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Burns, P.

Publications and source records attributed to Burns, P..

7 recordsLinked to original sources

Alterations in phototransduction timing, dark adaptation and GNAT1 trafficking in GNAT1-edited Xenopus laevis.

GNAT1 (also called -transducin) is the -subunit of a heterotrimeric G-protein present in rod photoreceptors that plays a critical role in phototransduction. Photoactivated rhodopsin binds GNAT1, which stimulates phosphodiesterase to hydrolyze cGMP, closing ion channels and hyperpolarizing the rod cell. To examine the effects of GNAT1 ablation on light-induced autophagy and light-exacerbated retinal degeneration, we previously generated genetically chimeric, GNAT1-edited Xenopus laevis using CRISPR technology. Here, we interbred these F0 animals to produce F1 animals with defined genotypes, including full knockouts, and characterized the F1 generation by Western blot, histology, and electroretinography (ERG). In X. laevis tadpoles with nonsense mutations in all four GNAT1 alleles, the GNAT1 protein was absent, and the scotopic ERG was absent, indicating full knockout. In animals with reduced GNAT1 expression, we observed increased A- and B-wave implicit times. Greater GNAT1 protein reduction was associated with greater ERG delay, demonstrating a role for GNAT1 in the timing of phototransduction. We also identified two unexpected phenotypes linked to distinct gene edits. The Q184L-GNAT1.L mutation conferred an ERG phenotype similar to that of a full knockout, but with minimal reduction in GNAT1 protein levels, consistent with loss of function. This mutation is also present in the human population. A three-base-pair deletion (T183,Q184[->]K183) in GNAT1.S caused dominantly inherited diminished ERG response and defective dark adaptation, and was associated with photoreceptor structural abnormalities and GNAT1 accumulation at the connecting cilium, consistent with a dominant-negative effect on GNAT1 trafficking.

neuroscience↗

Coordination-dynamics invariants from simultaneous vagus nerve electroneurogram and ECG: a Python pipeline applied to neonatal piglet endotoxaemia

HRV complexity metrics track the systemic cytokine response across mammalian inflammation models, but the dynamical mechanism translating molecular inflammation into HRV structure has remained unresolved, and no existing tool jointly extracts coordination-dynamics signatures from simultaneous vagus nerve electroneurogram (VENG) and ECG. We describe a modular open-source Python pipeline that (i) detects spectrally distinct latent states in 20 kHz whole-trunk VENG using a symmetric-Kullback-Leibler scan-statistic changepoint detector ported from earthquake seismology and verified against its R progenitor; (ii) places the inter-changepoint-interval series in the Haken-Kelso-Bunz coupled-oscillator framework, computes the Kuramoto order parameter R, fits the bistable potential V({varphi}) = -a cos{varphi} - b cos 2{varphi}, and maps each timepoint into the Arnold-tongue ({Omega}, K) plane; contrasts compound-action-potential band power between successive latent states; and (iii) couples the VENG analysis to a CIMVA HRV pipeline driven by a 5-algorithm Pro-MAC R-peak ensemble. Applied to a previously published two-animal neonatal piglet endotoxaemia cohort (Castel et al., 2020, 2024), the pipeline recovers known features of the (iv) preparation and surfaces three case-series observations that we frame as hypotheses for prospective replication: (1) a 6-8 s VENG state-switching period coincident with the HRV LF/HF spectral boundary; (2) qualitatively divergent coordination-dynamics trajectories under LPS versus LPS + VNS (Kuramoto R collapses from 0.69 to 0.12 without VNS, undergoes biphasic recovery to 0.99 with VNS, the two trajectories crossing at 60-75 min); (3) a regime-dependent empirical coupling between R and the HRV embedding scaling exponent eScalE (R {middle dot} eScalE {approx} 0.33 during moderate challenge, doubling to {approx}0.80 during VNS overshoot). Pre-specified null comparisons (Poisson and bootstrap surrogates) demonstrate that R and the critical-slowing-down indicators carry information beyond their most obvious null alternatives. With N = 2 animals no inferential statistics are possible, so these findings are reported as hypothesis-generating; the manuscript closes with a pre-registered prospective protocol designed specifically to falsify them. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=145 SRC="FIGDIR/small/728499v1_ufig1.gif" ALT="Figure 1"> View larger version (42K): org.highwire.dtl.DTLVardef@5ad100org.highwire.dtl.DTLVardef@4f6bb2org.highwire.dtl.DTLVardef@27a58aorg.highwire.dtl.DTLVardef@e52e15_HPS_FORMAT_FIGEXP M_FIG C_FIG Key PointsO_LIWe present an open-source Python pipeline that extracts coordination-dynamics invariants (Kuramoto phase coherence, Haken-Kelso-Bunz potential parameters, Arnold-tongue position, critical-slowing-down indicators) from simultaneously recorded vagus nerve electroneurogram (VENG) and ECG, starting from a spectral-KL scan-statistic changepoint detector ported from earthquake seismology. C_LIO_LIApplied to a previously published two-animal cohort (Castel et al., 2024), the pipeline reveals that VENG alternates between two spectrally distinct latent states at a baseline period of 6-8 s that coincides with the HRV low-frequency/high-frequency spectral boundary ([~]0.15 Hz). We propose the VENG latent-state oscillator as a candidate mechanistic generator of vagal LF HRV; this is a hypothesis motivated by the timescale match and is not established by the present data. C_LIO_LIIn this cohort, LPS endotoxaemia and vagus nerve stimulation drove qualitatively divergent trajectories in the coordination-dynamics phase space (Kuramoto R: 0.69 [->] 0.12 without VNS; biphasic to R [->] 0.99 with VNS at the IL-6/IL-8 cytokine peak). Because the design provides one animal per arm, these are case-series observations and not a between-arm statistical comparison. C_LIO_LIInter-changepoint-interval variance rose >100-fold roughly 15 min before overt state-switching collapse in the unmitigated animal. Bootstrap nulls drawn from the same animals pre-collapse ICI pool reject the same-distribution alternative ([§]2.6), motivating a critical-slowing-down early-warning hypothesis that requires prospective replication before any clinical use is warranted. C_LIO_LIThe pipeline surfaces a regime-dependent empirical coupling between VENG phase coherence (R) and HRV embedding scaling exponent (eScalE) in the VNS-treated animal: during moderate challenge R {middle dot} eScalE {approx} 0.33 (CV {approx} 0.20), during VNS-enhanced overshoot (45, 90, 105 min) the product doubles to {approx}0.80. The product is a post-hoc empirical construct, not a derived conservation law; we propose it as a falsification target for prospective cohorts ([§]6). C_LI

