Simvastatin inhibits planktonic cells and biofilms of Candida and Cryptococcus species.
The incidence of invasive fungal infections, especially those caused by opportunistic fungi of the genus Candida and Cryptococcus, has proportionally increased with the increase in the number of hosts with impaired immunity. (1-4) In addition, in vitro resistance to antifungal drugs among Candida spp. and Cryptococcus spp. strains recovered from humans and animals has been reported. (5-11)
This scenario motivates the search for new compounds with antifungal potential. Originally, the first statins were described as metabolites of microorganisms with the ability to lower blood cholesterol. (12) Later, it was demonstrated that these compounds reduce the growth of several fungal species, (13-15) including the yeasts Candida spp. and Cryptococcus neoformans (16) and the filamentous fungi Mucor spp. and Rhizopus spp. (17) In addition, it has also been reported that the administration of statins to hospitalized patients increases survival (18) and decreases Candida burden in diabetic patients. (19)
Although the antifungal potential of statins has already been addressed in previous reports, studies involving the effect of statins on fungal biofilms are needed to obtain a better knowledge on the antifungal potential of these compounds. Hence, this study evaluated the effect of the statins simvastatin, atorvastatin, and pravastatin on planktonic cells of Candida spp. and Cryptococcus spp. Considering that the best results were obtained for simvastatin, this drug was evaluated in combination with antifungal drugs against planktonic growth. In addition, simvastatin was tested against biofilms of Candida spp. and Cryptococcus spp.
Materials and methods
For this study, 51 strains of Candida spp. (16 Candida albicans; 12 Candida tropicalis; 11 Candida krusei; 12 Candida parapsilosis sensu lato), and 25 strains of Cryptococcus spp. (13 C. neoformans --serotypes A, D and AD; and 12 Cryptococcus gattii--serotypes B and C) isolated from animals were used. The isolates belong to the culture collection of the Specialized Medical Mycology Center, Brazil. The purity and identity of the Candida spp. strains were confirmed by growth on chromogenic medium and microscopical and biochemical features. (20) For the Cryptococcus spp. strains, capsule formation, melanin production, and biochemical testing were evaluated and the serotype of each strain was assessed by PCR. (21)
Susceptibility testing of planktonic cells
Susceptibility assays were performed using the broth microdilution method, as described by the document M27-A3 of the Clinical and Laboratory Standards Institute. (22) The tests were performed in duplicate and visually read after 48 h of incubation at 35[degrees]C. The strains C. parapsilosis ATCC 22019 and C. krusei ATCC 6258 were included as quality control for all tests. (22)
Inocula were prepared to obtain a final concentration of 0.5-2.5 x [10.sup.3] cells [mL.sup.-1]. (22) The statins simvastatin (Medley Industria Farmaceutica Ltda, Campinas, SP, Brazil), atorvastatin (Laboratorios Pfizer Ltda, Sao Paulo, SP, Brazil), and pravastatin (Bristol-Myers-Squibb, Nova York, NY, USA) and the antifungal drugs amphotericin B (Sigma Chemical Corporation, St Louis, USA), itraconazole (Janssen Pharmaceutica, Beerse, Belgium), and fluconazole (Pfizer Pharmaceuticals, New York, USA) were tested against all strains.
To obtain the stock-solutions of each drug, atorvastatin, pravastatin, and fluconazole were diluted with sterile distilled water, and amphotericin B and itraconazole were diluted with dimethylsulfoxide (DMSO). Simvastatin was activated from its lactone prodrug form through hydrolysis in ethanolic NaOH (15% (v/v) ethanol, 0.25% (w/v) NaOH), at 60[degrees]C, for 1h. (15) The concentration range tested was 3.9-2000 [micro]g [mL.sup.-1] for simvastatin, 19.5-10,000 [micro]g [mL.sup.-1] for atorvastatin, 97.6-50,000 [micro]g [mL.sup.-1] for pravastatin, 0.0312-64 [micro]g [mL.sup.-1] for amphotericin B and itraconazole, and 0.25-256 [micro]g [mL.sup.-1] for fluconazole. The minimum inhibitory concentration (MIC) was defined as the lowest drug concentration able to inhibit 100% of fungal growth for amphotericin B and 50% inhibition of fungal growth when compared to the free-drug azoles (22) and statins control.
