Next Article in Journal
Mechanical Characteristics and Failure Mode of Asphalt Concrete for Ballastless Track Substructure Based on In Situ Tests
Previous Article in Journal
Estimation of Wind Turbine Angular Velocity Remotely Found on Video Mining and Convolutional Neural Network
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Applied Sciences
Volume 10
Issue 10
10.3390/app10103546
applsci-logo
Submit to this Journal Review for this Journal Edit a Special Issue
► Article Menu

Article Menu

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

Ultrasonic Technology Applied against Mosquito Larvae

by
Kandasamy Kalimuthu
1,†,
Li-Chun Tseng
1,†,
Kadarkarai Murugan
2,
Chellasamy Panneerselvam
3,
Al Thabiani Aziz
3,
Giovanni Benelli
4 and
Jiang-Shiou Hwang
1,5,*
1
Institute of Marine Biology, National Taiwan Ocean University, Keelung 20224, Taiwan
2
Division of Entomology, Department of Zoology, School of Life Sciences, Bharathiar University, Coimbatore 641 046, Tamil Nadu, India
3
Department of Biology, Faculty of Science, University of Tabuk, Tabuk 71491, Saudi Arabia
4
Department of Agriculture, Food and Environment, University of Pisa, via del Borghetto 80, 56124 Pisa, Italy
5
Center of Excellence for the Oceans, National Taiwan Ocean University, Keelung 20224, Taiwan
*
Author to whom correspondence should be addressed.
†
Both authors contributed equally to the present contribution.
Appl. Sci. 2020, 10(10), 3546; https://doi.org/10.3390/app10103546
Received: 8 April 2020 / Revised: 14 May 2020 / Accepted: 18 May 2020 / Published: 20 May 2020
Browse Figures
Versions Notes

Abstract

:
The effective management of mosquito vectors is a timely challenge for medical and veterinary entomology. In this study, we evaluated the acoustic Larvasonic device to control young instars of the mosquito Aedes aegypti in diverse freshwater environments. Under laboratory conditions, we investigated the effect of exposure time and distance from the transducer on the mortality of larvae and pupae of Ae. aegypti. Furthermore, we evaluated the effectiveness of the ultrasound window of the electromagnetic spectrum under different field conditions. Results showed that first and second instar larvae were more sensitive to the frequency range of 18–30 kHz of the Larvasonic device. Ultrasonic waves applied for 180 s at a frequency from 18 to 30 kHz caused 100% larval mortality at a distance of 60 cm from the transducer. No mortality was observed in the non-target copepod Megacyclops formosanus. The exposure to the soundwaves produced by the acoustic larvicidal device over different distances effectively damaged Ae. aegypti through destruction of the larval dorsal tracheal trunk, thorax and abdomen. Overall, results indicated that the Larvasonic device tested can provide an alternative tool to reduce young instar populations of Ae. aegypti, without any effects on non-target aquatic invertebrates like copepods. It turned out to be a useful device for mosquito biocontrol. This technology has a relevant potential to fight the spread of mosquito-borne diseases.

1. Introduction

Mosquitoes (Diptera: Culicidae) transmit several of the most relevant life-threatening infectious diseases worldwide, including malaria, different types of encephalitis, lymphatic filariasis, West Nile virus, chikungunya, yellow fever, as well as Zika and dengue virus [1,2,3,4,5].
Recently, chikungunya and Zika virus emerged as two mosquito-borne viral diseases of major public health concern [6,7,8]. They are vectored by Aedes aegypti (L.) and Aedes albopictus (Skuse). Besides, a Flavivirus (Flaviviridae) mainly transmitted by the mosquito Ae. aegypti, is causing dengue fever, with significant human morbidity and mortality worldwide [9,10,11]. Annually, there are about 390 million humans infected with the dengue virus, with 96 million cases resulting in about 21,000 deaths. This worrying scenario urgently requires the development of effective measures for mosquito control [12,13]. The recent Zika virus outbreaks in many states of Brazil as well as on Pacific islands provide challenging examples [14,15,16]. In Brazil, Zika virus was ranked as one of the most serious public health issues, registering about 1.6 million cases in 2015 [17].
Mosquito vector control has the potential to reduce the impact of several mosquito-borne diseases [18,19]. Notably, since no effective vaccines against Aedes-vectored arboviruses are currently available, the control of vector populations at breeding sites remains crucial in urban and adjacent areas. Chemical insecticides are largely used for the management of mosquito populations, but they can be toxic to humans and non-target organisms, as well as for the environment [20]. They also led to the rapid development of insecticide resistance [21]. This situation demands new and safe mosquito control agents to reduce environmental and human health concerns [22,23,24]. In this study, we evaluated the efficacy of the Larvasonic apparatus based on ultrasound technology against Ae. aegypti larval instars developing in diverse aquatic breeding sites in Taiwan. Indeed, since Ae. aegypti widely exploits rather small water containers for oviposition and larval breeding, common in urban areas, it represents a suitable target for the Larvasonic device that was developed for acoustic transmission under water.
Ultrasound-based devices are used for other purposes, including microbiological control in aquaculture facilities, and for water treatment of ornamental water bodies and reservoirs [25]. Ultrasound was tested at strikingly different conditions on aquatic organisms, and effect studies are available from the earliest days of anti-mosquito ultrasound use [26]. It was observed that ultrasound can cause ruptures and bubbles that damage animal tissues. Tissue effects by cavitation are related to the duration, intensity, and frequency of acoustic waves [27]. The available ultrasound literature was already discussed by Colucci [28] in 2010, who applied ultrasound for algal control in a park pool of Austin, Texas, USA. Before that, ultrasound was used for wastewater treatment [29], as well as for anti-biofouling strategies in marine applications [30].
Concerning young instar management of mosquitoes, lower frequencies (20–50 kHz) are generally more effective in killing mosquito larvae than higher frequencies (>100 kHz), although the latter more efficiently produce free reactive radicals [31]. In another application, ultrasound-based technology was applied in the characterization of tissue and to evaluate animal carcass quality for human consumption. For instance, Morlein et al. [32] measured the intramuscular fat content using spectral analysis echo signals emitted by ultrasound treatment (at ~3.5 MHz). In pigs, backfat thickness and the length of the musculus longissimus, as well as fat thickness of the back was measured using an ultrasound scanner (at 3 MHz), as a prediction of meat quality [33]. In poultry, breast muscle thickness, as determined by ultrasonography (at 7 MHz), was shown to provide a reliable measurement of meatiness [34]. In addition, body measurements and ultrasound images (at 3–7.5 MHz) were used to classify carcass traits of ducks [35], sheep [36], cattle [37], and catfish [38].
In the present study, we adopted a technology employing acoustic waves generated by a transducer to control developmental stages of the mosquito vector Ae. aegypti. Experiments were conducted both in laboratory conditions and field conditions. Firstly, we assessed whether the Larvasonic exposure times as well as the distance from the ultrasound source can differentially affect the mortality of young instars of Ae. aegypti. Furthermore, the mode of action of ultrasound-based technology was investigated, providing insights on the damages caused by the selected ultrasound frequencies on mosquitoes exposed to treatment when compared to individuals of the control. Finally, since data about the non-target impact of ultrasound-based technology against mosquito natural enemies are scarce, herein the effect of the Larvasonic device on the non-target invertebrate copepod Megacyclops formosanus (Harada, 1931) was investigated. This cyclopoid copepod is known as one of the most effective predators of interest for mosquito biological control.

