2. Spirochaete
⢠Gram negative
⢠presence of varying number of endoflagella
⢠Pathogenic spirochetes belong to genera :
⢠1. Treponema
⢠2. Borrelia
⢠3. Leptospira
3. Treponeme
⢠Veneral treponemes
⢠Treponema pallidum ď syphilis
⢠Non veneral treponemes include :
⢠â T. endemicum(causative agent of endemic)
⢠â T. partenue (causative agent of yaws)
⢠â T. carateum (causative agent of pinta)
4. Staining
⢠Does not take ordinary stains
⢠Morphology & motility can be studied by dark ground or phase contrast
microscopy
⢠Silver impregnation method
6. Culture
⢠Pathogenic strain Cannot be cultured in artificical media
⢠Does not follow kochs postulate
⢠Reieter
⢠Non pathogenic strain
⢠cultivable
⢠Nichols strain
⢠Pathogenic hence non cultivable
⢠Serial testicular passage in rabbits
9. Treponema pallidum
⢠Spirochete
⢠Morphology / motility can be studied under
dark ground microscope
⢠Staining
⢠Silver impregnation method
⢠Light rose red with geimsa stain
⢠Fontanas method for Films
⢠Levaditis for tissue sections
10. Syphilis /veneral trepanomatosis
⢠IP 9- 90 days (avrg 21 days)
⢠Route of transmission
⢠Sexual
⢠Late d/s ď minimum transmission
⢠transplacental
14. Primary syphilis
⢠Hunterian or Hard chancre
⢠Single painless
⢠Indurated ulcer
⢠Highly infective
⢠At the site of inoculation
⢠b/l lymph node enlarged
⢠Firm /non tender/non suppurative (shotty enlargement of LN)
⢠After 1 wk of chancre
⢠heals with in 4- 8 weeks
FTA- ABS VDRL TPHA
First test to become positive After 1-2 weeks
15. Secondary syphilis
⢠Non-pruritic skin papules ď macular roseola
(palms and soles are involved ) c.f lichen plnus
⢠2-10 weeks after primary chancre
⢠Generalised non-tender lymphadenopathy +
⢠Perianal condyloma lata (infectious)
⢠Constitutional features like sore throat, malaise,
fever and joint pain may accompany the lesions
⢠All sero test +ve
⢠most contagious
16. Snail tract ulcer in secondary syphilis
Snail tract ulcer in secondary syphilis
17. ⢠1. Chancre redux is a recurrence of the primary sore at its original site
⢠In 1* syphilis
⢠2. Any lesion at the site of a healed primary has been labelled
pseudochancre redux in 3* syphilis
26. Neurosyphilis ď CSF Ab tests are positive
⢠Asymptomatic
⢠No clinical abnormality
⢠Abnormal CSF
⢠Meningovascular syphilis
⢠After 10 yrs of infection
⢠Diffuse inflammation of meninges
⢠Stroke is the most common presentation
⢠General paresis of insane
⢠20 yrs after infn
⢠Personality changesď dementia, memory loss,loss on insight, euphoria,paraparesis
⢠Hyperactive reflexes
⢠AR pupil,charcoats joint
⢠Tabes dorsalis
⢠Demyelination of posterior column
⢠ď ataxic gait , rombergs sign
⢠Loss of temperature/deep pain /position
27. Gumma / late benign syphilis in tertiary stage
⢠Painless deep granulomatous ulcers
⢠Noninfecctious
⢠Spirochetes cannot be demonstrated
⢠In face scalp
⢠Punched out ulcers
⢠With wash leather slough
⢠Typically scar with retractile scarring ď atrophic tissue paper scar
36. Congenital syphilis
⢠Transmitted in utero
⢠Transmission of Treponema pallidum from an infected woman to her
fetus across the placenta may occur at any stage of pregnancy,
⢠but the lesions of congenital syphilis usually develop after-the 4th month of
gestation, when "fetal immunologic" competence begins to develop
⢠Can be
⢠early or
⢠late congenital syphilis
37. Early congenital syphilis
⢠Similar to 2* syphilis ď highly infectious
⢠2-8 weeks after
⢠FTT
⢠Mucocutaneous lesion (vesiculo bullous lesions)
⢠Generalised lymphadenopathy
⢠nasal snufflesn(rhinitis)ď early symptom
⢠Skin rash
38. ⢠Earliest sign of congenital syphillis is rhinitis or snuffles.
⢠MC early manifestation are bone changes, hepatosplenomegaly,
lymphadenopathy.
⢠Cluttonâs joint (Bilateral knee effusion), interstitial keratitis are late
manifestation
43. Charcots joint/neuropathic joint
⢠a. progressive destructive arthritis associated with loss of pain sensation,
proprioception, or both.