As simvastatin provided the best antifungal results, we evaluated the interaction between this drug and the antifungal drugs against the tested yeasts. For drug interaction studies, simvastatin was tested with each azole by broth microdilution method, using the MIC of each tested drug alone as the highest concentrations tested in combination. The concentrations of the drugs in combination ranged from 0.03 to 1000, 0.00024 to 2, 0.00006 to 64 and 0.00048 to 256 [micro]g [mL.sup.-1] for simvastatin, amphotericin B, itraconazole and fluconazole, respectively. The reading criteria were the same as for the antifungal drugs alone, namely 100% inhibition when combined with amphotericin B and 50% inhibition when combined with azoles. The interaction between the drugs was analyzed by calculating the fractional inhibitory concentration index (FICI), with values [less than or equal to] 0.5 indicating synergism. (23)
Susceptibility test of sessile cells
Simvastatin was tested against growing biofilms and mature biofilms of Candida spp. and Cryptococcus spp. Amphotericin B and itraconazole were used in all tests as control drugs for biofilm inhibition. The tests were performed in triplicate using one biofilm-producing strain of each tested fungal species (C. albicans, C. tropicalis, C. parapsilosis, C. krusei, C. neoformans and C. gattii), according to the methodology described by Chatzimoschou et al., (24) with some modifications. Briefly, strains were grown on Sabouraud dextrose agar for 48 h at 30[degrees]C and then subcultured into Sabouraud dextrose broth for 24h, at 30[degrees]C, under agitation at 150rpm. After this period, the suspensions were centrifuged at 3000 rpm for 10 min, the supernatant was discarded, and the pellet was washed twice with sterile PBS. Then, the pellet was resuspended in RPMI 1640 medium (Gibco-BRL, USA), reaching a concentration of 1 x [10.sup.6] cells [mL.sup.-1]. Tests were performed in 96-well polystyrene plates.
To evaluate the effect of simvastatin, amphotericin B, and itraconazole on growing biofilm, 100 [micro]L of the fungal suspension was exposed to 100 [micro]L of simvastatin and incubated at 35[degrees]C for 48 h. The tested concentrations were based on the MIC obtained for each drug against fungal planktonic growth, including MIC, 10xMIC and 50xMIC. On the other hand, to evaluate the effect of simvastatin and the antifungals alone against mature biofilm, 100 [micro]L of the fungal suspension was added to 100 [micro]L of RPMI 1640 medium and incubated at 35[degrees]C for 48 h. Then, the mature biofilms were exposed to simvastatin, amphotericin B, and itraconazole and incubated at 35[degrees]C for 48 h. The tested concentrations against mature biofilms were 10xMIC, 50xMIC and 100xMIC. For all tests, drug-free growth control for each strain was included.
After 48 h of drug exposure, the growing and mature biofilms were submitted to the following procedures: supernatants were collected and reserved for further analysis, and plates were washed twice with sterile PBS Tween 20 (0.05%, v/v) solution to remove non-adhered cells. Then, the biofilm viability was evaluated through XTT assay, according to Martinez and Casadevall, (25) with modifications. Stock solutions of XTT (1 mg [mL.sup.-1]) were previously prepared, filtrated and stocked at -20[degrees]C, until used. Menadione (Sigma) (0.4mM in acetone) was prepared at the moment of use. Afterwards, 50 [micro]L of sterile PBS, 75 [micro]L of XTT solution, and 6 [micro]L of menadione solution were added to each well. Plates were incubated at 35[degrees]C during 5 h, in the dark, and then XTT was all transferred to a new plate and read in a spectrophotometer at 492 nm.
For analysis of the MIC data of drugs against planktonic cells, Student's t test for independent and paired samples was used. To check the variation of the MIC values of the drugs in combination, as well as the FICI value, Student's t test for paired samples was also used. Regarding the biofilm assay, all tests were made in triplicate and results were evaluated by ANOVA and Tukey's multiple comparison post-test. p-Values<0.05 were considered statistically significant.
