Evaluation of a novel immunochromatographic assay using silver ampli ﬁ cation technology for detection of Mycoplasma pneumoniae from throat swab samples in pediatric patients

Objectives: Mycoplasma pneumoniae is one of the common causative pathogens of community-acquired respiratory tract infections mainly in children and young adults. Rapid and accurate diagnostic techniques for identifying the causative pathogen would be useful for initiating treatment with an appropriate antibiotic. The purpose of the present study was to evaluate the sensitivity and speci ﬁ city of a novel immunochromatographic assay using silver ampli ﬁ cation technology using FUJI DRI-CHEM IMMUNO AG2 and FUJI DRI-CHEM IMMUNO AG cartridge Myco (FUJIFILM Co., Tokyo, Japan) for detection of M. pneumoniae . Methods: Throat swab samples were collected from 170 pediatric patients who were diagnosed with bronchitis or pneumonia. The silver amplification immunochromatographic (SAI) assay was performed using these samples and the results were compared with those of real-time PCR. The time required for the SAI assay is approximately 20 min (5 min for sample preparation and 15 min for waiting time after starting the assay). Results: The sensitivity and specificity of the SAI assay for detection of M. pneumoniae were 85.2 and 99.1%, respectively, and the assay showed positive and negative predictive values of 98.1 and 92.3%, respectively, compared with the results of real-time PCR. The diagnostic accuracy was 94.1%. Conclusions: FUJI DRI-CHEM IMMUNO AG2 and FUJI IMMUNO AG cartridge Myco are appropriate for clinical use. The optimal timing of this assay is five days or more after the onset of M. pneumoniae infection. However, PCR or other molecular methods are superior, especially with regard to sensitivity and negative predictive value.

Mycoplasma pneumoniae is one of the common causative pathogens of community-acquired respiratory tract infections mainly in children and young adults [1]. Macrolides are generally considered to be the drugs of choice for treatment of children with M. pneumoniae infection [2]. However, macrolide-resistant (MR) M. pneumoniae has been emerging in Asia, Europe, Canada and the USA since about 2000 [3][4][5][6]. Antimicrobial resistance (AMR) is a global public health concern and unnecessary use of antibiotics has contributed to the global emergence of antimicrobial resistance [7]. Rapid and accurate diagnostic techniques for identifying the causative pathogen would be useful for initiating treatment with an appropriate antibiotic. Nucleic acid amplification techniques (NAATs) including real-time PCR assay, multiplex real-time PCR assay and loopmediated isothermal amplification have been increasingly used for identification of respiratory pathogens including M. pneumoniae in clinical specimens due to their high levels of sensitivity and specificity [8]. However, it has been reported that NAATs were used in only 4% of patients who were suspected of having M. pneumoniae infection in Japan [9]. For the majority of patients, an antibody testing (64% of patients) and antigen testing including an immunochromatographic assay (32% of patients) were used [9]. Therefore, an immunochromatographic assay for detection of M. pneumoniae is important for clinical use in Japan. An immunochromatographic assay is generally inferior to NAATs with regard to sensitivity and specificity. However, an immunochromatographic assay can be performed easily in approximately 15 min and does not require an expert technologist or special instruments.
The purpose of the present study was to evaluate the sensitivity and specificity of a highly sensitive rapid immunochromatographic assay using silver amplification technology using FUJI DRI-CHEM IMMUNO AG2 and FUJI DRI-CHEM IMMUNO AG cartridge Myco (FUJIFILM Co., Tokyo, Japan) in pediatric patients infected with M. pneumoniae compared with the results of real-time PCR (Figure 1). Although the immunogen of a monoclonal antibody used in the FUJI DRI-CHEM IMMUNO AG cartridge Myco is undocumented, this assay does not cross-react with other species of Mycoplasma, at least 20 bacteria species, candida species and at least 19 viral species, according to the instructions of the assay.
Throat swab samples were collected from pediatric patients who were suspected of having respiratory tract infections associated with M. pneumoniae from May 2018 to March 2020 at Touei Hospital and Sapporo Kosei General Hospital in Hokkaido, Japan. The silver amplification immunochromatographic (SAI) assay was performed according to the manufacturer's instructions [10,11]. Sterile throat swabs provided in the kit were gently inserted into the throat through the mouth and rubbed against the back of the throat or tonsils several times to collect mucosal epidermis. The swab containing a specimen was placed directly in a dedicated soft extraction tube containing 600 μL of sample extraction reagent solution provided in the kit. The swab was then squeezed while rotating it several times to extract antigens from the swab. The sample was assayed using FUJI DRI-CHEM IMMUNO AG2 and FUJI DRI-CHEM IMMUNO AG cartridge Myco. The time required for the SAI assay is approximately 20 min (5 min for sample preparation and 15 min for waiting time after starting the assay).
