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39717659 2024 12 24 0166-0616 109 2024 Dec Studies in mycology Stud Mycol Known from trees and the tropics: new insights into the Fusarium lateritium species complex. 403 450 403-450 10.3114/sim.2024.109.06 The Fusarium lateritium species complex (FLSC) currently comprises 11 phylogenetic species, including accepted names such as F. lateritium , F. sarcochroum , and F. stilboides , which have mostly been reported in association with citrus and coffee. Many varieties were documented by Wollenweber & Reinking (1935), which is indicative of a wider diversity of species within this group. The lack of type material in some cases, especially for the older names, means that definition by molecular phylogeny is very difficult. In the present study, we examined 179 strains related to F. lateritium from different countries and substrates. Historic reference material, including representative strains from the Wollenweber & Reinking (1935) varieties were included in this study, DNA sequences were generated for comparison, and the morphology correlated with original descriptions to enable the correct application of older names. Strains were characterized by multi-gene phylogenetic analyses based on fragments of the β-tubulin (tub2 ), calmodulin (CaM ), RNA polymerase II second largest subunit (rpb2 ), and translation elongation factor 1-alpha (tef1 ) genes, evaluation of morphological characters and host-substrate preferences. The biological species concept was tested by crossings in vitro . Strains previously identified as F. lateritium , F. stilboides , or one of their varieties based on morphology, were found to belong to 16 species in the FLSC, but also to species from six other species complexes (SC), including the F. citricola SC, F. heterosporum SC, F. incarnatum-equiseti SC, F. redolens SC, F. sambucinum SC, and the F. tricinctum SC. Eleven new phylogenetic and two biological species are described in the FLSC, and emended descriptions are provided for four previously described species. An epitype is designated for F. lateritium , and F. lateritium var. longum , a former variety within the FLSC, is lecto- and epitypified, and elevated to species level with a replacement name. Taxonomic novelties: New species: F. aurantii M.M. Costa, Sand.-Den. & Crous, F. chlamydocopiosum M.M. Costa, Sand.-Den. & Crous, F. citri-sinensis L. Zhao & J.X. Deng, F. coffeibaccae M.M. Costa, L.H. Pfenning, Sand.-Den. & Crous, F. crocatum M.M. Costa, Sand.-Den. & Crous, F. malawiense M.M. Costa, Sand.-Den. & Crous, F. microcyclum M.M. Costa, Sand.-Den. & Crous, F. oliniae M.M. Costa, Sand.-Den. & Crous; F. rufum M.M. Costa, Sand.-Den. & Crous, F. stramineum M.M. Costa, Sand.-Den. & Crous, F. velutinum M.M. Costa, Sand.-Den. & Crous, F. verruculosum M.M. Costa, Sand.-Den. & Crous; Replacement name: F. hanswilhelmii M.M. Costa, Sand.-Den. & Crous; Epitype (basionym): F. lateritium Nees, F. lateritium var. longum Wollenw.; Lectotype (basionym): F. lateritium var. longum Wollenw. Citation: Costa MM, Sandoval-Denis M, Moreira GM, Kandemir H, Kermode A, Buddie AG, Ryan MJ, Becker Y, Yurkov A, Maier W, Groenewald JZ, Pfenning LH, Crous PW (2024). Known from trees and the tropics: new insights into the Fusarium lateritium species complex. Studies in Mycology 109 : 403-450. doi: 10.3114/sim.2024.109.06. © 2024 Westerdijk Fungal Biodiversity Institute. Costa M M MM Westerdijk Fungal Biodiversity Institute, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands. Sandoval-Denis M M Westerdijk Fungal Biodiversity Institute, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands. Moreira G M GM Department of Plant Pathology, Universidade Federal de Lavras, 37200-900, Lavras MG, Brazil. Kandemir H H Westerdijk Fungal Biodiversity Institute, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands. Kermode A A CAB International (CABI), Bakeham Lane, TW20 9TY Egham, Surrey, United Kingdom. Buddie A G AG CAB International (CABI), Bakeham Lane, TW20 9TY Egham, Surrey, United