physiology↗

RPE65 knockout Xenopus laevis have a compromised but detectable electroretinogram and altered visual responses, without retinal degeneration or altered melanophore dispersion

The isomerohydrolase RPE65 is a critical element of the visual cycle, the series of enzymatic reactions by which the chromophore of the visual pigments is regenerated following light exposure. In humans, mutations in the rpe65 gene cause a severe form of blindness called Lebers congenital amaurosis. Studies of RPE65-/- mice have shown dramatic depletion of 11- cis-retinal in the retina, resulting in a slow retinal degeneration. However, a number of studies suggest that RPE65 may not be necessary for the regeneration of photopigment in all photoreceptor types. Using CRISPR/Cas9 technology, we previously generated RPE65 knockout Xenopus laevis in order to test the involvement of rhodopsin chromophore in the cell death mechanisms associated with rhodopsin mutations and rhodopsin quality control. Here we further characterize the effects of RPE65 knockout in these animals, and show their rod photoreceptors have shortened outer segments that lack detectable rhodopsin photopigment. However, there is no progressive degeneration of rods or cones. Via electroretinography we found greatly reduced but significant responses to light under scotopic and photopic conditions. We also found reduced behavioral sensitivity to light, while light-induced melanophore dispersion was unaffected. RPE65 knockout X. laevis may be a useful system for examining RPE65-independent photosensation mechanisms in vertebrates.

cell biology↗

Using a multiscale lidar approach to determine variation in canopy structure from African forest elephant trails.

Recently classified as a unique species by the IUCN, African forest elephants (Loxodonta cyclotis) are critically endangered due to severe poaching. With limited knowledge about their ecological role due to the dense tropical forests they inhabit in central Africa, it is unclear how the Afrotropics would change if forest elephants were to go extinct. Although their role as seed dispersers is well known, they may also drive large-scale processes that determine forest structure, through the creation of elephant trails and browsing the understory and allowing larger, carbon-dense trees to succeed. Multiple scales of lidar were collected by NASA in Lope National Park, Gabon from 2015-2022. Utilizing two airborne lidar datasets and one spaceborne lidar in an African forest elephant stronghold, detailed canopy structural information was used in conjunction with elephant trail data to determine how forest structure varies on and off trails. Forest above elephant trails displayed different structural characteristics than forested areas off trails, with lower canopy height, canopy cover, and different vertical distribution of plant mass. Less plant area density was found on trails at 1 m in height, while more vegetation was found at 12 m, compared to off trail locations. Trails with previous logging history had lower plant area in the top of the canopy.

