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Vol. 62. Núm. 1.Janeiro - Março 2018
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Vol. 62. Núm. 1.Janeiro - Março 2018
Páginas 1-82
Biological Control and Crop Protection
DOI: 10.1016/j.rbe.2017.12.002
Effect of entomopathogens on Africanized Apis mellifera L. (Hymenoptera: Apidae)
Michele Potricha,
Autor para correspondência
, Rita T.L. da Silvaa, Fabiana M.C. Maiab, Everton R. Lozanoa, Robson M. Rossic, Fernanda C. Colomboa, Flavia G. Tedescoa, Alfredo de Gouveaa
a Universidade Tecnológica Federal do Paraná, Campus Dois Vizinhos (UTFPR-DV), Laboratório de Controle Biológico, Estrada para Boa Esperança, Paraná, PA, Brazil
b Universidade Tecnológica Federal do Paraná, Campus Dois Vizinhos (UTFPR-DV), Unidade de Ensino e Pesquisa (UNEPE) Apicultura, Paraná, PA, Brazil
c Universidade Estadual de Maringá (UEM), Departamento de Estatística, Maringá, PA, Brazil
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Tabelas (2)
Table 1. Lethal survival time (mean±SD a posteriori of the median parameter of the Weibull distribution (1)) of Africanized Apis mellifera workers in contact with entomopathogens. Temperature 27±2°C, 12-h photophase and relative humidity of 60±10%.
Table 2. Length (μm) (±SE) of Africanized Apis mellifera worker midgut (ventricle) cells after feeding with candy paste mixed with the entomopathogens. Temperature 27±2°C, 12-h photophase and relative humidity of 60±10%.
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This study aimed to evaluate the effect of commercially used entomopathogens on Africanized Apis mellifera L. (Hymenoptera: Apidae). Four bioassays were performed: 1) pulverized entomopathogens on A. mellifera; 2) entomopathogens sprayed on a smooth surface; 3) entomopathogens sprayed on soy leaves; and 4) entomopathogens mixed with candy paste (sugar syrup). Five treatments were prepared: sterile distilled water (control), distilled water sterilized with Tween® 80 (0.01%), and the commercial entomopathogens Metarhizium anisopliae E9 (1.0×109conidiamL−1), Beauveria bassiana PL63 (1.0×108conidia mL−1) and Bacillus thuringiensis var. kurstaki HD-1 (3.0×108sporesmL−1). Each treatment consisted of five repetitions, with 20 workers per repetition, which were stored in a plastic box and, later, in a biological oxygen demand (B.O.D.) incubator (27±2°C, RH of 60%±10%, 12-h photophase). The mortality of the workers was evaluated from 1h to 240h, and the data were analyzed using Bayesian inference. The workers killed by the ingestion of candy paste contaminated with the pathogens (products) were randomly separated and selected for the removal of the midgut. Each midgut was fixed in Bouin's solution and prepared for histology. B. bassiana was verified to reduce the survival of A. mellifera workers in all bioassays. Moreover, M. anisopliae reduced the survival of A. mellifera workers directly sprayed, on a smooth surface and mixed with candy. B. thuringiensis reduced A. mellifera survival on a smooth surface and mixed with candy paste. However, its effects were lower than that observed by B. bassiana. The treatments with the biological products did not induce morphometric alterations in the midgut of A. mellifera.

Bayesian statistics
Entomopathogenic fungi
Entomopathogenic bacteria
Texto Completo

Apis mellifera L. (Hymenoptera: Apidae), the honey bee, is a pollinating bee found in the most varied environments, and has outstanding importance in the cross-pollination of several plant species (Imperatriz-Fonseca et al., 2012). Aside from its important role in pollination, A. mellifera produces honey, propolis, wax, pollen, royal jelly and apitoxin, all products of interest to humans. The commercialization of these products helps in providing income to many producers and beekeepers (Wolff et al., 2008).

