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BackgroundRadiation induced sterility is the basis of the Sterile Insect Technique, by which a target insect pest population is suppressed by releasing artificially reared sterile males of the pest species in overflooding numbers over a target site. In order for the sterile males to be of high biological quality, effective standard irradiation protocols are required. Following studies investigating the effects of mosquito pupae irradiation in waterversusin air, there is a need to investigate the oxy-regulatory behavior of mosquito pupae in water to better understand the consequences of irradiation in hypoxic versus normoxic conditions.MethodsPupae ofAedes aegypti,Ae. albopictus, andAnopheles arabiensiswere submerged in water inside air-tight 2 ml glass vials at a density of 100 pupae/ml and the dissolved oxygen (DO) levels in the water were measured and plotted over time. In addition, male pupae ofAe. aegypti(aged 40–44 h),Ae. albopictus(aged 40–44 h) andAn. arabiensis(aged 20–24 h) were irradiated in a gammacell220 at increasing doses in either hypoxic (water with 2content) or normoxic (in air) conditions. The males were then mated to virgin females and resulting eggs were checked for induced sterility.ResultsAll three species depleted the water of DO to levels under 0.5% within 30 minutes, withAn. arabiensisconsuming oxygen the fastest at under 10 minutes. Following irradiation, the protective effect of hypoxia was observed across species and doses (P An. arabiensis.ConclusionsThe consumption of dissolved oxygen by pupae submerged in water was significantly different between species, indicating that their oxy-regulatory capacity seems to have possibly evolved according to their preferred breeding site characteristics. This needs to be considered when sterilizing male mosquitoes at pupal stage in water. Depending on species, their DO consumption rates and their density, irradiation doses needed to achieve full sterility may vary significantly. Further assessments are required to ascertain optimal conditions in terms of ambient atmosphere during pupal irradiation to produce competitive sterile males, and temperature and density dependent effects are expected.

Innovations in mosquito mass-rearing techniques are essential in the quest to develop SIT (sterile insect technique) methods to fight mosquito vectors of disease. This study reports modifications to the Food and Agriculture Organisation/International Atomic Energy Agency (FAO/IAEA) mass-rearing cage (MRC) for mosquitoes to support the behaviour of adult Anopheles arabiensis Patton (Diptera: Culicidae) and to maximize egg production. The effects of an improved sugar-feeding device, and the addition of resting sites and a black cloth shroud to create an artificial horizon (visual contrast of light vs. dark at the edge) were assessed for their effect on adult longevity and egg production. Egg production of adults resulting from larvae reared in individual free-standing trays vs. those reared in the same trays in the FAO/IAEA larval rearing rack was also compared. Finally, the effect of blood feeding and frequency of egg collection from the MRC on average egg production per batch was investigated. Overall, the modifications to the MRC enhanced adult longevity, and the improved cage prototype allowed the collection of more eggs overall from a cohort of adults than was possible using the original and previous cage prototypes. These stepwise improvements are important for the development of economical and logistically efficient mass-rearing systems for the malaria vector An. arabiensis.

Background Anopheles arabiensis is one of the major malaria vectors that put millions of people in endemic countries at risk. Mass-rearing of this mosquito is crucial for strategies that use sterile insect technique to suppress vector populations. The sterile insect technique (SIT) package for this mosquito species is being developed by the Insect Pest Control Subprogramme of the Joint FAO/IAEA Division of Nuclear Techniques in Food and Agriculture. To improve mass-rearing outcomes for An. arabiensis, the question of whether the egg production by females would be affected by the size of the adult holding cages, the source of the blood meal and the total number of pupae that could be loaded into the cages was addressed and finally the impact of adding additional pupae to the cage daily to maintain adult numbers on egg productivity assessed. Methods Mass production cages of two different volumes, two different sources of blood meal (bovine and porcine) and two different population densities (cages originally loaded with either 15,000 or 20,000 pupae) were tested and evaluated on the basis of eggs produced/cage or per female. Males and females pupae with a ratio of 1:1 were added to the cages at day 1 and 2 of pupation. The emerging adults had constant access to 5% sugar solution and blood fed via the Hemotek membrane feeding system. Eggs were collected either twice a week or daily. A generalized linear model was used to identify factors which gave significantly higher egg production. Results Neither cage volume nor blood meal source affected egg production per cage or per female. However, increasing population density to 20,000 pupae had a negative effect on eggs produced per cage and per female. Although high density negatively impacted egg production, adding 1000 daily additional pupae compensating for daily mortality resulted in a substantial increase in egg production. Moreover, in all tests the first and the third egg batches collected were significantly higher than others eggs batches. With the equipment and protocols described here and routinely used at the Insect Pest Control Laboratory (IPCL), it was possible to produce up to 120,000 eggs/cage/day. Conclusion These results demonstrated that 15,000 is the optimal number of pupae to be loaded into the Anopheles Mass production cages. Under this condition, an average of 40 eggs per female was obtained for five gonotrophic cycles. However, an improvement in egg production can be achieved by daily addition, to the original 15,000 pupae, of one thousand pupae a day. Interestingly, feeding females with bovine or porcine blood using both large and small versions of the mass production cage did not affect egg productivity.