Evaluation of the SLOMYCO Sensititre® panel for testing the antimicrobial susceptibility of Mycobacterium marinum isolates

Background The agar dilution method is currently considered as the reference method for Mycobacterium marinum drug susceptibility testing (DST). As it is time-consuming, alternative methods, such as the E-test, were evaluated for M.marinum DST, but without success. The SLOMYCO Sensititre® panel, recently commercialized by TREK Diagnostic Systems (Cleveland, OH), can be used for DST in slow-growing mycobacteria and for antimicrobial agents recommended by the Clinical and Laboratory Standards Institute (CLSI) for M.marinum DST. The main goal of this work was to evaluate the SLOMYCO Sensititre® panel method for DST in M.marinum isolates from human patients and fish relative to the reference agar dilution method. Methods/Results The reproducibility of the minimum inhibitory concentration (MIC) determination (±1 log2 dilution) was very good for both the agar dilution method and SLOMYCO Sensititre® panel (>90 % agreement). The percentage essential agreement between methods varied, depending on the drug: between 97 and 75 % for ciprofloxacin, moxifloxacin, linezolid, isoniazid, clarithromycin, amikacin, rifabutin and rifampin, 74 % for trimethoprim, 72 % for doxycycline, 70 % for sulfamethoxazole, 59 % for streptomycin, 33 % for ethambutol and only 2.2 % for ethionamide. When the agar dilution and SLOMYCO Sensititre® panel results were converted into interpretive criteria, the category agreement was 100 % for amikacin, ciprofloxacin, clarithromycin, moxifloxacin, rifabutin, sulfamethoxazole and trimethoprim, 98 % for ethambutol and 96 % for rifampin and no agreement for doxycycline. Conclusions The SLOMYCO Sensititre® panel method could provide a potential alternative to the reference agar dilution method, when DST in M.marinum is required, except for doxycycline.


Background
Mycobacterium marinum, a slow-growing nontuberculous photochromogenic mycobacteria, is an ubiquitous waterborne organism [9,10,17] that causes diseases in many fish species from cold or warm, fresh or salted water, and also in many other aquatic animals, such as amphibians, mammals and oysters [9,10,17]. In humans, M. marinum infection is commonly limited to the skin, but it can spread to deeper structures, resulting in tenosynovitis, arthritis and osteomyelitis [1,8,13] and, rarely, in disseminated infection in immunocompromised patients [13].
Mycobacterium marinum is naturally multi-drug resistant and there is no standardized antimicrobial treatment for M. marinum infections [7]. As the wild-type

Open Access
Annals of Clinical Microbiology and Antimicrobials susceptibility pattern of M. marinum is well known [2] and acquired resistance has not been described so far, antimicrobial susceptibility testing is not recommended except in the case of treatment failure and relapse [16]. The Clinical and Laboratory Standards Institute (CLSI) recommends microdilution for M. marinum drug susceptibility testing (DST) [16], but the agar dilution method is currently considered to be the reference method [2,4,19]. As this method is time-consuming, alternative methods, such as the E-test, were evaluated, but showed poor agreement with the reference method and therefore are not suitable for DST in M. marinum [2,11,19]. Recently, the SLOMYCO Sensititre ® panel was commercialized by TREK Diagnostic Systems (Cleveland, OH) [3]. This is a standard-order broth microdilution panel that can be used to evaluate the susceptibility of slow growing mycobacteria to 14 antimicrobial agents, including those recommended by CLSI for M. marinum DST [3].
The main goal of this work was to evaluate the SLO-MYCO Sensititre ® panel method for DST in M. marinum strains from humans and fish relative to the reference agar dilution method.

Bacterial strains and growth conditions
The origin and other information concerning the tested M. marinum isolates are described in Broutin et al. [5]. The 35 M. marinum isolates from human patients and nine from fish were collected in France between 1995 and 2007. None was from patients who experienced treatment failure or relapse. M. marinum identification was performed using GenoType Mycobacterium AS/CM, a commercial multiplex line-probe assay (Hain Lifescience GmbH, Nehren, Germany). Isolates were stored at −80 °C in Middlebrook 7H9 broth (DIFCO, Detroit, MI, USA) containing 5 % OADC (DIFCO, Detroit, MI, USA) until determination of the Minimum inhibitory concentrations (MICs). Mycobacteria were then cultured in Löwenstein-Jensen (LJ) slants (bioMérieux, Marcy l'Etoile, France) and in Middlebrook 7H10 agar (DIFCO, Detroit, MI, USA). The M. marinum ATCC 927 strain (from fish) and the M. marinum ATCC BAA-535/M strain isolated from an infected patient were used as controls for MIC determination.

