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Walsh, L.

Publications and source records attributed to Walsh, L..

6 recordsLinked to original sources

Conservation of a lateralized visuo-motor axis in hawkmoth proboscis probing

Lateralization of behaviour, including motor control and sensory processing, is widespread across bilaterians. In visually guided tasks it often manifests as an axis aligning eye, appendage, and a target within a shared reference frame, such as eye-hand coordination in humans or eye-beak coordination in birds. While studied intensively in a few vertebrate systems, whether similar control principles apply to invertebrates, and more generally, how sensory and motor lateralization are linked mechanistically, remains unclear. Using the proboscis inspection behaviour of hummingbird hawkmoth Macroglossum stellatarum as a model for visual appendage guidance, our study provides evidence for lateralized visuo-motor control in an invertebrate. Combining high-speed videography and markerless pose estimation, we establish the underlying control axis between the hawkmoths unpaired appendage and its eye. We demonstrate that individuals displayed stable, idiosyncratic proboscis lateralization, which was tightly linked to their instantaneous viewing angle of visual targets, thus forming a persistent eye- proboscis-target axis. This axis also had functional consequences for feature-targeting. Assessing the sensory-motor plasticity using monocular occlusion, we found that moths preserved their lateralized visuo-motor geometry by adjusting body posture during flower inspection. Our findings suggest convergent control principles with vertebrate models of lateralized visual appendage guidance, while highlighting stark differences in sensory-motor plasticity, thus adding to our general understanding of how lateralization shapes control strategies across nervous systems. Significance StatementLateralization is widespread across animals and shapes how sensation and action are coordinated. Visually guided reaching with appendages is frequently lateralized across taxa, reflecting biases like handedness and eye dominance. However, the mechanistic link between lateralized sensing and motor control, and the extent of their plasticity, remain poorly understood, particularly in invertebrates. Here we show that the hummingbird hawkmoth integrates individually lateralized vision and proboscis probing movements into a unified control axis. Upon sensory perturbation, moths adjusted their position and body posture to maintain this axis. The visuo-motor lateralization produced measurable functional consequences, revealing it as a form of sensory-motor optimization. These findings uncover convergent principles of lateralized visuo-motor control across insects, humans, birds, and elephants.

animal behavior and cognition↗

Recurrent connectivity supports carbon dioxide sensitivity in Aedes aegypti mosquitoes

The mosquito Aedes aegyptis human host-seeking behavior depends on the integration of multiple sensory cues. One of these cues, carbon dioxide (CO2), gates odorant and heat pathways and activates host-seeking behavior. The neuronal circuits underlying processing of CO2 information remain unclear. We used automated serial-section transmission electron microscopy (EM) to image and reconstruct the circuitry of the glomeruli that are innervated by the Ae. aegypti maxillary palp, including the glomerulus that responds to CO2. Notably, CO2-sensitive olfactory sensory neurons (OSNs) make high levels of recurrent synaptic connections with one another, while making a low density of feedforward synapses. At some of these contacts between CO2 OSNs, we observe ribbon- like presynaptic structures, which may further enhance recurrent signaling. We compared both feedforward and recurrent connectivity with all olfactory glomeruli in Drosophila melanogaster, and we found more recurrent connections between the Ae. aegypti CO2-responsive OSNs than in any D. melanogaster glomeruli. We developed a computational circuit model that demonstrates recurrent synapses are necessary for robust CO2 detection under normal physiological conditions. Together, elevated levels of recurrent connectivity and ribbon-like structures may amplify sensory information detected by CO2-sensitive OSNs to support mosquito activation and sensitization by CO2, even in the presence of high levels of other odorants in the environment. We propose that this circuit organization supports the salience of CO2 as a mosquito host cue. One Sentence SummaryConnectomic analysis of carbon dioxide circuitry in the disease-vector mosquito Aedes aegypti.

neuroscience↗

Methyl-CODEC enables simultaneous methylation and duplex sequencing

DNA mutations and methylation often contribute to disease development in a synergistic manner. While duplex sequencing is the most accurate method for detecting DNA mutations, it typically lacks the ability to simultaneously assess methylation or requires many reads. Here, we developed Methyl-CODEC to enable simultaneous methylation sequencing and duplex sequencing using single read pairs. To achieve this, Methyl-CODEC links an enzymatically deaminated sense strand to the reverse complement of the antisense strand, which is protected from conversion by using conversion-resistant dCTPs in the strand linking step of CODEC. Methyl-CODEC shows high concordance with standard enzymatic or bisulfite based whole genome methylation sequencing, while also uniquely preserving the original DNA sequence. This improves genetic sequencing accuracy, enables better alignment for next-generation sequencing (NGS), and distinguishes C>T mutations from unmethylated Cs. It also identifies rare mutations including those producing methylated Cs, which are enriched in CpG contexts. Methyl-CODEC opens new horizons for enhanced detection of biomarkers in cancer and molecular medicine.

