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Research Article

Indoor-Breeding of Aedes albopictus in Northern Peninsular Malaysia and Its Potential Epidemiological Implications

  • Hamady Dieng mail,

    hamachan1@yahoo.com

    Affiliation: School of Biological Sciences, Universiti Sains Malaysia, Penang, Malaysia

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  • Rahman G. M. Saifur,

    Affiliation: School of Biological Sciences, Universiti Sains Malaysia, Penang, Malaysia

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  • Ahmad Abu Hassan,

    Affiliation: School of Biological Sciences, Universiti Sains Malaysia, Penang, Malaysia

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  • M. R. Che Salmah,

    Affiliation: School of Biological Sciences, Universiti Sains Malaysia, Penang, Malaysia

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  • Michael Boots,

    Affiliation: Department of Animal and Plant Sciences, University of Sheffield, Sheffield, United Kingdom

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  • Tomomitsu Satho,

    Affiliation: Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka, Japan

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  • Zairi Jaal,

    Affiliation: School of Biological Sciences, Universiti Sains Malaysia, Penang, Malaysia

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  • Sazaly AbuBakar

    Affiliation: Department of Medical Microbiology, University of Malaya, Kuala Lumpur, Malaysia

    X
  • Published: July 27, 2010
  • DOI: 10.1371/journal.pone.0011790

Abstract

Background

The mosquito Ae. albopictus is usually adapted to the peri-domestic environment and typically breeds outdoors. However, we observed its larvae in most containers within homes in northern peninsular Malaysia. To anticipate the epidemiological implications of this indoor-breeding, we assessed some fitness traits affecting vectorial capacity during colonization process. Specifically, we examined whether Ae. albopictus exhibits increased survival, gonotrophic activity and fecundity due to the potential increase in blood feeding opportunities.

Methodology/Principal Findings

In a series of experiments involving outdoors and indoors breeding populations, we found that Ae. albopictus lives longer in the indoor environment. We also observed increased nighttime biting activity and lifetime fecundity in indoor/domestic adapted females, although they were similar to recently colonized females in body size.

Conclusion/Significance

Taken together these data suggest that accommodation of Ae. albopictus to indoor/domestic environment may increase its lifespan, blood feeding success, nuisance and thus vectorial capacity (both in terms of increased vector-host contacts and vector population density). These changes in the breeding behavior of Ae. albopictus, a potential vector of several human pathogens including dengue viruses, require special attention.

Introduction

The acquisition of indoor-breeding behavior can potentially increase the biting activity of mosquito vectors that opportunistically bite humans outdoors during the day. This may therefore have important implications to disease transmission. However, despite this epidemiological importance, there have been no previous studies of this issue in dengue vectors.

Dengue viruses infect up to 50 million people each year, causing more than 20,000 deaths [1], [2]. These flaviviruses are mainly transmitted by Aedes aegypti, but also Ae. albopictus [3]. Native to the Oriental Region and some islands in the Indian Ocean [3], Ae. albopictus has become well-established in the Western hemisphere where it is the second main vector of dengue [4]. It is also an important vector of yellow fever and various types of encephalitis virus, as well as a competent vector of at least 23 other arboviruses under laboratory conditions [5], [6], [7]. It is well adapted to peridomestic environments with its larvae breeding in artificial containers and adults aggressively biting humans and different animals during the day [3].

Efforts to control dengue have mainly involved insecticide spraying programs, but this strategy has proven ineffectual [8]. While a vaccine is currently under development, without immediate prospects for success, vector control remains the only viable method to prevent dengue transmission [9], [10], [11], [12]. Improved knowledge regarding egg-laying behavior is relevant because it underpins the primary surveillance method, i.e., ovitraping [13], [14]. However, the most commonly used ovitrap, the CDC gravid trap, is not appropriate for capturing Ae. albopictus [15], [16].

Blood feeding in mosquitoes represents phenotypic expression of reproductive investment as it is the acquisition of resources specifically for reproduction [17]. Reproductive output represents the energy allocated to egg production and oviposition that could otherwise be allocated to maintenance of somatic function, and the act of oviposition is associated with a risk to survival [18]. There has been a great deal of research regarding the variations of reproductive investment and outcome. Overall, increases in both number and size of blood meals result in increased individual egg mass and number of eggs [18]. Clearly, in the field an increased frequency of blood uptake will tend to require host – mosquito contact and expose hosts to a greater risk of disease transmission.

