Background Mycetoma is a chronic infectious disease of tropical and subtropical countries. It is produced by true fungi and actinobacteria. In México, Nocardia brasiliensis is the main causative agent of mycetoma, producing about 86% of the cases; the gold standard for the therapy of mycetoma by N. brasiliensis is the use of sulfonamides which give a 70% cure rate. The addition of amikacin to this regime increases to 95% the cure rate; however, the patients have to be monitored for creatinine clearance and audiometry studies because of the potential development of side effects. Because of that it is important to search for new active compounds. In the present work, we evaluated the in vivo effect of DA-7867, an experimental oxazolidinone, on the development of experimental mycetomas by N. brasiliensis in BALB/c mice. Methodology/Principal Findings In order to determine the optimal dose utilized to apply to the animals, we first determined by HPLC the plasma levels using several concentrations of the compounds. Based on these results, we used 10 and 25 mg/kg subcutaneously every 24 hr; DA-7867 was also supplied in the drinking water at a calculated dose of 25 mg/kg. As a control we utilized linezolid at 25 mg/kg, a compound active in murine and human infections, three times a day. The mice were infected in the right footpad with a young culture of N. brasiliensis HUJEG-1, and one week later we started the application of the antimicrobials for six more weeks. After that we compared the development of lesions in the groups injected with saline solution or with the antimicrobials; the results were analyzed by the variance ANOVA test. DA-7867 was able to reduce the production of lesions at 25 mg/kg, when given either subcutaneously or in the drinking water. Conclusions/Significance The experimental oxazolidinone DA-7867 is active in vivo against N. brasiliensis, which opens the possibility of using this drug once it is accepted for human application. Since oxazolidinones seem to be active against a wide spectrum of actinobacteria, it is possible they could be used in human cases of mycetoma by other actinomycetales, such as Streptomyces somaliensis, highly prevalent in Sudan, or Actinomadura madurae and A. pelletieri, which are commonly observed in Africa and India.
References
[1]
Lopez Martinez R, Mendez Tovar LJ, Lavalle P, Welsh O, Saul A, Macotela Ruiz E (1992) [Epidemiology of mycetoma in Mexico: study of 2105 cases]. Gac Med Mex 128: 477–481.
[2]
Welsh O, Vera-Cabrera L, Salinas-Carmona MC (2007) Mycetoma. Clin Dermatol 25: 195–202. doi: 10.1016/j.clindermatol.2006.05.011
[3]
Welsh O, Vera-Cabrera L (2003) Abstr. 15th Cong. Int. Soc. Human and Anim. Mycol., abstr. 354, San Antonio, Texas.
[4]
Bozdogan B, Appelbaum PC (2004) Oxazolidinones: activity, mode of action, and mechanism of resistance. Int J Antimicrob Agents 23: 113–119. doi: 10.1016/j.ijantimicag.2003.11.003
[5]
Vera-Cabrera L, Gonzalez E, Choi SH, Welsh O (2004) In vitro activities of new antimicrobials against Nocardia brasiliensis. Antimicrob Agents Chemother 48: 602–604. doi: 10.1128/AAC.48.2.602-604.2004
[6]
Vera-Cabrera L, Ochoa-Felix EY, Gonzalez G, Tijerina R, Choi SH, Welsh O (2004) In vitro activities of new quinolones and oxazolidinones against Actinomadura madurae. Antimicrob Agents Chemother 48: 1037–1039. doi: 10.1128/AAC.48.3.1037-1039.2004
[7]
Vera-Cabrera L, Castro-Garza J, Rendon A, Ocampo-Candiani J, Welsh O, Choi SH, Blackwood K, Molina-Torres C (2005) In vitro susceptibility of Mycobacterium tuberculosis clinical isolates to garenoxacin and DA-7867. Antimicrob Agents Chemother 49: 4351–4353. doi: 10.1128/AAC.49.10.4351-4353.2005
[8]
Gomez-Flores A, Welsh O, Said-Fernandez S, Lozano-Garza G, Tavarez-Alejandro RE, Vera-Cabrera L (2004) In vitro and in vivo activities of antimicrobials against Nocardia brasiliensis. Antimicrob Agents Chemother 48: 832–837. doi: 10.1128/AAC.48.3.832-837.2004
[9]
Moylett EH, Pacheco SE, Brown-Elliott BA, Perry TR, Buescher ES, Birmingham MC, Schentag JJ, Gimbel JF, Apodaca A, Schwartz MA, Rakita RM, Wallace RJ Jr (2003) Clinical experience with linezolid for the treatment of nocardia infection. Clin Infect Dis 36: 313–318. doi: 10.1086/345907
[10]
Park IN, Hong SB, Oh YM, Kim MN, Lim CM, Lee SD, Koh Y, Kim WS, Kim DS, Kim WD, Shim TS (2006) Efficacy and tolerability of daily-half dose linezolid in patients with intractable multidrug-resistant tuberculosis. J Antimicrob Chemother 58: 701–704. doi: 10.1093/jac/dkl298
[11]
Espinoza-González NA, Welsh O, de Torres NW, Cavazos-Rocha N, Ocampo-Candiani J, Said-Fernandez S, Lozano-Garza G, Choi SH, Vera-Cabrera L (2008) Efficacy of DA-7218, a new oxazolidinone prodrug, in the treatment of experimental actinomycetoma produced by Nocardia brasiliensis. Molecules 13: 31–40. doi: 10.3390/molecules13010031
[12]
Daw-Garza A, Welsh O, Said-Fernández S, Lozano-Garza HG, Waksman De Torres N, Cavazos-Rocha N, Ocampo-Candiani J, Vera-Cabrera L (2008) In vivo therapeutic effect of gatifloxacin on BALB/c mice infected with Nocardia brasiliensis. Antimicrob Agents Chemother 52: 1549–1550. doi: 10.1128/AAC.00148-08
[13]
Cavazos-Rocha N, Vera-Cabrera L, Welsh-Lozano O, Waksman-de-Torres N, de la Luz Salazar-Cavazos M (2007) Simultaneous determination and validation of antimicrobials in plasma and tissue of actinomycetoma by high-performance liquid chromatography with diode array and fluorescence detection. J Pharm Biomed Anal 43: 1775–1781. doi: 10.1016/j.jpba.2006.12.019
[14]
Bae SK, Chung WS, Kim EJ, Rhee JK, Kwon JW, Kim WB, Lee MG (2004) Pharmacokinetics of DA-7867, a new oxazolidinone, after intravenous or oral administration to rats: intestinal first-pass effect. Antimicrob Agents Chemother 48: 659–662. doi: 10.1128/AAC.48.2.659-662.2004
[15]
Park-Wyllie LY, Juurlink DN, Kopp A, Shah BR, Stukel TA, Stumpo C, Dresser L, Low DE, Mamdani MM (2006) Outpatient gatifloxacin therapy and dysglycemia in older adults. N Engl J Med 354: 1352–1361. doi: 10.1056/NEJMoa055191
[16]
Rustomjee R, Lienhardt C, Kanyok T, Davies GR, Levin J, Mthiyane T, Reddy C, Sturm AW, Sirgel FA, Allen J, Coleman DJ, Fourie B, Mitchison DA, Gatifloxacin for TB (OFLOTUB) study team (2008) A Phase II study of the sterilising activities of ofloxacin, gatifloxacin and moxifloxacin in pulmonary tuberculosis. Int J Tuberc Lung Dis 12: 128–138.