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Beattie, G. A.

Publications and source records attributed to Beattie, G. A..

2 recordsLinked to original sources

A Bioinformatic Pipeline for Consensus Taxonomic Classification of Long-Read Amplicons

Characterizing community composition is fundamental to understanding microbial community function. Recent advances in Oxford Nanopore Technology (ONT) long-read sequencing now allow community profiling using full-length gene amplicons, affording better taxonomic resolution than standard short-amplicon Illumina sequencing. However, robust ONT-compatible profiling workflows are lacking. To address this, we have created the Amplicon Consensus Taxonomy (ACT) pipeline for classifying long-read amplicons. ACT combines output from three existing pipelines - Emu, Sintax, and LACA - to leverage the strengths of each while offsetting their individual limitations. We also developed the ACT database (ACT-DB), a sequence-similarity-aware reference database that clusters highly similar sequences into multi-taxa groups to reduce overclassification. We benchmarked ACT performance against Emu and Sintax using a defined simple mock community, simulated datasets, and a complex rhizosphere community supplemented with novel species. While ACT exhibited generally comparable or superior performance across datasets, ACT demonstrated a marked advantage over Emu and Sintax in identifying novel and low-abundance taxa in both simple and complex communities, resulting in significantly higher species-richness estimates that better reflected those observed in prior Illumina amplicon studies. Furthermore, by clustering ambiguous reference sequences, ACT-DB allowed ACT to resolve reads to meaningful multi-species groups, improving resolution without coercing artificial precision. Together, ACT and ACT-DB form a robust long-read amplicon profiling workflow that confidently identifies known species while reducing overclassification and preserving low-abundance and unknown taxa. IMPORTANCEMicrobial communities are frequently characterized by amplicon sequencing of marker genes, such as the bacterial 16S rRNA gene and fungal ITS region. Historically, the standard profiling method has been Illumina sequencing of 200-300 bp amplicons, but improved accuracy of ONT long-read sequencing means it is now possible to sequence amplicons spanning full genes of any size, prompting the need for tools optimized for long amplicons. Here, we describe the ACT bioinformatic pipeline for assigning taxonomy to amplicons of any length. We evaluated ACT performance using full-length 16S amplicon data relative to that of two commonly used pipelines. Additionally, we developed a sequence ambiguity-aware ACT database (ACT-DB) of 16S rRNA sequences to further improve classification accuracy and resolution.

microbiology↗

Genotypic and Phenotypic Analyses Show Ralstonia solanacearum Cool Virulence is a Quantitative Trait Not Restricted to 'Race 3 biovar 2'

Most Ralstonia solanacearum species complex strains cause bacterial wilts in tropical or subtropical zones, but the group known as Race 3 biovar 2 (R3bv2) is cool virulent and causes potato brown rot at lower temperatures. R3bv2 has invaded potato-growing regions around the world but is not established in the United States. Phylogenetically, R3bv2 corresponds to a subset of the R. solanacearum phylotype IIB clade, but little is known about the distribution of the cool virulence phenotype within phylotype IIB. Therefore, genomes of 76 potentially cool virulent phylotype IIB strains and 30 public genomes were phylogenetically analyzed. A single clonal lineage within the sequevar 1 subclade of phylotype IIB that originated in South America has caused nearly all brown rot outbreaks worldwide. To correlate genotypes with relevant phenotypes, we quantified virulence of ten Ralstonia strains on tomato and potato at both 22{degrees}C and 28{degrees}C. Cool virulence on tomato did not predict cool virulence on potato. We found that cool virulence is a quantitative trait. Strains in the sequevar 1 pandemic clonal lineage caused the most disease, while other R3bv2 strains were only moderately cool virulent. However, some non-R3bv2 strains were highly cool virulent and aggressively colonized potato tubers. Thus, cool virulence is not consistently correlated with strains historically classified as R3bv2 group. To aid detection of sequevar 1 strains, this group was genomically delimited in the LINbase web server and a sequevar 1 diagnostic primer pair was developed and validated. We discuss implications of these results for the R3bv2 definition.

microbiology↗