Antimicrobial agents
Amikacin, ciprofloxacin, clarithromycin, doxycycline, ethambutol, ethionamide, isoniazid, rifampin, rifabutin, streptomycin and trimethoprim (Sigma-Aldrich, Lyon, France), linezolid (Pfizer, France) and moxifloxacin (Bayer, Wuppertal, Germany) were tested in this study. Stock solutions of each drug were prepared using the appropriate solvent and were filter-sterilized before storage at −80 °C. To prior testing, each drug was freshly diluted in sterile deionized water. The concentration ranges of the tested antimicrobial agents are indicated in Table 1.

MIC determination by using the agar dilution method
The agar dilution method was performed on Müller-Hinton agar (Becton-Dickinson, France) supplemented with 5 % OADC according to CLSI [16]. Twofold dilutions of the antibiotics to be tested were added to obtain the required final concentrations. Confluent colonies of the different bacteria in LJ slants were swept with a loop and emulsified in sterile water and the concentration was adjusted to the McFarland n. 1 standard turbidity. A 1/100 dilution of each suspension adjusted to the McFarland n. 1 standard was inoculated using a Steers replicator to deliver approximately 10 4 colony-forming units (CFU) per spot. Plates were incubated at 30 °C [16]. The MICs (i.e., the lowest concentration of antibiotic resulting in complete inhibition of growth) of the tested antibiotics were determined after 7 and 14 days of growth of the different M. marinum isolates/controls.

MIC determination using the SLOMYCO Sensititre ® panel (broth micro-dilution method)
Inocula for the SLOMYCO Sensititre ® panel were prepared according to the CLSI and the manufacturer's instructions [16]. SLOMYCO plates were incubated in a non-CO 2 incubator at 30 °C until the controls showed sufficient growth (7-14 days). The MICs were determined visually using an inverted mirror and read as the lowest concentration of the antibiotic showing 100 % growth inhibition.

Analysis of the results
The reproducibility of both methods was evaluated by performing two independent tests for each method and for each of the 44 isolates (a total of 176 tests) and five independent tests for the M. marinum ATCC 927 and ATCC BAA-535/M strains (a total of 30 tests). Each test result was independently interpreted by two blinded readers. The reproducibility value was defined as the percentage of strains with the same MIC value ±1 log 2 dilution at each test. The essential agreement between the agar dilution and SLOMYCO Sensititre ® panel results was expressed as the percentage of isolates that showed the same MIC value ±1 log 2 dilution with the two methods. Category agreement was evaluated using the breakpoints for determining the susceptibility and resistance categories recommended by CLSI [16]. For this study only very major errors (i.e., an isolate resistant [R] by the reference method, but susceptible [S] by the tested method) and major errors (S by the reference method and R by the test method) were considered. Minor errors (intermediate [I] by one method and S or R by the other method) were not considered because the CLSI breakpoints allow only two characterization categories (R or S) [16].

Results
The reproducibility of the results obtained with the agar dilution method (reference method) was very good ( Table 2) for all antibiotics. The MICs of the 14 antimicrobial agents determined by using the agar dilution method were distributed in a narrow range ( Table 1). Comparison of the MICs for the M. marinum isolates from infected humans and fish did not reveal any difference.
The MICs for the two reference M. marinum strains (ATCC 927 and ATCC BAA-535/M) were within 0-1 dilution of the MICs of the 44 tested isolates and within the expected range.
The relatively high MIC 90 of ethionamide (10 μg/mL), isoniazid (8 μg/mL) and streptomycin (16 μg/mL), for which breakpoints are not available, suggests that they are not good candidates for the treatment of M. marinum infection. In contrast, linezolid (MIC 90 : 2 μg/mL) was very effective against the different M. marinum isolates with MIC values among the lowest in our study.

