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Quality improvement of mitochondrial respiratory chain complex enzyme assays using Caenorhabditis elegans
Affiliation:1. Center for Developmental Therapeutics, Seattle Children’s Research Institute, Seattle, Washington;2. The Murdoch Childrens Research Institute and University of Melbourne Department of Pediatrics, Royal Children’s Hospital, Melbourne, Australia;3. Department of Molecular and Human Genetics, Medical Genetics Laboratories, Baylor College of Medicine, Houston, Texas;4. Departments of Pediatrics, Neurology and Pathology & Anatomical Sciences, Robert Guthrie Biochemical and Molecular Genetics Laboratory, State University of New York at Buffalo, New York;5. Department of Neurosciences and Pediatrics, The Mitochondrial and Metabolic Disease Center, University of California San Diego, La Jolla, California;6. Departments of Pharmacology and Medicine, Center for Mitochondrial Disease, Case Western Reserve University School of Medicine, Cleveland, Ohio;7. Department of Anesthesiology, Seattle, Washington.;8. Division of Genetic Medicine, Department of Pediatrics, University of Washington School of Medicine, Seattle, Washington.
Abstract:
PurposeThe diagnosis of a mitochondrial disorder relies heavily on the enzymatic analysis of mitochondrial respiratory chain complexes in muscle or other tissues. However, considerable differences exist between clinical laboratories in the protocols or particular tests used for evaluation. In addition, laboratories can encounter difficulties in consistent technique, as well as procurement of adequate positive or negative controls. Currently, there is no external quality assurance for respiratory chain complex assays. In this study, we explored the use of Caenorhabditis elegans mitochondria as a potential aid to diagnostic centers that perform respiratory chain complex assays.MethodFive diagnostic test centers in the United States and one from Australia comparatively analyzed enzyme activities of mitochondria from C. elegans. The first survey consisted of three open-labeled samples including one normal control and two mutants; the second survey consisted of one open-labeled normal control and two blinded samples.ResultsThere was very good concordance among laboratories in detecting the majority of the defects present in the mutant specimens. Despite the ability to detect respiratory chain complex defects, the scatter between centers for certain enzymatic assays, particularly I + III, II, III, and IV, led to different diagnostic interpretations between the centers.ConclusionThe data strongly support the need for comparative testing of mitochondrial enzyme assays between multiple laboratories. Our overall results are encouraging for the use of nematode mitochondria as a tool that might provide a virtually inexhaustible supply of mitochondria with defined defects for development of assays and as a potential source of control specimens.
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