Genome Sequence of the Deep-Rooted Yersinia pestis Strain Angola Reveals New Insights into the Evolution and Pangenome of the Plague Bacterium

Author:

Eppinger Mark1,Worsham Patricia L.2,Nikolich Mikeljon P.3,Riley David R.1,Sebastian Yinong4,Mou Sherry2,Achtman Mark5,Lindler Luther E.6,Ravel Jacques1

Affiliation:

1. Institute for Genome Sciences (IGS) and Department of Microbiology and Immunology, University of Maryland, School of Medicine, Baltimore, Maryland 21201

2. U.S. Army Medical Research Institute of Infectious Diseases (USAMRIID), Bacteriology Division, Fort Detrick, Maryland 21702

3. Walter Reed Army Institute of Research (WRAIR), Division of Bacterial & Rickettsial Diseases, Silver Spring, Maryland 20910

4. J. Craig Venter Institute, Rockville, Maryland 20850

5. Environmental Research Institute (ERI), University College Cork, Lee Road, Cork, Ireland

6. Department of Defense, Global Emerging Infections Surveillance and Response System, 503 Robert Grant Ave., Silver Spring, Maryland 20910

Abstract

ABSTRACT To gain insights into the origin and genome evolution of the plague bacterium Yersinia pestis , we have sequenced the deep-rooted strain Angola, a virulent Pestoides isolate. Its ancient nature makes this atypical isolate of particular importance in understanding the evolution of plague pathogenicity. Its chromosome features a unique genetic make-up intermediate between modern Y. pestis isolates and its evolutionary ancestor, Y. pseudotuberculosis . Our genotypic and phenotypic analyses led us to conclude that Angola belongs to one of the most ancient Y. pestis lineages thus far sequenced. The mobilome carries the first reported chimeric plasmid combining the two species-specific virulence plasmids. Genomic findings were validated in virulence assays demonstrating that its pathogenic potential is distinct from modern Y. pestis isolates. Human infection with this particular isolate would not be diagnosed by the standard clinical tests, as Angola lacks the plasmid-borne capsule, and a possible emergence of this genotype raises major public health concerns. To assess the genomic plasticity in Y. pestis , we investigated the global gene reservoir and estimated the pangenome at 4,844 unique protein-coding genes. As shown by the genomic analysis of this evolutionary key isolate, we found that the genomic plasticity within Y. pestis clearly was not as limited as previously thought, which is strengthened by the detection of the largest number of isolate-specific single-nucleotide polymorphisms (SNPs) currently reported in the species. This study identified numerous novel genetic signatures, some of which seem to be intimately associated with plague virulence. These markers are valuable in the development of a robust typing system critical for forensic, diagnostic, and epidemiological studies.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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