4.5 Article

Morphological changes of the dermatophyte Trichophyton rubrum after photodynamic treatment: a scanning electron microscopy study

期刊

MEDICAL MYCOLOGY
卷 46, 期 4, 页码 315-325

出版社

OXFORD UNIV PRESS
DOI: 10.1080/13693780701836977

关键词

Trichophyton rubrum; antifungal; photodynamic treatment; SEM; morphology

向作者/读者索取更多资源

Treatment strategies for superficial mycosis caused by the dermatophyte Trichophyton rubrum consist of the use of topical or oral antifungal preparations. We have recently discovered that T. rubrum is susceptible to photodynamic treatment (PDT), with 5,10,15-tris(4-methylpyridinium)-20-phenyl-[21H,23H]-porphine trichloride (Sylsens B) as a photosensitizer. The susceptibility appeared to depend on the fungal growth stage, with PDT efficacy higher with microconidia when compared to mycelia. The aim of this study was to investigate, with the use of scanning electron microscopy, the morphological changes caused by a lethal PDT dose to T. rubrum when grown on isolated human stratum corneum. Corresponding dark treatment and light treatment without photosensitizer were used as controls. A sub-lethal PDT dose was also included in this investigation The morphologic changes were followed at various time points after the treatment of different fungal growth stages. Normal fungal growth was characterized by a fiber-like appearance of the surface of the hyphae and microconidia with the exception of the hyphal tips in full mycelia and the microconidia shortly after attachment to the stratum corneum. Here, densely packed globular structures were observed. The light dose (108 J/cm(2)) in the absence of Sylsens B, or the application of the photosensitizer in the absence of light, caused reversible fungal wall deformations and bulge formation. However, after a lethal PDT, a sequence of severe disruptions and deformations of both microconidia and the mycelium were observed leading to extrusion of cell material and emptied fungal elements. In case of a non-lethal PDT, fungal re-growth started on the remnants of the treated mycelium.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Engineering, Biomedical

Biocompatibility of a fish scale-derived artificial cornea: Cytotoxicity, cellular adhesion and phenotype, and in vivo immunogenicity

T. H. van Essen, L. van Zijl, T. Possemiers, A. A. Mulder, S. J. Zwart, C. -H. Chou, C. C. Lin, H. J. Lai, G. P. M. Luyten, M. J. Tassignon, N. Zakaria, A. El Ghalbzouri, M. J. Jager

BIOMATERIALS (2016)

Article Hematology

Weibel-Palade Body Localized Syntaxin-3 Modulates Von Willebrand Factor Secretion From Endothelial Cells

Maaike Schillemans, Ellie Karampini, Bart L. van den Eshof, Anastasia Gangaev, Menno Hofman, Dorothee van Breevoort, Henriet Meems, Hans Janssen, Aat A. Mulder, Carolina R. Jost, Johanna C. Escher, Ruediger Adam, Tom Carter, Abraham J. Koster, Maartje van den Biggelaar, Jan Voorberg, Ruben Bierings

ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2018)

Article Geriatrics & Gerontology

Postmortem MRI and histology demonstrate differential iron accumulation and cortical myelin organization in early- and late-onset Alzheimer's disease

Marjolein Bulk, Walid M. Abdelmoula, Rob J. A. Nabuurs, Linda M. van der Graaf, Coen W. H. Mulders, Aat A. Mulder, Carolina R. Jost, Abraham J. Koster, Mark A. van Buchem, Remco Natte, Jouke Dijkstra, Louise van der Weerd

NEUROBIOLOGY OF AGING (2018)

Article Biochemistry & Molecular Biology

Loss of CRB2 in Muller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype

Peter M. Quinn, Aat A. Mulder, C. Henrique Alves, Melissa Desrosiers, Sharon I. de Vries, Jan Klooster, Deniz Dalkara, Abraham J. Koster, Carolina R. Jost, Jan Wijnholds

HUMAN MOLECULAR GENETICS (2019)

Article Multidisciplinary Sciences

Inducing fluorescence of uranyl acetate as a dual-purpose contrast agent for correlative light-electron microscopy with nanometre precision

Maarten W. Tuijtel, Aat A. Mulder, Clara C. Posthuma, Barbara van der Hoeven, Abraham J. Koster, Montserrat Barcena, Frank G. A. Faas, Thomas H. Sharp

SCIENTIFIC REPORTS (2017)

Article Oncology

Antibody-Neutralized Reovirus Is Effective in Oncolytic Virotherapy

Robert A. Berkeley, Lynette R. Steele, Aat A. Mulder, Diana J. M. van den Wollenberg, Timothy J. Kottke, Jill Thompson, Matthew Coffey, Rob C. Hoeben, Richard G. Vile, Alan Melcher, Elizabeth J. Ilett

CANCER IMMUNOLOGY RESEARCH (2018)

Article Cell & Tissue Engineering

Human iPSC-Derived Retinas Recapitulate the Fetal CRB1 CRB2 Complex Formation and Demonstrate that Photoreceptors and Muller Glia Are Targets of AAV5

Peter M. Quinn, Thilo M. Buck, Aat A. Mulder, Charlotte Ohonin, C. Henrique Alves, Rogier M. Vos, Monika Bialecka, Tessa van Herwaarden, Elon H. C. van Dijk, Mays Talib, Christian Freund, Harald M. M. Mikkers, Rob C. Hoeben, Marie-Jose Goumans, Camiel J. F. Boon, Abraham J. Koster, Susana M. Chuva de Sousa Lopes, Carolina R. Jost, Jan Wijnholds

STEM CELL REPORTS (2019)

Article Biochemistry & Molecular Biology

CRB2 Loss in Rod Photoreceptors Is Associated with Progressive Loss of Retinal Contrast Sensitivity

