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Brazilian Journal of Poultry Science

versão impressa ISSN 1516-635Xversão On-line ISSN 1806-9061

Rev. Bras. Cienc. Avic. vol.18 no.1 Campinas jan./mar. 2016

http://dx.doi.org/10.1590/1516-635X1801041-046 

Articles

Melaleuca alternifolia Essential Oil against the Lesser Mealworm (Alphitobius diaperinus) and Its Possible Effect on the Soil Fauna

A VolpatoI 

WR LorenzettiI 

T ZorteaI 

LCDD GiombelliI 

D BarettaI 

RCV SantosII  III 

RA VaucherII 

RP RaffinIV 

ME SouzaII  III 

LM StefaniI 

AA BoligonV 

ML AthaydeV 

AS da SilvaI 

IAnimal Science Department, Universidade do Estado de Santa Catarina, Chapecó, SC, Brazil.

IIMicrobiology and Parasitology Department, Universidade Federal de Santa Maria, Santa Maria, RS, Brazil.

IIIMicrobiology Laboratory, Programa de Pós-Graduação em Nanociências, Centro Universitário Franciscano, Santa Maria, RS, Brazil.

IVNanotechnology Laboratory, Programa de Pós-Graduação em Nanociências, Santa Maria, RS, Brazil.

VPhytochemistry Laboratory, Universidade Federal de Santa Maria, Santa Maria, RS, Brazil.


ABSTRACT

The aim of this study was to evaluate the in vitro bioactivity of tea tree (Melaleuca alternifolia) essential oil against larvae and adult forms of lesser mealworms (Alphitobius diaperinus) and its influence on the soil fauna. Tests were performed in triplicate using pure tea tree oil (TTO; 1, 5, 10, 25, 50, and 100%), TTO nanoparticles (1, 3, and 7.5%), or terpinen-4-ol, the main compound of the tea tree oil, at the same concentrations of TTO. Larvae and adult mortality occurred at concentrations up to 10 and 50% of TTO, respectively. No larvicidal or insecticidal effect of TTO nanoparticles was observed. Terpinen-4-ol showed insecticidal and larvicidal effect at concentrations higher than 25%. The evaluation of TTO effect on soil organisms was performed by standard ecotoxicological tests (ISO) with the springtail species Folsomia candida. Only TTO was used for ecotoxicological tests in doses of 1, 5, 10, 25, 50, and 100 mg kg-1 of soil. TTO had no negative effects on F. candida survival or reproduction. Therefore, it was concluded that M. alternifolia oil may be a new alternative for control of the lesser mealworm.

Keywords: Alphitobius diaperinus; essential oil; natural products; nanotechnology; pest management

INTRODUCTION

The lesser mealworm Alphitobius diaperinus , Panzer, is one of the most common pests of poultry industry. Poultry housing provide optimal temperature and humidity conditions for its development, and the lesser mealworm feeds on poultry feed residues, fecal material, and dead birds (Gazoni et al., 2012). A. diaperinus is a potential carrier of several pathogens (viruses, fungi, bacteria, and protozoa) and it can be found everywhere inside poultry houses, hidden in cracks, beneath feeders and other areas (Silva et al., 2005). Pest management practices are routinely adopted, and the lesser mealworm control has been based on chemical insecticides applied on wood shavings used as litter. However, some flaws in these sanitary measures leads to litter re-infestation by A. diaperinus (Santos et al., 2009). It is known that these chemicals can also cause environmental contamination, affecting soil fauna survival and reproduction (Santos et al. , 2012). Natural products may become alternative treatments, and therefore ecotoxicology tests are needed.

