There are four species of blood flukes that are primarily associated with disease in humans (known as
schistosomiasis, bilharziasis, or snail fever), all belonging to the genu Schistosoma. These four species are
Schistosoma haematobium, S. japonicum (Oriental blood fluke), S. mekongi, and S. mansoni. A fifth species, S.
intercalatum, is a pathogen primarily in animals but has been associated with human disease. The blood flukes
differ
in morphology and life cycle characteristics from the other trematodes, but because they all belong to the same
genus, they are very similar, and may be difficult to distinguish from each other. They do, however, require a
freshwater snail as the only intermediate host.
Figure 58: Paragonimus westermani egg.
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General characteristics
Unlike the other trematodes, adult schistosomes are not flattened, but are rather long, thin, and rounded in
shape. There is an oral sucker surrounding the mouth and a ventral sucker located just slightly below the oral
sucker. The adult male averages 1.5 cm in length and is wider than the female, having a ventral fold that wraps
around the female when they mate (Figure 59). The adult female averages 2 cm in length and is very thin.
The eggs of each species are distinct, and can be distinguished by size, spine morphology, and sometimes
specimen type (Figure 60). The size range for eggs of S. haematobium is 110 to 170 μm long by 40 to 70 μm
wide and they have a sharply pointed terminal spine. They are fully embryonated without an operculum. The size
range for the eggs of S. japonicum is 70 to 100 μm long by 50 to 65 μm wide, and they have a small lateral spine
that is sometimes difficult to detect .
S. mekongi eggs are smaller than those of S. japonicum, ranging in size from 50 to 65 μm long by 30 to 55 μm
wide. They are fully embryonated without an operculum and have a small lateral spine. The size range for eggs of
S. mansoni is 115 to 180 μm long by 40 to 75 μm wide, and they have a large lateral spine. S. mansoni eggs are
unoperculate, immature when released, and take up to 8 to 10 days to develop a miracidium. S. intercalatum eggs
are fully embryonated without an operculum, have a terminal spine, and range in size from 140 to 240 μm long by
50 to 85 μm wide. S. intercalatum eggs resemble those of S. haematobium and can be differentiated by ZiehlNeelsen acid-fast positivity. In addition, S. intercalatum eggs are only found in feces, not in urine specimens
One of the main differences in the schistosomes from other trematodes is that instead of being hermaphroditic,
there are separate male and female adult worms. In human infection, the adult worms live in either the veins that
supply the intestine (S. japonicum and S. mansoni) or the veins that supply the urinary bladder (S. haematobium).
The eggs are passed from the body in either the feces or the urine. To reach the inside of the intestine or bladder,
the eggs must penetrate the tissue from the veins. This is accomplished via a spine that is distinctive among the
major species. The embryonated egg will release the miracidium (Figure 62) once it reaches freshwater, and will
enter the snail host, where it will develop into the infectious cercaria. The freeswimming cercariae are capable of
penetrating through the human skin directly and do not encyst on aquatic vegetation or other aquatic wildlife
(Figure 63). The cercariae penetrate the host tissue until they reach a vein; then they travel to capillaries near the
lungs and then to the portal vein of the liver, where they mature. When they are mature, the adult males will pair
with the females and then travel to the veins of either the intestine or thebladder, where the eggs are produced.
Pathology and spectrum of disease
Infection with only a small number of worms may be asymptomatic. Quite often, penetration of the skin by
the cercariae causes localized swelling and itching. The migration of the larvae through the body may cause
transient symptoms of fever, malaise, cough (when they migrate in the lungs), or hepatitis (when in the liver).
The adults are able to acquire some host antigens on their outer surface, and so may not elicit an immune
response, although the eosinophil count may be high.
Severe tissue damage, with associated pain, fever, and chills, may occur when the eggs travel through the
tissue to reach the intestine or bladder. There may also be bloody diarrhea or blood in the urine (hematuria).
Necrosis, lesions, and granulomas may develop, as well as obstruction of the bowel or ureters. Penetration of
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human skin by the cercariae of blood flukes that commonly infect other mammals or aquatic birds may cause a
schistosomal dermatitis known as “swimmer’s itch.” Erythema, edema, and intense itching may develop that
usually disappear within 1 week. The cercariae of these species are not able to complete the life cycle by
entering the human bloodstream, and are destroyed by the host immune system.
Figure 59: Mating of Schistosoma mansoni male and femaleWorms.
Figure 60, Schistosoma mansoni egg. B, Schistosoma japonicum egg. C, Schistosoma haematobium egg.
Figure 61 :S. japonicum egg. Figure 62 :S. mansoni miracidium.
