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Letter
Nature Genetics  21, 385 - 389 (1999)
doi:10.1038/7716

Comparative genomes of Chlamydia pneumoniae and C. trachomatis

Sue Kalman1, Wayne Mitchell2, 3, Rekha Marathe1, Claudia Lammel2, Jun Fan1, Richard W Hyman1, Lynn Olinger2, 3, Jane Grimwood3, Ronald W Davis1 & Richard Stephens2, 3

1  Stanford DNA Sequencing and Technology Center, Stanford University, Stanford, California 94305, USA.

2  Program in Infectious Diseases, University of California, Berkeley, California 94720, USA.

3  Francis I. Proctor Foundation, University of California, San Francisco, California 94143, USA.

Correspondence should be addressed to Richard Stephens ctgenome@socrates.berkeley.edu
Chlamydia are obligate intracellular eubacteria that are phylogenetically separated from other bacterial divisions. C. trachomatis and C. pneumoniae are both pathogens of humans but differ in their tissue tropism and spectrum of diseases. C. pneumoniae is a newly recognized species of Chlamydia that is a natural pathogen of humans1, and causes pneumonia and bronchitis. In the United States, approximately 10% of pneumonia cases and 5% of bronchitis cases are attributed to C. pneumoniae infection2. Chronic disease may result following respiratory-acquired infection, such as reactive airway disease3, adult-onset asthma4 and potentially lung cancer5. In addition, C. pneumoniae infection has been associated with atherosclerosis6, 7, 8, 9, 10, 11. C. trachomatis infection causes trachoma, an ocular infection that leads to blindness, and sexually transmitted diseases such as pelvic inflammatory disease, chronic pelvic pain, ectopic pregnancy and epididymitis12. Although relatively little is known about C. trachomatis biology13, even less is known concerning C. pneumoniae. Comparison of the C. pneumoniae genome with the C. trachomatis genome14 will provide an understanding of the common biological processes required for infection and survival in mammalian cells. Genomic differences are implicated in the unique properties that differentiate the two species in disease spectrum. Analysis of the 1,230,230-nt C. pneumoniae genome revealed 214 protein-coding sequences not found in C. trachomatis, most without homologues to other known sequences. Prominent comparative findings include expansion of a novel family of 21 sequence-variant outer-membrane proteins, conservation of a type-III secretion virulence system, three serine/threonine protein kinases and a pair of parologous phospholipase-D-like proteins, additional purine and biotin biosynthetic capability, a homologue for aromatic amino acid (tryptophan) hydroxylase and the loss of tryptophan biosynthesis genes.

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Nature Genetics
ISSN: 1061-4036
EISSN: 1546-1718
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