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Lactoferrin Is Broadly Active against Yeasts and Highly Synergistic with Amphotericin B
Lactoferrin (LF) is a multifunctional milk protein with antimicrobial activity against a range of pathogens. While numerous studies report that LF is active against fungi, there are considerable differences in the level of antifungal activity and the capacity of LF to interact with other drugs. Here...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7179636/ https://www.ncbi.nlm.nih.gov/pubmed/32094132 http://dx.doi.org/10.1128/AAC.02284-19 |
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author | Fernandes, Kenya E. Weeks, Kerry Carter, Dee A. |
author_facet | Fernandes, Kenya E. Weeks, Kerry Carter, Dee A. |
author_sort | Fernandes, Kenya E. |
collection | PubMed |
description | Lactoferrin (LF) is a multifunctional milk protein with antimicrobial activity against a range of pathogens. While numerous studies report that LF is active against fungi, there are considerable differences in the level of antifungal activity and the capacity of LF to interact with other drugs. Here we undertook a comprehensive evaluation of the antifungal spectrum of activity of three defined sources of LF across 22 yeast and 24 mold species and assessed its interactions with six widely used antifungal drugs. LF was broadly and consistently active against all yeast species tested (MICs, 8 to 64 μg/ml), with the extent of activity being strongly affected by iron saturation. LF was synergistic with amphotericin B (AMB) against 19 out of 22 yeast species tested, and synergy was unaffected by iron saturation but was affected by the extent of LF digestion. LF-AMB combination therapy significantly prolonged the survival of Galleria mellonella wax moth larvae infected with Candida albicans or Cryptococcus neoformans and decreased the fungal burden 12- to 25-fold. Evidence that LF directly interacts with the fungal cell surface was seen via scanning electron microscopy, which showed pore formation, hyphal thinning, and major cell collapse in response to LF-AMB synergy. Important virulence mechanisms were disrupted by LF-AMB treatment, which significantly prevented biofilms in C. albicans and C. glabrata, inhibited hyphal development in C. albicans, and reduced cell and capsule size and phenotypic diversity in Cryptococcus. Our results demonstrate the potential of LF-AMB as an antifungal treatment that is broadly synergistic against important yeast pathogens, with the synergy being attributed to the presence of one or more LF peptides. |
format | Online Article Text |
id | pubmed-7179636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-71796362020-04-27 Lactoferrin Is Broadly Active against Yeasts and Highly Synergistic with Amphotericin B Fernandes, Kenya E. Weeks, Kerry Carter, Dee A. Antimicrob Agents Chemother Susceptibility Lactoferrin (LF) is a multifunctional milk protein with antimicrobial activity against a range of pathogens. While numerous studies report that LF is active against fungi, there are considerable differences in the level of antifungal activity and the capacity of LF to interact with other drugs. Here we undertook a comprehensive evaluation of the antifungal spectrum of activity of three defined sources of LF across 22 yeast and 24 mold species and assessed its interactions with six widely used antifungal drugs. LF was broadly and consistently active against all yeast species tested (MICs, 8 to 64 μg/ml), with the extent of activity being strongly affected by iron saturation. LF was synergistic with amphotericin B (AMB) against 19 out of 22 yeast species tested, and synergy was unaffected by iron saturation but was affected by the extent of LF digestion. LF-AMB combination therapy significantly prolonged the survival of Galleria mellonella wax moth larvae infected with Candida albicans or Cryptococcus neoformans and decreased the fungal burden 12- to 25-fold. Evidence that LF directly interacts with the fungal cell surface was seen via scanning electron microscopy, which showed pore formation, hyphal thinning, and major cell collapse in response to LF-AMB synergy. Important virulence mechanisms were disrupted by LF-AMB treatment, which significantly prevented biofilms in C. albicans and C. glabrata, inhibited hyphal development in C. albicans, and reduced cell and capsule size and phenotypic diversity in Cryptococcus. Our results demonstrate the potential of LF-AMB as an antifungal treatment that is broadly synergistic against important yeast pathogens, with the synergy being attributed to the presence of one or more LF peptides. American Society for Microbiology 2020-04-21 /pmc/articles/PMC7179636/ /pubmed/32094132 http://dx.doi.org/10.1128/AAC.02284-19 Text en Copyright © 2020 Fernandes et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Susceptibility Fernandes, Kenya E. Weeks, Kerry Carter, Dee A. Lactoferrin Is Broadly Active against Yeasts and Highly Synergistic with Amphotericin B |
title | Lactoferrin Is Broadly Active against Yeasts and Highly Synergistic with Amphotericin B |
title_full | Lactoferrin Is Broadly Active against Yeasts and Highly Synergistic with Amphotericin B |
title_fullStr | Lactoferrin Is Broadly Active against Yeasts and Highly Synergistic with Amphotericin B |
title_full_unstemmed | Lactoferrin Is Broadly Active against Yeasts and Highly Synergistic with Amphotericin B |
title_short | Lactoferrin Is Broadly Active against Yeasts and Highly Synergistic with Amphotericin B |
title_sort | lactoferrin is broadly active against yeasts and highly synergistic with amphotericin b |
topic | Susceptibility |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7179636/ https://www.ncbi.nlm.nih.gov/pubmed/32094132 http://dx.doi.org/10.1128/AAC.02284-19 |
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