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Detection and measurement of blood-feeding activity

a technology of blood feeding activity and detection and measurement, applied in the direction of chemiluminescene/bioluminescence, instruments, material analysis, etc., can solve the problems of reducing productivity, annoyance, discomfort, health problems, economic losses, etc., and the management practices have not been eliminated

Active Publication Date: 2010-05-13
CYTOSIGNET
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The wide biological diversity of hematophagous organisms presents a challenge to detecting and controlling these pests.
Infestations by hematophagous ectoparasites can cause annoyance, discomfort, health problems, and economic losses.
For example, pests in structures other than those for human habitation, including but not limited to hen houses for avian egg production, barns housing domestic animals, mammalian breeding facilities, or other structures for continued occupation by birds or mammals, may cause reduced productivity.
Subsequently, current pest management practices have not eliminated hematophagous ectoparasites from shelters: school children still are infected by head lice (Pediculus capitas); bedbugs (Cimex lectularius) infest henhouses and are being found with increasing frequency in homes and lodging facilities in the United States; fleas (Ctenocephalides sp.) and several genera of ticks enter structures inhabited by humans, mice, dogs, cats, and other mammals alone or in combination; and companion animals of humans are frequently hosts for are variety arachnid and insect ectoparasites.
Thus, while detection assays are know in the art, such assays have not been successfully adapted to the detection of hematophagous ectoparasites that live outside of the body of the host by the methods and compositions of this invention.

Method used

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  • Detection and measurement of blood-feeding activity
  • Detection and measurement of blood-feeding activity
  • Detection and measurement of blood-feeding activity

Examples

Experimental program
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Effect test

example 1

Detecting Heme-Iron in Bedbug Culture Substrate

[0046]Cultures of bedbugs (Cimex lectularius) were maintained in glass jars containing a pressed paper cardboard substrate (FIG. 1) at room temperature and were allowed to feed at 7 to 14-day intervals on human blood. The bedbugs were allowed access to human skin through a 200-mesh nylon screen attached over the top of their jars. The skin was allowed to be in contact with the mesh for at least 10 minutes with each jar during which time the bedbugs fed to repletion. Cardboard substrate was removed from each jar at least 10 days after feeding, put into plastic bags, sealed, and stored in the freezer at temperatures below −10° C. until processed.

[0047]Fecal occult blood tests (FOBT) of two different peroxidase activity visualization chemistries were used from three different commercial suppliers (guaiac from Immunostics, Inc., Ocean, N.J. and Care Products, Waterbury, Conn. and 3,3′,5,5′-tetramethyl benzidine (TMB) from Biomerica, Inc., N...

example 2

Detection of Blood in Bedbug Cultures Using Luminol

[0050]Debris collected from bedbug cultures as in Example I was placed on absorbent plastic-backed paper (FIG. 9) and sprayed with a commercially available luminol blood visualization solution (BlueStar, ROC Import, Monte Carlo, Monaco). The resultant chemiluminescence was seen to be associated with the debris and not with the molted exoskeletons (FIG. 10). This visualization technique can be used as in initial step to identify individual or clusters of particles emitting light to be isolated and subjected to further testing to confirm hematophage activity.

example 3

Detection of Blood in Bedbug Cultures Using Urine Test Strips

[0051]Debris collected from bedbug cultures as in Example I was dissolved in water and tested for the presence of blood using commercially available urine dipsticks (such as from Roche or Bayer). With each test the presence of detectable blood was indicated by positive reaction on the appropriate pads.

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PUM

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Abstract

This invention provides compositions and methods for detection of hematophagous ectoparasitic activity in an enclosure or area. The compositions comprise a reagent or reagents which are reactive against antigens or markers as they appear in the excrement or other ectoparasitic materials. Such markers or antigens may be produced by the ectoparasite itself or may have been introduced into the ectoparasite because of its blood feeding activity. The method of the present invention comprises collecting from the enclosure or area, a sample comprising environmental dust or materials and subjecting the sample to tests for detecting the presence of hematophagous ectoparasitic markers, host markers or both.

Description

[0001]This application claims priority to U.S. Provisional application No. 60 / 702,914, filed on Jul. 27, 2005, the disclosure of which is incorporated herein by reference.FIELD OF THE INVENTION[0002]This invention relates to environmental sampling and testing in structures, shelters, or dwellings for markers associated with the presence of free-living organisms that feed on vertebrate blood.BACKGROUND OF THE INVENTION[0003]Hematophagy is a behavior of feeding on blood taken from vertebrate hosts. It is practiced by about 15,000 species and about 400 genera of arthropods (Mans, Louw et al. 2002). It has also been reported that blood-feeding has evolved independently at least six times. In addition to arthropods, members of other phyla including annelids such as worms and leeches are hematophagous. While independent evolution and wide-spread occurrence of taking blood-meals have resulted in considerable biological diversity, there are consistent characteristics pertinent to strategies...

Claims

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Application Information

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IPC IPC(8): G01N33/569
CPCG01N21/76G01N33/5308G01N33/72G01N33/68G01N2333/43586G01N2333/43591G01N2333/76G01N2333/43582
Inventor SMITH, NATHAN L.
Owner CYTOSIGNET
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