Bioelectronic Sensor Technology for Detection of Cystic Fibrosis and Hereditary Hemochromatosis Mutations

Author:

Bernacki Susan H.1,Farkas Daniel H.1,Shi Wenmei1,Chan Vivian1,Liu Yenbou1,Beck Jeanne C.1,Bailey Karen Snow1,Pratt Victoria M.1,Monaghan Kristin G.1,Matteson Karla J.1,Schaefer Frederick V.1,Friez Michael1,Shrimpton Antony E.1,Stenzel Timothy T.1

Affiliation:

1. From the Department of Pathology, Duke University Medical Center, Durham, NC (Drs Bernacki and Stenzel); Motorola Life Sciences, Pasadena, Calif (Drs Farkas and Shi, Ms Chan, and Mr Liu); Coriell Institute for Medical Research, Camden, NJ (Dr Beck); the Department of Laboratory Medicine, Mayo Clinic, Rochester, Minn (Dr Snow Bailey); Laboratory Corporation of America, Research Triangle Park, NC (

Abstract

Abstract Context.—Bioelectronic sensors, which combine microchip and biological components, are an emerging technology in clinical diagnostic testing. An electronic detection platform using DNA biochip technology (eSensor) is under development for molecular diagnostic applications. Owing to the novelty of these devices, demonstrations of their successful use in practical diagnostic applications are limited. Objective.—To assess the performance of the eSensor bioelectronic method in the validation of 6 Epstein-Barr virus–transformed blood lymphocyte cell lines with clinically important mutations for use as sources of genetic material for positive controls in clinical molecular genetic testing. Two cell lines carry mutations in the CFTR gene (cystic fibrosis), and 4 carry mutations in the HFE gene (hereditary hemochromatosis). Design.—Samples from each cell line were sent for genotype determination to 6 different molecular genetic testing facilities, including the laboratory developing the DNA biochips. In addition to the bioelectronic method, at least 3 different molecular diagnostic methods were used in the analysis of each cell line. Detailed data were collected from the DNA biochip output, and the genetic results were compared with those obtained using the more established methods. Results.—We report the successful use of 2 applications of the bioelectronic platform, one for detection of CFTR mutations and the other for detection of HFE mutations. In all cases, the results obtained with the DNA biochip were in concordance with those reported for the other methods. Electronic signal output from the DNA biochips clearly differentiated between mutated and wild-type alleles. This is the first report of the use of the cystic fibrosis detection platform. Conclusions.—Bioelectronic sensors for the detection of disease-causing mutations performed well when used in a “real-life” situation, in this case, a validation study of positive control blood lymphocyte cell lines with mutations of public health importance. This study illustrates the practical potential of emerging bioelectronic DNA detection technologies for use in current molecular diagnostic applications.

Publisher

Archives of Pathology and Laboratory Medicine

Subject

Medical Laboratory Technology,General Medicine,Pathology and Forensic Medicine

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