genomics↗

Enteric nervous system regeneration and functional cure of experimental digestive Chagas disease with trypanocidal chemotherapy

Digestive Chagas disease (DCD) is an enteric neuropathy caused by Trypanosoma cruzi infection. There is a lack of evidence on the mechanism of pathogenesis and rationales for treatment. We used a mouse model that recapitulates key clinical manifestations to study how infection dynamics shape DCD pathology, and the impact of treatment with the front-line drug benznidazole. Curative treatment at 6 weeks post-infection resulted in sustained recovery of GI transit function, whereas sub-curative treatment led to infection relapse and gradual return of DCD symptoms. Neuro-immune gene expression profiles shifted from chronic inflammation to a tissue repair signature after cure, accompanied by increased glial cell activity and regenerative neurogenesis in the myenteric neuronal plexus. Delaying treatment until 24 weeks post-infection led to a partial reversal of the DCD phenotype, suggesting the accumulation of permanent tissue damage over the course of chronic infection. Our study shows that murine DCD pathogenesis is sustained by chronic T. cruzi infection and is not an inevitable consequence of acute stage denervation. The risk that irreversible enteric neuromuscular tissue damage and dysfunction will develop highlights the importance of prompt diagnosis and treatment. Finally, these findings support the concept of treating asymptomatic T. cruzi infected individuals with benznidazole to prevent DCD development.

microbiology↗

Development of a large-scale computer-controlled ozone inhalation exposure system for rodents

Complete systems for laboratory-based inhalation toxicology studies are typically not commercially available; therefore, inhalation toxicologists utilize custom-made exposure systems. Here we report on the design, construction, testing, operation, and maintenance of a newly developed in vivo rodent ozone inhalation exposure system. Key design requirements for the system included large-capacity exposure chambers to facilitate studies with large sample sizes, automatic and precise control of chamber ozone concentrations, as well as automated data collection on airflow and environmental conditions. The exposure system contains two Hazelton H-1000 stainless steel and glass exposure chambers, each providing capacity for up to 180 mice or 96 rats. We developed an empirically tuned proportional-integral-derivative (PID) control loop that provides stable ozone concentrations throughout the exposure period (typically 3h), after a short ramp time ([~]8 minutes), and across a tested concentration range of 0.2 to 2 ppm. Specific details on the combination analog and digital input/output system for environmental data acquisition, control, and safety systems are provided, and we outline the steps involved in maintenance and calibration of the system. We show that the exposure system produces consistent ozone exposures both within and across experiments, as evidenced by low coefficients of variation in chamber ozone concentration and consistent biological responses (airway inflammation) in mice, respectively. Thus, we have created a large and robust ozone exposure system, facilitating future studies on the health effects of ozone in rodents.

pharmacology and toxicology↗

Multi-dimensional genomic analysis of myoepithelial carcinoma identifies prevalent oncogenic gene fusions

Myoepithelial carcinoma (MECA) is an aggressive type of salivary gland cancer with largely unknown molecular features. MECA may arise de novo or result from oncogenic transformation of a pre-existing pleomorphic adenoma (MECA ex-PA). We comprehensively analyzed the molecular alterations in MECA with integrated genomic analyses. We identified a low mutational load (0.5/MB), but a high prevalence of fusion oncogenes (28/40 tumors; 70%). We found FGFR1-PLAG1 in 7 (18%) cases, and the novel TGFBR3-PLAG1 fusion in 6 (15%) cases. TGFBR3-PLAG1 was specific for MECA de novo tumors or the malignant component of MECA ex-PA, was absent in 723 other salivary gland tumors, and promoted a tumorigenic phenotype in vitro. We discovered other novel PLAG1 fusions, including ND4-PLAG1, which is an oncogenic fusion between mitochondrial and nuclear DNA. One tumor harbored an MSN-ALK fusion, which was tumorigenic in vitro, and targetable with ALK inhibitors. Certain gene fusions were predicted to result in neoantigens with high MHC binding affinity. A high number of copy number alterations was associated with poorer prognosis. Our findings indicate that MECA is a fusion-driven disease, nominate TGFBR3-PLAG1 as a hallmark of MECA, and provide a framework for future steps of diagnostic and therapeutic research in this lethal cancer.

cancer biology↗