Evaluation of Saline, Phosphate-Buffered Saline, and Minimum Essential Medium as Potential Alternatives to Viral Transport Media for SARS-CoV-2 Testing

Abstract

S evere acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of coronavirus disease 2019 , has caused a global pandemic since being discovered in late 2019.In response, clinical microbiology and public health laboratories have worked to develop, validate, and implement molecular assays to detect SARS-CoV-2 from respiratory samples.The preferred and most commonly collected specimen is a nasopharyngeal (NP) swab placed in viral transport media (VTM).As testing demand has increased, specimen collection and transportation supplies, including VTM, are decreasing nationwide.Due to these shortages of collection supplies and transport media, we assessed the feasibility of placing NP swabs in sterile 0.9% saline (Baxter, Deerfield, IL), sterile phosphate-buffered saline without calcium and magnesium (PBS), or minimum essential medium (MEM) (Corning, Corning, NY) prior to testing for SARS-CoV-2 by a commercially available (emergency use authorized [EUA]) FDA platform (cobas SARS-CoV-2; Roche Diagnostics, Indianapolis, IN) and a SARS-CoV-2 laboratory-developed test (LDT) that has been validated and submitted to the Food and Drug Administration for EUA approval.The Roche cobas SARS-CoV-2 test is performed on the cobas 6800 platform (Roche) per the manufacturer's protocol.The SARS-CoV-2 LDT is performed as described in the supplemental material, targeting the nucleocapsid (NUC) and open reading frame (ORF) regions of the virus.For this study, samples were prepared by placing analyte-negative NP swabs (patient swabs previously tested by the LDT) into twelve 15-ml conical tubes (Corning) containing 3 ml of either M4-RT VTM (Remel Inc., San Diego, CA), MEM, saline, or PBS for a total of 48 samples.Subsequently, each sample was spiked with SARS-CoV-2positive patient material at a concentration of 2,500 copies/ml.Two 15-ml conical tubes containing 3 ml of each medium (i.e., 8 total samples) functioned as negative controls.On day 0 (i.e., the day the samples were prepared), six contrived samples in each of the four types of media listed above (i.e., 24 samples), as well as negative controls, were tested by the Roche cobas and LDT SARS-CoV-2 methods (Table 1).Following initial testing, half of the contrived samples were stored refrigerated (2°to 8°C), while the remaining aliquots were stored frozen (Ϫ15°to -25°C).The aliquots were pulled from storage on days 1, 3, and 7 and tested by both methods.Equivalence (i.e., qualitative results as well as Ϯ2 cycle threshold [C T ] values) and stability (Ϯ2 C T values over 7 days) of the alternative transport media were compared to those of VTM.The SARS-CoV-2 results of both assays showed equivalence (i.e., 100% qualitative agreement and C T variation of Ͻ 2 cycles) when swabs were stored in MEM, PBS, saline, and VTM over 7 days under both refrigerated and frozen storage conditions (Table 1).No evidence of loss in sensitivity or stability (Ͼ2 C T value increase) was observed for any of the transport media.One sample stored in PBS at 2°C to 8°C and tested by the LDT

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