@ARTICLE{TreeBASE2Ref23694,
author = {Abdullah Mohammed Al-Hatmi and Alexandro Bonifaz and G. Sybren De Hoog and Leticia Vazquez-Maya and Karla Garcia-Carmona and Jacques F Meis and Anne van diepeningen},
title = {Keratitis by Fusarium temperatum, a novel opportunist },
year = {2014},
keywords = {keratitis, Fusarium temperatum, maize, molecular phylogenetics, infection},
doi = {},
url = {http://},
pmid = {},
journal = {BMC Infectious Diseases},
volume = {},
number = {},
pages = {},
abstract = {Abstract
Background: Fusarium species are among the most common fungi present in the environment and some species have emerged as major opportunistic fungal infection in human. However, in immunocompromised hosts they can be virulent pathogens and can cause death. The pathogenesis of this infection relies on three factors: colonization, tissue damage, and immunosuppression. A novel Fusarium species is reported for the first time from a keratitis in a 63-year-old male farmer who acquired the infection from plant material of maize. Maize plants are the natural host of this fungus where it causes stalk rot and seeding malformation under temperate and humid climatic conditions. The clinical manifestation, microbiological morphology, physiological features and molecular data are described.
Methods: Diagnosis was established by using polymerase chain reaction of fungal DNA followed by sequencing portions of translation elongation factor 1 alpha (TEF1 α) and beta-tubulin (BT2) genes. Susceptibility profiles of this fungus were evaluated using CLSI broth microdilution method.
Results: The analyses of these two genes sequences support a new opportunist Fusarium temperatum designation. Phylogenetic analyses showed that the reported clinical isolate was nested within the Fusarium fujikuroi species complex. Antifungal susceptibility testing demonstrated that the fungus had low MICs for micafungin (0.031 ?g/ml), posaconazole (0.25 ?g/ml) and amphotericin B (0.5 ?g/ml).
Conclusion: The present case extends the significance of genus of Fusarium as agents of keratitis and underscores the utility of molecular verification of these emerging fungi in the human host.
}
}
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Citation title: "Keratitis by Fusarium temperatum, a novel opportunist ".
Study name: "Keratitis by Fusarium temperatum, a novel opportunist ".
This study is part of submission 16415
(Status: Published).
Citation
Al-hatmi A.M., Bonifaz A., De hoog G., Vazquez-maya L., Garcia-carmona K., Meis J.F., & Diepeningen A.V. 2014. Keratitis by Fusarium temperatum, a novel opportunist. BMC Infectious Diseases, .
Authors
Al-hatmi A.M.
(submitter)
Bonifaz A.
De hoog G.
Vazquez-maya L.
Garcia-carmona K.
Meis J.F.
Diepeningen A.V.
Abstract
Abstract
Background: Fusarium species are among the most common fungi present in the environment and some species have emerged as major opportunistic fungal infection in human. However, in immunocompromised hosts they can be virulent pathogens and can cause death. The pathogenesis of this infection relies on three factors: colonization, tissue damage, and immunosuppression. A novel Fusarium species is reported for the first time from a keratitis in a 63-year-old male farmer who acquired the infection from plant material of maize. Maize plants are the natural host of this fungus where it causes stalk rot and seeding malformation under temperate and humid climatic conditions. The clinical manifestation, microbiological morphology, physiological features and molecular data are described.
Methods: Diagnosis was established by using polymerase chain reaction of fungal DNA followed by sequencing portions of translation elongation factor 1 alpha (TEF1 α) and beta-tubulin (BT2) genes. Susceptibility profiles of this fungus were evaluated using CLSI broth microdilution method.
Results: The analyses of these two genes sequences support a new opportunist Fusarium temperatum designation. Phylogenetic analyses showed that the reported clinical isolate was nested within the Fusarium fujikuroi species complex. Antifungal susceptibility testing demonstrated that the fungus had low MICs for micafungin (0.031 ?g/ml), posaconazole (0.25 ?g/ml) and amphotericin B (0.5 ?g/ml).
Conclusion: The present case extends the significance of genus of Fusarium as agents of keratitis and underscores the utility of molecular verification of these emerging fungi in the human host.
