Publications by authors named "Ana C Colabardini"

Article Synopsis
  • 53 isolates of Aspergillus section Nidulantes fungi were studied, revealing that 30 clinical isolates, including four from COVID-19 patients, were misidentified as the cryptic pathogen A. latus, which resulted from a hybridization event.
  • The research showed that A. latus displays significant genetic diversity and that both parental subgenomes are actively expressed in clinical isolates, responding to different environmental conditions.
  • Key differences in drug resistance and growth in oxidative stress were found between A. latus hybrids and related species, along with four features that could help in accurately identifying A. latus in the future.
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  • - Cryptic fungal pathogens are difficult to identify and manage because they closely resemble known pathogens but have distinct genetic traits and differences in their infection profiles.
  • - An investigation of 44 fungal isolates revealed that common identification methods often misidentify these pathogens, emphasizing the need for accurate diagnostics to improve epidemiological studies and treatment plans.
  • - The study highlighted significant genetic diversity within the pangenome and provided insights into the evolutionary origin of a specific hybrid pathogen, suggesting five new markers for species identification and enhancing understanding of these challenging pathogens.
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  • Aspergillus fumigatus is a dangerous fungal pathogen linked to around 100,000 deaths annually, and resistance to common antifungal treatments, like azoles, complicates effective treatment.
  • Caspofungin serves as a second-line therapy for severe infections, but can exhibit a paradoxical effect where higher doses lead to alternative growth patterns and greater resistance due to chitin replacing an essential component of the fungal cell wall.
  • Using genomewide association analysis and CRISPR/Cas9 techniques, researchers identified 48 genetic variants related to this paradoxical effect and demonstrated that certain gene deletions significantly affected growth rates and sensitivity to caspofungin.
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  • - Aspergillus fumigatus is the primary cause of aspergillosis, a serious fungal infection.
  • - The antifungal drug caspofungin (CSP) can treat this infection, but some strains show tolerance to it.
  • - The transcription factor FhdA plays a crucial role in regulating genes essential for mitochondrial function in response to CSP, revealing a new mechanism of interaction.
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  • In cystic fibrosis, mucus buildup in the lungs creates a low-oxygen environment that facilitates the growth of microorganisms, including the harmful bacteria Pseudomonas aeruginosa and the fungus Aspergillus fumigatus.
  • Despite P. aeruginosa’s ability to produce inhibitory compounds against A. fumigatus, the fungal response and metabolites in this competitive environment are not well understood.
  • The study identified multiple secondary metabolites produced by both organisms during biofilm formation under varying oxygen conditions, revealing complex interactions that influence their growth and persistence in cystic fibrosis patients.
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Cell responses against antifungals other than resistance have rarely been studied in filamentous fungi, while terms such as tolerance and persistence are well-described for bacteria and increasingly examined in yeast-like organisms. Aspergillus fumigatus is a filamentous fungal pathogen that causes a disease named aspergillosis, for which caspofungin (CAS), a fungistatic drug, is used as a second-line therapy. Some A.

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Aspergillus fumigatus causes a range of human and animal diseases collectively known as aspergillosis. A. fumigatus possesses and expresses a range of genetic determinants of virulence, which facilitate colonisation and disease progression, including the secretion of mycotoxins.

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Invasive Pulmonary Aspergillosis, which is caused by the filamentous fungus Aspergillus fumigatus, is a life-threatening infection for immunosuppressed patients. Chromatin structure regulation is important for genome stability maintenance and has the potential to drive genome rearrangements and affect virulence and pathogenesis of pathogens. Here, we performed the first A.

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Aspergillus fumigatus is the main causative agent of invasive pulmonary aspergillosis (IPA), a severe disease that affects immunosuppressed patients worldwide. The fungistatic drug caspofungin (CSP) is the second line of therapy against IPA but has increasingly been used against clinical strains that are resistant to azoles, the first line antifungal therapy. In high concentrations, CSP induces a tolerance phenotype with partial reestablishment of fungal growth called CSP paradoxical effect (CPE), resulting from a change in the composition of the cell wall.

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Article Synopsis
  • Aspergillus fumigatus is a major fungal pathogen that causes aspergillosis, which can become severe in immunocompromised individuals.
  • The treatment options for aspergillosis are limited, mainly relying on azole drugs, but resistance to these drugs is increasing, highlighting the need for new antifungal strategies.
  • By screening over 1,100 compounds, researchers found miltefosine as a potential antifungal, with a transcription factor called SmiA identified as crucial for the fungus’s response to the drug, affecting sphingolipid regulation.
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  • Invasive pulmonary aspergillosis is a serious fungal infection affecting mainly those with weakened immune systems, highlighting global concerns over antifungal resistance and limited treatment options.
  • Caspofungin, a second-line antifungal therapy, may not be effective due to resistance mechanisms, and understanding how fungi respond to it is crucial.
  • This study identifies ZnfA, a transcription factor that plays a significant role in fungal responses to calcium and caspofungin, bridging cellular responses to different stressors and enhancing our understanding of fungal biology.
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The fungal zinc finger transcription factor NsdC is named after, and is best known for, its essential role in sexual reproduction (ever in exual evelopment). In previous studies with , it was also shown to have roles in promotion of vegetative growth and suppression of asexual conidiation. In this study, the function of the homologue in the opportunistic human pathogen was investigated.

