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An improved method for in vitro feeding of adult female Dermanyssus gallinae (poultry red mite) using Baudruche membrane (goldbeater’s skin)
Parasites & Vectors volume 13, Article number: 585 (2020)
Dermanyssus gallinae, or poultry red mite (PRM), is an important ectoparasite in laying hen, having a significant effect on animal welfare and potentially causing economic loss. Testing novel control compounds typically involves in vitro methodologies before in vivo assessments. Historically, in vitro methods have involved PRM feeding on hen blood through a membrane. The use of hen blood requires multiple procedures (bleeds) to provide sufficient material, and the use of a larger species (e.g. goose) could serve as a refinement in the use of animals in research.
The in vitro feeding device used was that which currently employs a Parafilm™ M membrane (Bartley et al.: Int J Parasitol. 45:819–830, 2015). Adult female PMR were used to investigate any differences in mite feeding, egg laying and mortality when fed goose or hen blood. Effects on these parameters when PRM were fed through either the Parafilm™ M membrane or the Baudruche membrane alone or through a combination of the membrane with an overlaid polyester mesh were tested using goose blood.
Poultry red mites fed equally well on goose or hen blood through the Parafilm™ M membrane, and there were no significant differences in mortality of PRM fed with either blood type. A significant increase (t test: t = 3.467, df = 4, P = 0.03) in the number of eggs laid per fed mite was observed when goose blood was used. A 70% increase in PRM feeding was observed when the mites were fed on goose blood through a Baudruche membrane compared to when they were fed goose blood through the Parafilm™ M membrane. The addition of an overlaid polyester mesh did not improve feeding rates. A significant increase (analysis of variance: F(3, 20) = 3.193, P = 0.04) in PRM egg laying was observed in mites fed on goose blood through the Baudruche membrane compared to those fed goose blood through the Parafilm™ M membrane. A mean of 1.22 (standard error of the mean ± 0.04) eggs per fed mite was obtained using the Baudruche feeding device compared to only 0.87 (SEM ± 0.3) eggs per fed mite using the Parafilm™ M device when neither was combined with a polyester mesh overlay.
The in vitro feeding of adult female PRM can be readily facilitated through the use of goose blood in feeding devices with the Baudruche membrane.
Infestation of laying hen houses with the poultry red mite (PRM), Dermanyssus gallinae, is a major animal welfare and economic problem for the egg-producing industry worldwide, costing the poultry industry in excess of €231 million per year in the EU alone . Current treatment options are limited and often ineffective. PRM infestations cause serious welfare and production issues in the birds as a result of their nocturnal blood-feeding activities and potential as competent vectors for bacterial and viral pathogens [1,2,3]. Novel methods of controlling PRM (novel biopesticides and plant-derived products; semiochemicals and growth-regulators; vaccines etc.) are typically tested initially using small numbers of PRM in in vitro efficacy assays, followed by field testing using large numbers of both parasites and hens [4,5,6]. The in vitro feeding devices employed in these assays contain the mites, allowing them to feed on hen blood through a membrane, such as day-old chick skin [7, 8], or artificial membranes, such as the Parafilm™ M membrane [9, 10]. This methodology has technical limitations, not least due to the requirement for high numbers of replicates to overcome variable feeding rates when using Parafilm™ M and issues around supply, uniformity and quality when using chick skin [7, 8]. In addition, to supply sufficient hen blood for these assays, multiple invasive procedures are required involving venepuncture on hens’ wing veins. The aim of this study was to investigate the use of goose blood (which can be obtained in far higher volumes per procedure than hen blood) as a higher welfare alternative food source for the assays and goldbeater’s skin (also known as Baudruche membrane) as an alternative feeding membrane that may enable improved feeding of adult female PRM.
Chicken and goose whole blood samples were collected by wing vein venepuncture into a 1.5-ml capacity Eppendorf tube or syringe containing heparin, respectively (Sigma-Aldrich Co. Ltd., Dorset, UK), to give a final heparin concentration of 20 units/ml blood. Hen blood from four hens was pooled for further use; individual goose bleeds were used for each in vitro experiment. Trials were carried out on the day of blood collection, and blood was kept at room temperature (RT) until needed. The hens used were pullets aged approximately 20 weeks, housed in groups in floor pens. Male geese approximately 12 months old were used and housed in predator-proofed, enriched paddocks.
Poultry red mites were collected and stored as previously described . Briefly, D. gallinae of mixed stage and sex were collected at 3-weekly intervals from a commercial egg-laying unit. Prior to the feeding assays, mites were stored in vented 75-cm2 canted tissue culture flasks (Corning Inc., Corning, NY, USA) at RT for 7 days to allow blood digestion to occur, after which they were stored at 4 ℃ for up to 3 weeks.