2. Materials and Methods

2.1. Mosquito Rearing

The Institute of Epidemiology, National Taiwan University, Taipei, Taiwan, provided eggs of Ae. aegypti. Following Suresh et al. [39], eggs were allowed to hatch in 18 (L) × 13 (W) × 4 (D) cm enamel trays containing 500 mL of water. Mosquito larvae were subsequently reared at 27 ± 2 °C and 75%–85% R.H. at a 14:10 (L:D) photoperiod. Larvae were fed brewer’s yeast (Sigma Aldrich, Germany) and ground dog biscuits (Pedigree Company, MA, USA) at a 3:1 daily ratio.

2.2. Copepod Culture

Culture of the freshwater cyclopoid copepod M. formosanus was started by transferring 10 gravid females to a quartz glass aquarium filled with 3 L of culture medium consisting of ciliates, rotifers, and the alga Chlorella vulgaris Beijerinck 1890 in dechlorinated tap water. Copepods were then maintained at 27 ± 3 ºC, pH 7, and a photoperiod of 12:12 h (L:D) in an incubator at the Zooplankton and Coral Reef Laboratory, Institute of Marine Biology, National Taiwan Ocean University, Taiwan.

2.3. Efficacy of Ultrasonic Treatment at Laboratory Conditions

We adopted a technology employing acoustic waves generated by an ultrasound transducer, the Larvasonic apparatus (New Mountain Innovations Inc, Old Lyme, NY, USA) [5]. The transducer distributes acoustic energy uniformly in the horizontal plane and has a 360-degree volume of vertical coverage. In our study, the tested frequency range was 18–30 kHz. The transducer elements were made of piezoceramics with an output of 100 W. Experiments were conducted in an open fish tank 87 × 44 × 44 cm3 filled with water up to a height of 20 cm, 100 mosquito larvae (instars I, II, III, and IV, or pupae) were transferred to a net (150 µm mesh size; 2.3 × 44 × 44 cm3) and placed inside a fish tank at 13 test points of distance (0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, and 60 cm) from the transducer immediately after starting the exposure to Larvasonic, lasting 30, 60, 90, 120, 150, 180 s. Every experiment was replicated 5 times with new larvae or pupae. After each replicate, the number of dead mosquito larvae or pupae was noted. Non-target adults of the cyclopoid copepod M. formosanus were tested independently at the same distance and exposure time described above for Ae. aegypti larvae.

2.4. Efficacy of Ultrasonic Treatment in the Field

Field experiments were conducted in three selected areas (i.e., vegetable gardens, ditches, and waste tire stock sites) in Donggan, Nantou, and Keelung, Taiwan (Figure 1). Control samples of Ae. aegypti larvae were taken before treatment and after treatment by dipper sampling (100 mL), followed by larval counts. Several key factors that might impact experimental results were considered. These included the distance between the treatment device and the larvae that were collected in the field, and the size of the larval habitats. It was assured that the dipper samplings were able to collect larvae that sunk to the ground. Repeated collections were carried out to determine the differences in larval instar composition of the three collection sites. The selected environments were exposed to Larvasonic ultrasound pulses for 30 s. Then, the collected samples were brought back to the laboratory to count live and dead mosquitoes daily for one week. Three replicates were conducted for each area from southern to northern Taiwan.

2.5. Statistical Analysis

For statistical analysis, descriptive statistical parameters such as mean and standard deviation values were calculated. Mortality (%) data were then arcsine transformed to show that the data set had normality and homogeneity of variances. The effects of distance and period of exposure on each stage of mosquito larvae were analyzed using a two-way analysis of variance (ANOVA) followed by Tukey’s honestly significant difference (HSD) test. Furthermore, the relation between mortality (%), distance, and exposure time of all mosquito instars to the Larvasonic device were examined by regression analysis [40]. Distance and exposure time were used as predictors of mortality in a multiple regression analysis. SPSS software version 17.0 was used for the analysis.