ecology↗

Accurate simultaneous sequencing of genetic and epigenetic bases in DNA

DNA comprises molecular information stored via genetic bases (G, C, T, A) and also epigenetic bases, principally 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC). Both genetic and epigenetic information are vital to our understanding of biology and disease states. Most DNA sequencing approaches address either genetics or epigenetics and thus capture incomplete information. Methods widely used to detect epigenetic DNA bases typically fail to capture common C-to-T mutations or distinguish 5mC from 5hmC. Here, we present a single-base-resolution sequencing methodology that will simultaneously sequence complete genetics and complete epigenetics in a single workflow. The approach is non-destructive to DNA and provides a digital readout of bases, which we exemplify by simultaneous sequencing of G, C, T, A, 5mC and 5hmC; 6-Letter sequencing. We demonstrate sequencing of human genomic DNA and also cell-free DNA taken from a blood sample of a cancer patient. The approach is accurate, requires low DNA input and has a simple workflow and analysis pipeline. We envisage it will be versatile across many applications in life sciences.

genomics↗

Factors determining success of the chronically instrumented unanesthetized fetal sheep model of human development: a retrospective cohort study

AimChronically instrumented non-anesthetized fetal sheep (CINAFS) have been the mainstay model of human fetal development for 60 years. As a large "two for one" animal model, with instrumentation of the ewe and her fetus, the model poses challenges to implement de novo and to maintain overtime at the highest standards of operating procedures to ensure its ongoing performance. A common, yet conventionally underreported issue researchers face is the rate of animal loss. Here, we investigate what determines the success of the pregnant sheep model. MethodsWe conducted a retrospective cohort study consisting of 82 experiments spanning the course of six years. Our team identified ten variables that we anticipated were likely to influence the experimental outcome, such as the time of year, animal size, and surgical complexity. ResultsThe single variable identified in this study as determining the successful outcome of the experiments is the experience level of the team. ConclusionThe CINAFS model offers enormous potential to further our understanding of human fetal development and to create interventional technologies. However, to improve the outcomes of CINAFS models, improved communication and training are needed. We discuss the implications of our findings for the successful implementation of this challenging yet scientifically advantageous animal model of human physiology. Key pointsO_LIThe fetal sheep model closely mirrors the physiology of human fetal development C_LIO_LIIn addition to its high translational potential, this model is known to have some generally not reported rate of experimental failure C_LIO_LIWe show that factors such as animal characteristics & surgical complexity do not influence the experimental outcomes C_LIO_LIInstead, the key factor in model experimental success is the level of the research teams experience C_LIO_LIThe key factors to improve the animal model outcomes are an intra- and inter-team communication C_LI

physiology↗

α7 nicotinic acetylcholine receptor signalling modulates the inflammatory and iron homeostasis in fetal brain microglia

Neuroinflammation in utero may result in life-long neurological disabilities. Microglia play a pivotal role, but the mechanisms are poorly understood. No early postnatal treatment strategies exist to enhance neuroprotective potential of microglia. We hypothesized that agonism on 7 nicotinic acetylcholine receptor (7nAChR) in fetal microglia will augment their neuroprotective transcriptome profile, while the antagonistic stimulation of 7nAChR will achieve the opposite. Using an in vivo - in vitro model of developmental programming of neuroinflammation induced by lipopolysaccharide (LPS), we validated this hypothesis in primary fetal sheep microglia cultures re-exposed to LPS in presence of a selective 7nAChR agonist or antagonist. Our RNAseq and protein level findings show that a pro-inflammatory microglial phenotype acquired in vitro by LPS stimulation is reversed with 7nAChR agonistic stimulation. Conversely, antagonistic 7nAChR stimulation potentiates the pro-inflammatory microglial phenotype. Surprisingly, under conditions of LPS double-hit an interference of a postulated 7nAChR - ferroportin signaling pathway may impede this mechanism. These results suggest a therapeutic potential of 7nAChR agonists in early re-programming of microglia in neonates exposed to in utero inflammation via an endogenous cerebral cholinergic anti-inflammatory pathway. Future studies will assess the role of interactions between inflammation-triggered microglial iron sequestering and 7nAChR signaling in neurodevelopment.

neuroscience↗