Beekeeping is a prominent occupation in the Brazilian economy, with around 350,000 beekeepers, most of them family farmers (SEBRAE, 2014). One of the factors of this success is the correct management of the colonies and the specialization of the labor force, which remains incipient.

Despite the care taken in the apiary at the moment of foraging, worker bees may come into contact with plant products that are toxic to them, to the colony, or are contaminants for honey (Codling et al., 2016). They can also be contaminated by products used to control the mite Varroa destructor Anderson and Trueman (Acari: Mesostigmata) (Medici et al., 2012) or the wax moth Galleria mellonella L. (Lepidoptera: Pyralidae) (James, 2011; Ferreira et al., 2017). In addition, chemicals used in disease and insect control (Lu et al., 2012) and beekeeping pest control may contribute to colony collapse disorder (CCD) (Rucker and Thurman, 2012).

In this sense, studies have also been carried out to evaluate the safety of biological insecticides on A. mellifera, especially on indirect action on the health and development of the colony. The main biological insecticides tested are the entomopathogenic fungi Beauveria bassiana (Alves, 1998; Shaw et al., 2002; Al Mazra’awi, 2007; Meikle et al., 2009; Hamiduzzaman et al., 2012; James et al., 2012; Abdelaal and Hany, 2013) and Metarhizium anisopliae (Alves et al., 1996; Shaw et al., 2002; Kanga et al., 2002, 2003, 2006, 2010; Hamiduzzaman et al., 2012; Abdelaal and Hany, 2013) and the entomopathogenic bacterium Bacillus thuringiensis (Alves, 1998; Brighenti et al., 2007; Alquisira-Ramírez et al., 2014; Lez et al., 2014; D’Urso et al., 2017). While several tests have been conducted, few have reported the effects of these entomopathogens on Africanized A. mellifera, which is the species used in Brazilian beekeeping.

While these entomopathogens, of natural origin or applied in the environment, are considered safe, studies are necessary to evaluate the different methods in which these entomopathogens may come into contact with Africanized A. mellifera and interfere with their biology. In addition, different isolates must be tested, since the market for organic products is not static, and new isolates are constantly found, tested and made available. The aim of this study was to evaluate the effect of the entomopathogens B. bassiana, M. anisopliae and B. thuringiensis on Africanized A. mellifera in different contact methods.

Material and methods

The Africanized A. mellifera workers were obtained from brood frames from Langstroth hives for capped brood, from the Experimental Apiary of the Unidade de Ensino e Pesquisa – Apicultura (UNEPE) at UTFPR-DV. The brood frames were allocated to hives selected based on the quality and quantity of the queen's oviposition and were provided a daily artificial diet (17.5g of soy protein isolate, 4.0g of flax oil, 4.0g of palm oil, 17.5g of yeast extract, 40.9g of sugar, 10.0g of honey, 5.0g of pollen, 1.0g of soy lecithin and 0.1g of vitamin nucleus) until oviposition began. When the presence of 1-day-old eggs was observed, feeding occurred three times a week and counting continued until the 21st day (usually the time when the workers emerge) (Couto and Couto, 2002). On the 19th day, the brood frames were removed from the apiary, packed in Kraft paper bags (60cm×70cm, 50mm thick), sealed, drilled and transported to the Biological Control Laboratory II. The brood frames were placed in a B.O.D. incubator (30±2°C, RH of 70±10% and 12-h photophase) to simulate the environment of the origin hive, until its emergence, thus providing workers of standardized age. After 48h, the bees were collected (age zero) with the aid of a tube using the suction method. To feed the bees, pure candy paste was prepared by mixing 50g of icing sugar with 10mL of pure honey, until a homogeneous mass was formed.

The entomopathogens (treatments) used were M. anisopliae E9 (1.0×109conidiamL−1), B. bassiana PL63 (1.0×108conidiamL−1) and B. thuringiensis var. kurstaki HD-1 (3.0×108sporesmL−1), which were obtained from commercial products and used at concentrations recommended by manufacturers for target pest insects.

