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Jaworska, K.

Publications and source records attributed to Jaworska, K..

5 recordsLinked to original sources

Working memory operations emerge from dynamic changes in neural subspace geometry

Working memory representations of multiple items are maintained within quasi-orthogonal neural subspaces, a mechanism thought to reduce interference between memory contents. Previous studies in both non-human and human primates have demonstrated the existence of such subspaces, but it remains unclear how cognitive operations are performed on the information they encode. One hypothesis proposes that these operations are implemented through dynamic changes in subspace geometry, yet direct empirical evidence for this idea in the context of working memory is lacking. Furthermore, the neural mechanisms underlying such geometric reconfigurations remain unknown, particularly the role of oscillatory and aperiodic neural activity. Here, we addressed these questions using simultaneous magneto- and electroencephalography (M/EEG) recordings from healthy human participants performing a multi-item, multi-feature delayed match-to-sample visual WM task. Neural subspaces were estimated using dimensionality reduction techniques, and their geometry was characterized by quantifying the orthogonality between subspaces, distances between memory representations and subspace shapes. Participants maintained orientation and shape information simultaneously while task demands required either deprioritizing one feature or updating the representation of the prioritized feature. We found that subspace geometry was flexibly reshaped according to task demands: prioritization expanded representational subspaces, whereas de-prioritization shrunk them. In addition, subspaces representing different feature domains were generally oblique and became more orthogonal only under high cognitive demands. Finally, these task-dependent changes in subspace geometry were largely driven by interactions between aperiodic neural activity and slow oscillations in the delta and theta frequency bands.

neuroscience↗

Inactivation of lmo0946 (sif) induces the SOS response and MGEs mobilization and silences the general stress response and virulence program in Listeria monocytogenes

Bacteria have evolved numerous regulatory pathways to survive in changing environments. The SOS response is an inducible DNA damage repair system that plays an indispensable role in bacterial adaptation and pathogenesis. Here we report a discovery of the previously uncharacterized protein Lmo0946 as an SOS response interfering factor (Sif) in the human pathogen Listeria monocytogenes. Functional genetic studies demonstrated that sif is indespensible for normal growth of L. monocytogenes in stress-free as well as multi-stress conditions, and sif contributes to susceptibility to {beta}-lactam antibiotics, biofilm formation and virulence. Absence of Sif promoted the SOS response and elevated expression of mobilome genes accompanied by mobilization of the A118 prophage and ICELm-1 mobile genetic elements (MGEs). These changes were found to be associated with decreased expression of general stress response genes from the {sigma}B regulon as well as virulence genes, including the PrfA regulon. Together, this study uncovers an unexpected role of a previously uncharacterized factor, Sif, as an inhibitor of the SOS response in L. monocytogenes. SUMMARYThis study uncovers an unexpected role of a previously uncharacterized factor, Sif, as an inhibitor of the SOS response in L. monocytogenes.

microbiology↗

Spatio-temporal dynamics of visual information representation and transformation in brain networks resolving algorithmic functions

A key challenge in systems neuroscience remains to understand where, when and now particularly how brain networks compute over sensory inputs to achieve behavior. We used XOR, OR and AND functions as behavioral tasks, because each requires a different computation over the same inputs to produce correct outputs. In each task, source-localized magnetoencephalographic activity progresses through four systems-level computations identified within individual participants (N = 10/task): (1) linear discrimination of each visual input, first contra-laterally in occipital cortex then (2) jointly in midline occipital cortex and right fusiform gyrus, followed by (3) nonlinear task-dependent input integration in temporal-parietal cortex and finally (4) behavioral response representation in post-central gyrus. Our results show how network algorithms differently compute over the same inputs to produce different behaviors. One sentence summaryFour stages of task-specific computations over the same visual inputs achieve different behaviors in dynamic brain networks

neuroscience↗

TMAO, a seafood-derived molecule, produces diuresis and reduces mortality in heart failure rats

BackgroundThere is an ongoing debate whether trimethylamine-oxide (TMAO), a molecule present in seafood and a derivate of microbiota metabolism, is beneficial or harmful for the circulatory system. Interestingly, deep-water animals accumulate TMAO that protects proteins such as lactate dehydrogenase (LDH) against high hydrostatic pressure. We hypothesized that TMAO may benefit the circulatory system by protecting cardiac LDH exposed to hydrostatic stress (HS) produced by contracting heart. Methods and ResultsMale, 6-week-old, Sprague-Dawley (SD, n=40) and Spontaneously-Hypertensive-Heart-Failure (SHHF n=18) rats were divided into either Water or TMAO oral treatment. After 56 weeks, half of Water and TMAO SD rats were given isoprenaline (ISO) to produce catecholamine stress. In vitro, LDH with or without TMAO was exposed to HS (changes in pressure 0-250mmHg x 280min-1) and was evaluated using fluorescence correlation spectroscopy. After 58 weeks of the treatment survival was 100% in SD-Water, SD-TMAO, ISO-TMAO and 90% in ISO-Water. In SHHF-Water survival was 66% vs 100% in SHHF-TMAO. In general, TMAO-treated rats showed higher diuresis and natriuresis. In comparison to SHHF-Water, SHHF-TMAO showed significantly lower diastolic arterial blood pressure, plasma NT-proBNP and expression of angiotensinogen and AT1 receptors in the heart. In separate experiments, intravenous TMAO but not vehicle or urea significantly increased diuresis in SD. In vitro, exposure of LDH to HS with or without TMAO did not affect the protein structure. ConclusionsTMAO reduces mortality in SHHF rats that is associated with diuretic, natriuretic and hypotensive effects. HS produced by the contracting heart is neutral for cardiac LDH structure.

physiology↗

Neural Processing of the Same, Behaviourally Relevant Face Features is Delayed by 40 ms in Healthy Ageing

Fast and accurate face processing is critical for everyday social interactions, but it declines and becomes delayed with age, as measured by both neural and behavioural responses. Here, we addressed the critical challenge of understanding how ageing changes neural information processing mechanisms to delay behaviour. Young (20-36 years) and older (60-86 years) adults performed the basic social interaction task detecting a face vs. noise while we recorded their electroencephalogram (EEG). In each participant, using a new information theoretic framework we reconstructed the features supporting face detection behaviour, and also where, when and how EEG activity represents them. We found that occipital-temporal pathway activity dynamically represents the eyes of the face images for behaviour [~]170 ms post-stimulus, with a 40 ms delay in older adults that underlies their 200 ms behavioural deficit of slower reaction times. Our results therefore demonstrate how ageing can change neural information processing mechanisms that underlie behavioural slow down.\n\nAuthor summaryOlder adults are consistently slower than young adults in a variety of behavioural perceptual tasks. So far, it has been unclear if the underlying cause of the behavioural delay relates to attentional or perceptual differences in encoding visual information, or slower neural processing speed, or other neural factors. Our study addresses these questions by showing that in a basic social interaction task (discriminating faces from noise), young and older adults encoded the same visual information (eyes of the face) to perform the task. Moreover, early brain activity (within 200 ms following stimulus onset) encoded the same visual information (again, eyes of the face) in both groups, but was delayed and weaker in older adults. These early delays in information encoding were directly related to the observed behavioural slowing in older adults, showing that differences in early perceptual brain processes can contribute to the motor response.

neuroscience↗