Ae. albopictus has been occasionally incriminated in dengue epidemics in Asian countries [19], [20], [21]. The first report of a dengue epidemic in Malaysia was on Penang Island, and dengue fever with hemorrhagic manifestations was also reported from this Island [22]. These epidemics were accompanied by increased populations of Ae. albopictus. Increased invasiveness [23] and increased population densities of [24] have been recently been reported in the Malaysian peninsula. Ae. albopictus females was commonly observed developing in indoor/domestic sites throughout Penang Island during our 2009 entomological survey at Balik Pulau (Sungai Pinang and Sg. Burung), Gelugor, Jelutong, Air Itam (Kampung Relau), and other sites. This shift from outside to inside human dwellings is likely to increase the opportunities for females to obtain blood meals. This indoor immature breeding has raised the question of whether this mosquito may exhibit increased gonotrophic activity (GA) in response to potentially greater blood meal sources.

Given the potentially crucial interactions between reproduction, blood feeding, and vectorial capacity, we examined the GA and fecundity of Ae. albopictus using females derived from wild mosquitoes collected from outdoor containers in Kampung Teluk Tempoyak and Balik Pulau, Malaysia, with their daughters after they had spent five generations under laboratory conditions.

Materials and Methods

Occurrence of Ae. albopictus larvae in indoor containers

A survey of Aedes was carried out from February to June 2009 in Penang province, Malaysia, located between latitudes 5°8′N and 5°35′N and longitudes 100°8′E and 100°32′E [25], covering nine residential areas (townships and villages) on Penang Island (Figure 1). The survey zone is surrounded by hills on the northwest with the rest of the zone opening up into low-lying areas occupied by human populations. Immature mosquito stages were collected in household containers.

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Figure 1. Map of Malaysia and locations of the Aedes survey areas on the Island of Penang.

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Statement on ethic issues

This study was carried out in accordance with the principles expressed in the Declaration of Helsinki. The study was approved by the Biological Research Ethics Committee at University Sains Malaysia (Projects # 07-05-16-MG1-GMB15, # 1001/PBIOLOGI/842004 and Fellowship grant # RU:1001/229/29301/CIPS/AUPE001).

Colonization of wild Ae. albopictus

The Aedes mosquitoes used in this study were derived from wild pupae collected from outdoor containers in the survey zone. A colony was established in the insectarium at the School of Biological Sciences, Universiti Sains Malaysia, Penang. Larvae were reared routinely on a diet of dried yeast. Adults had access to 10% glucose solution, and females were blood-fed at two days old on restrained mice. Eggs were processed, dried, and stored under laboratory conditions (temperature 29°C±3°C, relative humidity 75%±10% and photoperiod 13:10 h, 1h dusk provided by an electrical lighting from a 60 and 25-watt incandescent bulbs.

Bioassays

Bioassays were carried out using females derived from wild mosquitoes (FWMs) and females derived from FWMs after five generations (d5FWMs) under laboratory conditions. In all bioassays, disposable plastic cups (9×11.5 cm) filled with 30 mL of tap water and lined with filter papers (#1, Whatman®; Whatman International, Maidstone, UK) as an oviposition substrate, were used to provide females with sites for egg deposition. The filter papers were folded into a double-chambered cone and placed such that the mosquitoes could lay their eggs inside or outside the cone. A sugar meal source was supplied from cotton wads soaked in 10% glucose solution placed at the top of the cages. A rearing cage containing 100 males was used as a mating source for experimental females. Male cage was supplied with individual males from field-collected pupae.

Experiments

The first experiment was performed to determine the oviposition responses of wild Ae. albopictus in the laboratory in relation to blood feeding time. Fifty two-day-old FWMs were blood-fed at 09:00 am on restrained mice. Similarly, a group of fifty two-days old FWMs were offered blood meals on the same day, but at 17:00. In both cases, females were provided with 10% glucose solution for two days. After they became gravid, they were placed individually in oviposition cages holding oviposition cups. Egg deposition was checked two days later at five time points during the day starting at 08:00 (09:00, 11:30, 17:00, 20:30, and 23:30). At each time point, cups with eggs were removed, eggs were counted, and new cups were placed in the cages.

