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. 2012 Jul;25(3):420–449. doi: 10.1128/CMR.05038-11

Table 1.

Prevalence of protozoa as described by various studies from developed countries

Reference Study location; period Cases and samples Lab method(s) Overall pathogen isolation rate (%) No. of samples Parasites detected (%)a,b
184 Melbourne, Australia; 1997 Fecal specimens from community-based asymptomatic individuals Modified iron-hemotoxylin stain to detect Giardia, Cryptosporidium, Blastocystis, Entamoeba, and other protozoa 11.8 1,091 Protozoa (8.3), Giardia spp. (1.6), Blastocystis spp. (6.0), Cryptosporidium (0.4), D. fragilis (0.4)
335 Helsinki, Finland; 1985-1986 Diarrhea in adult out- and inpatients attending three health centers and a municipal hospital Formalin-ether concentration method and modified Ziehl-Neelsen method for Cryptosporidium 35.2 253 G. intestinalis (2.0), Cryptosporidium sp. (2.8), E. histolytica/E. dispar (0.4) (majority of isolates were imported from other countries)
452 Madrid, Spain; 1980–1983 Fecal samples from infected persons (50% children) in hospital Microscopic examination for parasitesc 46.1 5,022 cases Giardia intestinalis (2.7), Entamoeba histolytica/E. dispar (<1)
247 Ljubljana, Slovenia; 1992-1993 Patients with diarrhea Permanent staining, Gomori's trichrome modification for Blastocystis sp., and safranin-methylene blue stain for Cryptosporidium, with bright-field microscopy 3.7 (39/1,066 patients) 1,066 cases, 150 controls Blastocystis spp. (3.7 [cases] and <1 [controls])
11 Population of England; 1993-1996 Fecal samples from patients with diarrhea and controls Novel real-time PCR for Giardia sp., real-time nested PCR for Cryptosporidium sp. 20 (population), 51 (pathogen isolated) 2,422 cases, 2,205 controls Cases: Giardia (2), Cryptosporidium spp. (2); controls: Giardia (1), Cryptosporidium spp. (0.5)
396 Sydney, Australia; 2003–2006 HIV-positive and HIV-negative MSM with diarrhea, presenting at general medical practice (GP) Molecular methods, modified iron-hematoxylin stain, and a carbol-fuschin staining step to detect coccidian parasites 23.98 (448 pathogens isolated) 1,868 total, 628 from HIV-negative patients, 618 from HIV-positive patients, 622 from non-MSM Entamoeba histolytica/E. dispar complex (2.9), Cryptosporidium species (1), Giardia intestinalis (2.9), Dientamoeba fragilis (0.8), Blastocystis spp.(16.9)
425 Northeast region of England; 2003–2005 Humans Cryptosporidium screen using auramine staining, microscopic examination for OCP NA 279 outbreaks, 2,889 cases tested Cryptosporidium (3.0)
90 Ankara, Turkey; 2005–2007 Hospital patients presenting with IBS, inflammatory bowel disease (5), and chronic diarrhea Native Lugol's, trichrome, and Kinyoun's acid-fast staining; genomic DNA preparation; subtyping by PCR with STS primers 18.1 (cases), 16.7% (controls) 105 cases, 96 controls Blastocystis (18 [cases]) and 16.7 [controls])
442 Uppsala, Sweden; 1981 Hospital inpatients and outpatient Swedish children of <15 years of age with acute gastroenteritis Parasitic studies, formalin-ether concentration method; Cryptosporidium detected by light microscopy and Kinyoun's acid-fast stainingd 68 416 cases, 200 controls Giardia intestinalis (1 [cases] and 1 [controls])
355 Brisbane, QLD, Australia; circa 1992 260 nonhospital patients with diarrhea sent to a private laboratory in Brisbane Fecal culture and microscopy (trichrome staining for identification by oil immersion microscopy) 15 260 specimens G. intestinalis (1.5), Blastocystis spp. (10.8), G. intestinalis (1.5)
416 Stockholm, Sweden; 1996-1997 Consecutive adult patients of >15 years of age with diarrhea and healthy control subjects OCP by direct microscopy and Cryptosporidium oocysts by a modified Ziehl-Nielsen technique 56 (cases), 16 (controls), 8 (protozoa) 851 cases, 203 controls Cases: E. histolytica (1), G. intestinalis (2), Blastocystis spp. (4), Cryptosporidium (2), microsporidia (<1); controls: E. histolytica (<1), Blastocystis spp. (9)
417 42 specialized travel or tropical medicine sites located on six continents; 1996–2005 Returned travelers diagnosed with an “infectious gastrointestinal disease” Best available reference diagnostics; there was considerable heterogeneity between centers in terms of availability and sophistication of diagnostic (e.g., molecular) testing 39 (65% of isolates were parasitic) 7,442; 2,902 tested for parasites Giardia (27.9), E. histolytica (12.5), Dientamoeba fragilis (4.0), Cryptosporidium spp. (1.1), Cyclospora (1.1), Cystoisospora belli (0.1)
12 26 U.S. states and two Canadian provinces; 1996 Fecal samples from infected and noninfected persons Formalin-ethyl acetate concentration sedimentation procedure and confirmatory permanent smears when necessary 5,250 cases C. cayetanensis (4.3); note that 91% of infected patients had gastroenteritis symptoms
144 Noumea, New Caledonia; 1990-1991 Patients of all ages with diarrhea Formalin-ether concentrates/smears stained with merthiolate-iodine-formaldehyde solution and examined microscopicallye 40.4 2,088 cases E. histolytica/dispar (3.5), Giardia intestinalis (7.8)
60 Republic of Korea; 2004–2006 Diarrheal patients hospitalized in 96 hospitals Enzyme immunoassay kit 36.8 76,652 cases Protozoa (2.3), Cryptosporidium spp. (0.8), Entamoeba histolytica/E. disparf (0.6), Giardia (1.7)
