Parasites and Diarrhea. I: Protozoans and Diarrhea

Transcription

1 Parasites and Diarrhea. I: Protozoans and Diarrhea Rayhan Hashmey, Robert M. Genta, and A. Clinton WhiteJr. Intestinal parasitism is extremely common, with approximately 70% of all people harboring one or more intestinal parasite. Parasitism and diarrhea are both hyperendemic in areas where sanitation is suboptimal. Many clinicians assume that the identification of intestinal parasites in patients with diarrhea implies that the parasites are the cause. This approach is frequently misguided. Some intestinal parasites such as Giardia lamblia and Entamoeba histolytica certainly do cause diarrhea. Others, for example Entamoeba coli and Ascaris lumbricoides, almost certainly do not. In addition, there are a number of other organisms that have been associated with diarrheal illness in some cases, which may or may not be important pathogens. In this article, we will review the role ofprotozoans as definite and possible causes of diarrhea. In Part 11, we review the role of helminths in diarrhea. Protozoans as Definite Causes of Diarrhea Table 1 lists the major protozoan parasites that have been associated with diarrhea. G. lamblia and E. histolytica are well-known causes of diarrheal illness while Cryptosporidium, Isospora belli, microsporidia and Cyclospora species have been increasingly recognized in association with diarrhea, especially in patients with AIDS. Balantidium coli is a well-recognized but less fiequent cause of diarrhea. Blastocystis horninis and Dientamoebafvagilis have also been identified in diarrheal illness, but their causal role is less clear. Other organisms such as Entamoeba dispar almost certainly do not cause diarrhea. Giardiasis Organism and Life Cycle G. lamblia is a binucleate, flagellated intestinal protozoan. Giardia are primitive eukaryotes and lack mitochondria.the life cycle is simple and consists of cyst and trophozoite stages. The trophozoite, which measures Rayhan Hashmey, MD, Robert M. Genta, MD, and A. Clinton White Jr., MD: Departments of Medicine, Pathology, and Microbiology and Immunology, Baylor College of Medicine, Houston, Texas. Reprint requests: A. Clinton White Jr., MD, Department of Infectious Diseases, Baylor College of Medicine, Rm 561E. One Baylor Plaza, Houston, TX J Travel Med 1996;4: pm long, is tear-drop shaped and on stained smears has a characteristic face-like appearance, due to the presence of symmetrically placed nuclei with large karyosomes.the dorsal surface is convex, while the ventral surface has a cytoskeletal disc made up of microtubules linked by microribbons.'.* Four pairs of posteriorly directed flagella help in 1ocomotion.Trophozoites multiply by longitudinal binary fission. Encystation occurs in the small bowel and is facilitated by neutral ph and bile salts. Ingesting as few as 1G25 mature cysts can establish infection. Excystation requires a low ph as well as the presence of pancreatic enzymes.3 Epidemiology G. lamblia is one of the major causes of parasitic diarrhea worldwide. In the developing world giardiasis is pandemic, with peak prevalence rates of up to 20% in children less than 10 years of age.4 In the United States G. lamblia is among the most frequently isolated intestinal parasites and has been identified in up to 7.2% of stool specimens submitted for parasitologic examination.'a6 Giardiasis often occurs in the setting of waterborne outbreaks.' It is an important cause of chronic diarrhea in travelers returning from developing countries.' Most studies estimate infection rates of 1-3% in short-term visitors to endemic area^.^.^ In a large series from Switzer- Table 1 Protozoan Parasites and Diarrhea Dejnite Causes of Diarrhea Causing bloody dnrrhea / dysentery Entamoeba kistolytica Balantidium coli Causing watery diarrhea / malabsorption Giardia lamblia Cryptosporidium parvum isospora belli Cyclospora cayetanensis Microsporidia Possible Causes of Diarrhea Dientamoeba fragilis Blastocystis hominis Not Associated with Diarrhea Entamoeba dispar Entamoeba coli Entamoeba hartmanni iodamoeba biitschlii Endolimax nana Trichomonas horninis

2 18 Journal of Travel Medicine, Volume 4, Number 1 land, G. lamblia was found in 0.4% of returning travelers who had chronic diarrhea."'travelers usually get infected after consumption of contaminated water." Although infrequent, several outbreaks of giardiasis have been associated with contaminated f~od.~*-'~ Person-to-person transmission is also important, especially in groups such as children in day care centers, sexually active male homosexuals, and institutionalized patient^.'^ These groups may have very high cyst carriage rates, up to 50% in some studies, and can transmit disease to friends and family.'' Animal-to-human transmission has been postulated as a common source ofinfection but has only been documented in a Canadian outbreak traced to beavers." Pathology and Pathogenesis The trophozoite adheres to the mucosal surface using the ventral disc. This results in distortion of the micmvih and disruption of the brush b~rder.'~.'~the parasite also elaborates several cytopathic substances including cysteine pmteinases, enterotoxin, and a surface binding le~tin.~j~,'~ In addition, infiltration of the lamina propria with lymphocytes has been noted and may lead to villus atrophy. These processes contribute to the development of disaccharidase deficiencies commonly associated with Giardia infection. Isozyme electrophoresis and genetic studies have demonstrated considerable phenotypic and genotypic heterogeneity among G. lamblia isolates. Analysis of sequential isolates suggests that this heterogeneity is due to the hgh rate of genetic rearrangement within the Giardia genome.20 Chronic infection has been associated with hypogammaglobulinemia, proteincalorie malnutrition, previous gastrectomy, and use of immunosuppressive medication.3~'*~19 Both systemic and mucosal antibody production occurs in giardiasis.21 Secretory IgA interferes with the adhesion mechanism of the parasite and may help clear the infection. The greater prevalence of disease in younger patients suggests a partial imrn~nity.~ Clinical Manifestations The clinical manifestations of giardiasis are remarkably &verse, including asymptomatic carriage, acute diarrheal disease, severe chronic diarrhea with malabsorption, and growth failure in Patients with acute symptomatic giardiasis complain of diarrhea, abdominal cramps, bloating, flatulence, malaise, nausea, and anorexia. Stools may be greasy or foul smelling. Fever and tenesmus are uncommon and point toward other pathogens that are invasive. Extraintestinal manifestations have been described in rare cases and include urticaria, reactive arthritis, and biliary tract di~ease.'