Next Article in Journal
Ultrastructure of Antennal Sensilla in Adults of Dioryctria rubella Hampson (Lepidoptera: Pyralidae)
Previous Article in Journal
Comparative Mitogenomic Analysis of Two Longhorn Beetles (Coleoptera: Cerambycidae: Lamiinae) with Preliminary Investigation into Phylogenetic Relationships of Tribes of Lamiinae
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Insects
Volume 12
Issue 9
10.3390/insects12090822
insects-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Effects of Selection to Diflubenzuron and Bacillus thuringiensis Var. Israelensis on the Overwintering Successes of Aedes albopictus (Diptera: Culicidae)

by
Charalampos S. Ioannou
1,2,
Christos Hadjichristodoulou
1,
Varvara A. Mouchtouri
1 and
Nikos T. Papadopoulos
2,*
1
Laboratory of Hygiene & Epidemiology, Faculty of Medicine, School of Health Science, University of Thessaly, 41222 Larissa, Greece
2
Laboratory of Entomology & Agricultural Zoology, Department of Agriculture Crop. Production and Rural Environment, School of Agricultural Sciences, University of Thessaly, 38446 Volos, Greece
*
Author to whom correspondence should be addressed.
Insects 2021, 12(9), 822; https://doi.org/10.3390/insects12090822
Submission received: 9 August 2021 / Revised: 5 September 2021 / Accepted: 8 September 2021 / Published: 13 September 2021
(This article belongs to the Section Insect Pest and Vector Management)
Browse Figure
Versions Notes

Abstract

:

Simple Summary

Aedes albopictus is an invasive mosquito species that is well established in many parts of Europe and poses high risks of autochthonous transmission of chikungunya and dengue viruses. The high dependency on commonly used larvicides such as Diflubenzuron (DFB) and Bacillus thuringiensis var. israelensis (Bti) to control its populations raise concerns for resistance development. Although studies addressing the potential for development of resistance in Ae. albopictus against these two important larvicides are essential for planning control programmes, no such data are available. Here, by imposing an increasing selective pressure to DFB and Bti over nine successive generations on a recently laboratory established Ae. albopictus population we determined the subsequent resistance levels and corresponding overwintering success of the selected populations relative to control (colonies that received no selection). Our findings revealed a moderate and a minor increase on the resistance levels following selection with DFB and Bti, respectively. No significant differences were observed regarding the overwintering successes between the two selected populations and the control, which suggests that the selected individuals retain an equal ability to persist in the wild on an annual base.

Abstract

Aedes albopictus is an invasive mosquito species responsible for local transmission of chikungunya and dengue viruses in Europe. In the absence of available treatments, insecticides-based control remains one of the most important viable strategies to prevent emerging problems. Diflubenzuron (DFB) and Bacillus thuringiensis var. israelensis (Bti) are among the most commonly used larvicides for Ae. albopictus control with consequent concerns for the potential development of resistance. Studies on the resistance emergence in Ae. albopictus and its persistence in the wild to both DFB and Bti are essential for the efficient and sustainable planning of the control programmes. In this context, larvae from a recently laboratory established population were subjected to increasing selective pressure for nine successive generations using both DFB and Bti. The resistance levels and the overwintering success of the selected populations relative to control (colonies that received no selection) were determined. Results revealed an 8.5- and 1.6-fold increase on the resistance levels following selection with DFB and Bti, respectively. The selection process to both larvicides had no apparent impacts on the overwintering capability relative to control, suggesting the successful persistence of the selected individuals in the wild on an annual base.