Kingdom. Ryan M J MJ CAB International (CABI), Bakeham Lane, TW20 9TY Egham, Surrey, United Kingdom. Becker Y Y Institute for Epidemiology and Pathogen Diagnostics, Julius Kühn Institute (JKI), Federal Research Centre for Cultivated Plants, Messeweg 11-12, 38104 Braunschweig, Germany. Yurkov A A Department of Bioresources for Bioeconomy and Health Research, Leibniz Institute DSMZ - German Collection of Microorganisms and Cell Cultures GmbH, Inhoffenstraße 7B, 38124 Braunschweig, Germany. Maier W W Institute for Epidemiology and Pathogen Diagnostics, Julius Kühn Institute (JKI), Federal Research Centre for Cultivated Plants, Messeweg 11-12, 38104 Braunschweig, Germany. Groenewald J Z JZ Westerdijk Fungal Biodiversity Institute, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands. Pfenning L H LH Department of Plant Pathology, Universidade Federal de Lavras, 37200-900, Lavras MG, Brazil. Crous P W PW Westerdijk Fungal Biodiversity Institute, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands. Department of Biochemistry, Genetics and Microbiology, Forestry and Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria, South Africa. 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Full characterization of members of this compound class is challenging due to the intrinsic complexity of byproducts during synthesis by fermentation. Moreover, when method validation is targeted for a regulated environment, a robust chromatographic separation of the highly polar oligosaccharides needs to be addressed, including isomers and compounds relevant for potential product adulteration. We present a combined approach of validated chromatography and NMR spectroscopy, which allows for full mass balancing of industrially produced 2'-fucosyl-d-lactose. A combination of NMR spectroscopy, mass spectrometry, and action IR spectroscopy tackles structural elucidation of monoacetylated species as a new class of byproducts. Neu Volker V 0009-0009-7662-3152 Analytical and Materials Science, BASF SE, Carl-Bosch-Strasse 38, Ludwigshafen am Rhein 67056, Germany. Hoffmann Waldemar W Analytical and Materials Science, BASF SE, Carl-Bosch-Strasse 38, Ludwigshafen am Rhein 67056, Germany. Weiß Thomas D TD Agricultural Solutions, BASF SE, Speyerer Strasse 2, Limburgerhof 67117, Germany. Puhl Michael M Chemicals and Catalysis Research, BASF SE, Carl-Bosch-Strasse 38, Ludwigshafen am Rhein 67056, Germany. Abikhodr Ali A Isospec Analytics SA, Renens CH-1020, Switzerland. Warnke Stephan S Isospec Analytics SA, Renens CH-1020, Switzerland. Ben Faleh Ahmed A Isospec Analytics SA, Renens CH-1020, Switzerland. Klinck Sandra S Analytical and Materials Science, BASF SE, Carl-Bosch-Strasse 38, Ludwigshafen am Rhein 67056, Germany. Pommer Maria M Analytical and Materials Science, BASF SE, Carl-Bosch-Strasse 38, Ludwigshafen am Rhein 67056, Germany. Kellner Sarah S Analytical and Materials Science, BASF SE, Carl-Bosch-Strasse 38, Ludwigshafen am Rhein 67056, Germany. Maier Walter W Analytical and Materials Science, BASF SE, Carl-Bosch-Strasse 38, Ludwigshafen am Rhein 67056, Germany. eng Journal Article Validation Study 2024 11 14 United States Anal Chem 0370536 0003-2700 0 Oligosaccharides XO2533XO8R 2'-fucosyllactose 0 Trisaccharides J2B2A4N98G Lactose IM Milk, Human chemistry Humans Oligosaccharides chemistry analysis Trisaccharides chemistry Magnetic Resonance Spectroscopy Lactose chemistry Mass Spectrometry 2024 11 26 6 34 2024 11 14 17 38 2024 11 14 6 53 ppublish 39540461 10.1021/acs.analchem.4c01926 39470297 2024 10 29 1552-485X 2024 Oct 29 American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics Am J Med Genet B Neuropsychiatr Genet Optimizing the Prediction of Depression Remission: A Longitudinal Machine Learning Approach. e33014 e33014 10.1002/ajmg.b.33014 Decisions about when to change antidepressant treatment are complex and benefit from accurate prediction of treatment outcome. Prognostic accuracy can be enhanced by incorporating repeated assessments of symptom severity collected during treatment. Participants (n = 714) from the Genome-Based Therapeutic Drugs for Depression study received escitalopram or nortriptyline over 12 weeks. Remission was defined as scoring ≤ 7 on the Hamilton Rating Scale. Predictors included demographic, clinical, and genetic variables (at 0 weeks) and measures of symptom severity (at 0, 2, 4, and 6 weeks). Longitudinal descriptors extracted with growth curves and topological data analysis were used to inform prediction of remission. Repeated assessments produced gradual and drug-specific improvements in predictive performance. By Week 4, models' discrimination in all samples reached levels that might usefully inform treatment decisions (area under the receiver operating curve (AUC) = 0.777 for nortriptyline; AUC = 0.807 for escitalopram; AUC = 0.794 for combined sample). Decisions around switching or modifying treatments for depression can be informed by repeated symptom assessments collected during treatment, but not until 4 weeks after the start of treatment. © 2024 The Author(s). American Journal of Medical Genetics Part B: Neuropsychiatric Genetics published by Wiley Periodicals LLC. Carr Ewan E Department of Biostatistics & Health Informatics, Institute of Psychiatry, Psychology and Neuroscience (IoPPN), London, UK. Rietschel Marcella M Department of Genetic Epidemiology in Psychiatry, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany. Mors Ole O Psychosis Research Unit, Aarhus University Hospital-Psychiatry, Aarhus, Denmark. Henigsberg Neven N Croatian Institute for Brain Research, Medical School, University of Zagreb, Zagreb, Croatia. Aitchison Katherine J KJ College of Health Sciences, Department of Psychiatry and Medical Genetics, University of Alberta, Edmonton, Alberta, Canada. Neuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada. Women and Children's Health Research Institute, University of Alberta, Edmonton, Alberta, Canada. Northern Ontario School of Medicine, Thunder Bay, Ontario, Canada. Maier Wolfgang W Department of Neurodegenerative Diseases and Geriatric Psychiatry, University Hospital Bonn, Bonn, Germany. German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany. Uher Rudolf R Department of Psychiatry, Dalhousie University, Halifax, Nova Scotia, Canada. Farmer Anne A Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK. McGuffin Peter P Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK. Iniesta Raquel R 0000-0003-1153-5417 Department of Biostatistics & Health Informatics, Institute of Psychiatry, Psychology and Neuroscience (IoPPN), London, UK. 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Through this, we identified and rated indicators relevant for walkability for older adults, additionally focusing on their functional status. The expert workshop and the review led to an extensive list of potential indicators, which we hope will be useful in future research. Those indicators were then adapted and rated in a three-stage Delphi expert survey. A fourth additional Delphi round was conducted to assess the relevance of each indicator for the different frailty levels, namely "robust," "pre-frail," and "frail." Between 20 and 28 experts participated in each round of the Delphi survey. The Delphi process resulted in a list of 72 indicators deemed relevant for walkability in older age groups, grouped into three main categories: "Built environment and transport infrastructure," "Accessibility and meeting places," and "Attractiveness and sense of security." For 35 of those indicators, it was suggested that functional status should be additionally considered. This framework represents a significant step forward in comprehensively covering indicators for subjective and objective walkability in older age, while also incorporating aspects of functioning relevant to older adults. It would be beneficial to test and apply the indicator set in a community setting. © 2024. The Author(s). Koller Daniela D 0000-0002-3203-7188 Institute of Medical Information Processing, Biometry, and Epidemiology, Faculty of Medicine, LMU