LETTER
Mycoplasma genitalium is an important sexually transmitted infection that can cause acute and/or chronic urethritis in males and females, and its prevalence is approximately 16% in females and 17% in males (1). Globally, macrolide resistance is estimated to exceed 50% in most urban centers (1–6), and in our local region of Queensland, Australia, it exceeds 60% (7). PCR is routinely used for diagnosis of M. genitalium and macrolide resistance mutations at positions 2058 and 2059 of the 23S rRNA gene; however, the turnaround times of laboratory-based methods often exceed 24 h and so may not be sufficiently timely to inform clinical management for symptomatic patients. Here, we evaluated the performance of the ResistancePlus MG FleXible cartridge test on the Cepheid GeneXpert (hereafter termed MG-Flex), which offers the potential for near-point-of-care testing.
A bank of 181 clinical samples (M. genitalium positive, n = 63, and negative, n = 118) from 145 males and 36 females was used in this study. Original patient samples were stored at 4°C for 4 weeks, then at −20°C for longer-term storage. Nucleic acid samples were stored at −20°C until required. Full details of the samples are provided in Table S1 in the supplemental material. The samples had all been submitted for routine M. genitalium testing to Pathology Queensland (Brisbane, Australia) where they were tested using an in-house PCR that detects the MgPa gene of M. genitalium (hereafter termed in-house MgPa-PCR) (8). For the purposes of this evaluation, all samples were tested using the MG-Flex near-point-of-care assay (which detects the macrolide resistance mutations A2058T, A2058C, A2058G, and A2059G) as well as the SpeeDx ResistancePlus MG test (hereafter termed RPMG, which detects the macrolide resistance mutations A2058T, A2058C, A2058T, A2059C, and A2059G). The RPMG test is a Therapeutic Goods Administration (TGA, Australia) cleared and CE-IVD-marked (i.e., Conformité Européene-marked for in vitro diagnostic) laboratory-based test.
The MG-Flex assay was prepared per the kit instructions. Briefly, 44 μl of MG-Flex mastermix, 1 ml of neat (unextracted) clinical sample, and 10 μl of internal control were added to the FleXible cartridge (Cepheid). In some instances, swab specimens (n = 17; Table S1) had less than 1 ml of sample, so the volume was made up to 1 ml with sterile molecular-grade water. The RPMG assay was performed per the manufacturer’s instructions using stored DNA extracts from the routine testing in the in-house MgPa-PCR.
This study was approved by the Children’s Health Queensland human research ethics committee (HREC/12/QRCH/139).
The results are summarized in Table 1 and further detailed in Table S1. The MG-Flex assay detected M. genitalium in 61 of 63 known positive samples, providing a sensitivity of 96.8%. The two samples providing negative results by the MG-Flex assay (samples 62 and 63; Table S1) were both from males. For sample 62, a reduced starting volume of sample likely contributed to discordance, and in both samples, low M. genitalium load was observed. One hundred sixteen M. genitalium-negative samples were negative in the MG-Flex assay, while two samples provided invalid results (samples 180 and 181; Table S1), and there was insufficient sample to repeat testing. MG-Flex assay specificity for evaluable samples was therefore 100%. The detection of macrolide resistance mutations by the MG-Flex assay correlated 100% with that of the RPMG assay, with the exception of two samples providing negative results for M. genitalium in the MG-Flex assay (samples 62 and 63; Table S1). The overall agreement between the RPMG and MG-Flex assays was 98.9%, with a kappa value of 0.98. The detection limit was also assessed by testing 10-fold dilutions of an M. genitalium-positive sample, and the MG-Flex test was able to reliably detect an additional dilution over the RPMG assay (Table S1).
Summary of results of the RPMG and MG-Flex assaysa
In summary, we found that the MG-Flex cartridge test was highly sensitive and specific for the detection of M. genitalium and 23S rRNA mutations.
ACKNOWLEDGMENTS
We thank Pathology Queensland staff for their assistance with this study.
D.M.W. reports research funding from SpeeDx Pty Ltd. The RPMG and MG-Flex assays were provided by SpeeDx Pty Ltd. Co-authors from SpeeDx Pty Ltd. (S.E. and L.Y.T.) participated in the study conception and design, data analysis, and manuscript writing.
This work was supported by The University of Queensland strategic funding.
FOOTNOTES
- Accepted manuscript posted online 2 January 2020.
Supplemental material is available online only.
- Copyright © 2020 American Society for Microbiology.