In today's world, Rickettsia conorii has become a topic of great relevance and interest both on a personal level and in society in general. With the advancement of technology and globalization, Rickettsia conorii has acquired unprecedented importance in our daily lives. In this article, we will explore in detail Rickettsia conorii and its impact on various aspects, from its influence on the economy to its role in popular culture. Through deep and insightful analysis, we will unravel the mysteries and complexities surrounding Rickettsia conorii, providing a clear and comprehensive view of its relevance in today's world.
Rickettsia conorii | |
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Rickettsia conorii observed in Vero cells (red rods; magnification ×1,000)[1] | |
Scientific classification ![]() | |
Domain: | Bacteria |
Kingdom: | Pseudomonadati |
Phylum: | Pseudomonadota |
Class: | Alphaproteobacteria |
Order: | Rickettsiales |
Family: | Rickettsiaceae |
Genus: | Rickettsia |
Species group: | Spotted fever group |
Species: | R. conorii
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Binomial name | |
Rickettsia conorii |
Rickettsia conorii is a Gram-negative, obligate intracellular bacterium of the genus Rickettsia that causes human disease called boutonneuse fever, Mediterranean spotted fever, Israeli tick typhus, Astrakhan spotted fever, Kenya tick typhus, Indian tick typhus, or other names that designate the locality of occurrence while having distinct clinical features.[3][4] It is a member of the spotted fever group and the most geographically dispersed species in the group, recognized in most of the regions bordering on the Mediterranean Sea and Black Sea, Israel, Kenya, and other parts of North, Central, and South Africa, and India.[3] The prevailing vector is the brown dog tick, Rhipicephalus sanguineus. The bacterium was isolated by Emile Brumpt in 1932[5] and named after A. Conor, who in collaboration with A. Bruch, provided the first description of boutonneuse fever in Tunisia in 1910.[6]
The genome of the bacterium has been sequenced and four subspecies have been identified.[7][8][9][10][11]
Genomes of intracellular or parasitic bacteria undergo massive reduction compared to their free-living relatives. Examples include Rickettsia for alpha proteobacteria, T. whipplei for Actinobacteria, Mycoplasma for Firmicutes (the low G+C content Gram-positive), and Wigglesworthia and Buchnera for gamma proteobacteria.[12]
Some of the largest virions like Megavirus chilense, Pandoravirus, Pithovirus and Mimivirus are comparable in size to miniature bacteria like T. whipplei and Rickettsia conorii.
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