Genome Sequence of <i>Yersinia pestis</i> KIM

Wen Deng(Laboratory of Molecular Genetics), Valerie Burland(Laboratory of Molecular Genetics), Guy Plunkett(Laboratory of Molecular Genetics), Adam T. Boutin(Laboratory of Molecular Genetics), George F. Mayhew(Laboratory of Molecular Genetics), Paul Liss(Laboratory of Molecular Genetics), Nicole T. Perna(New York Genome Center), Debra J. Rose(Laboratory of Molecular Genetics), Bob Mau, Shiguo Zhou(University of Wisconsin–Madison), David C. Schwartz(University of Wisconsin–Madison), Jaqueline D. Fetherston(University of Kentucky), Luther E. Lindler(Walter Reed Army Institute of Research), Robert R. Brubaker(Michigan State University), Gregory V. Plano(University of Miami), Susan C. Straley(University of Kentucky), Kathleen A. McDonough(Wadsworth Center), Matthew L. Nilles(University of North Dakota), Jyl S. Matson(University of North Dakota), Frederick R. Blattner(Laboratory of Molecular Genetics), Robert D. Perry(University of Kentucky)
Journal of Bacteriology
August 15, 2002
Cited by 540Open Access
Full Text

Abstract

We present the complete genome sequence of Yersinia pestis KIM, the etiologic agent of bubonic and pneumonic plague. The strain KIM, biovar Mediaevalis, is associated with the second pandemic, including the Black Death. The 4.6-Mb genome encodes 4,198 open reading frames (ORFs). The origin, terminus, and most genes encoding DNA replication proteins are similar to those of Escherichia coli K-12. The KIM genome sequence was compared with that of Y. pestis CO92, biovar Orientalis, revealing homologous sequences but a remarkable amount of genome rearrangement for strains so closely related. The differences appear to result from multiple inversions of genome segments at insertion sequences, in a manner consistent with present knowledge of replication and recombination. There are few differences attributable to horizontal transfer. The KIM and E. coli K-12 genome proteins were also compared, exposing surprising amounts of locally colinear "backbone," or synteny, that is not discernible at the nucleotide level. Nearly 54% of KIM ORFs are significantly similar to K-12 proteins, with conserved housekeeping functions. However, a number of E. coli pathways and transport systems and at least one global regulator were not found, reflecting differences in lifestyle between them. In KIM-specific islands, new genes encode candidate pathogenicity proteins, including iron transport systems, putative adhesins, toxins, and fimbriae.


Related Papers

No related papers found

Powered by citation graph analysis