Susceptibility test of planktonic cells
Among the tested statins, simvastatin showed the lowest MIC, with geometric means varying from 29.45 to 567.16 and from 62.5 to 500 mg [L.sup.-1] against the genera Candida and Cryptococcus, respectively (Table 1). Atorvastatin showed better results against Candida species, when compared to Cryptococcus spp., with MIC geometric means varying from 52.06 to 1682.37 mg [L.sup.-1] against Candida spp. and from 3886.02 to >10,000 [micro]g [mL.sup.-1] against Cryptococcus spp. (Table 1). As for pravastatin, the MIC geometric means varied from 2159.24 to >50,000 mg [L.sup.-1] against Candida spp. and from 44079.56 to >50,000 mg [L.sup.-1] against Cryptococcus (Table 1). MIC geometric means for the classic antifungals against Candida spp. varied from 0.343 to 1.624 mg [L.sup.-1] for amphotericin B, from 0.046 to 15.021 mg [L.sup.-1] for itraconazole, and from 0.659 to 82.346 mg [L.sup.-1] for fluconazole. MIC geometric means for classic antifungals against Cryptococcus spp. varied from 0.125 to 0.735 mg [L.sup.-1] for amphotericin B, from 0.189 to 1 mg [L.sup.-1] for itraconazole, and from 6.498 to 64 mg [L.sup.-1] for fluconazole (Table 1).
Results for the in vitro interaction between simvastatin and antifungal drugs against these yeasts are shown in Table 2. In general, a synergistic interaction was observed between simvastatin and both azoles against C. albicans (n = 10/10), C. tropicalis (n = 11/11) and C. parapsilosis sensu lato (n = 12/12) (p < 0.05). Concerning C. krusei, only the combination of simvastatin and itraconazole was synergistic (n = 9/10) (p < 0.05). As for Cryptococcus spp., synergistic interactions were observed between simvastatin and the three antifungals tested against C. gattii (simvastatin/amphotericin B and simvastatin/fluconazole: n = 7/7; simvastatin/itraconazole: n = 5/7) and C. neoformans (simvastatin/amphotericin B: n = 11/11; simvastatin/itraconazole: n = 9/11; simvastatin/fluconazole: n =10/11) (p < 0.05).
Susceptibility test of sessile cells
Regarding the action of simvastatin against biofilm of Candida spp., simvastatin inhibited growing biofilms at concentrations greater than 10xMIC (Fig. 1). Amphotericin B caused significant decrease in metabolic activity of growing biofilms at 10xMIC and 50xMIC, while itraconazole caused inhibition at all tested concentrations (p < 0.05). As for mature biofilms, simvastatin caused significant decrease in metabolic activity (Fig. 1) (p < 0.05), at concentrations above 50xMIC. Amphotericin B inhibited mature biofilms at all tested concentrations, while itraconazole only at 50xMIC and 100xMIC (p < 0.05).
Regarding the genus Cryptococcus, simvastatin inhibited growing biofilms at all tested concentrations (Fig. 2) (p < 0.05), similar to what was observed when amphotericin B and itraconazole were used (p < 0.05). Concerning mature biofilms, simvastatin caused significant decrease in metabolic activity of Cryptococcus biofilm at 50xMIC and 100xMIC (Fig. 2) (p < 0.05). Amphotericin B inhibited mature biofilms at all tested concentrations (p < 0.05), while itraconazole did not decrease biofilm metabolic activity at any tested concentration.