~ Chronic infection is associated with profound malaise, lassitude, epigastric discomfort, headaches, and steatorrhea. Patients who develop recurrent diarrhea after treatment for Giardia infection may have associated lactose intolerance rather than relapse of their infection. Diagnosis The most common method for diagnosis of giardiasis is microscopic examination of the stools for trophozoites using either wet mount or trichrome ~tain.~~three consecutive stool specimens when properly examined yield a diagnosis in 80-90% of cases.25 Iodine staining is used for better identification of the cysts.the stool sample may be preserved in 10% buffered formalin and examined later using trichrome or iron hematoxylin stains.the duodenal string test (Entero-Test) may increase the yield, but this procedure is not well-tolerated by patients. In selected patients, endoscopic aspiration and biopsy may be considered. Giardia antigen detection assays are commercially available and are highly sensitive and specific.2h Treatment and Prevention Metronidazole is the most frequently used drug for the treatment of giardiasis in the United States and is associated with a cure rate of 8c-90%." The adult dosage is 250 mg PO t.i.d. for 5-7 days; children should receive 5 mg/kg PO t.i.d. for 7 days. Quinacrine, which has a comparable efficacy, is associated with far more side effects and is no longer available in the United States. Tinidazole is frequently used worldwide but is not available in the US. It has excellent efficacy when given in a single oral dose of 2 g.28 Furazolidone mg PO q.i.d. is available as a liquid suspension. Recommended duration of therapy is for 7 days. It is well-tolerated by children, but the efficacy is lower. Pregnant women may be treated with paromomycin, a nonabsorbable aminoglycoside, which is effective in 60-70% of cases.treatment of asymptomatic cyst passers has been advocated in developed countries and returning travelers. Such an approach is futile in hyperendemic areas due to rapid reinfection.2' Travelers to developing countries should be advised against the ingestion of untreated surface water. Bringing water to boil is adequate to kill Giardia cysts, though boiling for a few minutes may be required at higher altitudes. Halogenation with iodine- or chlorinebased agents is generally effective.6 Person-to-person transmission can be reduced by practicing strict handwashing. '() Amebiasis (Entamoeba histolyfica and Entamoeba dispar) Organisms and Life Cycle Amebiasis is caused by infection with the enteric protozoan E. histolytiru.the existence of pathogenic and nonpathogenic strains of E. kistolytica has been postulated for some time based on studies showing differences in isozyme electrophoretic patterns (zymodemes).31,32 More recently, genomic differences in DNA polymerase chain reaction amplification products, rrna probe studies, and cloned genes have confirmed the existence of two distinct species that are morphologically identi~al.~'~"'the non-

3 Hashrney et al.. Parasites and Diarrhea. I: Protozoans and Diarrhea 19 pathogenic species, now named Entamoeba dispar, is only associated with the asymptomatic carrier state, while E. histolytica causes tissue invasion and symptomatic disease. The genus Entamoebu also includes five other species (E. coli, E. gingivulis, E. moshkovskii, E. hartmanni and E. polecki] known to infect humans. None of these species cause disease in humans.34 The life cycle of E. histolyticu includes trophozoite and cystic stages. Cysts are excreted into the environment and can remain viable for several weeks.the mature cyst is quadrinucleate and ranges in size fi-om prn in diameter. Infection is acquired by ingestion of the cyst form. Excystation occurs in the small bowel and results in eight motile trophozoites ranging from p.m in size. Epidemiology Both species have a worldwide distribution with approximately 12% of the world s population infected with one of the E. dispar has never been associated with disease and does not elicit any specific serologic response. In contrast, E. histolyticu causes serum antiamebic antibody production in -90% of patients with invasive disease.35 Since E. histolytica and E. dispar are morphologically identical, most of the data on prevalence includes both. In most areas E. dispav is 10 times as common as E. histolyticu. Amebiasis is endemic in countries such as Mexico, India,West and South Africa, and Central and South America, where up to 50% of the population may be infected. Serologic surveys in endemic areas indicate that up to 25% of the population have had prior asymptomatic infection with E. histolyti~a.~~ Epidemiologic risk factors include lower socioeconomic status, migration from areas of high endemicity, institutionalization (especially in mentally retarded individuals) and living in a communal setting. Patients with amebic liver abscess have a high prevalence (>75%) of asymptomatic intestinal colonization with E. histolytica that may result in a prolonged carrier state if inappropriately treated. Invasive amebic disease carries an annual worldwide mortality of 40, ,000. The overall prevalence of intestinal amebiasis in the United States was about 4% of clinical stool specimens, but this appears to be decreasing.36 In the southwestern United States there is a higher prevalence of invasive disease, especially among immigrants from Mexico. E. histolytiu is not a common cause of traveler s diarrhea. However, amebiasis can be a cause of chronic diarrhea in travelers returning from developing countries. The risk of acquiring infection is proportional to the duration of stay in the endemic area. Ninety-five percent of travelers or immigrants who develop liver disease will present within 5 months after returning from an area of endemicity. Pathology and Pathogenesis E. histolyticu trophozoites attach to the colonic epithelium by means of a galactose inhibitable adherence lectin (GIAL), a 260 kd surface protein.this adherence lectin protects the parasite against complement-mediated lysis by inhibiting the assembly of C8 and C9 components with the membrane attack ~omplex. ~~~*~~ The cytolytic activity of E. histolyticu is dependent upon direct contact to the target cell, binding by the GIAL, and the presence of extracellular calcium ions.4 Proteolytic disruption of tissue planes is mediated by a variety of parasite enzyme^.