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Establishment of a medium-scale mosquito facility: tests on mass production cages for Aedes albopictus (Diptera: Culicidae)
Parasites & Vectorsvolume 11, Article number: 189 (2018)
Mass egg production is an important component of Aedes albopictus mosquito control programs, such as the sterile insect technique and incompatible insect technique, which requires the releases of large number of sterile males. Developing standard operating procedures and optimized cages for adult maintenance of Ae. albopictus can improve the mass rearing efficiency.
Three different sex ratios of females to males with a total number of 4,000 mosquitoes were tested by evaluating the insemination rate, egg production (total number of eggs per cage), female fecundity and egg hatch rate in small cage (30 × 30 × 30 cm). Blood meals with adenosine triphosphate (ATP, 0.05 g/ml), cage structures (Big cage A: 90 × 30 × 30 cm; Big cage B: 90 × 30 × 50 cm or 90 × 50 × 30 cm) and rearing densities (12,000, 16,000 and 20,000 mosquitoes, corresponding to 0.9 cm2/mosquito, 0.675 cm2/mosquito and 0.54 cm2/mosquito, respectively) were also tested and evaluated on the basis of egg production, female fecundity and egg hatch rate. An adult rearing unit holding 15 of Big cage A with optimal egg production was designed to produce 10 million eggs per rearing cycle in a 1.8 m2 space.
Female to male ratios at 3:1 in small cages resulted in higher egg production but did not affect insemination rate, female fecundity and egg hatch rate. A concentration of 0.05 g/ml of ATP added to blood meals improved the blood-feeding frequency and thus increased the overall egg production per cage. Cage structures affected the egg production per cage, but not egg hatch rate. A medium rearing density at 0.675 cm2/mosquito (16,000 mosquitoes) resulted in higher egg production compared to both low and high densities. An adult rearing unit for Ae. albopictus on the basis of Big cage A has been developed with the capacity of producing 10 million eggs within 15 days.
Our results have indicated that the adult rearing methods and adult maintenance unit are recommended for Ae. albopictus mass rearing in support of the establishment of a medium-sized mosquito factory.
As a major vector for arbovirus diseases such as dengue, chikungunya and Zika, Aedes albopictus is responsible for a huge burden to public health worldwide . The current control strategies relying on the reduction of breeding sites and insecticide application are unsustainable and can become an economic and environmental burden on both public administration and human health [2, 3]. Vector control strategies such as the sterile insect technique (SIT), the incompatible insect technique (IIT), or a combination of both techniques, are currently under development for mosquito control . Both the SIT and IIT are species-specific and environmental friendly approaches for vector control and are based on the induction of sterility into the natural population by releasing a large number of irradiation-sterilized or Wolbachia-incompatible males . Aedes albopictus has been considered to be a suitable candidate for large suppression programs , and the feasibility of such a suppression program has been successfully tested in past field trials using either SIT  or IIT . As stated by the WHO in March 2017, the combined SIT/IIT technology has potential for long-term control of Ae. albopictus and Aedes aegypti mosquitoes .
