Article:Alternative strategies for mosquito-borne arbovirus control (6317787)
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Title: PLoS Neglected Tropical Diseases
Alternative strategies for mosquito-borne arbovirus control
Alternative Title: Alternative Strategies for Arbovirus Control
- Nicole L. Achee
- John P. Grieco
- Hassan Vatandoost
- Gonçalo Seixas
- Joao Pinto
- Lee Ching-NG
- Ademir J. Martins
- Waraporn Juntarajumnong
- Vincent Corbel
- Clement Gouagna
- Jean-Philippe David
- James G. Logan
- James Orsborne
- Eric Marois
- Gregor J. Devine
- John Vontas
Department of Biological Sciences, Eck Institute for Global Health, University of Notre Dame, Notre Dame, Indiana, United States of America
Department of Medical Entomology & Vector Control, School of Public Health, Tehran University of Medical Sciences (TUMS), Tehran, Iran
Global Health and Tropical Medicine, GHTM, Instituto de Higiene e Medicina Tropical, IHMT, Universidade Nova de Lisboa, UNL, Lisboa, Portugal
Environmental Health Institute (EHI), National Environment Agency (NEA), Singapore
Instituto Oswaldo Cruz (IOC), Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro, Brazil
Department of Entomology, Kasetsart University (KU), Bangkok, Thailand
Institut de Recherche pour le Développement (IRD), Maladies Infectieuses et Vecteurs, Ecologie, Génétique, Evolution et Contrôle, University of Montpellier, Montpellier, France
Centre National de la Recherche Scientifique (CNRS), Laboratoire d'Ecologie Alpine (LECA), Université Grenoble-Alpes, Domaine universitaire de Saint Martin d'Hères, Grenoble, France
Department of Disease Control, London School of Hygiene and Tropical Medicine, London, United Kingdom
ARCTEC, London School of Hygiene and Tropical Medicine, London, United Kingdom
Université de Strasbourg, CNRS UPR 9022, INSERM U963, Strasbourg, France
QIMR Berghofer Medical Research Institute, Brisbane, Australia
Institute Molecular Biology and Biotechnology (IMBB), Foundation for Research and Technology (FORTH), Crete, Greece
Pesticide Science Lab, Agricultural University of Athens, Athens, Greece
- Pattamaporn Kittayapong (Editor)
Faculty of Science, Mahidol University, THAILAND
Publication date (epub): 1/2019
Publication date (collection): 1/2019
Mosquito-borne viruses—such as Zika, chikungunya, dengue fever, and yellow fever, among others—are of global importance. Although vaccine development for prevention of mosquito-borne arbovirus infections has been a focus, mitigation strategies continue to rely on vector control. However, vector control has failed to prevent recent epidemics and arrest expanding geographic distribution of key arboviruses, such as dengue. As a consequence, there has been increasing necessity to further optimize current strategies within integrated approaches and advance development of alternative, innovative strategies for the control of mosquito-borne arboviruses.
Methods and findings
This review, intended as a general overview, is one of a series being generated by the Worldwide Insecticide resistance Network (WIN). The alternative strategies discussed reflect those that are currently under evaluation for public health value by the World Health Organization (WHO) and represent strategies of focus by globally recognized public health stakeholders as potential insecticide resistance (IR)-mitigating strategies. Conditions where these alternative strategies could offer greatest public health value in consideration of mitigating IR will be dependent on the anticipated mechanism of action. Arguably, the most pressing need for endorsement of the strategies described here will be the epidemiological evidence of a public health impact.
As the burden of mosquito-borne arboviruses, predominately those transmitted by Aedes aegypti and A. albopictus, continues to grow at a global scale, new vector-control tools and integrated strategies will be required to meet public health demands. Decisions regarding implementation of alternative strategies will depend on key ecoepidemiological parameters that each is intended to optimally impact toward driving down arbovirus transmission.
International public health workers are challenged by the burden of arthropod-borne viral diseases, to include mosquito-borne arboviruses transmitted by Aedes aegypti and A. albopictus due in part to lack of sustainable vector control and insecticide resistance (IR), as well as the inability to scale up and sustain existing interventions for prevention of urban epidemics. As a consequence, there has been increasing interest to advance the development of alternative methods. This review provides a general overview of alternative vector-control strategies under development for the control of arbovirus mosquito vectors and highlights how each could offer innovative public health value. Considerations to regulations, acceptance, and sustainability are also provided.
International public health workers are challenged by a burden of mosquito-borne arboviral diseases despite best efforts in control programs. An estimated 4 billion people live in areas at risk for dengue virus transmission alone . Well-documented successes indicate that rigorously applied vector control using existing interventions can reduce arbovirus transmission and disease [,]; however, the degree to which such strategies may have prevented epidemics and the spread of arbovirus diseases is not well understood due to lack of evidence . Despite existing interventions, epidemics and spread of arbovirus diseases continue. The reasons for this are complex but include inadequate program implementation; ineffective coverage; lack of human, financial and infrastructural capacity; insecticide resistance (IR); political will; and inability to scale. Integrated approaches and advancements in development of alternative strategies have been of renewed focus. This review provides an overview of strategies under development for the control of arbovirus mosquito vectors, focusing primarily on Aedes aegypti and A. albopictus.
Rationale for developing alternative strategies
A primary strategy for arbovirus outbreak control, such as dengue, is the use of synthetic chemicals with quick-action killing of adult vectors using space spraying [,,]. The majority of recommended insecticides are of the pyrethroid chemical class, creating challenges to preventing selection pressure on susceptible mosquito populations as well as the control of pyrethroid-resistant vectors . Regarding arbovirus vector population management, specifically of A. aegypti, larval control has long been proposed and implemented as a primary strategy , including applications of chemical and microbial larvicides, insect growth regulators (IGRs), and bacterial toxins . Biological agents used against immatures include predatory copepods, fish, and Toxorhynchites larvae. Arguably, the greatest obstacle to A. aegypti larval control success is dependency on the ability to detect, access, and eliminate or treat domiciliary—often cryptic—breeding sites, a challenging and costly task that often leads to low coverage. In addition, their reduced efficiency in some occasions limits their widespread adoption .
Outlook on alternative strategy development
New tools are being developed on the premise that significant health benefit can be demonstrated in at least two endemic settings, aiming at niche roles rather than becoming the default intervention across a wide range of settings. Priority is given to tools that will improve current interventions in areas where they are challenged, either due to vector behaviors that prevent mosquito interaction with the intervention, IR, and/or residual disease transmission . Several new strategies and product classes are under review by the World Health Organization Vector Control Advisory Group (WHO VCAG)  (Fig 1).10.1371/journal.pntd.0006822.g001Fig 1
WHO VCAG overview of new vector control product classes and status of evaluation.
We have used the current VCAG portfolio as a basis for our “inclusion criteria” for interventions described in this review. Specifically, we review strategies for which evaluations (1) have previously been conducted against arbovirus mosquito vectors demonstrating evidence of entomological success (e.g., autodissemination using entomopathogenic fungi or pyriproxyfen, pyrethroid treated traps, attractive targeted sugar baits [ATSB], Wolbachia, genetic manipulation) and/or (2) are actively underway against arbovirus vectors (e.g., spatial repellents, treated materials, sterile insect technique [SIT]). We did not include strategies currently being evaluated only against anopheline vectors (e.g., insecticide-treated eave tubes). The exception is gene drive due to historical theory and/or evaluations of entomological impact, expectation of broad utility of this strategy across disease vectors, and potential to overcome challenges posed by traditional genetic manipulation. In addition, the VCAG met in Geneva in November 2016 to review new potential vector control based on “genetic manipulation of mosquitoes through gene drive technology to reduce vector populations and transmission”; therefore, gene drive is part of the portfolio of vector control tools (VCTs) under consideration by WHO .
WHO has formally recognized some of these strategies for arbovirus control and encouraged testing in affected countries following appropriate monitoring and evaluation procedures . Among the VCAG criteria for facilitating WHO recommendation, arguably the most critical is epidemiological evidence to endorse full-scale implementation. Funding to support rigorous pilot trials for generating preliminary evidence supportive of large-scale clinical trials as well as for randomized cluster trials themselves must be forthcoming. Where funding is not made available, support for delivering the requisite evidence base by other means, such as analyses of historical data captured during public health exercises, must be advocated. Other VCAG criteria include entomological correlates of protection, acceptability, and manufacturability (Table 1).10.1371/journal.pntd.0006822.t001Table 1
Example epidemiological−entomological parameters intended to demonstrate public health value of a new vector-control tool1.
|Epidemiology||A significant reduction in incidence of pathogen infections compared to control using randomized cluster trial. Level of compliance and coverage required in relation to efficacy detected.|
|Entomology||Trends indicating significantly reduced vector population density, longevity/population age structure (parity rates), and/or arbovirus infection over time between treatment arms.|
|Economics||Projected cost per unit protected similar to, or less than, currently deployed arbovirus vector-control strategy in trial setting.|
|Technology development||Prototype or product is essentially ready to manufacture at scale; may require minor changes to improve the method in response to trial outcomes.|
|Manufacturability sustainability||Confirmation of commercial sustainability by manufacturer/producer; early manufacturing/production runs at volume; intellectual property issues resolved and commercial production possible. Product procurements and pre- and post-marketing QA|
|User compliance/acceptability||User acceptability/compliance estimated.|
|Delivery and feasibility of implementation||Feasibility of intervention implementation demonstrated.|
|Regulatory/safety/ethical and environmental impact||Adverse events monitored during trial; registration of product.|
1Adapted from the WHO VCAG (http://www.who.int/neglected_diseases/vector_ecology/Operational_procedures_for_VCAG.pdf?ua=1)
Abbreviations: QA, quality assurance; VCAG, Vector Control Advisory Group; WHO, World Health Organization.