^^^^^ Proteinases cause extracellular tissue destruction and degradation of secretory 1gA.The spectrum of colonic lesions range from nonspecific thickening of the mucosa to frank ~lceration.~ The classic description of flask-shaped ulcers is seen in less than half of cases. After invadmg the colonic epithelium, the amebic trophozoites can reach the liver via the ascending portal venous system. In the liver, extracellular proteinases digest the hepatic tissues, thereby resulting in focal areas of tissue destruction that can coalesce into necrotic areas termed liver abscesses. Immunity to amebic infection is incomplete, although patients cured of invasive disease rarely have reinfection. Clinical Manifestations Noninvasive lumenal infection with E. histolytica may result in asymptomatic infection or nonspecific gastrointestinal complaints such as bloating, cramps, decreased appetite, and flatulence. Amebic colitis on the other hand has a subacute onset characterized by bloody mucoid diarrhea, abdominal pain, weight loss, bloating, tenesmus, cramps, and fever. Amebic colitis can occur in a chronic nondysenteric syndrome with intermittent diarrhea, mucus, and abdominal ~ ain.~.~~ Complications of intestinal infection include fulminant colitis, toxic megacolon, intestinal perforation, stricture formation, and ameboma (annular lesion of the colon, usually near the cecal area, inhstinguishable fi-om carcinoma of the Chronic amebic colitis is clinically indistinguishable from idiopathic inflammatory bowel disease. Because corticosteroid therapy may result in perforation, stool examination for trophozoites and serologic test for amebic disease should be performed prior to making a diagnosis of inflammatory bowel disease. Extraintestinal disease most commonly presents as amebic liver abscess. Patients present with fever and right upper quadrant abdominal pain. Laboratory findings include leukocytosis and elevated liver enzymes. Liver abscesses occasionally rupture into the pleural space, resulting in pleural efisions. Extraintestinal disease rarely involves the pericardium, genitourinary system, and the brain. Diagnosis The diagnosis of intestinal infection is made by finding cysts or trophozoites in the stool. A saline wet mount of the stool should be made kom a fi-esh stool specimen, as trophozoites disintegrate in 30 minutes at room

4 20 Journal of Travel Medicine, Volume 4, Number 1 temperat~re.~' If immediate evaluation cannot be performed, the specimen should be fixed in polyvinyl alcohol and examined later using trichrome or iron hematoxylin stains. Stool examination is positive in >85% ofpatients when at least three stool specimens are examined on alternate days.46 Hematophagous trophozoites when seen are pathognomonic of E. hi~tolytica.~' Endoscopy with scraping or biopsy is a useful technique in evaluation of difficult to diagnose cases. In nonendemic areas, serum antiamebic antibody tests may be useful in the diagnosis of invasive disease. Over 85% of patients with biopsy-proven disease have detectable antibody by the seventh day of illness." In endemic areas a positive serology is less helpful. Up to 25% of the population may have serologic evidence of prior infecti~n.~~ Several new stool and serum antigen detection techniques appear promising in the identification of pathogenic versus nonpathogenic strain^.^' The presence of an amebic liver abscess is suggested by a history of fever and right upper quadrant pain, hepatic tenderness on physical examination, and an elevation in liver enzymes. Diagnosis requires the demonstration of the abscess by ultrasonography or computerized tomcgraphy scan. Trea tmenf Amebicidal drugs have been divided into intralumenal agents (e.g., diloxanide furoate, paromomycin, iodoquinol, and tissue agents metronidazole, tinidazole, and emetine).48ti~~ue amebicides lull amebae in host tissues and organs, whereas the poorly absorbed lumenal amebicides are active only in the intestinal l~men.~' "E. histolytica" cysts found in the stool of asymptomatic cyst passers are usually those of E. dispar. Since this parasite has never been shown to cause invasive infection, treatment is unnecessary. Serologic tests are negative and cysts are excreted in the stool for a limited period, usually 6-8 months. An enzyme-linked immunosorbent assay (ELISA) test to distinguish between E. histolytica and E. dispar is being developed. Symptomatic patients should be treated. In patients without evidence of invasive disease, diloxanide furoate 500 mg PO t.i.d. for I0 days is the therapy of choice. In the United States this drug is available only from the Centers for Disease Control and Prevention (CDC). Iodoquinol 650 mg PO t.i.d. for 20 days is also effective but has bothersome side effects and a longer duration of therapy. Paromomycin can be used as an alternative for lumenal or mild colonic disease. Invasive disease should be treated with metronidazole 750 mg PO t.i.d. for 10 days (tinidazole is also available outside the United States) followed by a lumenal amebicidal agent in order to eradicate intestinal disease.'') Tetracycline or erythromycin may be used in patients unable to tolerate metronidazole, but these drugs are not effective in hepatic disease. Dehy- droemetine is available from the CDC. Due to the occurrence of serious side effects such as prolongation of the Q-T interval, it should be administered in a monitored hospital setting. Chloroquine may be added to metronidazole in extraintestinal disease. Fine needle aspiration is indicated in left-sided abscesses and those unresponsive to medical therapy. Cryptosporidium panrum Organism and Life Cycle The protozoan parasites of the genus Cryptosporidium are closely related to other coccidian parasites such as TDxoplasma and Isospora. Although many species were named based on presumed host-species specificity, there is little host specificity for the strains infecting mammals.s1 Most organisms infecting mammals probably belong to a single species, C. parvum. Humans are infected after ingestion of oocysts (4-6 p,m in diameter).5' After excystation in the small intestines, the motile sporozoites attach to the host cells via their anterior end.they are enveloped by the microvilli and subsequently develop along the lumenal surface of the enterocyte within a parasitophorous vacuole separated from the host cytoplasm by a dense organelle (intracellular but extracytoplasinic).the parasite enlarges to form the trophozoite and divides forming meronts with four to eight nierozoites. When nierozoites are released they invade other host cells, and a portion of the merozoites develop into the