As any large-scale suppression program relies on continuous releases of a large number of competitive sterile males, efficient and effective approaches for mass rearing the target insects is essential. In a mosquito factory, mass rearing can be divided into two independent parts: rearing for male releases and rearing for colony egg production . The latter should not only provide a sufficient number of eggs for male releases but also for colony maintenance. For Ae. albopictus mass rearing, 90% of eggs may be used to produce males for releases and 10% for colony maintenance. Many studies have been performed to develop standardized rearing methods for Ae. albopictus at the egg [11, 12] or larval stage [13,14,15,16,17]. However, few studies have been performed to develop optimal rearing methods for Ae. albopictus at the adult stage, especially under mosquito mass rearing conditions. In addition, selecting a suitable cage structure for rearing adults is also a key for mass egg production. A prototype of a mass production cage (MPC), based on the cage design used for Medflies in Guatemala, which has been modified to allow blood-feeding, sugar-feeding and oviposition for simplified collection of the eggs, has been tested for both Ae. albopictus  and Anopheles arabiensis . The MPC cage was designed to reduce handling and the opening of the cages during operation such as for blood-feeding and egg collection, but the egg production of Ae. albopictus per cage was found to be quite low (average 16 eggs per female per blood meal). The cage structure seems to be the main factor resulting in low egg production; for example, the position of the two blood-feeders were positioned to one side of the cage which may cause a reduced blood-feeding rate as the mosquitoes on the other side may not have been attracted by the blood source. In addition to cage structure, mosquito density is another important factor that will influence the egg production. The number of adults per cm2 of vertical resting surface in a cage, defined as density-resting surface (DRS), is generally reported to be an important parameter for mating, feeding and longevity and a DRS value of 1.8 (1.8 cm2/adult) is considered suitable for mosquitoes maintenance in the laboratory . Mamai et al.  found decreased An. arabiensis egg production when overloading the cage with pupae (20,000 pupae, DRS ≈ 2.0 cm2/adult) compared to cages with optimized density (15,000 pupae). However, for Aedes mosquitoes, it is reported that they can be maintained at a relative high density in laboratory conditions. A DRS value of 0.9 is used for Ae. aegypti mass production in Brazil . Thus, it is important to develop standardized operation methods and cages for adult maintenance in any mosquito factory.
In this study, three sex ratios of females to males in small cages were evaluated to find an optimal sex ratio for adult maintenance. In addition, blood meals supplemented with ATP were tested for its impacts on egg production, female fecundity and egg hatch rate. Moreover, three different structures of large adult rearing cages were assessed by evaluating the egg production and egg hatch rate, with the aim to find a suitable cage structure and size for adult mass rearing. Lastly, egg production under three different mosquito densities was compared to find an optimal density for adult mass rearing. Based on these results, we discuss the design of an adult rearing unit for Ae. albopictus adults in terms of mass egg production in support of establishing a medium-sized mosquito factory.
Mosquito strain and rearing conditions
The triple Wolbachia-infected Ae. albopictus (HC) strain was used in this study . The HC line has been maintained in the mass rearing factory in Guangzhou, China for three years and experiments were conducted in a climate-controlled room at 27 ± 1 °C, 80 ± 10% RH, and a photoperiod of 12:12 h (L:D). The HC strain was reared as previously described .
Effects of adults sex ratios on insemination rate, egg production, female fecundity and egg hatch rate
Three different sex ratios of females to males with a total number of 4000 mosquitoes were tested in small stainless steel cages (L × W × H = 30 × 30 × 30 cm, volume = 27,000 cm3, Density-Resting Surface (DRS) = 3600 cm2, Fig. 1a): 1:1 (2000:2000), 2:1 (2667:1333) and 3:1 (3000:1000) ratios. Pupae were sexed and counted individually and then transferred into each cage for eclosion. Cotton soaked in 10% sugar solution was placed on top of the cages and provided to adults ad libitum. Thirty females (three to four days old) were randomly selected from each ratio to check the insemination status under the microscope before blood-feeding . The blood meals were prepared on an aluminum plate covered with Parafilm  and were provided to female adults 5–6 days post-eclosion. Oviposition cups were placed into each cage 48 h after blood-feeding. Eggs were collected for 48 h and allowed to mature for 5–6 days. The second blood meal was provided to females after the first egg collection and eggs were collected as described above. The schedule of the experimental rearing procedure for adult Ae. albopictus is shown in Additional file 1: Figure S1. Eggs were brushed by soft brush and weighed, and then hatched in hatch solution (1000 ml filtered water containing 0.12 g yeast powder) for 24 h. Egg hatch rate was assessed under the stereoscope as previously described [21, 23, 24]. Five replicates were conducted for each sex ratio.
Effects of ATP on egg production, female fecundity and egg hatch rate
To assess the effects of blood meals supplemented with adenosine triphosphate (ATP, Sigma-Aldrich, St. Louis, USA) on egg production, individual female fecundity and egg hatch rate, a 0.05 g/ml concentration of ATP was added to the blood meals. The small cages holding 4000 mosquitoes with the 3:1 sex ratio (females:males) were tested for effects of ATP on the reproductive parameters of females. Blood meals without ATP were used as controls. Three replicates were performed for both treatment and control cages.
