Rickettsia chlamydia presentation
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This document discusses Rickettsia and Chlamydia, which are obligate intracellular organisms. It describes the genera of Rickettsia including Rickettsia, Ehrlichia, Coxiella, and Bartonella. Key differences between Rickettsiae and Chlamydiae include that Rickettsiae contain cytochromes and have aerobic metabolism while Chlamydiae do not contain cytochromes and have anaerobic metabolism. Both multiply within host cells. The document also discusses pathogenesis, diagnosis, treatment, and control of diseases caused by these organisms.
Rickettsia chlamydia presentation
- 1. RICKETTSIA & CHLAMYDIA Hoza, A.S BLS 206
- 2. Introduction. • Rickettsiae and Chlamydiae- obligate intracellular organisms.(classif. as bacteria) • Rickettsia General features: -parasites of gut cells of athropods. -transmittion- athropod to animal.
- 3. Genera of the Family Rickettsiaceae: 1.Rickettsia -11 spp (do not multiply within vacuoles & do not parasitize wbcs. 2. Ehrlichia: - 2 spp obligate intracellular parasites – do not multiply within vacuoles but do parasitize wbcs.
- 4. Rickettsia. • 3. Coxiella: – (1 spp) obligate parasite –grows preferentially in vacuoles of host cells. • 4. Baartonella – 3 spp - intracellular parasite which attacks the rbc.
- 5. Fundamental differences btn Chlamydiae and rickettsiae. Rickettsiae Chlamydiae Cytochromes +ve No cytochromes Aerobic metabolism Anaerobic metabolism. Multiply by binary fision. Single development cycle.
- 6. Similarities Small, pleomorphic coccobacillary forms Obligate intracellular parasites. All contain DNA and RNA. Susceptible to various antibiotics. Cell walls resemble those of Gram –ve bacteria. Require exogenous cofactors from animal cells. Most grow readily in the yolk sac of embryonated eggs and in cell cultures.
- 7. Structure of Rickettsia. • Typical rickettsia – Very similar to that of gram-negative bacteria. • Typical envelope: – Innermost cytoplasmic membrane, a thin electron dense rigid cell wall & outer layer • Cell wall – Chemically similar to Gram-ve bacteria i.e contains diamino pimelic acid and no techoic acid. • No discrete nuclear structure.
- 8. Metabolism In dil.buffered salt soln: – Unstable, losing both metabolic activity and infectivity for animal cell. In enriched medium: – Can survive for may hrs. Basis for obligate parasitism: – Require rich cytoplasm to stabilize unusually permeable cell membrane. Require exogenous supply of cofactors.
- 9. Growth and Multiplication. Transverse binary fission. Under poor nutrition: long filamentous forms. Immediately after division: – Extensive movements through the cytoplasm of the cell. NB: C.burnetii: – Enclosed in a persistent vacuole during growth and division. 6-10 daughter cells form within the host cell before ruptures and releases them.
- 10. Host defenses • Both Cellular and Humoral immunity may be important.
- 11. Epidemiology • Endemic (murine) typhus: – primarily maintained in rodent populations. – transmitted via the flea. – Humans ( accidental host). • Spotted fever: – Found predominantly in animals. – Transmitted by the tick. – Humans (accidental hosts). • Q fever: – Mostly in animals. – Humans acquire disease primarily by inhalation of contaminated aerosols. • Epidemic typhus and trench fever: – transmitted from human to human via the louse.
- 12. Pathogenicity – Transmittion: via arthropod vectors; • Q fever : – via inhalation or ingestion of contaminated milk or food. • The bacteria enter host endothelial cells via an induced phagocytosis. – Phospholipase A may help in penetration. • Replication of the bacteria causes lysis of the host cell and consequent spread to other cells. • Initial replication: – At the site of entry producing a local lesion. – Followed by dissemination via the vascular system producing vasculitis and a skin rash.
- 13. Pathogenesis... – The lesions may become necrotic • Virulence : – Probably due to many factors including: • release of endotoxin, • production of immune complexes • hypersensitivity reactions. • A characteristic triad of symptoms include: – fever, – headache and – rash (no rash with Q fever).
- 14. Diagnosis. • Clinical: • These diseases present as: – febrile illnesses after exposure to arthropods or animal hosts or aerosols ( endemic areas). – High mortality from Spotted fever (delayed diagnosis). • The spread of the rash ( characteristic): – spread from the trunk to the extremities (centrifugal)- typical for typhus; – spread from the extremities to the trunk (centripetal) -typical for spotted fever.
- 15. Diagnosis… Laboratory: 1. Macchiavello stain: - organisms bright red V blue background. 1. Castaneda stain: - blue organisms V red background. 1. Giemsa stain: - bluish purple organisms. 4. Use of immunofluorescent antibodies: NB: The organism can be inoculated into tissue culture and grown over 4-7 days (very hazardous to personnel).
- 16. Diagnosis… Confirmative diagnosis: • Serological reaction:(Weil-Felix test): – The production of serum antibody reactive against Proteus OX19, OX2 or OXK antigens is determined • Embryonated eggs. – (Q- Fever) • Cell cultures.