The use of natural products can be an alternative to control the lesser mealworm, as shown by Prado et al. (2013) using Cunila angustifolia. Plants from the Meliaceae family, particularly Melaleuca alternifolia, can be used for controlling parasites (Mulla & Su 1999, Neves et al., 2012). The M. alternifolia oil is extracted from leaves and it is rich in terpinen-4-ol, the most likely chemical compound responsible for antifungal and antibacterial activities (Carson & Riley, 1993), as well as trypanocidal (Baldissera et al., 2014), insecticidal (Klauck et al., 2014) and acaricidal (Walton et al., 2004) effects. On the other hand, the oil has problems due to its high volatility and insolubility in water. In order to manage these problems, increasing its efficacy, nanoparticles have been used quite often (Pazinato et al., 2014). This technology consists of the manipulation of the molecule to a nanometric size, organizing oil atoms into a desirable form, which has several advantages over conventional products, such as slow, gradual and controlled release, increased bioavailability and lower toxicity (Roco, 2001).

This study was performed to investigate the bioactivity of pure M. alternifolia oil (TTO), nanoparticles form (TTO nanoparticles) of this same oil, and its major compound (terpinen-4-ol) on larvae and adult forms of A. diaperinus . TTO effects on soil fauna were also assessed by means of ecotoxicity tests.

MATERIALS AND METHODS

Oil forms and compounds

Tea tree oil (TTO), TTO nanoparticles and terpinen-4-ol were evaluated for their larvicidal and insecticidal activites. TTO was purchased from Importadora Química Delaware Ltda, Brazil. Terpinen-4-ol was purchased from Sigma Company. TTO nanoparticles were provided with the company Inventiva (Porto Alegre, Brazil), and the process of nanoparticle preparation was previously described by Pazinato et al. (2014). Solid lipid carriers were prepared with 7.5% of M. alternifolia essential oil using a patented process (Inventiva) based on high-pressure homogenization. Cetyl palmitate was used as the solid lipid and polysorbate 80 as surfactant. The total solid concentration was 18.6%. The particle size and zeta potential were evaluated on diluted samples (500x) using Zetasizer Nanoseries, Malvern. The pH was directly measured by use of a potentiomenter (Digimed, Brazil).

TTO characterization

Gas chromatography (GC) analyses were carried out using an Agilent Technologies 6890N GC-FID system, equipped with DB-5 capillary column (30mm x 0.25mm; film thickness of 0.25mm) connected to a flame ionization detector (FID). The injector and detector temperatures were set at 280°C. Helium was used as the carrier gas, at a flow rate of 1.3 mL/min. The thermal programmer was 50-300°C at a rate of 5°C/min. Two replicates of oil samples were processed in the same way. Relative component concentration was calculated based on GC peak areas without correction factors. The injection volume of the M. alternifolia (tea tree) essential oil was 1µL (Boligon et al., 2013).

Gas chromatography mass (GC-MS) analyses were performed on an Agilent Technologies Auto System XL GC-MS system operating in the EI mode at 70 eV, equipped with a split/split less injector (250°C). The transfer line temperature was 280°C. Helium was used as carrier gas (1.5mL/min) and the capillary columns used were a HP 5MS (30m x 0.25mm; film thickness of 0.25mm) and a HP Innowax (30m x 0.32mm i.d., film thickness of 0.5mm). The temperature program and the injected volume of oil were the same as used for GC analyses. The injected volume of the essentials oils was 1 µL. Component identification of both oils was based on the retention index (RI), using as reference of the homologous series of n-alkanes, C7-C30, under identical experimental conditions, and comparing with the mass spectra library search (NIST and Wiley), and with the mass spectra literature data (Adams, 1995). The relative amounts of the individual components were calculated based on the CG peak area (FID response).

Lesser mealworms

Lesser mealworms larvae (L8) and adults were obtained from naturally infested poultry farms located in the city of Concordia, State of Santa Catarina, Brazil. On the farms, insects were manually collected, placed in plastic bottles, and transported to the laboratory, where they were reared under controlled conditions (25ºC; 70% R.H.).The insects were kept in plastic pots with poultry litter and wet cottons, and were fed with poultry feed.