1. Introduction

Aedes albopictus Skuse (Diptera: Culicidae) also known as the Asian tiger mosquito is classified as one of the 100 most invasive species in the world [1]. During the last 50–60 years, largely facilitated by human activities and climate change, it has extended its geographic distribution from its native range in tropical and subtropical Southeast Asia to all over the world [2]. Successful invasion and colonization of the northern temperate areas have been attributed to the remarkable ecological and physiological plasticity of this species [3]. In temperate regions, Ae. albopictus overwinters at the egg stage containing pharate first instar larvae in facultative diapause that occurs when maternal females experience short day photoperiod as pupae and adults [4]. In Europe, Ae. albopictus was recorded for the first time in Albania in 1979 [5], however awareness only spread in the early 1990s after the discovery of established populations in Italy [6]. Recently, it has displayed a wide distribution in both the Mediterranean basin and central Europe having established itself in at least 19 countries [7]. Due to its aggressive biting behavior, Ae. albopictus causes important nuisance problems that negatively affect the welfare levels while they may also act as an important discouraging factor for the tourism industry [8]. Moreover, as a competent vector of more than 32 arboviruses, including chikungunya and dengue, Ae. albopictus poses a major threat for public health [9]. In Europe, its presence has been associated with autochthonous transmission of dengue in Croatia (2010), France (2010, 2013–2015), and Spain (2014–2016) and of chikungunya in Italy (2007 and 2017) and southeastern France (2010 and 2014) [10]. Furthermore, as a consequence of its highly opportunistic feeding behavior on different animal species, Ae. albopictus has the potential to act as a bridge-vector of zoonotic pathogens from animal-to-animal and from animal-to-human [11].
As there no available drug treatments, Ae. albopictus-borne diseases such as dengue and chikungunya are managed mainly through vector control [12]. In recent years, new control approaches have been proposed including the Sterile Insect Technique (SIT), the Release of Insects carrying a Dominant Lethal (RIDL), the release of Wolbachia-infected mosquitoes and pyriproxyfen autodissemination, i.e., a self-delivery technique that manipulates mosquitoes’ behavior to carry and disseminate the killing agent (the IGR insecticide pyriproxyfen) to potential breeding sites [13]. Despite the encouraging results, certain limitations prevent the wide application of these approaches in the field. Among others, the main limitations in the area-wide application of SIT are the high production and transportation costs of sterilized males required to achieve successful suppression of the wild mosquito populations [14]. On the other hand, the implementation of both RIDL and Wolbachia-based strategies are under strict prohibition in many countries including the European Union due to environmental/ecological concerns, whereas the efficacy of pyriproxyfen autodissemination highly depends on the availability of breeding sites in a given area [13]. Therefore, conventional spray applications of insecticides still remain the principal mean for dealing with Ae. albopictus related problems.
In general, insecticide interventions prioritize larval over adult control, due to the higher anticipated efficacy and the lower human health and environmental risks. Currently in Europe, larval control relies almost exclusively on the Insect Growth Regulator (IGR) Diflubenzuron (DFB) and the microbial control agent Bacillus thuringiensis var. israelensis (Bti) [15]. DFB is a chitin biosynthesis inhibitor that interrupts insects’ normal development during the immature stages [16]. During sporulation Bti produces a mixture of Cry (Cry11Aa, Cry4Ba, Cry 4Aa and Cry10Aa) and Cyt (Cyt1Aa and Cyt2Ba) toxins [17]. The Cry toxins act synergistically with the Cyt by disrupting the integrity of the larvae midgut membrane [18,19]. The synergistic interactions between the Cyt and the Cry toxins are considered the key factor for the drastic enhancement of the larvicidal activity of the later (Cry toxins) [20] as well as for the delay and the low risk of resistance selection to Bti in mosquitoes [17,21].
The intensive use of both DFB and Bti for mosquitoes’ control pose potential risks for the development of resistance. While a recent study suggests their suitability for the effectiveness control of Ae. albopictus [22], findings regarding other species do not fully confirm this point of view. In particular, high levels (up to 128-fold) of DFB resistance associated with specific mutations in the Chitin synthase gene have been identified in wild Cx. pipiens populations from different countries with a high focal distribution in areas characterized by intensive applications of this product for both mosquitoes and agricultural pests control [23,24,25]. On the other hand, there is only a single record to support for substantial (33-fold) Bti resistance development in Cx. pipiens mosquito natural populations [26]. Despite these findings, no efforts have been made so far to explore the potential resistance development in Ae. albopictus to DFB and Bti.
Insecticide resistance development is often accompanied with significant fitness costs as a result of trade-offs associated with the function of the resistance mechanisms [27]. Moreover, adverse abiotic conditions may largely affect the expression of these costs in mosquitoes [28]. In this regard, winter in temperate regions represents a very challenging season for the survival of mosquitoes and therefore potential insecticide resistance associated fitness costs may reduce their overwintering capacity. The ability of the insecticide tolerant/resistant individuals to survive during the cold period is crucial for both the stability and evolution of acquired resistance in the wild from year to year. While the effects of DFB and Bti selection on the overwintering success of the medically important mosquito species Cx. pipiens have recently been elucidated [28], no such information is available for Ae. albopictus given its different winter biology. Considering the above mentioned knowledge gaps regarding the potential performance of Ae. albopictus to DFB and Bti extensive exposure, the aim of the present study was to explore how selection of both larvicides affects the resistance development as well as the overwintering success of this species.

2. Materials and Methods

2.1. Mosquitoes Used and Rearing Methods

An Ae. albopictus population was established during early September to mid-October of 2017 from approximately 2000 eggs that were collected using a network of 20 ovitraps set up at the vicinity of Volos (39°21′39.71″ N, 22°56′32.93″ E) and Larisa (39°38′12.80″ N, 22°25′3.40″ E) city, Thessaly county, Greece. Over the past 10 years, regional mosquito control interventions, including the collection sites, are mainly based on the routine use of DFB and Bti [28]. The ovitraps consisted of glossy black, cylindrical (15 cm high and 11 cm diameter) plastic pots filled with 800 mL tap water up to an overflow hole. Ten wooden strips (tongue depressors of 15 × 1.8 cm2) with one side properly scratched by a serrated knife, were attached with paper clips vertically in the inner of each pot serving as oviposition substrates. Strips from each ovitap were collected every 8–10 days, placed in plastic sealing bags and transferred to the laboratory. Mosquitoes’ colonization took place under standard conditions (25 ± 1 °C, 65 ± 5% relative humidity and a photoperiod of 14L:10D with a simulated dusk and dawn for 45 min). Upon adult emergence, specimens’ identification was performed using a dichotomous key [29] to avoid possible colony contamination by the relative Ae. cretinus species, which is also present in some regions of Greece but at extremely low densities [22]. Larvae and adult rearing procedures of the established population were identical of that described for Cx. pipiens by Ioannou et al. [28]. In brief, groups of approximately 1000 larvae were reared inside plastic containers provided with 3 L of water and 2 g of dry cat food while adults were maintained in 32 × 32 × 32 cm3 screened cages at a density of 600–700 individuals having constant access to 10% sugar solution. Mosquitoes were offered an arm feeding by a volunteer (C. Ioannou) until all responding females (usually 80–90% of total) in each cage completed a full blood meal. Females had access to oviposit on moist filter papers submerged in 500 mL of tap water inside black, plastic cylindrical containers. Before the initiation of any experimental procedure, the mosquito population was reared for three generations to establish a uniform genetic background.