To determine the reason how ATP may enhance egg production, the female blood-feeding rate, volume, fecundity and egg hatch rate were additionally assessed: fifty fasting female adults (5–6 days old, not engorged with a recent sugar meal, assessed by personal observation) were selected, anaesthetized and measured with an analytical balance. Then females were placed into an empty cage (30 × 30 × 30 cm) for recovery. After 3–4 h, blood meals with ATP were provided to the females. Blood meals without ATP were used as negative control. After 1 h, all of the females in each cage were collected and the number of engorged females was recorded. females Three replicates were performed for both treatment and control cages. Thirty randomly selected engorged were anaesthetized and individually weighed using an analytical balance and the other thirty engorged females were placed into individual oviposition tubes with moist paper for egg collection. The individual female fecundity and fertility were assessed as described above.
Effects of cage structure on egg production, female fecundity and egg hatch rate
Three different structures of large stainless steel cages were used: Big cage A (Fig. 1b), Big cage B-1 (Fig. 1c), and Big cage B-2 (Fig. 1d). Cage specifications of the three cages tested are shown in Table 1. The Big cage B-1 and Big cage B-2 were the same cage design but set up in different orientation (vertically for B-1 and horizontally for B-2) to test if the inversion of height and width of the cage would affect the egg production.
The adult maintenance ratio of females to males was 3:1 for all of the following experiments. As described above, each small cage contained 3000 female and 1000 male mosquitoes, corresponding to 6.75 cm3/mosquito (calculated by volume) and 0.9 cm2/mosquito (calculated by DRS). To attain the same rearing density indices for both Big cages A and B, 9000 female and 3000 male mosquitoes, or 15,000 female and 5000 male mosquitoes were placed in Big cages A and B, respectively (volume = 6.75 cm3/mosquito and DRS = 0.9 cm2/mosquito). The rearing schedule and data recorded were the same as described above.
Effects of adult rearing density on egg production, female fecundity and egg hatch rate
Big cages A with a 120° “v” angle stainless steel base, which was used for holding the pupae for eclosion and subsequently for draining out any dead pupae after emergence, was used in this study (Fig. 2). Two pieces of (15 × 60 cm) nets were added to the inside of the cage to increase the DRS to 10,800 cm2 as described above. Three adult rearing densities at a maintenance ratio of 3:1 (females:males were tested: 12,000 mosquitoes (corresponding to DRS = 0.9 cm2/mosquito, low rearing density), 16,000 mosquitoes (DRS = 0.675 cm2/mosquito, medium rearing density) and 20,000 mosquitoes (DRS = 0.54 cm2/mosquito, high rearing density). Blood meals with ATP were provided to females in each cage. The rearing schedule and data recorded were the same as described above.
Data collected and statistical analysis
Females were considered to be successfully inseminated if one or more spermathecae was filled with sperm. The insemination rate was recorded as the number of females successfully inseminated divided by the total number of females tested. The egg production per cage was calculated as the sum of the eggs produced from the first and second gonotrophic cycles. The relationship between the number of eggs and their weight for Ae. albopictus HC strain was: 150,000 = 1 g eggs, which was close to figures described in our previous study . The female fecundity per cage was calculated as the egg production per cage divided by the number of females placed inside each cage, where we ignored the non-blood-fed and dead females during rearing. Individual female fecundity was calculated from the engorged females. The blood-feeding volume per female was calculated as the weight of engorged females minus the mean weight of fasting females, and then divided by the density of blood with ATP.
Data analysis was conducted using IBM SPSS 20.0 and Graph Pad Prism 6.0 software. To compare the insemination rates, egg hatch rates and blood-feeding rates, the values were first arcsin transformed. ANOVA analysis and Tukey post-hoc test were used to compare the egg production, female fecundity and egg hatch rates. Student t-test or Mann Whitney U-test were used to compare the egg production, blood-feeding rates, blood volume, individual female fecundity and egg hatch rates between blood meals with and without ATP. The results were presented as (mean ± SEM) in this study.