This study shows the inhibitory activity of simvastatin on the growth of yeasts of the genera Candida and Cryptococcus with an inhibitory effect against both planktonic cells and biofilms. The MICs of simvastatin against C. albicans and C. tropicalis were similar to the serum levels of the drug, when administered to control blood cholesterol. (26) C. albicans and C. tropicalis are important fungal pathogens commonly isolated from candidemia. (27,28) Simvastatin and atorvastatin have been described inhibiting Candida spp. and the filamentous fungus Aspergillus fumigatus. (13) This work confirms the action of these two drugs, especially simvastatin against Candida spp. and Cryptococcus spp. However, the growth of these fungi was not inhibited by pravastatin. The use of statins deregulates cellular production of isoprenoid, (13) which leads to mitochondrial dysfunction, respiratory deficit, (29) and changes in lipid structure and in the dynamics of plasma membrane of C. albicans cells. (30)
There is no synergistic interaction when simvastatin is associated with amphotericin B against most Candida spp. strains. Statins reduce the amount of fungal ergosterol, which may lead to decreased activity of amphotericin B, since ergosterol is the target molecule for this antifungal drug and a decrease in the amount of this molecule is one of the mechanisms developed by amphotericin B resistant Candida spp. However, synergism between simvastatin and amphotericin B was observed against strains of Cryptococcus spp., in line with previous reports with the filamentous fungi Rhizopus oryzae and Aspergillus flavus. (31) These contradictory findings still need to be elucidated.
[FIGURE 1 OMITTED]
In general, when simvastatin is associated with azoles (i.e. itraconazole or fluconazole) there is synergism against strains of Candida spp. and Cryptococcus spp. However, probably due to the intrinsic resistance of C. krusei to fluconazole, synergism between simvastatin and fluconazole was not observed against this Candida species. The interaction between statins and azoles has been reported against the yeasts Saccharomyces cerevisiae (32) and Candida spp., (33) and the filamentous fungi Aspergillus spp., Mucor spp. and Rhizopus spp. (17,33) Synergism between these two pharmacological groups is most likely associated with the combined action of the drugs in reducing fungal ergosterol, by acting at different moments in the pathway of ergosterol biosynthesis. (11) In addition, the reduction of endogenous sterol due to the action of statins increases cell membrane permeability in order to increase absorption of exogenous sterol, as a compensatory mechanism, and, simultaneously, the entrance of azoles in the cell is facilitated. (34)
Biofilm production is considered an important virulence factor of Candida spp. (35) and it contributes for the persistence of infections. (36) It has been demonstrated that simvastatin also inhibits growing and mature biofilms of Candida spp. and Cryptococcus spp. strains when used alone. Liu et al. (37) showed that simvastatin inhibited biofilm production of C. albicans after 16-h-incubation, suggesting that at least one mechanism of inhibition involves interference with ergosterol biosynthesis. On the other hand, there are no reports of the effect of simvastatin on biofilms of Cryptococcus spp. Additional studies are needed to better understand the action of simvastatin against yeast biofilms.
[FIGURE 2 OMITTED]
Studies have shown that amphotericin B inhibits fungal biofilms (25,38) causing apoptosis of the cells in Candida biofilms. (39) In our study, growing and mature biofilms of Candida spp. and Cryptococcus spp. were inhibited by amphotericin B. Although many authors have reported that azoles do not inhibit fungal biofilms, (25,38) the present study demonstrated the inhibition of growing and mature biofilms of Candida spp. by itraconazole. As for Cryptococcus spp., itraconazole only inhibited growing biofilms.
Although several reports have demonstrated in vitro activity of statins agents against many clinical relevant yeast and mold species, as well as the synergistic effect of statins with different antifungal drugs, clinical studies are scarce. (40) Spanakis et al. (19) showed that use of statins decreased the incidence of cultures positive for Candida species among patients with type 2 diabetes mellitus who underwent gastrointestinal surgery. In contrast, no beneficial effects were observed for statins in a study of patients with candidemia. (41) However, these studies were performed with different patient groups and were inconclusive. Thus, further studies aiming to evaluate the benefits of statin in antifungal therapy are required.
The present study showed the activity of statins against Candida and Cryptococcus species, with particular emphasis on simvastatin, isolated and combined with classical antifungals. In addition, it was also demonstrated that simvastatin was able to inhibit growing and mature biofilms of Candida spp. and Cryptococcus spp.
Conflicts of interest
The authors declare no conflicts of interest.
