Synergic effect of simvastatin in combination with amphotericin B against environmental strains of Cryptococcus neoformans from northeastern Brazil: a prospective experimental study
Statins are used as cholesterol-lowering drugs and may also have direct antimicrobial effects. To evaluate synergic interactions between simvastatin and both amphotericin B and fluconazole, against environmental strains of Cryptococcus neoformans isolated from captive birds' droppings. Experime...
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Published in: | São Paulo medical journal Vol. 138; no. 1; pp. 40 - 46 |
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Abstract | Statins are used as cholesterol-lowering drugs and may also have direct antimicrobial effects.
To evaluate synergic interactions between simvastatin and both amphotericin B and fluconazole, against environmental strains of Cryptococcus neoformans isolated from captive birds' droppings.
Experimental study conducted at Federal University of Piauí, Parnaíba, in collaboration with Federal University of Triângulo Mineiro, Uberaba, Brazil.
Statin susceptibility tests of Cryptococcus neoformans samples were performed as prescribed in standards. Interactions of simvastatin with amphotericin and fluconazole were evaluated using the checkerboard microdilution method. Presence of these interactions was quantitatively detected through determining the fractional inhibitory concentration index (FICI).
Isolates of Cryptococcus neoformans were obtained from 30 of the 206 samples of dry bird excreta (14.5%) that were collected from pet shops and houses. Ten isolates were selected for susceptibility tests. All of them were susceptible to amphotericin and fluconazole. All presented minimum inhibitory concentration (MIC) > 128 µg/ml and, thus, were resistant in vitro to simvastatin. An in vitro synergic effect was shown through combined testing of amphotericin B and simvastatin, such that six isolates (60%) presented FICI < 0.500. Two isolates showed considerable reductions in MIC, from 1 µg/ml to 0.250 µg/ml. No synergic effect was observed through combining fluconazole and simvastatin.
These results demonstrate that simvastatin should be considered to be a therapeutic alternative, capable of potentiating the action of amphotericin B. However, further studies are necessary to clarify the real effect of simvastatin as an antifungal agent. |
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AbstractList | Statins are used as cholesterol-lowering drugs and may also have direct antimicrobial effects.
To evaluate synergic interactions between simvastatin and both amphotericin B and fluconazole, against environmental strains of Cryptococcus neoformans isolated from captive birds' droppings.
Experimental study conducted at Federal University of Piauí, Parnaíba, in collaboration with Federal University of Triângulo Mineiro, Uberaba, Brazil.
Statin susceptibility tests of Cryptococcus neoformans samples were performed as prescribed in standards. Interactions of simvastatin with amphotericin and fluconazole were evaluated using the checkerboard microdilution method. Presence of these interactions was quantitatively detected through determining the fractional inhibitory concentration index (FICI).
Isolates of Cryptococcus neoformans were obtained from 30 of the 206 samples of dry bird excreta (14.5%) that were collected from pet shops and houses. Ten isolates were selected for susceptibility tests. All of them were susceptible to amphotericin and fluconazole. All presented minimum inhibitory concentration (MIC) > 128 µg/ml and, thus, were resistant in vitro to simvastatin. An in vitro synergic effect was shown through combined testing of amphotericin B and simvastatin, such that six isolates (60%) presented FICI < 0.500. Two isolates showed considerable reductions in MIC, from 1 µg/ml to 0.250 µg/ml. No synergic effect was observed through combining fluconazole and simvastatin.