Effects of sex ratio on insemination rate, egg production, female fecundity and egg hatch rate
Under the same rearing density (DRS), the higher the number of female mosquitoes maintained in one cage, the more eggs will be produced, which is beneficial for mass rearing efficiency. Thus it is recommended to stock the cage with a higher ratio of females to males in each cage, but without affecting the insemination rate. In this study, we first tested effects of different sex ratios of females to males on insemination rates (1:1, 2:1 and 3:1) and we observed the three tested ratios resulted in similar insemination rates in the small cage, with more than 96% females that had been successfully inseminated by males (Table 2). As we expected, higher total egg production per cage was observed correlating with the increased number of females introduced into cages (F(2, 12) = 38.3, P < 0.0001). For example, an average of 37.9% higher egg production was achieved at a 3:1 ratio when compared to a 1:1 ratio (Table 2). However, as the number of female mosquitoes maintained in the cages were different, the individual female fecundity (total egg production divided by the number of females introduced into the cage) showed no significant difference between the three tested ratios (F(2, 12) = 2.72, P = 0.1063). Similarly, we observed no significant difference on egg hatch rate between the three tested ratios (F(2, 12) = 0.11, P = 0.8988). These results indicate that a female biased ratio (of up to 3:1) in adult cages will improve egg production without negative impacts on female insemination rate, individual female fecundity and egg hatch rate (Table 2).
Effects of ATP on egg production, female fecundity and egg hatch rate
To improve egg production per cage, we added ATP to stimulate female blood-feeding. As shown in Table 3, an average of 30.0% higher egg production and female fecundity were both observed in small cages where females were provided with 2 blood meals supplemented with ATP (egg production: t = 3.37, df = 4, P = 0.028; female fecundity: t = 3.37, df = 4, P = 0.028), which indicated that an average of 15% higher egg production could be achieved with one blood-feeding with ATP. There was no significant difference between hatch rates in eggs produced by females that were fed on blood meals with and without ATP (t = 0.77, df = 4, P = 0.487).
To further investigate the causative reason for the ATP-associated increase in egg production, we repeated the above experiment with one blood-feeding and measured blood-feeding rate, blood-feeding volume, individual female fecundity and egg hatch rate. As shown in Fig. 3a, a significant difference was observed on blood-feeding rates of females when providing blood meals with ATP (74.5%) and without ATP (56.0%) (t = 3.23, df = 4, P = 0.030): there was an approximately 18.5% increase in the feeding rate on blood with ATP compared to without ATP. The improved blood-feeding rate correlated with the above-mentioned improvement in egg production. However, no significant differences were observed in blood-feeding volume (U = 375.0, P = 0.2701, Fig. 3b), individual female fecundity (U = 389.5, P = 0.9967, Fig. 3c) and egg hatch rate (U = 323.0, P = 0.2751, Fig. 3d) between blood meals with ATP and without ATP. These results indicate that ATP improves female feeding rate and thus increases egg production per cage.
Effects of cage structure on egg production, female fecundity and egg hatch rate
Compared to smaller cages for mosquito maintenance, the larger ones can reduce human handling and improve mass rearing efficiency. In this study we set up three different big cage structures (Fig. 1b-d) to test the effects of cage shape on egg production, female fecundity and egg hatch rate, aiming to find a suitable cage structure for mosquito maintenance. Among the three tested cages, Big cage A, Big cage B-1 and Big cage B-2, the latter cage design resulted in the highest egg production (egg production: F(2, 6) = 29.3, P = 0.0008) while Big cage A resulted in the highest individual female fecundity (F(2, 6) = 139.0, P < 0.0001) (Table 4). No significant difference was observed on egg hatch rate among these three cage structures (F(2, 6) = 1.68, P = 0.2633) (Table 4).