3. Results

3.1. Laboratory Experiments

In the laboratory, the effect of the ultrasonic wave spectrum at a frequency of 18 to 30 kHz caused 100% mortality on Ae. aegypti larvae and pupae at 20 cm distance from the transducer after an exposure of 30 s, and 100% mortality of instars I, II, and III at 35 cm after an exposure of 30 s. It takes 180s to kill all pupae at a distance of 60 cm (Figure 2). The mortality rates of Ae. aegypti were direct positively proportional to the exposure time (p < 0.05). All instars and pupae had 100% mortality at 20 cm after an exposure of 60 s (p < 0.05). With increasing exposure time and fixed distance to the transducer, the percentage of Ae. aegypti larval mortality also increased (p < 0.05) (Figure 2). Two-way ANOVA results showed that the distance, exposure time, and their interaction significantly impacted each young instar stage of Ae. aegypti (p < 0.001, Table 1). Among younger instars of this species, the fitted regression model revealed that mortality (%) was significantly correlated to distance and exposure time (p < 0.001, Table 2). The coefficient values of distance were negative and showed a decreasing trend with extended space, whereas positive coefficient values of time indicated that accumulated effects increased the control efficiencies.
In our research, we used different life stages (I–IV larval instars and pupae) of the mosquito Ae. aegypti, as well as adults of the copepod M. formosanus (Figure 3). No mortality was found on the non-target copepod M. formosanus, as well as in pretreatments of mosquito larvae. The mortality of Ae. aegypti larvae caused by the Larvasonic device probably resulted from the sound energy transmitted into the water at a high frequency, leading to ruptures of the dorsal tracheal trunk in young mosquito instars, thus resulting in major tissue damage and death (Figure 4).

3.2. Field Experiments

In the field among the three selected study sites, the highest population of mosquito larvae was collected in a vegetable garden pond (42.31%), followed by 38.46% in ditches, and 19.23% in waste tire sites of Donggan, Nantou, and Keelung (Figure 5a,b). In this research, we analyzed 26 field samples. Among them, the larval density was lower than 10 (individuals per liter) in 14 samples, followed by 20 to 40 (individuals per liter) in 3 samples, and 50 to 80 (individuals per liter) in only 1 sample (Figure 5c,d). The total sample analysis showed the presence of 21.36% of I instar larvae, 15.43% of II instar larvae, 28.62% of III instar larvae, 22.21% of IV instar larvae, and 12.36% of pupae. The reduction of the larval population after treatment was 95%, which was highly significant (p < 0.001) (Figure 6a). Overall, data collected here showed that the ultrasonic waves at frequencies ranging from 18 to 30 kHz were effective in controlling larvae and pupae of Ae. aegypti (Figure 6b).

4. Discussion

Ultrasound-based devices have been tested in a number of pest control attempts, developing several tools that provide sounds aiming to repel, deter, or kill unwanted animals such as arthropods, birds, rodents, and even larger mammals [41]. In particular, acoustic devices of various sizes and power levels were used successfully for insect pest management [42]. In our experiments, the morphological analysis of treated and killed Ae. aegypti larvae confirmed our hypothesis that the acoustic energy from the transducer broke the mosquito tracheal trunk in this species (Figure 4). It should also be noted that no matter the source and visibility by their avoidance, mosquitoes are able to detect ultrasound at a wavelength range of 38–44 kHz [43]. In agreement with our findings, Fredregill et al. [44] recently reported the efficacy of a Larvasonic Field Arm Mobile Wetlands Unit and SD-Mini in controlling Culex spp. mosquito populations, without any harmful effect on non-target organisms, including damselflies and dragonflies. Furthermore, Quraishi et al. [45] highlighted that ultrasonic waves at a frequency of 0.5 mc/s effectively inhibited the egg hatchability in Ae. aegypti. Also, Britch et al. [46] noticed that the Larvasonic SD-Mini acoustic larvicide achieved 90% mortality against Ae. aegypti. Besides, Foster and Lutes [47] reported that five ultrasonic waves at frequencies of 20–70 kHz were effective in repelling mosquitoes.
From a mechanistic point of view at the cellular level, ultrasounds can cause membrane blubbing, shrinkage of cells, fragmentation of nuclei, chromatin condensation, and the fragmentation of apoptotic bodies [48,49,50]. Mehier-Humbert et al. [51] observed cuticle holes that were likely caused by ultrasound cavitation. Such porations can damage or kill mosquito larvae if the tissue holes are too large or if the tissues cannot reseal fast enough. In our research, we noticed that the tested sound waves resonate at the frequency of mosquito larva internal air volume, causing the larvae to burst. As a result, 98% of larvae and pupae were dead and the remaining 2% were alive with morphological deformation, ultimately resulting in their mortality within a short span of time. Concerning the impact of ultrasound on non-target organisms, we observed that ultrasonic waves employed at a frequency of 18 to 30 kHz did not exhibit noticeable harmful effects on the copepod M. formosanus, which is a useful natural predator of mosquito young instars [52,53,54].
Vibrations caused by sound waves lead to the formation of gas vesicles that then resonate within and among the cells. Bubbles develop within cells, expand, and contract in a process of cavitational extension. Ultrasonic treatment leads to ruptures of the bubbles that are damaging the cells. Cavitational extension and with it the damaging effect on cells, is regulated by the frequency, intensity, and duration of sound waves [27]. These effects of ultrasonic waves do not only hold for mosquito young instar management but also for algal control. Other effects of ultrasonic waves include additional damage of cell membranes due to lipid peroxidation, and effects on the cell division cycle as evidenced from cyanobacteria [55,56]. Ma et al. [57] investigated the dynamics of microcystin release and degradation when Microcystis suspensions were treated with different ultrasound intensities and frequencies. Donskoy and Ludiyanskiy [58] showed that ultrasound can induce cavitation and mortality in veliger, juvenile, and adults of the invasive zebra mussel, applying 20–380 kHz.
Some aquatic insects are known to communicate by ultrasounds. Water boatmen (Hemiptera: Corixidae: Micronecta), for example, produce courtship songs which are partially in the ultrasonic range (about 5–22 kHz) [59]. Therefore, further research is required to understand the impact of ultrasound-based mosquito larvicidal treatments on the mating outcomes of aquatic Hemiptera. It should be noted that ultrasound may cause negative effects on some amphibians, since Pashovkin et al. [60] tested a variety of frequencies inducing striking mortality of Rana temporaria L. embryos after 5 to 15 min at 0.88 MHz and 0.2–0.7 W/cm2. However, compared to the latter, our results are highly promising, since the Larvasonic device tested in this study at a frequency range of 18–36 kHz did not lead to noticeable mortality on non-target cyclopoid crustaceans, which are also of interest for mosquito biocontrol [61].
Overall, in the present work we presented selected ultrasonic frequencies from 18 to 30 kHz leading to high mortality of different young instars of Ae. aegypti. This supports the approach using acoustic waves for the management of mosquito larval populations. The present results showed that mosquito mortality is related to exposure time and distance from the transducer. The chemical and physical forces provided by ultrasonic cavitation lead to severe damage to cell membranes that subsequently kills developmental instars of the targeted mosquito species. Based on our results, ultrasound-based devices can be considered as a viable technology for mosquito control. Ecofriendly characteristics include that they are harmless to non-target invertebrates, such as the copepod M. formosanus. This particular copepod species could be used as an additional biocontrol agent, since we preliminarily also observed that its predation rates against mosquito larvae were not affected in our trials.