Four bioassays were used, employing direct spray techniques, contact with treated surfaces (soy leaves and plastic boxes) and the supply of a contaminated diet. As a control, sterilized distilled water was used in the bioassays of direct spray techniques and contact with treated surfaces. In the bioassays that incorporated entomopathogens with candy paste, pure candy paste was used as a control.

Entomopathogens sprayed on A. mellifera

Each group, containing A. mellifera workers previously anesthetized with carbon dioxide (CO2) (120s), was sprayed with 1mL of the treatment using a PneumaticSagyma® airbrush coupled with a Fanem® constant pressure pump (1.2kgfcm2). The same procedure was performed for all treatments/repetitions. The bees sprayed with the treatments were transferred into plastic boxes (11×11×3.5cm, L×W×H) sealed with voile fabric, on which a piece of cotton wool soaked in distilled water and candy paste was laid.

All bioassays in this study were maintained in a B.O.D. incubator (27±2°C, RH of 60±10%). The mortality of the workers was evaluated from 1h to 240h after the beginning of their exposure to the treatments to estimate the survival period (methodology adapted from Baptista et al., 2009). The experimental design was completely randomized with four treatments and five repetitions with 20 bees each. Each bee was considered an experimental unit.

The dead workers, verified in the treatments with the use of the entomopathogenic fungi, in all the bioassays, were placed in a humidity chamber to confirm mortality by fungus (Alves, 1998).

Entomopathogens on a smooth surface

One milliliter of the treatment was sprayed onto the base of a sterilized plastic box using a Pneumatic Sagyma® airbrush coupled with a Fanem® constant pressure pump (1.2kgf/cm2). The box was subsequently arranged in a horizontal laminar flow chamber for the evaporation of water. The A. mellifera workers, previously anesthetized, were housed inside each box, in groups of 10 individuals, for the entire experimental period. These boxes were sealed with voile fabric, on which cotton soaked in water and candy paste was laid.

Entomopathogens on soy leaves

Soy leaves (Glycine max) were immersed for 5s in each treatment, and then placed in a horizontal laminar flow chamber for the evaporation of water. These leaves were subsequently arranged in plastic boxes. The A. mellifera workers, previously anesthetized, were housed inside each box in groups of 10 individuals. These boxes were sealed with voile fabric, on which cotton soaked in water and candy paste was laid.

Entomopathogens mixed with candy paste

Using the calculated dosage as a function of the weight:volume ratio, the entomopathogens were incorporated into honey. Icing sugar was then added to the honey to obtain a homogeneous diet. The A. mellifera workers, previously anesthetized, were housed in groups of 10 individuals, inside plastic boxes sealed with voile fabric, on which cotton soaked in water and candy paste with the entomopathogens was laid.

Histological analysis of the A. mellifera midgut

To perform histological analysis by repetition/treatment, the midguts of five bees from the bioassay with candy paste incorporated with entomopathogens were used. The samples were fixed in Bouin's fixative and stored in 70% alcohol. They were then dehydrated (alcohol), diaphonized (Xylol), paraffinized and embedded in Histological Paraffin (Cruz-Landim, 2009).

The material embedded in paraffin was cut [2–7μm] in a manual rotating microtome and subsequently stained using hematoxylin/eosin (H/E). The cuts were observed in a TNB-40T-PL Trinocular Opton Light Microscope, and the images were captured with a digital camera (ScopePhoto 2.04).

A quantitative evaluation was performed, by measuring the heights of the bees’ ventricular cells, and a qualitative evaluation was performed by observing tissue alterations. Compared with the samples from the control, they had no alterations in the midgut tissues.

Statistical analyses

Survival analysis for the lifetime (days) of bees during the bioassays was applied, using non-parametric (Kaplan–Meier) and parametric adjustments (Weibull model (1), f(t), S(t) and tp are, respectively, the probability density function, survival function and p-percentile tp=100p% of the distribution, where p=0.5 is the median). Estimates of these parameters were obtained by Bayesian inference.