2.2. Larval Bioassays

The susceptibility of the established Ae. albopictus population was evaluated against technical grade DFB (Purity ≥ 99.8%, Pestanal®, Sigma-Aldrich, Taufkirchen, Germany) and formulated Bti (Vectobac® 12AS, 11.61% w/w Bti serotype H-14, strain AM65-52, 1200 ITU/mg, Valent BioSciences Corporation, Libertyville, IL, USA) following the standard WHO guidelines [30]. Stock solutions were prepared in 99.5% acetone for DFB and distilled water for Bti and stored at –22 °C until use for a maximum of two weeks before being replaced by new ones. Bioassays for DFB and Bti were performed using late third and early fourth instar larvae, respectively. Each time, 25 larvae were transferred into plastic cups provided with 99 mL of distilled water and 1 mL of larvicide solution at the desired concentration. Control cups received 1 mL of acetone and distilled water in the case of DFB and Bti, respectively. Due to the slow mode of DFB action, in this case larvae were provided with cat food powder at a concentration of 100 mg/L to allow development. Six and five concentrations at the mortality range 10–95% were used for DFB and Bti bioassays. For each concentration and the respective controls six replicates (cups with 25 larvae) were performed. Bioassays were repeated three times on different days using new batches of larvae and larvicide solutions. Larval mortality for Bti was recorded after 24 h while determination of adult emergence inhibition for DFB was completed when all larvae in the control cups emerged as adults or died. EI50, EI80, and EI90 values (EI: Adult emergence inhibition) for DFB and LC50, LC80, and LC90 values (LC: Lethal concentration) for Bti were estimated using log-probit analysis [31].

2.3. Larval Selection

Larvae were selected for six successive generations to fixed IE80 and LC80 concentrations of DFB and Bti, respectively. At this point, the induced susceptibility levels were recalculated and the selection process was continued for three additional generations by applying the new IE80 and LC80 fixed doses. The selection process was identical of that described for Cx. pipiens by Ioannou et al. [28]. In brief, groups of approximately 1000 larvae, of appropriate developmental stage, were placed into rearing containers provided with 3 L of water and the fixed doses, while the resulting adults were reared following standard procedures. During the selection process, two additional larvae groups (≈1000 individuals each) were manipulated in exactly the same way but in the absence of DFB and Bti exposure serving as the control population. At the end of the selection process (F9 generation), new bioassays were performed to establish the induced resistance levels against both DFB and Bti. Moreover, the winter survival of diapausing eggs originating from each selected population and the control was determined.

2.4. Winter Survival

To induce Ae. albopictus females from each experimental population to lay diapausing eggs, both immature and adult stages were reared in an environmental chamber set at 20 °C, 8L:16D, and 70% RH [32]. Seven to 10 days after adult emergence, females were offered a blood meal (arm feeding). Soon after, 200 blood fed females from each population were allocated in 2 rearing cages (100/cage) and allowed to lay their eggs for 15 days in 2 ovitraps (one/cage), each containing 15 wooden strips. Ovitraps were then removed from the cages and held for 7 days inside the environmental chamber to permit embryonation. Then, eggs were cold acclimated for a week inside a dark incubator set at 10 ± 1 °C and RH 75 ± 5% to enhance their cold hardiness [4]. Before being exposed outdoors, each wooden strip was pictured under a binocular stereoscope (ZEISS, SteREO, Discovery.V12, Oberkochen, Germany) equipped with a digital camera (ZEISS, AxioCam, ERc 5s, Göttingen, Germany) to facilitate eggs counting. Then, strips were clipped to the inner edge of ovitrap pots with a single drainage hole placed 4.5 cm from the bottom. This configuration allowed ambient rain water to remain and moisten the wooden strips inside the pots but not flood the eggs. Two such pots were considered for each experimental population hosting a total of 30 wooden strips (15 each). Pots were covered, including the drainage hole, with a mesh screen (mesh size 1.0 mm) and fitted randomly side by side into a black, plastic, mesh box (mesh size 1 cm). To prevent access of macroscopic organisms, a second box was fastened on the top serving as a cover. Pots were positioned in the corner of a concrete wall at the University facilities, well protected from both direct sun light and strong winds. Eggs exposure took place on 12 November 2019. An outdoor data logger (HOBO Pro v2, Onset Computer Corporation, Bourne, MA, USA) set to receive 4 recordings of both temperature and RH per 24 h was attached at the bottom plastic box that hosted the pots. Based on empirical evidences suggesting the first appearance of Ae. albopictus adults in the area at the beginning of May overwintered egg strips were collected on 10 April 2020 and transferred to the laboratory. Strips were again pictured under the stereoscope and intact eggs were counted. To stimulate larval hatching, each egg strip was submerged for a week in a white, plastic container with 300 mL stale tap water provided with 0.05 g of cat food. After that, egg strips were removed from the water and left to dry for 72 h before a subsequent flooding was performed for another week. This procedure was repeated four times, until no more hatching events were observed, while the remaining unhatched eggs were considered dead. For each experimental population, survival of overwintered eggs under the ambient natural conditions was determined.

2.5. Statistical Analysis

Dose-response larval bioassays were subjected to Probit Analysis by transforming dose to log after corrections for control mortality according to Abbott’s formula [33]. Emergence inhibition (EI) and lethal concentrations (LC) values for DFB and Bti, respectively, where considered significantly different when 95% of confidence limits (CL) failed to overlap (p < 0.01). For the two selected populations and the control, the numbers of intact eggs in wooden strips before and after outdoor exposure and the respective proportions of hatched larvae were determined. Female fecundity and overwintered eggs hatchability data were analyzed using one-way analysis of variance after appropriate transformations for normality and homoscedasticity when necessary followed by Tukey’s HSD post hoc to separate means (p < 0.05). Data analysis was performed using IBM SPSS 25 (IBM Corp., Armonk, NY, USA).

3. Results

Larval bioassay results are given in Table 1 and Table 2 for DFB and Bti, respectively. The selection process with DFB for six successive generations by applying the EI80 corresponding dose, as determined for the established population, resulted in 3.6 and 4.4 Resistance Ratio (RR) values relative to the control as far as EI50 and EI90 are concerned. Selection for three additional generations with the new established EI80 corresponding dose, as determined at the end of the previous selection process (F6 generation), nearly doubled these values (Table 1). In contrast, selection to Bti had a little impact on the observed susceptibility levels (Table 2). Selection against both DFD and Bti reduced female fecundity relative to the control, however no significant differences were observed (Table 3). Recovery rates of diapaused eggs after outdoor exposure reached more than 95% for all tested populations (Table 3). Ambient temperature and relative humidity data during eggs’ overwintering are depicted in Figure 1. Temperatures ranged between 3.8 and 19.3 °C with a mean value of 10.9 °C indicating a rather mild cold period. Selection to Bti significantly increased the survival rates of overwintered eggs relative to control and the DFB selected population (Table 3). Moreover, the hatching rates of viable eggs (i.e., those that yielded larvae) following the first immersion in the water were significantly higher in the two selected populations relative to control.

