Toxin synergism is a complex biochemical phenomenon, where different animal venom proteins interact either directly or indirectly to potentiate toxicity to a level that is above the sum of the toxicities of the individual toxins. This provides the animals possessing venoms with synergistically enhanced toxicity with a metabolic advantage, since less venom is needed to inflict potent toxic effects in prey and predators. Among the toxins that are known for interacting synergistically are cytotoxins from snake venoms, phospholipases A from snake and bee venoms, and melittin from bee venom. These toxins may derive a synergistically enhanced toxicity formation of toxin complexes by hetero-oligomerization. Using a human keratinocyte assay mimicking human epidermis , we demonstrate and quantify the level of synergistically enhanced toxicity for 12 cytotoxin/melittin-PLA combinations using toxins from elapids, vipers, and bees. Moreover, by utilizing an interaction-based assay and by including a wealth of information obtained a thorough literature review, we speculate and propose a mechanistic model for how toxin synergism in relation to cytotoxicity may be mediated by cytotoxin/melittin and PLA complex formation.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7221120PMC
http://dx.doi.org/10.3389/fphar.2020.00611DOI Listing

Publication Analysis

Top Keywords

toxin synergism
12
synergistically enhanced
12
enhanced toxicity
12
unity strength
4
strength exploring
4
exploring intraspecies
4
intraspecies interspecies
4
toxin
4
interspecies toxin
4
synergism phospholipases
4

Similar Publications

The increasing use of products for medicinal, dietary, and recreational purposes has raised concerns about mycotoxin contamination in cannabis and hemp. Mycotoxins persist in these products' post-processing, posing health risks via multiple exposure routes. This study investigated cytotoxic and genotoxic interactions between cannabidiol (CBD) and the mycotoxin citrinin (CIT) using human cell models: SH-SY5Y, HepG2, HEK293, and peripheral blood lymphocytes.

View Article and Find Full Text PDF
Article Synopsis
  • Vitamin D (VD) plays a key role in bone health and immune function and may help protect against chronic inflammatory diseases.
  • The study involved treating THP-1 cells with VD and a chickpea protein hydrolysate (H30BIO) to assess their effects on inflammation and cytokine production.
  • Results showed that while VD alone reduced pro-inflammatory gene expression and cytokine levels, combining VD with H30BIO enhanced certain gene expressions, indicating a potential synergistic effect in modulating inflammation.
View Article and Find Full Text PDF
Article Synopsis
  • Research indicates that SARS-CoV-2 infection can increase the risk of developing parkinsonian symptoms when combined with the mitochondrial toxin MPTP, particularly in genetically modified mice expressing human ACE2 receptors.
  • The study found that while both mRNA and protein-based vaccines can mitigate neurodegeneration in wild-type (WT) mice, only the protein-based vaccine was effective in protecting G2019S LRRK2 mutant mice from SARS-CoV-2 related neurological damage.
  • Overall, the findings emphasize how environmental toxins and genetic predisposition contribute to the development of neurological diseases after viral infections, as well as the potential protective effects of vaccines.
View Article and Find Full Text PDF

Background: Different approaches have been adopted to manage Spodoptera frugiperda resistance to Bt toxins. However, studying the synergism among these practices applied directly in crop fields is a major challenge. We used a computational model to investigate how the proportion of refuge strips [crop area occupied by non-Bt corn (maize): 5%, 10%, 15%, or 20%] and the presence of naturally occurring parasitoid, affected or not by a pesticide with different selectivities applied in the field, could influence the dynamics of the resistance allele (R) in a S.

View Article and Find Full Text PDF

Background: Literature and data mining found abnormal induction of chemokine (C-X-C motif) ligand 1 (CXCL1) and CXCL8 and down-regulation of CXCL2 in inflammatory liver diseases. This study was performed to understand the glucocorticoid receptor's (GR's) effects on chemokine and acute-phase protein expression in human liver, in settings of bacterial infection (modeled using LPS) or inflammation (modeled using TNF).

Methods: Primary human hepatocytes (PHH) were treated with combinations of tumor necrosis factor alpha (TNF), lipopolysaccharide (LPS), and dexamethasone (DEX) for 24 h, following which chemokine mRNA and protein expression were analyzed using qPCR and enzyme-linked immunosorbent assay assays.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!