Literature DB >> 32233140

Application of carbon dioxide as a novel approach to eradicate poultry red mites.

JeongWoo Kang1, Md Akil Hossain1, Jiyeon Jeong2, Haechul Park1, Jin Hyun Kim2, Min Su Kang2, Yong Kuk Kwon2, Yong Sang Kim1, Sung Won Park3.   

Abstract

Poultry red mites (PRMs), Dermanyssus gallinae, are one of the most harmful ectoparasites of laying hens. Because of their public health impact, safe, effective methods to eradicate PRMs are greatly needed. Carbon dioxide (CO₂) was shown to eradicate phytophagous mites; however, there is no evidence that PRMs can be eradicated by CO₂. Thus, the efficacy of CO₂, applied by direct-spraying and dry ice-generated exposure, for eradicating PRMs was investigated. Both treatments eradicated > 85% of PRMs within 24 h and 100% of PRMs by 120 h of post-treatment. Therefore, these novel approaches may be useful for eradicating PRMs in clinical settings.
© 2020 The Korean Society of Veterinary Science.

Entities:  

Keywords:  Acaricides; Dermanyssus gallinae; asphyxiator; carbon dioxide

Year:  2020        PMID: 32233140      PMCID: PMC7113580          DOI: 10.4142/jvs.2020.21.e37

Source DB:  PubMed          Journal:  J Vet Sci        ISSN: 1229-845X            Impact factor:   1.672


INTRODUCTION

The poultry red mite (PRM), Dermanyssus gallinae (De Geer, 1778), is an important hematophagous ectoparasite that attacks resting hens, mainly at night, for a blood meal [1]. After feeding, the mites hide in cracks and crevices, where they mate and lay eggs. PRM infestations have several negative effects on the hens. Because an adult mite ingests approximately 0.2 μL of blood [2]. The PRM infestation and the mortality of hens are strongly related, and it is mentioned in some reports that the mortality rate of hens increases ten-times following severe infestation [3]. In addition to the direct physiological effects, PRMs may also be carriers of several important disease-causing agents, such as Salmonella [4] and the microbial agents that cause spirochetosis [5] and encephalitis. PRMs are considered to be the most damaging pests in poultry egg production [678], and as the number of infections increase, controlling PRMs is becoming very complicated. A range of acaricides, including organophosphates, carbamate, amidine and pyrethroid-based acaricides, are widely used to control PRMs [678]. However, many acaricides are not specifically labeled for use against PRMs [678]. Fipronil is an acaricide that is authorized for use in plant protection but is not approved for use as a veterinary medicinal product on food-producing animals [9]; however, in many countries, it is illegally used on laying hens to eradicate red mites [9]. Fipronil-contaminated eggs were detected in Belgium in July 2017, which was attributed to the illegal use of fipronil on poultry farms [9]. Furthermore, in various parts of the world, resistance against all classes of acaricides has developed [10]. Another important aspect to consider in the development of treatments for PRMs is the safety of non-targets, such as humans, the hosts (hens), and their eggs [10]. In recent years, several alternatives for the safe eradication of PRMs have been developed, including essential oils, biological compounds, predator mites, heat treatments, intermittent lighting programs, inert dusts and even vaccines [10]. It has been reported that the application of carbon dioxide (CO2) significantly reduced several species of phytophagous mites by asphyxiation [11]. Therefore, we hypothesized that CO2 would reduce the viability of PRMs. Therefore, this study was designed to evaluate the efficacy of CO2 treatment for the eradication of PRMs by exposing PRMs to CO2 both in a chamber for different durations and by direct spraying.

MATERIALS AND METHODS

Cardboard traps (100 mm × 70 mm × 3 mm) were prepared in-house using cardboard (Hansol Papertech Company Limited, Korea). To collect mites, cardboard traps were installed at a poultry farm located in Mungyeong city, Republic of Korea as described previously [12]. Then, the traps were collected in plastic zip-lock bags (Perfect Packing Company Limited, China). In one experiment, 20 individual PRMs each were transferred to 4 different petri dishes (SPL Life Sciences Company Limited, Korea) as described previously [13]. Then, CO2 was sprayed onto the PRMs in petri dishes for 10 sec by using a CO2 cylinder equipped with a sprayer (Catalina Cylinders, USA). The density of CO2 in the cylinder was 449,901 ppm or g/m3, and the exposure time was 10 sec. Then, the petri dishes were kept in normal experimental condition (25°C ± 2°C, < 65% related humidity) without sealing and the percentage of killed PRMs was determined after 2, 24, 48, and 120 h of CO2 spraying. The mites were classified as dead if they were in a dorsal position or if no motility was detected by touching with a fine-tipped artist's paintbrush. In another experiment, 3 different amounts (100, 300 and 500 g) of dry ice were used in 3 different chambers (Semadeni Plastics Group, Switzerland) to generate CO2. The CO2 densities in the chambers containing 100, 300, and 500 g of dry ice were 833, 2,500 and 4,167 ppm or g/m3, respectively. Twelve petri dishes containing 20 PRMs each were separately placed in 3 different CO2 chambers (4 petri dishes/chamber) for 1, 2, 5, 10, and 30 min. The densities of CO2 inside those respective petri dishes were same as in those chambers. After exposing the PRM in CO2 inside the chambers for the above mentioned duration, those petri dishes were kept in normal experimental condition without sealing. The percentages of killed PRMs after exposing for certain times (1, 2, 5, 10, and 30 min) in the chambers were determined at 4 different times (2, 24, 48, and 120 h) using the procedure described above. Petri dishes that contain 20 PRMs in each were separately kept at normal experimental condition without CO2 exposing was considered as control, and the mortality rate of control PRM was determined as mentioned for CO2 treated groups. These experiments were conducted as illustrated in Fig. 1 and were repeated 3 times.
Fig. 1

