Biology subjects

Taddei, F.

Publications and source records attributed to Taddei, F..

4 recordsLinked to original sources

bioRxiv2018

A cortical route for face-like pattern processing in human newborns

Humans are endowed with an exceptional ability for detecting faces, a competence that in adults is supported by a set of face-specific cortical patches. Human newborns already shortly after birth preferentially orient to faces even when they are presented in the form of highly schematic geometrical patterns, over perceptually equivalent non-face-like stimuli. The neural substrates underlying this early preference are still largely unexplored. Is the adult face-specific cortical circuit already active at birth, or does its specialization develop slowly as a function of experience and/or maturation? We measured EEG responses in 1-4 days old awake, attentive human newborns to schematic face-like patterns and non-face-like control stimuli, visually presented with a slow oscillatory \"peekaboo\" dynamics (0.8 Hz) in a frequency-tagging design. Despite the limited duration of newborns attention, reliable frequency-tagged responses could be estimated for each stimulus from the peak of the EEG power spectrum at the stimulation frequency. Upright face-like stimuli elicited a significantly stronger frequency-tagged response than inverted face-like controls in a large set of electrodes. Source reconstruction of the underlying cortical activity revealed the recruitment of a partially right-lateralized network comprising lateral occipito-temporal and medial parietal areas largely overlapping with the adult face-processing circuit. This result suggests that the cortical route specialized in face processing is already functional at birth.\n\nSignificance statementNewborns show a remarkable ability to detect faces even minutes after birth, an ecologically fundamental skill that is instrumental for interacting with their conspecifics. What are the neural bases of this expertise? Using EEG and a slow oscillatory visual stimulation, we identified a reliable response specific to face-like patterns in newborns, which underlying cortical sources largely overlap with the adult face-specific cortical circuit. This suggests that the development of face perception in infants might rely on an early cortical route specialized in face processing already shortly after birth.

neuroscience↗

bioRxiv2018

Temporal scaling of ageing as an adaptive strategy of Escherichia coli

Natural selection has long been hypothesised to shape ageing patterns, but whether and how ageing contributes to life-history evolution remains elusive. The complexity of various ageing-associated molecular mechanisms and their inherent stochasticity hinder reductionist approaches to the understanding of functional senescence, i.e. reduced fecundity and increased mortality. Recent bio-demographic work demonstrated that high-precision statistics of life-history traits such as mortality rates could be used phenomenologically to understand the ageing process. We adopted this approach to study cellular senescence in growth-arrested E. coli cells, where damages to functional macromolecules are no longer diluted by fast de novo biosynthesis. We acquired high-quality longitudinal physiological and life history data of large environmentally controlled clonal E. coli populations at single-cell resolution, using custom-designed microfluidic devices coupled to time-lapse microscopy. We show that E. coli lifespan distributions follow the Gompertz law of mortality, a century-old actuarial observation of human populations, despite developmental, cellular and genetic differences between bacteria and metazoan organisms. Measuring the shape of the hazard functions allowed us to disentangle quantitatively the demographic effects of ageing, which accumulate with time, from age-independent genetic longevity-modulating interventions. A pathway controlling cellular maintenance, the general stress response, not only promotes longevity but also temporally scales the whole distribution by reducing ageing rate. We further show that E. coli, constrained by the amount of total biosynthesis, adapt to their natural feast-or-famine lifestyle by modulating the amount of maintenance investment, rendering ageing rate a highly evolvable life-history trait.

evolutionary biology↗

bioRxiv2018

Selection of horizontal gene transfer through public good production

In bacteria, cooperative genes encoding public good molecules are preferentially located on mobile genetic elements (MGEs), and horizontal transfer of MGEs favours the maintenance of public good cooperation. The rate of horizontal transfer itself can evolve in response to selective pressures acting on both MGEs and bacterial hosts: benefits and costs of infectious spread, but also indirect effects of MGE genes to the host. We show here that carriage of public good genes on MGEs can generate another indirect selection for MGE transfer. Transfer increases public good production and, when relatedness is sufficiently high, public goods benefit preferentially genotypes with high transfer ability. Both our simulations and experiments indicate that transfer is not required to occur among kin, provided that public goods still benefit kin. Public good gene mobility thus aligns the interests of chromosomes and MGEs concerning transfer, promoting gene exchange among bacteria.

evolutionary biology↗

bioRxiv2017

Two stochastic processes shape diverse senescence patterns in a single-cell organism

Despite advances in aging research, a multitude of aging models, and empirical evidence for diverse senescence patterns, understanding is lacking of the biological processes that shape senescence, both for simple and complex organisms. We show that for a isogenic Escherichia coli bacterial population senescence results from two stochastic processes. A primary random deterioration process within the cell, such as generated by random accumulation of damage, leads to an exponential increase in mortality early in life followed by a late age mortality plateau; a secondary process of stochastic asymmetric transmission of an unknown factor at cell fission influences mortality. This second process is required to explain the difference between the classical mortality plateaus detected for young mothers offspring and the near non-senescence of old mothers offspring as well as the lack of a mother offspring correlation in age at death. We observed that life span is predominantly determined by underlying stochastic stage dynamics. Our findings support models based on stage-specific actions of alleles for the evolution of senescence. This support might be surprising since these models that have not specifically been developed in the context of simple, single cell organisms. We call for exploration of similar stochastic influences beyond simple organisms.

systems biology↗