4. Discussion

Despite the recent advances in new management approaches, the control of Ae. albopictus still relies to a great extent on the utilization of insecticides, raising concerns over resistance development. Understanding both the establishment and evolution of acquired resistance in the wild is crucial for the sustainability of management programmes. In this context, the current study represents a detailed investigation on the resistance development and establishment against two widely used larvicides. By applying an increasing selective pressure with DFB and Bti to Ae. albopictus, over a relative small number of successive generations, we found a moderate and a minor decrease on the susceptibility levels, respectively. Interestingly, selection to both larvicides had no apparent fitness costs in terms of female fecundity and the winter survival of diapausing eggs relative to control (non-selected population), suggesting an equal ability of the selected individuals to persist in the wild. These findings provide important insights on the potential development of resistance in Ae. albopictus against these commonly used insecticides, as well as on its prevalence in the wild from year to year.
The EI50 value determined for the established Ae. albopictus population (0.0017 mg/L) in the current study is remarkably lower than the WHO recommended DFB concentration (0.25 mg/L) for potable water [34] as well as the respective EI50 value (0.376 mg/L) reported for field collected Ae. albopictus populations from southern Switzerland [12]. In support of our findings, a recent survey revealed 100% mortality of Ae. albopictus populations collected from different regions of Greece at DFB doses below 0.02 mg/L, suggesting also high susceptibility [22]. On the other hand, the estimated LC50 value for Bti was 4.8 to 7.5-fold lower compared to the respective values recorded for other Greek populations of this species according to the previously mentioned study. However, such variations are not uncommon as an earlier survey in the island of Cyprus revealed an over 10-fold range in Bti LC50 values for wild collected mosquito populations of Cx. pipiens [35]. Interestingly, the LC50 value determined in our study is less than reported for laboratory strains of Ae. albopictus [36,37] suggesting high susceptibility to Bti.
Despite the high DFB susceptibility of the established population, the selection process resulted in the development of moderate resistance levels. During the first six successive generations of selection to the fixed dose corresponding to EI80, only a slight increment on the RR50 and 90 values was observed. This is in line with the results obtained by Belinato and Valle [38] who applied exactly the same selection protocol on Aedes aegypti. However, selection for three additional generations with the new established EI80 corresponding dose nearly doubled these values, indicating that the resistance development and evolution to DFB is highly facilitated by the imposition of increasing selective pressure. Thus, it appears that under certain conditions, even highly susceptible populations of Ae. albopictus as in our case, are capable of developing appreciable resistance levels. Recent evidences suggest the high suitability of DFB for the Asian tiger mosquito control [22], and this is partially true for other medically important mosquito species. In particular, very high DFB resistance levels have already been detected in wild populations of Cx. pipiens [23,39]. Moreover, subsequent surveys revealed a high focal distribution of the resistant individuals in areas with a strong background of intensive DFB use [24]. Therefore, in the light of our findings, the possibility of similar DFB resistance patterns cannot be excluded in the case of Ae. albopictus, highlighting the need for systematic resistance surveillance, especially in high risk areas.
On the other hand, selection to Bti had a negligible impact on the resistance levels of the Ae. Albopictus-established population. With the exception of a single record in Cx. pipiens [26], there are no consistent data to support for substantial Bti resistance development in mosquitoes [40]. As previously mentioned, the synergistic interactions between the Cyt and the Cry toxins are considered the key element for both the delay and the low risk of resistance selection to Bti. Conversely, extensive exposure to single Cry toxins can result in substantial resistance [41,42,43]. Another interesting aspect that appears to facilitate the low risk of Bti resistance development following extensive selection, is the fact that in the absence of selective pressure, any acquired resistance declines rapidly within a few generations [44,45]. While the reasons underlying this phenomenon remain largely unknown, the related high fitness costs have been proposed as a possible explanation [45].
Although, selection against both DFD and Bti reduced female fecundity compared to control, no significant differences were observed, suggesting a moderate fitness cost. In contrast to our findings, selection of Cx. pipiens and Ae. aegypti for 20 and 6 successive generations to Bti and DFB, respectively, resulted in a significant decrease of female fecundity [38,44]. However, it should be stressed that in these studies, tested females were previously exposed during the larval stage to the respective insecticides. Therefore, these results indicate primarily delayed effects following larvae exposure to sub-lethal doses of Bti and DFB rather than actual fitness costs. On the other hand, the females in our study that laid the diapausing eggs had no prior contact as immatures to both larvicides and thus we are confident that their oviposition output reflects the net costs induced as a result of the imposed selective pressure.
Survival of overwintering Ae. albopictus eggs under natural conditions is highly affected by the exposure methods. In this regard, our exposure configuration resulted in a 60% average hatching rate of the control population eggs, which is almost identical with the highest rate determined in a recent study that assessed different overwintering exposure protocols [46]. Selection to DFB had no apparent effect on the hatching rates of the overwintered eggs relative to control, suggesting no differences in their winter physiology. However, most importantly, it means that the progenies of the DFB selected individuals have the same survival prospects as the controls, providing the background for further resistance development in the coming year. In this context, the appearance of resistance without evidence of a trade-off in overwintering survival may pose a major challenge to future management of Ae. albopictus with DFB. Interestingly, while selection against Bti had a minor impact on the susceptibility levels, it conferred a moderate, though significant advantage regarding the overwintering success of the tested population relative to control. To the best of our knowledge this is the first report of a potential advantage associated with Bti selection in mosquitoes. Similarly to our findings, a positive association between selection to Bacillus thuringiensis subsp. kurstaki and the overwintering survival of the agricultural pest Trichoplusia ni (Lepidoptera: Noctuidae) has been recorded [47]. Authors attributed this phenomenon to possible pleiotropic effects according to which an allele responsible for resistance is positively influencing one of the components related with increased winter survival. However, this justification is not valid in our case as there are no consistent recordings of mosquito resistance to Bti, as mentioned above, and therefore no such alleles have been described for any mosquito species so far. As has emerged from the current study, selection to Bti resulted in a lower fecundity output relative to the other two tested populations (control and DFB selected). Therefore, it is possible that a greater maternal investment in terms of eggs nutrition occurred in this case, providing the background for a better overwintering capacity.
In the present study, the vast majority of eggs from all tested populations hatched after the first inundation followed by subsequent minimal hatchings. This is in line with an earlier study where overwintered eggs also went into a first mass hatching followed by other minor ones [46]. Ae. albopictus as well as other species of the genus Aedes, has a distinctive hatching pattern known as installment hatching. According to this, some eggs may hatch readily following inundation, while others may remain dormant for varying periods despite being underwater [48]. Selection to both DFB and Bti resulted in a higher synchronization of larvae hatching during the first inundation relative to control. This is most likely because the selection process in both cases enabled the prevalence of individuals with this attribute. While the biological significance of this finding remains largely unknown, at least theoretically it could promote the co-occurrence of the selected individuals during spring, facilitating their interbreeding and therefore the establishment of resistant/tolerant populations in the wild.