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Aspergillus fumigatus is an opportunistic fungal pathogen that secretes an array of immune-modulatory molecules, including secondary metabolites (SMs), which contribute to enhancing fungal fitness and growth within the mammalian host. Gliotoxin (GT) is a SM that interferes with the function and recruitment of innate immune cells, which are essential for eliminating A. fumigatus during invasive infections.

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is the leading cause of pulmonary fungal diseases. Azoles have been used for many years as the main antifungal agents to treat and prevent invasive aspergillosis. However, in the last 10 years there have been several reports of azole resistance in and new strategies are needed to combat invasive aspergillosis.

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Aspergillus fumigatus causes invasive aspergillosis, the most common life-threatening fungal disease of immuno-compromised humans. The treatment of disseminated infections with antifungal drugs, including echinocandin cell wall biosynthesis inhibitors, is increasingly challenging due to the rise of drug-resistant pathogens. The fungal calcium responsive calcineurin-CrzA pathway influences cell morphology, cell wall composition, virulence, and echinocandin resistance.

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Two novel GH3 family thermostable β-glucosidases from the filamentous fungus Chaetomium atrobrunneum (CEL3a and CEL3b) were expressed in Trichoderma reesei, purified by two-step ion exchange chromatography, and characterized. Both enzymes were active over a wide range of pH as compared to Neurospora crassa β-glucosidase GH3-3, which was also expressed in T. reesei and purified.

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In filamentous fungi, intracellular signaling pathways which are mediated by changing calcium levels and/or by activated protein kinase C (Pkc), control fungal adaptation to external stimuli. A rise in intracellular Ca2+ levels activates calcineurin subunit A (CnaA), which regulates cellular calcium homeostasis among other processes. Pkc is primarily involved in maintaining cell wall integrity (CWI) in response to different environmental stresses.

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Background: The production of bioethanol from lignocellulosic feedstocks will only become economically feasible when the majority of cellulosic and hemicellulosic biopolymers can be efficiently converted into bioethanol. The main component of cellulose is glucose, whereas hemicelluloses mainly consist of pentose sugars such as D-xylose and L-arabinose. The genomes of filamentous fungi such as A.

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To characterize the mechanisms involved in glucose transport, in the filamentous fungus Aspergillus nidulans, we have identified four glucose transporter encoding genes hxtB-E. We evaluated the ability of hxtB-E to functionally complement the Saccharomyces cerevisiae EBY.VW4000 strain that is unable to grow on glucose, fructose, mannose or galactose as single carbon source.

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  • Mitochondria play a vital role in providing energy and adapting to metabolic stress, with the ATM kinase in mammals acting as a key regulator of mitochondrial function.
  • In the fungus Aspergillus nidulans, the ATM homolog AtmA controls mitochondrial activity, glucose uptake, and cellular responses via the TOR pathway, impacting processes like autophagy and enzyme secretion during carbon starvation.
  • AtmA also influences a p53-like factor, XprG, to reduce cell death and protease secretion, highlighting the connection between mitochondrial stress, nutrient availability, and overall cell growth.
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After dephosphorylation by the phosphatase calcineurin, the fungal transcription factor CrzA enters the nucleus and activates the transcription of genes responsible for calcium homeostasis and many other calcium-regulated activities. A lack of CrzA confers calcium-sensitivity to the filamentous fungus Aspergillus nidulans. To further understand calcium signaling in filamentous fungi and to identify genes that interact genetically with CrzA, we selected for mutations that were able to suppress crzAΔ calcium intolerance and identified three genes.

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Endosymbiont-bearing trypanosomatids have been considered excellent models for the study of cell evolution because the host protozoan co-evolves with an intracellular bacterium in a mutualistic relationship. Such protozoa inhabit a single invertebrate host during their entire life cycle and exhibit special characteristics that group them in a particular phylogenetic cluster of the Trypanosomatidae family, thus classified as monoxenics. In an effort to better understand such symbiotic association, we used DNA pyrosequencing and a reference-guided assembly to generate reads that predicted 16,960 and 12,162 open reading frames (ORFs) in two symbiont-bearing trypanosomatids, Angomonas deanei (previously named as Crithidia deanei) and Strigomonas culicis (first known as Blastocrithidia culicis), respectively.

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The serum- and glucocorticoid-regulated protein kinase (SGK) is an AGC kinase involved in signal cascades regulated by glucocorticoid hormones and serum in mammals. The Saccharomyces cerevisiae ypk1 and ypk2 genes were identified as SGK homologues and Ypk1 was shown to regulate the balance of sphingolipids between the inner and outer plasma membrane. This investigation characterized the Aspergillus nidulans YPK1 homologue, YpkA, representing the first filamentous fungal YPK1 homologue.

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The filamentous fungus Aspergillus nidulans has been used as a fungal model system to study the regulation of xylanase production. These genes are activated at transcriptional level by the master regulator the transcriptional factor XlnR and repressed by carbon catabolite repression (CCR) mediated by the wide-domain repressor CreA. Here, we screened a collection of 42 A.

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Article Synopsis
  • The calC2 mutation in the protein kinase C gene pkcA in Aspergillus nidulans increases tolerance to farnesol (FOH), which typically inhibits cell growth and induces cell death.
  • Overexpressing pkcA during FOH exposure leads to enhanced cell death and activates markers for endoplasmic reticulum (ER) stress and the unfolded protein response (UPR), indicating a significant interaction between PkcA and UPR pathways.
  • The study also finds that pkcA overexpression raises mRNA levels and metacaspase activity, and involves a genetic link between PkcA and the caspase-like protein CasA, with MAP kinases playing a role in the signaling processes
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