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Antifungal activity of miltefosine against both azole-susceptible and -resistant Aspergillus strains.
Haghani, Iman; Yahyazadeh, Zahra; Hedayati, Mohammad Taghi; Shokohi, Tahereh; Badali, Hamid; Khojasteh, Shaghayegh; Akhtari, Javad; Javidnia, Javad; Moazeni, Maryam; Al-Harrasi, Ahmed; Aghili, Seyed Reza; Kermani, Firoozeh; Hajheydari, Zohreh; Al Hatmi, Abdullah M S; Abastabar, Mahdi.
Affiliation
  • Haghani I; Invasive Fungi Research Centre, Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran.
  • Yahyazadeh Z; Department of Medical Mycology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Mazandaran Province, Iran.
  • Hedayati MT; Invasive Fungi Research Centre, Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran; Department of Medical Mycology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Mazandaran Province, Iran.
  • Shokohi T; Invasive Fungi Research Centre, Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran; Department of Medical Mycology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Mazandaran Province, Iran.
  • Badali H; Invasive Fungi Research Centre, Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran; Department of Molecular Microbiology & Immunology, South Texas Center for Emerging Infectious Diseases, The University of Texas at San Antonio, San Antonio, Texas, USA.
  • Khojasteh S; Department of Medical Mycology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Mazandaran Province, Iran.
  • Akhtari J; Department of Nano-biomedicine, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
  • Javidnia J; Department of Medical Mycology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Mazandaran Province, Iran.
  • Moazeni M; Invasive Fungi Research Centre, Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran; Department of Medical Mycology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Mazandaran Province, Iran.
  • Al-Harrasi A; Natural and Medical Sciences Research Centre, University of Nizwa, Nizwa, Oman.
  • Aghili SR; Invasive Fungi Research Centre, Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran; Department of Medical Mycology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Mazandaran Province, Iran.
  • Kermani F; Invasive Fungi Research Centre, Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran; Department of Medical Mycology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Mazandaran Province, Iran.
  • Hajheydari Z; Invasive Fungi Research Centre, Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran; Department of Dermatology, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
  • Al Hatmi AMS; Natural and Medical Sciences Research Centre, University of Nizwa, Nizwa, Oman; Centre of Expertise in Mycology, Radboud University Medical Centre/Canisius Wilhelmina Hospital, Nijmegen, The Netherlands. Electronic address: a.alhatmi@unizwa.edu.om.
  • Abastabar M; Invasive Fungi Research Centre, Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran; Department of Medical Mycology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Mazandaran Province, Iran. Electronic address: mabastabar@gmail.com.
Int J Antimicrob Agents ; 61(3): 106715, 2023 Mar.
Article in En | MEDLINE | ID: mdl-36640844
Miltefosine, an alkylphosphocholine, has been approved recently for the treatment of visceral leishmaniasis. Miltefosine has shown promise as a treatment for paracoccidioidomycosis, and has mixed activity against other fungi and yeast. There are limited data on the in-vitro activity of miltefosine against azole-resistant and -susceptible Aspergillus spp. As such, the aim of this study was to determine the in-vitro activity of miltefosine against Aspergillus strains. Miltefosine was tested against 108 azole-susceptible and -resistant Aspergillus strains isolated from Iran and other countries using the broth microdilution method. Miltefosine was found to be effective against azole-resistant Aspergillus isolates, with minimum inhibitory concentrations (MICs) ranging from 1.562 to 6.25 µg/mL. MIC50 and MIC90 were 1.562 and 3.125 µg/mL, respectively. Miltefosine had a higher geometric mean MIC (2.459 µg/mL) for wild-type Aspergillus isolates than itraconazole (0.220 µg/mL) and voriconazole (0.298 µg/mL). No significant difference was found between miltefosine MICs for azole-resistant Aspergillus isolates and azole-susceptible Aspergillus isolates (P>0.05). Miltefosine appears to have good in-vitro activity against azole-resistant Aspergillus strains, according to these findings. Furthermore, the findings suggest that miltefosine could be used to treat infections caused by azole-resistant Aspergillus spp.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Azoles / Antifungal Agents Language: En Journal: Int J Antimicrob Agents Year: 2023 Document type: Article Affiliation country: Iran Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Azoles / Antifungal Agents Language: En Journal: Int J Antimicrob Agents Year: 2023 Document type: Article Affiliation country: Iran Country of publication: Netherlands