Daily oviposition patterns of the African malaria mosquito Anopheles gambiae Giles (Diptera: Culicidae) on different types of aqueous substrates
© Sumba et al. 2004
Received: 31 August 2004
Accepted: 13 December 2004
Published: 13 December 2004
Anopheles gambiae Giles is the most important vector of human malaria in sub-Saharan Africa. Knowledge of the factors that influence its daily oviposition pattern is crucial if field interventions targeting gravid females are to be successful. This laboratory study investigated the effect of oviposition substrate and time of blood feeding on daily oviposition patterns of An. gambiae mosquitoes.
Greenhouse-reared gravid and hypergravid (delayed oviposition onset) An. gambiae sensu stricto and wild-caught An. gambiae sensu lato were exposed to three types of substrates in choice and no-choice cage bioassays: water from a predominantly anopheline colonised ground pool (anopheline habitat water), swamp water mainly colonised by culicine larvae (culicine habitat water) and distilled water. The daily oviposition pattern and the number of eggs oviposited on each substrate during the entire egg-laying period were determined. The results were subjected to analysis of variance using the General Linear Model (GLM) procedure.
The main oviposition time for greenhouse-reared An. gambiae s.s. was between 19:00 and 20:00 hrs, approximately one hour after sunset. Wild-caught gravid An. gambiae s.l. displayed two distinct peak oviposition times between 19:00 and 20:00 hrs and between 22:00 and 23:00 hrs, respectively. During these times, both greenhouse-reared and wild-caught mosquitoes significantly (P < 0.05) preferred anopheline habitat water to the culicine one. Peak oviposition activity was not delayed when the mosquitoes were exposed to the less preferred oviposition substrate (culicine habitat water). However, culicine water influenced negatively (P < 0.05) not only the number of eggs oviposited by the mosquitoes during peak oviposition time but also the overall number of gravid mosquitoes that laid their eggs on it. The differences in mosquito feeding times did not affect the daily oviposition patterns displayed.
This study shows that the peak oviposition time of An. gambiae s.l. may be regulated by the light-dark cycle rather than oviposition habitat characteristics or feeding times. However, the number of eggs laid by the female mosquito during the peak oviposition time is affected by the suitability of the habitat.
Although An. gambiae s.l. mosquitoes are nocturnal in their feeding and oviposition activities, the probable time of oviposition is determined by many factors including ambient temperature and light conditions, and the time the mosquito obtains its blood meal [1, 2]. In addition, we hypothesised that the availability of a suitable larval habitat would also affect the mosquito's predisposition to oviposit. Anopheles gambiae is discriminative in its oviposition behaviour . Its preferred larval habitats are fresh water pools that are generally small, transient and sunlit, devoid of vegetation and often turbid [4–6]. Oviposition tendency might therefore be related to location and availability of such sites. In this study, we compared the daily oviposition patterns and the number of eggs laid by An. gambiae s.s. and wild-caught An. gambiae s.l. on aqueous collections from habitats colonised by anopheline or culicine larvae respectively, and distilled water.
Anopheles gambiae s.s. (MBITA strain; colonised since February 2001) mosquitoes from Mbita Point, western Kenya, were reared in a greenhouse  in water obtained from a natural ground pool colonised by anopheline larvae. Average temperatures and relative humidities were 31°C, 52 % during the day and 24°C, 72% at night. The mosquitoes were exposed to the natural photoperiod, 00° 25' South of the equator. A data logger (HOBO™) was used to record ambient conditions. Larvae were fed on Tetramin® fish food. Adult mosquitoes were kept in standard mosquito rearing cages (30 × 30 × 30 cm) made of a metal wire frame with a solid metal base and covered with white nylon mosquito netting. They were offered a 6% glucose solution soaked in white paper towel wicks. Three-to-four-day-old females were offered two blood meals, one each day at 18.00 hrs, from the forearm of a human volunteer. The unfed mosquitoes were removed from the cage after each blood meal. Fully engorged females were left in the cages until they were gravid or hypergravid. Gravid mosquitoes are those that were provided with oviposition substrates on the third evening after their first blood meal. Hypergravid mosquitoes were provided with oviposition substrates one day later. Wild, indoor-resting, blood fed anopheline mosquitoes were collected during early morning hours from houses in Lwanda village of Suba district, western Kenya, by means of aspirators. They were immediately transported to the greenhouse, sorted out to obtain An. gambiae s.l. females and provided with 6% glucose solution. They were used in periodicity experiments on the second evening after collection, as described below.
