A New Insecticide Delivery Method for Control of Fur Mite Infestations in Laboratory Mice
By Thomas N. Mather and Niels C.G. Lausen
tigators placed treated cotton in captured Peromyscus leucopus cages, they found the animals readily accepted
Thomas N. Mather is affiliated with the Department of Population Sci-
the cotton and would create fluffy nests with the material
ences, Harvard School of Public Health. Niels C.G. Lausen is affiliated with the Animal Resources Center, Harvard Medical School.
We thought that permethrin might also kill mites in-
festing laboratory mice. To test the effectiveness of per-methrin for that purpose, we supplied laboratory mice
THE FUR MITES, Myobia musculi, Radfordia affinis with cotton balls impregnated with three concentrations
and Myocoptes musculinus (Acari: Myobiidae), are
important ectoparasites of laboratory mice. These mites can infest whole colonies of laboratory rodents and may
Materials and Methods
adversely affect the general health of mice1. Mite infesta-tions often cause hypersensitivity-induced skin lesions2
We conducted the study in a colony containing over
that can promote secondary bacterial infection. Infested
1200 transgenic mice (including about 20 strains). All
mice may have altered immune statuses3, and epider-
the mice were backcrossed to CD-1 or Balb/C mice. The
mis and hair regrowth may be affected in some mouse
colony had been in existence for about 24 months and
strains4. A mouse experiencing a severe or prolonged
was infested with fur mites. We housed all the mice in
mite infestation may permanently disfigure itself by vig-
standard shoebox cages, each holding 1-5 mice. We kept
the cages on five open stainless steel racks in one animal
The toxicity of mitacidal agents, both to animals and
room. We provided the mice with water and food ad li-
caretakers, and low treatment cost-effectiveness have
bitum. An animal technologist cleaned the cages weekly
hampered the control of fur mites in laboratory mice.
and lined the cage bottoms with fresh wood chip bedding
Though scientists have assessed many methods of fur
(Alphachip, Northeast Wood Products).
mite control2,5-7, most methods do not work in the long-
To begin the study, we randomly selected and marked
run. M. musculi infestations in laboratory mouse colo-
eight cages from each rack. We looked for mites and mite
nies can be effectively curbed with the permethrin, an
eggs on the heads and backs of 50% of the mice from
acaricide, as recent evaluations have shown8. Permethrin,
each of the marked cages. To perform this step, we used
the investigators discovered, provided satisfactory short-
the scotch tape impression method with microscopic in-
term reductions in mite infestations. When the investiga-
terpretation: we thoroughly rubbed each mouse sampled
tors applied permethrin directly onto the mice or mixed
with clear adhesive tape, affixed the hair-covered tapes to
it in powder form with wood shavings, it did not produce
glass microscope slides, and examined them at 40X mag-
any noticeable effect in the mice. Their histopathologic
nification. We have found this method to be as reliable as
findings in the mouse livers, lungs and kidneys were nor-
scraping or post-mortem examination for diagnosing fur
mal. Presumably, scientists would use permethrin as an
mite infestations. We examined mice from each marked
acaricide unless it was difficult to administer, or if it was
cage using the procedure described above both before,
and at one-, two-, and four-week intervals after the per-
Investigators found that permethrin-impregnated
cotton, intended as rodent nest material, effectively kept
Following the initial examination, we gave the animal
immature ticks from infesting natural populations of the
technologist bags of cotton balls. We had saturated some
white-footed mouse, Peromyscus leucopus9. The investi-
cotton balls with a range of permethrin and left some un-
gators distributed treated cotton in dispensing tubes and
treated. We then instructed the technologist to provide all
placed them at regular intervals throughout the wooded
the cages on a rack either with cotton balls containing
and brush-covered habitat frequented by this mouse. Cot-
the same concentration of permethrin or untreated cotton.
ton disappeared from the dispensing tubes (presumably
To prepare the cotton balls, we soaked them in aqueous
into mouse nests)-as it did, the investigators captured
solutions9 containing 0.16, 1.6 and 2.4% of commercial-
increasing numbers of tick-free mice. When the inves-
ly formulated permethrin (Permanone 40 Mfg-Fairfield
New Insecticide Delivery Method for Control of Fur Mites
American Corp., Frenchtown, NJ) to produce treated cot-
this treatment, the mite infestations persisted. The num-
ton containing 0.5, 5.0 or 7.4% active permethrin (w/w)
ber of mite-infested mice after four weeks was close to
when dried. The volume of liquid we used just saturated
the number of infested mice in cages receiving untreated
the cotton mass (about 10 times the weight of the cotton).