In vitro feeding device
Feeding devices (Fig. 1) were constructed as described previously [3, 9, 12]. For the initial experiments comparing hen and goose blood as food sources, the feeding membrane used was Parafilm™ M. For the experiments comparing feeding membranes, the membranes were either a 2 × 2-cm square of Parafilm™ M membrane or Baudruche membrane (Preservation Equipment Ltd, Diss, UK), with the latter held in place by wrapping a strip of Parafilm™ M over the edges of the Baudruche membrane, around the outside of the tube, before the modified pipette bulb goose blood reservoir was placed over the top (Fig. 1). In the experiments to assess the impact of an overlaid polyester mesh on the feeding membranes, to improve mite attachment, a polyester mesh (Plastok Ltd, Birkenhead, UK) with an aperture width of 105 µm and a depth of 63 µm  was overlaid on the ventral aspect of the membranes used in the devices and heparinised goose blood was used as the food source.
Mites removed from storage at 4 ℃ were maintained at RT for 20 min to allow motile mites to migrate to the cap of the flask. Only motile, adult female mites were collected from the flask caps and transferred to the feeding devices (50 mites per device), following which the devices were sealed. Once all feeding devices contained mites, heparinised blood was added to the devices, which were then incubated in the dark in an incubator (model MLR-351H; Sanyo, Osaka, Japan) at 39 ℃ and 85% relative humidity (RH) for 3 h. Following incubation, mites were recovered from the devices, and each fed mite was transferred into a single-well of a 96-well tissue culture plate (Costar, Corning, NY, USA) which was then sealed using AeraSeal™ tape (Sigma-Aldrich Co.). Plates were placed into an incubator at 25 ℃ and 85% RH, and the mites observed using a stereo microscope at 3, 24, 48 and 144 h to record mite egg laying and mortality.
For the comparison of adult female PRM feeding rates, egg laying and mortality when fed goose blood or hen blood through a Parafilm™ M membrane, we performed a single experiment with three replicate assays per food source. For the comparison of adult female PRM feeding rates, egg laying and mortality when the PRM were fed goose blood through either a Parafilm™ M or a Baudruche membrane (or each of these membranes overlaid with the polyester mesh), we performed two repetitions of the experiment with three replicate assays per device in each.
Unpaired Student’s t tests were performed on mite feeding, mortality and fecundity data for the comparison of mites fed on goose or hen’ blood. An analysis of variance (ANOVA) was used to determine variance between the two experiments, which were held on different days, to compare the different membranes. ANOVA using Dunnett’s multiple comparisons was used to compare any differences between the Parafilm™ M membrane and Parafilm™ M membrane + mesh, Baudruche membrane and Baudruche + mesh. To examine any difference between the Parafilm™ M membrane and Parafilm™ M membrane + mesh and Baudruche membrane and Baudruche + mesh, we used an ANOVA using Sidak’s multiple comparisons test. All analyses were carried out using GraphPad Prism v8 (GraphPad Software, San Diego, CA USA; www.graphpad.com).
Comparison of feeding between goose and hen blood
Goose and hen blood were equally successful in terms of the numbers of PRM feeding on each blood source and survival of the mites following feeding (Table 1). There was a 26% increase in total egg production in mites fed on goose blood compared to those fed on hen blood, and the number of eggs laid per fed mite was significantly higher in those mites fed on goose blood (t test: t = 3.467, df = 4, P = 0.03).
Comparison of PRM feeding on goose blood through Parafilm™ M, Baudruche membranes and in those membranes overlaid with polyester mesh
No statistically significant differences were demonstrated within the same treatment groups in the two repetitions of the experiment in terms of feeding, egg laying, progeny per fed mite or mortality; consequently, replicates from the two repetitions of the experiment were combined for further analysis. Comparison of feeding rates, fecundity and mortality between PRM fed with goose blood through the different membranes is shown in Table 2. The Parafilm™ M membrane in one of the feeding devices developed a split during the incubation period, which is common with this type of membrane, whereas none of the Baudruche membranes failed. No feeding occurred in the failed device, and so data from this replicate were not included in the analysis. A 70% increase in the mean number of PRM feeding was observed in mites fed on goose blood through a Baudruche membrane compared to a Parafilm™ M membrane (Fig. 2; Table 2); however, due to the high levels of variability in the feeding levels of mites feeding through a Parafilm™ M membrane, this increase was not statistically significant (P = 0.1). Addition of an overlaid polyester mesh did not improve feeding rates on either membrane; rather, a significant (ANOVA: F(3,20) = 3.1, P = 0.04) decrease in feeding was noted (Table 2) in the devices containing Baudruche + mesh compared to the Baudruche membrane alone. Mites which had fed through Baudruche membrane (without overlaid mesh) produced double the number of eggs of those fed through a Parafilm™ M membrane (ANOVA: F(3, 20) = 3.193, P = 0.04) over the course of the experiment (Table 2; Fig. 2).
