- Open Access
High-throughput sorting of mosquito larvae for laboratory studies and for future vector control interventions
- Eric Marois1,
- Christina Scali2,
- Julien Soichot1,
- Christine Kappler1,
- Elena A Levashina†1, 3Email author and
- Flaminia Catteruccia†4, 5Email author
© Marois et al.; licensee BioMed Central Ltd. 2012
Received: 25 May 2012
Accepted: 7 August 2012
Published: 28 August 2012
Mosquito transgenesis offers new promises for the genetic control of vector-borne infectious diseases such as malaria and dengue fever. Genetic control strategies require the release of large number of male mosquitoes into field populations, whether they are based on the use of sterile males (sterile insect technique, SIT) or on introducing genetic traits conferring refractoriness to disease transmission (population replacement). However, the current absence of high-throughput techniques for sorting different mosquito populations impairs the application of these control measures.
A method was developed to generate large mosquito populations of the desired sex and genotype. This method combines flow cytometry and the use of Anopheles gambiae transgenic lines that differentially express fluorescent markers in males and females.
Fluorescence-assisted sorting allowed single-step isolation of homozygous transgenic mosquitoes from a mixed population. This method was also used to select wild-type males only with high efficiency and accuracy, a highly desirable tool for genetic control strategies where the release of transgenic individuals may be problematic. Importantly, sorted males showed normal mating ability compared to their unsorted brothers.
The developed method will greatly facilitate both laboratory studies of mosquito vectorial capacity requiring high-throughput approaches and future field interventions in the fight against infectious disease vectors.
Vector-borne infectious diseases are a major scourge for humanity. Malaria alone, caused by Plasmodium parasites transmitted by the bite of infected female Anopheles mosquitoes, annually infects 250 million people worldwide and kills close to one million, mostly children in sub-Saharan Africa . Past attempts at curbing the disease by the massive use of insecticides and of insecticide-impregnated bed nets have promoted the spread of genetic resistance to a wide range of insecticides across mosquito populations. This is reducing the impact of insecticide-based control methods, and novel approaches to control vector populations are urgently needed to roll back the disease. A similar challenge is posed by the control of Aedes mosquito species transmitting viral diseases including yellow fever, dengue and chikungunya.
Vector control methods that specifically target the desired species represent a valid and environmentally friendly alternative to insecticides. Dating from the 1950s, the sterile insect technique (SIT) is a species-specific control strategy that has been successfully used to reduce the population size of insect pests such as the screw worm and the Mediterranean fruit fly . For mosquito SIT (; reviewed in [4, 5]), large numbers of male insects must be produced in breeding facilities, sterilized by γ-ray irradiation, and released in the field to compete with wild males for mating with wild females. The SIT approach is well suited for Anopheles mosquitoes, as the majority of females mate once in their lifetime and use the sperm stored in their spermatheca to fertilize egg batches produced every time they take a blood meal . This implies that if a female copulates with a sterile male, she will not mate again and will lay only infertile eggs. Repeated releases of sterile males over a given area would, therefore, achieve a local drop in vector populations and a consequent decrease in malaria transmission. However, labour-intensive procedures for selection of male-only populations and a large variability in the efficiency of sterilization have to date posed vast blocks for a massive application of this approach.
Since the turn of the century, vast progress has been made in the generation of molecular and genetic tools for studies on Anopheles mosquitoes. The sequencing of the Anopheles gambiae genome  has allowed the identification of thousands of genes that shape the biology and behaviour of this main malaria vector. These genomic advances, combined with the development of transgenic technologies  to modify the mosquito genome and the possibility of silencing gene expression through RNAi , are facilitating studies on the biological processes that are crucial to the ability of Anopheles mosquitoes to transmit malaria. Importantly, they also offer a basis for novel vector control strategies to complement insecticide treatments. Among the advocated novel approaches are genetic control strategies related to SIT, such as the release of insects carrying a dominant lethal (RIDL), that are currently being developed for the dengue vector, Aedes aegypti[10, 11]. In RIDL, released male mosquitoes carry a transgene that makes their female progeny unviable or infertile. Further alternative strategies propose to alter the genetic make-up of mosquito populations to reduce their vectorial capacity traits, for instance by rendering mosquitoes resistant to human pathogens [12–14]. The introgression of natural genetic traits or of synthetic transgenic constructs interfering with the mosquito vectorial capacity would lead to the replacement of natural disease-transmitting populations with mosquitoes that do not transmit infectious agents, a process that could be enhanced by artificial gene drive systems [15, 16].
