Literature DB >> 16973654

Comparison of antifungal treatments for murine fusariosis.

Brad Spellberg1, Julie Schwartz, Yue Fu, Valentina Avanesian, Jill Adler-Moore, John E Edwards, Ashraf S Ibrahim.   

Abstract

OBJECTIVES: Fusarium solani infections are notoriously difficult to treat. We compared the efficacy of polyenes and an echinocandin in treating murine fusariosis to identify the optimal therapeutic regimen.
METHODS: Neutropenic mice infected intravenously with F. solani were treated with amphotericin B (AmB), liposomal AmB (LAmB), amphotericin B lipid complex (ABLC), caspofungin acetate or a combination of LAmB and caspofungin. Treatment was initiated prior to infection (prophylactic therapy), 24 h post-infection (delayed therapy) or 2 days before infection and continued for 1 day after (continuous therapy).
RESULTS: Prophylaxis only with LAmB significantly reduced brain or kidney fungal burden compared with placebo. No prophylactic treatment improved survival. LAmB levels in the kidneys were higher than ABLC or AmB levels, which were often undetectable. In the delayed therapy model, neither polyenes nor caspofungin improved survival. In the continuous therapy model, LAmB or LAmB plus caspofungin did not improve survival even though they did decrease fungal burden. In contrast, continuous caspofungin at 1 but not 5 mg/kg/day improved survival, but did not decrease fungal burden. Kidney inflammation and tissue necrosis were markedly decreased in mice treated with caspofungin compared with other treatments.
CONCLUSIONS: These studies demonstrate a dissociation between survival and tissue fungal burden during murine fusariosis. Although prophylactic LAmB may be useful at reducing tissue fungal burden, polyenes had limited survival benefit for active fusariosis. Caspofungin at 1 but not 5 mg/kg/day mediated surprising improvements in survival during active fusariosis, despite lack of reduction in fungal burden. Further studies are warranted.

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Year:  2006        PMID: 16973654     DOI: 10.1093/jac/dkl378

Source DB:  PubMed          Journal:  J Antimicrob Chemother        ISSN: 0305-7453            Impact factor:   5.790


  6 in total

1.  Cross-reactivity of Fusarium spp. in the Aspergillus Galactomannan enzyme-linked immunosorbent assay.

Authors:  Anna Maria Tortorano; Maria Carmela Esposto; Anna Prigitano; Anna Grancini; Cristina Ossi; Caterina Cavanna; Giuliana Lo Cascio
Journal:  J Clin Microbiol       Date:  2012-01-11       Impact factor: 5.948

2.  Macrophage reporter cell assay for screening immunopharmacological activity of cell wall-active antifungals.

Authors:  Russell E Lewis; Guangling Liao; Katherine Young; Cameron Douglas; Dimitrios P Kontoyiannis
Journal:  Antimicrob Agents Chemother       Date:  2014-01-06       Impact factor: 5.191

Review 3.  Fusariosis, a complex infection caused by a high diversity of fungal species refractory to treatment.

Authors:  J Guarro
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2013-08-11       Impact factor: 3.267

4.  Murine model of disseminated fusariosis: evaluation of the fungal burden by traditional CFU and quantitative PCR.

Authors:  Gloria M González; Jazmín Márquez; Rogelio de J Treviño-Rangel; José P Palma-Nicolás; Elvira Garza-González; Luis A Ceceñas; J Gerardo González
Journal:  Mycopathologia       Date:  2013-08-13       Impact factor: 2.574

5.  Fosmanogepix (APX001) Is Effective in the Treatment of Immunocompromised Mice Infected with Invasive Pulmonary Scedosporiosis or Disseminated Fusariosis.

Authors:  Sondus Alkhazraji; Teclegiorgis Gebremariam; Abdullah Alqarihi; Yiyou Gu; Zeinab Mamouei; Shakti Singh; Nathan P Wiederhold; Karen J Shaw; Ashraf S Ibrahim
Journal:  Antimicrob Agents Chemother       Date:  2020-02-21       Impact factor: 5.191

6.  Update on the treatment of disseminated fusariosis: Focus on voriconazole.

Authors:  Marta Stanzani; Fabio Tumietto; Nicola Vianelli; Michele Baccarani
Journal:  Ther Clin Risk Manag       Date:  2007-12       Impact factor: 2.423

  6 in total

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