Pathogenic Fungi (12-13) Flashcards

1
Q

What are the properties of fungi?

A

Fungi are eukaryotic adidas → include yeasts, moulds and fleshy fungi
Have a rigid cell wall → consisting of layers of polysaccharides, forms a rigid matrix
Chemoheterotrophs → require organic compounds for both carbon and energy sources
Obtain nutrients as saprophytes (live off of decaying matter) or as parasites (live off living matter) → are recyclers
Some stimulate the plant roots to proliferate
Lichens → composed of fungi and a photosynthetic component - either a eukaryotic alga or a cyanobacterium
Disease causing bacteria → infect mostly skin, hair and nails - able to hydrolyse keratin a tough protein found in dead skin cells and nails
Several fungal pathogens can cause lung infections
Asperigillus species → produce a toxic compound called aflatoxin which causes liver cancer
Ergot → the active ingredient in the hallucinogenic drug LSD is produced by fungi

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2
Q

What is the effect of fungi in industry?

A

Used by industry to produce a variety of products → due to ability of recycling nutrients, produce enzymes which can degrade some matter
However, can cause undesirable economic effects → e.g. spoilage of fruits, grains and vegetables, destruction of wood and leather products
Over 100,000 species of fungi, only ~100 are pathogenic for animals

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3
Q

What kingdoms to fungi fit into?

A

Chromistan fungi → pseudo (non-tree) fungi with cellulosic hyphal walls - Phyla, Oomycota and Hyphochytriomycota
Eumycotan fungi → true fungi with chitinous hyphal walls - Phyla, Chytridiomycota, Zygomycota, Glomeromycota, Dikaryomycota

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4
Q

What are the 3 major mechanisms fungi can cause disease through?

A

Hypersensitivity → by causing immune responses that result in allergic reactions following exposure to specific fungal antigens
Toxins → by producing toxins e.g. mycotoxins - a large diverse group of fungal exotoxins
Infection → the growth of fungus on or in the body is a mycosis

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5
Q

What are the different groups of fungi that can cause disease?

A

Dermatophytes → a few fungi have evolved ability to attack the outer surface of human beings
Normally soil organisms → adapted to life in the unusual and rather hostile environment of the human body, often responding to this environment by developing a different morphology (thermal dimorphic saprobes)
Opportunistic saprobes → attack us only when our defences are down - when our immune system are diseased or deficient, or when artificially suppressed

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6
Q

What are the 3 main types of human fungal infections?

A

Cutaneous (superficial) mycoses → involve the outer layers of the skin and cause an allergic or inflammatory response
→ treatable - topical fungicides
Subcutaneous mycoses → involve fungi of low inherent virulence which have been introduced to the tissues through a wound of some kind
→ remain localised or spread only by direct mycelial growth
→ still treatable (more difficult) but give rise to more damaging lesions
Systemic mycoses → caused by either true pathogenic fungi which can establish themselves in normal hosts
→ or by opportunistic saprobic fungi which could not infect a health host, but can attack individuals whose immune system is not working
→ both kinds sometimes become widely disseminated through the body of the host
→ typically pulmonary - cause serious disease, inhalation of spores

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7
Q

What are the types of cutaneous (superficial) mycoses?

A

Superficial cosmetic fungi infections → skin or hair shaft where no living tissue is invaded and there is no cellular response from the host - no pathological changes are elicited e.g. dandruff caused by Malassezia furfur
More commonly superficial fungal infections of the skin, hair or nails → group of closely related mould fungi called dermatophytes
→ can colonise and digest keratin - a variety of pathological changes occur in the host because of the presence of the infectious agents and its metabolic products

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8
Q

What is ringworm?

A

A type of cutaneous mycoses also referred to as Tinea infections → e.g. Tinea pedis (feet) or Tinea capitis (scalp)
Caused by 20 species of dermatophyte fungi → 3 genera Trichophyton, Microsporum & Epidermophyton
Infections spread by direct or indirect contact with infected individual or animal → e.g. fragment of certain containing viable fungus (direct), floor of swimming pool, shower, combs (indirect)
→ spread through fungal spores - good for transmission, long living
Dermatophytes have ability to utilise keratin as a nutrient source → they invade keratin via enzymic digestion (keratinise) and mechanical pressure

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9
Q

Why is the disease process for ringworm unique?