One must take into account the absorbent properties of the dosing material to arrive at the permethrin concentra-
Discussion
After soaking the cotton, we air-dried it. We con-
Investigators have found that several formulations of
firmed the concentration of permethrin in the various
permethrin are effective acaricides against ectoparasites
batches of cotton by examining acetone extracts from
of rodents and other animals, in the wild9, or in labora-
treated cotton balls using reverse phase high pressure liq-
tory8 and commercial settings10,11. Many of the features
uid chromatography. For this step, we used a C18 column
of this acaricide, including its low degree of toxicity to
with the sample diluted in 80% methanol in water. We
the animals and their caretakers, make it more advanta-
monitored the effluent from the column at 280 nm and
geous than other products and methods for controlling fur
used a computer to calculate the area of each peak.
The technologist placed up to 25 cotton balls in each
Acute, short-term, and long-term studies show that
cage (about five cotton balls per mouse) and put fresh
dermal or oral exposure of up to 2000-5000 mg per-
cotton in all the cages at cleaning time. The animal tech-
methrin per kg body weight (that is up to 125 mg per
nologist, alone, knew the concentration of acaricide used
25 g mouse) is not toxic to mice12. We calculate that ef-
for each rack. We performed all sampling, examinations
fective application rates using our method – five cotton
and evaluations without that knowledge.
balls containing either 5% or 7.4% permethrin per 25 g mouse – would deliver just 1200-1800 mg permethrin per kg body weight, or a maximum exposure to about 46 mg
per 25 g mouse. Furthermore, impregnating cotton with
Eighty-eight percent of the mice we initially ex-
permethrin binds much of the toxicant (up to 80%) to the
amined (n = 76) were infested with mite eggs and 40%
cotton fiber so it is not readily available for absorption (B.
were infested with nymphal or adult mites: Ninety per-
McNally, personal communication). Most toxicological
cent of the mice we originally examined were infested
studies use application methods intended to maximally
with either eggs or mites. We identified mites of the M.
absorb solvents into the application material (i.e. oral and
musculi, R. affinis, and M. musculinus species, but made
dermal applications formulated in corn oil or solvents).
no attempt to separate these species in the actual counts.
Even considering the focused method of our per-
Heavy infestations more than 5 adult or nymphal mites or
methrin application, we apparently needed a relatively
more than 15 eggs per slide-occurred on about 20% of the
high concentration of this acaricide to completely control
mice. Only about 10% of the mice we sampled suffered
fur mites infesting mice in our study. Reportedly, other
skin lesions or other signs of severe mite infestation.
investigators have successfully controlled M. musculi
The mice readily accepted the treated and untreated
when directly applying as little as 0.5 mg permethrin per
cotton and used it to construct nests. After the first treat-
mouse either as a dust or liquid emulsion8. At our lowest
ment, the number of mice infested with either adult or
treatment level (cotton containing 0.5% permethrin, or
nymphal mites decreased in cages with treated cotton
about 120 mg per mouse) we failed to completely con-
(SeeTable 1), although we observed no reduction in the
trol adult and nymphal mites, although fewer of the mice
number of mite egg-infested mice. After two weeks of-
were mite-infested after 4 weeks of treatment than before
treatment, nearly all the mice nesting in cotton balls con-
taining either 5.0 or 7.4% permethrin were free of adult
Our treatment might require more permethrin due to
and nymphal mites. Additionally, the number of animals
the actual exposure degree of mites to the active ingredi-
infested with mite eggs decreased. After four weeks of
ent impregnated onto the treated fiber, the nature of the
treatment, all mice nesting in cotton balls containing ei-
impregnation process, or it may be due to different sus-
ther 5.0 or 7.4% permethrin were completely free of adult
ceptibilities of mite species or strains between studies. It
and nymphal mites, and less than half the original num-
may be that a combination of these three possibilities ac-
counted for the seemingly higher concentration required
In contrast, fewer of the mice treated with 0.5% per-
methrin-soaked cotton were mite-free. After 4 weeks of
Though our method seems to require more chemical
New Insecticide Delivery Method for Control of Fur Mites
than others, it has several advantages: treated nest material is odor-free; since the toxicant is
contained on the cotton fiber, problems such as
Summary of actual counts of mite eggs, nymphs and
overdosing, spillage or toxic dusts and fumes,
adults infesting mice treated with permethrin-impreg-
are reduced; animal technologists can routine-
ly add nest material to cages when they clean them; both the cotton and the permethrin are
Proportion of mice infested on Treatment Week 0 Week 1 Week 2 Week 4
biodegradable so technologists can dispose of them safely with other refuse; the natural nest-
building behavior of mice is satisfied by the
cotton supply, perhaps making them more se-
cure and less prone to other stresses.
