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Treponema SPP

Treponema spp. are thin, helical, gram-negative spirochetes responsible for diseases such as syphilis and yaws. Syphilis presents in stages, with primary, secondary, and tertiary forms, and can lead to severe complications if untreated. Diagnosis is primarily through serologic tests, and treatment typically involves penicillin, with prevention focused on safe sex practices.
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0% found this document useful (0 votes)
20 views21 pages

Treponema SPP

Treponema spp. are thin, helical, gram-negative spirochetes responsible for diseases such as syphilis and yaws. Syphilis presents in stages, with primary, secondary, and tertiary forms, and can lead to severe complications if untreated. Diagnosis is primarily through serologic tests, and treatment typically involves penicillin, with prevention focused on safe sex practices.
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TREPONEMA SPP.

Treponema
• These spirochetes are thin, helical, gram-negative bacteria.

• The order Spirochaetales is subdivided into three families and 13 genera, of which
three (Treponema, Borrelia, and Leptospira) are responsible for human diseases.
Spirochete
Treponema
• The two treponemal species that cause human disease are Treponema pallidum (with
three subspecies) and Treponema carateum.
• All are morphologically identical.
• Produce the same serologic response in humans.
• Susceptible to penicillin.
• The organisms are distinguished by their epidemiologic characteristics and clinical
presentation.
Treponema
• T. pallidum subspecies pallidum is the etiologic agent of the venereal disease syphilis
• T. pallidum subspecies and endemicum causes endemic syphilis (bejel).
• T. pallidum subspecies pertenue causes yaws
• T. carateum cause pinta.
• Bejel, yaws and pinta are nonvenereal diseases
Pinta
yaws
Treponema
• T .Pallidum and related pathogenic treponems are thin, tightly coiled spirochetes with pointed,
straight ends.
• Three flagellae are inserted at each end.
• These spirochetes do not grow in cell-free cultures/synthetic media.

• Are too thin to be seen with light microscopy in specimens stained with Gram or Giemsa stain.

• visualized by dark-field microscopy or by staining with specific antitreponemal antibodies


labeled with flourescent dyes.
Epidemiology
• Syphilis is found worldwide
• The third most common sexually transmitted bacterial disease
• incidence of disease has decreased since the advent of penicillin therapy.
• Periodic increases have been observed that correspond to changes in sexual
practices.
CLINICAL DISEASES
Primary Syphilis
• Syphilitic chancre develops at the site where the spirochete is inoculated. Lesion starts as a
papule but then erodes to become a painless ulcer with raised borders

• A painless regional lymphadenopathy develops 1 to 2 weeks after the appearance of the


chancre.

• This ulcer heals spontaneously within 2 months, gives the patient a false sense of relief.
Secondary syphilis
• Flulike
syndrome with sore throat , headache, fever, myalgias, anorexia,
lymphadenopathy and generalised mucocutaneous rash.

• The rash cover the entire skin surface (including the palms and soles).

• As with the primary chancre, the rash in secondary syphilis is highly infectious.
Tertiary (Late) Syphilis
• Cause a destruction of virtually any organ or tissues(arteritis, dementia, blindness).

• Granulomatous lesions (gummas) in bone, skin and other tissues.


• The nomenclature of late syphilis reflects the organs of primary involvement (Neurosyphilis,
cardiovascular syphilis).

• Tabes dorsalis/ syphilitic myelopathy: demyelination of dorsal columns. Responsible for


proprioception, vibration and discriminative touch.
Congenital Syphilis
• Can lead to latent infections , multiorgan malformations, death of the fetus.

• Teeth (Hutchinson teeth) and bone malformation, blindness, deafness, facial defects
are common in untreated infants.

• Seizures, hepatosplenomegaly, anemia, jaundice


LABORATORY DIAGNOSIS
• Dark-field examination of the exudate from the skin lesion.

• Reliable only when an experienced microscopist immediately examines the clinical


material with actively motile spirochetes.
• Fluorescent-labelled antitreponemal antibodies are used to stain the bacteria.
serology
• Syphilis is diagnosed in most patients on the basis of serologic tests.
• Two general types of tests are biologically nonspecific (non-treponemal) tests and
specific treponemal tests.
Nontreponemal tests
• Antigen used for the nontreponemal tests is cardiolipin

• Developed against lipids released from the damaged cells during the early stages of disease and
present on the cell surface of treponems.

• the Venereal disease Research Laboratory (VDRL) test and the Rapid plasma Reagin (RPR) test.
Nontreponemal tests
• Successful treatment of primary or secondary syphilis leads to reduced titers
measured in VDRL and RPR tests.

• These test can be used to monitor the effectiveness of therapy


Treponemal tests
• Are specific antibody tests used to confirm positive reactions with the VDRL or RPR
tests.

• The test most commonly used are the fluorescent treponemal antibody-absorption
(FTA-ABS) test and Treponema pallidum particle agglutination(TP-PA) test.
Serologic test in infants of the infected mothers
• Represent a passive transfer of antibodies or a specific immunologic response to
infection.
• These two possibilities are distinguished by measuring the antibody titers of the
infant during a 6 month period.

• Antibody titers in non-infected infants decrease to undetectable levels within 3


months of birth but remain elevated in infants who have congenital syphilis
Treatment
• Benzathine penicillin for early stages and Penicillin G for congenital and late syphilis.

• Tetracycline and doxycycline for patients allergic to penicillin


PREVENTION AND CONTROL
• No vaccines
• Safe-sex and treatment of sex partners.

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