Novel larvicides and applications: Entomopathogenic fungi, pyriproxyfen, and autodissemination
Entomopathogenic Ascomycetes fungi, especially Metarhizium anisopliae and Beauveria bassiana, have been suggested for control of both larval and adult stages of dengue vectors . Fungal longevity (duration of efficacy once applied) may be one obstacle, with another being delivery of killing dose to target insect; therefore, formulation optimization is critical. Additionally, entomopathogens have fared badly in agriculture because they simply cannot compete with the costs and efficacy of chemical insecticides. This may change as insecticide regulation becomes more difficult and IR begins to dominate.
An approach to circumvent the difficulty of locating and treating immature habitats is autodissemination, wherein dispersal and transfer of actives is carried out by contaminated adult mosquitoes . Contamination can occur through treated materials  or dissemination stations such as modified ovitraps [,]. Once contaminated, mosquitoes disperse the agent in subsequent contacts with untreated surfaces. Autodissemination can exploit polygamic behavior whereby treated males can contaminate multiple females during mating . It is important to note that there must be amplification in coverage between the lure and aquatic habitat to achieve benefit beyond killing offspring of only contaminated adults.
An efficacy trial recently conducted in the United States showed a decline of A. albopictus populations following the field release of males contaminated with pyriproxyfen compared to untreated field sites , and the combination of pyriproxyfen autodissemination with the SIT (see below), a concept termed “Boosted SIT,” is being explored . Pilot interventions with pyriproxyfen have given promising results [,,]. Design of new types of dissemination stations and other actives  as well as new formulations (e.g., IGRs in combination with bacterial toxins of spinosad or fungi B. bassiana) may further improve effectiveness of autodissemination. Despite growing evidence of entomological efficacy, data requirements to demonstrate public health value are lagging (Table 1).
Spatial repellents are products designed to release volatile chemicals into an air space, induce insect behavior modification to reduce human-vector contact, and thereby reduce pathogen transmission . A spatial repellent product category is currently in Stage 3 of the VCAG assessment scheme, establishing proof-of-principle of efficacy through clinical trials (Fig 1). The application of spatial repellents at the household level through a consumer product market offers a “bottom-up” user-centric strategy for enhanced uptake (coverage), potentially overcoming challenges of scale . Evidence that community-led campaigns can impact transmission is needed. Spatial repellents may also be implemented through a donor-subsidized market similar to that used for insecticide-treated bed nets against malaria.
Studies have demonstrated that chemicals currently recommended for vector control can elicit varied responses dependent on concentration . For example, pyrethroids used in space spraying are applied at predominantly toxic levels to kill mosquitoes that land on treated surfaces or through contact with forced dispersal of formulated droplets. Other pyrethroids—labeled spatial repellents—such as transfluthrin and metofluthrin, are highly volatile at ambient temperature and disperse passively to repel, inhibit host-seeking, or kill mosquitoes depending on the chemical concentration gradient in the air space [,]. A range of spatial repellent products has demonstrated reduction in human−vector contact, and coils have been shown to contribute to reduction in human malaria infection [,]. Historically, the mode of action (MoA) of spatial repellent products has been focused on “movement away from the chemical source without the mosquito making physical contact with the treated surface” (deterrency), an expanded concept that reflects the complexity in defining spatial repellents, includes chemical actions that interfere with host detection and/or disrupt blood-feeding, and was established by WHO in 2013” . Knowledge gaps exist about how spatial repellents work, including exact molecular and physiological mechanisms , the hereditary basis by which spatial repellent traits are maintained in populations, and the relationship of response intensity with IR . All are vital characterizations required in discovery and optimization of spatial repellent compounds and formulated products.
Despite this, demonstration of efficacy in pyrethroid-resistant A. aegypti , as well as enhanced A. aegypti attraction response of gravid females to experimental ovipostion sites following exposure , may offer insights into complementary or synergistic roles for spatial repellents in integrated vector management strategies.
Mosquito traps have served for decades as effective surveillance tools but have only recently been considered under VCAG as a control strategy (Fig 1). For a trap to be an efficient tool for vector elimination, it must be highly sensitive and specific for a target species. The most effective traps rely on a combination of attractant cues such as light, heat, moisture, carbon dioxide, and synthetic chemicals for host attraction . The Centers for Disease Control and Prevention (CDC) miniature light trap was introduced in 1962 , but major advances have been made with newer traps that have incorporated innovations such as carbon dioxide plumes and counter flow geometry . Another trap recently developed is the Mosquito Magnet Pro (MMPro), which is commercially available and uses propane, making it affordable and easily deployable for the general public.
Expanding on the trap concept for arbovirus mosquito vector population reduction was the introduction of the lethal ovitrap. These traps are designed to attract and kill egg-bearing females. The attractive baited lethal ovitrap (ALOT) has shown promise in both laboratory and field settings for significantly reducing Aedes populations. A prospective nonrandomized field trial of the ALOT trap was conducted in two cohorts of Iquitos, Peru. One year into the trial, dengue incidence as measured by febrile surveillance was 75% lower in the intervention area compared to the control cohort . Although there have been a number of unsuccessful attempts to document significant reductions in vector densities using lethal ovitraps, it appears that sufficient coverage with an appropriate number of traps per unit area is key to this strategy’s success . Other research has demonstrated potential of the baited gravid (BG)-Sentinel trap as a vector-control tool . Studies with area-wide use of autocidal gravid ovitrap (AGO) in Puerto Rico have shown 80% reduction in densities of female A. aegypti for up to 1 year . In Brazil, significant reductions in densities of gravid A. aegypti by the biogents passive gravid Aedes trap (BG-GAT)  was achieved.
Incorporating a distribution model of peridomestic lethal ovitraps to remove gravid females from the vector population is anticipated to complement current A. aegypti control campaigns focused on source reduction of larval habitats. As naturally preferred oviposition sites are removed from the environment, artificial traps may become more effective at reducing vector populations; however, routine monitoring and/or retrieving of traps, if no longer used, must be incorporated to avoid traps becoming potential breeding sites in scaled control programs. In anticipation of success based on this concept, WHO has currently developed guidelines for efficacy testing of traps against arbovirus vectors to include indicators [http://apps.who.int/iris/bitstream/handle/10665/275801/WHO-CDS-NTD-VEM-2018.06-eng.pdf?ua=1].
The ATSB product class is currently at Stage 2 of the VCAG evaluation pathway (Fig 1). The success of an ATSB strategy relies on attracting mosquitoes to and having them feed on toxic sugar meals sprayed on plants or used in bait stations. The use of sugar feeding to reduce mosquito populations was first reported by Lea in 1965  and then other studies [–] in A. albopictus, other culicines, and sand flies.
ATSBs for both indoor and outdoor control of mosquito vectors may impact populations by direct mortality induced by feeding on an insecticide bait, and/or, dissemination through a bait of mosquito pathogens or nonchemical toxins . Because both female and male mosquitoes require sugar throughout the adult lifespan, the potential effects of this intervention on a vector population may be dramatic but will depend on feeding behavior (e.g., readiness to sugar feed indoors). Bait solutions are composed of sugar, an attractant, and an oral toxin. Toxins tested include boric acid , spinosad, neonicotinoids, and fipronil , as well as several other classes of insecticide . Some attractants are focused on locally acquired sugars, juices, and fruit as mosquitoes may be selective toward carbohydrates originating from their geographic range, although more “general” attractants have been developed more recently [,].
A cumulative effect of ATSBs on an anopheline mosquito population was demonstrated for an area with alternative sugar sources resulting in delayed population level lethality as compared to sugar-poor areas , suggesting its utility in arid environments. A single application of an ATSB affected Anopheles sergentii density, parity, survival, and hence vectorial capacity . Potential drawbacks of this strategy might be the effects on nontarget sugar-feeding organisms, as well as the high coverage required. Environmental, safety, and cost estimates are being explored as part of the WHO VCAG requirements for demonstration of public health value (Table 1).
Insecticide-treated materials (ITMs) can provide bite protection by killing or repelling vectors. ITMs, in the form of clothing, can be worn outside during the day, at work, or in school, offering protection where current mosquito control strategies, such as bed nets, may not. Military and other commercial companies have used insecticide-treated clothing to protect their workers from biting arthropods, and ITMs have reduced the incidence of vector-borne diseases such as malaria and leishmaniasis .