A
  1. No living tissue is invaded → the keratinised stratum corner is simply colonised
    → however, the presence of the fungi and its metabolic products usually induces an allergic and inflammatory response in the host - type and severity related to the species and strain of dermatophyte
  2. Dermatophytes are the only fungi that have evolved a dependency on human or animal infection for the survival and dissemination of their species
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10
Q

What causes Tinea Pedis infection?

A

The shedding of skin scales containing viable infectious hyphal elements (arthroconidia) of the fungus (e.g. *T. rubrum)
→ scales may remain infectious in the environment for months or years, thus transmission may take place by indirect contact long after infective debris have been shed
→ substrates like carpet and matting that hold skin scales are good vectors

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11
Q

How are Tinea infections treated and prevented?

A

Topical therapy → usually fine for skin infections but oral antifungals e.g. fluconazole, are required for extensive skin infections or those of the nail or scalp
Prophylatic use of anti fungal foot powder → after bathing helps reduce the spread of infection among swimmers

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12
Q

What is fluconazole?

A

A widely used bis-triazole anti fungal agent
→ has 5-membered ring structure containing 3 nitrogen atoms

Action → inhibition of cytochrome P450 14a-demethylase - an enzyme in the sterol biosynthesis pathway that leads from lanosterol to ergosterol (as essential component of the fungal cytoplasmic membrane)

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13
Q

What are the properties of yeast?

A

Unicellular fungi → usually appear as oval cells 1-5um wide by 5-30um long
Have typical eukaryotic structures
Facultative anaerobes → get their energy through aerobic respiration as well as fermentation
Have a thick polysaccharide cell wall
Can cause superficial and systemic infections

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14
Q

How does the immune system respond to yeast?

A

Components of the yeast cell wall (PAMPs) bind to pattern-recognition receptors on a variety of defense cells
→ triggers innate immune defences such as inflammation, fever and phagocytosis
→ can also activate the alternative complement pathway and the lectin pathway

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15
Q

What allows yeast Candida albicans to invade deeper into tissues?

A

Pseudohyphae (branching filaments of attached elongated yeast cells) help the yeast to invade deeper tissues after it colonises the epithelium
→ in addition to its usual oval budding, is also able to produce pseudohyphae - buds elongate forming a tube-like structure called a germ tube which remain attached to one another eventually producing a filament called a pseudohypa

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16
Q

How do yeast reproduce?

A

Asexually by a process called budding
→ a bud is formed on the outer surface of the parent cell as the nucleus divides
→ one nucleus migrates into the elongating bud, cell wall material forms between the bud and the parents cells and the bud breaks away

Sexually → by means of sexual spores called ascospores
→ result from fusion of the nuclei from two cells followed by meiosis - recombination
→ less common than aseual but allows for genetic recombination

17
Q

Where is Candida albicans usually found?

A

As normal flora not he mucous membranes and in the GI tract
→ usually held in check by 1) normal flora bacteria, 2) normal body defences

Can cause a variety of opportunistic infection in people who are debilitates, immunosuppressed or have received prolonged antibacterial therapy
→ women who are diabetic, pregnant, taking oral contraceptives, or having menopause are more prone to vaginitis - these conditions alter the sugar conc and pH of the vagina making it more favourable for the growth of Candida

18
Q

What is candidiasis?

A

Any Candida infection → most commonly causes vaginitis - inflammation of the mucous membranes of the vagina, thrush - infection of the mucous membranes of the mouth, balantitis - lesions on the penis from a female with vaginitis and cutaneous infections - infections of moist skin or the nail beds
→ less commonly can infect the lungs, blood, heart and meninges (the membranes covering the brain and spinal cord) - especially in the compromised or immunosuppressed host
→ also causes 10% of all cases of septicaemia - where microorganisms enter the bloodstream

19
Q

How are Candida infections diagnosed?

A
  1. Collect samples → from skin (using blunt scalpel) from the edges of the lesions - where the most viable fungus is likely to be
    → from the mouth or vagina from areas of white plaques
  2. Direct microscopy → examination specimens for the presence of small, round to oval, thin-walled clusters of budding yeast cells and branching pseudohyphae - providing the clinical manifestations support the diagnosis
20
Q

How are Candida infections treated and prevented?

