The Journal of Allergy and Clinical Immunology
Volume 104, Issue 3 , Pages 707-709, September 1999

Quantitation of dust mites and allergen in small dust samples☆☆★★

Dayton, Ohio, and Racine, Wis

From the Department of Biological Sciences, Wright State University, Dayton, Ohio,a and S.C. Johnson & Son, Inc, Racine, Wis.b

Received 30 March 1999; received in revised form 11 May 1999; accepted 13 May 1999.

Article Outline

Abbreviations:  Der 2 , Dermatophagoides group 2 allergen

 

Exposure to mites and allergen involves multiple variables such as the concentration or quantity of allergen in each reservoir, the activity in the home that renders mite allergens airborne and inhalable, and the time an individual spends in areas with mite allergen. Central to exposure are the amounts of mites and allergen in each of the reservoirs in the home; hence it is critical that the best method of reporting these levels is used so that their relevance to sensitization and provocation of allergy symptoms can be evaluated and mite and mite allergen mitigation strategies can be used, if necessary. Mite and allergen levels have traditionally been reported as the number of mites or the amount of allergen per gram of dust collected by vacuum sampling of a finite surface area rather than by reporting the total mite or allergen content per sampled area. However, the total quantity of dust collected during sampling of a given surface area is greatly variable, yet it is important for evaluating exposure and identifying whether there is a mite allergen problem. In this study we investigated the total amount and concentration of mites and allergens on specific surfaces as well as the relationship between mite and allergen levels in various locations within homes.

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METHODS 

Dust samples were obtained from 19 homes in Houston, Tex, and from 24 homes in Dayton, Ohio, during July and August 1997 (high mite season). In each home dust was collected by vacuuming an upholstered couch or chair located in the family room and an unencased, regularly used mattress, pillow(s), and carpet next to the bed in the bedroom, as previously reported.1 The entire surface of the pillows and 1 m2 of area of the other sites was vacuumed for 2 minutes to collect the sample.

The number of mites (alive and dead) in a 50-mg aliquot of each sample was determined by our standard method.1 If <50 mg of dust was recovered, the entire sample was weighed and counted. Dermatophagoides group 2 allergen (Der 2) levels in pillow and mattress samples were assayed with use of a commercial ELISA kit (Indoor Biotechnologies, Charlottesville, Va) that recognizes a cross-reactive epitope present on both Der p 2 and Der f 2.

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RESULTS 

In comparable sites within a home the average densities of mites and allergen were greater in homes in the semitropical climate in Houston compared with the temperate climate in Dayton (Table I). The mean mite density and group 2 allergen concentration in mattresses was higher in Houston (393 mites/g and 1440 ng of Der 2/g) compared with Dayton (139 mites/g and 570 ng of Der 2/g). In both cities most homes (24/36) had mite counts in bedroom carpets > mattresses > pillows. Furthermore, there was no correlation between the mite densities in the various sampling sites (r 2 < 0.0032).

Table I. Total number of mites (live + dead) per gram of dust or per total surface area of the pillow, total weight of pillow dust (in milligrams), and amount of allergen (nanograms of Dermatophagoides group 2 allergen [Der 2]) collected from 19 homes in Houston, Tex (subjects 01-19), and from 24 homes in Dayton, Ohio (subjects 21-44)
SubjectsTotal mites/g dustPillow 1Pillow 2
CouchBedroom carpetMattressNo. of mitesDust (mg)Der 2 (ng)No. of mitesDust (mg)Der 2 (ng)
01803001206371061176551196
02400720401259641511556262
031406001407386362703155141186
0462088080136632511265355
0534020080472141330*ND
063206801740509050236190166
07860680148010079501859458318572
084802601607335263019028
0920960138017118155120132
1020062016022186348710884960
11380400607520723537116ND
12100104014024298592924119ND
131406080512351229046
1460700120736081861620483
15540660180325451526149437406
162209209002236817783293501361
1712062020402869202037
18140401606949278216980266
19601900420021169124389147
211605240100120ND330ND
2202020102011200
232020402300NSNSNS
24801600014810340ND
256040120010NDNSNSNS
26NS2016071142NDNSNSNS
27140560300963NDNSNSNS
2894010002601240NDNSNSNS
29401600783ND671ND
30NSNS140041ND18100
3120401600134NDNSNSNS
323206020030NDNSNSNS
33601801601140NDNSNSNS
34120401601273288992NSNSNS
35200NS20350237505
3638012080050ND320ND
37180NS600500NSNSNS
382205204801520NDNSNSNS
390100100650NDNSNSNS
40200NS281ND071ND
41560NS500130NDNSNSNS
42100640NS1320NDNSNSNS
4390042020120NDNSNSNS
444060NS140NDNSNSNS
*Sample weight was not determined.