⢠b. Normal muscular reflexes
⢠c. modulate joint movement are decreased.
⢠d. Without these protective mechanisms, joints are subjected to repeated
trauma, resulting in progressive cartilage and bone damage.
⢠Disorders Associated with Neuropathic Joint Disease
⢠1. Diabetes mellitus***
⢠2. Tabes dorsalis (2nd MC)
⢠3. Meningomyelocele
⢠4. Syringomyelia
⢠5. Amyloidosis
⢠6. Leprosy
⢠7. Peroneal muscular atrophy
45. Treponemal test
⢠For confirmation
⢠TPI
⢠FTA â Abs
⢠Ig M FTA Abs
Non-treponemal test
⢠Screening
⢠Monitoring response to Rx
⢠Cardiolipin Ag based
⢠VDRL (slide flocculation test)
⢠Wasserman (compliment fixation
test)
⢠Kahnâs test (tube flocculation test)
⢠RPR (rapid plasma regain)
46. Diagnostic tests
⢠Dark ground examination
⢠On 3 consecutive days
⢠Transudate from lesion
⢠Identfication of single motile organism ď sufficient for diagnosis
⢠Serological test
⢠VDRL test
⢠Non specific test
⢠Biological false positives can occur
⢠Determine response to Rx
⢠FTA â Abs
⢠Flurescent treponemal Ab
⢠It becomes positive earlier than VDRL test
⢠Most sensitive test
47. ⢠TPI test
⢠Most specific test
⢠Costly
⢠Once +ve always +ve
48. Serological tests
⢠a. Nontreponemal tests
⢠Nonspecifc (reagin antibody) tests using the cardiolipin antigen
(standard
⢠tests for syphilis or STS).
⢠1. Wassermann complement fxation test
⢠2.Kahn ďŹocculation test
⢠3. Venereal Disease Research Laboratory (VDRL) test
⢠4. Rapid Plasma Reagin (RPR) test
⢠5. Toluidine red unheated serum test (TRUST)
49. Non treponemal test
⢠Fall of 2 dilutions (4 fold)ď adequate treatment
⢠False positive non treponemal test
⢠Pregnancy
⢠Connective tissue ds
⢠RA
⢠SLE
⢠Malaria
⢠leprosy
⢠Non veneral trepanomatosis
⢠Relapsing fever
⢠IMN
⢠old age
⢠Intravenous drug use
⢠HCV
⢠HIV
50. RPR or VDRL
⢠It becomes positive 3-5 weeks of infection (7-10 days of appearance
of chancre)
⢠Used for follow up
⢠For monitoring response to therapy
⢠Testing of large number for screening purpose
51. Treponemal tests
⢠a. Group specifc test using cultivable treponemal (Reiter strain) antigen
⢠Reiter Protein CF (RPCF) test
⢠b. Specifc tests using pathogenic treponemes (T. palidum)
⢠I. Test using live T. pallidum
⢠Treponema pallidum Immobilization (TPI) test
⢠II. Tests using killed T. pallidum
⢠a. Treponema pallidum agglutination (TPA) test
⢠b. Treponema pallidum immune adherence (TPIA) test
⢠c. Fluorescent Treponemal Antibody Absorption (FTA-ABS) test
⢠III. Tests using T. pallidum extract
⢠a. Treponema pallidum Hemagglutination Assay (TPHA) Microhemagglutination test for
Treponema pallidum (MHA-TP)
⢠b. Treponema pallidum Enzyme Immunoassays (TP-EIA)
52. ⢠FTA ABS
⢠First test to become positive
⢠Most sensitive
⢠TPI
⢠Most specific
53. Non Treponemal test Treponemal test Interpretation
+ + Active ongoing syphilis
+ - False +ve non treponemal test
- + Past treated infection
54. ⢠For monitoring treatment- Ideal test is VDRL>RPR
⢠Primary syphilis- Most Sensitive : Western blot & EIA >TPPA> RP
⢠Secondary syphilis- âAll equally sensitive (100%)
⢠Latent syphilis- Most Sensitive : All treponemal test >TPHA
⢠Late syphilisâMost Sensitive : FTA-ABS >TPHA
⢠Overall most specifc- TPHA, EIA,USR,TRUST (All 99% )>TPPA
⢠First test to be positiveâFTA-ABS
⢠Rapid and mass screening-VDRL
55.
56.