Its notation is T∼Wα,γ, and α>0 and γ>0 are the scale and shape parameters, respectively. Assuming the parameterization, such that, λ=log(1/αγ), making β=eγ=1/αγ and, consequently, α=e(log(β)/γ), non-informative distributions were considered a priori for all parameters, that is, λN(0, 10−6) and γGama(10−3, 10−3) (OpenBugs parameterization). The subsequent marginal distributions for the parameters were obtained through the BRugs package of the software R Core Team (2013). The value “1” and the frequency estimator were considered initial values for γ and λ, respectively. A total of 1,100,000 values were generated in an MCMC process, considering a sampling period of 100,000 initial values. The final sample of 11,000 values was formed after applying jumps of 100 in size, in order to eliminate the autocorrelation between values generated in the process. The convergence of the chains was verified through the R coda package, using the criterion of Heidelberger and Welch (1983). The parameters of the models, as well as the effects of the contrasts between treatments, were considered significant if their respective intervals, with 95% credibility for the a posteriori means, did not include the value zero.

To perform the histological analysis, the data of the quantitative tests were submitted to an analysis of variance (ANOVA), and the means were compared via the Scott Knott test, with 5% significance in the Assistat software (Silva et al., 2012).

ResultsEntomopathogens sprayed on A. mellifera

The entomopathogens M. anisopliae and B. bassiana reduced the survival of A. mellifera workers (Table 1) when sprayed directly on them. M. anisopliae reduced A. mellifera survival to 104.7h, and B. bassiana to 62.6h, while the control survival was much greater (127.6h) (Fig. 1A).

Table 1.

Lethal survival time (mean±SD a posteriori of the median parameter of the Weibull distribution (1)) of Africanized Apis mellifera workers in contact with entomopathogens. Temperature 27±2°C, 12-h photophase and relative humidity of 60±10%.

Bioassay  Treatment  Survival (h) 
Entomopathogens sprayed on Apis melliferaControla  127.6±8.17b 
Metarhizium anisopliae  104.7±5.97c 
Beauveria bassiana  62.6±3.01d 
Bacillus thuringiensis  167.2±7.60a 
Entomopathogens on a smooth surfaceControla  197.8±4.80a 
Metarhizium anisopliae  128.0±5.80c 
Beauveria bassiana  97.3±1.10d 
Bacillus thuringiensis  144.9±8.00b 
Entomopathogens on soy leavesControla  133.9±6.91a 
Metarhizium anisopliae  134.4±6.90a 
Beauveria bassiana  89.1±3.18b 
Bacillus thuringiensis  136.1±8.03a 
Entomopathogens mixed with candy pasteControla  169.8±7.56a 
Metarhizium anisopliae  141.9±9.86b 
Beauveria bassiana  117.3±7.88d 
Bacillus thuringiensis  131.3±7.97c 

Sterilized distilled water.

Different letters in the column indicate significant differences between treatment averages, using Bayesian contrasts at a 95% credibility level.

Fig. 1.

Survival curve (hours) of Africanized Apis mellifera workers. (A) Entomopathogens sprayed on A. mellifera, (B) entomopathogens on a smooth surface, (C) entomopathogens on soy leaves and (D) entomopathogens mixed with candy paste. Kaplan–Meier vs Weibull survival test adjusted for time (h). Temperature 27±2°C, 12-h photophase and relative humidity of 60±10%. Sterilized distilled water.

Entomopathogens on a smooth surface

All the entomopathogens evaluated reduced the survival of A. mellifera workers when they came into contact with the smooth surface containing these agents (Table 1). B. bassiana was the entomopathogen that most reduced the survival of the workers, in which 50% of the population survived for 97.3h after the experiment began. M. anisopliae reduced survival to 128h and B. thuringiensis to 144.9h. In the control group, on the other hand, 50% of A. mellifera survived for 197.8h; that is, for 8 days (Fig. 1B).

