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Brazilian Journal of Poultry Science

Print version ISSN 1516-635XOn-line version ISSN 1806-9061

Rev. Bras. Cienc. Avic. vol.18 no.3 Campinas July/Sept. 2016

http://dx.doi.org/10.1590/1806-9061-2015-0120 

ARTICLES

ACTIVITY OF SOME BRAZILIAN ISOLATES OF ENTOMOPATHOGENIC FUNGI AGAINST THE POULTRY RED MITE DERMANYSSUS GALLINAE DE GEER (ACARI: DERMANYSSIDAE)

CR KasburgI 

LFA AlvesII 

DGP OliveiraIII 

C RohdeIV 

ILaboratório de Biotecnologia Agrícola - UNIOESTE, Cascavel

IIProfessor/Bolsista Produtividade em Pesquisa, CNPq - UNIOESTE, Cascavel

IIIProfessor - UTFPR, Santa Helena

IVProfessor - UTFPR, Medianeira

ABSTRACT

Poultry red mite Dermanyssus gallinae is a cosmopolitan and hematophagous species commonly found in layer houses around the world. Poultry mite infestations may cause anemia, stress, low body weight and egg production, and mortality. Mite control is typically based on chemical products, but they are not effective and leave residues in eggs; therefore, alternative control methods, such as entomopathogenic fungi, need to researched. This study aimed at evaluating, in the laboratory, the activity of Brazilian isolates of entomopathogenic fungi against D. gallinae. The mites were collected from a commercial layer house and were sprayed with conidial suspensions (1 × 108 conidia/mL) of five isolates of Beauveria bassiana and Metarhizium anisopliae. All tested isolates were pathogenic for the red mite, with confirmed mortality ranging from 22.9 to 52.4%. This demonstrate the potential of the tested entomopathogenic fungi isolates for mite control, and reinforces the need for further studies with other isolates, application strategies, and with fungal formulations.

Keywords: Hematophagous mites; microbial control; ectoparasites; laying hens

INTRODUCTION

Brazilian egg production is based on intensive farming systems, which ensure greater yield in a smaller physical space. However, it favors the development of arthropod pests, such as the red mite Dermanyssus gallinae (De Geer) (Acari, Dermanyssidae). This mite feeds on poultry, causing weight loss, reduced egg production, blood spoliation anemia and, in more severe cases, death. Studies have shown that the red mite can carry Escherichia coli, Salmonella and Coxiella burnetii, as well as viruses (Saint Louis encephalitis virus, avian poxvirus, avian paramyxovirus type I and Newcastle disease virus). In all these cases, the mite may acquire these microorganisms by feeding on the blood of infected birds (Moro et al., 2007; Harrington et al., 2011; Pereira, 2009; 2011; Sparagano et al., 2014).

Mite control in poultry houses is based on chemical acaricides that are apparently effective because they cause momentary reduction of the pest population. Misuse of these products can lead to residues in the eggs, poisoning of workers and poultry in layer houses, environmental contamination; and can also select individuals resistant to the active ingredients (Chauve, 1998; Pereira, 2009; Liebisch, 2011).

As an alternative to chemical control, entomopathogenic fungi Beauveria bassiana (Bals.) Vuill. and Metarhizium anisopliae (Metsch.) Sorok isolates from Europe were evaluated against red mites (Steenberg & Kilpinen 2003). In addition, studies conducted in the laboratory and in the field in Iran and Egypt confirmed the action of fungal isolates from Europe and Asia against D. gallinae (Steenberg et al. , 2006; Kaoud, 2010; Tavassoli et al., 2008; Steenberg & Kilpinen, 2014).

However, in Brazil, studies on alternative pest control are focused only in the in-vitro evaluation of plant extracts (Morrone et al., 2001; Soares, 2012; Oliveira et al., 2014). Therefore, the objective of the present study was to evaluate for the first time the pathogenicity of Brazilian isolates of B. bassiana and M. anisopliae against D. gallinae.

MATERIALS AND METHODS

Mites were collected from a commercial layer house. Engorged mite females were selected based on their description (Flechtmann, 1973), placed in glass tubes closed with gauze, and kept at 26ºC, 70% RH and 12 h photoperiod for acclimatization until use in the experiment (Soares, 2012). Isolates of the fungi B. bassiana (Unioeste 01, Unioeste 02, Unioeste 04 and Unioeste 05) and Metarhizium anisopliae (Unioeste 22) were evaluated (Table 1).