sexual forms (macrogamont and microgamont).mer fertihzation the macrogamont develops into an oocyst, which sporulates in situ. Most of the oocysts are coated with a thick wall and are environmentally hardy. About 20% of the oocysts are thin-walled and may be involved in an autoinfection cycle. Epidemiology The first human case of cryptosporidiosis was reported as recently as 1976 and only seven human cases were reported prior to The number of cases has risen dramatically since the description ofaids. Subsequently, cryptosporidiosis has been identified in over 50 countries on all six inhabited continents in both normal and immunocompromised hosts.s3 When clinical stool specimens are examined for Crptosporidium oocysts, approximately 1-3% are positive in studies from North America and Europe (range 0.1%-14.1%, mean of 1.6 and 2.6%, respectively). In contrast, rates of % are typical in developing countries (range %).53.'4 Seroprevalence rates, which presumably reflect active or prior infection, range from 25-35% in developed countries but up to 64% among the urban indigent population in Latin 5.56 Cryptosporidiosis has been identified as a common cause of diarrhea in developing c ~untries.~~~"~~ Infec-

5 Hashmey et al., Parasites and Diarrhea. I: Protozoans and Diarrhea 21 tion is more common in children than in adults, but is rare in breastfed infants.sy,6' Cryptosporidiosis appears to be more prevalent in warm, wet month^.'^^."^ Cryptosporidiosis has also been frequently identified as a cause of diarrhea in travelers returning from areas with poor ~anitation.'~+'the oocysts are very hardy and survive for prolonged periods in the environment. Cryptosporidiosis is associated with waterborne epidemics of diarrheal Chlorination of water supplies does not appreciably kill the oocysts. Initial descriptions of cryptosporidiosis in normal hosts stressed animal contact;74 however, epidemiologic data have strongly supported only calf-to-human transmission."' Subsequent studies suggest that person-toperson transmission is also common, especially in urban area^.^',^^ In developed countries, cryptosporidiosis is a frequent cause of outbreaks of diarrhea in the context of day-care center^.^^^^^^^' Person-to-person transmission has also been documented in secondary cases in household c ~ntacts~~~~~ and among health care ~orkers.~'the high prevalence of disease among homosexual males also suggests person-to-person transmission.*" Cryptosporidiosis is an increasingly recognized cause of diarrhea in travelers to developing countries. Cryptosporidium was found to be the cause of diarrhea in 5% of travelers to Leningrad and in short-term Peace Corps workers in West Africa.*','' The prevalence of cryptosporidiosis is high in immunocompromised hosts, particularly in patients with AIDS. In the United States, 3-4% of patients with AIDS have cryptosporidi~sis.'~ In contrast, in Africa more than half of AIDS patients have cryptosporidi~sis.'~ Prevalence rates in Latin America are intermediate.'s~x6 Pathology and Pathogenesis Cvyptosporidium has been detected throughout the gastrointestinal tract, in the biliary tract, and even in the respiratory tract.sh Intestinal changes include villus blunting, crypt hyperplasia, and infiltration of the lamina propria with polymorphonuclear leukocytes, lymphocytes, and plasma The parasites are found within the microdus layer within parasitophorous vacuoles.though most patients exhibit normal duodenal villous architecture, high intensity infections, as evidenced by histologic examination of biopsy specimens, were associated with severe morphologic abnormalities." The pathophysiology of diarrhea in cryptosporidiosis is complex and likely involves both host and parasite factors. Current data suggest that site specific alteration in the function of villus absorptive cells, as evidenced by alteration in glucose-mediated sodium transport and release by the host of proinflammatory cytokines as part ofthe mucosal immune response, are the primary mech- anism involved." Chloride dependent enterotoxic activity has also been described." The host immune response in cryptosporidiosis has not been clearly defined. Secretory antibodies have been noted to interfere with sporozoite and merozoite attachment, but the development of specific serum and mucosal antibodies in AIDS patients does not effect a In contrast, the cell mediated immune response, specifically CD4 T cells and IFN-y, appear to play an important role in limiting infection.y4y6 In patients with HIV, the CD4 count is the best marker of the ability of the immune system to clear infection."' Dose response studies in healthy volunteers, using one strain of C. parvum, have shown a low mean infective dose (ID5,) of 132 oocy~ts;'~ however, it is not known whether immunocompromised individuals are more susceptible to infection than normal hosts.the dose of the inoculum did not influence the incubation period or the severity of illness. Clinical Manifestations The clinical presentation of cryptosporidiosis varies depending on the host response. In normal hosts, initial symptoms follow an incubation period, usually 7-10 day^.^^.'^,^^^'' Onset is typically abrupt. The most commonly identified symptom is diarrhea, with watery stools that may be voluminous. Mucus is usually not present. Fecal leukocytes and blood are absent. Abdominal pain and cramping were frequently noted in some series.74," Weight loss, anorexia, and flatulence have been noted. Fever when noted is typically low grade. Nausea and vomiting are present only in a minority of patients. Respiratory symptoms have been frequently noted in some series.5',6z, In travelers and other immunocompetent hosts, symptoms typically resolve in days.64,74.76," However, C. parvum is among the most common causes of diarrhea persisting for over 2 weeks, and chronic cases lasting over 30 days are well described."" Oocysts are excreted in the stool for 1-2 weeks after resolution of symptoms.98 Cryptosporidiosis has been associated with malabsorption. Whether this reflects Cryptosporidium causing malabsorption or merely the increased severity and recognition of cryptosporidiosis in patients with malabsorption due to other causes is unclear. Asymptomatic shedding of oocysts has been noted in some lo' In immunocompromised hosts, disease onset is usually insidio~s.~~*~~.~~,'""j"~ Watery diarrhea may gradually increase over weeks to months. Weight loss and profound dehydration are common. Abdominal pain and cramping are also common. Symptoms typically persist unless there is improvement in the immunologic status.