We have demonstrated that goose blood is an excellent food source for laboratory-maintained PRMs and that the Baudruche membrane is a superior feeding membrane compared to the traditionally used ParafilmTM M membrane for in vitro feeding assays. Geese are well suited as blood donor animals as their size means they can donate more blood per procedure than hen (approx. 20 fold). Generally, blood collected from individual hen is pooled for use in feeding assays, and the amount collected can be limiting in terms of number of replicates and/or size of experiment. A statistically significant increase in eggs laid per fed mite was demonstrated using goose blood compared to hen blood in the initial experiment using the ParafilmTM M-only device.
To our knowledge, this is the first published report on the use of Baudruche membrane in the feeding of D. gallinae, although this membrane has been used for tick feeding in conjunction with silicone as recently as 2019  and for mosquitoes as early as 1964 . Chick skin has been used successfully to allow in vitro feeding of PRM [4, 7, 8], but the availability and ease of use of artificial membranes has led to more frequent use of the latter. Membranes such as Parafilm™ M  or Nescofilm coated with a hen skin extract  are used and can work well. However, Parafilm™ M membranes often fail due to the need to stretch the membrane to make it sufficiently thin for mites to be able to feed successfully, and Nescofilm is no longer commercially available. Fed mites are difficult to recover from a device with membrane failure, possibly leading to misleading mortality data . In addition, the rate of device failure and highly variable feeding rates require additional replicates, with the associated increased invasive sampling of hens. Therefore, a more reliable in vitro feeding device increases hen welfare in terms of refinement in number of procedures required for successful data collection.
Krull et al. 2017  suggested that thin membranes for the feeding of tick larvae and nymphs could be obtained using Baudruche membrane coated in silicone or even by using Baudruche membrane alone. As previous attempts at using silicone with lens tissue, as described by Kröber and Guerin , did not result in PRM feeding in our laboratory (data not shown), we hoped that the reported high tensile strength of the Baudruche membrane alone would suffice and that it would be thin enough to allow the mites to feed without damaging the membrane. The addition of a mesh support has been successfully used in previous tick studies [14, 16, 17], resulting in enhanced attachment times of ticks to membranes. We therefore decided to test a mesh that had already demonstrated utility in the feeding of PRM  to determine if attachment was enhanced. No difference was observed in the feeding rates or egg laying with the ParafilmTM M membrane-only system and the ParafilmTM M + mesh system. A significant decrease in feeding was demonstrated between the Baudruche membrane + mesh system and the Baudruche membrane alone, possibly due to a lack of tension in the Baudruche membrane in the latter system and the difficulty faced by mites trying to attach through both the mesh and membrane compared to membrane alone. Greater variability was observed in both feeding rates and in number of eggs laid per fed mite when using only ParafilmTM M when compared to ParafilmTM M + mesh, whereas neither feeding rates or eggs laid per mite were affected by the addition of the mesh. In addition, no membrane failures were observed when using the ParafilmTM M with the overlaid mesh.
We observed in this study that mites that had fed on goose blood through the Baudruche membrane were fully engorged when compared to those that had fed through the Parafilm™ M membrane. This repletion level may explain the differences in the trend of increased egg production in the mites fed in the Baudruche membrane system. Therefore, the textured surface of the Baudruche membrane may facilitate easier mite attachment, enabling them to feed to repletion, when compared to the smooth Parafilm™ M membrane. The robust performance, availability and good feeding rates indicates that the Baudruche membrane is a useful alternative to chick skin and artificial membranes for use in PRM feeding.
When applied to novel interventions being delivered to PRMs via hen blood (e.g. novel vaccines and systemic acaricides), in vitro studies have previously suffered from highly variable mite feeding rates and high background mortality of mites when using the in vitro feeding system [4, 5]. A more reliable in vitro feeding device reduces the necessity of higher replicates and therefore the volume of blood required, leading to a refinement in animal procedures.
A more reliable in vitro feeding method is ideal for initial screening of new control compounds and for those studies that do not require on-hen testing (e.g. RNAi studies). We have demonstrated the potential of using Baudruche membrane for in vitro feeding of adult PRM, with further studies planned to examine its use for the other hematophagous life stages of the parasite.
Availability of data and materials
The datasets supporting the conclusions of this article are provided within the article and can be acquired from the corresponding author on request.