Munich, Munich, Germany. daniela.koller@med.uni-muenchen.de. Bödeker Malte M Federal Centre for Health Education, Cologne, Germany. Dapp Ulrike U 0000-0001-9497-2860 Geriatrics Centre, Scientific Department at the University of Hamburg, Albertinen-Haus, Hamburg, Germany. Grill Eva E 0000-0002-0273-7984 Institute of Medical Information Processing, Biometry, and Epidemiology, Faculty of Medicine, LMU Munich, Munich, Germany. German Center for Vertigo and Balance Disorders, LMU University Hospital, Munich, Germany. Fuchs Judith J 0000-0003-1594-2319 Department of Epidemiology and Health Monitoring, Robert Koch Institute, Berlin, Germany. Maier Werner W 0000-0003-4356-7296 Institute of Medical Information Processing, Biometry, and Epidemiology, Faculty of Medicine, LMU Munich, Munich, Germany. Strobl Ralf R 0000-0002-7719-948X Institute of Medical Information Processing, Biometry, and Epidemiology, Faculty of Medicine, LMU Munich, Munich, Germany. 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PMC5649390 28819693 39217139 2024 09 03 2158-3188 14 1 2024 Aug 31 Translational psychiatry Transl Psychiatry Correction: Metabolic activity of CYP2C19 and CYP2D6 on antidepressant response from 13 clinical studies using genotype imputation: a meta-analysis. 350 350 350 10.1038/s41398-024-03064-x Li Danyang D 0000-0001-7470-6645 Social, Genetic and Developmental Psychiatry Centre, King's College London, London, GB, UK. Cancer Centre, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, CN, China. Pain Oliver O 0000-0001-5680-3281 Maurice Wohl Clinical Neuroscience Institute, Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, GB, UK. Fabbri Chiara C 0000-0003-0276-7865 Social, Genetic and Developmental Psychiatry Centre, King's College London, London, GB, UK. Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy. Wong Win Lee Edwin WLE 0000-0001-6905-6449 Social, Genetic and Developmental Psychiatry Centre, King's College London, London, GB, UK. Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore. Lo Chris Wai Hang CWH Social, Genetic and Developmental Psychiatry Centre, King's College London, London, GB, UK. Ripke Stephan S 0000-0003-3622-835X Department of Psychiatry and Psychotherapy, Universitätsmedizin Berlin Campus Charité Mitte, Berlin, DE, Germany. Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA. Cattaneo Annamaria A 0000-0002-9963-848X Biological Psychiatry Laboratory, IRCCS Fatebenefratelli, Brescia, Italy. Department of Pharmacological and Biomedical Sciences, University of Milan, Milan, Italy. Souery Daniel D Laboratoire de Psychologie Medicale, Universitè Libre de Bruxelles and Psy Pluriel, Centre Européen de Psychologie Medicale, Brussels, Italy. Dernovsek Mojca Z MZ 0000-0001-5344-7007 University Psychiatric Clinic, University of Ljubliana, Ljubljana, Slovenia. Henigsberg Neven N 0000-0002-5303-1834 Department of Psychiatry, Croatian Institute for Brain Research, University of Zagreb Medical School, Zagreb, HR, Croatia. Hauser Joanna J 0000-0002-6621-3493 Psychiatric Genetic Unit, Poznan University of Medical Sciences, Poznan, Poland. Lewis Glyn G 0000-0001-5205-8245 Division of Psychiatry, University College London, London, GB, UK. Mors Ole O Psychosis Research Unit, Aarhus University Hospital - Psychiatry, Aarhus, Denmark. Perroud Nader N Department of Psychiatry, Geneva University Hospitals, Geneva, CH, Switzerland. Rietschel Marcella M 0000-0002-5236-6149 Department of Genetic Epidemiology in Psychiatry, Medical Faculty Mannheim, University of Heidelberg, Central Institute of Mental Health, Mannheim, Denmark. Uher Rudolf R 0000-0002-2998-0546 Department of Psychiatry, Dalhousie University, Halifax, NS, Canada. Maier Wolfgang W Department of Psychiatry and Psychotherapy, University of Bonn, Bonn, Denmark. Baune Bernhard T BT Department of Psychiatry, University of Münster, Münster, Denmark. Florey Institute for Neuroscience and Mental Health, University of Melbourne, Melbourne, Australia. Department of Psychiatry, Melbourne Medical School, University of Melbourne, Melbourne, Australia. Biernacka Joanna M JM 0000-0001-9350-4440 Department of Psychiatry and Psychology, Mayo Clinic, Rochester, MN, USA. Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA. Bondolfi Guido G Department of Psychiatry, Geneva University Hospitals, Geneva, CH, Switzerland. Domschke Katharina K 0000-0002-2550-9132 Department of Psychiatry and Psychotherapy, Medical Center, University of Freiburg, Freiburg, Denmark. Kato Masaki M Department of Neuropsychiatry, Kansai Medical University, Osaka, Japan. Liu Yu-Li YL 0000-0001-7519-2965 Center for Neuropsychiatric Research, National Health Research Institutes, Miaoli, Taiwan. Serretti Alessandro A Department of Medicine and Surgery, Kore University of Enna, Enna, Italy. Tsai Shih-Jen SJ 0000-0002-9987-022X Department of Psychiatry, Taipei Veterans General Hospital, Taipei, Taiwan. Division of Psychiatry, School of Medicine, National Yang-Ming University, Taipei, Taiwan. Weinshilboum Richard R 0000-0002-4911-7985 Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, MN, USA. GSRD Consortium, the Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium McIntosh Andrew M AM 0000-0002-0198-4588 Division of Psychiatry, University of Edinburgh, Edinburgh, GB, UK. Lewis Cathryn M CM 0000-0002-8249-8476 Social, Genetic and Developmental Psychiatry Centre, King's College London, London, GB, UK. cathryn.Lewis@kcl.ac.uk. Department of Medical & Molecular Genetics, King's College London, London, GB, UK. cathryn.Lewis@kcl.ac.uk. eng Published Erratum 2024 08 31 United States Transl Psychiatry 101562664 2158-3188 IM Transl Psychiatry. 2024 Jul 19;14(1):296. doi: 10.1038/s41398-024-02981-1 39025838 2024 9 1 16 17 2024 9 1 16 16 2024 8 31 23 13 2024 8 31 epublish 39217139 PMC11366016 10.1038/s41398-024-03064-x 10.1038/s41398-024-03064-x trying2...
Publications by W Maier | LitMetric
Publications by authors named "W Maier"
The species complex (FLSC) currently comprises 11 phylogenetic species, including accepted names such as , , and , which have mostly been reported in association with citrus and coffee. Many varieties were documented by Wollenweber & Reinking (1935), which is indicative of a wider diversity of species within this group. The lack of type material in some cases, especially for the older names, means that definition by molecular phylogeny is very difficult.
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Human milk oligosaccharides are of high interest as active ingredients in infant formulas and dietary food supplements. Full characterization of members of this compound class is challenging due to the intrinsic complexity of byproducts during synthesis by fermentation. Moreover, when method validation is targeted for a regulated environment, a robust chromatographic separation of the highly polar oligosaccharides needs to be addressed, including isomers and compounds relevant for potential product adulteration.
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Am J Med Genet B Neuropsychiatr Genet
October 2024
Decisions about when to change antidepressant treatment are complex and benefit from accurate prediction of treatment outcome. Prognostic accuracy can be enhanced by incorporating repeated assessments of symptom severity collected during treatment. Participants (n = 714) from the Genome-Based Therapeutic Drugs for Depression study received escitalopram or nortriptyline over 12 weeks.
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J Urban Health
December 2024
While mobility in older age is of crucial importance for health and well-being, it is worth noting that currently, there is no German language framework for measuring walkability for older adults that also considers the functional status of a person. Therefore, we combined the results of an expert workshop, a literature review, and a Delphi consensus survey. Through this, we identified and rated indicators relevant for walkability for older adults, additionally focusing on their functional status.
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