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SPIROCHETES

• Spirochetes: Large, heterogeneous group of spiral, motile bacteria.


• Classification: Belong to the order Spirochaetales.
• Human Pathogens:
o Family Spirochaetaceae: Includes Borrelia and Treponema.
o Family Leptospiraceae: Contains the genus Leptospira.
• Shape: Long, slender, helically coiled, spiral, or corkscrew-shaped bacilli.
• Outer Sheath: Presence of a glycosaminoglycan coating.
• Outer Membrane: Contains peptidoglycan, maintains structural integrity.
• Endoflagella: Flagella-like organelles in the periplasmic space, encased by the outer membrane,
extending from both ends to the midpoint.
• Inner Membrane (Cytoplasmic Membrane): Provides osmotic stability, covers the protoplasmic
cylinder.
• Cytoplasmic Tubules (Body Fibrils): Located inside the cell near the inner membrane.
• Reproduction Method: Transverse fission.

Treponema pallidum
• "Treponema" combines Greek "trepo" (to turn) and "nema" (thread), referring to its spiral shape.
• "Pallidum" from Latin means "pale," describing its microscopic appearance.

MORPHOLOGY AND IDENTIFICATION


• Structure: Slender spirals, approximately 0.2 μm wide and 5–15 μm long, with regularly spaced
spiral coils.
• Movement: Actively motile, rotating around endoflagella; can form a circle temporarily.
• Visibility: Difficult to see without immunofluorescent stain or dark-field illumination; does not
stain well with aniline dyes but visible with silver impregnation.
(Dark field microscopy)

(modified Steiner silver stain method)

CULTURE
• Limitations: Pathogenic T. pallidum has never been successfully cultured in artificial media,
fertile eggs, or tissue culture.
• Viability: Remains motile for 3–6 days at 25°C in suitable fluids; viable for at least 24 hours in
whole blood or plasma at 4°C.

REACTION TO CHEMICAL AND PHYSICAL AGENTS


• Susceptibility: Rapidly killed by drying, high temperature (42°C), and certain chemical agents
(arsenical, mercury, bismuth).
• Penicillin: Treponemicidal at low concentrations; no resistance demonstrated, slow killing rate
due to organism's metabolic inactivity and slow multiplication.

GENOME
• Size and Structure: Circular chromosome of approximately 1,138,000 base pairs, relatively small
for bacteria.
• Characteristics: Lack of transposable elements suggests a highly conserved genome; reliant on
host for energy production and nutrient synthesis.

ANTIGENIC STRUCTURE
• Limited Characterization: Due to inability to culture in vitro.
• Outer Membrane: Contains proteins with covalently bound lipids, inaccessible to antibodies.
• Endoflagella: Contain core proteins and a sheath protein, play a role in organism's invasiveness.
• Enzymes: Hyaluronidase breaks down hyaluronic acid in tissues.
• Enzymes: Hyaluronidase breaks down hyaluronic acid in tissues.

IMMUNE RESPONSE IN HUMANS


• Antibodies: Capable of staining T. pallidum (indirect immunofluorescence), immobilizing and
killing live organisms, and fixing complement.
• Reagin: Antibody-like substance developed in response to spirochetes, used in serologic
diagnosis of syphilis.

IMMUNITY
• Resistance: Individuals with active or latent syphilis show resistance to superinfection with T.
pallidum.
• Post-Treatment Susceptibility: After effective treatment of early syphilis, susceptibility to the
infection is restored.
• Limitation: Immune responses generally fail to eradicate the infection or halt its progression.

TREATMENT
• Penicillin: Primary treatment with significant treponemicidal activity.
• Follow-Up: Essential, especially in neurosyphilis and patients with AIDS.
• Jarisch-Herxheimer Reaction: May occur after starting treatment due to toxin release from dying
spirochetes.
• Dosage and Administration:
o Early Syphilis: Single injection of benzathine penicillin G (2.4 million units IM).
o Older/Latent Syphilis: Benzathine penicillin G IM, three doses at weekly intervals.
o Neurosyphilis: Same therapy or higher doses of intravenous penicillin; alternative antibiotics like
tetracyclines or erythromycin possible.
EPIDEMIOLOGY, PREVENTION, AND CONTROL
• Transmission: Mainly through sexual contact; congenital syphilis and occupational exposures are
rare.
• Contagious Period: 3–5 years during early syphilis; late syphilis (over 5 years) usually non-
contagious.
• Control Measures: Prompt treatment of cases, follow-up on contacts, safe sex practices
(condoms), and consideration of syphilis in diagnoses of other sexually transmitted diseases.

Treponema pallidum
ACQUIRED SYPHILIS
• Transmission: Primarily through sexual contact, with infectious lesions on skin or mucous
membranes. Non-genital lesions occur in 10-20% of cases.
• Infection Entry: Via intact mucous membranes or breaks in the epidermis.
• Early Development: Spirochetes multiply locally, spread to lymph nodes, then bloodstream.

 Primary Stage: Papule formation at infection site, evolving into a hard-based ulcer (“hard
chancre”), healing spontaneously.

 Secondary Stage: Occurs 2-10 weeks later, presenting red maculopapular rash, condylomas, and
possible syphilitic meningitis, hepatitis, or nephritis. Lesions subside but are highly infectious.
 Tertiary Stage: In about 30% of untreated cases, characterized by granulomatous lesions
(gummas), CNS degeneration (meningovascular syphilis, paresis, tabes), or cardiovascular lesions.
Treponemes rare in these lesions.

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