6 22 Journal of Travel Medicine, Volume 4, Number 1 Diagnosis Since the symptoms of cryptosporidiosis are nonspecific, diagnosis usually depends on the demonstration of oocysts in stool specimens. Considerable experience i5 required to obtain reliable results.the sensitivity of stool examination may be increased by concentration techniques or by staining. Sheather's sucrose floatation is the most frequently used concentration te~hnique.'"~"'~ A number ofstaining techniques have been used for Cryptosporidiurn A cid-fast staining is most commonly employed (Fig. 1). A number of acid-fast stains are widely used, including modified Kenyoun, diniethyl sulfoxide-modified stains, and fluorescent stains. 'i)1,'ij4 In patients with diarrhea, oocysts can generally be identified by acid-fast staining without using concentration techniques. Monoclonal antibody based immunofluorescent tests to detect oocysts in stool specimens are commercially available and demonstrate >90% sensitivity and specificity.'"' In comparative studies, the immunofluorescence test is both more sensitive and more specific than acid-fast staining technique^."'^^'"^ Widespread application of this test may be limited by the additional cost. Tissue forms can be detected in biopsy specimens with routine histologic stains including hematoxylin and eosin or Giemsa.In8 Treatment Fluid and electrolyte replacement are of primary importance in all cases of diarrhea. Attention to nutrition may be critical since the immunosuppression associated with malnutrition may delay recovery."' In compromised hosts, nonspecific antidiarrheal agents such as loperamide or diphenoxylate may be required to limit voluminous fluid losses. In a recent controlled clinical trial, Figure 1 Oocysts of Cryptosporidiurn are visualized in a stool specimen stained by the modified acid-fast stain (with permission from Dr. Lynn Garcia). the somatostatin analogue octreotide was no more effective than placebo.'"' There are numerous reports of antiparasitic agents used in cryptosporidiosis. Spiramycin, a poorly absorbed macrolide antibiotic, was initially reported to affect cryptosporidiosis in patients with AIDS in anecdotal reports,"' but efficacy has not been demonstrated in controlled trials. "* Paromomycin, a poorly absorbed aminoglycoside antibiotic,"3 achieves effective concentrations along the lumenal surface of the intestines, where the organism is found in vivo."4 A small placebo-controlled trial demonstrated both clinical and parasitologic improvement with paromomycin treatment in patients with AIDS."' Patients experienced significant symptomatic improvement; however, a majority relapsed. HIV-infected individuals should be advised not to drink water directly from lakes or rivers. Currently there are no recommendations regarding the use of household tap water; however, persons who want to take independent precautions can reduce the risk of infection by boiling water for 1 minute, by using"abso1ute" 1 micron water filters, or by using high-quality bottled water.- Risk of infection during travel to endemic areas can be reduced by avoiding use of untreated surface and ground water and by boiling water prior to use. Isospora belli 1. belli is a coccidian parasite closely related to Cryptosporidium. The oocyst is elliptical and measures by pm in size.within the oocyst are two sporocysts, each ofwhich contains four sporozoites.the sporozoites are released in the intestines, invade the intestinal epithelium, and undergo asexual (merogony) and sexual (gametogony) division within cytoplasmic vacuoles of the enterocyte."6 The oocysts are excreted prior to sporulation, which occurs outside the host. Epidemiology 1. belli is widely distributed in the animal kingdom. Infections have been described from nearly all the countries in the Americas, as well as in subsaharan Africa, the Middle East,Asia and the Pacific islands, and E~rope."~,"~ Studies suggest an increased prevalence in tropical and subtropical climates and in areas with poor sanitation. Little is known about the prevalence of infection in humans. In a limited number of studies employing adequate techniques, % of stools were positive."' Prevalence among AIDS patients in the United States is approximately 1%."' This may be an underestimate; this organism was not routinely looked for, and cotrimoxazole is frequently prescribed in these patients. In contrast the prevalence rate in less developed countries is as high as 15%.K44,R5J20 The mechanisms of transmission are unknown, although spread from infected animals and humans is suspected.

7 Hashrney et al., Parasites and Diarrhea. I: Protozoans and Diarrhea 23 Pathology and Pathogenesis Biopsy and autopsy specimens show villus atrophy, crypt hyperplasia, and infiltration of the lamina propria with inflammatory cells, in particular eosinophils."'j2' Al of the life cycle stages are visible within biopsy specimens.the mechanisms responsible for diarrhea are not clear, but may relate to malabsorption, which has been well described in both normal and compromised Clinical Features The clinical features of isosporiasis in immunocompetent hosts have been well defined by several large series and from experimental and laboratory-acquired infections.'1x~'22-'zs Aft er an incubation period (6-12 days in experimental and laboratory infections), patients typically present with an acute onset of fever, headache, and malaise. Gastrointestinal complaints include diarrhea (both frequent and watery stools), abdominal pain, nausea, and vomiting. Initially the stools are watery, but subsequently they may be fatty. Stool specimens do not contain fecal leukocytes but frequently contain Charcot- Leyden crystals and fat. Peripheral eosinophilia is fi-equent. While symptoms are usually self limited, patients are often ill for 6 weeks to 6 months. Even in apparently normal hosts, a portion of patients go on to develop chronic diarrhea and malabsorption, which may persist for years.' l6.l2' Patients with AIDS and isosporiasis present with an insidious onset of diarrhea, weight loss, and abdominal Fever and vomiting are less frequently noted. Symptoms are usually present for months prior to diagnosis. Biliary disease, acalculous cholecystitis, and ulcerative colitis have been rep~rted.'~~.''~ Diagnosis Diagnosis depends on the identification of organisms in stool or biopsy specimens.while the oocysts can be identified in wet mounts of stool specimens, stool examinations are frequently negative unless they are concentrated. Zinc sulfate floatation has been highly successful in some laboratories.'23 Acid-fast stains appear to increase the sensitivity of stool examination.'2y Treatment Isosporiasis responds promptly to therapy with antifolate dr~gs.'