Isosporiasis
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Overview
Isosporiasis is a human intestinal disease caused by a parasite called Isospora belli.
Related Key Words and Synonyms:
Isospora infection
Epidemiology and Demographics
Geographic Distribution:
Worldwide, especially in tropical and subtropical areas. Infection occurs in immunodepressed individuals, and outbreaks have been reported in institutionalized groups in the United States.
Pathophysiology & Etiology
Etiologic agent:
The coccidian parasite, Isospora belli, infects the epithelial cells of the small intestine, and is the least common of the three intestinal coccidia that infect humans.
Life cycle:
At time of excretion, the immature oocyst contains usually one sporoblast (more rarely two) 1. In further maturation after excretion, the sporoblast divides in two (the oocyst now contains two sporoblasts); the sporoblasts secrete a cyst wall, thus becoming sporocysts; and the sporocysts divide twice to produce four sporozoites each 2. Infection occurs by ingestion of sporocysts-containing oocysts: the sporocysts excyst in the small intestine and release their sporozoites, which invade the epithelial cells and initiate schizogony 3. Upon rupture of the schizonts, the merozoites are released, invade new epithelial cells, and continue the cycle of asexual multiplication 4. Trophozoites develop into schizonts which contain multiple merozoites. After a minimum of one week, the sexual stage begins with the development of male and female gametocytes 5. Fertilization results in the development of oocysts that are excreted in the stool 1. Isospora belli infects both humans and animals.
Diagnosis
Microscopic demonstration of the large, typically shaped oocysts, is the basis for diagnosis. Because the oocysts may be passed in small amounts and intermittently, repeated stool examinations and concentration procedures are recommended. If stool examinations are negative, examination of duodenal specimens by biopsy or string test (Enterotest®) may be needed. The oocysts can be visualized on wet mounts by microscopy with bright-field, differential interference contrast (DIC), and UV fluorescence. They can also be stained by modified acid-fast stain.
History and Symptoms
Infection causes acute, non bloody diarrhea with crampy abdominal pain, which can last for weeks and result in malabsorption and weight loss. In immunodepressed patients, and in infants and children, the diarrhea can be severe. Eosinophilia may be present (differently from other protozoan infections).
Laboratory Findings
Microscopy:
A, B, C: Oocysts of Isospora belli. The oocysts are large (25 to 30 µm) and have a typical ellipsoidal shape. When excreted, they are immature and contain one sporoblast (A, B). The oocyst matures after excretion: the single sporoblast divides in two sporoblasts (C), which develop cyst walls, becoming sporocysts, which eventually contain four sporozoites each. Images contributed by Georgia Division of Public Health.
Oocysts of Isospora belli can also be stained with acid-fast stains, and can be visualized by UV fluorescence on wet mounts, as illustrated in Figure 2. Three coccidian parasites that most commonly infect humans, seen in acid-fast stained smears (2A, 2C, 2F), bright-field differential interference contrast (2B, 2D, 2G) and UV fluorescence (2E, 2H, C. parvum oocysts do not autofluoresce).
Treatment
Acute Pharmacotherapies
Trimethoprim-sulfamethoxazole is the drug of choice.
References
- http://www.cdc.gov/ncidod/dpd/parasites/isospora/default.htm
- http://www.dpd.cdc.gov/dpdx/HTML/isosporiasis.htm
- http://en.wikipedia.org/wiki/Isosporiasis
Acknowledgements
List of contributors:
Pilar Almonacid
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