This work was supported by grants from the National Council for Scientific and Technological Development (CNPq; Brazil; Processes 307606/2013-9; 443167/2014-1; 445670/2014-2) and CAPES (AE1--0052-000650100/11).
(1.) Santos ER, Dal Forno CF, Hernandez MG, et al. Susceptibility of Candida spp. isolated from blood cultures as evaluated using the M27-A3 and new M27-S4 approved breakpoints. Rev Inst Med Trop Sao Paulo. 2014;56:477-82.
(2.) Martins N, Ferreira ICFR, Barros L, Silva S, Henriques M. Candidiasis: predisposing factors, prevention, diagnosis and alternative treatment. Mycopathologia. 2014;177:223-40.
(3.) Martins MA, Brighente KBS, Matos TA, Vidal JE, Hipolito DDC, Pereira-Chioccola VL. Molecular diagnosis of cryptococcal meningitis in cerebrospinal fluid: comparison of primer sets for Cryptococcus neoformans and Cryptococcus gattii species complex. Braz J Infect Dis. 2015;19:62-7.
(4.) Sloan DJ, Parris V.Criptococcal meningitis: epidemiology and therapeutic options. Clin Epidemiol. 2014;6:169-82.
(5.) Pfaller MA, Boyken L, Hollis RJ, Messer SA, Tendolkar S, Diekema DJ. In vitro susceptibilities of Candida spp. to caspofungin: four years of global surveillance. J Clin Microbiol. 2006;44:760-3.
(6.) Costa AKF, Sidrim JJC, Cordeiro RA, Brilhante RSN, Monteiro AJ, Rocha MFG. Urban pigeons (Columba livia) as a potential source of pathogenic yeasts: a focus on antifungal susceptibility of Cryptococcus strains in northeast Brazil. Mycopathologia. 2010;169:207-13.
(7.) Sidrim JJC, Castelo-Branco DSCM, Brilhante RSN, et al. Candida species isolated from the gastrointestinal tract of cockatiels (Nymphicus hollandicus): in vitro antifungal susceptibility profile and phospholipase activity. Vet Microbiol. 2010;145:324-8.
(8.) Warkentien T, Crum-Cianflone NF. An update on Cryptococcus among HIV-infected patients. Int J STD AIDS. 2010;21:679-84.
(9.) Da Costa VG, Quesada RM, Abe AT, Furlaneto-Maia L, Furnaleto MC. Nosocomial bloodstream Candida infections in a tertiary-care hospital in South Brazil: a 4-year survey. Mycopathologia. 2014;178:243-50.
(10.) Brilhante RS, Alencar LP, Cordeiro RA, et al. Detection of Candida species resistant to azoles in the microbiota of rheas (Rhea americana): possible implications for human and animal health. J Med Microbiol. 2013;62:889-95.
(11.) Cordeiro RA, Teixeira CEC, Brilhante RSN, et al. Minimum inhibitory concentrations of amphotericin B, azoles and caspofungin against Candida species are reduced by farnesol. Med Mycol. 2013;51:53-9.
(12.) Galgoczy L, Nyilasi I, Papp T, Vagvolgyi. Statins as antifungal agents. Word J Clin Infect Dis. 2011;1:4-10.
(13.) Macreadie IG, Johnson G, Schlosser T, Macreadie PI. Growth inhibition of Candida species and Aspergillus fumigatus by statins. FEMS Microbiol Lett. 2006;262:9-13.
(14.) Wikhe K, Westermeyer C, Macreadie IG. Biological consequences of statins in Candida species and possible implications for human health. Biochem Soc Trans. 2007;35:1529-32.
(15.) Nyilasi I, Kocsube S, Pesti M, Lukacs G, Papp T, Vagvolgyi C. In vitro interactions between primycin and different statins in their effects against some clinically important fungi. J Med Microbiol. 2010;59:200-5.
(16.) Chin NX, Weitzman I, Della Latta P. In vitro activity of fluvastatin, a cholesterol-lowering agent, and synergy with flucanazole and itraconazole against Candida species and Cryptococcus neoformans. Antimicrob Agents Chemother. 1997;41:850-2.
