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Mckee, M.

Publications and source records attributed to Mckee, M..

3 recordsLinked to original sources

Assessment of variability in the human urinary nucleic acid adductome

Assessment of the urinary nucleic acid adductome provides a valuable, non-invasive approach for evaluating whole-body exposure to genotoxins. To support its application to exposome research, a clear understanding of biological variability independent of exposure is required. In this study, we analyzed a urine biobank from 40 healthy, non-smoking adults. Samples were processed using dual-phase solid-phase extraction, which retains a broad spectrum of nucleic acid adducts, and analyzed using an Orbitrap IQX platform. Data processing was performed using MZmine, FeatureHunter, and MetaboAnalyst. Across approximately 160 adducts per sample, the number of recovered adducts remained consistent between collection times, indicating that qualitative characterization of the urinary nucleic acid adductome is largely unaffected by diurnal variation. Most adducts exhibited stable abundances across sampling times. Diurnal variation was observed only in males, with 10 adducts showing significant differences between collection times, while females showed no temporal differences. Of the total adducts detected, only 32 differed significantly by age and/or sex. Age-related differences were more pronounced, particularly in males, where all significantly altered adducts were present at higher intensities in the younger cohort (20 to 29 y) compared with the older cohort (30 to 60 y). These findings support the use of spot urine samples for adductomic studies, favoring first-void urine. Collectively, these findings provide the first comprehensive assessments of biological variability within the human urinary nucleic acid adductome and support its application as a robust biomonitoring tool for investigating endogenous and environmental exposures across diverse human populations.

pharmacology and toxicology↗

Knock-in = knock-out: differential fitness effects of cardinal mutations in Anopheles stephensi

The kynurenine pathway metabolizes tryptophan into 3-hydroxykynurenine (3-HK), a precursor for ommochrome eye pigments synthesized via the cardinal (cd) gene in mosquitoes. While cd disruption was presumed neutral, we observed fitness costs in Anopheles stephensi knock-in but not knock-out cd mutants. Here we investigated this anomaly further by assessing survival, fecundity, and midgut integrity across multiple cd mutant lines. Heterozygous knock-in lines, expressing a fluorescent marker and guide RNA for CRISPR/Cas9, exhibited reduced survival post-blood feeding, larva-to-adult survival deficits, and midgut barrier dysfunction, whereas knock-outs showed no such costs. Oral supplementation with xanthurenic acid partially rescued knock-in mortality, implicating oxidative stress linked to 3-HK metabolism. Expression analyses suggest transgene insertion effects, rather than cd disruption, underlie these fitness costs. These findings highlight the importance of evaluating insertional effects in gene drive target selection and support cd as a viable target for genetic control strategies in An. stephensi.

genetics↗

Integrating multiplexing into confineable gene drives effectively overrides resistance in Anopheles stephensi

Anopheles stephensi is a major malaria vector mainly present in southern Asia and the Arabian Peninsula. Since 2012 it has invaded several countries of eastern Africa, stimulating urgent efforts to develop more efficient strategies for vector control such as CRISPR/Cas9-based homing gene drives. Target site resistance is a significant challenge to the deployment of these systems. When a double-stranded break is repaired by NHEJ, it can lead to mutations which destroy the target site, making that allele unrecognizable to the sgRNA and resistant to further cleavage. The use of multiple sgRNAs has the potential to solve this issue. We performed experimental crosses to assess the homing and cutting efficiency of two different multiplexing strategies targeting the cardinal locus, in the presence and absence of a resistance allele. We found pre-existing mutations at one sgRNA target site did not significantly reduce the homing efficiency for either strategy. Modelling indicates that while both strategies can overcome resistance allele formation, the fitness of the drive-carrying alleles is a critical factor in determining the overall performance and persistence of a split drive.

genetics↗