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Doster, E.

Publications and source records attributed to Doster, E..

2 recordsLinked to original sources

Target-enriched sequencing enables genomic characterization within diverse microbial populations - a preprint

Characterizing microbial genetic sequences and key variants is critical for understanding pathogen ecology, transmission, and clinical impact. Yet, conventional metagenomic sequencing often yields too few on-target reads to move beyond species-level identification. We developed a target-enriched (TE) metagenomic workflow, including bait design, an optimized TE shotgun protocol, and the VARIANT++ pipeline, to recover and classify reads at a clustered genomic sequence-variant (GSV) level (see Graphical abstract). The computational component clusters reference genomes by average nucleotide identity, builds a GSV database, and integrates Kraken2, Themisto, and mSWEEP to increase call confidence while reducing false positives. Using Mannheimia haemolytica (Mh), the primary cause of bovine respiratory disease, we designed 114,375 DNA baits targeting sequences across 70 reference genomes. TE libraries from nasopharyngeal swabs of feedlot cattle achieved >250-fold increases in on-target Mh reads ([~]2.5% of non-host reads on average) compared with conventional shotgun sequencing, despite using one-quarter the sequencing depth. This variant-level resolution revealed six GSVs; most samples contained at least two, indicating variant mixtures difficult to detect with culture- or shotgun-based surveys. Because the approach leverages available reference sequences, it can be reconfigured for other microbial targets. TE metagenomics paired with genome-similarity clustering provides a scalable approach to variant-level characterization from complex microbial populations. O_FIG O_LINKSMALLFIG WIDTH=159 HEIGHT=200 SRC="FIGDIR/small/684174v1_ufig1.gif" ALT="Figure 1"> View larger version (35K): org.highwire.dtl.DTLVardef@5a7247org.highwire.dtl.DTLVardef@4ccf1org.highwire.dtl.DTLVardef@12b0413org.highwire.dtl.DTLVardef@118a0ec_HPS_FORMAT_FIGEXP M_FIG O_FLOATNOGraphical abstractC_FLOATNO Overview of the components in our three-part workflow. C_FIG

genomics↗

Exploring associations between the teat apex metagenome and Staphylococcus aureus intramammary infection risk in primiparous cows under organic directives

The primary objective of this study was to identify associations between teat apex microbiome and Staphylococcus aureus intramammary infection (IMI) risk in primiparous cows during the first 5 weeks after calving. We performed a case-control study using shotgun metagenomics of the teat apex and culture-based milk data collected longitudinally from 710 primiparous cows on 5 organic dairy farms. We observed a strong association between S. aureus DNA in the metagenomic teat apex data prior to parturition and the odds of S. aureus IMI after parturition (OR = 38.9, 95% CI: 14.84-102.21). Differential abundance analysis confirmed this association, with cases having a 23.8 higher log fold change (LFC) in abundance of S. aureus in their samples compared to controls. Of the most prevalent microorganisms in controls, those associated with a lower risk of post-calving S. aureus IMI included Microbacterium phage Min 1 (OR = 0.37, 95% CI: 0.25-0.53), Corynebacterium efficiens (OR = 0.53, 95% CI: 0.30-0.94), Kocuria polaris (OR = 0.54, 95% CI: 0.35-0.82), Micrococcus terreus (OR = 0.64, 95% CI: 0.44-0.93) and Dietzia alimentaria (OR = 0.45, 95% CI: 0.26-0.75). Microcin B17 was the most prevalent antibacterial peptide on the teat apex of cases and controls (99.7% in both groups). The predicted abundance of Microcin B17 was also higher in cases compared to controls (LFC 0.26). Cow and farm random effects often explained a large proportion of the observed variability in the teat apex microbiome, suggesting that our results need to be interpreted within the context of the random effects. IMPORTANCEIntramammary infections (IMI) caused by Staphylococcus aureus remain an important problem for the organic dairy industry. The microbiome on the external skin of the teat apex may play a role in mitigating S. aureus IMI risk, in particular the production of antimicrobial peptides (AMPs) by commensal microbes. However, current studies of the teat apex microbiome utilize a 16S approach, which precludes detection of genomics features such as AMPs. Therefore, further research using a shotgun metagenomic approach is needed to understand what role pre-partum teat apex microbiome dynamics play in IMI risk.

ecology↗