| Literature DB >> 31678592 |
Jill Hager Cocking1, Michael Deberg2, Jim Schupp3, Jason Sahl4, Kristin Wiggins5, Ariel Porty6, Heidie M Hornstra7, Crystal Hepp8, Claire Jardine9, Tara N Furstenau10, Albrecht Schulte-Hostedde11, Viacheslav Y Fofanov12, Talima Pearson13.
Abstract
Whole genome sequencing (WGS) is a widely available, inexpensive means of providing a wealth of information about an organism's diversity and evolution. However, WGS for many pathogenic bacteria remain limited because they are difficult, slow and/or dangerous to culture. To avoid culturing, metagenomic sequencing can be performed directly on samples, but the sequencing effort required to characterize low frequency organisms can be expensive. Recently developed methods for selective whole genome amplification (SWGA) can enrich target DNA to provide efficient sequencing. We amplified Coxiella burnetii (a bacterial select agent and human/livestock pathogen) from 3 three environmental samples that were overwhelmed with host DNA. The 68- to 147-fold enrichment of the bacterial sequences provided enough genome coverage for SNP analyses and phylogenetic placement. SWGA is a valuable tool for the study of difficult-to-culture organisms and has the potential to facilitate high-throughput population characterizations as well as targeted epidemiological or forensic investigations.Entities:
Keywords: Coxiella burnetii; Selective whole genome amplification; Whole genome sequencing
Year: 2019 PMID: 31678592 PMCID: PMC7199880 DOI: 10.1016/j.ygeno.2019.10.022
Source DB: PubMed Journal: Genomics ISSN: 0888-7543 Impact factor: 5.736