Currently, an ITM strategy for vector control is in Stage 1 of VCAG evaluations (Fig 1), with permethrin (a pyrethroid) being the only active ingredient used in ITMs due to requirements of meeting human safety profiles . Permethrin ITMs have demonstrated personal protection against A. aegypti mosquitoes in various laboratory experiments [–], reduction of A. aegypti human biting rates by 50% (partial limb coverage) to 100% (when fully clothed) in semifield trials [,], and an 80% reduction in A. aegypti densities after just one month of children wearing permethrin treated school uniforms . Models have estimated permethrin-treated uniforms could reduce dengue infections by up to 55% in the most optimistic scenarios .
Despite the potential for ITMs to control arbovirus vectors, current application techniques and formulations have limited efficacy under general use as permethrin washes out of material after several washes and is degraded by UV and heat exposure [,]. Novel formulations are needed to achieve long-lasting, effective release of permethrin under anticipated use. A technology being developed to address this challenge is microencapsulation, which binds deeper within the fabric and increases insecticide stability, allowing for a more consistent and extended release of the active ingredient . Novel active ingredients that have far-ranging efficacy compared to permethrin and/or represent a different chemical class (including natural ingredients) will be needed to overcome biting on exposed skin not covered by ITMs, as well as to address pyrethroid resistance, respectively .
As with other alternative strategies under evaluation, it will be imperative that epidemiological evidence be generated in robust trial designs before wider implementation of ITMs can be recommended. Efficacy of ITMs will be dependent on user compliance; therefore wearable technologies must be acceptable to target populations (see “Acceptability and compliance of alternative methods” section).
The sterile insect technique (SIT) is based on the release of sterilized male insects, traditionally by means of irradiation, to suppress vector mosquito populations. SIT induces random lethal dominant mutations in the germ cells, which acts on the eggs in the female to prevent fertilization . The concept is that sterile males will mate with wild females without producing any offspring. A major challenge to scale implementation has been building infrastructure in endemic settings to support mass rearing of the target vector. New technologies for mass rearing of mosquitoes, especially Aedes, are currently available [–]; however, improvement in the sterilization process is still needed to avoid somatic damage, resulting in reduction of longevity, problems with sexual vigor, and overall male activity . Although encouraging results of SIT have been obtained with A. albopictus , operational cost still constitutes a significant barrier to large-scale rearing facilities in endemic countries.
Release of insects with dominant lethality
The release of insects with dominant lethality (RIDL) strategy reduces vector populations (self-limiting approach) through individuals carrying a transgenic construct, which acts on the late larval stage and the pupae to prevent survival to imago. In contrast to both SIT and Wolbachia-based population suppression (see “Gene drives” section), for RIDL technology, eggs must become fertilized for subsequent impact. The engineered effector gene is homozygous, repressible dominant lethal, and activates its own promoter in a positive feedback loop but can be regulated using an external activator. The construct also includes a reporter gene resulting in RIDL insects expressing a visible fluorescent marker for easy screening of transgenic and hybrid individuals before and after an intervention .
RIDL transgenic constructs have been successfully integrated into A. aegypti laboratory strains by Oxitec,which has performed open release trials with the OX513A strain since 2009 in Brazil, Cayman Islands, and Panama, with approvals pending for trials in the US and India. In Brazil, Panama, and Cayman, wild A. aegypti populations were reduced by more than 90% after release of the OX513A strain [,]. The sustainability of this reduction will depend on methods to avoid a new population increase from the remaining insects, hatching of dried eggs, and migration from uncontrolled areas. A continued monitoring system will provide a better overview of the impact of this method in long-term suppression of A. aegypti.
Although the RIDL strategy has advanced to VCAG Stage 3 (Fig 1), a concern was that the reduction of A. aegypti could favor its replacement by A. albopictus. It should be noted that suppression of a population by any technique might encourage invasion and replacement by competitors. In Panama, however, six months after the OX513A A. aegypti releases ceased, there was no evidence of either expansion or augmented density of A. albopictus where both species occurred in sympatry .
Wolbachia is a natural intracellular bacterial symbiont found in at least 60% of insects known to alter reproduction of its host. Present in the female germline of an infected insect, Wolbachia is maternally transmitted to offspring. It can induce cytoplasmic incompatibility (CI), where mating between Wolbachia-infected males and uninfected females yields eggs that fail to develop. Regular releases of male mosquitoes infected with a Wolbachia strain not present in the wild-type mosquito could theoretically reduce the viability of eggs in the field and lead to population suppression. Alternately, Wolbachia strains may cause a decrease in the vectorial capacity of the vector (pathogen interference)—directly by interfering with competence or indirectly by shortening lifespan . The wMel Wolbachia strain currently being assessed by VCAG, in Stage 3 of evaluations, is intended for population replacement that interferes with ability to transmit pathogens (Fig 1).
Regarding population suppression, though it was reported almost 50 years ago that Culex pipiens fatigans was eradicated via CI in a village in Myanmar (then Burma), it was only in 1971 that the involvement of Wolbachia was reported . Successes in species-specific suppression using inundative male releases have been demonstrated in semifield and full-field trials involving Aedes polynesiensis in French Polynesia  and A. albopictus in Lexington, Kentucky, US . Releases involving Wolbachia−A. aegypti have also started in California, Thailand, Singapore, and Australia. The safety of the approach has been thoroughly evaluated and reported . Although results of field studies have been promising, full-scale sustainable deployment of a Wolbachia strategy requires more developmental efforts. Besides the need for an arsenal of Wolbachia vector strains that offers excellent CI, there is a need for active community engagement to gain public acceptance and a need to scale up the production of large numbers of Wolbachia mosquitoes through automation and optimization.
The population replacement strategy is based on the capacity of Wolbachia to invade and persist in wild mosquito populations, decreasing their vector competence . Advantages of a replacement strategy, at its full potential, is the lack of requirement for consistent and continuing releases or reliance on community engagement to achieve near universal coverage. In the case of A. aegypti, the Wolbachia evaluation of a population replacement strategy has achieved important goals, such as a fruit fly Wolbachia strains can invade and sustain themselves in mosquito populations, reduce adult lifespan, affect mosquito reproduction, and interfere with pathogen replication . So far three Wolbachia transinfection strains have been used in A. aegypti: wAlbB  introduced from A. albopictus, and wMel and wMelPop from Drosophila melanogaster . The wMel Wolbachia strain has the ability to reduce A. aegypti vectorial capacity to dengue and chikungunya viruses [,], an encouraging result recently extended to Zika virus, as indicated by experimental infection and transmission assays in wMel-infected mosquitoes .
The World Mosquito Program aims to promote research in arbovirus control by releasing Wolbachia-infected A. aegypti in dengue-affected communities (www.eliminatedengue.com). The first release occurred in Australia in 2011. Two natural populations were successfully invaded after 10 weekly releases, nearly reaching fixation five weeks after releases stopped . This high infection rate has been maintained through 2017 without further input. The substitution of a natural A. aegypti population by a wMel-infected A. aegypti one prompted a scale up to other countries, including Vietnam, Indonesia, Brazil, and Colombia.
Gene drives are transgenic constructs that possess the property to invade populations of the target species, even when conferring a fitness cost. The concept applied to mosquito control was proposed by Austin Burt as early as 2003  and has since been a topic of research to spread a desired trait in mosquito species.
Current gene drive designs are based on the Clustered Regularly Interspaced Short Palindromic Repeats—CRISPR-associated protein 9 (CRISPR-Cas9) system. The transgenic element must be inserted precisely in the sequence that it is designed to cleave. To achieve this, a “cassette” is integrated by “gene knock-in” . The drive cassette thus becomes heritable and able to “drive” (Fig 2). Alternatively, docking sites can be knocked in the gene of interest and subsequently serve as acceptors for the gene drive cassette .10.1371/journal.pntd.0006822.g002Fig 2
Principle of a gene drive.
(A) Initial integration of a gene drive construct into the mosquito genome: Cas9 and the gRNAs encoded in the transgenic construct prepared as a plasmid can serve as molecular scissors mediating their own integration into the genomic target site they cut. Asterisks represent the cut sites determined by the gRNAs (three gRNAs in this example). Homologous recombination-mediated knock-in of the transgenic cassette occurs thanks to the target site flanking sequences cloned into the plasmid. (B) Spread of the gene drive in a mosquito population: mating between transgenic and nontransgenic mosquitoes places the transgenic construct in the presence of wild-type chromosomes that get cut by Cas9 at the target site determined by the gRNA(s). This break is repaired most frequently by homologous recombination with the intact chromosome, effectively copying the trans-gene into the broken wild-type chromosome and converting a heterozygous into homozygous cell. Cas9, CRISPR associated protein 9; gRNA, guide RNA.