~",'~','~~,'~' Trimethoprim (160 mg) combined with sulfamethoxazole (800 mg) four times a day for 10 days leads to prompt resolution of symptoms in normal hosts and in patients with AIDS. For AIDS patients, approximately half will relapse if not placed on secondary prophylaxis. Both trimethoprim (TMP)/sulfamethoxazole (SMX) (160 mg/800 mg three times a week) and sulfadoxine/pyrimethamine (500 mg/25 mg) once weekly can prevent relapse.'30 Cyclospora Cyclospora cayetanensis, a coccidian parasite, has recently been identified as causing human infe~ti0n.l~' Before its identification as a coccidian parasite, Cyclospora had been referred to as cyanobacteria-like bodies (CLB) and blue-green algae.132-'35 The appearance of oocysts is similar to those of Cryptosporidium, but the size is slightly larger (9-10 pm). Each oocyst contains two sporocysts, each of which contain two sporozoites.i3' Epidemiology There is a wide geographic hstribution of Cyclospora. Most of the reported cases have originated in tropical countries such as India, Nepal, and South America. Cases have been identified in travelers returning from the trop- ic~.'~~.'"~'~' Gascon et al. found Cyclospora in 2.8% of patients with traveler's diarrhea in their ~1inic.l~' Transmission occurs via the oral route, and local outbreaks have been traced to contaminated water or food supply. An outbreak of relapsing diarrhea among 17 physicians and three hospital employees in a Chicago hospital was traced to a contaminated water so~rce.'~~~~'~' Most outbreaks occur during the summer season. Pathology and Pathogenesis The site ofinfection is the small intestine. Endoscopic biopsy specimens show a diffuse inflammatory response, with an increase in intraepithelial leukocytes, mild to severe villus atrophy, and crypt hyperplasia. '42The pathogenesis of these lesions and the mechanism of diarrhea are unclear; however, both invasion as well as toxin production have been p~stulated.'~~ Clinical Presentation The clinical presentation is similar to that of Cryptosporidium and Isospora infections. Clinically, patients present with watery diarrhea, anorexia, and malaise. Approximately half experience abdominal cramps and up to a third have nausea, vomiting, and fever. Symptoms often wax and wane.the duration of illness in immunocompetent patients is variable but typically lasts several weeks (mean duration 43 days in one series).i3' In AIDS patients, Cyclospora results in chronic intestinal infection with prolonged diarrhea.137 Duration of symptoms correlates with the presence of Cyclospora in the stool. Control groups either with other causes of diarrhea or without symptoms only rarely have the organism in their stools. C. cayetanensis may be associated with biliary tract disease.'43 Diagnosis and Treatment Diagnosis requires a high index of suspicion. Diagnosis is dependent on microscopic demonstration of morphologic characteristics, staining properties, and autofluorescence under ultraviolet light. In contrast to Cryptosporidium, staining is variable with the modified acid-fast stain (Fig. 2). Oocysts autofluoresce when examined under ultraviolet light and do not cross-react with immunologic tests specific for Cr~pto~poridium.'~~.'~~ Measurement of oocysts is recommended to distinguish Cyclospora from Cryptosporidium.'44,'45 Cotrimoxazole

8 24 Journal of Travel Medicine, Volume 4, Number 1 Figure 2 A stool specimen demonstrating a variable uptake of modified acid-fast stain by oocysts of Cyclospara (kindly provided by Dr. Charles Stager). (TMP 160 mg/smx 800 mg) PO b.i.d. for 5-7 days is the treatment of choice, with recent studies reporting a significant response to therapy and improvement in both clinical and parasitologic parameter^.^'.'"^'^",'^' Microsporid ia ( Enterocytozoon bieneusi and Encephalitozoon intestinalis) Organism and Life Cycle Microsporidia are a group of obligate intracellular protozoan parasites belonging to the phylum Microspora, which consists of more than one hundred genera and over a thousand 14' Human infection was first reported in 1959 and thus far four genera have been implicated in human disease: Enterocytozoon sp. (E. bieneusz], Encephalitozoon sp. (E. hellurn, E. canaliculi, E. intestinalis), Nosema sp. (N. connori, N. ocularurn, N. corneurn), and Pleistophora sp.149a15fl The major species associated with enteric infection are Enterocytozoon bieneusi and Encephalitozoon intestinalis (previously called Septata intestinalis). Microsporidia are primitive eukaryotic unicellular parasites.they lack mitochondria and golgi membranes and possess small prokaryotic-sized rrna.'" They produce environmentally resistant spores that are characterized by coiled polar tubules. After entering the hosts, the polar tubules inject the sporoplasm (nucleus and cytoplasm) into the host cell.'48,149,152 Although there is significant intergeneric variation, the life cycle has three distinct phases: first, the spore or infective stage; second, the proliferative stage during which the organism divides by merogony (schizogony); and lastly, sporogony, the spore-forming stage. Epidemiology Little is known about the epidemiology of human microsporidiosis. Serologic surveys suggest that infection with these organisms is widespread. Spread of the organ- isms through environmental, person-to-person (fecal-oral, aerosolized respiratory secretions), and animal-to-person transmission have been postulated.'5"j53 Although there are few reported cases of microsporidial infection in nonhiv patients, these organisms are increasingly being recognized as etiologic agents of chronic disseminated disease in HIV-positive individuals. E. bieneusi and E. intestinalis have both been associated with chronic diarrhea in AIDS patients. However, studies have not been unanimous in demonstrating this association. In one casecontrolled prospective study, the investigators did not find a significant difference in the presence of microsporidia on intestinal biopsy specimens when comparing HIV infected patients with and without diarrhea.'54 In contrast, others have noted a clear association between infection and altered d-xylose absorption.'"* In the normal host, microsporidia have been associated with traveler's diarrhea.'55 It has been suggested that microsporidia transiently infect immunocompetent individuals causing disease only in immunosuppressed patient~.'~~,'~~j~~ Pathology and Pathogenesis E. bieneusi infections generally appear to be limited to the intestinal and biliary epithelium. The organisms are primarily found in the tips of the villi. Meronts are 4-6 pm in diameter. E. bieneusi was initially identified by electron micros~opy.~~~~'~~ E. bieneusi infections are limited to the intestinal and biliary epithelium. Histopathologic changes range from normal villus architecture to severe dus atrophy. Infiltration of the lamina propria with mononuclear cells has been noted. Little is known about the pathogenic basis of diarrhea in intestinal microsporidiosis. Malabsorption of both carbohydrates and fats has been demon~trated.