The second experiment was performed to examine the nocturnal biting activity of wild Ae. albopictus. Ten newly emerged FWMs were maintained on 10% glucose solution for 3 to 4 days, and thereafter starved for a brief period (12 h). The mosquitoes were then placed in cages containing a restrained mouse and observed continuously. Ten females of Ae. aegypti were treated as described above and used as a control group regarding its endophagic behavior [26] and nighttime biting activity [27], [28]. Engorgement was checked at eight time points during the night (20:00, 21:00, 22:00, 23:00, 24:00, 01:00, 02:00 and 03:00), and the feeding times were recorded for each female of both species. The experiment was run under laboratory photoperiod conditions.

The third experiment involved determining the effects of Ae. albopictus domestication time on the number of gonotrophic cycles (GCs) it can perform in its lifetime. A total of one hundred fully blood-fed FWMs and d5FWMs were used in this experiment. Each gravid female was placed singly in an oviposition cup holding a 10% glucose solution source. Egg deposition was confirmed by examining filter papers under a dissecting microscope at the end of the oviposition period. The same females were again given access to blood re-feeding, and provided with oviposition cups, which was repeated until their death. In addition to the possibility that the generation rank affects the number of times eggs are produced, we also examined whether there was any effect of generation rank on lifetime fecundity. Eggs oviposited in each GC of both FWMs and d5FWMs were counted by examining filter papers under a dissecting microscope. Body size was measured in all females used in the fecundity experiment due to the possibility that this parameter affects the number of eggs produced.

Data collection and analysis

Immature Aedes (larvae and pupae) collected from indoor containers were identified morphologically with reference to appropriate taxonomic keys [29]. In all bioassays, females in the experimental group were allowed to feed on blood for one day, to digest it for two days, and to lay eggs for 24 h. Blood feeding was scored based on distention of the abdomen. We recorded the number of GCs for each experimental female (FWMs and d5FWMs). Following previous studies [30], we considered a GC as the time between ingestion of blood and commencement of oviposition. In each GC, the number of eggs deposited was used as the score of fecundity, thus adopting others [31]. Eggs were counted under a dissecting microscope (Meiji EMZ; Meiji Techno Co. Ltd, Tokyo, Japan). We considered percentage female survival as the number of individuals that laid eggs divided by the initial number of individuals tested in each GC trial. As an indicator of body size, the length of one wing per female from the axillary incision to the apical margin excluding the fringe scales was measured under a light microscope (Olympus CX41; Olympus, Tokyo, Japan) as described by others [32]. The rate of oviposition was determined as the number of females that oviposited divided by the initial number of females tested. The differences in the number of GCs, fecundity, and body size between FWMs and d5FWMs were examined by analysis of variance using the statistical software package Systat v.11 (Systat Software, Inc., Richmond, CA, USA) [33]. In the fecundity experiment, Tukey's test was applied to separated means. In all statistical analyses, P<0.05 was taken to indicate statistical significance. Survival rates were compared based on differences in percentages.

Results

Survey Aedes inside houses

Indoor containers with immature Aedes stages consisted of drums, flower vases, ant-guards, buckets, cement tanks, empty paint cans, wells, hare pots, underground floor, and sinks (Table 1, Figure 2). The majority of mosquitoes collected were Ae. albopictus, but Ae. aegypti was also found. Between February and May, the sizes of immature stage populations remained high and constant in the five residential areas of the study. In some cases, larval instars of Ae. albopictus were persistent until June, suggesting that oviposition events did occur continuously (Table 1). The heterogeneity of larval developmental stages and their persistence suggested that Ae. albopictus has established populations within peoples' houses.

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Figure 2. Indoor breeding of Ae. albopictus.

Empty paint containers (A) and a cement tank (B) in residences in the township of Gelugor, Penang, Malaysia contained high numbers of larvae. Red arrows indicate the containers and tank.

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Table 1. Characteristics of Ae. albopictus collections from indoor/domestic containers from homes throughout Penang Island in 2009.

doi:10.1371/journal.pone.0011790.t001

Oviposition activity of wild Ae. albopictus

Figure 3 shows the oviposition responses of FWMs of Ae. albopictus given blood meals at two different times of the day. In both cases, oviposition activity was low to absent during the night. Ae. albopictus exhibited two distinct peaks of oviposition activity for all feeding times: a narrow peak in the morning and a wider peak during the afternoon. Females that took a blood meal in the early morning (09:00, Figure 3A) showed a narrow peak of oviposition at 11:00 two days later. Those that fed on blood in the late afternoon (17:00, Figure 3B) showed a weak and narrow peak around noon (13:00) and a larger wider peak in the afternoon (from 15:00 to 18:00).

