Biology subjects

Dunn, J. D.

Publications and source records attributed to Dunn, J. D..

5 recordsLinked to original sources

bioRxiv2026

Naturalistic face-directed attention predicts face recognition ability

Recognising people precedes and informs most social interactions, yet it is not clear why individuals differ so markedly in face recognition ability. Exposure-based accounts propose that it is shaped by visual experience with faces, known as 'face diet', but most prior work treats exposure as passively acquired, thereby masking the active and dynamic nature of visual attention in natural settings. Here we examined whether spontaneous attention to faces in everyday environments predicts face recognition ability. Eighty participants wore mobile eye-tracking glasses while walking through a busy university campus and during a face-to-face interaction, before completing standard measures of face recognition ability. Fixations directed to faces showed stable individual differences in both settings. People who looked more at faces scored higher on our composite measure of face recognition ability, and gaze in the two settings predicted ability independently, together accounting for 22% of its variance. These findings suggest that differences in how people actively sample visual information from their environments may be an overlooked source of variance in perceptual expertise.

animal behavior and cognition↗

bioRxiv2026

Enhanced neural encoding of individual exemplars in the Super-Recogniser brain is specific to faces

Super-Recognisers are known for their exceptional ability to encode and remember faces. Recent work has found robust neural codes for face identity in brain activity. Here we test whether the enhanced individuation of face identity in super-recogniser neural codes extends to exemplars from non-face categories. We recorded 64-channel electroencephalography (EEG) as 22 Super-Recognisers and 20 typical recognisers viewed rapid, randomised sequences of faces, dogs, houses, and cars (10 different images of 10 different exemplars per category). Using a neural decoding approach, we found that Super-Recognisers neural responses contained stronger and more temporally sustained information discriminating individual face identities. Moreover, Super-Recognisers displayed increased inter-individual consistency in the organisation of their face-identity representations, suggesting a more stable and/or canonical representational structure in individuals with superior face recognition abilities. Crucially, there was no evidence to suggest that these encoding advantages generalised to non-face categories: neural discrimination of individual dogs, cars, and houses was comparable across groups, and group-differences in inter-subject consistency were evident only for faces. Together, these findings suggest that enhanced perceptual encoding underlying exceptional face recognition is highly category-specific, supporting the view that expertise in this group reflects specialised mechanisms for processing facial identity rather than broadly enhanced visual discrimination capacities.

neuroscience↗

bioRxiv2026

Robust neural face identity codes in the Super-Recogniser brain

Super-Recognisers show exceptional ability in face recognition, providing a natural model of how perceptual systems optimise for individuating visually similar stimuli in variable viewing conditions. However, the neural representations supporting this extreme perceptual expertise are unknown. Here, we tested whether Super-Recognisers (n = 23) differed from typical recognisers (n = 21) in the dimensional organisation of neural face identity coding. We recorded 64-channel electroencephalography while participants viewed random and rapidly-presented sequences containing 10 naturally varying images of 40 unfamiliar identities. Using time-resolved representational similarity analysis we measured the geometry of identity representations, their consistency across observers, and how clearly they specified face identity. Although neural expression of identity information was robust in both groups, we found three key differences between Super-Recognisers and typical recognisers. First, the geometry of face identity representations differed between groups. Second, Super-Recognisers showed greater inter-individual consistency in representational geometry. Third, Super-Recognisers neural signals discriminated between face identities more strongly than those of typical recognisers. Differences in the coding of broader face categories (sex, age, ethnicity) were notably weaker, suggesting that the observed group differences reflected fine-scale differences in identity coding rather than global reshaping of representational geometry. Strikingly, all three differences emerged within a common mid-latency interval ([~]300-500ms), implicating higher-stages of face processing associated with representations that are sensitive to face familiarity and link between perceptual and semantic domains. Together, these findings indicate that individual differences in face recognition ability reflect higher-level differences in neural identity coding, rather than enhanced early sensory processing. Significance statementSuper-Recognisers have an exceptional ability to recognise unfamiliar faces, yet the neural basis of this advantage has remained unclear. We find brain activity expresses the identity of unfamiliar faces more strongly and consistently in Super-Recognisers than typical recognisers. These advantages were specific to individual identity and could not be explained by enhanced encoding of broader facial categories such as sex, age, or ethnicity. Critically, group differences emerged during a mid-latency stage of processing ([~]300-500 ms) associated with higher-level representations that support stable identity coding across variable images. The findings suggest that exceptional face recognition arises from more robust neural representations of individual identity rather than enhanced early visual processing, providing new insight into the neural basis of perceptual expertise.

neuroscience↗

bioRxiv2022

Intratumoral heterogeneity and clonal evolution induced by HPV integration

The human papillomavirus (HPV) genome is integrated into host DNA in most HPV-positive cancers, but the consequences for chromosomal integrity are unknown. Continuous long-read sequencing of oropharyngeal cancers and cancer cell lines revealed a unique form of structural variation, i.e., heterocateny, characterized by diverse, interrelated, and repetitive patterns of concatemerized virus and host DNA segments within a cancer. Unique breakpoint sequences shared across structural variants facilitated stepwise reconstruction of their evolution from a common molecular ancestor. This analysis revealed that virus and virus-host concatemers are unstable and, upon insertion into and excision from chromosomes, facilitate capture, amplification, and recombination of host DNA and chromosomal rearrangements. Evidence of heterocateny was detected in extrachromosomal and intrachromosomal DNA. The data indicate that heterocateny is driven by the dynamic, aberrant replication and recombination of an oncogenic DNA virus, thereby extending known consequences of HPV integration to include promotion of intratumoral heterogeneity and clonal evolution.

cancer biology↗

bioRxiv2019

Conidial melanin of the human pathogenic fungus Aspergillus fumigatus disrupts cell autonomous defenses in amoebae

The human pathogenic fungus Aspergillus fumigatus is a ubiquitous saprophyte that causes fatal infections in immunocompromised individuals. Following inhalation, conidia are ingested by innate immune cells and can arrest phagolysosome maturation. How such general virulence traits could have been selected for in natural environments is unknown. Here, we used the model amoeba Dictyostelium discoideum to follow the antagonistic interaction of A. fumigatus conidia with environmental phagocytes in real time. We found that conidia covered with the green pigment 1,8-dihydroxynaphthalene-(DHN)-melanin were internalized at far lower rates when compared to those lacking the pigment, despite high rates of initial attachment. Immediately after uptake of the fungal conidia, nascent phagosomes were formed through sequential membrane fusion and fission events. Using single-cell assays supported by a computational model integrating the differential dynamics of internalization and phagolysosome maturation, we could show that acidification of phagolysosomes was transient and was followed by neutralization and, finally, exocytosis of the conidium. For unpigmented conidia, the cycle was completed in less than 1 h, while the process was delayed for conidia covered with DHN-melanin. At later stages of infection, damage to infected phagocytes triggered the ESCRT membrane repair machinery, whose recruitment was also attenuated by DHN-melanin, favoring prolonged persistence and the establishment of an intracellular germination niche in this environmental phagocyte. Increased exposure of DHN-melanin on the conidial surface also improved fungal survival when confronted with the fungivorous predator Protostelium aurantium, demonstrating its universal antiphagocytic properties.

microbiology↗