A

Correct underlying conditions that allows it to colonise the skin or mucosa → i.e. restore the normal epithelial barrier function
Cutaneous candidiasis → control of excessive moisture, heat and friction which cause local skin maceration and treatment with a topical imidazole compound
Oral candidiasis → nystatin, amphotericin B or miconnazole are effective - azoles prevent the synthesis of ergosterol
→ polyenes (e.g. amphotericin B and nystatin) interferon with the integrity of the fungal cell membrane by binding to membrane sterols
Most cases of vaginal candidiasis can be treated with a topical imidazole or the oral fluconazole
Oral treatment is essential for the treatment of intractable chronic infections → prolonged therapy may be required and development of resistance can occur

21
Q

What is chromoblastomycosis?

A

A subcutaneous mycoses → chronic localised disease of the skin and subcutaneous tissues
→ causative organisms: *Cladophialophora sp., Fonsecasea sp., Phialophora sp.)
→ infections caused by the traumatic implantation of fungal elements into the skin and are chronic, slowly progressive and localised
→ characterised by crusted, warty lesions usually involving the limbs
→ world-wide distribution but more commonly in bare footed populations living tropical regions

22
Q

How is chromoblastomycosis diagnosed and treated?

A

Diagnosis → presence in skin scrapings and/or biopsy tissue of brown pigmented, planate-dividing, round sclerotic bodies from a patients supporting clinical symptoms
Treatment → surgical removal of tissue (though required removal of a margin of unaffected tissue to prevent local dissemination)
→ fluorocytosine (a pyrimidine analog) and the azaleas thiabendazole and itraconazole are effective

23
Q

What is sporotrichosis?

A

A subcutaneous mycoses → primarily a chronic mycotic infection of the cutaneous or subcutaneous tissues and adjacent lymphatics
→ characterised by nodular lesions which may ulcerate
→ infections caused by the dramatic implantation of the fungus into the skin, or very rarely, by inhalation into the lungs - more serious, non-specific symptoms
→ secondary spread to joints, bond and muscle is not infrequent and the infection may also involve the CNS, lungs or genitourinary tract

24
Q

How is sporotrichosis diagnosed and treated?

A

Diagnosis → tissue biopsy will contain very low numbers of narrow base budding yeast cells
Treatment → cutaneous lesions respond well to saturated potassium iodide, - itraconazole and terbinafine can also be effective

25
Q

What is terbinafine?

A

A type of synthetic anti-fungal agent → an allylamine
→ highly lipophilic in nature and tends to accumulate in skin, nails and fatty tissues

Action → inhibits ergosterol biosynthesis via inhibition of squalene epoxidase - enzyme part of the fungal sterol synthesis pathway for the fungal cell membrane

26
Q

What is Cryptococcus neoformans?

A

A serious pathogenic yeast → can cause systemic mycoses
→ yeast can also reproduce sexually - sexual form called Filobasidiella neoformans
→ appears as an oval yeast, forms buds with a thin neck and is surrounded by a thick capsule (enables it to resist phagocytic engulfment) - does not produce pseudphyphae and chlamydospores
→ infections usually mild or subclinical, but when symptomatic usually begin in the lungs after inhalation of the yeast in dried bird faeces
→ found in soil, actively grows in the bird faeces but not in the bird itself
→ usually infection doesn’t process beyond the pulmonary stage - but in immunosuppressed it may spread through the blood to the meninges and other body areas causing cryptococcal meningoencephalitis (often fatal)
→ cutaneous and visceral infections also found

27
Q

What is the infectious cycle of C. neoformans?

A

Reside in environment and has been found associated primarily with pigeon droppings
Infection of humans generally occurs when basidiospores produced by it in the nature are inhaled into the lungs
→ inhaled spores are deposited into the alveoli and germinate to establish a dormant infection or disseminate the CNS
→ once dissemination has occurred, viable cells can be culture from the cerebrospinal fluid of affected individuals

28
Q

What is Pneumocystis carinii?

A

Can cause systemic mycoses
→ thought to be transmitted from person to person by the respiratory route and is almost always asymptomatic
→ in persons which highly depressed immune responses e.g. leukemias or HIV can cause an often lethal pneumonia called PCP

29
Q

What is blastomycosis?

A

Disease caused by the dimorphic fungus Blastomyces dermatitidis → can cause systemic mycoses
Endemic in the southeastern and south central states of North America
→ outbreaks associated with occupational or recreation activities around streams or rivers which high content of moisture soil enriched with organic debris and/or rotting wood
Infection if acquired via inhalation of the conidia which transforms into the yeast form once in the lungs
After 30-45 days an acute pulmonary disease indistinguishable from a bacterial pneumonia may occur

30
Q

What is histoplasmosis?