C. Henrique Alves, Nanda Boon, Aat A. Mulder, Abraham J. Koster, Carolina R. Jost, Jan Wijnholds

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2019)

Article Clinical Neurology

Progression and Classification of Granular Osmiophilic Material (GOM) Deposits in Functionally Characterized Human NOTCH3 Transgenic Mice

Gido Gravesteijn, Leon P. Munting, Maurice Overzier, Aat A. Mulder, Ingrid Hegeman, Marc Derieppe, Abraham J. Koster, Sjoerd G. van Duinen, Onno C. Meijer, Annemieke Aartsma-Rus, Louise van der Weerd, Carolina R. Jost, Arn M. J. M. van den Maagdenberg, Julie W. Rutten, Saskia A. J. Lesnik Oberstein

TRANSLATIONAL STROKE RESEARCH (2020)

Article Biochemistry & Molecular Biology

Naturally occurring NOTCH3 exon skipping attenuates NOTCH3 protein aggregation and disease severity in CADASIL patients

Gido Gravesteijn, Johannes G. Dauwerse, Maurice Overzier, Gwendolyn Brouwer, Ingrid Hegeman, Aat A. Mulder, Frank Baas, Mark C. Kruit, Gisela M. Terwindt, Sjoerd G. van Duinen, Carolina R. Jost, Annemieke Aartsma-Rus, Saskia A. J. Lesnik Oberstein, Julie W. Rutten

HUMAN MOLECULAR GENETICS (2020)

Article Clinical Neurology

NOTCH3 variant position is associated with NOTCH3 aggregation load in CADASIL vasculature

Gido Gravesteijn, Remco J. Hack, Aat A. Mulder, Minne N. Cerfontaine, Remco van Doorn, Ingrid M. Hegeman, Carolina R. Jost, Julie W. Rutten, Saskia A. J. Lesnik Oberstein

Summary: CADASIL patients with an EGFr 7-34 variant have significantly less vascular NOTCH3 aggregation than patients with an EGFr 1-6 variant. This may be one of the factors underlying the difference in disease severity between NOTCH3(cys) EGFr 7-34 and EGFr 1-6 variants.

NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2022)

Article Multidisciplinary Sciences

High-impact FN1 mutation decreases chondrogenic potential and affects cartilage deposition via decreased binding to collagen type II

Marcella van Hoolwerff, Alejandro Rodriguez Ruiz, Marga Bouma, H. Eka D. Suchiman, Roman Koning, Carolina R. Jost, Aat A. Mulder, Christian Freund, Farshid Guilak, Yolande F. M. Ramos, Ingrid Meulenbelt

Summary: The study found that a pathogenic mutation in an early-onset osteoarthritis family affected the binding capacity of fibronectin to collagen type II, thus impacting chondrogenic capacity and propensity to an osteoarthritic state. Therefore, restoring or maintaining proper binding between fibronectin and collagen type II is crucial for effective treatment development for osteoarthritis.

SCIENCE ADVANCES (2021)

Article Clinical Neurology

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Family Members With a Pathogenic NOTCH3 Variant Can Have a Normal Brain Magnetic Resonance Imaging and Skin Biopsy Beyond Age 50 Years

Remco J. Hack, Gido Gravesteijn, Minne N. Cerfontaine, Ingrid M. Hegeman, Aat A. Mulder, Saskia A. J. Lesnik Oberstein, Julie W. Rutten

Summary: This study demonstrates that extremely mild small vessel disease (SVD) phenotypes can occur in individuals from Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) pedigrees harboring NOTCH3 EGFr 7-34 variants with normal brain magnetic resonance imaging up to age 58 years. These findings have important implications for CADASIL diagnosis, disease prediction, and counseling of individuals from EGFr 7-34 CADASIL pedigrees.

STROKE (2022)

Article Multidisciplinary Sciences

Interplay between calcium and sarcomeres directs cardiomyocyte maturation during regeneration

Phong D. Nguyen, Iris Gooijers, Giulia Campostrini, Arie O. Verkerk, Hessel Honkoop, Mara Bouwman, Dennis E. M. de Bakker, Tim Koopmans, Aryan Vink, Gerda E. M. Lamers, Avraham Shakked, Jonas Mars, Aat A. Mulder, Sonja Chocron, Kerstin Bartscherer, Eldad Tzahor, Christine L. Mummery, Teun P. de Boer, Milena Bellin, Jeroen Bakkers

Summary: Zebrafish hearts can regenerate by replacing damaged tissue with new cardiomyocytes. The cardiac dyad, a structure that regulates calcium handling and excitation-contraction coupling, plays a key role in the redifferentiation process.

SCIENCE (2023)

Article Cell & Tissue Engineering

CRB1 is required for recycling by RAB11A+vesicles in human retinal organoids

Thilo M. Buck, Peter M. J. Quinn, Lucie P. Pellissier, Aat A. Mulder, Aldo Jongejan, Xuefei Lu, Nanda Boon, Danielle Koot, Hind Almushattat, Christiaan H. Arendzen, Rogier M. Vos, Edward J. Bradley, Christian Freund, Harald M. M. Mikkers, Camiel J. F. Boon, Perry D. Moerland, Frank Baas, Abraham J. Koster, Jacques Neefjes, Ilana Berlin, Carolina R. Jost, Jan Wijnholds

Summary: In this study, patient-derived retinal organoids were used to model retinal degenerative diseases caused by CRB1 gene mutations. The results showed various abnormalities in CRB1 patient organoids at the retinal level, including downregulation of CRB1 and NOTCH1 expression, impaired endosome maturation and receptor recycling.

STEM CELL REPORTS (2023)

暂无数据