Table 1 Total and confirmed mortality of D. gallinae by different isolates of entomopathogenic fungi. 

Treatment Host1 Total mortality Confirmed mortality
Control 25.7 ± 1.29 b 0.0 ± 0.00 c
Beauveria bassiana
Unioeste 01 Astylus variegatus (adult) 49.5 ± 1.75 ab 43.8 ± 1.70 ab
Unioeste 02 Alphitobius diaperinus (larvae) 71.4 ± 1.22 a 65.7 ± 1.14 a
Unioeste 04 Alphitobius diaperinus (larvae) 37.2 ± 1.71 ab 22.9 ± 1.28 b
Unioeste 05 Alphitobius diaperinus (adult) 59.1 ± 1.10 ab 52.4 ± 1.07 ab
Metarhizium anisopliae
Unioeste 22 Soil, Ilex paraguaiensis plantation 52.4 ± 0.59 ab 38.1 ± 0.56 ab
CV (%) 36.3 42.5

1Entomopathogenic Fungi Collection - Laboratory of Agricultural Biotechnology, Unioeste-Cascavel, PR, Brazil. Astylus variegatus and Alphitobius diaperinus - Coleoptera: Melyridae and Tenebrionidae, respectively.

Means followed by the same letter incolumn do not differ by Tukey's test (p ≤0.05)

The fungi were grown in culture medium (sporulation medium) in Petri dishes (10 days at 26ºC; 12 h photoperiod) (Alves et al., 1998). After incubation, conidia were collected by scrapping the surface of the culture medium. A suspension of conidia was prepared (1 × 108 conidia/mL) in distilled water + Tween 80(r) at 0.01%. Fifteen adult female mites were transferred to a Petri dish and sprayed with 1 mL of the conidial suspension using a Potter spray tower (0.7 kgf/cm2). As control treatment, only distilled water + Tween 80(r) to 0.01% was applied. After spraying, mites were transferred to glass tubes closed with cotton gauze plug, and observed daily for seven days. The dead mites were removed using a fine-tipped brush and placed in a humid chamber and incubated under the above-mentioned conditions for the confirmation of mortality by the fungus. All treatments included seven replicates of 15 mites each. Experiments were repeated twice.

A completely randomized experimental design was applied. Total and confirmed mortality data were transformed into arcsen and analyzed for normality and variance homogeneity by the Shapiro-Wilk and Levene's tests, respectively. Means were compared by Tukey's test (p ≤0.05) using Sisvar statistical software (Ferreira, 2011).

RESULTS AND DISCUSSION

All B. bassiana isolates were pathogenic for the poultry red mite D. gallinae (confirmed mortality between 22.9 and 52.4%). Significant differences were detected only between Unioeste 2 and Unioeste 4 isolates. The M. anisopliae Unioeste 22 isolate caused 52.4% total mortality and only 38.1 % confirmed mortality (Table 1).

Steenberg & Kilpinen (2003) also found 60% mortality of the poultry red mite by B. bassiana and 30% by M. anisopliae in the laboratory. The acaricidal activity of a commercial product based on of B. bassiana conidia in a powder formulation was also demonstrated under laboratory conditions, with 65% mortality after five days of inoculation (Kaoud, 2010).

Isolates of M. anisopliae were also pathogenic against mite D. gallinae in the laboratory, with mortality ranging between 40 and 70% depending on the tested isolates, and, under field conditions, they were shown to be efficient in commercial poultry houses treated with a conidia suspension at a high concentration (1 × 109 conidia/mL) (Tavassoli et al., 2008, 2011).

The results of the present study demonstrate the potential of the tested entomopathogenic fungi isolates for the control of the poultry red mite. However, it should be noted that this is a preliminary test with Brazilian isolates, and further research is suggested to find more virulent isolates and to test application strategies and fungal formulations, both in the laboratory and in the field.

ACKNOWLEDGEMENTS

The authors are thankful to the Brazilian National Research Council (CNPq) and to the Coordination for the Improvement of Higher Education Personnel (CAPES) for providing the research grants.

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Received: November 2015; Accepted: June 2016

Corresponding author e-mail address Luis Francisco Angeli Alves Laboratório de Biotecnologia Agrícola - UNIOESTE, Rua Universitária, 2069 85819-110. Cascavel, PR, Brasil Tel: (005545) 32203288 Email:luis.alves@unioeste.br

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