MYCOLOGY - CHAPTER SIX 

  DIMORPHIC FUNGI 

WEB RESOURCES
CDC-Blastomycosis

Most of the systemic fungi have a specific niche in nature where they are commonly found. Blastomyces dermatitidis survives in soil that contains organic debris (rotting wood, animal droppings, plant material) and infects people collecting firewood, tearing down old buildings or engaged in other outdoor activities which disrupt the soil. In addition to an ecological niche, most fungi that cause systemic infections have a limited geographic distribution where they occur most frequently. Blastomycosis occurs in eastern North America (figure 6) and Africa. The vast majority of patients with blastomycosis in South Carolina  are infected in the northern part of the state, above the Fall Line (Augusta, GA, Aiken, Columbia, Cheraw, Raleigh, NC). 

Blastomycosis is a chronic granulomatous disease which means that it progresses slowly. Although the pulmonary and skin (figure 1) involvement is the most common, B. dermatitidis frequently affects bone, prostate and other organs. More frequently blastomycosis presents as a cutaneous or a respiratory disease. The cutaneous lesions may be primary (usually self-limiting) or secondary (a manifestation of systemic disease). The patient who presents with a complaint of respiratory symptoms will frequently remark about loss of appetite, loss of weight, fever, productive cough, and night sweats. While these symptoms resemble those of TB, it is not this disease. The X-ray shows obvious pulmonary disease. To make the specific diagnosis, the physician must be aware of blastomycosis. Sputum sent to the lab for "culture" will not grow the organism. The lab must be alerted to look for fungal organisms or to look specifically for blastomyces. Some patients have a sub-clinical or "flu-like" response to infection. B. dermatitidis can frequently be demonstrated in a KOH preparation of pus from a skin lesion. A typical cutaneous lesion shows central healing with microabscesses at the periphery. A pus specimen may be obtained by nicking the top of a microabscess with a scalpel, obtaining the purulent material and making the diagnosis in 5 min. by microscopic examination with KOH. This organism has a characteristic appearance of a double contoured wall with a single bud on a wide base (figures 2 - 5). There are no specific virulence factors for B. dermatitidis. Laboratory specimens depend on the manifestation of the disease: If there are skin lesions, send skin scrapings or pus. If there is pulmonary involvement, send sputum. Other specimens include biopsy material and urine. Occasionally, the organism can be isolated from urine as it often infects the prostate. 

Mycology

If you request a fungus culture from the microbiology lab, they will incubate the cultures at 37 degrees C and at 25 degrees C because most of the significant pathogenic fungi are dimorphic.

A culture of B. dermatitidis takes 2 to 3 weeks to grow at 25 degrees C. It appears as a white, cottony mold (mycelium) on Sabouraud dextrose agar. Most specimens for fungus culture are plated on Sabouraud's dextrose agar. Microscopically, the mycelia and the fruiting bodies are evident. However, the mold cannot be identified by its fruiting bodies. The fruiting bodies are called microconidia, but they are not distinctive. Other fungal saprophytes and pathogens have similar conidia. At 37 degrees C the yeast form grows in about 7-10 days. It appears as a buttery-like, soft colony with a tan color. Microscopically, we see the typical yeast form of a thick wall and a single bud with a WIDE BASE. This wide base is characteristic of B. dermatitidis, and it is important to be able to recognize this. The cells are 12-15 microns in diameter. The yeast will convert to the mycelial form when incubated at 25 degrees C, taking from 3 to 4 days up to a few weeks. Similarly, the mycelial growth can be converted to yeast form when incubated at 37 degrees C.In the past, the only way to identify the dimorphic fungi was to convert from one form to the other, but now it is possible to take the mycelial growth (which is the easiest to grow), and confirm the isolate with a DNA probe in a matter of hours.

Histopathology 

B. dermatitidis produces both a granulomatous and suppurative tissue reaction

Serology 

There are three serological tests used for blastomycosis:

1. Immunodiffusion test (precipitin). This requires 2 to 3 weeks to become positive. This test is positive in about 80% of the patients with blastomycosis. When it is positive, there is close to 100% specificity.

2. Complement fixation (CF) test. This test requires 2 to 3 months after the onset of disease to develop detectable antibody. Besides the long delay before there is measurable antibody, another disadvantage of the C-F is that it cross reacts with other fungal infections (coccidioidomycosis and histoplasmosis). The advantage is that it is a quantitative test. The physician can follow the patient's response to the disease by monitoring the antibody titer.

