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PMID: 10192388 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Comparative genomes of Chlamydia pneumoniae and C. trachomatis.

Nature genetics ·Vol. 21 ·No. 4 ·1999-04-00 ·Pages 385-9

Kalman S, Mitchell W, Marathe R, Lammel C, Fan J, Hyman RW, Olinger L, Grimwood J, Davis RW, Stephens RS

Abstract

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 humans, and causes pneumonia and bronchitis. In the United States, approximately 10% of pneumonia cases and 5% of bronchitis cases are attributed to C. pneumoniae infection. Chronic disease may result following respiratory-acquired infection, such as reactive airway disease, adult-onset asthma and potentially lung cancer. In addition, C. pneumoniae infection has been associated with atherosclerosis. 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 epididymitis. Although relatively little is known about C. trachomatis biology, even less is known concerning C. pneumoniae. Comparison of the C. pneumoniae genome with the C. trachomatis genome 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.

MeSH Terms
Amino Acid Sequence Bacterial Proteins/genetics,metabolism Chlamydia trachomatis/genetics,metabolism,pathogenicity Chlamydophila pneumoniae/genetics,metabolism,pathogenicity Conserved Sequence Enzymes/genetics,metabolism Genome, Bacterial Membrane Proteins/genetics,metabolism Molecular Sequence Data Operon Sequence Homology, Amino Acid Tryptophan/biosynthesis
Chemicals
Bacterial Proteins Enzymes Membrane Proteins Tryptophan
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Kalman S
Stanford DNA Sequencing and Technology Center, Stanford University, California 94305, USA.
Mitchell W
Marathe R
Lammel C
Fan J
Hyman R W
Olinger L
Grimwood J
Davis R W
Stephens R S
Article Info
Journal
Nature genetics
Abbr.
Nat Genet
ISSN
1061-4036
Published
1999-04-00
Pages
385-9
Language
English
Region
United States
NLM ID
9216904
Subset
IM
Databases
GENBANK
AE001273, AE001363
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