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بسم الله الرحمن الرحيم GENERA: TREPONEMA & BORREILIA Prof. Khalifa Sifaw Ghenghesh.

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Presentation on theme: "بسم الله الرحمن الرحيم GENERA: TREPONEMA & BORREILIA Prof. Khalifa Sifaw Ghenghesh."— Presentation transcript:

1 بسم الله الرحمن الرحيم GENERA: TREPONEMA & BORREILIA Prof. Khalifa Sifaw Ghenghesh

2   Unicellular helical or spiral rod- shaped spirochaetes.   Actively motile – –Flagella attached at each pole of the cell and wrap around the bacterial cell body – –Flagella are enclosed within the bacterial outer membrane

3 Treponema   Do not stain by Gram’s method   Pathogenic Treponema – –T. pallidum – –T. pertenue – –T. endemicum – –T. carateum – –Cannot be cultivated in laboraotry media – –Maintained by subculture in susceptible animals – –Differentiation of organisms is based primarily on clinical syndromes – –Micro-aerophilic

4 Treponema pallidum   Syphilis – –Acquired by sexual contact with infected person   Congenital Syphilis – –Infected mother to fetus in utero or during passage of neonates through infected canal (vertical transmission)

5 PATHOGENESIS   Untreated the disease may progress to Primary, Secondary, latent and Tertiary stages.   Primary syphilis – –Organism penetrates intact mucosae > lymphatics > disseminates via blood to any organ – –Multiplies at entry site > ~ 3 weeks > painless chancre (mainly on external genitalia). – –Chancre heals spontaneous in 3-6 weeks

6   Secondary syphilis – –Appear 2-12 weeks – – Symptoms are highly variable but mainly involve the skin (macular or pustular lesion) – –Lesions are highly infectious and gradually resolve   Latent syphilis – –No clinical manifestations are seen but serological evidence of infection remains – –Individuals are not generally infectious but can transmit infection to the fetus during pregnancy – –Their blood can be infectious

7   Tertiary syphilis – –May develop decades after primary syphilis – –A slowly progressive, destructive inflammatory disease > affects any organ   Neurosyphilis   Cardiovascular syphilis   Gummatous syphilis

8 Histopathology showing Treponema pallidum spirochetes. Modified Steiner silver stain.

9 Treponema pallidum darkfield preparation

10 Light microscope pictures showing tissue infected with the spirochete Treponema pallidum, the causative agent of syphilis.

11 Treponema organisms stained by fluorescent-tagged antibodies.

12 Treponema pertenue – –Yaws – –Rural population in subtropical countries – – Non-venereal, after contact of traumatized skin with exudate from early yaws lesion – –Primary yaws (3-5 weeks) > lesions on the legs >> papular lesions >> enlarge erode and heal spontaneously within 6 months > may erupt weeks or months later. – –Secondary lesions > bones (fingers, long bones and jaw) – –Late yaws > cutaneous plaques and ulcers and thickening of the skin on the palms and soles of the feet.   No neurological and cardiovascular damage – – No congenital yaws

13 Treponema endemicum – –Bejel (endemic syphilis) – –Non-venereal, affects mainly children rural populations in Africa, western Asia and Australia – –Direct person to person contact and by sharing contaminated eating and drinking utensils – –Initial lesion > oral – –Secondary lesions > oropharyngeal mucous patches, condyloma lata and periostitis – –Late lesion > gummata in the skin, nasopharynx and bones   No neurological and cardiovascular damage – – congenital bejel is rare

14 Treponema carateum   Pinta   Rural regions of Mexico, Central America and Colombia   Confined to the skin   Non-destructive lesion but cause disfigurement   Direct contact with infectious lesions resulting in depigmented lesions which are characteristic of late stages of pinta with no serious harm

15 LABORATORY DIGNOSIS   Direct Microscopy – –Specimen: fresh exudate from primary or secondary lesions – –Examine with dark-ground or phase contrast microscopy   Serological Tests - T. pallidum infection > 2 types of Abs – –Specific Abs against polypeptide Ags of the bacterium – –Non-specific Abs reacts with a non- treponemal Ag > Cardiolipin

16 1. Non-Specific Serological Test   The Venereal Disease Reference Laboratory (VDRL) Test - Mixture of Cardiolipin, cholestrol and licithin as Ag - IgM or IgG Ab in positive serum or CSF from neurosyphilis case causes a suspension of lipoidal Ag to flocculate > read by the eye - Used as a screening test > – –70% of primary and 99% of secondary syphilis cases are positive – –Negative in late syphilis - Quantitatively > diagnosis of congenital syphilis - To monitor the efficacy of antibiotic therapy

17 2. Tests for Specific Antibody i. Fluorescent treponemal Ab (FTA-Abs) test – –Indirect immunofluorescence assay – –T. pallidum = Ag – –Acetone-fixed treponemes incubated with heat- treated sera > bound Ab detected by fluorescin-labelled conjugate and UV microscopy – –Positive in 80% primary, 100% secondary and 95% late syphilis patients. – –Remain positive after treatment

18 ii. T. pallidum haemagglutination assay (TPHA) - RBCs coated with T. pallidum Ag - Specific Ab in test sera >> haemaggluination - Positive in 65% primary, 100% secondary and 95% late syphilis patients. -Remains positive for life iii. Other Antibody tests - Monoclonal ant-T. pallidum Abs > ELISA - Detects Ab response individual treponemal Ags - Rapid screening of large number of samples

19 TREATMENT   Primary and Secondary Syphilis – –Prolonged high dose of procaine penicillin – –Erythromycin, tetracycline or choramphenicol   Late Syphilis – –Aqueous benzylpenicillin

20 CONTROL   Treating index cases and any known contacts

21 Borrelia   Gram-negative   Cause Relapsing fevers   Transmitted by arthropod vectors   Characterized clinically by recurrent periods of fever and spirochaetaemia   Disease occur world-wide

22 Borrelia recurrentis   Cause epidemic or louse-borne Relapsing fever – – An obligate human pathogen – – Person-to-person transmission by the body louse Pediculus humanus

23 Other Borrelia   B. duttoni   B. hermsii   B. parkeri   B. turicatae   Cause endemic or thick-borne relapsing fever   Transmitted to humans by soft-bodied Ornithodorus ticks   Natural hosts – –Rodents and other small mammals

24 LABORATORY DIAGNOSIS   Specimen – –Peripheral blood   Thick or thin blood smears stained with Giemsa, acridine orange or other stains   Serological tests – –Not reliable (due to antigenic variation) and not widely available

25 TREATMENT AND CONTROL   Tetracycline, Erythromycin, chloramphenicol and penicillin   Prevention – –Avoidance or eradication of the insect vector – –Eradication of ticks from human dwellings using insecticides – –Louse-borne infection   Good personnel hygiene   If necessary >> delousing


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