Bioassays

In-vitro tests were conducted using test solutions prepared with pure TTO, nanoparticles, and terpinen-4-ol. Pure TTO was first dissolved in Triton solution (1:1) and then diluted in water to the concentrations of 1, 5, 10, 25, 50, and 100%. TTO nanoparticles were dissolved in water to the concentrations of 1, 3, and 7.5%. Terpinen-4-ol was dissolved only in water to the same concentrations as TTO. The solutions (300 µL) were added to filter paper-lined Petri dishes according to a completely randomized design and three replicates per treatment at 25 °C (±3) and 70% (±10) relative humidity, and submitted to a photoperiod of 12:12 (L:D). Three controls were used, and included water-treated mealworms, Triton-treated mealworms and nanoparticle-treated mealworms (only the capsule of cetyl palmitate and polysorbate 80).

Larvae and adults

Ten 8th instar larvae or adults were placed in a Petri dish. Solutions were then added and the dishes were transferred to an incubator with controlled environment (25ºC; 70% R.H.). The percentage of live larvae was monitored daily for 13 days. The percentage of live lesser mealworm adults on each disk was monitored daily for 24 or 31 days.

Ecotoxicity tests

The evaluation of the effect of TTO on soil organisms was performed by standard ecotoxicological tests (ISO 1999, ISO 2010) with the springtail species Folsomia candida. The springtails were obtained from cultures of the Laboratory of Soil and Sustainability at the University of the State of Santa Catarina (UDESC) and kept under controlled conditions at 20±2 °C, and a photoperiod of 16:8 (L:D).

This study was conducted using the tropical artificial soil (TAS) method, with humidity set at 65% of retention capacity and pH adjusted to 6.0±0.5. The treatments consisted of TAS enriched with TTO in the laboratory. Similarly to the in-vitro tests, the TTO was previously mixed with Triton solution (1:1), and the final doses were obtained by diluting this mixture with distilled water.

For survival tests, the soil was exposed to six concentrations of TTO (1, 5, 10, 25, 50 and 100 mg kg-1) using four replicates per concentration. Each plastic recipient contained 50g of soil, to which 10 springtails were added, along with 2mg of dried granular baker's yeast. The containers were opened to allow air contact for three seconds three times weekly, and 2mg of dry yeast granules were added again after 14 days of incubation. At the end of 28 days of testing, the contents of each test vessel was poured into a beaker of water. A few drops of blue ink were gently added and homogenized. The floating springtails were counted and missing adults were considered dead.

TTO concentrations used in the reproduction test were the same as those applied in the survival test. This test followed the procedures described by ISO (1999), and the methodology was based on the survival test, i.e., larvae that floated in the water were photographed for better counting.

Statistical analysis

The normality test was applied for the results of the bioassays with the lesser mealworm, and data showed normal distribution. Data were then submitted to analysis of variance (ANOVA) and Duncan test (p<0.05). The data on springtail survival and reproduction were subjected to ANOVA followed by Dunnett test (p<0.05). Untreated lesser mealworms were used as control group.

RESULTS

Components present in the essential oil of tea tree

The results of the components found in the TTO oil are shown in Table 1. The three main compounds were identified as terpinen-4-ol, g-terpinene, and a-terpineol.

Table 1 Qualitative and quantitative analyses of Melaleuca alternifolia essential oil (TTO) used in this study. 

Peak Compounds RIa RIb Amount (%) ISO4730 range (%) Mol. Formule
1 a-pinene 937 939 3.51 1-6 C10H16
2 Sabinense 976 976 0.46 Tr-3.5 C10H16
3 a-terpinene 1016 1018 9.85 5-13 C10H16
4 p-cymene 1025 1026 2.27 0.5-8.0 C10H14
5 Limonene 1032 1031 1.39 0.5-1.5 C10H16
6 1.8-cineole 1037 1038 6.03 Tr-15 C10H18O
7 g-terpinene 1062 1062 20.15 10-28 C10H16
8 terpinen-4-ol 1178 1177 41.98 30-48 C10H18O
9 Terpinolene 1089 1088 4.17 1.5-5 C10H16
10 a-terpineol 1190 1189 2.43 1.5-8 C10H18O
11 Aromadendrene 1440 1439 1.04 Tr-3 C15H24
12 Ledene 1521 1525 0.80 Tr-3 C15H24
13 d-cadinene 1539 1538 0.63 Tr-3 C15H24
14 Globulol 1583 1583 0.97 Tr-1 C15H26O
15 viridiflorol 1591 1590 0.18 Tr-1 C15H26O
Total identified (%) 95.86