(17.) Chamilos G, Lewis RE, Kontoyiannis DP. Lovastatin has significant activity against zygomycetes and interacts synergistically with voriconazole. Antimicrob Agents Chemother. 2006;50:96-103.
(18.) Forrest GN, Kopack AM, Perencevich EN. Statins in candidemia: clinical outcomes from a matched cohort study. BMC Infect Dis. 2010;10:152.
(19.) Spanakis EK, Kourkoumpetis TK, Livanis G, Peleg AY, Mylonakis E. Statin therapy and decreased incidence of positive Candida cultures among patients with type 2 diabetes mellitus undergoing gastrointestinal surgery. Mayo Clin Proc. 2010;85:1073-9.
(20.) Brilhante RS, Castelo-Branco DSCM, Soares GD, et al. Characterization of the gastrointestinal yeast microbiota of cockatiels (Nymphicus hollandicus): a potential hazard to human health. J Med Microbiol. 2010;59:718-23.
(21.) Cordeiro RA, Costa AKF, Brilhante RSN, et al. PCR-REA as an important tool for the identification of Cryptococcus neoformans and Cryptococcus gattii from human and veterinary sources. Vet Microbiol. 2011;154:180-4.
(22.) Clinical and Laboratory Standards Institute. Reference method for broth dilution antifungal susceptibility testing of yeasts. Approved standard M27-A3. Wayne, USA: CLSI; 2008.
(23.) Odds FC. Synergy, antagonism, and what the chequerboard puts between them. J Antimicrob Chemother. 2003;52:1.
(24.) Chatzimoschou A, Katragkou S, Simitsopoulou M, et al. Activities o triazole-echinocandin combinations against Candida species in biofilms and as planktonic cells. Antimicrob Agents Chemother. 2011;55:1968-74.
(25.) Martinez LR, Casadevall A. Susceptibility of Cryptococcus neoformans biofilms to antifungal agents in vitro. Antimicrob Agents Chemother. 2006;50:1021-33.
(26.) Schachter M. Chemical, pharmacokinetic and pharmacodynamic properties of statins: an update. Fundam Clin Pharmacol. 2004;19:117-25.
(27.) Pfaller MA, Diekema DJ. Epidemiology of invasive mycoses in North America. Crit Rev Microbiol. 2010;36:1-53.
(28.) Quindos G. Epidemiology of candidaemia and invasive candidiasis: a changing face. Rev Iberoam Micol. 2014;31: 42-8.
(29.) Westermeyer C, Macreadie IG. Simvastatin reduces ergosterol levels, inhibits growth and causes loss of mtDNA in Candida glabrata. FEMS Yeast Res. 2007;7:436-41.
(30.) Gyetvai A, Emri T, Takacs K, et al. Lovastatin possesses a fungistatic effect against Candida albicans, but does not trigger apoptosis in this opportunistic human pathogen. FEMS Yeast Res. 2006;6:1140-8.
(31.) Nyilasi I, Kocsube S, Galgoczy L, Papp T, Pesti M, Vagvolgyi C. Effect of different statins on the antifungal activity of polyene antimycotics. Acta Biol Szeged. 2010;54:33-6.
(32.) Lorenz RT, Parks LW. Effects of lovastatin (mevinolin) on sterol levels and on activity of azoles in Saccharomyces cerevisiae. Antimicrob Agents Chemother. 1990;34:1660-5.
(33.) Nyilasi I, Kocsube S, Krizsan K, et al. In vitro synergistic interactions of the effects of various statins and azoles against some clinically important fungi. FEMS Microbiol Lett. 2010;307:175-84.
(34.) Cabral ME, Figueroa LIC, Farina JI. Synergistic antifungal activity of statin-azole associations as witnessed by Saccharomyces cerevisiae and Candida utilis bioassays and ergosterol quantification. Rev Iberoam Micol. 2013;30:31-8.
(35.) Williams DW, Kuriyama T, Silva S, Malic S, Lewis MAO. Candida biofilms and oral candidosis: treatment and prevention. Periodontol 2000. 2011;55:250-65.
