015;13:230–9.
Michael B, Deen J, Buchy P, Gubler D, Harris E, Homach J. World Health Organization dengue guidelines for diagnosis, treatment, prevention, and control. Switzerland: WHO Publisher; 2009. p. 3.
Moyes CL, Vontas J, Martins AJ, Ng LC, Koou SY, Dusfour I, et al. Contemporary status of insecticide resistance in the major Aedes vectors of arboviruses infecting humans. PLoS Negl Trop Dis. 2017;11:e0005625.
Thomé RCA, Yang HM, Esteva L. Optimal control of Aedes aegypti mosquitoes by the sterile insect technique and insecticide. Math Biosci. 2010;223:12–23.
Black WC, Alphey L, James AA. Why RIDL is not SIT. Trends Parasitol. 2011;27:362–70.
Carvalho DO, McKemey AR, Garziera L, Lacroix R, Donnelly CA, Alphey L, et al. Suppression of a field population of Aedes aegypti in Brazil by sustained release of transgenic male mosquitoes. PLoS Negl Trop Dis. 2015;9:e0003864.
Phuc H, Andreasen MH, Burton RS, Vass C, Epton MJ, Pape G, et al. Late-acting dominant lethal genetic systems and mosquito control. BMC Biol. 2007;5:11–11.
Turelli M, Hoffmann AA. Cytoplasmic incompatibility in Drosophila simulans: dynamics and parameter estimates from natural populations. Genetics. 1995;140:1319–38.
Moreira LA, Iturbe-Ormaetxe I, Jeffery JA, Lu G, Pyke AT, Hedges LM, et al. A Wolbachia symbiont in aedes aegypti limits infection with dengue, chikungunya, and plasmodium. Cell. 2009;139:1268–78.
Hoffmann AA, Turelli M. Unidirectional incompatibility in Drosophila simulans: inheritance, geographic variation and fitness effects. Genetics. 1988;119:435–44.
Turelli M, Hoffmann AA. Rapid spread of an inherited incompatibility factor in California Drosophila. Nature. 1991;353:440–2.
Ye YH, Carrasco AM, Dong Y, Sgrò CM, McGraw EA. The effect of temperature on Wolbachia-mediated dengue virus blocking in Aedes aegypti. Am J Trop Med Hyg. 2016;94:812–9.
Carrington LB, Tran BCN, Le NTH, Luong TTH, Nguyen TT, Nguyen PT, et al. Field- and clinically derived estimates of Wolbachia-mediated blocking of dengue virus transmission potential in Aedes aegypti mosquitoes. Proc Natl Acad Sci USA. 2017;115:361–6.
Aliota MT, Peinado SA, Velez ID, Osorio JE. The wMel strain of Wolbachia reduces transmission of Zika virus in Aedes aegypti. Sci Rep. 2016;6:28792.
Dutra HLC, Rocha MN, Dias FBS, Mansur SB, Caragata EP, Moreira LA. Wolbachia Blocks Currently Circulating Zika Virus Isolates in Brazilian Aedes aegypti Mosquitoes. Cell Host Microbe. 2016;19:771–4.
van den Hurk AF, Hall-Mendelin S, Pyke AT, Frentiu FD, McElroy K, Day A, et al. Impact of Wolbachia on infection with chikungunya and yellow fever viruses in the mosquito vector Aedes aegypti. PLoS Negl Trop Dis. 2012;6:e1892.
Rocha MN, Duarte MM, Mansur SB, Silva BDME, Pereira TN, Adelino TÉR, et al. Pluripotency of Wolbachia against Arboviruses: the case of yellow fever. Gates Open Res. 2019;3:161.
Nazni WA, Hoffmann AA, NoorAfizah A, Cheong YL, Mancini MV, Golding N, et al. Establishment of Wolbachia strain wAlbB in Malaysian populations of Aedes aegypti for dengue control. Curr Biol. 2019. https://doi.org/10.1016/j.cub.2019.11.007.
Gilbert JA, Melton L. Verily project releases millions of factory-reared mosquitoes. Nat Biotechnol. 2018;36:781.