5. Conclusions

By using an Ae. albopictus population with high, inherent susceptibility to both DFB and Bti we showed that exposure to progressively increasing selective pressure resulted in a moderate and a minor increase of the resistance levels, respectively. Moreover, selection of both larvicides revealed no significant trade-offs on females’ fecundity as well as on the overwintering success of their descendants. These findings provide important insights regarding the potential risks of resistance development in Ae. albopictus against these two widely used larvicides as well as on its persistence in the wild on an annual base. Based on this, systematic monitoring for potential resistance development is imperative in order to maintain the current effectiveness of these two larvicides against Ae. albopictus populations and especially of DFB.

Author Contributions

Conceptualization, C.S.I., C.H. and N.T.P.; methodology and investigation, C.S.I. and V.A.M.; formal analysis and writing—original draft preparation, C.S.I.; resources and supervision, N.T.P. and C.H.; data curation, C.S.I. and N.T.P.; writing—review and editing, C.S.I., N.T.P., C.H. and V.A.M.; project administration, C.H.; funding acquisition, C.S.I. and C.H. All authors have read and agreed to the published version of the manuscript.

Funding

This research was exclusively funded by the Stavros Niarchos Foundation: Post-Doctoral Scholarships of Stavros Niarchos Foundation for the University of Thessaly. Grant number 5394.02.11, 2017–2020.

Institutional Review Board Statement

Not applicable.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Acknowledgments

We would like to thank Evagelia Mpakovassili for technical support.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