Two strategies are under evaluation in VCAG Step 1 based on gene drives—population replacement and population suppression (Fig 1). In the latter, a drive element can be designed to insert into and inactivate a sex-specific fertility gene, suppressing the population as the resulting “sterility allele” increases its frequency. This approach was illustrated by a recent proof-of-principle laboratory study in the African malaria vector Anopheles gambiae  and could rapidly be adapted to A. aegypti and A. albopictus. Gene drives may prove to function less efficiently in the field than in the laboratory  due to the selection of pre-existing refractory variants in the guide RNA (gRNA) targets. Should gene drives function almost as efficiently in the field as in theory, the suppression approach carries the potential to eradicate the target species altogether, although insect population substructuring would probably allow the existence of residual pockets of intact populations [,].
Gene-drive designs for population suppression are not yet optimal for release in the field; a female sterility-spreading gene drive will only function optimally if heterozygous females are fully fertile, which is not the case of the published designs. Optimized promoters that restrict Cas9 activity to germline tissues, or Cas9 variants with shorter half-lives, are avenues to explore to alleviate these limitations. A careful evaluation of the ecological impact of species eradication must be considered. Gene-drive animals represent a new class of genetically modified organism (GMO), the safety of which will need to be evaluated according to new criteria compared to traditional GMOs. This and other considerations, such as horizontal transfer, are the focus of a recent US National Academy of Sciences report on gene drives .
Gene drives can also be applied in population replacement strategies—using a drive construct to confer mosquito resistance to a given pathogen resulting in a population that becomes pathogen resistant as the genetic invasion progresses. Proof-of-principle has been demonstrated in the laboratory using the Asian malaria vector Anopheles stephensi . In Aedes, antiviral constructs could be designed similarly, targeting one or several viruses. Candidate antiviral factors include RNA interference (RNAi) constructs, overexpressed components of the antiviral response, or RNA-targeting molecular scissors such as the recently identified CRISPR-Cas-like system C2c2 . In all cases, it will be important to ascertain increasing resistance to a given virus does not render mosquitoes more susceptible to another.
Other alternative strategies outside the VCAG portfolio
Considerations for introducing alternative strategies
Resistance management potential
IR in arbovirus vectors, such as A. aegypti, is considered a major obstacle to successful control . The incidence of IR has increased rapidly in recent years , and concerns regarding environmental impact caused from insecticide residues continue . This highlights the need for alternative methods to better manage arbovirus vector populations while mitigating selection pressure on existing IR genes . Other WIN reviews will describe IR distribution, mechanisms, and management; we present here complementary considerations on the integration of alternative strategies for resistance. The use of nonchemicals, or chemicals with completely different MoAs (i.e., alternate target site), will potentially have a greater impact on insecticide resistance management (IRM), such as using IGRs for larval and pyrethroids for adult A. aegypti control, respectively . Combination or rotations of unrelated compounds can (in theory) mitigate the occurrence of resistance and/or delay the selection process if already present at low levels. This may not hold true when considering metabolic resistance mechanisms by which one enzyme degrading one insecticide with a particular MoA may also degrade another insecticide with a different MoA. Reciprocally, two insecticides with the same MoA may not be degraded by the same enzymes (no cross metabolic resistance). The authors acknowledge that any tool is vulnerable to resistance development; therefore, robust monitoring and evaluation should accompany implementation.
The potential of example alternative strategies to impact IRM is indicated in Table 2, whereas details of resistance risks are presented in Fig 3. There are a number of ways in which alternative strategies can control insecticide-resistant vectors, including different MoAs or different application methods (i.e., oral versus contact). Tests are available to measure and predict this "antiresistance" potential at several stages of product development; however, evidence is missing, for example, on the impact of target site resistance to pyrethroids on efficacy of transfluthrin (a pyrethroid spatial repellent) to reduce human infections in settings with resistant vector populations, or the efficacy of pyriproxyfen against insects overexpressing cytochrome P450s capable of metabolizing pyrethroids. In addition to cross resistance and efficacy assessments against pyrethroid-resistant mosquitoes, the introduction of novel active ingredients into VCTs requires careful monitoring of possible resistance development.10.1371/journal.pntd.0006822.g003Fig 3
Current and alternative arbovirus control methods in the context of the targeted life stage of implementation and anticipated impact on IRM.
IGR, insect growth regulator; IRM, insecticide resistance management; RIDL, release of insects with dominant lethality; ULV, Ultra-low volume spraying].10.1371/journal.pntd.0006822.t002Table 2
Summary description of alternative vector-control tools, primary challenges, and benefits to include probability of mitigating evolutionary response/impact in resistance management.
|Product category (strategy)||MoA1||Prototype product description||Intended application in operational deployment; primary challenge to success; primary benefit of operational deployment||Impact in resistance management based on MoA|
|Novel larvicide approaches||S/L||IGRs||Outdoors in immature habitats; presence of cryptic habitats; traditional deployment strategy||High|
|S/L||Microbial insecticides (Bacillus thuringiensis israelensis||Outdoors in immature habitats; presence of cryptic habitats; traditional deployment strategy/aerial spray||High|
|S/L||Entomopathogenic fungi||Indoors and outdoors; lethal effects to nontargets; can be applied on various surfaces||High|
|Spatial repellents||C||Passive emanator to reduce human−vector contact||Indoors and outdoors; resistance to currently available actives; can be delivered using consumer-product channels||Dependent on target site of actives|
|Traps||S||Captures and removes host seeking and/or gravid females||Indoors and outdoors; bulk; affordable and easy to use||Dependent on target site of actives|
|ATSBs||S/L||Attract and kill females and males (of all physiological status)||Outdoors; lethal effects to nontargets; easy to use||Dependent on target site of actives|
|ITMs||C||Clothing, blankets, screens, curtains with insecticides or spatial repellents||Indoors and outdoors; acceptability/behavior change by end-user; mobile technology||Dependent on target site of actives|
|Classical SIT||S/L||Release of radiated sterile male insects to sterilize females||Indoors and outdoors; colony maintenance, multiple releases, mating competitiveness; no nontarget effects||High|
|RIDL||S||Release of transgenic insects with dominant lethal construct to eliminate female progeny production||Indoors and outdoors; colony maintenance, multiple releases; no nontarget effects||High|
|Wolbachia||R||Population replacement (vectorial capacity)||Indoors and outdoors; colony maintenance, multiple releases, mating competitiveness; regulations for release||Moderate|
|S/L||Population suppression (CI)||Indoors and outdoors; colony maintenance, multiple releases, mating competitiveness; no nontarget effects||High|
|Gene drives||R||Population replacement (introduction and spread of pathogen effector gene)||Indoors and outdoors; off-target effects (molecular); rate of spread through population||Low|
|S/L||Population suppression (introduction and spread of lethal gene)||Indoors and outdoors; off-target effects (molecular); rate of spread through population||High|
1Primary Entomological MoA: S, population suppression; R, population replacement; L, reduction of mosquito longevity and density; C, reduction of human-vector contact.
Abbreviations: ATSB, attractant toxic sugar baits; CI, cytoplasmic incompatibility; IGR, insect growth regulators; ITM, insecticide-treated materials; MoA, mode of action; RIDL, release of insects with dominant lethality; SIT, sterile insect technique.
Strategies used for IRM and the introduction of new VCTs is adopted from agricultural practices , for which another WIN review is forthcoming. IRM should be applied within integrated vector management (IVM) approaches , which is defined as the rational decision-making process for the optimal use of resources for vector control  and includes the use of multiple complementary tools. An important point to stress is that a novel vector-control product may be more useful via its role in IRM in a certain setting with high levels of resistance risk, even if it is of a similar efficacy to existing interventions (“non inferior”).
Knowledge base on mosquito biology and behavior
The importance of characterizing the biological profile (genetic structure, insecticide susceptibility) of the local vector population should be considered in the context of IVM and IRM using alternative strategies. For instance, the first release of Wolbachia in Rio de Janeiro, Brazil, did not succeed, because the spread of the bacteria was not self-sustained. Although wMel Wolbachia was already hosted by around 60% of the local A. aegypti after 20 weeks of insertion, this frequency rapidly dropped when releases stopped. This may likely have occurred because the released wMel-infected A. aegypti strain was susceptible to pyrethroids, the class of insecticide largely used by residents in dwellings. It was known that the natural A. aegypti population of that locality was highly resistant to pyrethroids. When a new colony of A. aegypti, as resistant as the field population, was infected with wMel and released in the field for 24 weeks, 80% of local A. aegypti presented the bacteria, and this index is continually increasing [,]. Additional characterizations of importance include male feeding behavior for optimizing ATSB and genotyping key phenotypes to identify targets for gene drives.
Acceptability and compliance of alternative methods
Social science, effective training of staff, and capacity building have major roles in the deployment of novel VCTs. New interventions must be acceptable to the communities in which it will be used. One possible barrier is that homeowners might perceive the intervention as ineffective or harmful to themselves or their environment, and adoption of the strategy might be compromised. For example, populations may be reluctant to use juvenoids (e.g., pyriproxyfen) because the insecticide has a late killing action on pupae, leaving live larvae in the container. Regardless of how efficacious a control strategy may prove to be during proof-of-concept, it is critical to assess the potential barriers and/or acceptance of local populations in which implementation trials may occur early in the development phase, even within a limited participant population [,]. More robust surveys can be used once an intervention prototype is available . Such surveys can be used to assess factors associated with adoption and maintenance behaviors and identify barriers to its correct and consistent use to ensure (or improve) product sustainability.