5. Conclusions and Challenges for Future Research

This study provided three main results achieved through the employment of the Larvasonic device against Ae. aegypti young instars: (i) both the distance from the source of acoustic waves and the exposure time significantly affected mosquito larval mortality; (ii) the efficacy of the Larvasonic device was high even in the field over various Aedes breeding sites; and (iii) we did not detect negative impacts on the non-target copepod species M. formosanus, which is of interest for providing additional biological predatory control of mosquito larvae. The application of this method is particularly suitable for small urban and peri-urban water bodies where young instars of Ae. aegypti may develop at high densities. Therefore, the size of the experimental setup can be increased in future applications and research to assess the efficacy of this tool in large-scale real-world scenarios. Our laboratory and field studies suggest that an ultrasound-based technology has a good potential for future applications for mosquito larval control. Therefore, can be considered among integrated vector management tools to manage mosquito-borne diseases in an ecofriendly way.
As recommended by the World Health Organization in 2005, tests with new products and technologies should follow standard methodologies and should be carried out mainly with third and fourth instar mosquito larvae. In relation to the field experiment, another important factor affecting the efficacy of this tool is the volume of water at breeding sites, as already stressed in earlier researches [5]. Depending on the volume of water in the container, the effect can vary, thus decreasing larval mortality. Another factor is the timing of mortality after larval exposure in respective treatments. In addition, field tests should be carried out at larger scale.
The applied technology should be improved to minimize side effects on non-target species in aquatic ecosystems. In this framework, further research is still needed to assess the impact of the Larvasonic device on other aquatic non-target organisms. In addition, future in situ applications could include ultrasonic devices integrated in a remotely operating vehicle with a function similar to a vacuum cleaner. Furthermore, artificial intelligence could integrate signals of a laser sensor that would automatically detect and target mosquito larvae and pupae. This application would successfully manage mosquito populations, reducing environmental pollution and non-target effects of still widely used chemical insecticides.

Author Contributions

J.-S.H. conceived and designed the experiments. K.K. performed the laboratory experiments. K.K., L.-C.T., J.-S.H., and K.M. performed the field experiments. L.-C.T. and K.K. analyzed the data, prepared the figures, and wrote the original draft. J.-S.H. contributed reagents, materials, and analysis tools. K.K., L.-C.T., K.M., C.P., A.T.A., G.B. and J.-S.H. contributed to formal analysis, data curation and reviewed/edited the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

The authors are grateful for financial support from the Ministry of Science and Technology (MOST) of Taiwan through grant no. MOST 104–2611-M-019–004, MOST 105–2621-M-019-001, MOST 105–2918-I-019-001, MOST 106-2621-M-019-001, MOST 107-2621-M-019-001 and MOST 108-2621-M-019-003 to J.-S. Hwang, as well as the grant no. MOST 104–2811-M-019-005, MOST 105–2811-M-019-008, MOST 107-2811-M-019-004 and MOST 108-2811-M-019-504 to L.-C. Tseng. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Acknowledgments