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Figure 3. Oviposition responses of FWMs Ae. albopictus offered blood meals at 09:00 (A) and 17:00 (B) of the day.

The arrow indicates the 1h dusk period.

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Patterns of nocturnal blood feeding

The hourly nighttime biting activities of Ae. albopictus and Ae. aegypti were examined between 20:00 and 03.00. Ae. albopictus showed a constant pattern of biting activity at all time points examined, with higher percentage fed and longer feeding time in comparison to Ae. aegypti (Table 2).

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Table 2. Nocturnal biting frequencies of FWMs of Ae. albopictus and Ae. aegypti.

doi:10.1371/journal.pone.0011790.t002

Survival and gonotrophic activity period

The survival rate decreased when progressing from first to last GC for both FWMs and d5FWMs, although the pattern of the decrease varied with female generation. In FWMs, more than 50% of the females examined died at the third GC. Among the only two FWMs that survived and achieved a seventh GC, none showed subsequent survival. In d5FWMs, more than 50% of females survived and achieved a fourth GC. More than 20% of d5FWMs survived and reproduced a seventh time. Among these, six individuals reproduced an eleventh time and one individual reproduced a fourteenth time. Overall, survival decreased with time, but this was more pronounced among FWMs (Figure 4).

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Figure 4. Percentages of surviving FWMs and d5FWMs of Ae. albopictus and their gonotrophic activity periods.

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Patterns of gonotrophic activity

The number of GCs achieved by Ae. albopictus varied significantly with generation (F = 30.06, df = 1, P<0.001). The mean number of cycles for FWMs was 2.0±0.10 (range: 1–7), while that in d5FWMs was 4.0±0.10 (range: 1–14). Therefore, it is clear that females from d5FWMs had a greater number of GCs (Figure 5).

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Figure 5. Numbers of gonotrophic cycles (mean ± SD) of FWMs and d5FWMs of Ae. albopictus.

Bars labeled with the same letter are not significantly different (P<0.05).

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Fecundity

Figures 6A and 6B show the egg deposition patterns in FWMs and d5FWMs of Ae. albopictus, respectively. The overall egg production did not differ significantly between females from the two generations (Table 3). Pairwise comparisons using the Tukey test revealed no significant difference in egg production during the first (F = 0.015, df = 1, P = 0.905), second (F = 0.041, df = 1, P = 0.842), third (F = 0.195, df = 1, P = 0.663), fourth (F = 0.169, df = 1, P = 0.684), or fifth (F = 0.001, df = 1, P = 0.975) GC.

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Figure 6. Numbers of eggs (mean ± SE) laid by FWMs (A) d5FWMs (B) of Ae. albopictus.

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Table 3. Statistical analysis by ANOVA of the variations in fecundity and body size between FWMs and d5FWMs of Ae. albopictus.

doi:10.1371/journal.pone.0011790.t003

In FWMs, the level of egg production was maximal in the first GC (63.25±8.00). The number of eggs laid was not significantly different between the different GCs achieved (F = 0.707, df = 4, P = 0.591). There were more eggs deposited by FWMs at the first than at the fifth GC, but the difference in mean egg deposition between the first and last GCs was not significant (F = 2.001, df = 1, P = 0.171).

In d5FWMs, the peak of egg production was recorded at the third GC (65.77±8.60), and egg production varied significantly between GCs in these mosquitoes (Table 1). From the third GC, egg production tended to decrease as the rank of GC progressed. The mean number of eggs deposited by d5FWMs was significantly lower at the ninth than at the first GC (F = 7.444, df = 1, P = 0.012).

Body size

The mean wing lengths were 2.46±0.04 and 2.51±0.04 mm in FWMs and d5FWMs, respectively. Although d5FWMs tended to be slightly larger than FWMs, there was no significant difference in mean wing length between the two groups (Table 1, Figure 7).

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Figure 7. Wing length (mean ± SE) of FWMs and d5FWMs of Ae. albopictus.

Bars labeled with the same letter are not significantly different (P<0.05).