81 Netherlands; 1996–1999 Stool samples from patients who consulted with a GP regarding gastroenteritis Microscopic examination of SAF-fixated samplesg 37.5 (cases), 9.8 (controls) 857 cases, 574 controls Cases: G. intestinalis (5.4), Cryptosporidium spp. (2.1), Cyclospora (0.2), Entamoeba spp. (0.9), D. fragilis (10.3); controls: G. intestinalis (3.3), Cryptosporidium (0.2), Cyclospora (0.2), Entamoeba spp. (0.7), D. fragilis (14.6)
192 Gyeonggi-do, South Korea; 2004–2006 Gastroenteritis patients in hospital ELISA 3.4 6,071 cases Protozoa (3.4), G. intestinalis (2.5), E. histolytica/E. dispar (0.4), Cryptosporidium parvum (0.4)
301 16 Danish counties, Denmark; 2000-2001 Stool samples from children of less than 5 years of age from hospitals and general practice offices Microscopyh plus Ziehl-Neelsen acid-fast staining for Cryptosporidium and Cyclospora sp. 54 (cases), 22 (controls) 424 cases, 866 controls Cases: G. intestinalis (<1), Cryptosporidium (1.7), Blastocystis spp. (<1); controls: G. intestinalis (<1), Blastocystis spp. (1.3)
24 Melbourne, Victoria, Australia; 1980–1993 Hospitalized children (0 to 14 years old) Microscopyi for OCP, modified acid-fast smears for cryptosporidia 56.6 3,785 Cryptosporidium (0.5), G. intestinalis (0.3)
264 Sydney, Australia; 2001 412 children under 6 years of age with diarrhea, either hospitalized or outpatients at The Sydney Children's Hospital Giardia-specific enzyme immunoassay and microscopy with modified Ziehl-Neelsen stain for cryptosporidia 33 412 Cryptosporidium spp. (2.4), G. intestinalis (2.7)
370 Melbourne, Australia; 1997–1999 Fecal samples from family units (community) of at least two children (≤15 years old) and two adults each A modified iron-hematoxylin stain was used to detect Giardia and Cryptosporidium in concentrated specimens 25 791 Cryptosporidium spp. (1.6), Giardia intestinalis (2.5)
193 Neusiedl am See, rural eastern Austria; January to December 2007 Patients who consulted general practitioners for gastroenteritis Giardia intestinalis plus Cryptosporidium parvum (RIDA Quick Cryptosporidium/Giardia Combi test) 23.2 306 Protozoa (1.3), Cryptosporidium spp. (1.6), Giardia intestinalis (2.5)
128 Canadian hospital morbidity database (HMDB); 1995–2004 Population hospitalized in Canada for gastorintestinal illness (acute, chronic, and rehabilitation care) Not given 21.7 927,645 hospitalizations Entamoeba spp. (0.05), Giardia intestinalis (0.15), Cryptosporidium spp. (0.08)
467 England; 1993–1996 Patients with diarrhea in the community and seen by GP Microscopyj (12) 24 1,262 Protozoa (1.6), Cryptosporidium spp. (1.3), Giardia intestinalis (0.32)
204 Berlin, Germany; 2005–2007 Patients of ≥18 years of age hospitalized with community-acquired gastroenteritis SAF fixation-concentration and microscopy for OCP; direct immunofluorescence antibody test for G. intestinalis and Cryptosporidium; Kinyoun's staining method for Cryptosporidium, C. cayetanensis, and I. belli 59.8 132 Blastocystis spp. (7.6), Giardia intestinalis (7.6)
255 Parma, Italy; 1983-1984 Hospitalized patients with acute enteritis Microscopy 26.2 797 Protozoa (3.1), Giardia intestinalis (1.4)
225 Seattle, WA, USA; 1998–2001 Children with diarrhea who presented to a pediatric emergency department Trichrome stains and formalin-ethyl acetate sedimentation for OCPD and fluorescence antibody testing for Giardia and Cryptosporidium sp. 19.5 656 (from 1,626 patients) Protozoa (2.13), Blastocystis spp. (1.1), Cryptosporidium spp. (0.15), Giardia spp. (0.46), E. histolytica/E. dispar (0.15)
265 United States; 1996-1997 National surveillance data for food-borne illness cases Not given Not given Estimated 38,629,641 cases Parasites (6.6), Cryptosporidium parvum (0.8), Cyclospora cayetanensis (0.4), Giardia intestinalis (5.2)
215 Helsinki, Finland; 1982-1983 Fecal samples sent by GPs for routine parasitological examination Ritchie's formalin ether concentration method, used along with a modified Ziehl-Neelsen method Not given 154 Cryptosporidium spp. (9.1), Giardia (29.2), Blastocystis spp. (13), E. histolytica/E. dispar (2)
1 Tenerife, Canary Islands, Spain; ∼2004 Clinical samples (156 stools) Light microscopy, staining with Weber's chromotrope and PCR-hybridization for the identification of Enterocytozoon bieneusi 11.54 156 Protozoa (11.54), E. bieneusi (11.54)
96 United States (10 cities); 1998-1999 Diarrheal stool specimens from HIV-infected patients in 3 U.S. hospitals and a database Moura's quick-hot Gram chromotrope technique, modified trichrome blue stain (confirmed by chromotrope 2R staining and oil immersion microscopy) 1.5 737 Microsporidian species (1.5)
248 Vigo, Spain; ∼2001 Elderly HIV-negative patients; 47 of 60 had diarrhea Light microscopy with Weber's chromotrope-based stain and PCR-hybridization 17.02 60 E. bieneusi (17.02)
448 Central area of Brussels, Belgium; 2002-2003 Patients suspected of suffering from a parasitic gastrointestinal illness Bright-field microscopy and PCR 37 1,207 stool samples from 448 outpatients D. fragilis (6.3), G. intestinalis (7.1), C. parvum (1.6%), E. hystolytica (0.2%), Blastocystis sp. (9.8%), Entamoeba coli (5.4%)
a