Turbid water taken from a natural ground pool colonised by anopheline larvae (anopheline habitat water), yellow-brown water from a reed swamp colonised by culicine larvae (culicine habitat water), and distilled water were used as oviposition substrates. Presence of larvae was determined by making five random dips using a 350 ml standard dipper.
Oviposition substrate preference
The experiments were carried out under greenhouse conditions in 25 cm cubic Plexi®-glass cages, each fitted with a white netting top and a side sleeve opening. To determine oviposition substrate preference, individual gravid An. gambiae s.s. mosquitoes were exposed to 20 ml of each of the above substrates in a three-choice bioassay (n = 55). The substrates were held in black plastic oviposition cups (2 cm depth, 4 cm diameter), placed at equal distances from one another. Individual mosquitoes were released into the cages at about 17.00 hours and left overnight. The following morning, eggs oviposited on each substrate were counted under a dissection microscope. In subsequent replications, oviposition cups containing substrates were rotated such that they occupied different positions every time in the oviposition cages.
Daily oviposition patterns in a no-choice bioassay
Daily oviposition patterns of An. gambiae female mosquitoes on test oviposition substrates, which were offered individually, were determined as follows. Groups of five greenhouse-reared gravid and hypergravid An. gambiae s.s. females were held in separate cages into which anopheline or culicine habitat water or distilled water were introduced. Each mosquito and substrate combination treatment was replicated four times on each experimental day and the experiment repeated on three different days. At the end of the experiment, the mosquitoes that had laid in each group were identified by dissecting each under a dissection microscope and examining their ovaries for the presence of either retained eggs, coiled or uncoiled tracheolar skeins .
Daily oviposition patterns in a choice bioassay
Groups of five gravid and hypergravid An. gambiae s.s. (ten cages of each) were placed in separate cages and allowed to choose from the three types of oviposition substrates. Similarly, groups of five wild-caught An. gambiae s.l. mosquitoes were offered a choice of the three substrates and their daily oviposition patterns monitored. The experiment was replicated twice on each experimental day and repeated on five different days with new mosquito batches. Individual species within the wild-caught An. gambiae mosquitoes that had laid were identified using polymerase chain reaction (PCR) .
Effect of the time of blood feeding on daily oviposition patterns
The effect of the time of blood feeding of An. gambiae s.s. on its daily oviposition pattern was determined as follows. Four groups of three-to-four-day-old females were given two blood meals, one each day at 06.00 hrs, 18.00 hrs, 22.00 hrs or at 00.00 hrs, respectively. Unfed females were removed from the cages after every blood meal. Gravid mosquitoes were then provided with oviposition cups on the third day at 06.00 hrs and their daily oviposition patterns monitored.
In all experiments, the oviposition cups were removed from the cages after every hourly interval, for 24 hours, starting at 18.00 hrs and replaced with freshly prepared ones. The eggs laid on each substrate were counted under a dissection microscope. To minimise disturbance that might have been due to exposure to white light, red light was used at night while replacing the oviposition cups.
Since oviposition trends for gravid and hypergravid females were similar, data for the two were pooled for analysis. The differences in the number of eggs laid on different oviposition substrates were compared statistically by analysis of variance using the General Linear Model (GLM) procedure. The effect of oviposition substrate on the number of either gravid or hypergravid mosquitoes contributing to the total egg number was similarly compared. Means were separated by the least significant difference (LSD) procedure. Data were subjected to log10 (n+1) transformation to normalise their distribution. All the analyses were carried out using the SPSS® statistical package, version 11.0.
Oviposition substrate preference
The mean number ± standard error (39.4 ± 6.1) of eggs oviposited on anopheline habitat water was significantly higher than that on the culicine (16.1 ± 4.6; P = 0.01) or distilled water (23.7 ± 5.3; P = 0.02).
Daily oviposition patterns
The number of mosquitoes (Mean ± SE1) contributing to the total eggs laid in each mosquito/ substrate combination.