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Laboratory diagnosis
The standard method of diagnosis is by the detection of characteristic eggs in feces or rectal biopsy, for S.
japonicum, S. mekongi, S. mansoni, and S. intercalatum (and perhaps S. haematobium if these worms have
migrated to a bladder vein that is close to the intestine); and in urine (usually concentrated before examination)
or bladder tissue biopsy for S. haematobium.
A wet mount with/without iodine from a sedimentation or concentration method can be examined for eggs.
Figure provides images of three different schistosome eggs. To optimize recovery of S. haematobium in urine,
the specimen should be collected between noon and 2 pm. There are some antibody-based assays that are
available for diagnosis of schistosomal IgG antibody (enzyme immunoassay [EIA], enzyme-linked
immunosorbent assay [ELISA], and immunoblot), but these methods cannot distinguish between current and
previous infections. This type of assay may, however, be useful for travelers who have returned from endemic
areas.
Several nucleic acid-based testing methods have been developed that demonstrate high sensitivity and
specificity using genomic or mitochondrial sequences. In addition, schistosome DNA has been identified in
patients’ plasma using real-time polymerase chain reaction (PCR).
Therapy
The drug of choice for treatment of schistosome infections is praziquantel, given in two or three doses in a
day. Infection with S. mansoni may require a larger dose than that for the other species.
Prevention
Because human infection is by direct penetration of the cercariae, prevention of schistosome infection is more
difficult to achieve. Educational programs are required to help people in endemic areas understand how to help
prevent infection.
Sanitary conditions need to be improved with proper disposal not only of human wastes but also that of
domestic animals (in areas with S. japonicum and S. mekongi). A safe water supply for bathing and washing
Figure 63: S. mansoni cercaria.
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clothes is also necessary. Various snail control methods have been tried, but these methods are very costly and
would need to be repeated on a regular basis to have the desired effect.
Table Body Sites and Parasite Recovery (Trophozoites, Cysts, Oocysts, Spores, Adults, Larvae, Eggs,
Amastigotes,Trypomastigotes)
Site Parasites
Blood
Red cells
Plasmodium spp.
Babesia spp.
White cells Leishmania spp.
Toxoplasma gondii
Whole
blood/plasma
Trypanosoma spp.
Microfilariae
Bone marrow Leishmania spp.
Trypanosoma cruzi
Plasmodium spp.
Central
Nervous
System
Cutaneous
ulcers
Taenia solium (cysticerci)
Echinococcus spp.
Naegleria fowleri
Acanthamoeba spp.
Balamuthia mandrillaris
Sappinia diploidea
Toxoplasma gondii
Microsporidia
Trypanosoma spp
Intestinal tract Leishmania spp.
Acanthamoeba spp.
Entamoeba histolytica
Entamoeba dispar
Entamoeba coli
Entamoeba hartmanni
Endolimax nana
Iodamoeba bütschlii
Blastocystis hominis
Giardia lamblia
Chilomastix mesnili
Dientamoeba fragilis
Pentatrichomonas hominis
Balantidium coli
Cryptosporidium spp.
Cyclospora cayetanensis
Isospora belli
Microsporidia
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Ascaris lumbricoides
Enterobius vermicularis
Hookworm
Strongyloides stercoralis
Trichuris trichiura
Hymenolepis nana
Hymenolepis diminuta
Taenia saginata
Taenia solium
Diphyllobothrium latum
Clonorchis sinensis (Opisthorchis)
Paragonimus spp.
Schistosoma spp.
Fasciolopsis buski
Fasciola hepatica
Metagonimus yokogawai
Heterophyes heterophyes
Liver, spleen Echinococcus spp.
Entamoeba histolytica
Leishmania donovani
Microsporidia
Lung Cryptosporidium spp.*
Echinococcus spp.
Paragonimus spp.
Microsporidia
Muscle Taenia solium (cysticerci)
Trichinella spp.
Onchocerca volvulus (nodules)
Trypanosoma cruzi
Microsporidia
Skin Leishmania spp.
Onchocerca volvulus
Microfilariae
Urogenital
system
Trichomonas vaginalis
Schistosoma spp.
Microsporidia
Microfilariae
Eye Acanthamoeba spp.
Toxoplasma gondii
Loa loa
Microsporidia
Note: This table does not include every possible parasite that can be found in a particular body site; the most
likely organisms have been listed.
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*Disseminated in severely immunosuppressed individuals
Table Epidemiology of the More Common Groups of Human Parasites
Parasite
Group
Habitat (Reservoir Mode of Transmission Prevention
Protozoa,
Intestinal
Amebae
Single-celled organisms
generally found
in humans. Although certain
animals
harbor some of these
organisms,
they are not considered
important
reservoir hosts.