In some reports, some patients had multiple pathogens isolated; hence, the percentages may not add up to 100%.

b

The designation E. histolytica is reported as E. histolytica/E. dispar for consistency, unless the study's methodology indicated clearly that the test was specific for E. histolytica.

c

Incomplete techniques and no permanent stained smears used. The methods were described as follows. “Wet mounts of 5,022 freshly passed stools were examined for leukocytes or parasites or both. The samples which were not immediately processed were stored at 4degrees Celcius for a maximum of 36 h.”

d

Permanent stains were not performed for routine investigations of protozoa.

e

No permanent stains performed. Although the authors indicate the presence of E. histolytica, there is nothing in the article to indicate that the organisms were confirmed as E. histolytica versus E. histolytica/E. dispar.

f

A Ridascreen immunoassay kit was used, and this test detects E. dispar trophozoites. However, the authors reported that the organisms were E. histolytica.

g

Microscopic examination included a combination of (i) a wet film (iodine stained or unstained); (ii) Ridley concentration (iodine staining); (iii) modified Ziehl-Neelsen staining of Ridley concentrate; and (iv) permanent staining by hematoxylin.

h

Microscopy of concentration sediment wet mount for protozoa only, other than special stains for coccidia.

i

Microscopy for wet mount examination only, other than special stains for coccidia.

j

Microscopy not defined.