We appreciated the innovation and kind technical assistance of Herbert Nyberg (New Mountain Innovations, NY, USA), who developed the Larvasonic device. Finally, we thank Chih-Ming Lin for his assistance in manuscript submission.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Kilpatrick, A.M.; Randolph, S.E. Drivers, dynamics, and control of emerging vector-borne zoonotic diseases. Lancet 2012, 380, 1946–1955. [Google Scholar] [CrossRef][Green Version]
  2. Benelli, G.; Beier, J. Current vector control challenges in the fight against malaria. Acta Trop. 2017, 174, 91–96. [Google Scholar] [CrossRef]
  3. Mayer, S.V.; Tesh, R.B.; Vasilakis, N. The emergence of arthropod-borne viral diseases: A global prospective on dengue, chikungunya, and Zika fevers. Acta Trop. 2017, 166, 155–163. [Google Scholar] [CrossRef] [PubMed]
  4. Benelli, G.; Lo Iacono, A.; Canale, A.; Mehlhorn, H. Mosquito vectors and the spread of cancer: An overlooked connection? Parasitol. Res. 2016, 115, 2131–2137. [Google Scholar] [CrossRef] [PubMed][Green Version]
  5. Nyberg, H.J.; Muto, K. Acoustic tracheal rupture provides insights into larval mosquito respiration. Sci. Rep. 2020, 10, 2378. [Google Scholar] [CrossRef]
  6. Kindhauser, M.K.; Allen, T.; Frank, V.; Santhana, R.S.; Dye, C. Zika: The origin and spread of a mosquito-borne virus. Bull. World Health Org. 2016, 94, 675. [Google Scholar] [CrossRef]
  7. World Health Organization. Guidelines for Laboratory and Field Testing of Mosquito Larvicides. 2005. Available online: https://apps.who.int/iris/handle/10665/69101 (accessed on 18 May 2020).
  8. Lee, S.J.; Kim, J.H.; Lee, S.C. Effects of oil-film layer and surfactant of the siphonal respiration and survivorship in the fourth instar larvae of Aedes togoi mosquito in laboratory conditions. Sci. Rep. 2018, 8, 5694. [Google Scholar] [CrossRef][Green Version]
  9. Benelli, G. Research in mosquito control: Current challenges for a brighter future. Parasitol. Res. 2015, 114, 2801–2805. [Google Scholar] [CrossRef]
  10. Murugan, K.; Aruna, P.; Panneerselvam, C.; Madhiyazhagan, P.; Paulpandi, M.; Subramaniam, J.; Rajaganesh, R.; Wei, H.; Alsalhi, M.S.; Devanesan, S.; et al. Fighting arboviral diseases: Low toxicity on mammalian cells, dengue growth inhibition (in vitro) and mosquitocidal activity of Centroceras clavulatum-synthesized silver nanoparticles. Parasitol. Res. 2016, 115, 651–662. [Google Scholar] [CrossRef]
  11. Mendeiros-Sousa, A.R.; Fernandes, A.; Ceretti-Junior, W.; Wilke, A.B.B.; Marrelli, M.T. Mosquitoes in urban green spaces: Using an island biogeographic approach to identify drivers of species richness and composition. Sci. Rep. 2017, 7, 17826. [Google Scholar] [CrossRef][Green Version]
  12. Bhatt, S.; Gething, P.W.; Brady, O.J.; Messina, J.P.; Farlow, A.W.; Moyes, C.L.; Drake, J.M.; Brownstein, J.S.; Hoen, A.G.; Sankoh, O.; et al. The global distribution and burden of dengue. Nature 2013, 496, 504–507. [Google Scholar] [CrossRef] [PubMed]
  13. Schwab, S.R.; Stone, C.M.; Fonseca, D.M.; Fefferman, N.H. The importance of being urgent: The impact of surveillance target and scale on mosquito-borne disease control. Epidemics 2017, 23, 55–63. [Google Scholar] [CrossRef] [PubMed]
  14. Cardoso, C.W.; Paploski, I.A.; Kikuti, M.; Rodrigues, M.S.; Silva, M.M.; Campos, G.S.; Sardi, S.I.; Kitron, U.; Reis, M.G.; Ribeiro, G.S. Outbreak of exanthematous illness associated with Zika, chikungunya, and dengue viruses, Salvador, Brazil. Emerg. Infect. Dis. 2015, 21, 2274–2276. [Google Scholar] [CrossRef] [PubMed]
  15. Benelli, G.; Mehlhorn, H. Declining malaria, rising dengue and Zika virus: Insights for mosquito vector control. Parasitol. Res. 2016, 115, 1747–1754. [Google Scholar] [CrossRef] [PubMed]
  16. Boyer, S.; Calvez, E.; Chouin-Carneiro, T.; Diallo, D.; Failloux, A.B. An overview of mosquito vectors of zika virus. Microbes Infect. 2018, 20, 646–660. [Google Scholar] [CrossRef]
  17. Brazilian Health Ministry. Dengue. Bol. Epidem. 2016, 47, 1–5. [Google Scholar]
  18. Fernandes, J.N.; Moise, I.K.; Maranto, G.L.; Beier, J.C. Revamping mosquito-borne disease control to tackle future threats. Trends Parasitol. 2018, 34, 359–368. [Google Scholar] [CrossRef] [PubMed]
  19. Lambert, B.; Sikulu-Lord, M.T.; Mayagaya, V.S.; Devine, G.; Dowell, F.; Churcher, T.S. Monitoring the age of mosquito populations using near-infrared spectroscopy. Sci. Rep. 2018, 8, 5274. [Google Scholar] [CrossRef][Green Version]
  20. Benelli, G. Plant-borne ovicides in the fight against mosquito vectors of medical and veterinary importance: A systematic review. Parasitol. Res. 2015, 114, 3201–3212. [Google Scholar] [CrossRef]
  21. Naqqash, M.N.; Gökçe, A.; Bakhsh, A.; Salim, M. Insecticide resistance and its molecular basis in urban insect pests. Parasitol. Res. 2016, 115, 1363–1373. [Google Scholar] [CrossRef]
