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Hellewell, J.

Publications and source records attributed to Hellewell, J..

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Bayesian bacterial GWAS model reveals threshold-dependent genetic changes in antimicrobial resistance phenotypes

Genome-wide association studies (GWASs) utilize the association between genetic variants and phenotypic changes to identify causal variants underlying a phenotype of interest, and in some cases employ these correlations to perform phenotype prediction for novel genomes given their repertoire of genetic variants. Often utilizing a logistic or linear regression framework, bacterial GWAS methods have frequently been applied to infer variants associated with antimicrobial resistance (AMR) phenotypes measured using serial dilutions and recorded as minimum inhibitory concentrations (MICs). Beyond their increased granularity compared to resistant-sensitive classifications, MICs provide a more robust measure of AMR because they are not dependent on threshold values that can change over time and between data sources. One prominent challenge posed by both existing inference and prediction GWAS frameworks is the representation of MICs as censored ordered intervals rather than as binary resistant-sensitive or continuous approximations, a more suitable statistical model that has the potential to improve the discovery of lower-penetrance variants and MIC prediction. We show that Bayesian ordered logistic regression GWAS models can recover known antimicrobial resistance variants, identify variants with threshold-dependent effects without employing computationally-costly pairwise comparisons, and predict categorical MIC phenotypes. Specifically, the models recovered known resistance-conferring variants for {beta}-lactams (in the penicillin-binding protein genes pbp2x, pbp1a, and pbp2b) and trimethoprim (in the dihydrofolate reductase gene folA) in S. pneumoniae, and for rifampicin (in the rpoB gene encoding the beta subunit of bacterial RNA polymerase) for M. tuberculosis, in addition to numerous lower-penetrance resistance variants. We found that ordered categorical models that allow for non-proportionality in the effect of each genetic variant across different MIC categories replicate the pattern of stepwise accumulation of resistance mutations in pbp genes in their relative effects at different MIC thresholds, and can improve balanced accuracy for MIC prediction compared to a proportional-effects model, suggesting that nonlinear effects may play a role in missing heritability. We also describe the use of lineage clustering as an alternative method of reducing false positives induced by genetic relatedness within a bacterial population. The methods described here incorporate a more accurate representation of minimum inhibitory concentration phenotypes into a highly flexible bacterial GWAS methodology capable of capturing nonlinear variant effects and suitable for both causal variant inference and prediction of MIC phenotypes.

bioinformatics↗

A reusable model of pangenome selection informs optimal surveillance strategies over vaccine introductions

BackgroundThe human pathogen Streptococcus pneumoniae is a major cause of disease, including pneumonia and meningitis. The introduction of Pneumococcal Conjugate Vaccines (PCVs) initially reduced the burden of disease through a reduction of colonisation by vaccine-targeted serotypes. However, since PCVs only target a proportion of pneumococcal serotypes, they shift intraspecific competition, eventually allowing non-targeted types to replace vaccine types. Understanding the host and pathogen factors causing replacement is important for future vaccine development. Mechanistic understanding of vaccine replacement dynamics is crucial for forecasting and optimisation of genomic surveillance strategies to evaluate realised vaccine effectiveness. MethodsWe developed a mathematical model of the genomic and demographic factors which explain vaccine replacement, used this model to replicate serotype-frequency changes, and investigated cost-effective genomic surveillance strategies. We extended a forward-time model based on the Wright-Fisher model, developing a user-friendly model framework that describes the post-vaccine dynamics of S. pneumoniae populations. Our model describes vaccine replacement as a function of vaccine impact, immigration of new strains, and negative frequency-dependent selection (NFDS) on the accessory genome content. ResultsWe used our model to study vaccine replacement in newly sequenced genomic surveillance data from Nepal, and existing data from the US, and the UK, with distinct surveillance strategies. We showed that the model with NFDS better replicates replacement dynamics than a null model without NFDS, and that NFDS likely only acts on part of the S. pneumoniae accessory genome. We found consistent estimates for vaccination effectiveness across the different study locations and country-specific genes under NFDS, highlighting the importance of conducting genomic surveillance in each country of interest. By simulating data from the model, we showed that an optimal surveillance strategy prioritises per-sampling sample size over sampling frequency for small sampling budgets. ConclusionsOur model can be used to predict vaccine replacement dynamics after PCV introduction, and can be easily reapplied to analyse new data from vaccine introductions or new regions. Our model is available in the R package STUBENTIGER (Studying Balancing Evolution (NFDS) To Investigate Genome Replacement) on GitHub https://github.com/bacpop/Stubentiger.