Schematic representations of CO2 treatment methods to eradicate PRMs in this study. (A) Direct spraying of CO2. (B) Exposure to dry ice-generated CO2 in a closed chamber.

CO2, carbon dioxide; PRM, poultry red mite.

Schematic representations of CO2 treatment methods to eradicate PRMs in this study. (A) Direct spraying of CO2. (B) Exposure to dry ice-generated CO2 in a closed chamber.

CO2, carbon dioxide; PRM, poultry red mite.

RESULTS AND DISCUSSION

The chemicals used to control PRMs may have adverse effects on humans, both directly, when workers are exposed to the chemicals, and indirectly, through the consumption of pesticide residue-containing poultry eggs [14]. Therefore, we sought to develop an effective and convenient treatment that eradicates PRMs without causing any harm to chickens or other non-target individuals. In this study, we investigated the efficacy of 2 different CO2 treatment methods for eradicating PRMs. After CO2 treatment using either method, the survival rates of the parasites were reduced (Table 1) and the mortality rate increased with increased CO2 exposure time. This suggests that CO2 may affect one or more vital physiological processes of the PRMs such as respiration [11]. A significant percentage (26%–78%) of the PRMs were killed after 2 h of CO2 application by both spraying and exposure, and most or all of the remaining mites were killed (73%–100%) within 120 h after CO2 application. Importantly, the mites did not recover from the CO2 treatment.
Table 1

Efficacy of CO2 treatment for the eradication of poultry red mites using different application methods

CO2 treatment methodEradication rate (%) at different time intervals after CO2 treatment
2 h24 h48 h120 h
833 ppm2,500 ppm4,167 ppm833 ppm2,500 ppm4,167 ppm833 ppm2,500 ppm4,167 ppm833ppm2,500 ppm4,167 ppm
Control0.0 ± 0.00.0 ± 0.00.0 ± 0.01.7 ± 2.0
Exposure (1 min)25.8 ± 5.634.5 ± 6.542.5 ± 4.835.2 ± 5.441.0 ± 4.348.7 ± 10.150.5 ± 6.755.4 ± 4.360.2 ± 9.472.6 ± 8.592.5 ± 3.295.2 ± 5.5
Exposure (2 min)31.5 ± 9.948.7 ± 4.650.2 ± 5.835.6 ± 4.355.5 ± 5.759.5 ± 6.759.5 ± 10.068.7 ± 6.869.2 ± 5.673.7 ± 6.789.2 ± 9.597.7 ± 9.0
Exposure (5 min)45.4 ± 5.772.2 ± 5.470.7 ± 6.755.8 ± 2.676.7 ± 6.875.5 ± 6.057.4 ± 9.785.5 ± 7.480.6 ± 7.285.3 ± 8.492.2 ± 8.799.5 ± 8.5
Exposure (10 min)59.7 ± 7.177.5 ± 4.376.6 ± 4.364.5 ± 9.380.6 ± 5.482.8 ± 4.669.5 ± 2.785.6 ± 8.188.4 ± 11.284.2 ± 12.595.7 ± 7.597.5 ± 8.7
Exposure (30 min)62.5 ± 5.777.8 ± 5.877.2 ± 7.372.8 ± 10.082.2 ± 9.885.5 ± 6.378.5 ± 6.989.8 ± 3.591.5 ± 9.785.4 ± 11.796.2 ± 5.499.0 ± 2.0
Spray (10 sec)74.6 ± 15.289.4 ± 11.596.8 ± 12.8100.0 ± 0.0

Data represent the mean ± SD of 3 replicate analyses. The eradication rates of poultry red mites in CO2 treatment groups (both CO2 exposure and spraying) are significantly (p < 0.05) different than the control group at each observation time (2, 24, 48, and 129 h).

CO2, carbon dioxide.