Entomopathogens on soy leaves

When sprayed on soy leaves, the entomopathogen B. bassiana reduced the survival of A. mellifera workers (Table 1). In this bioassay, 50% of the workers survived for 89.1h after the experiment began (Fig. 1C).

Entomopathogens mixed with candy paste

When B. bassiana was mixed with the candy paste and offered to the workers as food, it caused a reduction in survival (117.3h) when compared to other treatments. However, in comparison to other bioassays, this technique least affected the longevity of A. mellifera (Table 1 and Fig. 1D).

Histological analysis of the A. mellifera ventricle

There were no changes in the ventricular cell length of A. mellifera workers fed with candy paste integrated with B. thuringiensis, B. bassiana, M. anisopliae or pure candy paste (Table 2).

Table 2.

Length (μm) (±SE) of Africanized Apis mellifera worker midgut (ventricle) cells after feeding with candy paste mixed with the entomopathogens. Temperature 27±2°C, 12-h photophase and relative humidity of 60±10%.

Treatments  Ventricle cells (μm) 
Controla  106.7±8.33a 
Metharizium anisopliae  92.0±0.17a 
Beauveria bassiana  83.2±16.10a 
Bacillus thuringiensis  102.3±18.42a 
CV%  11.86 

Sterilized distilled water.Mean (±SD) followed by the same lowercase letter did not differ statistically from one another by Scott–Knott test (p<0.05).


In the bioassays of entomopathogens sprayed on A. mellifera, on a smooth surface and on soy leaves, the entomopathogenic fungus B. bassiana caused the greatest reduction in survival of Africanized A. mellifera workers, especially in the spray bioassay. This is related to the mode of action of B. bassiana, which germinates upon contact with insect integument (Alves, 1998). In this case, the direct spray technique allows an even greater concentration of conidia on the body of A. mellifera, which can be evidenced by the survival of 50% of the workers for 62.6h.

The fungus B. bassiana 447, when applied topically on Africanized adult A. mellifera workers, negatively affected their survival, causing mortality in 50% of the bees (Alves et al., 1996). On the other hand, the isolates of B. bassiana, ARSEF 3769 (ARK), NY (NY; BB008, SCPFRC) and GHA, when tested via the contact method on the surface of canola leaves (Brassica napus L.), did not cause mortality in A. mellifera workers, and no insects infected with the fungus were observed (Al Mazra’awi et al., 2006).

However, the spraying of three other B. bassiana isolates (ARK, GHA and LON) (1.0×108conidiamL−1) mixed with corn flour on adult A. mellifera carnica workers, also resulted in a reduced survival rate, while the isolate NY did not affect survival (Al Mazra’awi, 2007). Another four isolates of B. bassiana (EABb 04/01-Tip, EABb 01/110-Su, Bb-1333, EABb 01/103-Su) sprayed on adult A. mellifera workers did not interfere in survival, while isolate Bb-1333 only reduced survival of pupae (García-Fernández et al., 2008).

Although no studies have been reported on the effect of B. bassiana on A. mellifera when sprayed on a smooth/vitreous surface, some studies have been carried out to verify the effect of this entomopathogen on other hymenopteran insects. These studies showed no interference in the survival of these insects, as verified for Oomyzus sokolowskii (Kurdjumov) (Hymenoptera: Eulophidae) (Santos Jr. et al., 2006).

Of the entomopathogens applied on soy leaves, only B. bassiana interfered negatively in the survival of A. mellifera workers, in which 50% of A. mellifera survived for 89.1h. The contact of the A. mellifera workers with B. bassiana on the surface of soy leaves, and the consequent contamination, showed that even when the fungus is on top of a leaf surface, it can adhere to the body of insects. This bioassay reproduces part of what can occur in the field when A. mellifera workers are foraging and come into contact with the leaves of plants.

