The Effects of Signal Erosion and Core Genome Reduction on the Identification of Diagnostic Markers

Author:

Sahl Jason W.12,Vazquez Adam J.1,Hall Carina M.1,Busch Joseph D.1,Tuanyok Apichai3,Mayo Mark4,Schupp James M.2,Lummis Madeline1,Pearson Talima1,Shippy Kenzie1,Colman Rebecca E.2ORCID,Allender Christopher J.1,Theobald Vanessa4,Sarovich Derek S.4ORCID,Price Erin P.4ORCID,Hutcheson Alex5,Korlach Jonas5,LiPuma John J.6,Ladner Jason7,Lovett Sean7,Koroleva Galina7,Palacios Gustavo7,Limmathurotsakul Direk89,Wuthiekanun Vanaporn8,Wongsuwan Gumphol8,Currie Bart J.4,Keim Paul12ORCID,Wagner David M.1

Affiliation:

1. Center for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, Arizona, USA

2. Translational Genomics Research Institute, Flagstaff, Arizona, USA

3. Emerging Pathogens Institute, University of Florida, Gainesville, Florida, USA

4. Global and Tropical Health Division, Menzies School of Health Research, Darwin, Northern Territory, Australia

5. Pacific Biosciences, University of Michigan, Ann Arbor, Michigan, USA

6. Division of Pediatric Infectious Diseases, University of Michigan, Ann Arbor, Michigan, USA

7. Center for Genome Sciences, USAMRIID, Fort Detrick, Maryland, USA

8. Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand

9. Department of Tropical Hygiene, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand

Abstract

ABSTRACT Whole-genome sequence (WGS) data are commonly used to design diagnostic targets for the identification of bacterial pathogens. To do this effectively, genomics databases must be comprehensive to identify the strict core genome that is specific to the target pathogen. As additional genomes are analyzed, the core genome size is reduced and there is erosion of the target-specific regions due to commonality with related species, potentially resulting in the identification of false positives and/or false negatives. IMPORTANCE A comparative analysis of 1,130 Burkholderia genomes identified unique markers for many named species, including the human pathogens B. pseudomallei and B. mallei . Due to core genome reduction and signature erosion, only 38 targets specific to B. pseudomallei /mallei were identified. By using only public genomes, a larger number of markers were identified, due to undersampling, and this larger number represents the potential for false positives. This analysis has implications for the design of diagnostics for other species where the genomic space of the target and/or closely related species is not well defined.

Funder

DOD | Defense Threat Reduction Agency

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

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