Fungal infections can cause different diseases, and nucleic acid extraction is a crucial step in assisting the diagnosis of fungal infections. Traditional methods and current commercial fungal nucleic acid extraction kits are often time-consuming and involve hazardous chemicals. We developed a nucleic acid extraction kit that is safe, rapid, and efficient, designated as FNA-REK (Fungal Nucleic Acid Extraction Kit), which facilitates the simultaneous extraction of DNA and RNA without the necessity for hazardous chemicals, liquid nitrogen, or glass beads. This kit is user-friendly and achieves complete extraction within a mere 10 min. The RNA from the culture of Cryptococcus neoformans, Candida albicans, Candida krusei, Aspergillus flavus, Aspergillus niger and Aspergillus fumigatus. Meanwhile, the RNA from Candida albicans, Candida glabrata and Candida tropicalis of mid-stream urine, vaginal discharge and sputum samples, respectively, Cryptococcus neoformans, genus Aspergillus and Pneumocystis jirovecii of sputum samples, genus Aspergillus of bronchoscopy rinsing fluid were extracted using both the FNA-REK and the BIO-TEK. The concentration and purity of the extracted RNA were measured by nanodrop photometer. The nucleic acid extracted from Cryptococcus neoformans and Candida albicans using FNA-REK showed higher concentration and purity compared to BIO-TEK following a 10 dilution. The maximum coefficients of variation for intra-run and inter-run replicates were 2.26% and 8.44%, respectively, significantly lower than 10%, indicating the high reproducibility of the FNA-REK. The FNA-REK yielded a lower cycle threshold (Ct value) than the BIO-TEK for cultured Candida krusei, Aspergillus niger and Aspergillus fumigatus obtained from clinical laboratory. Also, FNA-REK performed better than BIO-TEK for Candida albicans, Candida glabrata, Candida tropicalis, and genus Aspergillus in sputum samples from patients with severe pneumonia. The FNA-REK is a sensitive and stable nucleic acid extraction kit, offering an economical, efficient, and environmentally sustainable approach for fungal nucleic acid extraction. Its high extraction efficiency provides significant technical support for both laboratory and clinical applications, positioning it as a strong contender to become the most convenient and fastest fungal nucleic acid extraction kit currently available on the market.
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http://dx.doi.org/10.1007/s00203-025-04273-8 | DOI Listing |
It is known that inhibition of the endoplasmic reticulum transmembrane signaling protein (ERN1) suppresses the glioblastoma cells proliferation. The present study aims to investigate the impact of inhibition of ERN1 endoribonuclease and protein kinase activities on the , , and gene expression in U87MG glioblastoma cells with an intent to reveal the role of ERN1 signaling in the regulation of expression of these genes. The U87MG glioblastoma cells with inhibited ERN1 endoribonuclease (dnrERN1) or both enzymatic activities of ERN1 (endoribonuclease and protein kinase; dnERN1) were used.
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Center for Inflammation, Immunity and Infection, Institute for Biomedical Sciences, Georgia State University, Atlanta, GA, United States.
Current influenza vaccines are not effective in conferring protection against antigenic variants and pandemics. To improve cross-protection of influenza vaccination, we developed a 5xM2e messenger RNA (mRNA) vaccine encoding the tandem repeat conserved ectodomain (M2e) of ion channel protein M2 derived from human, swine, and avian influenza A viruses. The lipid nanoparticle (LNP)-encapsulated 5xM2e mRNA vaccine was immunogenic, eliciting high levels of M2e-specific IgG antibodies, IFN-γ+ T cells, T follicular helper cells, germinal center phenotypic B cells, and plasma cells.
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Department for Integrative Evolutionary Biology, Max Planck Institute for Biology Tübingen, Max-Planck Ring 9, Tübingen, 72076, Germany.
Environmental influences on traits and associated transgenerational epigenetic inheritance have widespread implications but remain controversial and underlying mechanisms poorly understood. We introduce long-term environmental induction experiments on alternative diets in , a nematode exhibiting mouth-form plasticity including predation, by propagating 110 isogenic lines for 101 generations with associated food-reversal experiments. We found dietary induction and subsequent transgenerational inheritance of the predatory morph and identified a role of ubiquitin ligase EBAX-1/ZSWIM8 in this process.
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The RNA Institute, University at Albany, State University of New York, Albany, NY 12222, USA.
DNA nanostructures are typically assembled by thermal annealing in buffers containing magnesium. We demonstrate the assembly of DNA nanostructures at constant temperatures ranging from 4° to 50°C in solutions containing different counterions. The choice of counterions and the assembly temperature influence the isothermal assembly of several DNA motifs and designed three-dimensional DNA crystals.
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