Interestingly, mosquitoes in Big cage B-1 and B-2 were controlled under the same rearing methods and density (DRS/mosquito and volume/mosquito), however, when Big cage B-1 was placed horizontally (referred to as Big cage B-2), an average of 36.5% higher egg production and female fecundity was observed (Table 4). In this study the egg production of Big cage B-2 was 19.3% higher than that of Big cage A, and this improvement in egg production was attributed to 4,500 more female mosquitoes which were placed in the former cage. However, when calculated into individual female fecundity, an average of 39.6% higher female fecundity was obtained in Big cage A compared to Big cage B-2 (Table 4). Taken together, these results indicate that cage structure (height and width) can influence egg production or individual female fecundity, but not egg hatch rate.
Effects of adult rearing density on egg production, female fecundity and egg hatch rate
Based on our results described above, we selected Big cage A as the potential cage structure for mosquito adult maintenance as it induced the highest level of individual female fecundity (Table 4). With the rearing methods (sex ratio and two blood-feedings with ATP) developed previously, we tested the effects of rearing density on egg production, female fecundity and egg hatch rate by using Big cage A. Three rearing densities were tested with Big cage A: 12,000 mosquitoes, 16,000 mosquitoes and 20,000 mosquitoes, corresponding to 0.9 cm2/mosquito (low density), 0.675 cm2/mosquito (medium density) and 0.54 cm2/mosquito (high density). As shown in Table 5, the medium density resulted in the highest egg production compared to both low and high densities (F(2, 7) = 8.18, P = 0.0147). An average of 20.8% higher egg production was observed with the medium density compared to low density as there were 4000 more mosquitoes placed in the medium density cage, however, there was a significant difference in female fecundity between medium and low densities (Table 5). Female fecundity decreased under the high rearing density compared to low and medium densities (F(2, 7) = 49.3, P < 0.0001) (Table 5). These three tested rearing densities had no significant impacts on egg hatch rate (F(2, 7) = 3.58, P = 0.0852) (Table 5). Our results show that medium rearing density with Big cage A is recommended for adult maintenance as higher egg production is achieved but without affecting female fecundity and egg hatch rate.
With an average production of approximately 0.7 million Ae. albopictus eggs at a density of 16,000 mosquitoes for Big cage A, an adult rearing unit was designed for holding 15 Big cages A with the capacity of producing 10 million eggs per rearing cycle, while only occupying a 1.8 m2 space (Fig. 4). A comparison between the adult rearing in a Small cage unit (holding 12 small cages) and a Big cage A unit for producing 10 million eggs is shown in Additional file 2: Table S1. The advantage of the Big cage A unit compared to the Small cage unit is the minimized number of cages required (15 vs 60), indicating less labor (stocking cages with pupae and subsequent removal of pupal emergence cups from cages, sugar-feeding, blood-feeding, egg collection and cage cleaning, etc.) needed by using the Big cage A unit when mass rearing Ae. albopictus in a factory setting.
In this study, we assessed the rearing method and cage structure for Ae. albopictus adults in support of the establishment of a medium-scale mosquito facility for the SIT/IIT strategy. Our results indicate that the optimal adult colony maintenance sex ratio lies at 3:1 of females to males. Blood meals supplemented with ATP can improve the egg production as ATP can increase the blood-feeding rate of the females. Cage structure and rearing density can also affect the egg production and overall female fecundity. Big cage A is suitable for adult mass rearing with an achievable egg production of more than 0.7 million eggs per two blood-feedings per rearing cycle. An adult rearing unit for Ae. albopictus based on 15 Big cage A has also been developed with the capacity of producing 10 million eggs per rearing cycle as determined by this study.
Aedes albopictus male mosquitoes can mate with several females in their lifetime, while it has been suggested that most of the females usually mate only one time [25,26,27]. Thus, higher egg production per cage can be achieved by increasing the number of females while maintaining the insemination rate. More than 96% insemination rate is observed in the three tested adult maintenance ratios 1:1, 2:1 and 3:1 (Table 2). Considering that a higher egg production is achieved at a 3:1 ratio of females to males compared to the other two ratios (Table 2), this maintenance ratio is recommended for Ae. albopictus adult mass rearing. Previous studies have reported that a 3:1 ratio of females to males is also suitable for Ae. ageypti mass rearing . For Ae. albopictus, males are always seeking to copulate with females, thus a higher ratio of males (e.g. females to males at 1:1) will exacerbate harassment of females, resulting in decreased blood-feeding rates, fecundity and survivorship of females (personal observation). Even though a maintenance ratio at 3:1 may carry the risk of reducing the diversity of the cage population after prolonged colonization, this risk can be minimized by periodically outcrossing the colony populations with wild type populations. Bellini et al.  has reported that a very minimal reduction in genetic variability is observed in an Italian Ae. albopictus laboratory strain by performing regular outcrosses.