3. Enzyme Immunoassay (EIA). The latter test has met with mixed acceptance by mycologists. However it is easy to perform and antibody is detected early in the disease process.

Amphotericin B remains is the drug of choice (DOC) although it is very toxic and must be administered intravenously for several weeks. Ketoconazole is also being used in mild cases.

Histoplasmosis is a systemic disease, mostly of the reticuloendothelial system, manifesting itself in the bone marrow, lungs (figure 12-17), liver, and the spleen. In fact, hepatosplenomegaly is the primary sign in children, while in adults, histoplasmosis more commonly appears as pulmonary disease. This is one of the most common fungal infections, occurring frequently in South Carolina, particularly the northwestern portion of the state. The ecological niche of H. capsulatum is in blackbird roosts, chicken houses and bat guano. Typically, a patient will have spread chicken manure around his garden and 3 weeks later will develop pulmonary infection. There have been several outbreaks in South Carolina where workers have cleared canebrakes which served as blackbird roosts with bulldozers. All who were exposed, workers and bystanders, contracted histoplasmosis. Histoplasmosis is a significant occupational disease in bat caves in Mexico when workers harvest the guano for fertilizer. In the endemic area the majority of patients who develop histoplasmosis (95%) are asymptomatic. The diagnosis is made from their history, serologic testing or skin test. In the patients who are clinically ill, histoplasmosis generally occurs in one of three forms: acute pulmonary, chronic pulmonary or disseminated. There is generally complete recovery from the acute pulmonary form (another "flu-like" illness). However, if untreated, the disseminated form of disease is usually fatal. Patients will first notice shortness of breath and a cough which becomes productive. The sputum may be purulent or bloody. Patients will become anorexic and lose weight. They have night sweats. This again sounds like tuberculosis, and the lung x- ray also looks like tuberculosis, but today radiologists can distinguish between these diseases on the chest film (histoplasmosis usually appears as bilateral interstitial infiltrates). Histoplasmosis is prevalent primarily in the eastern U.S. In S.C., a histoplasmin skin test survey of lifetime, one county residents, white males, 17 to 21 years old, was performed on Navy recruits. The greatest number of positive skin tests appeared in the northwestern part of the state. A similar study of medical students conducted at Medical University of  South Carolina, about 25 years ago, bore the same distribution (Goodman and Ever, J.S.C.M.A. 67:53-55, 1971).The skin test is NOT used for diagnostic purposes, because it interferes with serological tests. Skin tests are used for epidemiological surveys.

Clinical specimens sent to the lab depend on the presentation of the disease: Sputum or Bronchial alveolar lavage, if it is pulmonary disease, or Biopsy material from the diseased organ. Bone marrow is an excellent source of the fungus, which tends to grow in the reticulo-endothelial system. Peripheral blood is also a source of visualizing the organism histologically. The yeast (figures 7-11) is usually found in monocytes or in PMN's. Many times an astute medical technologist performing a white blood cell count will be the first one to make the diagnosis of histoplasmosis. In peripheral blood, H. capsulatum appears as a small yeast about 5-6 microns in diameter. (Blastomyces is 12 to 15 microns). Gastric washings are also a source of H. capsulatum as people with pulmonary disease produce sputum and frequently swallow their sputum.

Mycology 

When it is grown on Sabouraud dextrose agar at 25 degrees C, it appears as a white, cottony mycelium after 2 to 3 weeks. As the colony ages, it becomes tan. In the mold form, Histoplasma has a very distinct spore called a tuberculate macroconidium. The tubercles are diagnostic, however there are some non-pathogens which appear similar. A medical mycologist will be able to distinguish them. Grown at 37 degrees, C the yeast form appears. It is a white to tan colony. The yeast cell is 5-6 microns in diameter and slightly oval in shape. This is not diagnostic. To confirm the diagnosis, one must convert the organism from yeast to mycelium or vice-versa or use the DNA probe.

Serology for histoplasmosis is a little more complicated than for other mycoses, but it provides more information than blastomycosis serology.

