As one of the main pathogens of periodontitis, often forms mixed biofilms with other bacteria or fungi under the gingiva, such as . Heme is an important iron source for and that supports their growth in the host. From the perspective of heme competition, this study aims to clarify that the competition for heme enhances the pathogenic potential of during the interaction between and . single-species biofilm and - dual-species biofilm were established in a low- and high-heme environment. The results showed that the vitality of was increased in the dual-species biofilm under the condition of low heme, and the same trend was observed under a laser confocal microscope. Furthermore, the morphological changes in were observed by electron microscope, and the resistance of in dual-species biofilm was stronger against the killing effect of healthy human serum and antibiotics. The ability of to agglutinate erythrocyte was also enhanced in dual-species biofilm. These changes disappeared when heme was sufficient, which confirmed that heme competition was the cause of thepathogenicy change in . Gene level analysis showed that was in a superior position in the competition relationship by increasing the expression of heme utilization-related genes, such as HmuY, HmuR, HusA, and Tlr. In addition, the expression of genes encoding gingipains (Kgp, RgpA/B) was also significantly increased. They not only participate in the process of utilizing heme, but also are important components of the virulence factors of . In conclusion, our results indicated that the pathogenic potential of was enhanced by through heme competition, which ultimately promoted the occurrence and development of periodontitis and, therefore, subgingival colonization should be considered as a factor in assessing the risk of periodontitis.
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http://dx.doi.org/10.3389/fmicb.2020.596459 | DOI Listing |
bioRxiv
December 2024
Department of Pharmacology and Toxicology, Michigan State University, East Lansing, MI, United States.
Pirin is a non-heme iron binding protein with a variety of proposed functions including serving as a co-activator of p65 NFκB and quercetinase activity. We report here, failure to confirm pirin's primary proposed mechanism, binding of Fe(III)-pirin and p65. Analytical size exclusion chromatography (SEC) and fluorescence polarization (FP) studies did not detect an interaction.
View Article and Find Full Text PDFChemistry
October 2024
Department of Chemistry and Chemical Biology, Stevens Institute of Technology, 1 Castle Point Terrace, Hoboken, NJ 07030, United States.
Some pathogens use heme-containing nitric oxide reductases (NORs) to reduce NO to NO as their defense mechanism to detoxify NO and reduce nitrosative stress. This reduction is also significant in the global N cycle. Our previous experimental work showed that Fe and Co porphyrin NO complexes can couple with external NO to form NO when activated by the Lewis acid BF.
View Article and Find Full Text PDFSAR QSAR Environ Res
October 2024
Department of Gynecology and Obstetrics, the Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Dithiocarbamate fungicides have been widely used in agricultural practices due to their effective control of fungal diseases, thereby contributing to global food security and agricultural productivity. In this study, the inhibitory potency of eight compounds on human and rat aromatase (CYP19A1) activity was evaluated. The results revealed that zineb exhibited the highest inhibitory potency on human CYP19A1 (IC, 2.
View Article and Find Full Text PDFPLoS Pathog
October 2024
Laboratory of Tropical Diseases-Prof. Dr. Luiz Jacintho da Silva, Department of Genetics, Evolution, Microbiology and Immunology, University of Campinas-UNICAMP, Campinas, São Paulo, Brazil.
Artemisinin-based combination therapy (ACT) is the mainstay of effective treatment of Plasmodium falciparum malaria. However, the long-term utility of ACTs is imperiled by widespread partial artemisinin resistance in Southeast Asia and its recent emergence in parts of East Africa. This underscores the need to identify chemotypes with new modes of action (MoAs) to circumvent resistance to ACTs.
View Article and Find Full Text PDFBiochim Biophys Acta Proteins Proteom
January 2025
Department of Chemistry, North Carolina State University, Raleigh, NC 27695, United States of America. Electronic address:
At least two of the six methionine (Met) residues in dehaloperoxidase (DHP) are shown to act as electron donors in both autoreduction and protein-heme crosslinking. Autoreduction observed in the two isozymes, DHP-A and DHP-B, is explained by the high heme reduction potential and an endogenous source of electrons from methionine (Met) or cysteine (Cys). This study provides evidence of a connection to protein-heme crosslinking that occurs when DHP is activated by HO in competition with substrate oxidation and autoreduction.
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