  22. Benelli, G. Plant-mediated biosynthesis of nanoparticles as an emerging tool against mosquitoes of medical and veterinary importance: A review. Parasitol. Res. 2016, 115, 23–34. [Google Scholar] [CrossRef]
  23. Pavela, R.; Benelli, G. Ethnobotanical knowledge on botanical repellents employed in the African region against mosquito vectors—A review. Exp. Parasitol. 2016, 167, 103–108. [Google Scholar] [CrossRef] [PubMed]
  24. Hawkes, F.M.; Dabiré, R.K.; Sawadogo, S.P.; Torr, S.J.; Gibson, G. Exploiting Anopheles responses to thermal, odour and visual stimuli to improve surveillance and control of malaria. Sci. Rep. 2017, 7, 17283. [Google Scholar] [CrossRef] [PubMed]
  25. Gina, L.; Elizabeth, H. Literature review of the effects of ultrasonic waves on cyanobacteria, other aquatic organisms, and water quality. Wisconsin DNR 2014, 195, 1–14. [Google Scholar]
  26. Miller, D.L. The botanical effects of ultrasound: A review. Env. Exp. Bot. 1983, 23, 1–27. [Google Scholar] [CrossRef]
  27. Rajasekhar, P.; Fan, L.; Nguyen, T.; Roddick, F.A. Impact of sonication at 20 kHz on Microcystis aeruginosa, Anabaena circinalis, and Chlorella sp. Water Res. 2012, 46, 1473–1481. [Google Scholar] [CrossRef]
  28. Colucci, L.A. Ultrasonic algae control literature review. AWPD 2010, 7, 1–5. [Google Scholar]
  29. Madge, B.A.; Jensen, J.N. Disinfection of wastewater using a 20-kHz ultrasound unit. Water Env. Res. 2002, 74, 159–169. [Google Scholar] [CrossRef]
  30. Gómez Olmedilla, D. Preventing the Growth of Barnacles by Using Ultrasonic Sound. Master Thesis, Chalmers University of Technology, Göteborg, Sweden, 2012. [Google Scholar]
  31. Mason, T.J. Large scale sonochemical processing: Aspiration and actuality. Ultrason. Sono. Chem. 2000, 7, 145–149. [Google Scholar] [CrossRef]
  32. Morlein, D.; Rosner, F.; Brand, S.; Jenderka, K.V.; Wicke, M. Non-destructive estimation of the intramuscular fat content of the longissimus muscle of pigs by means of spectral analysis of ultrasound echo signals. Meat Sci. 2005, 69, 187–199. [Google Scholar] [CrossRef]
  33. Cisneros, F.; Ellis, M.; Miller, K.D.; Novakofski, J.; Wilson, E.R.; McKeith, F.K. Comparison of transverse and longitudinal real-time ultrasound scans for prediction of lean cut yields and fat-free lean content in live pigs. J. Anim. Sci. 1996, 74, 2566–2576. [Google Scholar] [CrossRef]
  34. Kleczek, K.; Wawro, K.; Wilkiewicz-Wawro, E.; Makowski, W.; Konstantynowicz, K. Relationships between breast muscle thickness measured by ultrasonography and meatiness and fatness in broiler chicken. Arch. Tierzucht. 2009, 52, 538–545. [Google Scholar] [CrossRef]
  35. Farhat, A. Carcass characteristics of Peking ducks selected for greater breast muscle thickness using ultrasound scanning in response to dietary protein. Res. J. Agric. Biol. Sci. 2009, 5, 731–739. [Google Scholar]
  36. Emenheiser, J.C.; Greiner, S.P.; Lewis, R.M.; Notter, D.R. Validation of live animal ultrasonic measurements of body composition in market lambs. J. Anim. Sci. 2010, 88, 2932–2939. [Google Scholar] [CrossRef] [PubMed][Green Version]
  37. Stelzleni, A.M.; Perkins, T.L.; Brown AHJr Pohlman, F.W.; Johnson, Z.B.; Sandelin, B.A. Genetic parameter estimates of yearling live animal ultrasonic measurements in Brangus cattle. J. Anim. Sci. 2002, 80, 3150–3153. [Google Scholar] [CrossRef] [PubMed][Green Version]
  38. Bosworth, B.G.; Holland, M.; Brazil, B.L. Evaluation of ultrasound imagery and body shape to predict carcass and fillet yield in farm-raised catfish. J. Anim. Sci. 2001, 79, 1483–1490. [Google Scholar] [CrossRef]
  39. Suresh, U.; Murugan, K.; Panneerselvam, C.; Rajaganesh, R.; Roni, M.; Aziz, A.T.; Al-Aoh, H.A.N.; Trivedi, S.; Rehman, H.; Kumar, S.; et al. Suaeda maritima-based herbal coils and green nanoparticles as potential biopesticides against the dengue vector Aedes aegypti and the tobacco cutworm Spodoptera litura. Physiol. Mol. Plant. Path. 2018, 101, 225–235. [Google Scholar] [CrossRef]
  40. Zar, J.H. Biostatistical Analysis, 4th ed.; Prentice Hall: Upper Saddle River, NJ, USA, 1999. [Google Scholar]
  41. Frings, H. Pest control with sound waves; Ultrasonics as a possibility in the future of rodent and insect control. Pest. Control. 1948, 16, 9. [Google Scholar]
  42. Mankin, R.W. Applications of acoustics in insect pest management. CAB Rev. 2012, 7, 1–7. [Google Scholar] [CrossRef][Green Version]
  43. Mohankumar, D. Ultrasound and Insects. 2010. Available online: http://www.electroschematics.com/3864/ultrasound-and-insects/ (accessed on 18 May 2020).
  44. Fredregill, C.L.; Motl, G.C.; Dennett, J.A.; Bueno, R.; Debboun, M. Efficacy of two larvasonic units against Culex larvae and effects on common aquatic non-target organisms in Harris County, Texas. J. Am. Mosq. Control. Assoc. 2015, 31, 366–370. [Google Scholar] [CrossRef]