These results demonstrate that simvastatin should be considered to be a therapeutic alternative, capable of potentiating the action of amphotericin B. However, further studies are necessary to clarify the real effect of simvastatin as an antifungal agent. BACKGROUND: Statins are used as cholesterol-lowering drugs and may also have direct antimicrobial effects. OBJECTIVE: To evaluate synergic interactions between simvastatin and both amphotericin B and fluconazole, against environmental strains of Cryptococcus neoformans isolated from captive birds’ droppings. DESIGNAND SETTING: Experimental study conducted at Federal University of Piauí, Parnaíba, in collaboration with Federal University of Triângulo Mineiro, Uberaba, Brazil. METHODS: Statin susceptibility tests of Cryptococcus neoformans samples were performed as prescribed in standards. Interactions of simvastatin with amphotericin and fluconazole were evaluated using the checkerboard microdilution method. Presence of these interactions was quantitatively detected through determining the fractional inhibitory concentration index (FICI). RESULTS: Isolates of Cryptococcus neoformans were obtained from 30 of the 206 samples of dry bird excreta (14.5%) that were collected from pet shops and houses. Ten isolates were selected for susceptibility tests. All of them were susceptible to amphotericin and fluconazole. All presented minimum inhibitory concentration (MIC) > 128 µg/ml and, thus, were resistant in vitro to simvastatin. An in vitro synergic effect was shown through combined testing of amphotericin B and simvastatin, such that six isolates (60%) presented FICI < 0.500. Two isolates showed considerable reductions in MIC, from 1 µg/ml to 0.250 µg/ml. No synergic effect was observed through combining fluconazole and simvastatin. CONCLUSION: These results demonstrate that simvastatin should be considered to be a therapeutic alternative, capable of potentiating the action of amphotericin B. However, further studies are necessary to clarify the real effect of simvastatin as an antifungal agent. |
Author | Silva, Tássio Henrique Sousa Gomes, Thayse Haylene Soares Damasceno Júnior, Evandro César Bezerra Ferreira, Thatiana Bragine Carvalho, Andressa Maria Aguiar de Ferreira-Paim, Kennio Silva, Nayra Cristina Lira Dos Santos Andrade-Silva, Leonardo Eurípedes Alves, Nathanael Dos Santos Caminha, Henrique Barros Fonseca, Fernanda Machado Araújo, Claudiane Vansoski Silva, Andressa Kelly Ferreira E Mendes, Maria Gabriela Araújo Daboit, Tatiane Caroline Santos, Khelvin Myner da Costa Silva-Vergara, Mario León |
AuthorAffiliation | V BSc. Biomedic, Department of Biomedicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil XVII PhD. Associate Professor, Department of Biomedicine, Universidade Federal do Triângulo Mineiro, Uberaba (MG), Brazil XV PhD. Associate Professor, Department of Infectious and Parasitic Diseases, Universidade Federal do Triângulo Mineiro, Uberaba (MG), Brazil XII PhD. Associate Professor, Department of Medicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil VII BSc. Biomedic, Department of Biomedicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil XIV PhD. Biomedic, Department of Clinical Pathology, Universidade Federal do Triângulo Mineiro, Uberaba (MG), Brazil IX MSc. Doctoral Student, Department of Biomedical Sciences, Universidade Federal do Piauí, Parnaíba (PI), Brazil XI MSc. Doctoral Student, Department of Biomedical Sciences, Universidade Federal do Piauí, Parnaíba (PI), Brazil IV BSc. Biomedic, Department of Biomedicine, Universidade Federal do Piauí, Parnaíba (PI), Brazi |