O’Neill SL. Dengue and Zika: control and antiviral treatment strategies. Adv Exp Med Biol. 2018;1062:355–60.
Zheng X, Zhang D, Li Y, Yang C, Wu Y, Liang X, et al. Incompatible and sterile insect techniques combined eliminate mosquitoes. Nature. 2019;572:56–61.
Sørensen JG, Addison MF, Terblanche JS. Mass-rearing of insects for pest management: challenges, synergies and advances from evolutionary physiology. Crop Prot. 2012;38:87–94.
Nguyen TH, Nguyen HL, Nguyen TY, Vu SN, Tran ND, Le TN, et al. Field evaluation of the establishment potential of wMelPop Wolbachia in Australia and Vietnam for dengue control. Parasit Vectors. 2015;8:563.
Harris AF, Nimmo D, McKemey AR, Kelly N, Scaife S, Donnelly CA, et al. Field performance of engineered male mosquitoes. Nat Biotechnol. 2011;29:1034–7.
Gorman K, Young J, Pineda L, Márquez R, Sosa N, Bernal D, et al. Short-term suppression of Aedes aegypti using genetic control does not facilitate Aedes albopictus. Pest Manag Sci. 2015;72:618–28.
Bouyer J, Culbert NJ, Dicko AH, Gomez Pacheco M, Virginio J, Pedrosa MC, et al. Field performance of sterile male mosquitoes released from an uncrewed aerial vehicle. Sci Robot. 2020. https://doi.org/10.1126/scirobotics.aba6251.
Bouyer J, Vreysen MJB. Yes, irradiated sterile male mosquitoes can be sexually competitive! Trends Parasitol. 2020;36:877–80.
Marina CF, Liedo P, Bond JG, Osorio RA, Valle J, Angulo-Kladt R, et al. Comparison of ground release and drone-mediated aerial release of aedes aegypti sterile males in Southern Mexico: efficacy and challenges. Insects. 2022. https://doi.org/10.3390/insects13040347.
Just Add Water: Oxitec’s New Friendly Mosquito Mini-Capsule Technology Rapidly Suppresses 95% of Disease-Spreading Aedes aegypti in Brazil Trial. M2 Presswire. Coventry: Normans Media Ltd; 2020 May 19; https://search.proquest.com/docview/2404270014?pq-origsite=primo.
Bier E. Gene drives gaining speed. Nat Rev Genet. 2021;23:5–22.
Ryan PA, Turley AP, Wilson G, Hurst TP, Retzki K, Brown-Kenyon J, et al. Establishment of wMel Wolbachia in Aedes aegypti mosquitoes and reduction of local dengue transmission in Cairns and surrounding locations in northern Queensland. Australia Gates Open Res. 2019;3:1547.
Tantowijoyo W, Andari B, Arguni E, Budiwati N, Nurhayati I, Fitriana I, et al. Stable establishment of wMel Wolbachia in Aedes aegypti populations in Yogyakarta Indonesia. PLoS Negl Trop Dis. 2020;14:e0008157–e0008157.
O’Neill SL, Ryan PA, Turley AP, Wilson G, Retzki K, Iturbe-Ormaetxe I, et al. Scaled deployment of Wolbachia to protect the community from dengue and other Aedes transmitted arboviruses. Gates Open Res. 2018;2:36.
Allman MJ, Slack AJ, Abello NP, Lin Y-H, O’Neill SL, Robinson AJ, et al. Trash to treasure: how insect protein and waste containers can improve the environmental footprint of mosquito egg releases. Pathogens. 2022;11:373.
Fraser JE, Bruyne JTD, Iturbe-Ormaetxe I, Stepnell J, Burns RL, Flores HA, et al. Novel Wolbachia-transinfected Aedes aegypti mosquitoes possess diverse fitness and vector competence phenotypes. PLoS Pathog. 2017;13:e1006751.
Joubert DA, Walker T, Carrington LB, Bruyne JTD, Kien DHT, Hoang NLT, et al. Establishment of a Wolbachia superinfection in Aedes aegypti mosquitoes as a potential approach for future resistance management. PLoS Pathog. 2016;12:e1005434.