Female mosquitoes require blood meals before laying eggs and they can produce eggs several times after each blood meal throughout their lifetime. Female fecundity and egg hatch rates will decrease as females age . Previous studies have reported that female fecundity and egg hatch rate are highest in the first two gonotrophic cycles and then decrease after the second gonotrophic cycle . In this study we only provide two blood meals to females with the aim of acquiring the maximum egg production within a short rearing period. Egg production efficiency in mosquito factories should be enhanced by reducing the number of blood meals and applied rearing cycles of a cage. The egg production after a third blood meal has been assessed and only 20% of the total egg production is achieved in the third gonotrophic cycle regardless of adult rearing densities (Additional file 3: Figure S2). Compared to a two-time blood-feeding schedule, feeding three times will increase the adult rearing cycle duration, human labor and will reduce the utilization rate of a cage and egg quality. Thus, two blood-feedings per rearing cycle are recommended for Ae. albopictus egg producing colonies in mosquito factories as almost 80% of possible egg production would be achieved while minimizing costs.
Artificial blood-feeding systems should be developed in any mosquito mass rearing facility. The uses of natural and artificial membranes, such as collagen sausage skins, bovine intestines (cleaned) and Parafilm, have been tested for several mosquito species [10, 18, 19, 30,31,32]. The blood temperature is an important parameter for feeding responses of females . Blood-feeding systems with electric temperature control have also been developed for Anopheles mosquito mass rearing cages [18, 19]. The Aedes MPC with two blood-feeding slots into which collagen sausage skins filled with blood can be inserted in vertical positions, has been shown to improve the feeding rate of females compared to blood sources placed on top of the cage [18, 34]. However, the blood-feeding method for the Aedes MPC requires the use of a larger volume of blood compared to the traditional artificial feedings methods . The average blood volume ingested by an individual female is approximately 0.7 μl, regardless of whether the blood meals contain ATP or not (Fig. 3). Hence, the volume of blood required for normal cage structures (cubes or cuboids) by using aluminum plate feeding systems is less than that required for the Aedes MPC, which can reduce the cost of blood considerably in a mosquito facility. The quality of blood will also affect the blood-feeding rate of females, especially for females of the Aedes genus, most of which do not feed on defrosted blood as it is likely that hemolysis happens after freezing. However, it has been reported that only the blood plasma plays a role in the processes of egg formation  and further studies should be performed on the effects of defrosted plasma on the blood-feeding of females.
To improve the blood-feeding response of females, attractants such as honey, glucose and ATP have been added to the blood meals [36, 37]. Our results have also indicated that blood supplemented with ATP can increase the blood-feeding rate of females, which is similar to previous studies [33, 37]. Higher feeding frequency can lead to higher egg production per cage, thus ATP is recommended to be added to blood meals to improve the egg production for Ae. albopictus. However, due to the high costs of ATP (laboratory use level), it is impossible to use it in a mosquito factory as this will increase the total costs of mass rearing. Thus finding other low cost supplements to improve the blood-feeding frequency are important for mosquito factories. Additional research is recommended to focus on the development of artificial blood meals, which has been proposed for both Ae. albopictus and Ae. aegypti [35, 38]. Compared to the use of animal blood, which should undergo testing for microbial contamination before feeding, artificial blood meals would be suitable for mosquito rearing as it might be safer in terms of quality control of both mosquitoes and insectary staff. This, however, requires more research before possible implementation [33, 38].