ND, Der 2 was not determined; NS, no sample was collected.

The quantity of dust collected by thoroughly vacuuming the pillow surfaces in both Dayton and Houston was very small. The Houston pillows yielded a mean of 378 mg of dust. The mean total number of mites on these pillow surfaces was 136 ± 37 (range = 0 to 1007) with 27 of the 38 pillows (71%) having <100 mites on the entire surface. Only 3 of the 35 pillows tested had >2 μg of Der 2 allergen on the entire surface (mean = 662 ± 228 ng).

Likewise, most pillow samples (27/32) from Dayton homes contained <100 mg of dust (Table I, mean = 82 mg), which was an insufficient quantity to conduct both a mite count and an allergen analysis, so only the mite count was performed. One >10-year-old pillow contained 1273 mites. If this pillow is excluded as an outlier, the mean number of mites recovered from the remaining 31 pillows was 7 ± 2 with a range 0 to 71. Twenty-five of 32 pillows (78%) had fewer than 10 mites on their surfaces and all but this outlier had fewer than 75 mites per pillow surface (Table I).

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DISCUSSION 

Our results indicate that mite breeding in specific sites in homes is independent of other sites and that dispersal of allergen from site to site does not result in a uniform distribution throughout the home. Therefore the levels of mite and allergen in one location within a home cannot be used to predict the levels in other areas or to determine occupant exposure to allergens.

Most studies report mite and allergen density (concentration) as the amount per gram of collectable dust, although considerably less than 0.2 g of dust is usually recovered by vacuuming the entire pillow surface.2, 3, 4 The practice of extrapolating and reporting dust mite and allergen concentrations per gram of dust when sampled areas or surfaces yield considerably less than 1 g of dust leads to the reporting of exaggerated mite and allergen levels on surfaces where there are few mites and little allergen. For example, one study2 reported averages of 10.85 and 27.58 μg of Der p 1 per gram of dust on pillow surfaces from 2 cohorts of homes. However, the same data analyzed in terms of the actual dust collected per total pillow surface (0.084 and 0.063 g, respectively) resulted in means of 0.91 and 1.74 μg of Der p 1 for the entire surface. Another study3 reported mean concentrations of Der p 1 of 22.28 and 8.24 μg/g, whereas the actual micrograms per pillow were 1.0 and 0.13 for synthetic and feather pillows, respectively. In our study, when the concentration was expressed per gram, 24 of 37 Houston pillows exceeded 100 mites per gram, yet only 2 pillows had > 1 g of collectable surface dust. Most had <0.5 g of dust (mean = 378 mg) and <100 mites on the entire surface. The results are even more striking for the Dayton pillows, where the mean number of mites per pillow was only 7 ± 2 (excluding 1 outlier) but extrapolated it was 137 mites per gram. Twenty-five of the 32 pillows had <10 mites on the entire pillow surface.

On the basis of the data presented here and the few data reported in the literature, we are recommending that, as a standard, the actual number of mites and the total quantity of allergen be reported when less than 0.5 g of dust is collected from a sampled surface. For pillow surfaces the total mite number and allergen amount should be reported.

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Acknowledgements 

We thank Camona Woodford and Dolores Rodriguez for helping to collect the dust samples and Jacqueline Neal, Christine Rapp, and DiAnn Vyszenski-Moher for performing the mite counts.

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References 

  1. Arlian LG, Bernstein D, Bernstein IL, Friedman S, Grant A, Lieberman P, et al.  Prevalence of dust mites in the homes of people with asthma living in eight different geographic areas of the United States. J Allergy Clin Immunol. 1992;90:292–300
  2. Frederick JM, Warner JO, Jessop WJ, Enarder I, Warner JA. Effect of a bed covering system in children with asthma and house dust mite hypersensitivity. Eur Respir J. 1997;10:361–366
  3. Kemp TJ, Siebers RW, Fishwick D, O’Grady GB, Fitzharris P, Crane J. House dust mite allergen in pillows [letter]. BMJ. 1996;313:916
  4. Hallum C, Simpson B, Houghton N, Simpson A, Craven M, Custovic A, et al.  Mite allergens in feather and synthetic pillows [abstract 719]. J Allergy Clin Immunol. 1999;103:S188

 Supported in part by S.C. Johnson & Son, Inc, the National Institutes of Health, and the US Environmental Protection Agency (USEPA R-825250-01-0).

☆☆ Reprint requests: Larry G. Arlian, PhD, Department of Biological Sciences, Wright State University, Dayton, OH 45435.

 J Allergy Clin Immunol 1999;104:707-9.

★★ 0091-6749/99 $8.00 + 0  1/54/99996

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The Journal of Allergy and Clinical Immunology
Volume 104, Issue 3 , Pages 707-709, September 1999