There was a reduction in the survival of A. mellifera workers who ingested candy paste incorporated with B. bassiana. Despite this, the survival was less affected than workers who came into contact with the product, or by spraying on different treated surfaces. Alves et al. (1996) evaluated the mortality of workers and found that this same fungus (B. bassiana isolate 447), when introduced into the diet of A. mellifera, caused 76% mortality.

The fungus M. anisopliae reduced the survival of A. mellifera workers when sprayed directly onto them, when in contact with a smooth surface, and during the candy paste ingestion bioassays. Despite having caused reduction, when compared to the survival of the control bees, no treatment showed a lower survival than that observed for B. bassiana.

No studies evaluating M. anisopliae on A. mellifera when sprayed on a smooth/vitreous surface have been reported, however, some studies have assessed the action of this entomopathogen on parasitoids. As in the example of O. sokolowskii (Kurdjumov) (Hymenoptera: Eulophidae), which did not have its survival/longevity altered when it came into contact with plastic cages sprayed (1.0×107conidiamL−1) with B. bassiana and M. anisopliae (447 and E9, respectively) (Santos Jr. et al., 2006). Furthermore, adult Cotesia flavipes parasitoid, exposed to isolates of the fungus M. anisopliae (UFGD 05, IBCB 348 and IBCB 425) (1.0×107, 0.5×108, 1.0×108, 0.5×109 and 1.0×109conidiamL−1) had little reduction in survival when they came into contact with a treated surface (filter paper), demonstrating low virulence of these isolates for this parasitoid (Hayashida et al., 2012).

Other biological A. mellifera parameters were evaluated when in contact with B. bassiana, in which Meikle et al. (2007) found that B. bassiana had no effect on colony weight, adult bee weight or honey production. Abdelaal and Hany (2013), in studies evaluating M. anisopliae (Bioranza®) on biological A. mellifera parameters, found that there was no negative effect on their weight gain when sprayed on the workers, and there was no effect on the larval, prepupal, pupal and adult stages. On other hand, Hamiduzzaman et al. (2012) found that the B. bassiana isolate GHA caused a reduction in worker emergence and mortality when they came into contact with the fungus-contaminated mite.

It should be noted that the confinement caused by bioassays creates stress that makes the bees more vulnerable to fungi (Al Mazra’awi, 2007). Another factor to be considered is the temperature in the bioassays, which favors infection (Alves, 1998) but is not the ideal temperature for bee development (Al Mazra’awi, 2007). B. bassiana and M. anisopliae present optimum germination temperatures between 23 and 30°C (90% moisture) (Alves, 1998). At temperatures out of this range, these fungi are less able to germinate and penetrate the insect, which may occur if the fungi were applied in the field.

In addition to these factors, it should be noted that younger bees have more pronounced grooming and self-grooming behaviors (Brighenti et al., 2007), which may lead to greater contact with the conidia of the fungus, resulting in conidia adhering to the integument of the mouthparts and causing infection.

Contrary to fungal infection mechanisms, B. thuringiensis infection occurs through its ingestion (Fiuza, 2009). As such, the spraying of this entomopathogen on insects should have little to no effect, as verified in the spray bioassay on A. mellifera. In the present study, B. thuringiensis did not reduce the survival of A. mellifera workers, only when mixed with candy paste. It was also verified, in other studies, that the entomopathogen B. thuringiensis reduces the survival of A. mellifera workers when mixed with candy paste (10 and 20g of the product/60g of candy paste), causing 100% mortality 72h after ingestion (Brighenti et al., 2007).

B. thuringiensis acts via ingestion and causes mortality in different insects 48h after ingestion, on average, but this effect was not observed in the present study, in which 50% of A. mellifera workers were still alive 131.3h after ingesting the candy paste. Dai et al. (2012) also verified that the toxin Cry1Ah, from B. thuringiensis, did not alter the survival, longevity, pollen consumption or weight of the hypopharyngeal gland of A. mellifera ligustica and Apis cerana cerana, when added to sugar syrup in different concentrations. The isolates EA3 and EA26 of B. thuringiensis, tested by Alquisira-Ramírez et al., 2014, did not affect the survival of A. mellifera when immersed in or ingesting the solution.

