Background Recently, the prevalence of invasive fungal infections has been on the rise, and one of the prevalent symptoms frequently observed is bone deterioration and bone loss.Materials and Methods Using an in vitro model we studied how Aspergillus fumigatus invades the bone. Pathological analysis was then employed to observe the structure and distinctive features of the invading fungal elements within the bone invasion model. Meanwhile, the antifungal effects of itraconazole, voriconazole, posaconazole, and amphotericin B were evaluated.Results The pathological findings showed that in the experimental group, fungal spores and hyphae invaded the bone tissue or were observed growing in the vicinity of the bone edge tissues, as indicated by both HE and PAS staining. In contrast, no fungal elements were observed in the control group, indicating that the in vitro bone invasion model of A. fumigatus was successfully constructed. Furthermore, the findings from the antifungal sensitivity test demonstrated that the lowest effective concentrations of antifungal drugs against the bone invasion model were as follows: 4 mu g/ml for itraconazole, 0.5 mu g/ml for voriconazole, 2 mu g/ml for posaconazole, and 2 mu g/ml for amphotericin B.Discussion The successful construction of the bone invasion model of A. fumigatus has provided a solid basis for future investigations into the mechanisms underlying A. fumigatus bone invasion and the study of its virulence factors. Utilizing bone models is of utmost importance in advancing the development of novel antifungal treatment approaches, as well as in effectively preventing and treating fungal bone invasion and osteolytic diseases.
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Univ Manchester, Fac Med & Hlth Sci, Manchester, Lancs, England
Univ S Manchester Hosp, Natl Aspergillosis Ctr, Manchester M23 9LT, Lancs, EnglandUniv Manchester, Fac Med & Hlth Sci, Manchester, Lancs, England
Denning, David W.
Ghnan, Nesrin
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Univ Manchester, Fac Med & Hlth Sci, Manchester, Lancs, EnglandUniv Manchester, Fac Med & Hlth Sci, Manchester, Lancs, England
Ghnan, Nesrin
Kwizera, Richard
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Univ Manchester, Fac Med & Hlth Sci, Manchester, Lancs, EnglandUniv Manchester, Fac Med & Hlth Sci, Manchester, Lancs, England
Kwizera, Richard
Osmanov, Ali
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Univ Manchester, Fac Med & Hlth Sci, Manchester, Lancs, EnglandUniv Manchester, Fac Med & Hlth Sci, Manchester, Lancs, England
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Baqiyatallah Univ Med Sci, Mol Biol Res Ctr, Tehran, IranBaqiyatallah Univ Med Sci, Mol Biol Res Ctr, Tehran, Iran
Kachuei, R.
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Khodavaisy, S.
Rezaie, S.
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Univ Tehran Med Sci, Sch Publ Hlth, Div Mol Biol, Dept Med Mycol & Parasitol, Tehran, IranBaqiyatallah Univ Med Sci, Mol Biol Res Ctr, Tehran, Iran
Rezaie, S.
Sharifynia, S.
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Univ Tehran Med Sci, Sch Publ Hlth, Div Mol Biol, Dept Med Mycol & Parasitol, Tehran, IranBaqiyatallah Univ Med Sci, Mol Biol Res Ctr, Tehran, Iran
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North Carolina State Univ, Ctr Integrated Fungal Res, Raleigh, NC USANorth Carolina State Univ, Dept Clin Sci, 1060 William Moore Dr, Raleigh, NC 27607 USA
Cotter, Henry Van T.
Cubeta, Marc
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North Carolina State Univ, Ctr Integrated Fungal Res, Raleigh, NC USANorth Carolina State Univ, Dept Clin Sci, 1060 William Moore Dr, Raleigh, NC 27607 USA
Cubeta, Marc
Gilger, Brian C.
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North Carolina State Univ, Dept Clin Sci, 1060 William Moore Dr, Raleigh, NC 27607 USANorth Carolina State Univ, Dept Clin Sci, 1060 William Moore Dr, Raleigh, NC 27607 USA