Regardless of the final goal of the control programme (population eradication through SIT/RIDL or population replacement), when targeting mosquito vectors male-only populations must be released, since females may (i) contribute to an unwanted increase of the mosquito populations if not sterile, (ii) mate with the released males thereby reducing the efficacy of the trial, and (iii) participate in disease transmission. This underlines the need for high-throughput sexing tools for mosquitoes: males carrying the desired sterility or disease-resistance trait need to be produced on an industrial scale to reach the vast numbers (millions) necessary for a release programme. It is essential that the released males, whether sterile or not, are fully competitive for mating with field females. Therefore, the mechanism utilized for inducing sterility/refractoriness, the mass rearing conditions and the sex sorting procedures must have no impact on overall male fitness.
Proof-of-principle evidence that automated separation of the sexes is achievable in A. gambiae mosquitoes was previously provided using a flow cytometry machine (COPAS®, Union Biometrica) to separate males from females based on the expression of a sperm-specific fluorescence marker in the testis . The usefulness of this system was limited by the fact that male individuals could be identified only during late larval stages, at the onset of sperm development. Here, the full potential of this high-throughput system is achieved by the use of early sex-specific transgenic markers. This system allows the efficient and fully accurate separation of the desired phenotypes at early stages of development. Large larval populations can be sorted into populations of males/females; transgenics/non-transgenics, heterozygous/homozygous, transgenic females/non-transgenic males. Further, the property of the system to quantify transgene copy number offers a new approach for mosquito sexing based on X-linked insertions at any stage of larval development. The sorting procedure has no impact on the mating ability of the resulting adult males. The system, here tested on A. gambiae mosquitoes, could be easily adapted to all mosquito species that are amenable to transgenesis.
Mosquito strains and rearing
Anopheles gambiae mosquitoes (G3 and Ngousso strains and their transgenic derivatives) were maintained at 28°C and 70-80% humidity in a 12/12 h day/night cycle. Anesthetized CD1 mice were used for blood feeding and larvae were fed finely ground Tetra Goldfish food (Tetra, Germany). The DSX transgenic strain, obtained in the G3 background, has been previously described .
The FK transgenesis plasmid was assembled by recombining three entry plasmids and one piggyBac destination plasmid using three-fragment Multisite Gateway cloning (Invitrogen) according to the manufacturer’s instructions. The resulting construct contained the attB1, attB2, attB3 and attB4 Gateway seam sites that delimit each of the three cassettes contributed by the entry plasmids (for the full annotated construct sequence refer to Additional file 1). The Vitellogenin (AGAP004203) promoter was amplified from A. gambiae genomic DNA using the following primers: 5’-TGACCTCGAGTTCAACTCGACC-3’ and 5’-GATATCGATGGTTCGGTTGTTCGCAGTTG-3’. The amplified fragment was cloned into Xho I and Cla I restriction sites of the YFP-containing entry vector. The AGAP002620 promoter region was amplified using primers: 5-CCGTCTAGACCGGGCTCTACAAAGTC-3’ and 5’-CAGCTCTCGAGCAGGAGGATCGTT-3’ and cloned as an Xba I - Xho I fragment into the tdTomato-containing entry vector. Embryos (n = 120) of the Ngousso strain were injected with a 200 ng/μl solution of the transgenesis plasmid