Humans acquire infections by
ingesting
food and water contaminated
with fecal
material containing the
resistant, infective cyst stage
of the protozoa.
Various sexual practices have
also been documented in
transmission.
Preventive measures
include
increased attention to
personal
hygiene and sanitation
measures; elimination of
sexual
activities that may
involve
fecal-oral contact.
Flagellates The flagellates are generally
found in
humans. Although certain
animals
harbor some of these
organisms,
they are not considered
important
reservoir hosts; one exception
may
be animals, such as the
beaver, that
harbor Giardia lamblia.
Contaminated
water supplies are also a
source.
Humans acquire infections by
ingesting
food and water contaminated
with fecal
material containing the
resistant,
infective cyst stage of the
protozoa; in
some cases (Dientamoeba
fragilis), no
cyst stage has been identified;
the
trophozoite forms may be
transmitted
from person to person in
certain
helminth eggs.
Preventive measures
include
increased attention to
personal
hygiene and sanitation
measures; elimination of
sexual
activities that may
involve
fecal-oral contact;
adequate
water treatment
(including
filtration) is required;
also
awareness of
environmental
sources of infection.
Ciliates Balantidium coli is generally
found in
humans, but it is also found in
pigs.
In some areas of the world,
Humans acquire infections by
ingesting
food and water contaminated
with fecal
material containing the
Preventive measures
include
increased attention to
personal
hygiene and sanitation
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pigs are
considered important reservoir
hosts.
resistant,
infective cyst stage of the
protozoa
measures, as well as
elimination of sexual
activities
that may involve fecaloral
contact.
Coccidia Coccidia are found in humans.
In some
cases (e.g., cryptosporidiosis)
animal
reservoirs (cattle) can serve as
important hosts. The muscle
of
various animals may contain
sarcocysts that are infective
for
humans through the
consumption of
raw or poorly cooked meat.
Numerous waterborne
outbreaks
with Cryptosporidium spp.
have been
reported throughout the world.
Coccidian oocysts are
extremely
resistant to environmental
conditions,
particularly if they are kept
moist
These protozoa are acquired
through
ingestion of various meats or
by
fecal-oral transmission through
contaminated food and/or
water. The
infective forms are called
oocysts
(Cryptosporidium spp.,
Isospora
(Cystoisospora) belli,
Cyclospora
cayetanensis) or sarcocysts
(Sarcocystis
spp.), which are contained in
infected
meat. Cryptosporidia have also
been
implicated in nosocomial
infections.
Preventive measures
include
increased attention to
personal
hygiene and sanitation
measures; elimination of
sexual
activities that may
involve
fecal-oral contact.
Adequate
water treatment
(including
filtration) is mandatory;
awareness of
environmental
sources of infection also
is
important.
Microsporidia Microsporidia can infect
every living
animal, some of which
probably
serve as reservoir hosts for
human
infection. However, host
specificity
Infection with microsporidial
spores usually
occurs through ingestion;
however,
inhalation of spores and direct
inoculation from the
environment almost
certainly occur.
Preventive measures
include
increased attention to
personal
hygiene and sanitation
measures; increased
awareness of
environmental
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has not been well defined to
date.
The spores are
environmentally
resistant and can survive years
if
kept moist.
exposure possibilities;
and
adequate water
treatment.
Protozoa,
Other
Sites
Amebae
Free-living amebae are
associated with
warm, freshwater
environments; they
are also found in soil.
Although
humans can harbor these
organisms,
person-to-person transfer is
thought
to be rare. Environmental
sources
are the primary link to human
infection. Contaminated eye
care
solutions have been linked to
organisms that cause keratitis.
Infection occurs through
contact with
contaminated water; organisms
enter
through the nasal mucosa and
may
travel via the olfactory nerve
to the
brain. Disease can be very
severe and
life-threatening; keratitis is
also caused
by these organisms, and
infection can
be linked to blindness or
severe corneal
damage. Eye infections can be
linked to
contaminated lens solutions or
direct,
accidental inoculation of the
eye from
environmental water and/or
soil sources.
Avoidance of
contaminated
environmental water and
soil
sources; adequate care of
contact lens systems
Flagellates Trichomonas vaginalis
infection is found
in a large percentage of
humans;
humans may present as
symptomatic or
asymptomatic.
T. vaginalis is found in the
genitourinary
system and is usually acquired
by
sexual transmission.
Awareness of sexual
transmission; treatment
of all
partners when infection
is
diagnosed in an
individual
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Person-to-person transfer is
very
common; reinfection is also
common, particularly if sexual
partners are not treated.
patient.