References

  1. Global Invasive Species Database. Available online: http://www.iucngisd.org/gisd/100_worst.php (accessed on 26 July 2021).
  2. Kraemer, M.U.G.; Reiner, R.C.; Brady, O.J.; Messina, J.P.; Gilbert, M.; Pigott, D.M.; Yi, D.; Johnson, K.; Earl, L.; Marczak, L.B.; et al. Past and future spread of the arbovirus vectors Aedes aegypti and Aedes albopictus. Nat. Microbiol. 2019, 4, 854–863. [Google Scholar] [CrossRef] [PubMed]
  3. Bonizzoni, M.; Gasperi, G.; Chen, X.; James, A.A. The invasive mosquito species Aedes albopictus: Current knowledge and future perspectives. Trends Parasitol. 2013, 29, 460–468. [Google Scholar] [CrossRef] [Green Version]
  4. Hanson, S.M.; Craig, G.B. Cold acclimation, diapause, and geographic origin affect cold hardness in eggs of Aedes albopictus (Diptera: Culicidae). J. Med. Entomol. 1994, 31, 192–201. [Google Scholar] [CrossRef] [PubMed]
  5. Adhami, J.; Reiter, P. Introduction and establisment of Aedes (Stegomia) albopictus Skuse (Diptera: Culicidae) in Albania. J. Am. Mosq. Control Assoc. 1998, 14, 340–343. [Google Scholar]
  6. Sabatini, A.; Raineri, V.; Trovato, G.; Coluzzi, M. Aedes albopictus in Italy and possible diffusion of the species into the Mediterranean area. Parassitologia 1990, 32, 301–304. [Google Scholar]
  7. Medlock, J.M.; Hansford, K.M.; Versteirt, V.; Cull, B.; Kampen, H.; Fontenille, D.; Hendrickx, G.; Zeller, H.; van Bortel, W.; Schaffner, F. An entomological review of invasive mosquitoes in Europe. Bull. Entomol. Res. 2015, 105, 637–663. [Google Scholar] [CrossRef]
  8. Kolimenakis, A.; Bithas, K.; Latinopoulos, D.; Richardson, C. On lifestyle trends, health and mosquitoes: Formulating welfare levels for control of the Asian tiger mosquito in Greece. PLoS Negl. Trop. Dis. 2019, 13, e0007467. [Google Scholar] [CrossRef]
  9. Pereira-dos-Santos, T.; Roiz, D.; Lourenço-de-Oliveira, R.; Paupy, C. A Systematic Review: Is Aedes albopictus an Efficient Bridge Vector for Zoonotic Arboviruses? Pathogens 2020, 9, 266. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  10. Gossner, M.C.; Ducheyne, E.; Schaffner, F. Increased risk for autochthonous vector-borne infections transmitted by Aedes albopictus in continental Europe. Eurosurveillance 2018, 23, 1800268. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  11. Paupy, C.; Delatte, H.; Bagny, L.; Corbel, V.; Fontenille, D. Aedes albopictus, an arbovirus vector: From the darkness to the light. Microbes Infect. 2009, 11, 1177–1185. [Google Scholar] [CrossRef]
  12. Suter, T.; Crespo, M.M.; de Oliveira, M.F.; de Oliveira, T.S.A.; de Melo-Santos, M.A.V.; de Oliveira, C.M.F.; Ayres, C.F.J.; Barbosa, R.M.R.; Araújo, A.P.; Regis, L.N.; et al. Insecticide susceptibility of Aedes albopictus and Ae. aegypti from Brazil and the Swiss-Italian border region. Parasit. Vectors. 2017, 10, 1–11. [Google Scholar] [CrossRef] [Green Version]
  13. Baldacchino, F.; Caputo, B.; Chandre, F.; Drago, A.; Della Torre, A.; Montarsi, F.; Rizzoli, A. Control methods against invasive Aedes mosquitoes in Europe: A review. Pest Manag. Sci. 2015, 71, 1471–1485. [Google Scholar] [CrossRef] [Green Version]
  14. Balatsos, G.; Puggioli, A.; Karras, V.; Lytra, I.; Mastronikolos, G.; Carrieri, M.; Papachristos, D.P.; Malfacini, M.; Stefopoulou, A.; Ioannou, C.S.; et al. Reduction of egg fertility of Aedes albopictus mosquitoes in Greece following releases of imported sterile males. Insects 2021, 12, 110. [Google Scholar] [CrossRef] [PubMed]
  15. Bellini, R.; Zeller, H.; Van Bortel, W. A review of the vector management methods to prevent and control outbreaks of West Nile virus infection and the challenge for Europe. Parasit. Vectors. 2014, 7, 323. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  16. Merzendorfer, H. Chitin synthesis inhibitors: Old molecules and new developments. Insect Sci. 2013, 20, 121–138. [Google Scholar] [CrossRef]
  17. Ben-Dov, E. Bacillus thuringiensis subsp. israelensis and Its Dipteran-Specific Toxins. Toxins 2014, 6, 1222–1243. [Google Scholar] [CrossRef]
  18. Cantón, P.E.; Zanicthe Reyes, E.Z.; Ruiz de Escudero, I.; Bravo, A.; Soberón, M. Binding of Bacillus thuringiensis subsp. israelensis Cry4Ba to Cyt1Aa has an important role in synergism. Peptides 2011, 32, 595–600. [Google Scholar] [CrossRef] [Green Version]
  19. Pérez, C.; Fernandez, L.E.; Sun, J.; Folch, J.L.; Gill, S.S.; Soberón, M.; Bravo, A. Bacillus thuringiensis subsp. israelensis Cyt1Aa synergizes Cry11Aa toxin by functioning as a membrane-bound receptor. Proc. Natl. Acad. Sci. USA. 2005, 102, 18303–18308. [Google Scholar] [CrossRef] [Green Version]
  20. Valtierra de Luis, D.; Villanueva, M.; Lai, L.; Williams, T.; Caballero, P. Potential of Cry10Aa and Cyt2Ba, Two Minority delta-endotoxins Produced by Bacillus thuringiens ser. israelensis, for the control of Aedes aegypti larvae. Toxins 2020, 12, 355. [Google Scholar] [CrossRef]
  21. Wirth, M.C.; Park, H.W.; Walton, W.E.; Federici, B.A. Cyt1A of Bacillus thuringiensis delays evolution of resistance to Cry11A in the mosquito Culex quinquefasciatus. Appl. Environ. Microbiol. 2005, 71, 185–189. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Balaska, S.; Fotakis, E.A.; Kioulos, I.; Grigoraki, L.; Mpellou, S.; Chaskopoulou, A.; Vontas, J. Bioassay and molecular monitoring of insecticide resistance status in Aedes albopictus populations from Greece, to support evidence-based vector control. Parasit. Vectors 2020, 13, 1–13. [Google Scholar] [CrossRef]