and 20 surviving adults were back-crossed to Ngousso mosquitoes. A single transgenic mosquito male was recovered from the back-cross progeny. Further genetic crosses revealed that the transgene insertion was X-linked. The piggyBac insertion was mapped by inverse PCR as follows: 500 ng of genomic DNA were digested with Sau 3AI or cocktails of blunt end restriction enzymes (Sca I Hinc II, Dra I, Sma I Pvu II, Fermentas), and re-ligated with T4 DNA ligase (Fermentas) in a final volume of 500 μl. The sample was ethanol-precipitated, re-suspended in 20 μl water, of which 2 μl were subjected to PCR. The piggyBac 5’ border of the insertion site was mapped by sequencing a product amplified with primers 5’-TGCACAGCGACGGATTCGCGCTATT-3’and 5’-AGGACATCTCAGTCGCCGCTTGGA-3’, followed by nested PCR with 5’-CGCGCTATTTAGAAAGAGAGAG-3’ and 5’-GAACTATAACGACCGCGTGAGTC-3’; or with 5’-GAACTATAACGACCGCGTGAGTC-3’ and 5’-CAGTGACACTTACCGCATTGACA-3’. The piggyBac 3’ border of the insertion site was mapped by sequencing the product amplified with primers 5’-CGAGGTTTATTTATTAATTTGAATAGATATTAAG-3’ and 5’-CGATATACAGACCGATAAAACACATGCGT-3’, followed by nested PCR with 5’-GCGTCAATTTTACGCATGATTATCTTT-3’ and 5’-ATTTACACTTACATACTAATAATAAATTCAAC-3’.
Amplified fragments were compared by BLAST to the Anopheles gambiae genome (VectorBase). The transposon insertion was mapped within a 232-base pair repeated element on the X chromosome. This short repeated element is broadly distributed in the genome, but at the position X: 22463464 is present in the Ngousso strain and absent from the G3 and PEST strains. The transgenic construct carried the EGFP gene under the control of a 3xP3 promoter  as a transgenesis selection marker, and two additional reporter genes: (i) YFPvenus under the control of the A. gambiae Vitellogenin (AGAP004203) promoter and (ii) tdTomato under the control of the AGAP002620 gene promoter . The detailed characterization of these additional reporter constructs will be described elsewhere. Mosquitoes were reared and blood-fed on anesthetized mice in compliance with French and European laws on animal house procedures (agreement #E67-482-2 of the Direction of Veterinary services of the French Ministry of Agriculture).
COPAS-assisted larval sorting
The blood-fed mosquitoes (two to four days after a blood meal) were offered an egg dish made of a conical, 90 mm diameter, hardened filter paper (#50 Whatman, GE Healthcare, UK) dipped in a glass bowl filled with water. Larvae were allowed to hatch directly in the egg dish and were recovered from water leaving most of the empty eggshells on the filter paper. Larvae were transferred to the reservoir of a Complex Object Parametric Analyzer and Sorter (COPAS) large particles flow cytometry SELECT instrument (Union Biometrica, Holliston, MA, USA), and analysed with the Biosort5281 software. For laser-assisted sorting, 488 or 514 nm emission filters were used indifferently with the following acquisition parameters: Green PMT 500, Yellow PMT 500, Red PMT 600, Delay 8; Width 6, pure mode selection with superdrops. Detection thresholds were set to 100 (signal) and 150 (time of flight). “Sheath” pressure (demineralized water was used instead of Sheath medium) was kept at a value of around 3, sorter pressure 3.3, while sample pressure varied between 3 and 4.5 depending on the density of the larvae. The flow rate was kept below 18 detected objects per second. Selected larvae were collected into a Petri dish placed underneath the flow cell outlet. Though result diagrams can be directly viewed in the COPAS® software, the LMD files generated by the COPAS analysis were imported in the WinMDI freeware for data analyses and diagram generation.