@ARTICLE{TreeBASE2Ref23694,
author = {Abdullah Mohammed Al-Hatmi and Alexandro Bonifaz and G. Sybren De Hoog and Leticia Vazquez-Maya and Karla Garcia-Carmona and Jacques F Meis and Anne van diepeningen},
title = {Keratitis by Fusarium temperatum, a novel opportunist },
year = {2014},
keywords = {keratitis, Fusarium temperatum, maize, molecular phylogenetics, infection},
doi = {},
url = {http://},
pmid = {},
journal = {BMC Infectious Diseases},
volume = {},
number = {},
pages = {},
abstract = {Abstract
Background: Fusarium species are among the most common fungi present in the environment and some species have emerged as major opportunistic fungal infection in human. However, in immunocompromised hosts they can be virulent pathogens and can cause death. The pathogenesis of this infection relies on three factors: colonization, tissue damage, and immunosuppression. A novel Fusarium species is reported for the first time from a keratitis in a 63-year-old male farmer who acquired the infection from plant material of maize. Maize plants are the natural host of this fungus where it causes stalk rot and seeding malformation under temperate and humid climatic conditions. The clinical manifestation, microbiological morphology, physiological features and molecular data are described.
Methods: Diagnosis was established by using polymerase chain reaction of fungal DNA followed by sequencing portions of translation elongation factor 1 alpha (TEF1 α) and beta-tubulin (BT2) genes. Susceptibility profiles of this fungus were evaluated using CLSI broth microdilution method.
Results: The analyses of these two genes sequences support a new opportunist Fusarium temperatum designation. Phylogenetic analyses showed that the reported clinical isolate was nested within the Fusarium fujikuroi species complex. Antifungal susceptibility testing demonstrated that the fungus had low MICs for micafungin (0.031 ?g/ml), posaconazole (0.25 ?g/ml) and amphotericin B (0.5 ?g/ml).
Conclusion: The present case extends the significance of genus of Fusarium as agents of keratitis and underscores the utility of molecular verification of these emerging fungi in the human host.
}
}
TY - JOUR
ID - 23694
AU - Al-Hatmi,Abdullah Mohammed
AU - Bonifaz,Alexandro
AU - De Hoog,G. Sybren
AU - Vazquez-Maya,Leticia
AU - Garcia-Carmona,Karla
AU - Meis,Jacques F
AU - diepeningen,Anne van
T1 - Keratitis by Fusarium temperatum, a novel opportunist
PY - 2014
KW - keratitis
KW - Fusarium temperatum
KW - maize
KW - molecular phylogenetics
KW - infection
UR - http://dx.doi.org/
N2 - Abstract
Background: Fusarium species are among the most common fungi present in the environment and some species have emerged as major opportunistic fungal infection in human. However, in immunocompromised hosts they can be virulent pathogens and can cause death. The pathogenesis of this infection relies on three factors: colonization, tissue damage, and immunosuppression. A novel Fusarium species is reported for the first time from a keratitis in a 63-year-old male farmer who acquired the infection from plant material of maize. Maize plants are the natural host of this fungus where it causes stalk rot and seeding malformation under temperate and humid climatic conditions. The clinical manifestation, microbiological morphology, physiological features and molecular data are described.
Methods: Diagnosis was established by using polymerase chain reaction of fungal DNA followed by sequencing portions of translation elongation factor 1 alpha (TEF1 α) and beta-tubulin (BT2) genes. Susceptibility profiles of this fungus were evaluated using CLSI broth microdilution method.
Results: The analyses of these two genes sequences support a new opportunist Fusarium temperatum designation. Phylogenetic analyses showed that the reported clinical isolate was nested within the Fusarium fujikuroi species complex. Antifungal susceptibility testing demonstrated that the fungus had low MICs for micafungin (0.031 ?g/ml), posaconazole (0.25 ?g/ml) and amphotericin B (0.5 ?g/ml).
Conclusion: The present case extends the significance of genus of Fusarium as agents of keratitis and underscores the utility of molecular verification of these emerging fungi in the human host.
L3 -
JF - BMC Infectious Diseases
VL -
IS -
ER -