There are 4 tests:

1. Latex agglutination

2. Complement Fixation

3. Immunodiffusion

4. EIA

Each of these serological tests has different characteristics that make them useful. The latex agglutination test is a very simple test involving agglutination in a test tube. The Ab is fairly specific and rises early in the disease (in the first 2 weeks), and disappears in about 3 months. The complement fixation test is like the one for blastomycosis, except there are 2 antigens, one to the yeast form of the organism and the other to the mycelial form. Some patients react to one form and not the other, while some individuals react to both. The reason for the different responses is not clear. One disadvantage is that complement fixing antibody develops late in the disease, about 2 to 3 months after onset. A second disadvantage is that it cross reacts with other mycotic infections. An advantage of the C-F test is that it is quantitative, so the physician can follow the course of the disease by observing the titer of several samples. The interpretation of the immunodiffusion test is a little more complicated than with blastomycosis because there are two bands which may appear. An H band indicates active disease and will appear in 2 to 3 weeks. An M band can indicate past or present disease, or result from a skin test. This is one reason why skin tests are not used for diagnosis because they can interfere with other tests. Skin tests will also affect the complement fixation test.

Recently, a radioimmunoassay for histoplasma polysaccharide antigen has been developed. This is a proprietary test so the evaluation of the results have been questioned. The drug of choice (DOC) is amphotericin B, with all its side effects. Itraconazole is now also being used.

WEB RESOURCES
CDC-Histoplasmosis

C. COCCIDIOIDOMYCOSIS (Coccidioides immitis) 

Coccidioidomycosis is primarily a pulmonary disease. About 60 % of the infections in the endemic area are asymptomatic. About 25 % suffer a "flu-like" illness and recover without therapy. This disease exhibits the typical symptoms of a pulmonary fungal disease: anorexia, weight loss, cough, hemoptysis, and resembles TB. CNS infection with C. immitis is more common while it is less frequent with the other fungal diseases. The ecological niche of C. immitis is the Sonoran desert, which includes the deserts of the Southwest (California, Arizona, New Mexico and Texas) and northern Mexico (figure 18). It is also found in small foci in Central and South America. 

Desert soil, pottery, archaeological middens, cotton, and rodent burrows all harbor C. immitis. C. immitis is a dimorphic fungus with 2 life cycles. The organism follows the SAPROPHYTIC cycle in the soil and the PARASITIC cycle in man or animals. The saprophytic cycle starts in the soil with spores (arthroconidia) that develop into mycelium. The mycelium then matures and forms alternating spores within itself. The arthroconidia are then released, and germinate back into mycelia. The parasitic cycle involves the inhalation of the arthroconidia by animals which then form spherules filled with endospores. The ambient temperature and availability of oxygen appear to govern the pathway The organism can be carried by the wind and therefore spread hundreds of miles in storms so the distribution is quite wide. In 1978, cases were seen in Sacramento 500 miles north of the endemic area, from a dust storm in Southern California. The spores of the organism are readily airborne. The cases that occur in South Carolina are usually in patients who have visited an endemic area and brought back pottery, or blankets purchase from a dusty roadside stand, or in Navy and Air Force personnel who were exposed when they were stationed in the endemic area. The disease manifests itself after they are transferred to a base in South Carolina. A few interesting cases occurred in cotton mills in Burlington and Charlotte, N.C. The cotton, grown in the desert of the Southwest, was contaminated with the fungus and the mill workers inhaled the spores while handling the raw cotton and developed coccidioidomycosis.

Clinical specimens include sputum, pus from skin lesions, gastric washings, CSF, and biopsy material from skin lesions.

Mycology
C. immitis is a dimorphic fungus (figure 19-23). Cultured on Sabouraud's agar at 25 degrees C it grows as a mold in 2 to 3 weeks. Characteristically, the mycelia develop arthroconidia. ("By their fruits ye shall know them"). It is a barrel-shaped (smaller at the edges, wider at the middle) asexual spore. Typically, the arthroconidia alternate with non spore-forming cells in the mycelium. When grown in vitro at 37 degrees C, there is no yeast form!! C. immitis is a dimorphic fungus; in vivo, (pus or tissue) one sees the pathogenic or invasive form B which is a spherule. The organism develops into spherules (30-60 microns) that are filled with endospores which are 3 to 5 microns in diameter (see figure above). A spherule will develop endospores within, then break apart, releasing the endospores. This is the tissue form seen in pus or histological sections: spherules and loose endospores. They can also be seen in a KOH preparation of sputum. It is pathognomonic for coccidioidomycosis.

Histopathology

The inflammatory reaction is both purulent and granulomatous. Recently released endospores incite a polymorphonuclear response. As the endospores mature into spherules, the acute reaction is replaced by lymphocytes, plasma cells, epithelioid cells and giant cells.