Small larvae were spotted in a drop of water in the wells of a CEL-LINE teflon-coated, 24-well diagnostic microscope slide (Erie Scientific, Menzel GmbH, Braunschweig; Germany) and observed with the 5x objective of an Axiovert 200 M Zeiss fluorescence microscope. To immobilize larvae for photography, an anaesthetics solution of final concentration 5% tricaine and 0.5% tetramizole was added to the water 15 min before observation.
Rapid and precise establishment of homozygous transgenic Anopheles gambiae lines by COPAS sorting
Next, male and female homozygous transgenic adults obtained from the sorting process were crossed and their progeny was screened (again using the COPAS instrument) to search for potential heterozygous individuals arising from inefficient sorting of homozygotes. Heterozygotes were absent, suggesting that the initial sorting of homozygous individuals by COPAS was 100% efficient, thereby permitting the establishment of a homozygous transgenic mosquito line in one generation. These results demonstrate the potential of the COPAS machine for compensating the lack of balancer chromosomes in mosquitoes for selection and maintenance of a desired transgenic genotype, thereby permitting a major gain in time and precision.
COPAS-assisted high-throughput sexing of early mosquito larvae
After sorting, 2,000 larvae of each population were raised separately to the pupal stage and resulting pupae were placed in two different cages. Careful and repeated visual examination of the adults emerged in each cage confirmed that all adults from the larvae displaying high GFP fluorescence were males and all adults from the larvae showing low GFP fluorescence were females (Figure 3B).
Efficiency of COPAS sorting and survival of sorted larvae
Number of COPAS sortings
COPAS sorting does not impair male mating competitiveness
Effect of COPAS on male reproductive competitiveness
Progenies of DSX male
Progenies of a competitor male
Total number of progenies
Three additional independent repeats of this experiment were performed with smaller mosquito numbers (45–60 mosquitoes for each group). These confirmed the absence of significant loss of fitness and mating competitiveness for males that passed through the machine compared to control males of the same genotype (data not shown). These results suggest that repeated COPAS sorting does not confer any obvious mating disadvantage to the males, at least in laboratory conditions.
Isolation of non-transgenic male-only populations from transgenic colonies
The possibility to employ genetic control strategies to roll back malaria and other mosquito-borne diseases calls for new technological approaches that overcome the current blocks in mass-rearing of mosquitoes with the desired phenotypes. The work reported here demonstrates that the technology of large particle flow cytometry provides an extremely efficient, fast and reliable method for the selection of male-only (or female-only) mosquito populations early in their developmental cycle, and for the rapid and effective establishment of homozygous transgenic lines. This work builds on an earlier report that provided a proof-of-principle demonstration of the potential of COPAS for genetic sexing of mosquito larvae . This initial study was restricted to the separation of the sexes and achieved incomplete accuracy and low speed of sorting due to the advanced stage of larvae development. Here, these limitations are overcome by exploiting a sex-specific fluorescent marker expressed at the very early stages of larval development. Moreover, it is shown here that X-linked transgenes efficiently substitute for early sex-specific markers for mosquito sexing. Currently, sexing in Culicidae is achieved manually by microscopic sorting of pupae based on the dimorphism of the male and female terminal abdominal segments. Another method for separation of the sexes exploits differences in size of male and female pupae characteristic of Aedes mosquitoes (http://www.oxitec.com/news-and-views/topic-pages-safety-and-sustainability/what-happens-if-female-mosquitoes-are-released/). This approach cannot be used for A. gambiae, a mosquito species in which the size difference between male and female pupae is too subtle to warrant accurate separation of females from males. Therefore, to date COPAS sorting is the only reliable method that allows high-throughput sexing in Anopheles.
The performance of the current COPAS sorters (40,000 male larvae per hour) would allow the separation of almost 2 million male mosquitoes per week (considering a 20% larval mortality rate and an 8-hour daily use of a single machine). Based on past SIT attempts , this number would be sufficient for most release strategies. For interventions requiring larger number of released males, the sorting method described here would need to be scaled up. The further improvement of sorters specifically designed for mosquitoes (upgraded COPAS instruments or similar sorters that may be developed by other manufacturers) may render this task achievable in the near future.
