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Haugh, K.

Publications and source records attributed to Haugh, K..

2 recordsLinked to original sources

The Contextual Specificity of Pausing: Interpreting Electromyographic Partial Responses During Action Cancellation and Attentional Capture

A prominent model of action stopping theorises that the reactive cancellation of movement is underpinned by two dissociable processes: a rapid, involuntary "pause" that transiently suppresses motor output, and a slower, voluntary cancellation of movement. As a fundamental component of motor control, the pause process has been posited to generalise broadly to infrequent and salient stimuli (irrespective of whether they bear an imperative to stop) and to be observable as suppression in electromyographical (EMG) recordings. Over two experiments (N = 24 in each), participants completed standard stop signal and flanker tasks, and novel task variants, where flanking arrows occurred infrequently, with or without a delay (relative to the central go stimulus), or coincident with a stop stimulus. Relative to a standard flanker task, presenting flankers infrequently specifically increased slowing in incongruent trials after at least three preceding trials without flanking stimuli, with no effect in congruent or neutral trials, indicating involuntary delays to infrequent events are sensitive to both stimulus features and the recency of perceptually similar events. Presenting flanker arrows of any congruence alongside a stop stimulus resulted in faster EMG suppression than stop stimuli alone, indicating that additional infrequent stimuli can facilitate inhibitory responses. However, presenting flanker stimuli at an equivalent frequency and delay outside of a stopping task did not reliably elicit EMG suppression or behavioural delays. The current findings challenge current models by demonstrating that physiological signatures previously interpreted as manifestations of a generalisable pause process are instead context specific, requiring the anticipation of action cancellation.

neuroscience↗

Longitudinal bioluminescent imaging of HIV-1 infection during antiretroviral therapy and treatment interruption in humanized mice

Non-invasive bioluminescent imaging (NIBLI) of HIV-1 infection dynamics allows for real-time monitoring of viral spread and the localization of infected cell populations in living animals. In this report, we describe full-length replication-competent GFP and Nanoluciferase (Nluc) expressing HIV-1 reporter viruses from two clinical transmitted / founder (T/F) stains: TRJO.c and Q23.BG505. By infecting humanized mice with these HIV-1 T/F reporter viruses, we were able to directly monitor longitudinal viral spread at whole-animal resolution via NIBLI at a sensitivity of as few as 30-50 infected cells. Bioluminescent signal strongly correlated with HIV-1 infection and responded proportionally to virus suppression in vivo in animals treated daily with a combination antiretroviral therapy (cART) regimen. Longitudinal NIBLI following cART withdrawal visualized tissue-sites that harbored virus during infection recrudescence. Notably, we observed rebounding infection in the same lymphoid tissues where infection was first observed prior to ART treatment. Our work demonstrates the utility of our system for studying in vivo viral infection dynamics and identifying infected tissue regions for subsequent analyses.\n\nAuthor SummaryNon-invasive bioluminescent imaging (NIBLI) in small animals allows for in vivo longitudinal imaging of infection spread and pathogenesis. We have taken advantage of the small luciferase reporter protein, Nanoluciferase (Nluc), to generate a replication-competent HIV-1 reporter virus to allow for NIBLI of viral infection in humanize mice. NIBLI via Nluc enabled us to directly visualize longitudinal spreading patterns before, during, and after interruption of daily doses of combined antiretroviral therapy (cART). We observed that rebounding infection often emerged in tissue regions originally associated with infected cells prior to cART treatment. Thus, Nluc-based NIBLI of HIV-1 infection can be used as an experimental tool to study early events involved in viral dissemination and spread from initial sites of infection to draining lymphoid tissues as well as locate infected tissues for subsequent cellular characterization of HIV-1 infected cells.

microbiology↗