genomics↗

CELEBRIMBOR: Pangenomes from metagenomes

SummaryMetagenome Assembled Genomes (MAGs) are often incomplete, with sequences missing due to errors in assembly or low coverage. Incomplete MAGs present a particular challenge for identification of shared genes within a microbial population, known as core genes, as a core gene missing in only a few assemblies will result in it being mischaracterized at a lower frequency. Here, we present CELEBRIMBOR, a snakemake pangenome analysis pipeline which uses a measure of genome completeness to automatically adjust the frequency threshold at which core genes are identified, enabling accurate core gene identification in MAGs. Availability and implementationCELEBRIMBOR is published under open source Apache 2.0 licence at https://github.com/bacpop/CELEBRIMBOR and is available as a Docker container. Supplementary material is available in the online version of the article.

bioinformatics↗

Seamless, rapid and accurate analyses of outbreak genomic data using Split K-mer Analysis (SKA)

Sequence variation observed in populations of pathogens can be used for important public health and evolution genomic analyses, especially outbreak analysis and transmission reconstruction. Identifying this variation is typically achieved by aligning sequence reads to a reference genome, but this approach is susceptible to reference biases and requires careful filtering of called genotypes. Additionally, while the volume of bacterial genomes continues to grow, tools which can accurately and quickly call genetic variation between sequences have not kept pace. There is a need for tools which can process this large volume of data, providing rapid results, but remain simple so they can be used without highly trained bioinformaticians, expensive data analysis, and long term storage and processing of large files. Here we describe Split K-mer Analysis (SKA2), a method which supports both reference-free and reference-based mapping to quickly and accurately genotype populations of bacteria using sequencing reads or genome assemblies. SKA2 is highly accurate for closely related samples, and in outbreak simulations we show superior variant recall compared to reference-based methods, with no false positives. We also show that within bacterial strains, where it is possible to construct a clonal frame, SKA2 can also accurately map variants to a reference, and be used with recombination detection methods to rapidly reconstruct vertical evolutionary history. SKA2 is many times faster than comparable methods and can be used to add new genomes to an existing call set, allowing sequential use without the need to reanalyse entire collections. Given its robust implementation, inherent absence of reference bias and high accuracy, SKA2 has the potential to become the tool of choice for genotyping bacteria and can help expand the uses of genome data in evolutionary and epidemiological analyses. SKA2 is implemented in Rust and is freely available at https://github.com/bacpop/ska.rust.

bioinformatics↗

Improving modelling for epidemic responses: reflections from members of the UK infectious disease modelling community on their experiences during the COVID-19 pandemic

The COVID-19 pandemic both relied and placed significant burdens on the experts involved from research and public health sectors. The sustained high pressure of a pandemic on responders, such as healthcare workers, can lead to lasting psychological impacts including acute stress disorder, post-traumatic stress disorder, burnout, and moral injury, which can impact individual wellbeing and productivity. As members of the infectious disease modelling community, we convened a reflective workshop to understand the professional and personal impacts of response work on our community and to propose recommendations for future epidemic responses. The attendees represented a range of career stages, institutions, and disciplines. This piece was collectively produced by those present at the session based on our collective experiences. Key issues we identified at the workshop were lack of institutional support, insecure contracts, unequal credit and recognition, and mental health impacts. Our recommendations include rewarding impactful work, fostering academia-public health collaboration, decreasing dependence on key individuals by developing teams, increasing transparency in decision-making, and implementing sustainable work practices. Despite limitations in representation, this workshop provided valuable insights into the UK COVID-19 modelling experience and guidance for future public health crises. Recognising and addressing the issues highlighted is crucial, in our view, for ensuring the effectiveness of epidemic response work in the future.

scientific communication and education↗