Serology  

There are four tests for diagnosis:

1. Complement-Fixation

2. Slide agglutination

3. Immunodiffusion

4. EIAC-F antibody is slow to rise and develop in about 1 month. This test is excellent for coccidioidomycosis because it is quantitative. However, these antibodies cross-react with some other fungi (Blastomyces and Histoplasma). The C-F test is also a PROGNOSTIC test. If the titer keeps rising, then the patient is responding poorly and the course may be fatal. If the C-F titer is dropping then the prognosis for that patient is favorable. A titer of greater than 1:128 usually indicates extensive dissemination. Life-long immunity usually follows infection with C. immitis. There is a much greater mortality rate in dark-skinned people (Mexicans, Filipinos, and Blacks). They are 25 times more likely to develop progressive disease and death. The reason for this is obscure.

Amphotericin B, fluconazole and itraconazole are the drugs of choice.

  Figure 26.
Tongue lesion of paracoccidioidomycosis. CDC/Dr. Lucille K. Georg

Histopathology 

Histologically, one sees multiple buds forming a "Captain's wheel." This is diagnostic of paracoccidioidomycosis. In this case, the mother cell is 40-50 microns in diameter and the buds are 2-5 microns in size (figure 29-31).

Serology

The best serological test for paracoccidioidomycosis is the immunodiffusion test. It is better than 99% specific and almost 85% sensitive.

Therapy

The D.O.C. is amphotericin B. Sulphonamide-trimethoprim and ketoconazole have also been used. Presently Itraconazole appear to provide the best recovery.

Figure 32.
This patient presented with sporotrichosis affecting the skin of the thumb.

Figure 33.
conidiophores and conidia of the fungus Sporothrix schenckii
CDC/Dr. Libero Ajello

Figure 34.
SABHI agar plate culture of Sporothrix schenckii grown at 20°C CDC/Dr. William Kaplan

Sporotrichosis is usually a chronic infection of the cutaneous or subcutaneous tissue which tends to suppurate, ulcerate and drain. In recent years, a pulmonary disease has been seen more frequently. Occasionally, infection with S. schenckii may result in a mycetoma. Sporotrichosis is caused by another dimorphic fungus. The infection is also known as "rose growers disease." The ecologic niche for this organism is rose thorns, sphagnum moss, timbers and soil. A study on the occupational distribution of sporotrichosis showed that forest employees accounted for 17% of the cases, gardeners and florists, 10%; and other soil-related occupations another 16%. Sporotrichosis occurs worldwide. Every aspect of this disease (clinical, pathology, mycology, ecology) was investigated during an epidemic of 3,000 patients in a gold mine in South Africa during the 1940's. Patient history is very important in this disease also. It is often seen in gardeners and begins with a thorn prick on the thumb (figure 32). A pustule develops and ulcerates. It infects the lymphatic system and then the disease progresses up the arm with ulceration (figure 37), abscess formation, break down of the abscess with large amounts of pus followed by healing. Progression usually stops at the axilla. Clinical material to be sent to the lab may be pus, biopsy material, or sputum from pulmonary patients. The yeast form of this fungus in tissue or in culture, can be round (6 - 8 um) or fusiform. The fusiform shape is not the usual form but if a cigar-shaped yeast is observed in tissue, it is usually diagnostic of sporotrichosis.  S. schenckii does not stain with the usual histopathological stains. If sporotrichosis is suspected, the pathologist must be informed so he can use special stains. Histologically asteroid bodies, a tissue reaction (also known as Splendori reaction) may be seen around the yeast cell. At 25 degrees C, this colony is white-cream and very membranous (figure 34 and 35), but as it ages for 2-3 weeks it becomes black and leathery (figure 36). Microscopically, the mycelium is branching, septate and very delicate, 2-3 um in diameter (figure 33). The pyriform conidia, 2-4 um form a typical arrangement in groups at the end of a conidiophore called "daisies" (figure 33). Serologic tests are not commercially available. The drug of choice for the cutaneous form is saturated iodides (e.g., potassium iodide) administered orally. The patient begins with 2-3 drops, 3-4/days until tolerance to the drug is built up, then the dose is increased. Potassium iodide may interact with the host immune system. For the systemic form the drug of choice is itraconazole or amphotericin B.

WEB RESOURCES
CDC-Sporotrichosis