bioRxiv Science⌕ Search

Biology subjects

Ryan, J. L.

Publications and source records attributed to Ryan, J. L..

2 recordsLinked to original sources

Mechanisms of carbon dioxide detection in the earthworm Dendrobaena veneta.

Carbon dioxide (CO2) is a critical biological signal that is noxious to many animals at high concentrations. The earthworm Dendrobaena veneta lives in subterranean burrows containing high levels of CO2 and respires through its skin. Despite the ecological and agricultural importance of earthworms, relatively little is known about how they make decisions in their environment, including their response to elevated levels of CO2. To examine CO2 detection in this species, we designed the exudate assay, in which we placed an earthworm in a sealed container, exposed it to varying concentrations of CO2 for one minute, and recorded the amount of exudate secreted. Because earthworms excrete exudate in response to noxious stimuli, we hypothesized that the amount of exudate produced was proportional to the amount of irritation. We repeated these experiments after treatment with several blockers for molecules with potential involvement in CO2 detection, including carbonic anhydrases, guanylate cyclase, TRPA1, ASICs, and OTOP channels. We also confirmed the presence of homologous transcripts for each of these gene families in an epithelial transcriptome for D. veneta. Additionally, since organisms often detect CO2 levels indirectly by monitoring the conversion to carbonic acid (a weak acid), we used the exudate assay to evaluate aversion to additional weak acids (formic acid, acetic acid, and propionic acid). Earthworms excreted significantly more exudate in response to CO2 in a dosage-dependent manner, and this response was muted by the general carbonic anhydrase inhibitor acetazolamide, the carbonic anhydrase IX/XII inhibitor indisulam, the calcium channel blocker ruthenium red, the sodium channel blocker amiloride, and the acid-sensing ion channel blocker diminazene aceturate. These data provide evidence of the role of carbonic anhydrase and epithelial sodium channels in earthworm CO2 detection, establish that, similar to other subterranean-dwelling animals, earthworms are extremely tolerant of CO2, and contribute to our understanding of the mechanisms used by earthworms to detect and react to weak acids in their environment. Contribution to the field statementCarbon dioxide (CO2) is a major byproduct of cellular respiration and an important biological signal. The metabolism of animals living underground in burrows can cause the concentration of CO2 to increase above atmospheric CO2. Most animals have multiple molecular mechanisms that detect CO2 and find high concentrations aversive or noxious; some subterranean animals have adaptations that make them more tolerant of concentrated CO2. Earthworms live in burrows, are a keystone species for subterranean ecosystems, and in their lightless environment must rely primarily on tactile and chemical signals. Despite the profound importance of earthworms, few if any of the molecular mechanisms they use to detect these signals have been characterized. Here we use RNA sequencing to develop a list of candidate mechanisms that the European nightcrawler may use to respond to CO2. We also have developed an assay for comparing how noxious different concentrations of volatile compounds are to earthworms. In the present study, we utilize that assay with inhibitors to further narrow the possible multiple molecular mechanisms responsible for the detection of CO2. We suspect that our study is among the first attempts to combine RNA-sequencing technology and pharmacology to describe earthworm sensory biology.

physiology↗

Genetic mapping in Diversity Outbred mice identifies a Trpa1 variant influencing late phase formalin response

Identification of genetic variants that influence susceptibility to chronic pain is key to identifying molecular mechanisms and targets for effective and safe therapeutic alternatives to opioids. To identify genes and variants associated with chronic pain, we measured late phase response to formalin injection in 275 male and female Diversity Outbred (DO) mice genotyped for over 70 thousand SNPs. One quantitative trait locus (QTL) reached genome-wide significance on chromosome 1 with a support interval of 3.1 Mb. This locus, Nociq4 (nociceptive sensitivity inflammatory QTL 4; MGI:5661503), harbors the well-known pain gene Trpa1 (transient receptor potential cation channel, subfamily A, member 1). Trpa1 is a cation channel known to play an important role in acute and chronic pain in both humans and mice. Analysis of DO founder strain allele effects revealed a significant effect of the CAST/EiJ allele at Trpa1, with CAST/EiJ carrier mice showing an early, but not late, response to formalin relative to carriers of the seven other inbred founder alleles (A/J, C57BL/6J, 129S1/SvImJ, NOD/ShiLtJ, NZO/HlLtJ, PWK/PhJ, and WSB/EiJ). We characterized possible functional consequences of sequence variants in Trpa1 by assessing channel conductance, Trpa1/Trpv1 interactions, and isoform expression. The phenotypic differences observed in CAST/EiJ relative to C57BL/6J carriers were best explained by Trpa1 isoform expression differences, implicating a splice junction variant as the causal functional variant. This study demonstrates the utility of advanced, high-precision genetic mapping populations in resolving specific molecular mechanisms of variation in pain sensitivity.

bioinformatics↗