Relative proportions of the essential oil components are expressed as percentages. Tr = Trace amounts. aExperimental retention indices (based on homologous series of n-alkane C7-C30). bRetention indices from literature (Adams, 1995). International Organization for Standardization (ISO), standard number 4730.

TTO nanoparticles

The TTO nanoparticles were evaluated for their physical and chemical properties. The particle size was 287 (±2nm) and polydispersity index of 0.2 (±0.022) with a zeta potential of-14,2 ± 1,7 mV.

In-vitro tests

The three controls were used this study (water-treated mealworms, triton-treated mealworms and nanocapsule-treated mealworms) validated in vitro tests, i.e., water, triton and nanocapsule are not harmful to lesser mealworm larvae or adults. The controls are described below each Figure.

TTO oil

The results of the percentage of live adults and larvae are presented in Figure 1. The tests lasted 13 days for larvae, and 31 days for adults. The larvae were not affected by TTO at 1%, similarly to what was observed in the control group (Fig. 1a). A significant percentage of larval mortality (over 60%) was observed with 10% of TTO. TTO was efficient to eliminate all larvae at 25, 50, and 100%, demonstrating great larvicidal potential. The mortality rate was lower in adults when compared with the larvae, i.e., 40% adult mortality was observed with TTO at 50% (Fig. 1b). Adult mortality was not significantly different among lower TTO concentrations (1, 5, 10, and 25%); however, TTO concentrations of 50 and 100% demonstrated high insecticidal effect. In adults, observations were carried out until 50 days, but no changes were observed after 31 days; therefore, only data until 31 days were included in the analyses.

Figure 1 Percentage of live larvae (A) and adults (B) of Alphitobius diaperinus after treatment with Melaleuca alternifolia essential oil (1, 5, 10, 25, 50, and 100%). Means within a circle are similar by the Duncan's test (p>0.05). "Control" used to triton-treated lesser mealworms. 

TTO nanoparticles

TTO nanoparticles had no effect on A. diaperinus larvae and adult when compared with the control group, independent of the concentration (Figure 2). The experimental periods were 13 days for the larvae and 24 days for the adults. Thus, TTO nanoparticles had neither larvicidal nor insecticidal effect at these concentrations.

Figure 2 Percentage of live larvae (A) and adults (B) of Alphitobius diaperinus after treatment with Melaleuca alternifolia nanoparticles (1, 3, and 7.5%). Means within a circle are similar by the Duncan's test (p>0.05). "Control" used refers to nanoparticle-treated lesser mealworms (only the capsule of cetyl palmitate and polysorbate 80). 

Terpinen-4-ol

The results obtained with terpinen-4-ol were similar to those verified with pure TTO (Figure 3). Terpinen-4-ol at 1, 5, and 10% promoted similar results as those of the control group (Fig. 3a), whereas concentrations of 25, 50 and 100% had both larvicidal and insecticidal effects (Fig. 3b).

Figure 3 Percentage of live larvae (A) and adults (B) of Alphitobius diaperinus after treatment with terpinen-4-ol (1, 5, 10, 25, 50, and 100%). Means within a circle are similar by the Duncan's test (p>0.05). "Control" refers to water-treated lesser mealworms. 

Ecotoxicity tests

The results of springtail survival and reproduction tests are reported in Figure 4. TTO had no lethal effect on the adult springtails submitted to the survival test, which indicates it is not toxic to the soil fauna. The reproduction test showed no statistical differences among the treatments. TTO doses of 10 and 25 mg kg-1 resulted in the lowest number of juveniles, despite the lack of statistical differences (p>0.05).

