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Biology subjects

Chan, B. W.

Publications and source records attributed to Chan, B. W..

2 recordsLinked to original sources

Unexpected levels of antibiotic resistance in marine bacterial communities not solely explained by urban river discharge

Driven by anthropogenic pressures, antibiotic resistance has become more prevalent within urban bacterial communities over recent decades. In general, resistance is expected to spread from highly impacted areas into surrounding environments as the spatial patterns of resistance reflect the balance between the ability of dispersal and horizontal gene transfer to spread resistance, and the effects of dilution or selection driven by other environmental or ecological factors that change along these gradients. However, the strength and scale of this effect is less clear, especially in coastal environments. We investigated antibiotic resistance of bacterial communities along a transect from a freshwater site in the Los Angeles River (surrounded by high-density urban development) out into the San Pedro Basin in the Pacific Ocean. We determined the minimum concentration of twelve different antibiotics needed to inhibit the growth of bacterial communities across eight sites. We also examined community composition and the prevalence of known genes related to antibiotic resistance from anthropogenic sources in each sample using 16S rRNA sequencing and qPCR. In contrast to our expectations, marine bacteria communities displayed higher resistance than the freshwater LA River community. Rather than the presence of known resistance genes or proximity to urban impacts, patterns of resistance were more strongly associated with the higher species diversity found in marine communities. These unexpected results open new opportunities to determine why marine bacterial communities possess high resistance and the repercussions for potentially pathogenic bacteria and their impacts on the health of humans and wildlife.

microbiology↗

A genome-wide association study finds genetic variants associated with neck or shoulder pain in UK Biobank

BackgroundCommon types of musculoskeletal conditions include pain in the neck and shoulder areas. This study seeks to identify the genetic variants associated with neck or shoulder pain based on a genome-wide association approach using 203,309 subjects from the UK Biobank cohort and look for replication evidence from the Generation Scotland: Scottish Family Health Study (GS:SFHS) and TwinsUK. MethodsCases in the UK Biobank were determined by a question which asked the participants if they had experienced pain in the neck or shoulder in the previous month influencing daily activities. Controls were the UK Biobank participants who reported no pain anywhere in the last month. A genome-wide association study was performed adjusting for age, sex, BMI and 9 population principal components. Significant and independent genetic variants were then sent to GS:SFHS and TwinsUK for replication. ResultsWe identified 3 genetic loci that were associated with neck or shoulder pain in the UK Biobank samples. The most significant locus was in an intergenic region in chromosome 17, rs12453010, having P = 1.66 x 10-11. The second most significant locus was located in the FOXP2 gene in chromosome 7 with P = 2.38 x 10-10 for rs34291892. The third locus was located in the LINC01572 gene in chromosome 16 with P = 4.50 x 10-8 for rs62053992. In the replication stage, among 4 significant and independent genetic variants, rs2049604 in the FOXP2 gene and rs62053992 in the LINC01572 gene were weakly replicated in GS:SFHS (P = 0.0240 and P = 0.0202, respectively). None of the single nucleotide polymorphisms (SNPs) were replicated in the TwinsUK cohort (P > 0.05). ConclusionsWe have identified 3 loci associated with neck or shoulder pain in the UK Biobank cohort, two of which were weakly supported in a replication cohort. Further evidence is needed to confirm their roles in neck or shoulder pain. SignificanceThis is the first genome-wide association study on neck or shoulder pain. We have identified 3 genetic loci (an intergenic region in chromosome 17, the FOXP2 gene in chromosome 7, and the LINC01572 gene in chromosome 16) that are associated with neck or shoulder pain using the UK Biobank cohort, among which the FOXP2 gene and the LINC01572 gene were weakly replicated by the Generation Scotland: Scottish Family Health Study (P < 0.05). The SNP heritability was 0.11, indicating neck or shoulder pain is a heritable trait. The tissue expression analysis suggested that neck or shoulder pain was related to multiple brain tissues, indicating the involvement of neuron function. The results will inform further research in the characterisation of the mechanisms of neck or shoulder pain.

genetics↗