  45. Quraishi, S.M.; Osmani, M.H.; Ahmad, H.S. Effect of ultrasonic waves on the hatching of Aedes aegypti eggs at a frequency of 0.5 mc./s. J. Econ. Entomol. 1963, 56, 668–670. [Google Scholar] [CrossRef]
  46. Britch, S.C.; Nyberg, H.; Aldridge, R.L.; Swan, T.; Linthicum, K. Acoustic control of mosquito larvae in artificial drinking water containers. J. Am. Mosq. Control. Assoc. 2016, 32, 341–344. [Google Scholar] [CrossRef] [PubMed]
  47. Foster, W.A.; Lutes, K.L. Tests of ultrasonic emissions on mosquito attraction to hosts in a flight chamber. J. Am. Mosq. Control. Assoc. 1985, 1, 199–202. [Google Scholar] [PubMed]
  48. Ashush, H.; Rozenszajn, L.A.; Blass, M.; Barda-Saad, M.; Azimov, D.; Radnay, J.; Zipori, D.; Rosenschein, U. Apoptosis induction of human myeloid leukemic cell by ultrasound exposure. Cancer Res. 2000, 60, 1014–1020. [Google Scholar] [PubMed]
  49. Lagneaux, L.; de Meulenaer, E.C.; Delforge, A.; Dejeneffe, M.; Massy, M.; Moerman, C.; Hannecart, B.; Canivet, Y.; Lepeltier, M.F.; Bron, D. Ultrasonic low-energy treatment: A novel approach to induce apoptosis in human leukemic cells. Exp. Hematol. 2002, 30, 1293–1301. [Google Scholar] [CrossRef]
  50. Tian, Z.M.; Wan, M.X.; Lu, M.Z.; Wang, X.D.; Wang, L. The alteration of protein profile of Walker 256 carinosarcoma cells during the apoptotic process induced by ultrasound. Ultrasound Med. Biol. 2005, 31, 121–128. [Google Scholar] [CrossRef]
  51. Mehier-Humbert, S.; Guy, R.H. Physical methods for gene transfer: Improving the kinetics of gene delivery into cells. Adv. Drug. Deliv. Rev. 2005, 57, 733–753. [Google Scholar] [CrossRef] [PubMed]
  52. Dhanker, R.; Kumar, R.; Hwang, J.S. How effective are Mesocyclops aspericornis (Copepoda: Cyclopoida) in controlling mosquito immatures in the environment with an application of phytochemicals? Hydrobiologia 2013, 716, 147–162. [Google Scholar] [CrossRef]
  53. Awasthi, A.K.; Wu, C.H.; Tsai, K.H.; King, C.-C.; Hwang, J.S. How does ambush predatory copepod Megacyclops formosanus (Harada 1931) capture mosquito larvae, Aedes aegypti? Zool. Stud. 2012, 51, 927–936. [Google Scholar]
  54. Awasthi, A.K.; Molinero, J.C.; Wu, C.-H.; Tsai, K.-H.; King, C.-C.; Hwang, J.-S. Behavioral changes in mosquito larvae induced by copepod predation. Hydrobiologia 2015, 749, 113–123. [Google Scholar] [CrossRef]
  55. Tang, J.W.; Wu, Q.Y.; Hao, H.W.; Chen, Y.; Wu, M. Effect of 1.7 MHz ultrasound on a gas-vacuolate cyanobacterium and a gas-vacuole negative cyanobacterium. Coll. Surf. B Biointer. 2004, 36, 115–121. [Google Scholar] [CrossRef]
  56. Zhang, G.; Zhang, P.; Liu, H.; Wang, B. Ultrasonic damages on cyanobacterial photosynthesis. Ultrason. Sonochem. 2006, 13, 501–505. [Google Scholar] [CrossRef] [PubMed]
  57. Ma, B.; Chen, Y.; Hao, H.; Wu, M.; Wang, B.; Lv, H.; Zhang, G. Influence of ultrasonic field on microcystins produced by bloom-forming algae. Coll. Surf. B. 2005, 41, 197–201. [Google Scholar] [CrossRef] [PubMed]
  58. Donskoy, D.M.; Ludiyanskiy, M.L. Low frequency sound as a control measure for zebra mussel fouling. In Proceedings of the Fifth International Zebra Mussel and Other Aquatic Nuisance Organisms Conference, Toronto, ON, Canada, 14–21 February 1995; pp. 103–112. [Google Scholar]
  59. Sueur, J.; Mackie, D.; Windmill, J.F.C. So small, so loud: Extremely high sound pressure level from a pygmy aquatic insect (Corixidae, Micronectinae). PLoS ONE 2011, 6, e21089. [Google Scholar] [CrossRef] [PubMed][Green Version]
  60. Uteshev, V.K.; Pashovkin, T.N.; Sevirov, A.N.; Mel′nikova, E.V.; Sadikova, D.G.; Karnaukhov, V.N.; Gakhova, E.N. The survival of amphibian embryos after continuous ultrasonic treatment. Biofizika 2006, 51, 539–544. [Google Scholar] [CrossRef] [PubMed]
  61. Awasthi, A.K.; Wu, C.H.; Hwang, J.S. Diving as an anti-predator behavior in mosquito pupae. Zool. Stud. 2012, 51, 1225–1234. [Google Scholar]
Applsci 10 03546 g001 550
Figure 1. Map showing the field sample collection and study areas in Taiwan.
Figure 1. Map showing the field sample collection and study areas in Taiwan.
Applsci 10 03546 g001
Applsci 10 03546 g002 550
Figure 2. Mosquito mortality (%) achieved by the Larvasonic treatment over different conditions on Aedes aegypti young instars.
Figure 2. Mosquito mortality (%) achieved by the Larvasonic treatment over different conditions on Aedes aegypti young instars.
Applsci 10 03546 g002
Applsci 10 03546 g003 550
Figure 3. Young instars of Aedes aegypti before Larvasonic treatment: (a) I instar, (b) II instar II, (c) III instar, (d) IV instar, (e) pupae; and (f) non-target cyclopoid copepod Megacyclops formosanus.
Figure 3. Young instars of Aedes aegypti before Larvasonic treatment: (a) I instar, (b) II instar II, (c) III instar, (d) IV instar, (e) pupae; and (f) non-target cyclopoid copepod Megacyclops formosanus.
