The main objective of this study is to identify unique DNA sequences within the genome of human scabies that can be utilized to identify the parasite through PCR.
The main objective of this proposed study is to identify unique DNA sequences within the genome of human scabies that can be utilized to identify the parasite through polymerase chain reaction or PCR. The goal of the project is to design an assay that can distinguish samples from skin scrapings containing scabies mites, eggs, or fecal material confirmed by clinic based microscopic evaluation (gold standard) from negative controls (i.e. scrapings for tinea and/or demodex folliculitis) that do not contain Sarcoptes scabiei. We hypothesize that specifically amplifying the unique regions of the Scabies genome using PCR can serve as a means to diagnosis infestations in humans. To address this question, we will optimize PCR amplification of known scabies samples then apply our procedure to DNA extracted from patient samples.
Study Type
OBSERVATIONAL
Enrollment
17
Seton Family of Hospitals- Trinity and Hays Clinic
Austin, Texas, United States
University Medical Center Brackenridge and Paul Bass Clinic
Austin, Texas, United States
University of Texas Physicians at Trinity
Austin, Texas, United States
Seton Family of Hospitals- Dell Children's Medical Center of Central Texas and Specially for Children
Austin, Texas, United States
Identification of DNA sequences within scabies that can be used to identify the parasite through PCR
Time frame: 1 year
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Seton Family of Hospitals- Seton Luling Family Medicine Clinic and Lockhart Specialty Clinic
Lockhart, Texas, United States