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Discussion

The most important observation in the present survey was that Ae. albopictus breeds inside peoples' houses in many parts of Penang Island, Malaysia. Larval populations were heterogeneous and most developmental stages were present over the five-month period of the survey. As this mosquito typically shows outdoor breeding behavior [34], [3], [35], the persistence of its larval and pupal stages in indoor containers over a long period suggests that Ae. albopictus is being adapted to the indoor environment. A similar observation was recently reported in neighboring Thailand [36], but there have been no studies regarding the epidemiological significance of these observations. Here, we examined the gonotrophic performance of wild Ae. albopictus with regard to the crucial interactions between biting activity and vectorial capacity [37].

As the present study was begun with a wild population, it was first necessary to determine whether they could oviposit under laboratory conditions. Oviposition trials indicated that FWMs can lay eggs in the laboratory and that the patterns of egg–laying were associated with blood feeding time. The findings of the present study were consistent with the natural oviposition behavior of this mosquito [38], [39], [40], [41], therefore allowing the long-term experiments required for this study.

We found a major effect of level of adaptation to indoor/domestic environment on the number of GCs in the laboratory. d5FWMs showed a much higher number of GCs than their FWMs counterparts. In mosquitoes, the nutritional history of the parents is influential in determining the fecundity of daughters [42]. This study showed that daughters from parents reared in a food-limited environment produced more eggs than those from parents reared under high food conditions. They suggested that this increased fecundity arose to compensate for expected decreased longevity in stressing environments. Here, females derived from wild mosquitoes (FWMs) and females derived from these FWMs after five generations achieved 7 and 14 GCs, respectively. d5FWMs survival rate was higher than that of FWMs mosquitoes. Although the mechanisms underlying these observations are not yet clear, they could be the result of at least two processes. First, the highly nutritious food conditions in the laboratory could lengthen the mosquito lifespan, and thus increase the probability that it reproduces. Second, the shift from a complex wild environment to a simple environment, such as that in the laboratory, may result in physiological changes that increase the allocation of energy to functions other than egg production, thereby increasing the probability of survival. Longer living females may take more blood meals and reproduce more simply because of the increased availability of meals. Epidemiologically, an increased number of GCs will tend to increase the probability of disease occurrence. With an extended period of GA, females have a higher probability of picking up and transmitting a disease agent as well as an increased lifespan as blood provides an alternative energy source for survival [43]. The increased period of reproduction of the d5FWMs will also lead to a higher mosquito population density, which is also likely to be associated with increased occurrence of disease. Population levels expressed as larval [44], [45], [46], pupal [47], and adult indices [48] are often associated with levels of risk for dengue transmission. Dengue outbreaks occurred in Singapore [49] but not in Brazil [50] when the national overall percentage of houses positive for larvae (HI) was below 1%. In Puerto Rico, the incidence of dengue increased one month after larval density peaked [51], whereas in Brazil, dengue seroincidence increased when the HI was above 3% [52]. The present study was prompted by the permanent presence of biting adults and immature stages of Ae. albopictus within residences in Teluk Tempoyok and Balik Pulau located in northern peninsular Malaysia and a lack of information regarding the epidemiological implications. Although we did not determine whether these populations were infected with dengue viruses, the focal point of this study was that the presence of larvae strongly suggests that at least a GC has been achieved. Thus, infection would occur if the virus was present. Note that this species is competent for many viruses [6], [7], but has only occasionally been incriminated in minor dengue epidemics all the world, e.g., in Hawai in 2001–2002 [53].