Regulatory considerations for alternative control strategies
Regulatory considerations are required early in the development process to ensure data requirements are met for safety and use (Table 1). If a tool under investigation does not fall under an existing product category (i.e., is a new class), a new regulatory framework and/or data requirements may be warranted. It is important to note, regulation can be as substantial an obstacle to an effective intervention as any gap in research and development (R&D). Where regulations are prohibitive, options for arbovirus control will become even more constrained; this may be most evident when a lack of expertise and/or infrastructure exists around the new tool (e.g., biotechnology and gene drives).
Historically, the WHO Pesticide Evaluation Scheme (WHOPES) was the body responsible for review of product evaluation and recommendations . However, a reform in the regulatory process for evaluation of new products has been made with the recent agreement by WHO to adopt the Innovation to Impact (I2I) initiative in 2017 . The I2I is expected to accelerate the evaluation process, increase transparency, and improve quality assurances, similar to the framework already adopted for drug and vaccine prequalifications . Development of new guidelines or modifications of existing ones for efficacy testing of alternative VCTs are anticipated to be needed as novel MoA are exploited. Likewise, if the formulated product under investigation is not registered in the study area for which it will be evaluated, experimental use permits or similar must be obtained before investigations begin. Proprietary protection for evaluation of product formats still under development should follow industry specifications.
Arboviruses transmitted by Aedes mosquitoes represent major international public-health concerns that will surely require a range of integrated interventions to be effectively controlled. As the scope of arboviruses continues to grow, development and evaluation of alternative vector-control products and strategies are critical to pursue. Following endorsement by global, national, and local authorities, effective strategies will have to be locally adapted to take into account the biology of the vector and virus transmission intensity, as well as human and financial resources. This review focuses on alternative strategies mainly for control of A. aegypti and A. albopictus because these two species are arguably the primary arbovirus vectors in the world. Alternative strategies will provide additional options for arbovirus control and potentially add value to existing strategies; however, until operational effectiveness and frameworks for use are in hand, further optimization of current strategies is warranted, to include innovative delivery methods of existing products (e.g., targeted indoor residual spraying ).
Top five papers
Novel larvicides and/or autodissemination: Devine GJ, Perea EZ, Killeen GF, Stancil JD, Clark SJ, Morrison AC. Using adult mosquitoes to transfer insecticides to Aedes aegypti larval habitats. Proceedings of the National Academy of Sciences. (2009);106(28):11530–4. 
Spatial repellents: Norris, Edmund J., and Joel R. Coats. Current and Future Repellent Technologies: The Potential of Spatial Repellents and Their Place in Mosquito-Borne Disease Control. Int. J. Environ. Res. Public Health (2017): 14(2), 124; 10.3390/ijerph14020124. 
Traps: Barrera R, Acevedo V, Felix GE, Hemme RR, Vazquez J, Munoz JL, Amador M. Impact of autocidal gravid ovitraps on chikungunya virus incidence in Aedes aegypti (Diptera: Culicidae) in areas with and without traps. Journal of medical entomology. (2016);54(2):387–95. 
ATSBs: Fiorenzano J. M., Philip G. Koehler P. G., Xue R-D. Attractive Toxic Sugar Bait (ATSB) For Control of Mosquitoes and Its Impact on Non-Target Organisms: A Review. Int J Environ Res Public Health. (2017); 14(4): 398. 
ITMs: Banks, S. D., Murray, N., Wilder-Smith, A. and Logan, J. G. Insecticide-treated clothes for the control of vector-borne diseases: a review on effectiveness and safety. Med Vet Entomol. (2014): 28: 14–25. doi:10.1111/mve.12068. 
SIT/ RIDL:Alphey L., McKemey A., Nimmo D., Oviedo M.N., Lacroix R., Matzen K., Beech C. Genetic control of Aedes mosquitoes. Pathog Glob Health. (2013); 107(4): 170–179. 
Gene drives: Hammond A, Galizi R, Kyrou K, Simoni A, Siniscalchi C, Katsanos D, et al. A CRISPR-Cas9 gene drive system targeting female reproduction in the malaria mosquito vector Anopheles gambiae. Nature biotechnology (2016): 34(1): 78–83. 
Key learning points
Arboviruses such as dengue, Zika, and chikungunya are reemerging worldwide with increasing prevalence and/or severity.
Decades of efforts have failed to consistently control Aedes spp. mosquito populations and/or to curtail the cycle of arbovirus epidemics. Reasons are complex and include inadequate program implementation; lack of human, financial, and infrastructural capacity; IR; and inability to scale up existing interventions.
Several alternative Aedes spp. arbovirus vector-control strategies are in the development pipeline and under evaluation, including biological and chemical approaches, but lack evidence with regards to when and where such strategies and/or products could offer greatest public health value and contribute to managing IR.
Alternative strategies will need to be introduced using an approach of integrated vector management to include optimization of current methods, such as innovative delivery of existing products.
An alternative vector-control strategy may be more useful via its role in integrated resistance management, even if it is of a similar efficacy to existing interventions.
The paper was written based on consultations during a Worldwide Insecticide resistance Network (WIN) meeting held in Montpelier, France, in May 2016, plus additional literature searches. Additional editorial support was provided by Ms. Claire Durot of WIN, Ms. Marianne Krebs and Ms. Diane Choi of the University of Notre Dame.
- OJ Brady, PW Gething, S Bhatt, JP Messina, JS Brownstein, AG Hoen, et alRefining the Global Spatial Limits of Dengue Virus Transmission by Evidence-Based Consensus. PLoS Negl Trop Dis2012;6(8):e176010.1371/journal.pntd.000176022880140
- NL Achee, F Gould, T Perkins, RC Reiner, AC Morrison, SA Ritchie, et alA Critical Assessment of Vector Control for Dengue Prevention. PLoS Negl Trop Dis2015;9(5):e000365510.1371/journal.pntd.000365525951103
- D Roberts, R Tren, R Bate, J Zambone. The Excellent Powder: DDT's Political and Scientific History. Dog Ear Publishing; 2016.
- O Horstick, S Runge-Ranzinger, MB Nathan, A Kroeger. Dengue Vector-Control Services: How Do They Work? A Systematic Literature Review and Country Case Studies. Trans R Soc Trop Med Hyg2010;104(6):379–386. 10.1016/j.trstmh.2009.07.02720400169
- V Corbel, NL Achee, F Chandre, MB Coulibaly, I Dusfour, DM Fonseca, et alTracking Insecticide Resistance in Mosquito Vectors of Arboviruses: The Worldwide Insecticide Resistance Network (WIN). PLoS Negl Trop Dis2016;10(12):e000505410.1371/journal.pntd.000505427906961
- World Health Organization. Dengue: Guidelines for Diagnosis, Treatment, Prevention and Control. 200923762963
- MA Rodríguez-Pérez, AF Howard, F Reyes-Villanueva. Integrated Pest Management and Pest Control-Current and Future Tactics Rijeka, Croatia. Integrated Pest Management and Pest Control—Current and Future Tactics2012.
- S Poopathi. and S Abidha. Mosquitocidal Bacterial Toxins (Bacillus sphaericus and B. thuringiensis serovar israelensis): Mode of Action, Cytopathological Effects and Mechanism of Resistance. Journal of Physiology and Pathophysiology2010;1(3):22–38.
- BA Federici. Bacteria as Biological Control, Agents for Insects: Economics, Engineering, and Environmental SafetyNovel Biotechnologies for Biocontrol Agent Enhancement and Management: Springer, Dordrecht; 2007 p. 25–51.
- World Health Organization. Vector Control Advisory Group (VCAG) on New Paradigms. Available from: http://www.who.int/neglected_diseases/vector_ecology/VCAG/en/ [cited 2018 Nov 26].
- World Health Organization-VCAG. Fifth Meeting of the Vector Control Advisory Group. Available from: http://apps.who.int/iris/bitstream/handle/10665/255824/WHO-HTM-NTD-VEM-2017.02-eng.pdf. [cited 2018 Nov 26].
- World Health Organization. Mosquito Control: Can it Stop Zika at Source? WHO 2017. Available from: http://migre.me/tDWVe. [cited 2018 Nov 26].