  23. Grigoraki, L.; Puggioli, A.; Mavridis, K.; Douris, V.; Montanari, M.; Bellini, R.; Vontas, J. Striking diflubenzuron resistance in Culex pipiens, the prime vector of West Nile virus. Sci. Rep. 2017, 7, 11699. [Google Scholar] [CrossRef] [Green Version]
  24. Porretta, D.; Fotakis, E.; Mastrantonio, V.; Chaskopoulou, A.; Michaelakis, A.; Kioulos, I.; Weill, M.; Urbanelli, S.; Vontas, J.; Bellini, R. Focal distribution of diflubenzuron resistance mutations in Culex pipiens mosquitoes from Northern Italy. Acta Trop. 2019, 193, 106–112. [Google Scholar] [CrossRef] [Green Version]
  25. Guz, N.; Cagatay, N.S.; Fotakis, E.A.; Durmusoglu, E.; Vontas, J. Detection of diflubenzuron and pyrethroid resistance mutations in Culex pipiens from Mugla, Turkey. Acta Trop. 2020, 203, 105294. [Google Scholar] [CrossRef]
  26. Paul, A.; Harrington, L.; Zhang, L.; Scott, J. Insecticide resistance in Culex pipiens from New York. J. Am. Mosq. Control. Assoc. 2005, 21, 305–309. [Google Scholar] [CrossRef]
  27. Belinato, T.A.; Martins, A.J. Insecticide Resistance and Fitness Cost. In Insecticides Resistance; Trdan, S., Ed.; InTech: Rijeka, Croatia, 2016; pp. 243–261. [Google Scholar]
  28. Ioannou, C.S.; Hadjichristodoulou, C.; Kyritsi, M.A.; Papadopoulos, N.T. Short term selection to Diflubenzuron and Bacillus thuringiensis var. Israelensis differentially affects the winter survival of Culex pipiens f. pipiens and Culex pipiens f. molestus (Diptera: Culicidae). Insects 2021, 12, 527. [Google Scholar] [CrossRef] [PubMed]
  29. Voyatzoglou-Samanidou, A. The Mosquitoes of Greece: Morphology, Biology, Public Health, Identification Keys, Control; Agrotypos: Maroussi, Greece, 2011; ISBN 978-960-7667-43-4. [Google Scholar]
  30. WHO. Guidelines for Laboratory and Field Testing of Mosquito Larvicides; World Health Organisation: Geneva, Switzerland, 2005. [Google Scholar]
  31. Finney, D.J. Probit Analysis; Cambridge University Press: London, UK, 1971. [Google Scholar]
  32. Thomas, S.M.; Obermayr, U.; Fischer, D.; Kreyling, J.; Beierkuhnlein, C. Low-temperature threshold for egg survival of a post-diapause and non-diapause European aedine strain, Aedes albopictus (Diptera: Culicidae). Parasit. Vectors 2012, 5, 1–7. [Google Scholar] [CrossRef] [Green Version]
  33. Abbott, W. A method of computing the effectiveness of an insecticide. J. Econ. Entomol. 1925, 18, 265–267. [Google Scholar] [CrossRef]
  34. WHO. Guidelines for Drinking-Water Quality 3rd Edition Incorporating 1st and 2nd Addenda. Geneva: World Health Organization. 2008. Available online: https://www.who.int/watersanitationhealth/dwq/fulltext.pdf (accessed on 3 August 2021).
  35. Wirth, M.C.; Ferrari, J.A.; Georghiou, G.P. Baseline susceptibility to bacterial Insecticides in populations of Culex pipiens Complex (Diptera: Culicidae) from California and from the Mediterranean Island of Cyprus. J. Econ. Entomol. 2001, 94, 920–928. [Google Scholar] [CrossRef]
  36. Li, Y.; Xu, J.; Zhong, D.; Zhang, H.; Yang, W.; Zhou, G.; Su, X.; Wu, Y.; Wu, K.; Cai, S.; et al. Evidence for multiple-insecticide resistance in urban Aedes albopictus populations in southern China. Parasit. Vectors 2018, 11, 1–10. [Google Scholar] [CrossRef] [PubMed]
  37. Su, X.; Guo, Y.; Deng, J.; Xu, J.; Zhou, G.; Zhou, T.; Li, Y.; Zhong, D.; Kong, L.; Wang, X.; et al. Fast emerging insecticide resistance in Aedes albopictus in Guangzhou, China: Alarm to the dengue epidemic. PLoS Negl. Trop. Dis. 2019, 13, e0007665. [Google Scholar] [CrossRef]
  38. Belinato, T.A.; Valle, D. The impact of selection with diflubenzuron, a chitin synthesis inhibitor, on the fitness of two Brazilian Aedes aegypti field populations. PLoS ONE 2015, 10, e0130719. [Google Scholar] [CrossRef]
  39. Fotakis, E.A.; Mastrantonio, V.; Grigoraki, L.; Porretta, D.; Puggioli, A.; Chaskopoulou, A.; Osório, H.; Weill, M.; Bellini, R.; Urbanelli, S.; et al. Identification and detection of a novel point mutation in the Chitin Synthase gene of Culex pipiens associated with diflubenzuron resistance. PLoS Negl. Trop. Dis. 2020, 14, e0008284. [Google Scholar] [CrossRef]
  40. Carvalho, K.D.S.; Crespo, M.M.; Araújo, A.P.; da Silva, R.S.; de Melo-Santos, M.A.V.; de Oliveira, C.M.F.; Silva-Filha, M.H.N.L. Long-term exposure of Aedes aegypti to Bacillus thuringiensis svar. israelensis did not involve altered susceptibility to this microbial larvicide or to other control agents. Parasit. Vectors. 2018, 11, 1–11. [Google Scholar] [CrossRef]
  41. Georghiou, G.P.; Wirth, M.C. Influence of exposure to single versus multiple toxins of Bacillus thuringiensis subsp. israelensis on development of resistance in the mosquito Culex quinquefasciatus (Diptera: Culicidae). Appl. Environ. Microbiol. 1997, 63, 1095–10101. [Google Scholar] [CrossRef] [Green Version]
  42. Cadavid-Restrepo, G.; Sahaza, J.; Orduz, S. Treatment of an Aedes aegypti colony with the Cry11Aa toxin for 54 generations results in the development of resistance. Memo. Inst. Oswaldo Cruz. 2012, 107, 74–79. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Stalinski, R.; Tetreau, G.; Gaude, T.; Despres, L. Pre-selecting resistance against individual Bti Cry toxins facilitates the development of resistance to the Bti toxins cocktail. J. Invertebr. Pathol. 2014, 119, 50–53. [Google Scholar] [CrossRef]
  44. Saleh, M.S.; El-Meniawi, F.A.; Kelada, N.L.; Zahran, H.M. Resistance development in mosquito larvae Culex pipiens to the bacterial agent Bacillus thuringiensis var. israelensis. J. Appl. Entomol. 2003, 127, 29–32. [Google Scholar] [CrossRef]
  45. Paris, M.; David, J.P.; Despres, L. Fitness costs of resistance to Bti toxins in the dengue vector Aedes aegypti. Ecotoxicology 2011, 20, 1184–1194. [Google Scholar] [CrossRef]