Mean ± SE1
Gravid/ Distilled water
3.3 ± 0.4bc
Gravid/ Anopheline habitat water
3.5 ± 0.4ab
Gravid/ Culicine habitat water
2.5 ± 0.4c
Hypergravid/ Distilled water
3.8 ± 0.4ab
Hypergravid/ Anopheline habitat water
4.4 ± 0.3a
Hypergravid/ Culicine habitat water
3.6 ± 0.4ab
In the present study, the daily oviposition patterns of greenhouse-reared An. gambiae s.s. were well defined with oviposition peak times between 19:00 and 20:00 hrs, regardless of the type of oviposition substrate used. Haddow and Ssenkubuge  obtained comparable results using An. gambiae s.s. (KISUMU strain, western Kenya): about half of the eggs were laid during the first three hours of the night (18:00 – 21:00 hrs). On the other hand, oviposition by wild-caught mosquitoes from the coast of Kenya used by McCrae , comprising mostly An. gambiae s.s., peaked much later at night in the hour following midnight. This suggests differences in oviposition patterns between our strain and that of Haddow and Ssenkubuge representing Lake Victoria populations, on one hand, and that used by McCrae representing the Kenyan coastal population, on the other. Studies of oviposition patterns of populations from different parts of eastern Africa may help shed further light on the question.
In the current study, wild-caught An. gambiae s.l., which were shown to contain a mixture of An. gambiae s.s. and An. arabiensis gravid females, displayed two distinct oviposition peak times in the first half of the night. The two peaks may be attributed to the two sibling species and suggests that this may also be an important factor in the diversity of oviposition patterns in the field in different geographical locations.
The differences in the mosquito feeding times did not affect the timing of peak oviposition, although females that obtained their blood meals later in the night displayed a somewhat broader oviposition peak interval. Peak oviposition consistently occurred approximately one hour after sunset; therefore, a fall in light intensity might be one of the important cues that trigger oviposition in female An. gambiae that are physiologically ready to oviposit. On the other hand, McCrae  observed that the time of oviposition was a function of the time of blood feeding and not a result of an endogenous rhythm. Given the uniform oviposition peak times of mosquitoes that were fed at different times, daily oviposition among An. gambiae s.l. may also be endogenously regulated. Detailed experiments to demonstrate a free-running oviposition periodicity would clarify this. There was no difference in oviposition patterns displayed by gravid and hypergravid mosquitoes. Since significantly more gravid females exposed to the preferred substrate oviposited their eggs than those exposed to the less preferred one, gravid females that fail to find a suitable oviposition site on the night they are due may retain their eggs and oviposit early the next night as hypergravids.
Gravid mosquitoes are generally attracted to water; however, the decision to oviposit may depend on additional olfactory signals  and /or contact stimuli received when the insects land on the water surface . In this study and others , the gravid mosquitoes showed marked preference for the water taken from a site naturally inhabited by anopheline larval populations. This suggests 'memory' of similar information gathered by contact with the oviposition water at emergence or during larval period as in the case of Culex quinquefasciatus . In this regard, gravid females might associate specific site characteristics from conspecific and heterospecific immatures, soil microbial activity , colour and turbidity of the oviposition substrate  with their suitability for sustaining progeny development.
This study shows that the peak oviposition time of An. gambiae s.l. may be regulated by the light-dark cycle rather than oviposition habitat characteristics or feeding times. However, the number of eggs laid during the peak oviposition time is affected by the suitability of the habitat. This suggests that there is a relationship between the investment made by the female mosquito with respect to the number of eggs laid in a given habitat and the potential fitness of the progeny. Females may use a series of site characteristics, including olfactory cues, to locate and oviposit at such sites. Our results on oviposition patterns differ from those reported on a coastal population, and suggest that a lot more work needs to be done to elucidate differences in this regard between different populations.
We thank, E. Obudho, J. Wauna and the staff of the malaria vector programme at ICIPE-Mbita for their support, P. Seda, J. Mutunga, J. Kongere and N. Gitonga for assistance with mosquito identification, and L. Gouagna, D. Impoinvil and D. Chadee for their comments on an earlier version of this manuscript. This research was supported by funds from the National Institutes of Health (NIH) grant U19 AI45511 and the ABC Fogarty through grant number D43TWØ1142. LS wishes to acknowledge the PhD scholarship from the German Academic Exchange Service (DAAD) through the African Regional Post-graduate Programme in Insect Science (ARPPIS). Approval for feeding the mosquitoes on human subjects was sought and obtained from the Kenya National Ethical Review Board, protocol number KEMRI/RES/7/3/1.
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