- E Scholte, BGJ Knols, RA Samson, W Takken. Entomopathogenic Fungi for Mosquito Control: a Review. Journal of insect science (Online)2004;4(1):19.15861235
- T Itoh, H Kawada, A Abe, Y Eshita, Y Rongsriyam, A Igarashi. Utilization of Bloodfed Females of Aedes aegypti as a Vehicle for the Transfer of the Insect Growth Regulator Pyriproxyfen to Larval Habitats. J Am Mosq Control Assoc1994;10(3):344–347. 7807075
- Takashi Tsunoda, Hitoshi Kawada, Loan Le Luu Trang TT Huynh, Huu Ngoc Tran San Hoang Le, et alField Trial on a Novel Vontrol Method for the Dengue Vector, Aedes aegypti by the Systematic Use of Olyset? Net and Pyriproxyfen in Southern Vietnam. Parasites & Vectors2013;6(1):6.23312018
- B Caputo, A Ienco, D Cianci, M Pombi, V Petrarca, A Baseggio, et alThe "Auto-Dissemination" Approach: a Novel Concept to Fight Aedes albopictus in Urban Areas. PLoS Negl Trop Dis2012;6(8):e179310.1371/journal.pntd.000179322953015
- Devine Gregor J, Perea Elvira Zamora, Killeen Gerry F., Stancil Jeffrey D., Suzanne J. Clark, Morrison Amy C., et alUsing Adult Mosquitoes to Transfer Insecticides to Aedes Aegypti Larval Habitats. Proceedings of the National Academy of Sciences of the United States of America2009;106(28):11530–11534. 10.1073/pnas.090136910619561295
- JW Mains, CL Brelsfoard, SL Dobson. Male Mosquitoes as Vehicles for Insecticide. PLoS Negl Trop Dis2015;9(1):e000340610.1371/journal.pntd.000340625590626
- J Bouyer, T Lefrançois. Boosting the Sterile Insect Technique to Control Mosquitoes. Trends in parasitology2014;30(6):271–273. 10.1016/j.pt.2014.04.00224746400
- F Abad-Franch, E Zamora-Perea, G Ferraz, SD Padilla-Torres, SLB Luz. Mosquito-Disseminated Pyriproxyfen Yields High Breeding-Site Coverage and Boosts Juvenile Mosquito Mortality at the Neighborhood Scale. PLoS Negl Trop Dis2015;9(4):e000370210.1371/journal.pntd.000370225849040
- Kartzinel Mark A, Alto Barry W, Deblasio Michael W, Burkett-Cadena Nathan D. Testing of Visual and Chemical Attractants in Correlation with the Development and Field Evaluation of an Autodissemination Station for the Suppression of Aedes aegypti and Aedes albopictus in Florida. Journal of the American Mosquito Control Association2016;32(3):19410.2987/16-6555.127802398
- NL Achee, MJ Bangs, R Farlow, GF Killeen, S Lindsay, JG Logan, et alSpatial Repellents: from Discovery and Development to Evidence-Based Validation. Malar J2012;11:16410.1186/1475-2875-11-16422583679
- E Norris, J Coats. Current and Future Repellent Technologies: The Potential of Spatial Repellents and Their Place in Mosquito-Borne Disease Control. International Journal of Environmental Research and Public Health2017;14(2):124.
- JP Grieco, NL Achee, T Chareonviriyaphap, W Suwonkerd, K Chauhan, MR Sardelis, et alA New Classification System for the Actions of IRS Chemicals Traditionally Used For Malaria Control. PLoS ONE2007;2(8):e71610.1371/journal.pone.000071617684562
- N Achee, P Masuoka, P Smith, N Martin, T Chareonviryiphap, S Polsomboon, et alIdentifying the Effective Concentration for Spatial Repellency of the Dengue Vector Aedes aegypti. Parasit Vectors2012;5:30010.1186/1756-3305-5-30023273133
- SA Ritchie, GJ Devine. Confusion, Knock-Down and Kill of Aedes aegypti Using Metofluthrin in Domestic Settings: a Powerful Tool to Prevent Dengue Transmission?Parasit Vectors2013;6(1):26210.1186/1756-3305-6-26224025232
- N Hill, HN Zhou, P Wang, X Guo, I Carneiro, SJ Moore. A Household Randomized, Controlled Trial of the Efficacy of 0.03% Transfluthrin Coils Alone and in Combination with Long-Lasting Insecticidal Nets on the Incidence of Plasmodium falciparum and Plasmodium vivax Malaria in Western Yunnan Province, China. Malar J2014;13:20810.1186/1475-2875-13-20824885993
- D Syafruddin, MJ Bangs, D Sidik, I Elyazar, PBS Asih, K Chan, et alImpact of a Spatial Repellent on Malaria Incidence in Two Villages in Sumba, Indonesia. Am J Trop Med Hyg2014;91(6):1079–1087. 10.4269/ajtmh.13-073525311699
- World Health Organization, WHO Pesticide Evaluation Scheme. Guidelines for Efficacy Testing of Spatial Repellents. 2013.
- JD Bohbot, JC Dickens. Odorant Receptor Modulation: Ternary Paradigm for Mode of Action of Insect Repellents. Neuropharmacology2012;62(5–6):2086–2095. 10.1016/j.neuropharm.2012.01.00422269900
- JM Wagman, NL Achee, JP Grieco. Insensitivity to the Spatial Repellent Action of Transfluthrin in Aedes aegypti: A Heritable Trait Associated with Decreased Insecticide Susceptibility. PLoS Negl Trop Dis2015;9(4):e000372610.1371/journal.pntd.000372625879206
- S Horstmann, R Sonneck. Contact Bioassays with Phenoxybenzyl and Tetrafluorobenzyl Pyrethroids Against Target-Site and Metabolic Resistant Mosquitoes. PLoS ONE2016;11(3):e014973810.1371/journal.pone.014973826930058
- DB Choi, JP Grieco, CS Apperson, C Schal, L Ponnusamy, DM Wesson, et alEffect of Spatial Repellent Exposure on Dengue Vector Attraction to Oviposition Sites. PLoS Negl Trop Dis2016;10(7):e000485010.1371/journal.pntd.000485027428011
- J Spitzen, RC Smallegange, W Takken. Effect of Human Odours and Positioning of CO2 Release Point on Trap Catches of the Malaria Mosquito Anopheles gambiae Sensu Stricto in an Olfactometer. Physiological Entomology2008;33(2):116–122.
- DD Stamm, RW Chamberlain, WD Sudia. Arbovirus Studies in South Alabama, 1957–1958. Am J Hyg1962;76:61–81. 13916153
- DL Kline. Comparison of Two American Biophysics Mosquito Traps: the Professional and a New Counterflow Geometry Trap. J Am Mosq Control Assoc1999;15(3):276–282. 10480115
- D Wesson, A Morrison, V Paz Soldan, R Moudy, K Long, L Ponnusamy, et alLethal Ovitraps and Dengue Prevention: Report from Iquitos, Peru. International Journal of Infectious Diseases2012;16:e473.
- OD Lorenzi, C Major, V Acevedo, J Perez-Padilla, A Rivera, BJ Biggerstaff, et alReduced Incidence of Chikungunya Virus Infection in Communities with Ongoing Aedes Aegypti Mosquito Trap Intervention Studies—Salinas and Guayama, Puerto Rico, November 2015-February 2016. MMWR Morb Mortal Wkly Rep2016;65(18):479–480. 10.15585/mmwr.mm6518e327171600
- CM Degener, AE Eiras, TMF Azara, RA Roque, S Rösner, CT Codeço, et alEvaluation of the Effectiveness of Mass Trapping with BG-Sentinel Traps for Dengue Vector Control: a Cluster Randomized Controlled Trial in Manaus, Brazil. J Med Entomol2014;51(2):408–420. 24724291
- R Barrera, M Amador, V Acevedo, RR Hemme, G Felix. Sustained, Area-Wide Control of Aedes aegypti Using CDC Autocidal Gravid Ovitraps. American Journal of Tropical Medicine and Hygiene2014;91(6):1269–1276. 10.4269/ajtmh.14-042625223937
- AO Lea. Sugar-Baited Insecticide Residues Against Mosquitoes. Mosquito News1965;25(1).