Data represent the mean ± SD of 3 replicate analyses. The eradication rates of poultry red mites in CO2 treatment groups (both CO2 exposure and spraying) are significantly (p < 0.05) different than the control group at each observation time (2, 24, 48, and 129 h). CO2, carbon dioxide. Under normal experimental condition, without any treatment (control), the PRMs remained stable until 24 h of observation; however, by 120 h of observation, 1.7% of red mites dead. In contrast, direct CO2 spraying resulted in high killing rates (75, 89, 97, and 100%) within 2, 24, 48, and 120 h, respectively. In the CO2 exposure method, the PRM killing rates were lower when the CO2 density in the chamber was lower and higher when the CO2 density was higher. Exposure of the PRMs to both 2,500 and 4,167 ppm CO2 for ≥ 10 min killed > 75% of the test parasites within 2 h and > 80% of PRMs within 24 h, respectively. The killing rates of PRMs obtained by exposing to both 2,500 and 4,167 ppm CO2 for 10 min were similar to the killing rate obtained by the spraying method. Moreover, the findings of this study demonstrated that both the CO2 spraying and exposure methods can completely eradicate PRM. Using the spraying method, complete eradication of the PRMs was observed within 120 h of CO2 treatment. PRMs exposed to 2500 ppm CO2 for ≥ 10 min were completely eradicated within 120 h of CO2 treatment. PRMs exposed to 4,167 ppm CO2 were also completely eradicated within 120 h of CO2 treatment, regardless of the duration of CO2 exposure. It is also clearly evident that the PRM killing rate was dependent on the CO2 density in the chamber. The killing trends for both methods were nearly the same. Furthermore, ≥ 80% mortality in 24 h is normally considered to be sufficiently effective according to the “Guideline for testing efficacy of insecticide for prevention of infectious diseases (Ministry of Food and Drug safety of Korea)” [15]. Based on this guideline, the spraying of CO2 for 10 sec is effective enough to eradicate red mites. Similarly, exposing the PRMs in CO2 for at least 10 min confirm the efficacy of this treatment method. To completely eradicate PRMs (100%) in a closed environment, like a chicken room on a farm, CO2 exposure in a sealed room for 30 min may be a preferable treatment method.The CO2 spraying method can be applied to birds to eradicate PRMs before introducing them to a farm. Moreover, spraying CO2 in local environments where PRM colonies are located, including walls, floors, roosts, nests, boxes, cracks, and crevices, may lead to their rapid eradication. PRMs can be completely eradicated from chicken rooms by exposing the rooms to CO2 under closed conditions at a time when they are “all in all out.” These novel PRM eradication methods can be further optimized for application in clinical settings. For this purpose, a spray bottle or can of CO2 could be used for rapid application and ease of transport. However, further studies are needed to determine the specific mechanisms underlying the eradication of PRMs by CO2.
  9 in total

1.  Traps containing acaricides for the control of Dermanyssus gallinae.

Authors:  Jan Chirico; Ragnar Tauson
Journal:  Vet Parasitol       Date:  2002-12-11       Impact factor: 2.738

2.  Laboratory observations on three species of bird mites.

Authors:  R K SIKES; R W CHAMBERLAIN
Journal:  J Parasitol       Date:  1954-12       Impact factor: 1.276

3.  Resistance of the red poultry mite to pyrethroids in France.

Authors:  F Beugnet; C Chauve; M Gauthey; L Beert
Journal:  Vet Rec       Date:  1997-05-31       Impact factor: 2.695

4.  Encounter the poultry red mite resistance to acaricides in Czechoslovak poultry-farming.

Authors:  P Zeman
Journal:  Folia Parasitol (Praha)       Date:  1987       Impact factor: 2.122

5.  Potential role of Dermanyssus gallinae De Geer, 1778 in the circulation of the agent of pullurosis-typhus in hens.

Authors:  P Zeman; V Stika; B Skalka; M Bártík; F Dusbábek; M Lávicková
Journal:  Folia Parasitol (Praha)       Date:  1982       Impact factor: 2.122

Review 6.  Significance and control of the poultry red mite, Dermanyssus gallinae.

Authors:  O A E Sparagano; D R George; D W J Harrington; A Giangaspero
Journal:  Annu Rev Entomol       Date:  2014       Impact factor: 19.686

7.  Anaemia in poultry infested with the red mite Dermanyssus gallinae.

Authors:  A C Kirkwood
Journal:  Vet Rec       Date:  1967-04-29       Impact factor: 2.695

8.  Determination of phoxim residues in eggs by using high-performance liquid chromatography diode array detection after treatment of stocked housing facilities for the poultry red mite (Dermanyssus gallinae).

Authors:  G Hamscher; B Priess; H Nau
Journal:  Anal Chim Acta       Date:  2006-09-28       Impact factor: 6.558

9.  Evaluation of the poultry red mite, Dermanyssus gallinae (Acari: Dermanyssidae) susceptibility to some acaricides in field populations from Italy.

Authors:  M Marangi; M A Cafiero; G Capelli; A Camarda; O A E Sparagano; A Giangaspero
Journal:  Exp Appl Acarol       Date:  2008-12-17       Impact factor: 2.380

  9 in total
  1 in total

Review 1.  Parasitic Mite Fauna in Asian Poultry Farming Systems.

Authors:  Olivier A E Sparagano; Jeffery Ho
Journal:  Front Vet Sci       Date:  2020-07-09
  1 in total

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