Figure 4 Survival (A) and reproduction (B) tests with Folsomia candida exposed to tropical artificial soil (TAS) with different concentrations of Melaleuca alternifolia essential oil (TTO - tea tree oil). Treatments were similar by the Dunnet's test (p>0.05). 

DISCUSSION

The lesser mealworm control in poultry houses is typically controlled by an intense use of chemicals; however, these insects eventually become resistant to these products (Chernaki-Leffer et al., 2011). This has motivated the search for efficient alternative control methods and that also have lower environmental impact. These requirements can be met using natural products, including essential oils, which have attracted the interest of many researchers (Prado et al., 2013; Pazinato et al., 2014; Klauck et al., 2014).

In the present study, we showed for the first time the efficacy of M. alternifolia oil against both larval and adult forms of the lesser mealworm, with promising results. TTO showed potent larvicidal effect at concentrations greater than 10%, as well as against adults at concentrations greater than 25%. It is likely that the mortality of the lesser mealworm with the use of pure oil was related to the presence of its main compound, known as terpinen-4-ol, which promoted results similar to TTO when tested alone. However, we cannot exclude the application of other compounds, which may act in synergism for the control of this pest. Other oil compounds, such as thymol and carvacrol, have been shown to have strong toxic properties on some parasites (Szczepanik et al., 2012).

Studies have demonstrated that M. alternifolia oil has toxic effects against horn flies (Haematobia irritans), and repelent effect at concentration of 5% (Klauck et al., 2014). In addition, TTO has acaricidal effect on cattle ticks (Rhipicephalus microplus), and damages their reproductive system, both in its pure and nanoparticle forms, but the nanoparticles potentiated its lethal effect (Pazinato et al., 2014), which was not observed in this study with A. diaperinus. Nanotechnology has been used to improve the efficiency of essential oils and to reduce the need for large oil volumes (Martinez et al., 2011).

Other studies have shown insecticidal effect of different essential oils on some A. diaperinus life stages. Tests demonstrated that thyme essential oil (Thymus vulgaris) was harmful to this insects, as well as when two compounds (carvacrol and thymol) of this oil were individually tested (Szczepanik et al., 2012). Anise oil (Illiciumverum) showed 100% efficacy against A. diaperinus larvae and adults at the concentrations of 3.12, 6.25, 12.5, and 25.0 mg ml-1 (Szczepanik & Szumny, 2011), similarly to the effects obtained with the higher TTO concentrations used in the present study. Our findings suggest that other formulations of the oil, in addition of nanoparticles, may be useful and need to be tested both in-vitro and under field conditions, since no toxicity to the soil fauna was detected.

Cypermethrin is the main insecticide used to control A. diaperinus; however, this drug may be toxic to the soil fauna (Styrishave et al., 2010; Zortéa et al., 2015), and consequently cause environmental damage. Therefore, it is important to evaluate the environmental impact of new treatments because contamination may affect many ecology systems. In the present study, the M. alternifolia oil had no significant toxic effect on the soil fauna, differently from the essential oil of E. globulus, which resulted in a 76% reduction in reproduction of F. candida at 60 mg kg-1(Martins et al., 2013). The overall results of the present study show that poultry litter can be used as organic fertilizer after TTO application to control A. diaperinus.

CONCLUSIONS

Both TTO and terpinen-4-ol have insecticidal and larvicidal effect against the lesser mealworm A. diaperinus. In addition, it was demonstrated that TTO does not negatively affect the soil fauna, and consequently, there is no environmental impact when this essential oil is mixed with soil. Therefore, the tea tree oil is an option to control of A. diaperinus, particularly its larval stage.

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Received: April 2015; Accepted: October 2015

Mail Address Corresponding author e-mail address Aleksandro da Silva Rua Beloni Trombeta Zanin, 68E Bairro Santo Antonio, Chapecó, SC, Brazil. Postal code: 8981-630. Phone: (049) 2049-9560 Email:aleksandro_ss@yahoo.com.br

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