- LL Robert, MJ Perich, Y Schlein, RL Jacobson, RA Wirtz, PG Lawyer, et alPhlebotomine Sand Fly Control Using Bait-Fed Adults to Carry the Larvicide Bacillus sphaericus to the Larval Habitat. Journal of the American Mosquito Control Association1997;13(2):140–144. 9249650
- Y Schlein, H Pener. Bait-Fed Adult Culex pipiens Carry the Larvicide Bacillus sphaericus to the Larval Habitat. Med Vet Entomol1990;4(3):283–288. 2132993
- R Xue, DL Kline, A Ali, DR Barnard. Application of Boric Acid Baits to Plant Foliage for Adult Mosquito Control. J Am Mosq Control Assoc2006;22(3):497–500. 10.2987/8756-971X(2006)22[497:AOBABT]2.0.CO;217067052
- Y Schlein, GC Müller. An Approach to Mosquito Control: Using the Dominant Attraction of Flowering Tamarix jordanis Trees Against Culex pipiens. J Med Entomol2008;45(3):384–390. 18533430
- EE Revay, GC Müller, WA Qualls, DL Kline, DP Naranjo, KL Arheart, et alControl of Aedes albopictus with Attractive Toxic Sugar Baits (ATSB) and Potential Impact on Non-Target Organisms in St. Augustine, Florida. Parasitol Res2014;113(1):73–79. 10.1007/s00436-013-3628-424122115
- DP Naranjo, WA Qualls, GC Müller, DM Samson, D Roque, T Alimi, et alEvaluation of Boric Acid Sugar Baits Against Aedes albopictus (Diptera: Culicidae) in Tropical Environments. Parasitology Research2013;112(4):1583–1587. 10.1007/s00436-013-3312-823388730
- GC Müller, JC Beier, SF Traore, MB Toure, MM Traore, S Bah, et alSuccessful Field Trial of Attractive Toxic Sugar Bait (ATSB) Plant-Spraying Methods Against Malaria Vectors in the Anopheles gambiae Complex in Mali, West Africa. Malar J2010;9:21010.1186/1475-2875-9-21020663142
- G Müller, Y Schlein. Plant Tissues: the Frugal Diet of Mosquitoes in Adverse Conditions. Med Vet Entomol2005;19(4):413–422. 10.1111/j.1365-2915.2005.00590.x16336306
- SA Allan. Susceptibility of Adult Mosquitoes to Insecticides in Aqueous Sucrose Baits. J Vector Ecol2011;36(1):59–67. 10.1111/j.1948-7134.2011.00141.x21635642
- R Xue, DR Barnard. Boric Acid Bait Kills Adult Mosquitoes (Diptera: Culicidae). J Econ Entomol2003;96(5):1559–1562. 14650531
- R Xue, A Ali, DL Kline, DR Barnard. Field Evaluation of Boric Acid- and Fipronil-Based Bait Stations Against Adult Mosquitoes. J Am Mosq Control Assoc2008;24(3):415–418. 10.2987/5683.118939695
- PR Grimstad, GR DeFoliart. Nectar Sources of Wisconsin Mosquitoes. J Med Entomol1974;11(3):331–341. 4152968
- JC Beier, GC Müller, W Gu, KL Arheart, Y Schlein. Attractive Toxic Sugar Bait (ATSB) Methods Decimate Populations of Anopheles Malaria Vectors in Arid Environments Regardless of the Local Availability of Favoured Sugar-Source Blossoms. Malar J2012;11:3110.1186/1475-2875-11-3122297155
- SD Banks, N Murray, A Wilder-Smith, JG Logan. Insecticide-Treated Clothes for the Control of Vector-Borne Diseases: a Review on Effectiveness and Safety. Med Vet Entomol2014;28Suppl 1:14–25.24912919
- SD Banks, J Orsborne, SA Gezan, H Kaur, A Wilder-Smith, SW Lindsey, et alPermethrin-Treated Clothing as Protection Against the Dengue Vector, Aedes aegypti: Extent and Duration of Protection. PLoS Negl Trop Dis2015;9(10):e000410910.1371/journal.pntd.000410926440967
- James Orsborne, Adam Hendy Sarah DeRaedt Banks, Harparkash Kaur Salvador A Gezan, Wilder-Smith Annelies, et alPersonal Protection of Permethrin-Treated Clothing Against Aedes aegypti, the Vector of Dengue and Zika Virus, in the Laboratory. PLoS ONE2016;11(5):e015280510.1371/journal.pone.015280527187593
- B Most, V Pommier de Santi, F Pagès, M Mura, WM Uedelhoven, MK Faulde. Long-Lasting Permethrin-Impregnated Clothing: Protective Efficacy Against Malaria in Hyperendemic Foci, and Laundering, Wearing, and Weathering Effects on Residual Bioactivity After Worst-Case Use in the Rain Forests of French Guiana. Parasitol Res2017 02;116(2):677–684. 10.1007/s00436-016-5333-627942961
- P Kittayapong, P Olanratmanee, P Maskhao, P Byass, J Logan, Y Tozan, et alMitigating Diseases Transmitted by Aedes Mosquitoes: A Cluster-Randomised Trial of Permethrin-Impregnated School Uniforms. PLoS Negl Trop Dis2017;11(1):e000519710.1371/journal.pntd.000519728103255
- E Massad, M Amaku, FAB Coutinho, P Kittayapong, A Wilder-Smith. Theoretical Impact of Insecticide-Impregnated School Uniforms on Dengue Incidence in Thai Children. Global health action2013;6(1):20473–6.23541045
- MK Faulde, F Pages, W Uedelhoven. Bioactivity and Laundering Resistance of Five Commercially Available, Factory-Treated Permethrin-Impregnated Fabrics for the Prevention of Mosquito-Borne Diseases: the Need for a Standardized Testing and Licensing Procedure. Parasitol Res2016;115(4):1573–1582. 10.1007/s00436-015-4892-226738734
- T Yao-, L Wang-, J Cheng-, Y Hu-, J Zhao-, G Zhu-. Optimization of Pyrethroid and Repellent on Fabrics Against Stegomyia albopicta (= Aedes albopictus) Using a Microencapsulation Technique. Med Vet Entomol2015;29(1):37–43. 10.1111/mve.1208825429906
- JG Logan, NM Stanczyk, A Hassanali, J Kemei, AEG Santana, KAL Ribeiro, et alArm-In-Cage Testing of Natural Human-Derived Mosquito Repellents. Malar J2010;9:23910.1186/1475-2875-9-23920727149
- MD Proverbs. Induced Sterilization and Control of Insects. Annu Rev Entomol1969;14:81–102. 10.1146/annurev.en.14.010169.0005014882184
- DO Carvalho, D Nimmo, N Naish, AR McKemey, P Gray, ABB Wilke, et alMass Production of Genetically Modified Aedes aegypti for Field Releases in Brazil. J Vis Exp2014(83):e357910.3791/357924430003
- M Zheng, D Zhang, DD Damiens, H Yamada, JRL Gilles. Standard Operating Procedures for Standardized Mass Rearing of the Dengue and Chikungunya Vectors Aedes aegypti and Aedes albopictus (Diptera: Culicidae)—I—Egg Quantification. Parasit Vectors2015;8:4210.1186/s13071-014-0631-225614052
- M Zheng, D Zhang, DD Damiens, RS Lees, JRL Gilles. Standard Operating Procedures for Standardized Mass Rearing of the Dengue and Chikungunya Vectors Aedes aegypti and Aedes albopictus (Diptera: Culicidae)—II—Egg Storage and Hatching. Parasit Vectors2015;8:34810.1186/s13071-015-0951-x26112698
- MEH Helinski, AG Parker, BGJ Knols. Radiation Biology of Mosquitoes. Malar J2009;8Suppl 2:S6.
- R Bellini, A Medici, A Puggioli, F Balestrino, M Carrieri. Pilot Field trials with Aedes albopictus Frradiated Sterile Males in Italian Urban Areas. J Med Entomol2013;50(2):317–325. 23540120
- HK Phuc, MH Andreasen, RS Burton, C Vass, MJ Epton, G Pape, et alLate-Acting Dominant Lethal Genetic Systems and Mosquito Control. BMC Biol2007;5:1110.1186/1741-7007-5-1117374148
- DO Carvalho, AR McKemey, L Garziera, R Lacroix, CA Donnelly, L Alphey, et alSuppression of a Field Population of Aedes aegypti in Brazil by Sustained Release of Transgenic Male Mosquitoes. PLoS Negl Trop Dis2015;9(7):e000386410.1371/journal.pntd.000386426135160
- K Gorman, J Young, L Pineda, R Márquez, N Sosa, D Bernal, et alShort-Term Suppression of Aedes aegypti Using Genetic Control Does Not Facilitate Aedes albopictus. Pest Manag Sci2016;72(3):618–628. 10.1002/ps.415126374668
- EP Caragata, HLC Dutra, LA Moreira. Exploiting Intimate Relationships: Controlling Mosquito-Transmitted Disease with Wolbachia. Trends Parasitol2016;32(3):207–218. 10.1016/j.pt.2015.10.01126776329
- JH Yen, AR Barr. New Hypothesis of the Cause of Cytoplasmic Incompatibility in Culex pipiens L. Nature1971;232(5313):657–658. 4937405
- L O'Connor, C Plichart, AC Sang, CL Brelsfoard, HC Bossin, SL Dobson. Open Release of Male Mosquitoes Infected with a Wolbachia Biopesticide: Field Performance and Infection Containment. PLoS Negl Trop Dis2012;6(11):e179710.1371/journal.pntd.000179723166845
- JW Mains, CL Brelsfoard, RI Rose, SL Dobson. Female Adult Aedes albopictus Suppression by Wolbachia-Infected Male Mosquitoes. Sci Rep2016;6:3384610.1038/srep3384627659038
- L Ng, C Liew, R Gutierrez, C Chong, C Tan, G Yap, et alHow Safe is Wolbachia for Aedes Control?Entomological News Bulletin2017.