  46. Jiang, Y. Survival of overwintering Aedes albopictus eggs under natural conditions in North-central Florida. J. Am. Mosq. Control. Assoc. 2018, 34, 255–359. [Google Scholar] [CrossRef] [Green Version]
  47. Caron, V.; Myers, J.H. Positive association between resistance to Bacillus thuringiensis and overwintering survival of cabbage loopes, Trichoplusia ni (Lepidoptera: Noctuidae). Bull. Entomol. Res. 2008, 98, 317–322. [Google Scholar] [CrossRef]
  48. Edgerly, J.; Willey, M.S.; Livdahl, T.P. The community ecology of Aedes egg hatching: Implications for mosquito invasion. Ecol. Entomol. 1993, 18, 123–128. [Google Scholar] [CrossRef]
Insects 12 00822 g001 550
Figure 1. Temperature (a) and humidity (b) profiles at the study site during winter 2019/2020.
Figure 1. Temperature (a) and humidity (b) profiles at the study site during winter 2019/2020.
Insects 12 00822 g001
Table
Table 1. Emergence inhibition (EI) values of diflubenzuron (DFB) against Ae. albopictus before and after the selection process for six and nine successive generations, respectively.
Table 1. Emergence inhibition (EI) values of diflubenzuron (DFB) against Ae. albopictus before and after the selection process for six and nine successive generations, respectively.
PopulationN *EI50
(95% CL) a		RR50EI90
(95% CL) a		RR90SlopeX2 (df)
Pre-selection
Colony31500.0017
(0.0014–0.0019)		–0.0039
(0.0036–0.0041)		–3.56119.24 (105)
Post-selection
Control27000.0022
(0.0016–0.0026)		–0.0041
(0.0037–0.0045)		–4.68156.25 b (87)
F6 DFB 27000.0080
(0.0070–0.0089)		3.60.0182
(0.0170–0.0196)		4.43.5862.23 (87)
Control27000.0022
(0.0019–0.0025)		–0.0040
(0.0038–0.0043)		–4.8699.94 (87)
F9 DFB27000.0188
(0.0174–0.0200)		8.50.0301
(0.0288–0.0319)		7.56.2824.73 (87)
* Number of larvae tested. a EI values are expressed in milligrams per liter, and they are considered significantly different when 95% of confidence limits (CL) fail to overlap (p < 0.01). b Since goodness-of-fit test is significant (p < 0.05), a heterogeneity factor was used in the calculation of confidence limits (CL).
Table
Table 2. Lethal concentration (LC) values of Bti against Ae. albopictus before and after the selection process for six and nine successive generations, respectively.
Table 2. Lethal concentration (LC) values of Bti against Ae. albopictus before and after the selection process for six and nine successive generations, respectively.
PopulationN *LC50
(95% CL) a		RR50LC90
(95% CL) a		RR90SlopeX2 (df)
Pre-selection
Colony27000.027
(0.024–0.034)		–0.051
(0.047–0.056)		–4.5994.44 (87)
Post-selection
Control27000.032
(0.030–0.034)		–0.046
(0.044–0.050)		–8.08132.02 b (87)
F6 Bti27000.041
(0.031–0.048)		1.30.067
(0.062–0.071)		1.56.0459.86 (87)
Control27000.030
(0.028–0.032)		–0.045
(0.043–0.047)		–7.7058.39 (87)
F9 Bti27000.047
(0.036–0.055)		1.60.083
(0.076–0.088)		1.85.2080.62 (87)
* Number of larvae tested. a LC values are expressed in milligrams per liter, and they are considered significantly different when 95% of confidence limits (CL) fail to overlap (p < 0.01). b Since goodness-of-fit test is significant (p < 0.05), a heterogeneity factor was used in the calculation of confidence limits (CL).
Table
Table 3. Female fecundity and winter larvae survival parameters of Ae. albopictus diapausing eggs originated from populations that either were selected against diflubenzuron (DFB) and Bti for nine successive generations or not (control). For each population, 200 blood fed females were allowed to lay their eggs in 30 wooden strips.
Table 3. Female fecundity and winter larvae survival parameters of Ae. albopictus diapausing eggs originated from populations that either were selected against diflubenzuron (DFB) and Bti for nine successive generations or not (control). For each population, 200 blood fed females were allowed to lay their eggs in 30 wooden strips.
Mean ± SE
PopulationEggs/Wooden Strip Before Outdoor Exposure Eggs/Wooden Strip after Outdoor ExposureHatching Rates of Recovered Eggs%Hatching Rates of Viable Eggs% during the First Water Immersion
Control304.47 ± 23.70 a294.10 ± 23.14 a59.98 ± 1.31 b85.50 ± 1.80 b
F9 DFB279.63 ± 17.36 a273.57 ± 17.20 a60.15 ± 1.35 b91.71 ± 0.87 a
F9 Bti266.47 ± 25.07 a257.60 ± 24.73 a66.17 ± 1.96 a93.35 ± 1.32 a
F0.750.735.058.96
df2.872.872.872.87
P0.4760.4850.008<0.0001
Means in the same column followed by the same letter indicate no significant differences (Tukey’s HSD test, p > 0.05).
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Ioannou, C.S.; Hadjichristodoulou, C.; Mouchtouri, V.A.; Papadopoulos, N.T. Effects of Selection to Diflubenzuron and Bacillus thuringiensis Var. Israelensis on the Overwintering Successes of Aedes albopictus (Diptera: Culicidae). Insects 2021, 12, 822. https://doi.org/10.3390/insects12090822

AMA Style

Ioannou CS, Hadjichristodoulou C, Mouchtouri VA, Papadopoulos NT. Effects of Selection to Diflubenzuron and Bacillus thuringiensis Var. Israelensis on the Overwintering Successes of Aedes albopictus (Diptera: Culicidae). Insects. 2021; 12(9):822. https://doi.org/10.3390/insects12090822

Chicago/Turabian Style

Ioannou, Charalampos S., Christos Hadjichristodoulou, Varvara A. Mouchtouri, and Nikos T. Papadopoulos. 2021. "Effects of Selection to Diflubenzuron and Bacillus thuringiensis Var. Israelensis on the Overwintering Successes of Aedes albopictus (Diptera: Culicidae)" Insects 12, no. 9: 822. https://doi.org/10.3390/insects12090822

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop