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Systemic Mycoses
By Dr. Rakesh Prasad Sah
Assistant Professor, Microbiology
Introduction
• Systemic mycoses are fungal infections affecting internal
organs.
• Fungi enter the body via lungs, through the gut, para-nasal
sinuses or skin
• Then spread via bloodstream to multiple organs including the
skin
• Can cause a tremendous variety of health problems
including digestive difficulties, skin problems , asthma,
breathing difficulties etc.
• Often causing multiple organs to fail and eventually
resulting in the death of the patient
Classification of systemic mycosis
Histoplasmosis
• Causative agent  Histoplasma capsulatum
• Ds of R.E. system
• Is an intracellular parasite
• ds worldwide in distribution but is most common in America
• Source of Infection 
– spores +nt in soil enriched with excreta of birds or bats
– Inhalation of spores
Clinical features-
• Infection is asymptomatic.
• Some individual develop pulmonary disease which resembles
tuberculosis.
• Disseminated histoplasmosis develope in infected individuals.
• Involvement of reticuloendothelial system results in
lymphadenopathy, hepatosplenomegaly,fever, anaemia and
high fatality rate.
• Granulomatous and ulcerative lesion develop on skin and
mucosa.
Lab diagnosis-
• Sputum
• Bone marrow aspirate
• Peripheral blood
• Scrapping from dermal or mucosal ulcer
• Biopsis of lymph nodes.
1) Direct examination-smear stained with Giemsa stain or wright
stains, it shows small oval yeast cells.
2) Culture- SDA or brain heart infusion with cycloheximide &
chloramphenical.The yeast phase is formed at 37˚c .white cottony
mycelial growth contain large, thick walled, spherical spores with
tubercles or finger like projections at 250
C.
H.capsulatum-mycelial form.
Serological tests-
• Latex agglutination,precipitation and complement fixation test
is positive two weeks after infection.
• Increase in titre of antibodies shows progessive disease
•
• Histoplasmin test-delayed hypersensitivity test.it is similar to
tuberculin test bt antigen histoplasmin is used.Histoplasmin is
filterate antigen of H.capsulatum.
 Treatment- Amphoterin B.
 AFRICAN HISTOPLASMOSIS-causative agent-
H.duboisii..involve skin & subcutaneous tissues.
H.capsulatum-yeast cells in
macrophages.
Blastomycosis
• Causative agent- Blastomyces dermatitidis (dimorphic fungi)
• Chronic infection of the lungs but may spread to other tissues,
particularly skin, bone & genitourinary tract.
• Sources of infection -inhalation of conidia of fungus.
• Clinical features-
• Asymptomatic
• Mild primary pulmonary disease.
• Disseminated disease.
• Disseminated lesions found in AIDS.
• Cutaneous blastomycosis observe on skin of face.
– Initial lesion is a papule  around this secondary nodules develop
and colaesce  large elevated ulcerative lesions
MORPHOLOGY
• Appear spherical or oval budding yeast cells with thick walls
at 370
C, at 250
C , culture is filamentous with septate and oval
conidia.
 Lab diagnosis-
• Sputum
• Pus
• Scraping from skin lesion.
• Direct microscopy-10% KOH mount-thick walled yeast cells
with a single broad based bud.
• H&E and PAS show yeast cells.
B.dermititidis-yeast forms.
Culture
• SDA & Blood agar.
• Mycelial phase-25˚C
• Yeast phase-37˚C
• Culture incubate for 6 weeks.
Treatment-Amphoterin B.
Paracoccidiomycosis.
• Causative agent- Paracoccidioides brasiliences.
• Chronic granulomatous- lungs, mucosa,skin & lymphatic drainage.
• Source of infection-Inhalation of spores.
• Clinical features-
• Primary pulmonary infections spread by mucous membrane of
nose,mouth,lymph nodes,produce chronic granulomatous reaction.
• Ulcerative granulomas of buccal and nasal mucosa.
Morphology
• Yeast phase-37˚C with multiple buds in tissue.
• Mycelial phase-25˚C.
 Lab diagnosis-
• Specimens-pus,sputum,biopsis from granulomatous lesions.
 Direct microscopy-
• Examination in KOH mount show yeast cells with multiple
bud.
• Tissue stain with H&E and PAS stains.
• Culture-
• Mycelial phase-on SDA at 25˚C
• Yeast phase – on BHI at 37˚c.
• Treatment- Amphotericin B.
P.Brasiliensis : yeast form.
Coccidioidomycosis.
• Causative fungus- Coccidioides immitis.
• Primary infections of the lungs.
• Source of infections -inhalation of
arthrospores.
• Clinical features-
• Asymptomatic
• Primary pulmonary diseases-influenza like
fever(valley fever),severe pneumonia.
• Disseminated disease-CNS,skin,& bones.
• Mophology-
• It is spherule with thick doubly refratile wall with
endospores.
• Mycelial phase contains pseudohyphae which is
highly infectious.
• Laboratory diagnosis-
• Specimens-sputum,pus,biopsy material.
• Direct microscopy –detect mature spherules
• Culture-
• Use SDA medium.
• Petri dish not used.
• Incubate 25˚c for 3 weeks.
Skin test -coccidiodin antigen is used.
• Positive test-between 3-21 days of symptoms.
Coccidioides immitis
CRYPTOCOCCOSIS.
• Causative agent - Cryptococcus neoformans.
• Abundant in faeces of pigeons.
• MORPHOLOGY –
• Spherical budding cell, have capsule.
• True yeast.
• Capsule can be demonstrated by india ink preparation.
• SOURCE OF INFECTION –
• Inhalation of dust containing yeast cells.
Pathogenesis -
• Pathogenic in humans & animals.
• Occurs in immuno compromised host.
• Asymptomatic.
• Pulmonary cryptococcosis – leads to pneumonitis
• Cryptococcal meningitis occurs by haematogenous
spread, mostly seen in AIDS patients.
• Skin,lymph-nodes,bones & other organs alse gets to
affected.
• Cutaneous cryptococcus varies from small ulcers to
large granulomas.
• Visceral forms of cryptococcal infection stimulate
tuberculosis and cancer clinically
Lab diagnosis
• Specimen - CSF, sputum ,pus, brain tissue.
• Direct microscopy-
1) Specimen mixed with drop of india ink-round budding yeast
cells.
2) Gram staining –gram positive yeast cells.
• Culture
• On SDA, it shows
smooth, mucoid, cream
colored colonies.
• NIGER SEED AGAR is
differential medium for
presumptive
identification.  Brown
colonies at 300
C within 1
week.
Phenoloxidase
Caffeic acid
Melanin
• Latex agglutination test .
• Animal inoculation test – intracerebral or intraperitoneal
inoculation.
• Other tests – C. neoformans hydrolyses urea.
Differentiation of C.neoformans from other
non-pathogenic cryptococci –
C.neoformans has ability to –
– Grow at 37˚C.
– Hydrolyse urea
– Produce brown colonies on niger seed agar.
– Produce disease in mice.
C.neoformans – India ink
preparation.
C.neoformans.
Systemic mycoses by Dr. Rakesh Prasad Sah

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Systemic mycoses by Dr. Rakesh Prasad Sah

  • 1. Systemic Mycoses By Dr. Rakesh Prasad Sah Assistant Professor, Microbiology
  • 2. Introduction • Systemic mycoses are fungal infections affecting internal organs. • Fungi enter the body via lungs, through the gut, para-nasal sinuses or skin • Then spread via bloodstream to multiple organs including the skin
  • 3. • Can cause a tremendous variety of health problems including digestive difficulties, skin problems , asthma, breathing difficulties etc. • Often causing multiple organs to fail and eventually resulting in the death of the patient
  • 5. Histoplasmosis • Causative agent  Histoplasma capsulatum • Ds of R.E. system • Is an intracellular parasite • ds worldwide in distribution but is most common in America • Source of Infection  – spores +nt in soil enriched with excreta of birds or bats – Inhalation of spores
  • 6. Clinical features- • Infection is asymptomatic. • Some individual develop pulmonary disease which resembles tuberculosis. • Disseminated histoplasmosis develope in infected individuals. • Involvement of reticuloendothelial system results in lymphadenopathy, hepatosplenomegaly,fever, anaemia and high fatality rate. • Granulomatous and ulcerative lesion develop on skin and mucosa.
  • 7. Lab diagnosis- • Sputum • Bone marrow aspirate • Peripheral blood • Scrapping from dermal or mucosal ulcer • Biopsis of lymph nodes. 1) Direct examination-smear stained with Giemsa stain or wright stains, it shows small oval yeast cells. 2) Culture- SDA or brain heart infusion with cycloheximide & chloramphenical.The yeast phase is formed at 37˚c .white cottony mycelial growth contain large, thick walled, spherical spores with tubercles or finger like projections at 250 C.
  • 9. Serological tests- • Latex agglutination,precipitation and complement fixation test is positive two weeks after infection. • Increase in titre of antibodies shows progessive disease • • Histoplasmin test-delayed hypersensitivity test.it is similar to tuberculin test bt antigen histoplasmin is used.Histoplasmin is filterate antigen of H.capsulatum.  Treatment- Amphoterin B.  AFRICAN HISTOPLASMOSIS-causative agent- H.duboisii..involve skin & subcutaneous tissues.
