Publication | Open Access
Complete genome sequence of the Q-fever pathogen<i>Coxiella</i><i>burnetii</i>
566
Citations
49
References
2003
Year
Coxiella burnetii is an obligate intracellular acidophile adapted to the eukaryotic phagolysosome, and its genome architecture differs markedly from related pathogens such as Rickettsiae and Chlamydiae in mobile elements, genome reduction, metabolism, and transporters. The 1,995,275‑bp genome of Coxiella burnetii (Nine Mile phase I RSA493) was sequenced using random shotgun sequencing. Genome analysis identified numerous genes involved in adhesion, invasion, intracellular trafficking, host‑cell modulation, and detoxification, including a novel 13‑member ankyrin repeat protein family, 83 pseudogenes, and 32 dispersed insertion sequences, indicating ongoing gene degradation, genomic plasticity, and a relatively recent evolution of its intracellular lifestyle.
The 1,995,275-bp genome of Coxiella burnetii , Nine Mile phase I RSA493, a highly virulent zoonotic pathogen and category B bioterrorism agent, was sequenced by the random shotgun method. This bacterium is an obligate intracellular acidophile that is highly adapted for life within the eukaryotic phagolysosome. Genome analysis revealed many genes with potential roles in adhesion, invasion, intracellular trafficking, host-cell modulation, and detoxification. A previously uncharacterized 13-member family of ankyrin repeat-containing proteins is implicated in the pathogenesis of this organism. Although the lifestyle and parasitic strategies of C. burnetii resemble that of Rickettsiae and Chlamydiae , their genome architectures differ considerably in terms of presence of mobile elements, extent of genome reduction, metabolic capabilities, and transporter profiles. The presence of 83 pseudogenes displays an ongoing process of gene degradation. Unlike other obligate intracellular bacteria, 32 insertion sequences are found dispersed in the chromosome, indicating some plasticity in the C. burnetii genome. These analyses suggest that the obligate intracellular lifestyle of C. burnetii may be a relatively recent innovation.
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