(36.) Martinez LR, Fries BC. Fungal biofilms: relevance in the setting of human disease. Curr Fungal Infect Rep. 2010;4:266-75.
(37.) Liu G, Vellucci VF, Kyc S, Hostetter MK. Simvastatin inhibits Candida albicans biofilm in vitro. Pediatr Res. 2009;66:600-4.
(38.) Inigo M, Peman J, Del Pozo JL. Antifungal activity against Candida biofilms. Int J Artif Organs. 2012;35:780-91.
(39.) Rawya S, Al-Dhaheri Douglas LJ. Apoptosis in Candida biofilms exposed to amphotericin B. J Med Microbiol. 2010;59:149-57.
(40.) Bergman PW, Bjorkhem-Bergman L. Is there a role for statins in fungal infections. Expert Rev Anti Infect Ther. 2013;11:1391-400.
(41.) Welch ML, Liappis AP, Kan VL. Candidemia outcomes not improved with statin use. Med Mycol. 2013;51:219-22.
Raimunda Samia Nogueira Brilhante (a,b), *, Erica Pacheco Caetano (a), Jonathas Sales de Oliveira (a), Debora de Souza Collares Maia Castelo-Branco (a), Elizabeth Ribeiro Yokobatake Souza (a), Lucas Pereira de Alencar (a), Rossana de Aguiar Cordeiro (a,b), Tereza de Jesus Pinheiro Gomes Bandeira (a), Jose Julio Costa Sidrim (a,b), Marcos Fabio Gadelha Rocha (a,c)
(a) Centro Especializado em Micologia Medica, Programa de Pos-Graduacao em Microbiologia Medica, Universidade Federal do Ceara (UFC), Fortaleza, CE, Brazil
(b) Programa de Pos-Graduacao em Ciencias Medicas, Universidade Federal do Ceara (UFC), Fortaleza, CE, Brazil
(c) Programa de Pos-Graduacao em Ciencias Veterinarias, Universidade Estadual do Ceara (UECE), Fortaleza, CE, Brazil
Received 2 April 2015
Accepted 1 June 2015
Available online 26 June 2015
* Corresponding author at: Rua Barao de Caninde, 210, Montese, CEP: 60425-540 Fortaleza, CE, Brazil.
E-mail address email@example.com (R.S.N. Brilhante).
Table 1--Geometric means of the minimum inhibitory concentrations (MIC) of statins and antifungal agents against Candida spp. and Cryptococcus spp. Strains (n) MIC geometric mean ([micro]g [mL.sup.-1]) Statins Simvastatin Atorvastatin Pravastatin Candida species C. albicans (16) 29.45 52.06 2159.24 C. tropicalis (12) 70.12 165.34 21022.41 C. krusei (11) 567.16 755.06 >50,000 C. parapsilosis 235.97 1491.37 >50,000 sensu lato (12) Cryptococcus species C. neoformans A 500 3886.02 44079.56 (a) (11) C. neoformans D (1) 250 >10,000 >50,000 C. neoformans AD (1) 62.5 >10,000 >50,000 C. gatti B (11) 500 5325.21 44079.56 C. gatti C (1) 500 >10,000 >50,000 Strains (n) MIC geometric mean ([micro]g [mL.sup.-1]) Antifungals Amphotericin B Itraconazole Fluconazole Candida species C. albicans (16) 0.561 5.992 21.357 C. tropicalis (12) 0.343 15.021 82.346 C. krusei (11) 1.624 0.072 12.126 C. parapsilosis 0.707 0.059 0.891 sensu lato (12) Cryptococcus species C. neoformans A 0.536 0.189 6.498 (a) (11) C. neoformans D (1) 0.25 0.25 8 C. neoformans AD (1) 0.125 0.5 8 C. gatti B (11) 0.735 0.315 34.562 C. gatti C (1) 1 1 64 (a) Serotypes. Table 2--Geometric means of the minimum inhibitory concentrations (MIC) of the combination of simvastatin and the antifungal amphotericin B, itraconazole, or fluconazole against Candida spp. and Cryptococcus spp. Species (n) Drugs MIC (isolated) ([micro]g [mL.sup.