Ordinarily when a new transgenic mosquito line is obtained, inaccurate and lengthy visual screening of larvae from a heterogeneous F2 population must be performed by fluorescence microscopy to select homozygous individuals based on their stronger fluorescence phenotype. This process is subjective and prone to human error; in addition, given the limited speed of the manual process, only a small number of homozygous larvae can be obtained by one operator in a few hours. These limitations make obtaining stable homozygous transgenic lines a lengthy, tedious and inefficient process. As illustrated here for the DSX line, COPAS usage revolutionizes this step and yields a large population of homozygous individuals in one sorting session lasting less than 30 min, based on the differential expression level of the selectable marker in heterozygous and homozygous individuals. This method, now routinely used in the laboratory, facilitated the establishment of more than 20 distinct transgenic lines in two distinct A. gambiae genetic backgrounds, the G3 and Ngousso strains (data not shown), illustrating its general value for the development of transgenic mosquito lines.
The availability of an effective and high-throughput technology to rapidly select homozygous individuals from mixed populations offers the possibility to increase the fitness of released insects. It is particularly important when considering the problems posed by mass-rearing transgenic insects, where inbreeding of the population causes large fitness costs. As a way to increase the genetic pool of inbred populations with a consequent positive effect on fitness, field mosquitoes can be introduced into the mass-reared population every few generations. Moreover, the sorting technology allows purifying a transgenic line in case of contamination with wild-type individuals, a frequently occurring problem even in the most experienced laboratories.
The selection procedure described here and the use of multiple fluorescent markers such as GFP, YFP, CFP and DsRed proteins in transgenic larvae enable novel experimental schemes now routinely used by the authors. For example, multiple transgenes can be rapidly combined into a single mosquito line, or the frequency dynamics of multiple transgenes present in a single population can be monitored over generations and corrected at will.
When using transgenic lines that allow separation of the sexes based on fluorescent phenotypes, COPAS-assisted sexing can produce large single-sex mosquito populations. In addition to enabling particular laboratory studies that require considerable numbers of virgin females or males, such a tool will be invaluable for the selection of male-only mosquito populations for genetic control strategies against vector-borne diseases such as malaria. In the current experiments, a limitation on the number of screened individuals (up to 20,000 in 30 min) is only imposed by the size of the mosquito colony and not by the throughput characteristics of the COPAS instrument used. Importantly, COPAS-selected males are as competitive for mating as their unsorted peers in cage conditions. In addition, the authors’ empirical experience in managing more than 20 independent transgenic A. gambiae strains using routine COPAS sorting indicates that sorted populations are often healthier than their unsorted peers, possibly because COPAS sorting eliminates microbe-rich debris from progenitor mosquitoes.
The powerful capacity of the COPAS system to distinguish gene copy number by intensity of fluorescence is not limited to the use of DSX-like sex-specific constructs, and is applicable to a large number of insect species that are amenable to transgenesis. Novel COPAS-based strategies will certainly further assist the development of transgenic applications, such as large-scale larval seeding in multi-well plates for high-throughput drug or small molecule screening.
We are now entering a new era in which much anticipated genetics-based disease control strategies are finally taking shape. Considerable laboratory work is urgently needed to evaluate their promises and risks, and to determine the practical aspects of their implementation. The tools presented here remove many of the hurdles related to inaccurate and low-throughput sorting of mosquito populations and thereby pave the way for both laboratory studies and future field releases of sterile or disease-resistant vectors.
This work was supported by the Institut National de la Santé et de la Recherche Médicale (INSERM U963) and by the Centre National de la Recherche Scientifique (CNRS UPR9022), the European Commission FP7 projects INFRAVEC (grant agreement no. 228421) and EVIMalar (grant agreement no. 242095), by a Medical Research Council Career Development Award (Agreement ID 78415, File G0600062), by the European Research Council FP7 ERC Starting Grant project ‘Anorep’ (Grant ID: 260897).
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