  • 11. Blastomycosis • Causative agent- Blastomyces dermatitidis (dimorphic fungi) • Chronic infection of the lungs but may spread to other tissues, particularly skin, bone & genitourinary tract. • Sources of infection -inhalation of conidia of fungus. • Clinical features- • Asymptomatic • Mild primary pulmonary disease. • Disseminated disease. • Disseminated lesions found in AIDS. • Cutaneous blastomycosis observe on skin of face. – Initial lesion is a papule  around this secondary nodules develop and colaesce  large elevated ulcerative lesions
  • 12. MORPHOLOGY • Appear spherical or oval budding yeast cells with thick walls at 370 C, at 250 C , culture is filamentous with septate and oval conidia.  Lab diagnosis- • Sputum • Pus • Scraping from skin lesion. • Direct microscopy-10% KOH mount-thick walled yeast cells with a single broad based bud. • H&E and PAS show yeast cells.
  • 14.
  • 15. Culture • SDA & Blood agar. • Mycelial phase-25˚C • Yeast phase-37˚C • Culture incubate for 6 weeks. Treatment-Amphoterin B.
  • 16. Paracoccidiomycosis. • Causative agent- Paracoccidioides brasiliences. • Chronic granulomatous- lungs, mucosa,skin & lymphatic drainage. • Source of infection-Inhalation of spores. • Clinical features- • Primary pulmonary infections spread by mucous membrane of nose,mouth,lymph nodes,produce chronic granulomatous reaction. • Ulcerative granulomas of buccal and nasal mucosa.
  • 17. Morphology • Yeast phase-37˚C with multiple buds in tissue. • Mycelial phase-25˚C.  Lab diagnosis- • Specimens-pus,sputum,biopsis from granulomatous lesions.  Direct microscopy- • Examination in KOH mount show yeast cells with multiple bud. • Tissue stain with H&E and PAS stains. • Culture- • Mycelial phase-on SDA at 25˚C • Yeast phase – on BHI at 37˚c. • Treatment- Amphotericin B.
  • 19.
  • 20. Coccidioidomycosis. • Causative fungus- Coccidioides immitis. • Primary infections of the lungs. • Source of infections -inhalation of arthrospores. • Clinical features- • Asymptomatic • Primary pulmonary diseases-influenza like fever(valley fever),severe pneumonia. • Disseminated disease-CNS,skin,& bones.
  • 21. • Mophology- • It is spherule with thick doubly refratile wall with endospores. • Mycelial phase contains pseudohyphae which is highly infectious. • Laboratory diagnosis- • Specimens-sputum,pus,biopsy material. • Direct microscopy –detect mature spherules • Culture- • Use SDA medium. • Petri dish not used. • Incubate 25˚c for 3 weeks. Skin test -coccidiodin antigen is used. • Positive test-between 3-21 days of symptoms.
  • 23.
  • 24. CRYPTOCOCCOSIS. • Causative agent - Cryptococcus neoformans. • Abundant in faeces of pigeons. • MORPHOLOGY – • Spherical budding cell, have capsule. • True yeast. • Capsule can be demonstrated by india ink preparation. • SOURCE OF INFECTION – • Inhalation of dust containing yeast cells.
  • 25.
  • 26. Pathogenesis - • Pathogenic in humans & animals. • Occurs in immuno compromised host. • Asymptomatic. • Pulmonary cryptococcosis – leads to pneumonitis • Cryptococcal meningitis occurs by haematogenous spread, mostly seen in AIDS patients.
  • 27. • Skin,lymph-nodes,bones & other organs alse gets to affected. • Cutaneous cryptococcus varies from small ulcers to large granulomas. • Visceral forms of cryptococcal infection stimulate tuberculosis and cancer clinically
  • 28. Lab diagnosis • Specimen - CSF, sputum ,pus, brain tissue. • Direct microscopy- 1) Specimen mixed with drop of india ink-round budding yeast cells. 2) Gram staining –gram positive yeast cells.
  • 29. • Culture • On SDA, it shows smooth, mucoid, cream colored colonies. • NIGER SEED AGAR is differential medium for presumptive identification.  Brown colonies at 300 C within 1 week. Phenoloxidase Caffeic acid Melanin
  • 30. • Latex agglutination test . • Animal inoculation test – intracerebral or intraperitoneal inoculation. • Other tests – C. neoformans hydrolyses urea.
  • 31. Differentiation of C.neoformans from other non-pathogenic cryptococci – C.neoformans has ability to – – Grow at 37˚C. – Hydrolyse urea – Produce brown colonies on niger seed agar. – Produce disease in mice.
  • 32. C.neoformans – India ink preparation.