AuthorAffiliation_xml | – name: III BSc. Biomedic, Department of Biomedicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil – name: X MSc. Doctoral Student, Department of Biomedical Sciences, Universidade Federal do Piauí, Parnaíba (PI), Brazil – name: XVII PhD. Associate Professor, Department of Biomedicine, Universidade Federal do Triângulo Mineiro, Uberaba (MG), Brazil – name: V BSc. Biomedic, Department of Biomedicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil – name: XII PhD. Associate Professor, Department of Medicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil – name: II BSc. Biomedic, Department of Biomedicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil – name: IV BSc. Biomedic, Department of Biomedicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil – name: I BSc. Biomedic, Department of Biomedicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil – name: IX MSc. Doctoral Student, Department of Biomedical Sciences, Universidade Federal do Piauí, Parnaíba (PI), Brazil – name: XIII MSc. Doctoral Student, Department of Infectious and Parasitic Diseases, Universidade Federal do Triângulo Mineiro, Uberaba (MG), Brazil – name: XIV PhD. Biomedic, Department of Clinical Pathology, Universidade Federal do Triângulo Mineiro, Uberaba (MG), Brazil – name: VIII BSc. Biomedic, Department of Biomedicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil – name: XI MSc. Doctoral Student, Department of Biomedical Sciences, Universidade Federal do Piauí, Parnaíba (PI), Brazil – name: VI BSc. Biomedic, Department of Biomedicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil – name: XV PhD. Associate Professor, Department of Infectious and Parasitic Diseases, Universidade Federal do Triângulo Mineiro, Uberaba (MG), Brazil – name: XVI PhD. Associate Professor, Department of Microbiology, Universidade Federal do Triângulo Mineiro, Uberaba (MG), Brazil – name: VII BSc. Biomedic, Department of Biomedicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil – name: Universidade Federal do Triângulo Mineiro – name: Universidade Federal do Piauí |
Author_xml | – sequence: 1 givenname: Tássio Henrique Sousa orcidid: 0000-0002-7792-2535 surname: Silva fullname: Silva, Tássio Henrique Sousa organization: BSc. Biomedic, Department of Biomedicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil – sequence: 2 givenname: Claudiane Vansoski orcidid: 0000-0002-7763-9190 surname: Araújo fullname: Araújo, Claudiane Vansoski organization: BSc. Biomedic, Department of Biomedicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil – sequence: 3 givenname: Khelvin Myner da Costa orcidid: 0000-0002-1550-7512 surname: Santos fullname: Santos, Khelvin Myner da Costa organization: BSc. Biomedic, Department of Biomedicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil – sequence: 4 givenname: Nathanael Dos Santos orcidid: 0000-0001-6945-6282 surname: Alves fullname: Alves, Nathanael Dos Santos organization: BSc. Biomedic, Department of Biomedicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil – sequence: 5 givenname: Thayse Haylene Soares orcidid: 0000-0003-0369-2690 surname: Gomes fullname: Gomes, Thayse Haylene Soares organization: BSc. Biomedic, Department of Biomedicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil – sequence: 6 givenname: Andressa Kelly Ferreira E orcidid: 0000-0002-8606-1407 surname: Silva fullname: Silva, Andressa Kelly Ferreira E organization: BSc. Biomedic, Department of Biomedicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil – sequence: 7 givenname: Nayra Cristina Lira Dos Santos orcidid: 0000-0002-6067-239X surname: Silva fullname: Silva, Nayra Cristina Lira Dos Santos organization: BSc. Biomedic, Department of Biomedicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil – sequence: 8 givenname: Evandro César Bezerra orcidid: 0000-0002-6548-913X surname: Damasceno Júnior fullname: Damasceno Júnior, Evandro César Bezerra organization: BSc. Biomedic, Department of Biomedicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil – sequence: 9 givenname: Andressa Maria Aguiar de orcidid: 0000-0001-5415-1670 surname: Carvalho fullname: Carvalho, Andressa Maria Aguiar de organization: MSc. Doctoral Student, Department of Biomedical Sciences, Universidade Federal do Piauí, Parnaíba (PI), Brazil – sequence: 10 givenname: Maria Gabriela Araújo orcidid: 0000-0002-4733-9170 surname: Mendes fullname: Mendes, Maria Gabriela Araújo organization: MSc. Doctoral Student, Department of Biomedical Sciences, Universidade Federal do Piauí, Parnaíba (PI), Brazil – sequence: 11 givenname: Henrique Barros orcidid: 0000-0002-4965-1643 surname: Caminha fullname: Caminha, Henrique Barros organization: MSc. Doctoral Student, Department of Biomedical Sciences, Universidade Federal do Piauí, Parnaíba (PI), Brazil – sequence: 12 givenname: Tatiane Caroline orcidid: 0000-0001-5186-7382 surname: Daboit fullname: Daboit, Tatiane Caroline organization: PhD. Associate Professor, Department of Medicine, Universidade Federal do Piauí, Parnaíba (PI), Brazil – sequence: 13 givenname: Thatiana Bragine orcidid: 0000-0002-4038-0744 surname: Ferreira fullname: Ferreira, Thatiana Bragine organization: MSc. Doctoral Student, Department of Infectious and Parasitic Diseases, Universidade Federal do Triângulo Mineiro, Uberaba (MG), Brazil – sequence: 14 givenname: Leonardo Eurípedes orcidid: 0000-0002-0485-229X surname: Andrade-Silva fullname: Andrade-Silva, Leonardo Eurípedes organization: PhD. Biomedic, Department of Clinical Pathology, Universidade Federal do Triângulo Mineiro, Uberaba (MG), Brazil – sequence: 15 givenname: Mario León orcidid: 0000-0003-1020-2119 surname: Silva-Vergara fullname: Silva-Vergara, Mario León organization: PhD. Associate Professor, Department of Infectious and Parasitic Diseases, Universidade Federal do Triângulo Mineiro, Uberaba (MG), Brazil – sequence: 16 givenname: Kennio orcidid: 0000-0002-6035-8392 surname: Ferreira-Paim fullname: Ferreira-Paim, Kennio organization: PhD. Associate Professor, Department of Microbiology, Universidade Federal do Triângulo Mineiro, Uberaba (MG), Brazil – sequence: 17 givenname: Fernanda Machado orcidid: 0000-0002-5326-0776 surname: Fonseca fullname: Fonseca, Fernanda Machado organization: PhD. Associate Professor, Department of Biomedicine, Universidade Federal do Triângulo Mineiro, Uberaba (MG), Brazil |
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Cites_doi | 10.1086/597039 10.1111/j.1439-0507.2010.01901.x 10.1007/s11046-011-9500-0 10.1128/AAC.41.4.850 10.1016/j.bjid.2015.06.001 10.1093/jac/dkh434 10.1093/jac/dkn019 10.1590/S0036-46652005000500003 10.1007/s11046-009-9245-1 10.3201/eid0902.020246 10.1080/13693780802378853 10.1146/annurev.pharmtox.45.120403.095748 10.1080/13693780410001712025 10.1590/S0100-736X2008000700004 10.1093/jac/dkg301 10.1128/JCM.43.8.3807-3810.2005 10.1111/j.1574-6968.2010.01972.x 10.3201/eid1001.020779 10.1007/s10096-004-1136-2 10.1016/S1567-1356(03)00038-2 10.1007/s11046-012-9528-9 10.1111/j.1567-1364.2006.00128.x 10.3109/13693786.2010.530697 10.1093/femsyr/fow045 |
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Keywords | Antifungal therapy Cryptococcosis treatment Cryptococcus neoformans Fractional inhibitory concentration index Drug resistance, fungal Drug interactions Cryptococcosis Antifungal agents HIV infection |
Language | English |
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Microbiol contributor: fullname: Pfaller, MA; Boyken, L; Hollis, RJ |
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Snippet | Statins are used as cholesterol-lowering drugs and may also have direct antimicrobial effects.
To evaluate synergic interactions between simvastatin and both... BACKGROUND: Statins are used as cholesterol-lowering drugs and may also have direct antimicrobial effects. OBJECTIVE: To evaluate synergic interactions between... |
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SubjectTerms | Antifungal agents Antifungal therapy Cryptococcosis Cryptococcosis treatment Cryptococcus neoformans Drug interactions Drug resistance, fungal Fractional inhibitory concentration index HIV infection MEDICINE, GENERAL & INTERNAL Original |
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Title | Synergic effect of simvastatin in combination with amphotericin B against environmental strains of Cryptococcus neoformans from northeastern Brazil: a prospective experimental study |
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