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Hans, J.

Publications and source records attributed to Hans, J..

2 recordsLinked to original sources

Spiders as natural DNA samplers recover arthropod community diversity and biotic interactions across space and time

Global arthropod decline demands effective biodiversity monitoring strategies. However, most current monitoring approaches do not provide an exhaustive picture of arthropod community structure. In particular, biotic interactions and temporal patterns of biodiversity change are still poorly understood. Here we explore the possibility of addressing these two shortfalls using spiders, one of the most important predators of terrestrial arthropods, as natural samplers for arthropod community DNA. We conducted several experiments comparing the recovered community composition between spider gut contents and traditional monitoring methods. Additionally, we used archived spiders from long-term collections to assess the preservation of prey DNA over time. Spiders proved to be highly efficient natural DNA samplers, with gut content metabarcoding revealing similar community composition and alpha- and beta-diversity like traditional methods. Unique arthropod taxa were detected by spider gut contents and traditional methods respectively, indicating that these two approaches can serve as valuable complements to each other. Well-preserved archived spiders effectively reconstructed historical diets up to 20 years back in time, showing that historical spider collections can act as time capsules of the wider diversity that occurred in the spider's habitat. Spiders as natural samplers overcome critical shortfalls in biodiversity monitoring and contribute to our future understanding of community assembly across space and time.

ecology↗

Agonists of orally expressed TRP channels stimulate salivary secretion and modify the salivary proteome

Natural compounds that can stimulate salivary secretion are of interest in developing treatments for xerostomia, the perception of a dry mouth, that affects between 10 and 30% of the adult and elderly population. Chemesthetic transient receptor potential (TRP) channels are expressed in the surface of the oral mucosa. The TRPV1 agonists capsaicin and piperine have been shown to increase salivary flow when introduced into the oral cavity but the sialogogic properties of other TRP channel agonists have not been investigated. In this study we have determined the influence of different TRP channel agonists on the flow and protein composition of saliva.Mouth rinsing with the TRPV1 agonist nonivamide or menthol, a TRPM8 agonist, increased whole mouth saliva (WMS) flow and total protein secretion compared to unstimulated saliva, the vehicle control mouth rinse or cinnamaldehyde, a TRPA1 agonist. Nonivamide also increased the flow of labial minor gland saliva but parotid saliva flow rate was not increased. The influence of TRP channel agonists on the composition and function of the salivary proteome was investigated using a multi-batch quantitative mass spectrometry method novel to salivary proteomics. Inter-personal and inter-mouth rinse variation was observed in the secreted proteomes and, using a novel bioinformatics method, inter-day variation was identified with some of the mouth rinses. Significant changes in specific salivary proteins were identified after all mouth rinses. In the case of nonivamide, these changes were attributed to functional shifts in the WMS secreted, primarily the over representation of salivary and non-salivary cystatins which was confirmed by immunoassay.This study provides new evidence of the impact of TRP channel agonists on the salivary proteome and the stimulation of salivary secretion by a TRPM8 channel agonist, which suggests that TRP channel agonists are potential candidates for developing treatments for sufferers of xerostomia.AbbreviationsCARD10CAspase Recruitment Domain-containing protein 10DTTDiThioThreitolLC-MS/MSLiquid Chromatography - tandem Mass SpectrometryGOGene OntologyIEFIsoElectric FocusingLDSLithium Dodecyl SulphateMSMass SpectrometryPGPropylene GlycolPGK1PhosphoGlycerate Kinase 1TCEPTris (2-CarboxyEthyl) PhosphineTEABTriEthylAmmonium BicarbonateTMTTandem Mass TagTRPTransient Receptor PotentialTRPA1Transient Receptor Potential cation channel, subfamily A, member 1TRPM8Transient Receptor Potential cation channel subfamily M member 8TRPV1Transient Receptor Potential cation channel subfamily V member 1WMSWhole Mouth SalivaUWMSUnstimulated Whole Mouth SalivaView Full Text

physiology↗