Sigognault Flochlay A, Thomas E, Sparagano O. Poultry red mite (Dermanyssus gallinae) infestation: a broad impact parasitological disease that still remains a significant challenge for the egg-laying industry in Europe. Parasites Vectors. 2017;10:357.
Sparagano OA, George DR, Harrington DW, Giangaspero A. Significance and control of the poultry red mite Dermanyssus gallinae. Annu Rev Entomol. 2014;59:447–66.
Sommer D, Heffels-Redmann U, Köhler K, Lierz M, Kaleta EF. Role of the poultry red mite (Dermanyssus gallinae) in the transmission of avian influenza A virus. Tierarztl Prax Ausg G Grosstiere Nutztiere. 2016;44:26–33.
Thomas E, Chiquet M, Sander B, Zschiesche E, Flochlay AS. Field efficacy and safety of fluralaner solution for administration in drinking water for the treatment of poultry red mite (Dermanyssus gallinae) infestations in commercial flocks in Europe. Parasites Vectors. 2017;10:457.
Wright HW, Bartley K, Nisbet AJ, et al. The testing of antibodies raised against poultry red mite antigens in an in vitro feeding assay; preliminary screen for vaccine candidates. Exp Appl Acarol. 2009;48:81–91.
Bartley K, Turnbull F, Wright HW, et al. Field evaluation of poultry red mite (Dermanyssus gallinae) native and recombinant prototype vaccines. Vet Parasitol. 2017;244:25–34.
Arkle S, George DR, Guy JH, Sparagano OAE. Comparison of in vitro survival and fecundity rates or the poultry red mite Dermanyssus gallinae. Res Vet Sci. 2010;88:279–80.
Bruneau A, Dernburg A, Chauve C, Zenner L. First in vitro cycle of the chicken mite, Dermanyssus gallinae (DeGeer 1778), utilizing an artificial feeding device. Parasitology 2001;123(Pt 6):583–9.
Bartley K, Wright HW, Huntley JF, et al. Identification and evaluation of vaccine candidate antigens from the poultry red mite (Dermanyssus gallinae). Int J Parasitol. 2015;45:819–30.
Harrington D, Guy J, Robinson K, Sparagano O. Comparison of synthetic membranes in the development of an in vitro feeding system for Dermanyssus gallinae. Bull Entomol Res. 2010;100:127–32.
Nunn F, Bartley K, Palarea Albaladejo J, et al. A novel, high-welfare methodology for evaluating poultry red mite interventions in vivo. Vet Parasitol. 2019;267:42–6.
McDevitt R, Nisbet AJ, Huntley JF. Ability of a proteinase inhibitor mixture to kill poultry red mite, Dermanyssus gallinae in an in vitro feeding system. Vet Parasitol. 2006;141(3–4):380–5.
Trentelman JJA, Teunissen H, Kleuskens JAGM, et al. A combination of antibodies against Bm86 and Subolesin inhibits engorgement of Rhipicephalus australis (formerly Rhipicephalus microplus) larvae in vitro. Parasites Vectors. 2019;12(1):362.
Schmidt ML. Laboratory culture of two Phlebotomous species, P. papatasi and P. orientalis. Bull WHO. 1964;31(4):577–8.
Krull C, Böhme B, Clausen PH, Nijhof AM. Optimization of an artificial tick feeding assay for Dermacentor reticulatus. Parasites Vectors. 2017;10(1):60.
Kröber T, Guerin PM. In vitro feeding assays for hard ticks. Trends Parasitol. 2007;23(9):445–9.
Kuhnert F, Diehl PA, Guerin PM. The life-cycle of the bont tick Amblyomma hebraeum in vitro. Int J Parasitol. 1995;25(8):887–96.
We thank the Bioservices Group at Moredun Research Institute for their ongoing help and expertise.
We gratefully acknowledge funding from the National Centre for the Replacement, Refinement and Reduction of Animals in Research (NC3Rs) project reference NC/R001081/1 and from Scottish Government Rural & Environment Science & Analytical Services (RESAS).
Ethical approval and consent to participate
All experimental procedures described here were approved by the Moredun Animal Welfare and Ethical Review Body. Goose bleeds were conducted under the legislation of UK Home Office Project License (reference P33D3D364 for geese and P46F495BD for hen) and in accordance with the Animals (Scientific Procedures) Act of 1986.
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Nunn, F., Baganz, J., Bartley, K. et al. An improved method for in vitro feeding of adult female Dermanyssus gallinae (poultry red mite) using Baudruche membrane (goldbeater’s skin). Parasites Vectors 13, 585 (2020). https://doi.org/10.1186/s13071-020-04471-x
- Baudruche membrane
- Dermanyssus gallinae
- In vitro feeding
- Goldbeater’s skin
- Poultry red mite