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Preston, L.

Publications and source records attributed to Preston, L..

2 recordsLinked to original sources

Stability of phoneme-related potentials across testing sessions and stimulus presentation conditions

ObjectivesObjective and ecologically valid measures of speech processing can complement conventional audiologic assessments. Phoneme-related potentials (PRPs), derived by averaging listeners electroencephalography (EEG) responses time-locked to phonemes in continuous speech, have emerged as a promising approach for capturing cortical processing of speech in naturalistic listening conditions. Importantly, PRPs reveal speech perception challenges even when conventional audiograms are clinically normal, positioning them as a promising neural marker for suprathreshold listening difficulties that standard audiometry often misses. As a critical step toward clinical translation, this study examined the extent to which PRP-derived measures remain stable across real-world contexts relevant to clinical implementation, including monaural versus binaural presentation, stimulus intensity level, and repeated testing sessions. The study also assessed cortical tracking of lower-level speech acoustics to determine whether the PRP findings could be attributed to acoustic processing. DesignEEG was recorded from 18 young adults with normal hearing as they listened to audiobook speech presented monaurally or binaurally at 60 or 75 dB across two sessions separated by approximately one week. Neural differentiation of phoneme manner-of-articulation classes (vowels, nasals/approximants, fricatives, and stops) in PRPs was quantified using two measures: an F-statistic reflecting between-manner relative to within-manner variability, and classification accuracy from a machine-learning model trained to predict manner class from PRPs. Temporal response function modeling assessed neural tracking of continuous acoustic envelope and onset features of the audiobook speech. ResultsNeither PRP-derived measure of manner differentiation showed significant effects of session, presentation modality, intensity level, or their interactions. Intraclass correlation analyses further indicated moderate-to-good reliability across all three factors. In contrast, neural tracking of the acoustic envelope and acoustic onsets was stronger under binaural than monaural presentation, with binaural presentation eliciting more pronounced cortical responses to the envelope. ConclusionsPRP-derived measures remained relatively stable across modest procedural variations that are common in clinical testing contexts, positioning PRPs as a potent objective index of naturalistic speech processing. This stability may reflect cortical processing of abstract, linguistically relevant speech categories and suggest that PRPs provide complementary information beyond audiologic assessments of peripheral auditory functions and EEG measures that primarily capture lower-level acoustic processing.

neuroscience↗

A Panel of Diverse Klebsiella pneumoniae Clinical Isolates for Research and Development

Klebsiella pneumoniae are a leading cause of healthcare associated infections worldwide. In particular, strains expressing extended-spectrum {beta}-lactamases (ESBLs) and carbapenemases pose serious treatment challenges, leading the World Health Organization (WHO) to designate ESBL and carbapenem-resistant Enterobacteriaceae (CRE) as "critical" threats to human health. Research efforts to combat these pathogens can be supported by accessibility to diverse and clinically relevant isolates for testing novel therapeutics. Here, we describe a panel of 100 diverse K. pneumoniae isolates publicly available to assist the research community in this endeavor. Whole-genome sequencing (WGS) was performed on 3,878 K. pneumoniae clinical isolates housed at the Multidrug-Resistant Organism Repository and Surveillance Network. The isolates were cultured from 63 facilities in 19 countries between 2001 and 2020. Core-genome multilocus sequence typing and high-resolution single nucleotide polymorphism based phylogenetic analyses captured the genetic diversity of the collection and were used to select the final panel of 100 isolates. In addition to known multi-drug resistant (MDR) pandemic lineages, the final panel includes hypervirulent lineages and isolates with specific and diverse resistance genes and virulence biomarkers. A broad range of antibiotic susceptibilities ranging from pan-sensitive to extensively drug resistant isolates are described. The panel collection, all associated metadata and genome sequences, are available at no additional cost and will be an important for the research community and for the design and development of novel antimicrobial agents and diagnostics against this important pathogen. ImportanceKlebsiella pneumoniae is a major cause of healthcare-associated infections that are increasingly difficult to treat due to the emergence of multi-drug resistant strains. In particular, strains expressing extended-spectrum {beta}-lactamases and carbapenemases have attained global notoriety, with the World Health Organization listing these strains as a "critical-priority" for the development of new therapeutics. Access to a diverse collection of strains for testing is critical for this endeavor, but few resources currently exist. Similarly, pivotal research of the genetic determinants underlying the pathogenesis of hypervirulent lineages is hampered by the lack of standardized, comparator strains. Herein we describe a panel of 100 diverse K. pneumoniae constructed to maximize genetic and phenotypic diversity from a repository of over 3,800 clinical isolates collected over 19 years. The panel, and all associated metadata and genome sequences, is provided at no cost and will greatly assist efforts by academic, government, and industry research groups.

microbiology↗