- 17. Important Rickettsial diseases of animals Heartwater: Tropical canine Pancytopenia. Equine and Canine Ehrlichiosis. Q- Fever Potomac horse Fever. Salmon poisoning.
- 18. Rickettsia of Public health significance Tick-borne:- • Rocky mountain spotted fever (R.rickettsii) – Reservoir (Dog, rodents) • Q-Fever (C. burnetii) – Reservoir (cattle, shoat) • Spotted Fever (R.rhipicephali) – Reservoir (dogs) • Ehrlichiosis (E.canis) – Reservoir (dogs)
- 19. Public health… Louse-borne: 1. European epidemic typhus (R.prowazekii) -No animal reservoir 1. Trench Fever (Bartonella) - No animal reservoir. Flea-borne: 1. Endemic murine typhus (R.typhi) -Reservoir- Wild rodents
- 20. Public health…. 2.Cat scratch fever/bacillary angiomatosis (Bartonella henselae) Reservoir (domestic cat) Mite-borne: • Scrub typhus(R. tsutsugamushi)reservoir- wild rodents. • Rickettsialpox (r.akari) reservoir House mice. Fly-borne: • Oroyo fever/ Verruga peruana (B. bacilliformis) Reservoir ??
- 21. Treatment & Control • Chemotherapeutic: – Tetracycline or – Chloramphenicol • Sanitary: – Arthropod and rodent control are possible but difficult. • Immunological: – No vaccines - currently available.
- 22. Chlamydia General characteristics • Species: trachomatis, psittaci • The Chlamydia – Obligate intracellular parasites. • C. trachomatis – Trachoma, – Inclusion conjunctivitis, – Lymphogranuloma venereum (LGV) – nongonococcal urethritis (NGU). I.e, oculourogenital infections. • C. psittaci produces systemic diseases: – psittacosis, – ornithosis and – pneumonitis.
- 23. Distinctive properties. • Have two distinct forms:- – Infectious elementary bodies and – Intracellular reticulate bodies. • Elementary bodies attach and are internalized by susceptible host cells. • Once inside, they reorganize into a replicative form (the reticulate body) • Over a 24 hour period: – Reticulate bodies divide and begin to reorganize back into elementary bodies.
- 24. Distinctive properties… • 48-72 hours after infection: – The cell is lysed and – numerous infectious elementary bodies released. • The genome of Chlamydia is only 25% the size of E. coli (i.e one of the smallest prokaryotes). • The pathogenic mechanisms employed by Chlamydia - not well understood.
- 26. Metabolism. • No detectable flavoproteins or cytochrome. • Basis of obligate intracelluar parasitism – lack of ATP-generating ability – Obtain ATP from the host cell. • The cells can synthesize : – DNA – RNA and – Protein.
- 27. Pathogenesis. • C. psittaci is acquired from infected birds, usually via the respiratory route. • C. trachomatis is spread via the fingers to the urogenital area and vis versa. • Trachoma: – Infection of the epithelial cells of the conjunctiva, producing inclusion bodies. – Vascularization and clouding of cornea along with trichiasis (inward growth of eyelashes) ---- produce scarring leading to blindness.
- 28. Pathogenesis…. • Inclusion conjunctivitis – Milder form, – Occurs in both children and adults. • Sexually transmitted nongonococcal urethritis (NGU): – Similar to gonorrhea – Occurs with greater frequency. • Lymphogranuloma venereum (LGV) involving inguinal lymphadenopathy ("buboes") can occur in men
- 29. Host defenses. • Chlamydia induce interferon and are sensitive to it. • During infection, antibodies are synthesized but recovery is not generally protective.
- 30. Epidemiology. • Trachoma: – prevalent in Africa and Asia, – generally in hot and dry areas. • The organisms are very persistent. – Their habitat : similar to that of Neisseria and Haemophilus. • Infection can occur via: – swimming in unchlorinated pools, – sharing towels or – by passage through the birth canal.
- 31. Diagnosis • Clinical: – Diagnosis of trachoma is usually good. – Genital vesicles associated with LGV are characteristic. – NGU can only be suspected in the absence of laboratory findings. • Laboratory: – Iodine stained specimens usually show inclusion bodies. • Tissue culture: – Chlamydia can be cultured in tissue culture and appropriate serological tests performed
- 32. Diagnosis Serological diagnosis: • Micro-immunofluorescent tests in tears of patients with eye infections for presence of anti-chlamydia Ab. • Delayed –type skin rexn (hypersensitivity Type IV) (Frei-test) • Rising titer of Ab V chlamydial family Ag in lung infections.
- 33. Treatment and Control. • Chlamydia exhibit low pathogenicity in a compromised host. • Chemotherapeutic: – Tetracycline or erythromycin are drugs of choice. • Sanitary: – Good hygiene, – Treatment of sexual partners and – Quarantine of birds all reduce the incidence.
- 34. Treatment and control. • Immunological: – No vaccine – available since specific antibodies fail to neutralize elementary bodies in vivo. NB: • Chlamydial d’ses –relatively easy to treat, but: 1.Latency of infection 2.Susceptibility to reinfection.