Genome sequence of Yersinia pestis KIM

被引:427
作者
Deng, W
Burland, V
Plunkett, G
Boutin, A
Mayhew, GF
Liss, P
Perna, NT
Rose, DJ
Mau, B
Zhou, SG
Schwartz, DC
Fetherston, JD
Lindler, LE
Brubaker, RR
Plano, GV
Straley, SC
McDonough, KA
Nilles, ML
Matson, JS
Blattner, FR
Perry, RD
机构
[1] Univ Wisconsin, Genet Lab, Madison, WI 53706 USA
[2] Univ Wisconsin, Genome Ctr, Madison, WI 53706 USA
[3] Univ Wisconsin, Dept Anim Hlth & Biomed Sci, Madison, WI 53706 USA
[4] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
[5] Univ Kentucky, Dept Microbiol & Immunol, Lexington, KY 40536 USA
[6] Walter Reed Army Inst Res, Div Communicable Dis & Immunol, Dept Bacterial Dis, Washington, DC 20307 USA
[7] Michigan State Univ, Dept Microbiol & Mol Genet, E Lansing, MI 48824 USA
[8] Univ Miami, Sch Med, Dept Microbiol & Immunol, Miami, FL 33176 USA
[9] Wadsworth Ctr, David Axelrod Inst, Albany, NY 12201 USA
[10] Univ N Dakota, Sch Med & Hlth Sci, Dept Microbiol & Immunol, Grand Forks, ND 58202 USA
关键词
D O I
10.1128/JB.184.16.4601-4611.2002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
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页码:4601 / 4611
页数:11
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