The difference found between studies is influenced by 1) different isolates tested, which is important, since new isolates are constantly being released and found in different parts of the world, demonstrating the need for selectivity tests; 2) different concentrations of the fungus used in the bioassays; 3) culture medium in which the fungi were produced, or in the case of commercial fungi, the different adjuvants; 4) subspecies of A. mellifera submitted to bioassays; and 5) stage of development and age of the bees used in the tests.

In the analysis of the midgut cells of Africanized A. mellifera workers that ingested candy paste containing the entomopathogens, no significant difference was observed between the treatments in the midgut sample analyzed by light microscopy. The midgut is the only organ of the digestive tract of endodermal origin, and is the region of this tube where most of the food digestion and absorption of nutrients takes place. In bees, the midgut is a long and thick cylindrical tube located inside the abdominal cavity. Its wall is formed by the epithelium (constituted of prismatic cells) and by visceral muscular fibers (Cruz-Landim, 2009).

The B. thuringiensis proteins, cry1C and cry2C, in an artificial diet (royal jelly, glucose, fructose, distilled water and yeast extract) supplied to the larvae of A. mellifera, did not cause damage to the border of the midgut when analyzed via light microscopy (Wang et al., 2015).

B. thuringiensis, at the concentrations denominated as field concentration (100.0g/hL), low concentration (40.00g/hL) and high concentration (24,000.00g/hL) caused irregularities in the midgut epithelium of A. mellifera workers after 96h. These changes were verified after the first 24h at the two highest concentrations, when analyzed by scanning and transmission electron microscopy (D’Urso et al., 2017).

The method of spray application in the laboratory occurs with the exposure of bees to the products, simulating the contact of these insects at the time of foraging in the field. To avoid contact of the pollinators with the entomopathogens while spraying these products in the field, farmers should, preferably, carry out the applications late in the afternoon, in periods when the foraging rate is lower. It is also necessary to close the hive in order to avoid drift contamination.

In addition, bees can generate more heat in response to an infection in the environment, as seen with Ascosphaera apis (Maassen ex Claussen) Olive & Spiltoir in A. mellifera (Starks et al., 2000). They can also reduce the impact of pathogens and parasites through hygiene behavior, in which workers identify and remove diseased or infected larvae to avoid or combat these agents (Ibrahim and Spivak, 2006; Richard et al., 2008).

Many studies point out that, even with the changes to A. mellifera workers, B. bassiana can be used in Integrated Pest Management programs with little to no effect on bees (Alves, 1998; Al Mazra’awi, 2007). In addition, A. mellifera has the ability to disseminate B. bassiana, which is advantageous to the field (Al Mazra’awi et al., 2006).

The concentrations of entomopathogens applied to Africanized A. mellifera in this study are concentrations higher than those recommended by the manufacturers, and the workers are exposed to forced spraying, causing A. mellifera to come into contact with these agents, which differs from normal conditions in the field.

Thus, studies of the selectivity of entomopathogens to A. mellifera should be continuously carried out, evaluating different species, isolates, concentrations, and temperatures. Further studies should also assess biological, morphological and morphometric parameters. There is also a need for field trials on the production of queens and brood.


B. bassiana reduced the survival of A. mellifera workers in the four bioassays tested (spraying on A. mellifera, contact on a smooth surface, contact on soy leaves, and mixed with candy paste) in the laboratory.

The entomopathogens B. bassiana, B. thuringiensis and M. anisopliae did not cause morphometric changes in the midgut of A. mellifera fed with candy paste.

Conflicts of interest

The authors declare no conflicts of interest.


This work was supported by the Fundação Araucária (project 25.383 – Agreement 229/2013) and Universidade Tecnológica Federal do Paraná (PAPCDT 7/2015).

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