Applsci 10 03546 g003
Applsci 10 03546 g004 550
Figure 4. Post-treatment efficacy of Larvasonic under laboratory conditions against larvae (a–g) and pupae (h) of Aedes aegypti.
Figure 4. Post-treatment efficacy of Larvasonic under laboratory conditions against larvae (a–g) and pupae (h) of Aedes aegypti.
Applsci 10 03546 g004
Applsci 10 03546 g005 550
Figure 5. Number of mosquito larval samplings from different habitats surveyed in Taiwan (a,b). Aedes aegypti larval density over different samplings (c,d).
Figure 5. Number of mosquito larval samplings from different habitats surveyed in Taiwan (a,b). Aedes aegypti larval density over different samplings (c,d).
Applsci 10 03546 g005
Applsci 10 03546 g006 550
Figure 6. (a) Aedes aegypti larval mortality after of Larvasonic treatment. Asterisks indicate significant differences between control and treatment mortalities (ANOVA, Tukey’s honestly significant difference (HSD) test, p < 0.05). (b) Total mosquito larval mortality and survival after Larvasonic treatments. Data and statistical analysis consider the proportion of larvae/pupae killed or surviving and not absolute numbers that were killed.
Figure 6. (a) Aedes aegypti larval mortality after of Larvasonic treatment. Asterisks indicate significant differences between control and treatment mortalities (ANOVA, Tukey’s honestly significant difference (HSD) test, p < 0.05). (b) Total mosquito larval mortality and survival after Larvasonic treatments. Data and statistical analysis consider the proportion of larvae/pupae killed or surviving and not absolute numbers that were killed.
Applsci 10 03546 g006
Table
Table 1. Results of two-way ANOVA testing the effect of distance and exposure time on Aedes aegypti young instars. The values of d.f. = degree of freedom, significance level p < 0.05.
Table 1. Results of two-way ANOVA testing the effect of distance and exposure time on Aedes aegypti young instars. The values of d.f. = degree of freedom, significance level p < 0.05.
SourceType III Sum of Squaresd.f.Mean SquareFp-value
I instar larva
Distance (cm)0.99120.0818.24<0.001
Time (s)0.3550.0715.36<0.001
Distance (cm) × Time (s)1.23600.024.54<0.001
Error1.41312<0.01
II instar larva
Distance (cm)1.66120.1447.86<0.001
Time (s)0.7650.1552.79<0.001
Distance (cm) × Time (s)2.27600.0413.09<0.001
Error0.90312< 0.01
III instar larva
Distance (cm)2.29120.1937.74<0.001
Time (s)0.9850.2038.81<0.001
Distance (cm) × Time (s)2.16600.047.15<0.001
Error1.573120.01
IV instar larva
Distance (cm)5.69120.4768.03<0.001
Time (s)1.9450.3955.75<0.001
Distance (cm) × Time (s)3.67600.068.78<0.001
Error2.173120.01
Pupa
Distance (cm)9.06120.7624.30<0.001
Time (s)3.2150.6420.64<0.001
Distance (cm) × Time (s)6.11600.103.27<0.001
Error9.703120.03
Table
Table 2. Fitted mixed contribution model for mortality (ŷ) of mosquito young instars (%), evaluating the effect of the distance from the source of sound waves (cm) and the exposure time (s). The numbers in parentheses are standard errors of the estimated coefficients shown above. Dist. = distance, ET = exposure time.
Table 2. Fitted mixed contribution model for mortality (ŷ) of mosquito young instars (%), evaluating the effect of the distance from the source of sound waves (cm) and the exposure time (s). The numbers in parentheses are standard errors of the estimated coefficients shown above. Dist. = distance, ET = exposure time.
Treatment Group and Fitted Model
I instar larva
ŷ = 98.95 − 0.074 (Dist.) + 0.021 (ET)
   (0.53)  (0.010)       (0.004)
II instar larva
ŷ = 98.31 − 0.104 (Dist.) + 0.032 (ET)
   (0.59)  (0.011)       (0.004)
III instar larva
ŷ = 98.01 − 0.129 (Dist.) + 0.037 (ET)
   (0.62)  (0.012)       (0.004)
IV instar larva
ŷ = 96.46 − 0.235 (Dist.) + 0.063 (ET)
   (1.00)  (0.019)       (0.007)
Pupa
ŷ = 96.60 − 0.377 (Dist.) + 0.070 (ET)
   (2.08)  (0.040)       (0.015)

Share and Cite

MDPI and ACS Style

Kalimuthu, K.; Tseng, L.-C.; Murugan, K.; Panneerselvam, C.; Aziz, A.T.; Benelli, G.; Hwang, J.-S. Ultrasonic Technology Applied against Mosquito Larvae. Appl. Sci. 2020, 10, 3546. https://doi.org/10.3390/app10103546

AMA Style

Kalimuthu K, Tseng L-C, Murugan K, Panneerselvam C, Aziz AT, Benelli G, Hwang J-S. Ultrasonic Technology Applied against Mosquito Larvae. Applied Sciences. 2020; 10(10):3546. https://doi.org/10.3390/app10103546

Chicago/Turabian Style

Kalimuthu, Kandasamy, Li-Chun Tseng, Kadarkarai Murugan, Chellasamy Panneerselvam, Al Thabiani Aziz, Giovanni Benelli, and Jiang-Shiou Hwang. 2020. "Ultrasonic Technology Applied against Mosquito Larvae" Applied Sciences 10, no. 10: 3546. https://doi.org/10.3390/app10103546

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

Article Metrics

Back to TopTop