Comparison of ESwab and Wound Fiber Swab Specimen Collection Devices for Use with Xpert SA Nasal Complete Assay

Paired nasal swab specimens were collected from patients who were undergoing routine methicillin-resistant Staphylococcus aureus (MRSA) screening prior to elective cardiac or orthopedic procedures. Each patient was swabbed using a traditional wound fiber liquid Stuart swab and an ESwab device, a flocked swab with a modified liquid Amies microbiology transport medium. The two specimens were tested using the Cepheid Xpert SA Nasal Complete assay. Results demonstrated a 95.5% agreement between the ESwab and the FDA-cleared wound fiber swab collection device.

M ethicillin-resistant Staphylococcus aureus (MRSA) is an important cause of postsurgical infection. Several recent studies have shown that preoperative screening with nucleic acid amplification tests and subsequent decolonization of MRSA can significantly reduce the rate of postsurgical MRSA infection (1,2). The Xpert SA Nasal Complete assay (SA Complete) (Cepheid, Sunnyvale, CA) is a molecular test that is approved for screening nasal specimens for the presence of MRSA and methicillin-susceptible S. aureus (MSSA).
As automation of the microbiology laboratory becomes more common, the use of liquid-based microbiology (LBM) specimen transport systems is also increasing. To standardize collection devices across all testing platforms, laboratories must consider validating the use of these devices with molecular tests in addition to culture-based microbiology (3). In our facility, MRSA screening is frequently performed by collecting nasal swab specimens using a liquid Stuart BBL Dual Culture-Swab (traditional swab) (BD Diagnostics, Sparks, MD), and testing is performed using the SA Nasal Complete test (one swab is broken off directly into the SA Complete assay elution reagent vial). A previous analytical study indicated that ESwab is a suitable collection device for use with the Xpert MRSA assay (Cepheid) (4). The purpose of the current study was to determine whether an ESwab collection device (ESwab) (Copan Diagnostics, Murrieta, CA) could be used in lieu of a traditional swab for routine MRSA screening from patient nasal swab specimens using the SA Complete assay.
Specimens from patients undergoing MRSA/MSSA screening were collected in parallel with a traditional swab (the FDAcleared specimen collection device for this assay) and an ESwab. Each swab was placed in both nostrils, with the collection being made in a randomized order (at the collector's discretion). The ESwab collection device consists of a flocked swab, which is used to collect the specimen, and a vial containing 1 ml of modified liquid Amies bacterial transport medium. Following collection, the swab was broken off into the transport medium, which was in turn used as input for the molecular assays. Upon receipt in the laboratory, one of the two traditional swabs from the dual swab collection device was used for testing with the SA Complete assay according to the manufacturer's protocol. ESwab specimens were vortexed, and 200 l (20% of the ESwab volume) was added to an SA Complete elution reagent vial in lieu of the wound fiber liquid Stuart swab; the remainder of the procedure was carried out according to the manufacturer's product insert (5).
Following testing, the performance of the ESwab was determined by assessing positive and negative percent agreements using the results from the traditional swab as the gold standard. The Xpert MRSA test (performed on the remaining traditional swab from the dual swab collection device) was used as the discriminator for any differences observed in the MRSA result of the SA Complete assay (MSSA discrepant analysis was not were compared to determine if either collection device had a significantly lower C T value (i.e., more sensitive). The average C T values were compared using a two-tailed student's t test and were considered significant if the t test returned a P value of Ͻ0.05. A total of 223 paired specimens were obtained for the study. Seventeen specimens had invalid results that could not be resolved with traditional swabs. Five specimens were invalid with ESwab devices. One specimen was invalid with both swabs. Two specimens were excluded due to inaccurately labeled containers. The final analysis contained 198 specimens that could be compared directly using traditional and ESwab collection devices in the SA Complete assay.
The SA Complete assay provides two separate qualitative results, one for the presence of S. aureus (positive if the SPA target is detected) and one for the presence of methicillin resistance (positive if the SPA, mecA, and SCC targets are detected). Specimens that were collected using the ESwab showed a 93.7% and 96.3% positive and negative percent agreement, respectively, with traditional swabs for the detection of S. aureus (Table 1), which is not statistically significant (P ϭ 1.0). ESwab showed an 85.7% positive percent agreement and a 100% negative percent agreement for detection of methicillin resistance (Table 2). Discrepant analysis of the MRSA result was performed using the Xpert MRSA assay with the remaining traditional swab, which was taken to be the true result. Following discrepant analysis, the positive and negative percent agreement for methicillin resistance resolved to 92.3% and 100%, respectively (Table 2), which was not statistically significant (P ϭ 0.5). A significant limitation of this study was the limited number of positive MRSA specimens (n ϭ 13). Future studies of this nature should focus on populations with an increased prevalence of MRSA.
In addition to the qualitative results, the C T values for all of the positive staphylococcal targets (spa, mecA, and SCC) were recorded. The average C T values for each target were compared between the two collection devices, and no significant differences in the C T values were observed despite the fact that only 20% of the ESwab specimens were used as input for the molecular test, while the entire traditional swab specimen is consumed by the assay. The internal process control (SPC) consists of Bacillus globigii spores that are present as a dried cake in each test cartridge to ensure that lysis and thermal cycling conditions are sufficient to release and amplify S. aureus DNA if it is present in the specimen. Because the SPC comes in the test cartridge, the amount present in the assay should be the same for the two collection devices despite the fact that only 20% of the ESwab specimen is loaded into the test. Interestingly, the average C T value for the SPC was significantly lower (i.e., more sensitive) for the ESwab collection device specimens (P ϭ 1.42 ϫ 10 Ϫ7 ) ( Table 3). A more detailed investigation is required to determine the exact nature of this observation. However, some possibilities include a more efficient amplification process with ESwabs, a more complete rehydration of the dried cake and better extraction of the SPC due to an increased volume of liquid being added to the test cartridge, or a decrease in the amount of inhibitors present in the specimen, as only 20% of the ESwab specimen goes into the test.
In this study, the ESwab device had 66% fewer invalid results than traditional swabs (6 versus 18, respectively) in the SA Complete assay with no significant differences in sensitivity and specificity. This study suggests that the ESwab collection device is at least equivalent to traditional wound fiber swabs for sample collection and analysis using the Cepheid Xpert SA Nasal Complete assay.