~"~~'~~*'~~ E. intestinalis infects enterocytes, macrophages, fibroblasts, and endothelial cells of the lamina propria. In contrast to E. bieneusi, widespread dissemination often Clinical Presentation Microsporidia have been associated with a self-liniited diarrheal illness in a few apparently immunocompetent patients. 155 Ophthalmologic involvement and central nervous system disease have also been reported. E. bieneusi appears to be associated with chronic diarrhea in AIDS patients.is4 In this group, the clinical presentation consists of diarrhea that is watery, without blood or mucus, and of variable volume. Weight loss is common. Since diagnosis was initially limited to patients who underwent intestinal biopsy, self-limited cases and milder cases may have been overlooked. Asymptomatic intestinal colonization by microsporidia has also been reported. ls4 Microsporidial infection of the biliary mucosa is associated with AIDS ~holangiopathy.'~'~'~ Clinical presentation of E. intestinalis resembles that of E. bieneusi, except that extraintestinal disease is common.'6'

9 Hashmey et al., Parasites and Diarrhea. I: Protozoans and Diarrhea 25 tions, and electron microscopy have been used to increase sensitivity. Treatment There is no proven curative therapy currently available for E. bieneusi infections.as in all diarrheal illnesses, attention to fluid and electrolyte management and nutrition are the mainstay of therapy. Symptomatic improvement may be achieved by the use of antidiarrheals.there have been anecdotal reports of clinical responses to treatment with albendazole.16' Controlled trials are in progress. E. intestinulis infection, on the other hand, shows a dramatic clinical and parasitologic response to albendazole therapy.16' Figure 3 Modified-trichrorne stain of a stool specimen showing microsporidial spores. Diagnosis The primary means of diagnosing intestinal microsporidial infection is demonstration of the spores in stool.the spores are small (1-3pm in diameter) and not easily identified without special staining techniques. Weber developed a modified trichrome stain that facilitates identification of spores in stool (Fig. 3).'62 The cysts can also be stained by fluorescent stains including calcofluor white (Fig. 4) and indirect immunofluores- ~ence.'~',~~~ Cytologic evaluation of readily obtainable specimens (stool, duodenal aspirates, urine, sputum, nasal discharge, and bronchoalveolar lavage) using light microscopic staining techniques such as Giemsa and modified trichrome are becoming routine practice.i5' On intestinal biopsy specimens, organisms stain with hematoxylin and eosin. The spores also stain with toluidine blue, brown-brenn or Giemsa stains. They are frequently overlooked in routine sections due to their small size and limited numbers. Thin plastic sections, touch prepara- Balanfidium coli B. coli is the only ciliate associated with human infection. It has a widespread distribution, but is only rarely found in human stool samples (<1% in all surveys).' Humans appear to be an incidental host with the primary reservoir in domestic and wild animals, including pigs. The trophozoites are p,m in length and p,m wide, ovoid in shape, and actively motile in fi-esh specimens.the cyst stage is p,m in diameter. The predominant site of infection is the colon, especially the rectosigmoid. 167 Histologically, the lesions resemble those seen with amebiasis, including flaskshaped ulcers with undermined edges and few neutrophils.the lesions may coalesce, involving most of the colon. Most organisms are found at the periphery of lesions. Occasionally, lesions may perforate. Clinically many cases are a~ymptornatic.'"~'~~ A chronic form has been described with loose bowel movements, abdominal pain, tenesmus, mucus in the stools, and weight ~ oss.~~~j~~ Finally, dysentery has been described in a minority of patients. Patients present with sudden onset of diarrhea with blood and/or leukocytes in the stool. Abdominal pain and tenderness and weight loss are frequent. Symptoms may last for months. Diagnosis is by demonstration of the trophozoites in stools. Fresh stools examined for motile trophozoites are probably more sensitive than are preserved specimens.'66 Tetracyclines are recommended as treatment.'69 Metronidazole, diiodohydroxyquin, and paromomycin also have some activity.'66a160 Protozoans as Possible Causes of Diarrhea Figure 4 Microsporial spores visualized under ultraviolet light using a modified flurochrome calcofluor white stain (photograph kindly provided by Dr. Charles Stager). Dienfamoeba fragilis D.fragilis is a flagellate, closely related to the trichomonads. It has been identified in most areas of the world with a prevalence of % in stool specimen~.~~" An association of D.fragi!is and Enterobius uermicularis (pinworm) has been noted, and some suggest that they are transmitted t~gether.'~" D.jagUis is considered

10 26 Journal of Travel Medicine, Volume 4, Number 1 by some to be a cause of diarrheal illness. Most information on D.frugi/is-associated illness comes from retrospective studies. Several studies identified the organism in stool samples of patients that lacked other recognized pathogen~.'~+''~ In a recent survey, D.jiagilis was the only parasite found in two-thirds of the cases.173 It occurred more frequently in children 5-9 years old. Eighty percent of the patients reported diarrheal symptoms. Anal pr~ritis'~",'~' and eosinophilia have been reported in a substantial portion of ca~es.'~~~'~~these symptoms may in part be due to concomitant pinworm infection. None of these studies looked carefully for other organisms that might have accounted for the symptoms (e.g., Esherichia coli, Stronnloides stercoralis, G. lamblia, Ctyptosporidium, and Isospora). Furthermore, D.jiagilis has never been shown to be invasive.while pathologic abnormalities have been described in infected patients (e.g., fibrosis of the appendix),i7* other explanations seem more likely than parasitism.therapy with metronidazole, iodoquinol, or paromomycin is effective, but eradicating the organism has only inconsistent effects on ~ymptoms.'~",'~~ Blastocystis hominis B. hominis is a common component of the human intestinal flora. In the past, it was mistakenly believed to be a yeast. Elegant studies, primarily by Zierdt and coworkers, have conclusively demonstrated that B. hoininis is a protozoan.'74 The role of ths organism in the pathogenesis of diarrhea is contr~versial.'