In FWMs and d5FWMs, the number of eggs oviposited tended to decrease as GC rank progressed, but this effect was most marked in the second group. As in most anautogenous mosquitoes, the production of eggs in Ae. albopictus requires the ingestion of blood [54], [55]. The female converts about 20% of the ingested blood meal into egg constituents [56]. Several groups have reported that the degree to which eggs are produced depends largely on meal size [32], [57], [58]. Indeed, a female that ingests a large blood meal size will tend to invest more in egg production than a female with a small blood meal. In the present study, we have used females adapted to laboratory conditions and females derived from wild pupae. It is often assumed that wild insects are subject to much harsher environmental conditions that trigger small body size and that they have lower levels of energetic reserves than laboratory strains. Clearly, in the laboratory, the highly nutritious larval diet will tend to produce large bodied mosquitoes capable of blood feeding for long periods due to little or no host defense behavior from anesthetized hosts [32]. Here, FWMs and d5FWMs were similar in body size and had the same feeding time, so differential egg production due to differences in meal size is unlikely. These discrepancies may be explained by differential utilization of blood. Adult mosquitoes feed on blood for immediate energy needs [57], [59], but in some cases, they use blood as an alternative energy source for survival [43]. There is evidence that colonization alters reproductive traits [60], in particular offspring fecundity [42]. Therefore, it is tempting to suggest that the accommodation of the wild strain to the laboratory environment has occurred in addition to physiological changes relative to blood use. It is possible that the reduced level of egg production observed with increasing generations represented a compensation for better acclimation to the laboratory environment. Presumably, protein use by d5FWMs offsets the costs associated with egg production and facilitates population maintenance in this environment. In support of this suggestion, it has been reported that Ae. albopictus may use some blood proteins for maintenance [61].

The pattern of egg production was similar between females of both types, but lifetime fecundity was greater in d5FWMs. This difference was the result of their greater survival. Females with a long lifespan may take more blood meals and reproduce more simply because of the increased availability of meals. Easy access to blood sources in any host – vector interaction can be of crucial epidemiological significance because increased frequency of host-biting may favor the spread of infectious disease present. The presence of Ae. albopictus inside houses, that was observed in many residences throughout Penang Island, appears to facilitate human blood feeding. In this context, biting activity during both the day and night may increase mosquito – human contact. In addition, dengue viruses can be transmitted sexually from male to female Ae. albopictus [62]. Therefore, the increased fecundity of d5FWMs may contribute to virus propagation.

This study emphasizes the invasive properties of Ae. albopictus and importantly shows the acquisition of an indoor breeding behavior by this major vector of dengue viruses. This behavioral change may lead to increased vectorial capacity. Several parameters come into play when the vectorial capacity of a mosquito for an arbovirus is considered [63]. In particular, host availability and population density are very influential to the competence of a vector. Indeed the more individual vectors are present, the more likely they will be able to transmit a pathogen. Adaption to the indoor/domestic environment, which triggers increased human-vector contacts, will presumably stimulate feeding behavior. In the neighboring Thailand, 100% of field-collected populations of this mosquito fed on humans [64]. Theoretically, such an affinity for feeding on human blood in a wild context will tend to increase inside residences. Ae. albopictus exhibited a high biting activity, showing a shorter feeding time and a greater blood feeding success when compared to Ae. aegypt at night. This period is the time when residents exhibit low defensive responses to mosquito feeding. In our study, the epidemiological implications were also approached from gonotrophic performance and survival because biting activity is a pivotal factor in the continuation of both pathogen transmission and vector generation [65]. Furthermore, the mosquito individuals that are most easily infected and most likely to incubate a pathogen to an infectious level are those that live long enough [66]. Clearly, adaption to the indoor/domestic environment may produce more competent vectors, since it favors long life and increased lifetime reproductive output.

There is one factor related to our approach that should be discussed in light to keep away from misinterpretations of the obtained results. We have used mice as the blood host. This can appear as a drawback of our method, because the attitudes of a restrained mouse differ from those exhibited by a human under mosquito attacks. We assumed that during sleep, a human may exhibit little defensive responses as a retrained mouse. Experimental mosquitoes were derived from wild pupae collected in a dengue epidemic context. To avoid any infection risks, as no data on dengue infection of Ae. albopictus was available, we used mouse as animal model. Although, there are differences in the fitness ramifications for the host species that a mosquito takes blood from, evidence also exist that mice under some conditions mimic well human responses to dengue infection [67], [68].

Acknowledgments

We thank the team of the Vector Control Unit of the School of Biological Sciences, University Sains Malaysia, the populations of the townships and villages where the survey was carried out. We also thank Steven Neeve of John Innes Centre, Norwich, UK, for his comments on an earlier version of this manuscript. The authors are grateful to the students and drivers of the School of Biological Sciences for their assistance in the field survey.

Author Contributions

Conceived and designed the experiments: HD RGMS. Performed the experiments: HD RGMS. Analyzed the data: HD RGMS AAH MCS TS MB ZJ SA. Contributed reagents/materials/analysis tools: HD. Wrote the paper: HD RGMS AAH MCS TS MB ZJ SA.

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