A

Condition caused by infection with the dimorphic endemic fungus Histoplasma capsulatum → can cause systemic mycoses
Most common cause of fungal infections in the world
→ majority of acute cases of infection with this fungus follow a subclinical and benign course in normal hosts
Fatal in immunosuppressed individuals, children <2, the elderly and people exposed to a very large inoculum
Infection acquired through inhalation of microconidia → thus lungs are the most frequently affected site and chronic pulmonary disease may occur
→ frequently associated with pre-existing chronic lung diseases like emphysema

31
Q

What is aspergillosis?

A

Broad range of disease states whose etiologic agents are membrane of the genus Aspergillus
→ ubiquitous organisms, progressively associated with a growing spectrum of infections in immunocompromised hosts
Aspergillus fumigatus → responsible for over 90% of cases of invasive aspergillosis
Three most prevalent diseases: allergic bronchopulmonary aspergillosis, pulmonary aspergilloma and invasive aspergillosis

32
Q

What is allergic bronchopulmonary aspergillosis?

A

Produces an allergy to the spores of Aspergillus moulds
→ common in asthmatics and cystic fibrosis patients
Symptoms: intermittent eposides of feeling unwell, coughing and wheezing, cough up brown-coloured plugs of mucus
Diagnosis: X-ray or by sputum, skin and blood tests
Long term → can lead to permanent lung damage (fibrosis) if untreated

33
Q

What is Aspergilloma?

A

Disease in which Aspergillus grows within a cavity of the lung which was previously damages during an illness e.g. tuberculosis - burns into scar from previous problem
→ any lung diseases which cause cavities leave people vulnerable
→ spored penetrate the cavity and germinate forming a fungal ball
Illness caused by secretion of toxins/other products (elastase, proteases)
Symptoms: maybe none early on, weight changes, chronic cough, brain fog, feeling rundown, coughing of blood
Diagnosis: X-rays, scans of lungs and blood tests

34
Q

What is invasive aspergillosis?

A

Often fatal - no good diagnostic test, often treatment has to be started when the condition is only suspected
→ usually clinically diagnosed in people with low defences e.g. bone marrow transplant, cancer patients, AIDs or major burns - rare inherited condition that gives people low immunity (chronic granulomatous disease - phagosomes inefficient killers)
Symptoms: fever, cough, chest pain, breathlessness - don’t respond to normal antibiotics
Diagnosis: bronchoscopy - inspection of the inside of the lung with a small tube inserted via the nose, X-rays and scans usually abnormal but can help localise the disease

35
Q

What is the treatment and control used against systemic pathogenic fungi?

A

Effective chemotherapy against systemic fungal infections is very difficult
Amphotericin B → one of the most effective antibiotics - binds to membrane sterols and affects the integrity of the fungal cell membrane, punches holes
→ can give rise to serious side effects e.g. kidney toxicity
Exposure of fungi can rarely be eliminated using air filtration in restricted local environment

36
Q

What contributes to fungal pathogenicity?

A

Fungal virulence factors can be divided into 2 categories
1 → virulence factors that promote fungal colonisation of the host
2 → virulence factors that damage the host

37
Q

What are virulence factors that promote fungal colonisation?

A

Adherence → the ability to adhere plays a role in fungal virulence
Capsules → some fungi produce capsules allowing them to resist phagocytic engulfment
→ e.g. yeast Crytococcus neoformans
Cytokines → Candida albicans stimulates the production of cytokine GM-CSF - surpassed the production of complement by monocytes and macrophages
→ can also acquire iron from red blood cells
Resistance → some fungi are resistant to phagocytic destruction
→ e.g. more difficult for phagocytes to engulf Candida albicans when its in pseudohyphal form

38
Q

What are some fungal virulence factors that damage the host?

A

Enzymes → as fungi grow in the body they can secrete enzymes to digest cells
→ in response to the fungus and cell injury cytokines are released - leads to inflammation and extracellular killing by phagocytes causing further destruction of host tissues
Mycotoxins → many moulds secrete mycotoxins (common when growing on grains, nuts and beans) - may cause a variety of effects in humans and animals if ingested e.g. loss of muscle coordination, weight loss and tremors, some are mutagenic and carcinogenic
→ aflatoxins are especially carcinogenic
→ mycotoxin symptoms: dermatitis, inflammation of mucous membranes, cough, fever, headache and fatigue