- AA Hoffmann, I Iturbe-Ormaetxe, AG Callahan, BL Phillips, K Billington, JK Axford, et alStability of the wMel Wolbachia Infection Following Invasion Into Aedes aegypti Populations. PLoS Negl Trop Dis2014;8(9):e311510.1371/journal.pntd.000311525211492
- I Iturbe-Ormaetxe, T Walker, SL O' Neill. Wolbachia and the Biological Control of Mosquito-Borne Disease. EMBO Rep2011;12(6):508–518. 10.1038/embor.2011.8421546911
- Z Xi, SL Dobson. Characterization of Wolbachia Transfection Efficiency by Using Microinjection of Embryonic Cytoplasm and Embryo Homogenate. Appl Environ Microbiol2005;71(6):3199–3204. 10.1128/AEM.71.6.3199-3204.200515933022
- T Walker, PH Johnson, LA Moreira, I Iturbe-Ormaetxe, FD Frentiu, CJ McMeniman, et alThe wMel Wolbachia Strain Blocks Dengue and Invades Caged Aedes aegypti Populations. Nature2011;476(7361):450–453. 10.1038/nature1035521866159
- LA Moreira, I Iturbe-Ormaetxe, JA Jeffery, G Lu, AT Pyke, LM Hedges, et alA Wolbachia Symbiont in Aedes aegypti Limits Infection with Dengue, Chikungunya, and Plasmodium. Cell2009;139(7):1268–1278. 10.1016/j.cell.2009.11.04220064373
- HLC Dutra, MN Rocha, FBS Dias, SB Mansur, EP Caragata, LA Moreira. Wolbachia Blocks Currently Circulating Zika Virus Isolates in Brazilian Aedes aegypti Mosquitoes. Cell Host Microbe2016;19(6):771–774. 10.1016/j.chom.2016.04.02127156023
- AA Hoffmann, BL Montgomery, J Popovici, I Iturbe-Ormaetxe, PH Johnson, F Muzzi, et alSuccessful Establishment of Wolbachia in Aedes Populations to Suppress Dengue Transmission. Nature2011;476(7361):454–457. 10.1038/nature1035621866160
- A Burt. Site-Specific Selfish Genes as Tools for the Control and Genetic Engineering of Natural Populations. Proc Biol Sci2003;270(1518):921–928. 10.1098/rspb.2002.231912803906
- Ethan Bier Valentino M Gantz. The Mutagenic Chain Reaction: A Method for Converting Heterozygous to Homozygous Mutations. Science2015;348(6233):442–444. 10.1126/science.aaa594525908821
- A Hammond, R Galizi, K Kyrou, A Simoni, C Siniscalchi, D Katsanos, et alA CRISPR-Cas9 Gene Drive System Targeting Female Reproduction in the Malaria Mosquito Vector Anopheles gambiae. Nat Biotechnol2016;34(1):78–83. 10.1038/nbt.343926641531
- RL Unckless, AG Clark, PW Messer. Evolution of Resistance Against CRISPR/Cas9 Gene Drive. Genetics2017;205(2):827–841. 10.1534/genetics.116.19728527941126
- A Beaghton, PJ Beaghton, A Burt. Gene Drive through a Landscape: Reaction-Diffusion Models of Population Suppression and Elimination by a Sex Ratio Distorter. Theor Popul Biol2016;108:51–69. 10.1016/j.tpb.2015.11.00526704073
- A Beaghton, A Hammond, T Nolan, A Crisanti, HCJ Godfray, A Burt. Requirements for Driving Antipathogen Effector Genes into Populations of Disease Vectors by Homing. Genetics2017;205(4):1587–1596. 10.1534/genetics.116.19763228159753
- National Academies of Sciences, Committee on Gene Drive Research in Non-Human Organisms. Gene Drives on the Horizon: Advancing Science, Navigating Uncertainty, and Aligning Research with Public Values. 2016.
- VM Gantz, N Jasinskiene, O Tatarenkova, A Fazekas, VM Macias, E Bier, et alHighly Efficient Cas9-Mediated Gene Drive for Population Modification of the Malaria Vector Mosquito Anopheles stephensi. Proc Natl Acad Sci U S A2015;112(49):6736.25971728
- OO Abudayyeh, JS Gootenberg, S Konermann, J Joung, IM Slaymaker, DBT Cox, et alC2c2 is a Single-Component Programmable RNA-Guided RNA-Yargeting CRISPR Effector. Science2016;353(6299):aaf557310.1126/science.aaf557327256883
- SC Britch, H Nyberg, RL Aldridge, T Swan, KJ Linthicum. Acoustic Control of Mosquito Larvae In Artificial Drinking Water Containers. J Am Mosq Control Assoc2016;32(4):341–344. 10.2987/16-6606.128206869
- S Whyard, CNG Erdelyan, AL Partridge, AD Singh, NW Beebe, R Capina. Silencing the Buzz: a New Approach to Population Suppression of Mosquitoes by Feeding Larvae Double-Stranded RNAs. Parasit Vectors2015;8:9610.1186/s13071-015-0716-625880645
- CL Moyes, J Vontas, AJ Martins, LC Ng, SY Koou, I Dusfour, et alContemporary Status of Insecticide Resistance in the Major Aedes vectors of Arboviruses Infecting Humans. PLoS Negl Trop Dis2017;11(7):e000562510.1371/journal.pntd.000562528727779
- CA Damalas, IG Eleftherohorinos. Pesticide Exposure, Safety Issues, and Risk Assessment Indicators. Int J Environ Res Public Health201105;8(5):1402–1419.
- P Sirisopa, T Kanutcharee, C Theeraphap, J Waraporn. Resistance to Synthetic Pyrethroids in Aedes aegypti (Diptera: Culicidae) in Thailand. Kasetsart J. (Nat. Sci.)2014.
- NM Endersby-Harshman, JR Wuliandari, LG Harshman, V Frohn, BJ Johnson, SA Ritchie, et alPyrethroid Susceptibility Has Been Maintained in the Dengue Vector, Aedes aegypti (Diptera: Culicidae), in Queensland, Australia. J Med Entomol2017;54(6):1649–1658. 10.1093/jme/tjx14528981684
- World Health Organization. Global Plan for Insecticide Resistance Management in Malaria Vectors. 2012.
- WHO. Handbook for Integrated Vector Management. Eastern Mediterranean Health Journal2012;18(4):392.
- JC Beier, J Keating, JI Githure, MB Macdonald, DE Impoinvil, RJ Novak. Integrated Vector Management for Malaria Control. Malar J2008;7Suppl 1:S4.19091038
- G Garcia, R Maciel-de Frietas, M Petersen, M Turelli, D Villela. How Pyrethroids Resistance in Aedes aeygpti Populations from Brazil Affects Wolbachia Invasion? Evidences from Simulations and Field Releases. American Society for Tropical Medicine and Hygiene2016.
- R Maciel-de Freitas. Why Wolbachia Was Not Able to Invade a Local Aedes aegypti Population on its First Release in Brazil?Entomol VI—SOVE2016.
- VA Paz-Soldan, V Plasai, AC Morrison, EJ Rios-Lopez, S Guedez-Gonzales, JP Grieco, et alInitial Assessment of the Acceptability of a Push-Pull Aedes aegypti Control Strategy in Iquitos, Peru and Kanchanaburi, Thailand. Am J Trop Med Hyg2011;84(2):208–217. 10.4269/ajtmh.2011.09-061521292886
- VA Paz-Soldan, J Yukich, A Soonthorndhada, M Giron, CS Apperson, L Ponnusamy, et alDesign and Testing of Novel Lethal Ovitrap to Reduce Populations of Aedes Mosquitoes: Community-Based Participatory Research between Industry, Academia and Communities in Peru and Thailand. PLoS ONE2016;11(8):e016038610.1371/journal.pone.016038627532497
- VA Paz-Soldán, AC Morrison, JJ Cordova Lopez, A Lenhart, TW Scott, JP Elder, et alDengue Knowledge and Preventive Practices in Iquitos, Peru. Am J Trop Med Hyg2015;93(6):1330–1337. 10.4269/ajtmh.15-009626503276
- World Health Organization. WHO Pesticide Evaluation Scheme.
- WHO Malaria Policy Advisory Committee Meeting. Innovation to Impact–WHO Change Plan for Strengthening Innovation, Quality and Use of Vector-Control Tools. 2015. Available from: http://www.who.int/malaria/mpac/mpac-sept2015-vector-control-innovation.pdf. Access date: 2018 Nov 26.
- World Health Organization. WHO Prequalification. Available from: http://www.who.int/topics/prequalification/en/. [cited 2018 Nov 26].
- GM Vazquez-Prokopec, BL Montgomery, P Horne, JA Clennon, SA Ritchie. Combining Contact Tracing with Targeted Indoor Residual Spraying Significantly Reduces Dengue Transmission. Sci Adv2017;3(2):e160202410.1126/sciadv.160202428232955
- R Barrera, V Acevedo, GE Felix, RR Hemme, J Vazquez, JL Munoz, et alImpact of Autocidal Gravid Ovitraps on Chikungunya Virus Incidence in Aedes aegypti (Diptera: Culicidae) in Areas With and Without Traps. J Med Entomol2017;54(2):387–395. 10.1093/jme/tjw18728031347
- JM Fiorenzano, PG Koehler, R Xue. Attractive Toxic Sugar Bait (ATSB) For Control of Mosquitoes and Its Impact on Non-Target Organisms: A Review. Int J Environ Res Public Health2017;14(4).
- L Alphey, A McKemey, D Nimmo, M Neira Oviedo, R Lacroix, K Matzen, et alGenetic control of Aedes mosquitoes. Pathog Glob Health2013;107(4):170–179. 10.1179/2047773213Y.000000009523816508