Compared to small adult rearing cages (e.g. 30 × 30 × 30 cm), large cages can not only hold more mosquitoes leading to higher egg production, but can also reduce requirements for rearing space, manual labor and mosquito escapes when in operation. However, cage size and design should not negatively affect female fecundity and egg hatch rate [18, 19]. In this study, we found that the cage structure had no impacts on egg hatch rate (Table 4), but affected the egg production and female fecundity (Table 4). It is interesting to note that higher egg production was achieved in Big cage B-2 compared to Big cage B-1 even though the same number of mosquitoes was used (Table 4). This difference may be due to the structure of the cage, as the lower height (30 cm) of the cage results in a higher blood-feeding rate compared to the taller height (50 cm). Thus, a good balance should be determined between the height and width of the cage aiming at finding an optimal cage structure for mosquito adult colony maintenance. The average fecundity of Aedes females has been found to range between 42–88 eggs per female in the first gonotrophic cycle under laboratory conditions, however, the female fecundity ranges between 30–74 eggs per female regardless of cage structure and rearing density after two blood-feedings (Tables 2–5) in this study, which is lower than reported in a previous study . Even though female fecundity can be affected by many factors, such as the quality of blood, blood volume ingested by the female and female insemination status, in this study, the female fecundity is calculated as the total number of eggs divided by the number of females added to the cage, where the blood-feeding frequency and fatalities of females are neglected, resulting in a lower female fecundity in the mosquito mass rearing factory than in laboratory conditions. Carvalho et al.  has also reported that an average of 48 eggs per Ae. aegypti individual female can be acquired within two weeks (twice blood-feedings per week) in a mosquito factory. However, the description of egg production or female fecundity within one rearing cycle in each cage is much clearer for mass production. Too high rearing densities for mosquitoes in cages will decrease the egg production and female fecundity . Thus, a balance should be determined between the rearing density and egg production/female fecundity for each adult rearing cage.
Our study has indicated that the sex ratio, rearing density and cage structure are important parameters for mass egg production under factory conditions. High levels of egg production can be achieved using Big cage A with an introduction of 16,000 mosquitoes at 3:1 ratio of females to males within 15 days with two blood meals supplemented with ATP. Based on the cage structure and rearing schedule developed in this study, we have designed an adult rearing unit for Ae. albopictus with the capacity of producing 10 million eggs. Results from this study can significantly contribute to mosquito mass rearing in support of the establishment of a medium-sized mosquito facility for any genetic control strategy requiring the mass production of the target species.
Triple Wolbachia-infected Aedes albopictus
Incompatible insect technique
Mass production cage
Standard error of mean
Sterile insect technique
World Health Organization
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The authors would like to thank Xiaohua Wang, Jixin Zhang, Chunping Chen, Yun Peng and Guangmin Yan for rearing the mosquito samples for this experiment.
This study was supported by the National Natural Science Foundation of China (No. 31372263), the National Key R & D Program of China (No. 2016YFC1200500), the National Institutes of Health/National Institute of Allergy and Infectious Disease (No. R01AI080597), the Guangdong Innovative Research Team Program (No. 2011S009), the Scientific and Technological Leading Talents of Guangzhou Development District (No. 2016-2414), the 111 Project (No. B12003) and the Coordinated Research Project of International Atomic Energy Agency (D44002 (No. 19115) & D42016 (No. 18816)).
Availability of data and materials
All data are disclosed in the text or in tables in the article.
Ethics approval and consent to participate
Research on mosquitoes (Ae. albopictus) does not require a specific permit in Guangzhou, China. All of the experiments were performed from April to August 2016 based on standard operating procedures in the Sun Yat-sen University - Michigan State University Joint Center of Vector Control for Tropical Diseases, Guangzhou, China. The blood used for routine blood-feeding of mosquitoes was bought from Weilai Biotechnology Co., Ltd, Guangzhou, China during routine slaughtering of sheep or goats in a nationally authorized abattoir according to the highest possible standards and strictly following Chinese laws and regulations.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Figure S1. Design of experimental rearing procedures for adult Aedes albopictus. (TIFF 139 kb)
Table S1. Comparison between rearing modules using small cages and Big cage A for the production of 10 million eggs of Aedes albopictus. (DOCX 13 kb)
Figure S2. Percentage of egg production at different egg collection points with different adult rearing densities using Big cage A. (TIFF 159 kb)