Complete Genome Sequence ofRickettsia typhiand Comparison with Sequences of Other Rickettsiae

作者
Michael P. McLeod,Xiang Qin,Sandor E. Karpathy,Jason Gioia,Sarah K. Highlander,George E. Fox,Thomas Z. McNeill,Huaiyang Jiang,Donna M. Muzny,Leni S. Jacob,Alicia Hawes,Erica Sodergren,Rachel Gill,Jennifer Hume,Maggie Morgan,Guangwei Fan,Anita G. Amin,Richard A. Gibbs,Chao Hong,Xue‐jie Yu
出处
期刊:Journal of Bacteriology [American Society for Microbiology]
卷期号:186 (17): 5842-5855 被引量:240
标识
DOI:10.1128/jb.186.17.5842-5855.2004
摘要

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 Inversions in this region are also seen in the unpublished genome sequences of R. sibirica and R. rickettsii, indicating that this region is a hot spot for rearrangements.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.

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