Axford JK, Callahan AG, Hoffmann AA, Yeap HL, Ross PA. Fitness of wAlbB Wolbachia infection in Aedes aegypti: Parameter estimates in an outcrossed background and potential for population invasion. Am J Trop Med Hyg. 2016;94:507–16.
Walker T, Johnson PH, Moreira LA, Iturbe-Ormaetxe I, Frentiu FD, McMeniman CJ, et al. The wMel Wolbachia strain blocks dengue and invades caged Aedes aegypti populations. Nature. 2011;476:450.
McMeniman CJ, O’Neill SL. A virulent Wolbachia infection decreases the viability of the dengue vector Aedes aegypti during periods of embryonic quiescence. PLoS Negl Trop Dis. 2010;4:e748.
Yeap HL, Mee P, Walker T, Weeks AR, O’Neill SL, Johnson P, et al. Dynamics of the “popcorn” Wolbachia infection in outbred Aedes aegypti informs prospects for mosquito vector control. Genetics. 2011;186:583–95.
Allman MJ, Fraser JE, Ritchie SA, Joubert DA, Simmons CP, Flores HA. Wolbachia’s deleterious impact on aedes aegypti egg development: the potential role of nutritional parasitism. Insects. 2020;11:735.
Ant TH, Herd CS, Geoghegan V, Hoffmann AA, Sinkins SP. The Wolbachia strain wAu provides highly efficient virus transmission blocking in Aedes aegypti. PLoS Pathog. 2018;14:e1006815.
Lau M-J, Ross PA, Hoffmann AA. Infertility and fecundity loss of Wolbachia-infected Aedes aegypti hatched from quiescent eggs is expected to alter invasion dynamics. bioRxiv. 2021. https://doi.org/10.1101/2020.11.25.397240v1.
Byttebier B, Majo MSD, Majo MSD, Fischer S. Hatching response of Aedes aegypti (Diptera: Culicidae) eggs at low temperatures: effects of hatching media and storage conditions. J Med Entomol. 2014;51:97–103.
WMP. World Mosquito Program Website. 2022. https://www.worldmosquitoprogram.org/. Accessed 16 Aug 2022.
Flores HA, Taneja de Bruyne J, O’Donnell TB, Tuyet Nhu V, Thi Giang N, Thi Xuan Trang H, et al. Multiple Wolbachia strains provide comparative levels of protection against dengue virus infection in Aedes aegypti. PLoS Pathog. 2020;16:e1008433.
Puggioli A, Balestrino F, Damiens D, Lees RS, Soliban SM, Madakacherry O, et al. Efficiency of three diets for larval development in mass rearing Aedes albopictus (Diptera: Culicidae). J Med Entomol. 2013;50:819–25.
Braig HR, Zhou W, Dobson SL, O’Neill SL. Cloning and characterization of a gene encoding the major surface protein of the bacterial endosymbiont Wolbachia pipientis. J Bacteriol. 1998;180:2373–8.
Zhou W, Rousset F, O’Neil S. Phylogeny and PCR-based classification of Wolbachia strains using wsp gene sequences. Proc Biol Sci. 1998;265:509–15.
Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCT method. Methods. 2001;25:402–8.
Shapiro SS, Wilk MB. An analysis of variance test for normality (complete samples). Biometrika Oxford Academic. 1965;52:591–611.
Kruskal WH, Wallis WA. Use of ranks in one-criterion variance analysis. J Am Stat Assoc. 1952;47:583–621.
Crawley MJ. Proportion Data. The R Book. 2012;628–49.
Mann HB, Whitney DR. On a test of whether one of two random variables is stochastically larger than the other. aoms. 1947;18:50–60.
Girden ER. ANOVA: Repeated measures. Sage University papers Quantitative applications in the social sciences, Vol 84. 1992;77. https://psycnet.apa.org/fulltext/1992-97020-000.pdf.