Discussion
The manufacturer's guidelines (TREK Diagnostic Systems, Cleveland, OH) recommend the SLOMYCO Sensititre ® method for antibiotic susceptibility testing in M. marinum, but studies evaluating the concordance with the reference agar dilution method have not been published yet. As the SLOMYCO Sensititre ® panel technique presents several advantages (commercial availability; standardization; easy to set up and to interpret; and amenable to automation [2,19] compared to the timeconsuming and cumbersome agar dilution method, our objective was to compare the performance of these two methods. The lack of difference between the MICs for the M. marinum isolates from infected humans and fish could be explained by the fact that most of the clinical samples were from patients who handled infected fish (from aquarium tanks or fish-related work) and, therefore, the antibiotic susceptibility profiles of the human isolates reflected those of the fish isolates.
Our results show that the reproducibility of the SLO-MYCO Sensititre ® results for the reference strains and the M. marinum isolates (from human and fish) was very good. All results of the independent tests were within the ±1 log 2 dilution acceptable level of variation. Moreover, the level of agreement (±1 log 2 dilution) between the results (MICs and interpretive categories) obtained with the SLOMYCO Sensititre ® panel and the agar dilution methods was good for most of the antibiotics recommended by CLSI and ATS [12] for the treatment of (rifampin, rifabutin, amikacin, clarithromycin and sulfamethoxazole-trimethoprim) or with therapeutic potential (linezolid, isoniazid) for M. marinum infections. It should be noted that two very major errors were observed for rifampin in isolates in which the MIC for rifampin was just above the breakpoint (2 μg/mL) and that still belong to the wild type population [2]. The clinical significance of these data is unclear. Moreover, the MIC of the only rifampin-resistant M. marinum reported until now [14] was clearly above the breakpoint (>16 µg/  Conversely, poor agreement was observed for ethambutol. The MICs for ethambutol obtained with the SLO-MYCO Sensititre ® panel were 2-3 dilutions lower than those obtained with the reference method. However, this poor agreement resulted in only one very major error, when MICs were converted into interpretive categories. This discrepancy corresponds to a strain with a MIC just above the breakpoint (16 µg/mL) ( Table 1).
In the case of doxycycline, no agreement was observed between methods resulting in 46 major errors. This could be explained by (i) the overestimation of doxycycline MICs by the SLOMYCO Sensititre ® panel that could be due to the medium or pH, and (ii) the fact that the MIC 50 and MIC 90 were similar to the breakpoint value. Among the antibiotics recommended by CLSI and on the basis of in vitro susceptibility testing, our results confirm that rifampin, rifabutin, amikacin, clarithromycin and sulfamethoxazole-trimethoprim are good options for the treatment of M. marinum infections, as reported in previous studies [2,4,11,14,15,19]. Sulfamethoxazole and trimethoprim showed good in vitro activity against M. marinum and could be considered as an alternative treatment [19]. The present study brings new data on M. marinum susceptibility pattern to ethionamide, streptomycin and linezolid. The American Thoracic Society recommendations for the treatment of some nontuberculous mycobacteria (NTM) infections include the use of streptomycin (for rifampin-resistant M. kansassii infection) and ethionamide (for M. malmoense infection) [7,12]. However, the lack of clinical experience in M. marinum infections and the absence of breakpoints for NTM susceptibility and resistance to these two antibiotics did not allow predicting their potential efficiency in M. marinum infections [16]. Linezolid has been reported to be effective against mycobacteria (M. chelonae and M. marinum) [6,7] and for treating skin and soft tissue infections [6,7]. In our study, linezolid was one of the most active antimicrobial agents in agreement with the low MIC determined in a previous study [4]. Despite the lack of breakpoint values for M. marinum, linezolid may be an interesting alternative therapeutic agent due to its pharmacological properties. This study confirmed that M. marinum is resistant to isoniazid and ethambutol [7] and the observed M. marinum susceptibility pattern corresponded to the wild type phenotype, as previously reported [2,7,14,18,19]. As the ethambutol MIC 90 was close to the breakpoint and clear evidence on the clinical efficacy of this antibiotic are lacking, it should not be recommended as a first-line drug for M. marinum infection treatment.

Conclusion
In this study, we evaluated the SLOMYCO Sensititre ® panel method for susceptibility testing in 44 M. marinum isolates (from humans and fish) relative to the reference agar dilution method. Our results indicate that the SLOMYCO Sensititre ® panel method could provide a potential alternative to the reference agar dilution method, when DST in M. marinum is required, except for doxycycline. If doxycycline susceptibility needs to be tested, the use of another method (broth microdilution) is more appropriate.

Consent
Written informed consent was obtained from the patients for the publication of this report.