Rickettsia Presentation
Rickettsia Presentation
Rickettsia Presentation
The supervisors: Mr. Abed Elkader Elottol Collected by: Ahmad al-Aswad
Content
Name of the pathogen General characteristics Virulence factors Diseases Cultural characters Sample collection world distribution Vaccine Discovery Classification Pathogenicity transmission routes Weil-Felix test Identification Treatment References
Discovery
Discovered form of tick-borne typhus first described in the Rocky Mountain section of the United States, caused by a specific microorganism (Rickettsia rickettsii). Discovery of the microbe of Rocky Mountain spotted fever in 1906 by Howard Taylor Ricketts led to the understanding of other rickettsial diseases.
General characteristics
Highly pleomorphic bacreria that can present as cocci (0.1 m in diameter), rods (14 m long) or thread-like (10 m long). Rickettsiaceae are Gram-negative, obligate intracellular bacteria (except Rochlimaea) that infect mammals and arthropods. Gram stain poorly, but appear to be G Stain readily with Giemsa . Traditional biochemical tests are useless because it cant cultivated in ordinary medias.
Classification
Usually rickettsia classified by the disease it cause to two groups : 1. Spott fever group (SFG)
Rickettsia
species Typhus group: Disease Epidemic typhus Recrudescent typhus
Human Humans body lice None Fleas Fleas Fleas Ticks Ticks Humans Rodents Opossums Opossums
Murine typhus (Endemic typhus) Murine typhus like Rocky Mountain spotted fever Boutonneuse fever
Spotted Fever group: Small mammals, North & South dogs, rabbits, birds America Rodents, dogs Africa, Southern Europe, India
R. sibirica
R. japonica R. australis R. akari
Ticks
Ticks Ticks Mites
Rodents
Rodents, dogs Rodents House mice, rats
Eurasia, Asia
Japan Australia Worldwide
Virulence factors
1. Group specific soluble antigens compose from lipopolysaccharide and consider from the major cell wall component, used in vaccine production. 2. Species specific antigen Used to differentiate between rickettsia species, heat labile antigen. 3. Alkali stable polysaccharide antigen Found in many rickettsiae and is shared by certain strains of Proteus vulgaris.
5. The enzyme phospholipase A may help penetration. 6. Induced phagocytosis and recruitment of actin for intracellular spread. 7. R. Canadensis haemolyses red blood cells, is susceptible to erythromycin.
Pathogenicity
On entry to human body
Organism multiplies locally & enters the blood stream
Epidemic typhus
Causative organism: R.prowazekii . Vector: Pediculus humanus corporis (human body louse). Transmission: Autoinoculation by the person while scratching the bite of infected body louse produce abrasion- which is portal of entry for the organisms. Incubation Period: 6-15 days. It is associated with wars & poverty. It is found in Africa & South America but not in United States. Symptoms: Chills, fever, headache, pain, stupor and delerium. Signs of severe meningoencephalitis, begin with rash. If untreated - death occurs due to peripheral vascular collapse or due to bacterial pneumonia. R. prowazekii is the agent of epidemic typhus. During World War I, approximately 3 million deaths resulted from infection by this bacterium. In World War II, the numbers were similar. This agent is carried by the human louse; therefore, disease is a consequence of overcrowding and poor hygiene.
Cultural characters
Do not grow on cell-free media. They can be cultivated in the yolk sacs of embryonated eggs. Can be cultivated on cell cultures HeLa, HEp2, Detroit 6 etc. Laboratory animal like mice is used for primary isolation . The following nutrients are added to cell media : serine , glycine , Other nonessential amino acids, additional glucose, and potential products.
Weil-Felix test
Weil-Felix test is based on cross reaction of the rickettsial antigen with the O antigen polysaccharide found in Proteus vulgaris OX-19, OX-2 and OX-K. The test measures the antiricketssial Ab in patients serum.
Sample collection
Coetaneous lesions are the symptoms which is in common between all rickettsial diseases, so, sample obtain mainly from skin lesions.
Identification
If you do a skin biopsy, you can make a diagnosis in a day or so. Some people dont bother to do a biopsy. Although the biopsy is 100% specific, it sometimes gives dangerous false negative reports. Later, you can confirm your diagnosis by doing tests for antibodies, or serology. The old tests, the Weil-Felix tests, are now archaic. Laboratories now have immunofluorescent antibody (IFA), or ELIZA assays. The problem is that you have to wait a couple weeks before you can expect the antibodies to develop and draw the blood for the convaslescent titers.
world distribution
R. conorii Astrakhan R. helvetica R. sibirica R. mongolotimonae
R. heilongjiangii
R. slovaca
R. conorii Isral
R. conorii R. rickettsii R. conorii R. australis R. africae R. honei
R. japonica
References
MIMS: chapter 21. Levinson: chapter 26. Bairley: chapter 39. Emanuel: chapter 28. Jawetz: chapter 27. Kayser: unit 4. http://www.textbookofbacteriology.net/Rick ettsia_2.html. http://en.wikipedia.org/wiki. http://www.cehs.siu.edu/fix/medmicro/ricke. htm. others.