Haynes W. Tukey’s Test. In: Dubitzky W, Wolkenhauer O, Cho K-H, Yokota H, editors. Encyclopedia of systems biology. New York: Springer New York; 2013. p. 2303–4.
Denton JA, Joubert DA, Goundar AA, Gilles JRL. International shipments of Wolbachia-infected mosquito eggs: towards the scaling-up of world mosquito program operations. Rev Sci Tech. 2022;41:91–9.
Zheng M-L, Zhang D-J, Damiens DD, Lees RS, Gilles JRL. Standard operating procedures for standardized mass rearing of the dengue and chikungunya vectors Aedes aegypti and Aedes albopictus (Diptera: Culicidae)—II—egg storage and hatching. Parasit Vectors. 2015;8:348.
Juliano SA, O’Meara GF, Morrill JR, Cutwa MM. Desiccation and thermal tolerance of eggs and the coexistence of competing mosquitoes. Oecologia. 2002;130:458–69.
Zhang D, Zhang M, Wu Y, Gilles JRL, Yamada H, Wu Z, et al. Establishment of a medium-scale mosquito facility: Optimization of the larval mass-rearing unit for Aedes albopictus (Diptera: Culicidae). Parasites and Vectors. 2017;10:569.
Lau M-J, Ross PA, Endersby-Harshman NM, Hoffmann AA. Impacts of low temperatures on Wolbachia (Rickettsiales: Rickettsiaceae)-infected Aedes aegypti (Diptera: Culicidae). J Med Entomol. 2020. https://doi.org/10.1093/jme/tjaa074.
Farnesi LC, Martins AJ, Valle D, Rezende GL. Embryonic development of Aedes aegypti (Diptera: Culicidae): influence of different constant temperatures. Mem Inst Oswaldo Cruz. 2009;104:124–6.
Gunasekaran K, Sadanandane C, Panneer D, Kumar A, Rahi M, Dinesh S, et al. Sensitivity of wMel and wAlbB Wolbachia infections in Aedes aegypti Puducherry (Indian) strains to heat stress during larval development. Parasit Vectors. 2022;15:221.
Ross PA, Ritchie SA, Axford JK, Hoffmann AA. Loss of cytoplasmic incompatibility in Wolbachia-infected Aedes aegypti under field conditions. PLoS Negl Trop Dis. 2019;13:e0007357.
Ross PA, Wiwatanaratanabutr I, Axford JK, White VL, Endersby-Harshman NM, Hoffmann AA. Wolbachia infections in Aedes aegypti Differ Markedly in their response to cyclical heat stress. PLoS Pathog. 2017;13:e1006006.
We gratefully acknowledge Peter Kyrylos of the World Mosquito Program for developing and providing the wAlbB141 qPCR assay and providing the primer sequences.
This research was supported by funding from the Australian Government Research Training Program (RTP) Scholarship.
Ethical approval and consent to participate
To produce eggs used in these experiments, mosquito colonies were blood fed on adult human volunteers in accordance with Monash University Human Research Ethics permit number 27690, or provided human blood obtained from the Australian Red Cross, under Supply Agreement 22-05VI-04 with the World Mosquito Program Ltd.
Consent for publication
All authors read and approved the final manuscript.
The authors declare no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Additional file 1: Table S1.
qPCR primer and probe sequences. Fig. S1. Repeat experiment of data in Fig. 1: Encapsulating eggs for storage at 22 °C does not exacerbate impacts on egg viability, adult emergence or Wolbachia density compared to controls. Fig. S2. Repeat experiment of data in Fig. 2. Encapsulating eggs for storage at 18 °C does not improve egg fitness compared to 22 °C.
Additional file 2:
Dataset S1: Statistical outputs.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
About this article
Cite this article
Allman, M.J., Lin, YH., Joubert, D.A. et al. Enhancing the scalability of Wolbachia-based vector-borne disease management: time and temperature limits for storage and transport of Wolbachia-infected Aedes aegypti eggs for field releases. Parasites Vectors 16, 108 (2023). https://doi.org/10.1186/s13071-023-05724-1
- Aedes aegypti
- Insect releases
- Egg release