The principle of the immunochromatographic assay is based on silver halide photography technology. The sample is dropped onto the sample instilling section of the cartridge. The cartridge is set in the analyzer and then measurement starts. The result is displayed automatically after 15 min.
In order to evaluate the sensitivity and specificity of the FUJI DRI-CHEM IMMUNO AG2 and FUJI DRI-CHEM IMMUNO AG cartridge Myco in comparison with real-time PCR, DNA was extracted with a DNA extraction kit (Smitest EX-R&D, Medical & Biological Laboratories Co., Nagoya, Japan) from 100 μL of sample extraction reagent solution in the kit and was finally resuspended in 15 μL of buffer. One μL of DNA solution was quantified by real-time PCR using Mp181-F (TTTGGTAGCTGGTTACGGGAAT) and Mp181-R (GGTCGGCACGAATTTCATATAAG) primers and an Mp181-P probe ([FAM]-TGTACCAGAGCACCCCA-GAAGGGCT-[BHQ-1]) as described elsewhere [12][13][14]. The plasmid containing PCR products of the real-time PCR in the vector pT7Blue (Novagene, Madison, WI, USA) was used as a positive control and for standard curves. The minimum concentrations of M. pneumoniae that would allow reproducible quantification were 10 copies per reaction. The results of real-time PCR were confirmed by two persons (NI and RS).
In order to investigate whether the assay could detect macrolide-resistant strains of M. pneumoniae, mutations associated with resistance to macrolides at sites 2,063, 2,064, and 2,617 in the M. pneumoniae 23S rRNA domain V gene region were detected by a sequencing method described elsewhere [15]. M. pneumoniae showing a point mutation in domain V of the 23S rRNA gene was defined as MR M. pneumoniae. All statistical analyses were performed using JMP software version 13.2.1 (SAS Institute, Cary, NC, USA).
According to the sentinel surveillance of M. pneumoniae infection by the National Institute of Infectious Diseases in Japan, the weekly numbers of M. pneumoniae patients were more than 0.2 from July 23, 2018 to February 3, 2019 and from August 12, 2019 to April 26, 2020 [16]. In these periods, 56 (91.8%) of 61 M. pneumoniae patients were diagnosed with a high probability.
Each dot represents the copy number of M. pneumoniae detected by real-time PCR. The first row shows copy numbers of M. pneumoniae that were negative by the SAI assay and the second row shows copy numbers of M. pneumoniae that were positive by the SAI assay. The dotted line shows the level of 1 × 10 3 copies per 100 μL of sample extraction reagent solution. The horizontal line inside the box represents the median, the lower and upper borders of the box represent the 25th and 75th percentiles, respectively, and the whiskers correspond to extension to 1.5 times the box width (i.e., the interquartile range) from both ends of the box.
Fourteen of the 61 patients with M. pneumoniae PCR-positive results were found to be infected with MR M. pneumoniae. All of those 14 patients had an A-to-G transition at position 2,063 in domain V of the 23S rRNA gene (A2063G). No mutations at site 2,064 or 2,617 in domain V of the 23S rRNA gene were observed. Twelve (85.7%) of 14 M. pneumoniae with A2063G mutation cases and 40 (85.1%) of 47 M. pneumoniae without mutation cases were detected by the SAI assay.
In the present study, the SAI assay showed sensitivity and specificity of 85.2% (52/61) and 99.1% (108/109), respectively, compared with the results of real-time PCR. The pooled sensitivity and specificity of other immunochromatographic assay kits for detecting M. pneumoniae in throat swabs have been reported to be 70 and 92%, respectively [1].
M. pneumoniae antigen level in the nasal cavity was significantly lower than that in the pharynx. This suggests that proliferating M. pneumoniae in the lower respiratory tract may have been transferred by coughing to the pharynx but not to the nasal cavity [17,18]. Therefore, we used throat swab samples for the assay. Additionally, nonadherence to the validated technique is one reason why the performance of the assay often decrease in the setting of point of care testing.
The time from onset of M. pneumoniae infection to the SAI assay and results of the real-time PCR assay are shown in Figure 3. M. pneumoniae in the real-time PCR-positive and SAI assay-negative samples (gray dots) was detected within four days after the onset of M. pneumoniae infection but was not detected in those samples 5-15 days after the onset of M. pneumoniae infection. These results suggest that the optimal timing of the SAI assay is five days or more after the onset of M. pneumoniae infection. There was no statistically significant difference in the copy numbers of M. pneumoniae between patients with bronchitis and those with pneumonia or between patients in different age groups.
This study showed high sensitivity and high specificity of the SAI assay for detecting M. pneumoniae from throat swab samples. FUJI DRI-CHEM IMMUNO AG2 and FUJI DRI-CHEM IMMUNO AG cartridge Myco (FUJIFILM Co., Tokyo, Japan) are therefore appropriate for clinical use. However, PCR or other molecular methods are superior,