Protozoa,
Blood
and Tissue
Malaria,
Babesiosis
Humans harbor the five
species of
malaria (Plasmodium vivax,
P. ovale,
P. malariae, P. knowlesi, and
P.
falciparum). Other animals
can carry
Babesia spp., and animal
reservoir
hosts play a large role in
human
transmission.
These organisms are
arthropod-borne,
Plasmodium spp. by the
female
anopheline mosquito and
Babesia spp.
by one or more genera of ticks.
These
infections can also be
transmitted
transplacentally, via shared
needles,
through blood transfusions,
and from
organ transplants.
Vector control;
awareness of
transmission through
blood
transfusions, shared drug
needles, congenital
infections,
and organ transplants.
Careful
monitoring of the blood
supply.
Malaria prophylaxis if
traveling
to endemic areas.
Flagellates
(leishmaniae
Some strains of leishmaniae
have
reservoir hosts (e.g., dogs for
the
Mediterranean strain of
Leishmania
donovani and wild rodents for
the
African strains of L.
donovani.) L.
tropica also has been linked to
the
same two animal reservoirs
Transmission is through the
bite of infected
sandflies. Infection can also
occur from
person to person (cutaneous
lesions),
from blood transfusion, shared
needles,
and organ transplants.
Vector control; avoiding
environmental sources
(e.g.,
dogs, wild rodents);
careful
handling of all clinical
specimens from infected
patients.
Flagellates
(trypanosomes
Humans are the only known
hosts for
Trypanosoma brucei
gambiense
(West African
Transmission is through the
bite of the
infected tsetse fly and through
blood
transfusion, shared needles,
Vector control;
awareness of
potential
exposure/infection
from blood sources
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trypanosomiasis);
Trypanosoma brucei
rhodesiense
(East African
trypanosomiasis)
infections are found in a
number of
antelope and other ungulates
that
act as reservoir hosts. Rodents
and
some mammals are reservoir
hosts
for Trypanosoma cruzi
and organ
transplants.
Transmission of T. cruzi is
through the
infected feces of the triatomid
bug; the
bug takes a blood meal,
immediately
defecates, and the human host
scratches the infected feces
into the
bite site; bug saliva contains
an irritant
that stimulates scratching
(transfusions, shared
needles,
organ transplants).
Laboratory
accidents while handling
infected blood have been
reported.
Nematodes,
intestinal
These roundworms generally
do no
have animal reservoirs
relevant to
human infection. One
exception is
the pig ascarid; human
infections
have been reported. These
worms
are found worldwide; Ascaris
lumbricoides is probably the
most
common parasite of humans,
although some would argue
that
Enterobius vermicularis is
number
one. Strongyloides stercoralis
is
particularly important as the
causative agent of severe
disease in
the compromised host.
A. lumbricoides and Trichuris
trichiura eggs
must undergo development in
the soil
before they are infective; thus
children
who play in the dirt are a
particularly
high-risk group. Ingestion of
food and
water contaminated with
infective eggs
is the primary route of
infection.
Hookworm and S. stercoralis
infections are
initiated by larval penetration
of the skin
from contaminated soil.
Pinworm infection (E.
vermicularis) is
acquired through ingestion of
infective
eggs from the environment
Avoiding ingestion of
contaminated soil and/or
avoiding frequenting soil
contaminated with
hookworm
eggs (pets, soil, water,
warmth,
warm weather);
treatment for
pinworm is
recommended, but
reinfection is common
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(hand-tomouth).
Nematodes,
Tissue
Trichinella spp. have a
number of
animal reservoir hosts,
including
bears, walruses, pigs, rodents,
and
other animals. Dog and cat
hookworms cause cutaneous
larva
migrans (CLM), and the dog
and cat
ascarid, Toxocara spp., causes
visceral and ocular larva
migrans
(VLM, OLM). These
infections can be
serious and cause severe
disease if
not treated.
Trichinella organisms are
acquired by
ingestion of raw or poorly
cooked
infected meat.
CLM is caused by skin
penetration of
infective larvae from the soil;
children
should avoid sandboxes where
dogs and
cats are known to defecate.
Larval
migration is limited to the
skin.
VLM and OLM are caused by
accidental
ingestion of Toxocara spp.
eggs from
contaminated soil; larval
migration
occurs throughout the body,
including
the eyes.
Adequate cooking of
infected
meat; awareness of
possibility
of contaminated soils for
dog
and cat hookworms
and/or
ascarids; covering of all
sandboxes where pets
have
access to defecation and
children play.
Nematodes,
filarial
Wuchereria bancrofti, Loa
loa, and
Onchocerca volvulus have no
animal
reservoirs and are found only
in
humans, whereas Brugia spp.
can
also be found in cats and
monkeys.
Dracunculus medinensis can
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