In our study, mice in cages with 5%- and
7.4%-permethrin-soaked cotton balls were
mite-free after four weeks, although a few em-bryonated and empty mite eggs remained on
the fur of some mice. We observed that eggs
present prior to the initial treatment and eggs
on control mice could be distributed anywhere
along the entire hair shaft. Most of the eggs we found on treated mice later in the study were usually nearer the distal end of the hair. Eggs that we ob-
References
served close to the base of the hair shaft were more likely
1. Weisbroth. S.H., et al. The parasitic ecology of the rodent mite Myobia
embryonated, while eggs we observed near the distal end
musculi: I. Grooming factors. Lab. Anim. Sci.; 24:510-516, 1974.
were most often empty. Additionally, after three and four
2. Weisbroth, S.H. Friedman, S., and Scher S. The parasitic ecology of the
weeks of treatment, we found eggs on fewer of the mice
rodent mite Myobia musculi: III. Lesions in certain host strains. Lab. Anim. Sci.; 26:25-735, 1976.
treated with 5% and 7.4% permethrin-soaked cotton than
3. Friedman, S., and Weisbroth, S.H. The parasitic ecology of the rodent
at the beginning of the study. Taken together, these obser-
mite Myobia musculi: II. Genetic factors. Lab. Anim. Sci.; 25:440-445,
vations suggest that new oviposition ceased near the time
4. Whiteley. H.J., and Horton, D.L. The effect of Myobia musculi on the
epidermis and hair regrowth cycle in the aging CBA mouse. J. Path.
Given the 23-day natural life-cycle of these mites13,
Bact.; 83:509-514, 1962.
the fact that egg hatching is nonsynchronous and con-
5. Wagner, J.E. Control of mouse ectoparasites with resin vaporizer strips
containing vapona. Lab. Anim. Care; 19:804-807, 1969.
tinuous, and that permethrin treatment is not ovicidal, a minimum of four to five treatment weeks for an infested
6. Tarshis, B. The use of silica aerogel compounds for the control of ec-
toparasites. Proc. Anim. Care Panel; 12:217-258, 1962.
mouse colony is apparently necessary to prevent reinfes-
7. Constantin, M.L. Effects ofinsecticides on acariasis in mice. Lab Anim.;
tation. Furthermore, supplying mice colonies with treated
62:279-286, 1972.
nest material over an extended period of time can prevent
8. Bean-Knudsen, D.E., Wagner, J.E., and Hall, R.D. Evaluation of the con-
new infestations in settings when one introduces outside
trol of Myobia musculi infestations on laboratory mice with permethrin. Lab. Anim. Sci.; 36:268-270, 1986.
mice into the colony, or if feral animals could contami-
9. Mather, T.N., Ribeiro, J.M.C., and Spielman, A. Lyme disease and babe-
siosis: Acaricide focused on potentially infected ticks. Am. J. Trop. Med. Hyg.; 36:609-614, 1987. Acknowledgements
10. Hall, R.D., et al. Comparative efficacy of plastic strips impregnated
with permethrin and permethrin dust for northern fowl mite control on caged laying hens. Poult. Sci.; 62:612-615, 1983.
The authors appreciated the assistance of Jose M.C.
11. Taylor, S.M., et al. Efficacy of pyrethroid impregnated ear tags for
Ribeiro and Rachael Wallace. Supported in part by a grant
prophylaxis of tickborne diseases of cattle. Vet. Record; 114:454-455,
from The Arthritis Foundation (to TNM). Permethrin-
treated nesting material is manufactured under the trade
12. NRCC. Pyrethroids: Their effects on aquatic and terrestrial ecosystems.
Nat. Res. Coun. Can. Pub. No. 24376:303 pp., 1986.
name MiteArrest® and will be available commercially
13. Friedman, S., and Weisbroth, S.H. The parasitic ecology of the rodent
pending registration by the Environmental Protection
mite Myobia musculi: IV. Life cycle. Lab. Anim. Sci.; 27:34-37, 1977.
Agency. The product is manufactured by EcoHealth, Inc.,
14. Levine, J.F., and Lage, A.L. House mouse mites infesting laboratory
33 Mt. Vernon Street, Boston, MA 02108.
rodents. Lab. Anim. Sci.; 34:393-394, 1984.
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