PT - JOURNAL ARTICLE AU - Evans, Jason AU - Bankhead, Kyler AU - Dagostin, Justin AU - Rocco LaSala, P. TI - Innate Errors of Quantitative Streaking Methodologies AID - 10.29074/ascls.2019001974 DP - 2019 Jul 01 TA - American Society for Clinical Laboratory Science PG - 107--107 VI - 32 IP - 3 4099 - http://hwmaint.clsjournal.ascls.org/content/32/3/107.short 4100 - http://hwmaint.clsjournal.ascls.org/content/32/3/107.full SO - Clin Lab Sci2019 Jul 01; 32 AB - The objective of this study was to assess the variability of quantitative streaking between and within groups of laboratory professionals and students and an automated spiral plater. In today’s clinical laboratories, advances in technology present an everchanging landscape that mandates adaptations, and the microbiology laboratory is no exception. Despite these advancements, one of the most quintessential manual techniques employed by laboratory professionals and taught to clinical laboratory science and technician students is quantitative streaking of bacterial cultures. Although few, there are studies detailing the accuracy of a 0.001-ml calibrated loop, perhaps the most common tool for quantitative streaking; however, there has been a lack of work addressing the variability associated with laboratory personnel’s individual techniques and inherent variability. Our study analyzed the number of bacterial colony-forming units (CFUs) per milliliter that resulted from sequential plating by our control groups and automatic spiral plater from a common sample. The sample was a dilution of bacteria in saline from an initial 0.5 McFarland standard (approximation of 1.5 × 108 CFU/ml). Preliminary data indicate that in most instances, there were significant differences seen (via analysis of variance and Tukey post hoc tests; P < 0.05) within the test groups and considerable variations within each individual’s plating results (measured by coefficient of variation) for both the gram-positive and gram-negative organism dilutions tested, Staphylococcus aureus and Escherichia coli, respectively. Although this result is not unexpected, our work also shows that there are manual streaking procedural changes that more closely mimic the results obtained by our automated plating, circumventing potential lab budgetary constraints with purchasing automated platers. Collectively, our data demonstrate that manual quantitative streaking protocols are an area of the clinical microbiology lab that should be regularly assessed for quality control to ensure accuracy and reproducibility between laboratory professionals.