Complete Genome Sequence of Rickettsia typhi and Comparison with Sequences of Other Rickettsiae

Author:

McLeod Michael P.12,Qin Xiang1,Karpathy Sandor E.12,Gioia Jason3,Highlander Sarah K.3,Fox George E.4,McNeill Thomas Z.14,Jiang Huaiyang1,Muzny Donna1,Jacob Leni S.1,Hawes Alicia C.1,Sodergren Erica1,Gill Rachel1,Hume Jennifer1,Morgan Maggie1,Fan Guangwei1,Amin Anita G.1,Gibbs Richard A.1,Hong Chao5,Yu Xue-jie5,Walker David H.5,Weinstock George M.132

Affiliation:

1. Human Genome Sequencing Center

2. Department of Microbiology and Molecular Genetics, University of Texas Health Science Center at Houston, Houston

3. Department of Molecular Virology and Microbiology, Baylor College of Medicine

4. Department of Biology and Biochemistry, University of Houston

5. Department of Pathology, University of Texas Medical Branch, Galveston, Texas

Abstract

ABSTRACT Rickettsia typhi , the causative agent of murine typhus, is an obligate intracellular bacterium with a life cycle involving both vertebrate and invertebrate hosts. Here we present the complete genome sequence of R. typhi (1,111,496 bp) and compare it to the two published rickettsial genome sequences: R. prowazekii and R. conorii . We identified 877 genes in R. typhi encoding 3 rRNAs, 33 tRNAs, 3 noncoding RNAs, and 838 proteins, 3 of which are frameshifts. In addition, we discovered more than 40 pseudogenes, including the entire cytochrome c oxidase system. The three rickettsial genomes share 775 genes: 23 are found only in R. prowazekii and R. typhi , 15 are found only in R. conorii and R. typhi , and 24 are unique to R. typhi . Although most of the genes are colinear, there is a 35-kb inversion in gene order, which is close to the replication terminus, in R. typhi , compared to R. prowazekii and R. conorii . In addition, we found a 124-kb R. typhi -specific inversion, starting 19 kb from the origin of replication, compared to R. prowazekii and R. conorii . Inversions in this region are also seen in the unpublished genome sequences of R. sibirica and R. rickettsii , indicating that this region is a hot spot for rearrangements. Genome comparisons also revealed a 12-kb insertion in the R. prowazekii genome, relative to R. typhi and R. conorii , which appears to have occurred after the typhus ( R. prowazekii and R. typhi ) and spotted fever ( R. conorii ) groups diverged. The three-way comparison allowed further in silico analysis of the SpoT split genes, leading us to propose that the stringent response system is still functional in these rickettsiae.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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