-1]) SIM Antifungal Candida albicans (10) SIM/AMB 29.11 0.616 SIM/ITC 29.11 9.189 SIM/FLC 29.11 21.112 Candida tropicalis (11) SIM/AMB 75.47 0.3426 SIM/ITC 75.47 15.021 SIM/FLC 75.47 82.347 Candida krusei (10) SIM/AMB 574.35 1.624 SIM/ITC 574.35 0.072 SIM/FLC 574.35 12.126 Candida parapsilosis sensu lato (12) SIM/AMB 235.97 0.707 SIM/ITC 235.97 0.059 SIM/FLC 235.97 0.891 Cryptococcus neoformans (11) Serotypes: A(9); D(1); AD(1) SIM/AMB 388.6 0.4139 SIM/ITC 388.6 0.1943 SIM/FLC 388.6 6.622 Cryptococcus gattii (7) Serotypes: B(6); C(1) SIM/AMB 500 0.8203 SIM/ITC 500 0.4102 SIM/FLC 500 39.008 Species (n) Drugs MIC (combination) ([micro]g [mL.sup.-1]) SIM Antifungal Candida albicans (10) SIM/AMB 24.06 0.595 SIM/ITC 1.042 0.329 SIM/FLC 1.695 0.116 Candida tropicalis (11) SIM/AMB 55.637 0.354 SIM/ITC 1.327 0.266 SIM/FLC 4.425 4.832 Candida krusei (10) SIM/AMB 435.28 1.231 SIM/ITC 116.61 0.014 SIM/FLC 233.26 4.925 Candida parapsilosis sensu lato (12) SIM/AMB 78.74 0.236 SIM/ITC 41.68 0.010 SIM/FLC 49.58 0.187 Cryptococcus neoformans (11) Serotypes: A(9); D(1); AD(1) SIM/AMB 35.42 0.0377 SIM/ITC 70.86 0.0354 SIM/FLC 21.38 0.3648 Cryptococcus gattii (7) Serotypes: B(6); C(1) SIM/AMB 19.025 0.0312 SIM/ITC 84.0803 0.0689 SIM/FLC 38.051 2.972 Species (n) Drugs FICI Number of strains showing synergism Candida albicans (10) SIM/AMB 1.741 0/10 SIM/ITC 0.071 10/10 SIM/FLC 0.116 10/10 Candida tropicalis (11) SIM/AMB 1.37 1/11 SIM/ITC 0.035 11/11 SIM/FLC 0.117 11/11 Candida krusei (10) SIM/AMB 1.515 0/10 SIM/ITC 0.416 9/10 SIM/FLC 0.812 3/10 Candida parapsilosis sensu lato (12) SIM/AMB 0.667 7/12 SIM/ITC 0.353 12/12 SIM/FLC 0.420 12/12 Cryptococcus neoformans (11) Serotypes: A(9); D(1); AD(1) SIM/AMB 0.182 11/11 SIM/ITC 0.365 9/11 SIM/FLC 0.11 10/11 Cryptococcus gattii (7) Serotypes: B(6); C(1) SIM/AMB 0.076 7/7 SIM/ITC 0.336 5/7 SIM/FLC 0.152 7/7 SIM, simvastatin; AMB, amphotericin B; ITC, itraconazole; FLC, fluconazole; MIC, minimum inhibitory concentration; FICI, fractional inhibitory concentration index.
|Printer friendly Cite/link Email Feedback|
|Title Annotation:||Original article|
|Author:||Brilhante, Raimunda Samia Nogueira; Caetano, Erica Pacheco; de Oliveira, Jonathas Sales; Castelo-Bra|
|Publication:||The Brazilian Journal of Infectious Diseases|
|Date:||Sep 1, 2015|
|Previous Article:||Evaluation of short-interfering RNAs treatment in experimental rabies due to wild-type virus.|
|Next Article:||Molecular epidemiology of heteroresistant vancomycin-intermediate Staphylococcus aureus in Brazil.|