57. Rx
⢠1*,2* and early latent syphilis
⢠Benzathine penicillin G single IM dose of 2.4 million U
⢠Late latent
⢠Benzathine penicillin G single IM dose of 2.4 million U weekly * 3 weeks
⢠CNS syphilis & congenital syphilis
⢠Aqueous crystalline penicillin/ procaine penicillin G
58.
59.
60.
61. Non veneral / endemic trepanomatosis
Ds Caused by Affects Rx
Bejel (endemic syphilis ) T.Endemicum Skin bones mucus
membranes
BPG
0.6 mega U (<10 year)
1.2 mega U(>10 year)
Yaws T.Pertenue Skin and bone (periostitis) BPG
Pinta T.Carateum Skin alone (non
destructive)
BPG
There are two types of serologic test for syphilis:
nontreponemal and treponemal. Both types of test are reactive
in persons with any treponemal infection, including yaws,
pinta, and endemic syphilis.
62.
63.
64. Jarisch herscheimer reaction
⢠Intensifiction of symptoms
because of the release of
antigenic protein (when
spirochaete is killed by
penicillin )
⢠With in 12 hours after 1st dose
⢠MC in secondary syphilis
⢠Most dangerous in tertiary ď
given under steroid cover
⢠Brucellosis
⢠Borrelia
⢠Lyme ds
⢠Tick borne relapsing fever
⢠Cat scratch ds
⢠Q fever
⢠Syphilis (2*>1*>early latent)
⢠Typhoid fever
66. ⢠Large, refractile spirochetes which can be stained by ordinary method
and are Gram (â) ve.
⢠Cork screw motility
⢠⢠Pathogenic species are :
⢠B.burgodorferi - Causes Lymeâs disease
⢠B.recurrentis - Causes Relapsing fever
⢠B.vincenti - Causes Vincent angina
71. ⢠Diagnosis
⢠â ELISA followed by western blot is best investigation.
⢠â Culture in BSK medium gives definitive diagnosis but not useful
clinically.
⢠â PCR particularly in persistant infection
72. ⢠Treatment
⢠â For nervous manifestation and 30 heart block â Ceftriaxone is DOC.
⢠â For skin manifestation, arthritis 10 and 20 AV block â Doxycycline is DOC.
73. Relapsing fever
⢠Causative agent B.recurrentis.
⢠Relpases occur d/t antigenic variation of borrelia in vivo
⢠It is of 2 types :
⢠â Louse borne
⢠â Louse borne relapsing fever occur as epidemic
⢠Transmitted by body lice by crushing & rubbing in to abraded skin
⢠â Tick borne occur as sporadic / endemic cases
⢠Transmitted by bite of tick
⢠Treatment : Erythromycin is DOC
75. Vincent angina
⢠Causative agent B.vincenti
⢠Normal mouth commensal, but when associated with fusiform bacilli
(Fusobacterium fusiform) causes ulcerative gingivostomatitis or
oropharyngitis called vincent angina.
⢠Treatment : Penicillin and Metronidazole
78. ⢠Leptospirosis (sewer workers disease, Weilâs disease,
icterohemorrhagic fever) is zoonotic infection manifesting as fever,
jaundice and haemorrhage.
⢠Rats are the important hosts
79. ⢠Leptospirosis is a zoonosis with rodents being most important
reservoir.
⢠Transmission results from ingestion or contact with urine, blood or
tissue from infected animal but not from bite.
⢠Since leptospires are excreted in urine of infected rat, water is
important vehicle.
⢠Human to human transmission donât occur
80.
81. ⢠Incubation period averages 5â14 days
⢠Anicteric (90%) stage
⢠Present with fever & conjunctival congestion
⢠- Biphasic-
⢠â Septicemic or acute stage(1st week)
⢠â Immune stage (meningitis, uveitis, rash)- after 2nd week, excreted in urine
⢠Icteric
⢠Elevated bilirubin BUN & PT
⢠Icteric-(10%)- (Weilâs/hepatorenal hemorrhagic syndrome)-
⢠â Hepatomegaly & jaundice
⢠â Acute tubular injury(oliguric, with serum electrolyte abnormalities)
⢠â Hemorrhages (MC âpulmonary)
⢠â Hypotension
83. ⢠1. Isolation of organism
⢠â From blood or CSF during 1st 10 days
⢠â From urine after 1 week
⢠â For isolation
⢠EMJH medium is useful
⢠Korthof medium
⢠2.microscopy
⢠Dark ground microscopy
⢠3. Serology
⢠â Microscopic agglutination test [MAT]
⢠Gold standard
⢠â ELISA
84. Rx
⢠Mild cases
⢠Doxycycline ampicillin or amoxicillin
⢠Moderate or severe
⢠Penicillin G
⢠DOC
⢠Doxycyline