Tiled Amplicon Sequencing Enables Culture-free Whole-Genome Sequencing of Pathogenic Bacteria From Clinical Specimens
Chaney C. KalinichiD, Freddy L. GonzaleziD, Alice OsmastoniD, Mallery I. BrebaniD, Isabel DistefanoiD, Candy Leon, Patricia SheeniD, Mirko ZimiciD, Jorge CoroneliD, Grace Tan, Valeriu CruduiD, Nelly CiobanuiD, Alexandru CodreanuiD, Walter Solano, Jimena Ráez, Orchid M. AllicockiD, Chrispin ChaguzaiD, Anne L. WyllieiD, Matthew BrandtiD, Daniel M. WeinbergeriD, Benjamin SobkowiakiD, Ted CoheniD, Louis GrandjeaniD, Nathan D. GrubaughiD, Seth N. RedmondiD
Abstract
Pathogen sequencing is an important tool for disease surveillance and demonstrated its high value during the COVID-19 pandemic. Viral sequencing during the pandemic allowed us to track disease spread, quickly identify new variants, and guide the development of vaccines. Tiled amplicon sequencing, in which a panel of primers is used for multiplex amplification of fragments across an entire genome, was the cornerstone of SARS-CoV-2 sequencing. The speed, reliability, and cost-effectiveness of this method led to its implementation in academic and public health laboratories across the world and adaptation to a broad range of viral pathogens. However, similar methods are not available for larger bacterial genomes, for which whole-genome sequencing typically requires in vitro culture. This increases costs, error rates and turnaround times. The need to culture poses particular problems for medically important bacteria such as Mycobacterium tuberculosis, which are slow to grow and challenging to culture. As a proof of concept, we developed two novel whole-genome amplicon panels for M. tuberculosis and Streptococcus pneumoniae. Applying our amplicon panels to clinical samples, we show the ability to classify pathogen subgroups and to reliably identify markers of drug resistance without culturing. Development of this work in clinical settings has the potential to dramatically reduce the time of diagnosis of drug resistance for multiple drugs in parallel, enabling earlier intervention for high priority pathogens.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 1
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Same-day diagnostic and surveillance data for tuberculosis via whole genome sequencing of direct respiratory samples.
A. A. Votintseva, P. Bradley, … Z. Iqbal·bioRxiv·Dec 19, 2016
- Whole genome amplification and sequencing of low cell numbers directly from a bacteria spiked blood model
Catherine Anscombe, Raju.V Misra, Saheer Gharbia·bioRxiv·Apr 26, 2018
- Direct nanopore sequencing of M. tuberculosis on sputa and rescue of suboptimal results to enhance transmission surveillance
Sheri M. Saleeb, Andrea Marcos-Abellán, … Darı́o Garcı́a de Viedma·bioRxiv·Sep 23, 2025
- Genomic Sequencing from Sputum for Tuberculosis Disease Diagnosis, Lineage Determination and Drug Susceptibility Prediction
K. Nilgiriwala, M.-S. Rabodoarivelo, … T. M. Walker·bioRxiv·Oct 31, 2022
- MinION Nanopore Sequencing of Multiple Displacement Amplified Mycobacteria DNA Direct from Sputum
Sophie George, Yifei Xu, … Kate Elizabeth Dingle·bioRxiv·Dec 7, 2018
- Target-enrichment sequencing yields valuable genomic data for difficult-to-culture bacteria of public health importance
Tristan P. W. Dennis, Barbara K. Mable, … Taya Forde·Microbial GenomicsPeer-reviewed·May 27, 2022