~~ B. hominis is present in 10-20% of stools from both normal and ill populations. Several series have been reported of patients with B. hominis in their stools, the absence of other identified pathogens, and gastrointestinal symptoms.'7"'7y A recent prospective case-controlled study among tourists in Nepal failed to show a difference in prevalence or heavy colonization (>I0 organisms per high power field) of B. hominis between study subjects and controls.'x".'x' Symptoms attributed to B. hominis include diarrhea, abdominal pain and bloating, and anorexia. Duration of illness has been variable. Eosinophilia has been noted in some cases. Response to therapy with antiprotozoal agents has been variable. Eradication of the organism does not correlate well with clinical response. Not all commonly recognized pathogens were sought in these studies, nor were noninfectious causes of diarrhea excluded. On careful evaluation, three groups found that most patients with diarrhea and Blastocystis in their stool have another explanation for their symptom~.'~'-'~~ Biopsy specimens have usually shown normal ti~sue."~ Studies in gnotobiotic animals have demonstrated colonization only when infected with other stool organisms as well as B. hominis. Finally, purportedly infected humans lacked a significant serologic response to the organism."' Other Protozoa A number of nonpathogenic protozoa may be identified by routine parasitologic examination of stool specimens. The most frequently encountered are Endolimax nana and Entamoeba coli, each identified in approximately 4% of specimens. Others include Entamoeba hartmanrzi, Iodamoeba butchlii and Trichomonas hominis.' References Soltys B, Gupta R. Immunoelectron microscopy of Giardia lamblia cytoskeleton using antibody to acetylated alpha-tubulin. J Eukar Microbiol 1994;41(6): Chavez B, Martinezpalonio A. Ciardia lanrblia: freeze fracture structure of the ventral disc plasma membrane. J Eukar Microbiol 1995;42: Farthing M. Diarrheal disease: current concepts and future challenges. Pathogenesis of giardiasis.trans R SOC Trop Med Hyg 1993;87: Gilman R, Brown K. Epidemiology and serology of Giardia lamblia in a developing country: Bangladesh 1985.Trans 1\ SOC Trop Med Hyg 1985;79: Kappus KD, Lundgen KJ,Juranek D, et al. Intestinal parasitism in the United States: update on a continuing problem. Am J Trop Med Hyg 1994;50: Hill 13 Giardiasis: itsues in diagnosis and management. Infect Dis Clin North Am 1994;7(3): Craun G. Waterborne giardkasis in the United States. Lancet 1986;2: Kelsall BL, Guerrant RL. Evaluation of diarrhea in the returning traveler. Infect Dis Clin North Am 1992;6: Brodsky K, Spencer HJ, Schultz M. Giardiasis in American travelers to the Soviet Union. J Infect Dis 1974;130:319. Steffan R, Richenback M,Wilheni U. Health problems after travel to developing countries. 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11 Hashrney et al., Parasites and Diarrhea. I : Protozoans and Diarrhea Owen R, Nemanic F, Stevens D. Ultrastructural observations of giardiasis in a murine model. Intestinal distribution, attachment and relationship to the immune system of Giardia muris. Gastroenterol 1979;76: Nash T, Keister D. Differences in excretory-secretory products and surface antigens among 19 isolates of Giardia. J Infect Dis 1985;152: Meloni BP, Lymbery AJ,Thompson RCA. Genetic characteristics of isolates of Giardia duodenalis by enzyme electrophoresis: implications for reproductive biology, population structure, taxonomy and epidemiology. J Parasitol 1995; 81 : Heyworth M. Immunology of Ciardia and Cryptosporidium infections. J Infect Dis 1992;166: Hill D. Giardia tamblia. In: Mandell G, ed. Principles and practice of infectious &seases.vol. 2. NewYork: Churchill Livingstone, 1995: Shaw R, Stevens M.The reactive arthritis of giardiasis. JAMA 1987;258:2734. Adam R. 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In: Ravdin J, ed.amebiasis: human infection by E. histolytica.vo1. 1. New York:Wiley,l988. Haque R, NeviUe LM, Hahn P, et al. Rapid hagnosis of Enfamoeba infection by using Entamoeba and Entamoeba histolytica stool antigen detection kits. J Clin Microbiol 1995;33: , Cooperstock M, DuPont H, Corrado M, et al. Evaluation of new anti-infective drugs for the treatment of diarrhea caused by E. histolytica. Clin Infect Dis 1991;15:S254-S258. Khaw M, Panosian C. Human antiprotozoal therapy: past, present and future. Clin Microbiol Rev 1995;8: Simjee A, GaithiramV,JacksonT, et a1.a comparative trial of metronidazole vs. tinidazole in the treatment of amebic liver disease. S Afr Med J 1985;68:923. Fayer R, Speer CA, Dubey JP. General biology of Cryptosporidium. In: Dubey JP, Speer CA, Fayer K, eds. Cryptosporidiosis of man and animals. Boca Raton, FL: CKC Press, 199O:l-29. Fayer R, Ungar BLP Cryptosporidium spp. and cryptosporidiosis. Microbiol Rev 1986;50: Ungar BLP. 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12 28 Journal of Travel Medicine, Volume 4, Number Bogaerts J, Lepage P, Rouvony D, et al. Cryptosporidium species, a frequent cause of diarrhoea in Central Africa. J Clin Microbiol 1984;20: Mata L, Bolanos H, Pizarro D, et al. Cryptosporidiosis in chddren from some highland Costa Rican rural and urban areas. Am J Trop Med Hyg 1984;33: Mathan MM,Venkatesan S, George R, et al. Cryptosporidiosis and diarrhoea in southern Indian children. Lancet 1985;2: Pape JW, Levine E, Beaulieu ME, et al. Cryptosporidiosis in Haitian children. Am J Trop Med Hyg 1987;36: Shahid NS, Rahman ASMH, Anderson BC, et al. Cryptosporidiosis in Bangladesh. BMJ 1985;290: Weikel CS, Johnston L, DeSousa A, et al. Cryptosporidiosis in northeastern Brazil. J Infect Dis 1985;151: Wolfion JS, Richter JM,Waldron MA, et al. Cryptosporidiosis in immunocompetent hosts. N Engl J Med 1985;312: Soave R, Ma E? Cryptosporidiosis.Trave1er s diarrhea in two families. Arch Intern Med 1985;145: Ma P, Kaufman DL, Helmick CG, et al. 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13 Hashmey et al., Parasites and Diarrhea. 1: Protozoans and Diarrhea Jokipii L, Jolului AMM.Timing of symptoms and oocyst excretion in human cryptosporidiosis. N Engl J Med 1986;315: Egger M, Mausezahl D, Odermatt P, et al. Symptoms and transmission of intestinal cryptosporidiosis. Arch Dis Child 1990;65: Soave R. Cryptosporidiosis and isosporiasis in patients with AIDS. Infect Dis Clin North Am 1988;2: Fang GD, Lima AAM, Martins CV, et al. Etiology and epidemiology of persistent diarrhea in Northeastern Brazil: a hospital-based, prospective, case-controlled study. J Pediatr Gastroenterol Nutr 1995;21: Roberts WG, Green PHR, Ma J, et a]. Prevalence of cryptosporidiosis in patients undergoing endoscopy: evidence for an asymptomatic carrier state.am J Med 1989;87: Garcia LS, Current WL. Cryptosporidiosis: clinical features and diagnosis. Crit Rev Clin Lab Sci 1989;6: CurrentWL.Techniques in laboratory maintenance of Cryptosporidium. In: Dubey JP, Speer CA, Fayer R, eds. 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