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Diagnosis and control of endoparasites in wild animals and Birds.pptx
1.
2. Diagnosis and control of endoparasites in
wild animals and Birds
Submitted to
Respected Prof. Dr. Asif Raza
Submitted by
FOUZIA TABASSUM
SHAHEEN
Course code: 715
Parasitology
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4. Content List
Most prevalent endoparasites in wild animals, Birds and Mammals
Diagnosis in Wild Animals
Diagnosis in Birds
Diagnosis in Mammals
Control of endoparasites in wild animals and Birds
13. Internal Parasite Diagnosis
in Small Animals
Diagnosis of internal parasites in small animals is
typically performed by examination of feces for parasite
eggs.
Fecal samples should be fresh, preferably collected from
the animal during the act of defecation or from the
rectum using a fecal loop during the physical
examination
Specimens should be submitted to a diagnostic
laboratory in a sealed container, labeled with proper
identification.
Specimens should be fixed in 10% formaldehyde
solution or sent chilled.
Other preservative solutions (eg, sodium acetate
formalin, polyvinyl alcohol, available in commercial
mailer kits) better preserve protozoa and facilitate
special staining (eg, trichrome, iron hematoxylin).
14. Cont…
Routine examinations should be done by both direct fecal smear and fecal flotation.
Direct smears are prepared by mixing feces (an amount of feces fitting on one-half the tip of a
wooden applicator stick) with 1 drop each of saline (for motile organisms) and Lugol’s iodine stain
(to see internal morphologic structures, eg, those of Giardia), and covering with separate coverslips
on the same slide.
Flotation methods concentrate diagnostic stages and provide a cleaner final preparation, using ~2 g
of feces.
Sugar (specific gravity [SG] 1.27) and sodium nitrate (SG 1.39) are commonly used flotation media.
Zinc sulfate flotation (SG 1.18), repeated on 3 consecutive days, is the method of choice to
reveal Giardia cysts, which are intermittently shed in feces.
15. Cont…
Motile nematode larvae may be collected and concentrated by Baermann sedimentation; a
convenient method is to place ~2 g of feces on several sheets of cotton gauze in a tea strainer
suspended in the wide end of a large, conical funnel fitted with a rubber tube and stopcock.
The funnel is filled with warm tap water or saline for 1 hr before sediment examination.
Larvae descend within the funnel due to gravity and are collected from the end of the stopcock
for microscopic examination.
Special procedures, such as formalin-ethyl acetate sedimentation, may be used for parasitic
larval stages that do not float well.
Sheather’s sugar (SG 1.30) can be used to detect small oocysts of Cryptosporidium (4–6 μ)
or Toxoplasma (12 μ) by focusing just under the coverslip.
Oocysts “float up” to the under-surface of a coverslip placed on the slide for 10 min before
examination.
16. Cont…
A direct smear using 1 drop of blood can be used to detect motile microfilariae of Dirofilaria immitis, but
this should not be the sole means of detection.
More accurate examination of blood may be done by a modified Knotts’ test: 1 mL blood is added to 9
mL of 2% formalin solution in a 15-mL tube and centrifuged at 1,500 rpm.
The supernatant is discarded and a drop of methylene blue stain is mixed with the sediment “button,”
which is pipetted onto a microscope slide, covered with a coverslip, and examined to differentiate
microfilariae of D immitis from those of the nonpathogenic Dipetalonema reconditum.
Commercial filtration and staining procedures are effective alternatives to the modified Knotts’ test.
Animals on heartworm preventive become amicrofilaremic, and an occult heartworm test using a
commercially available ELISA for circulating uterine antigen of adult female Dirofilaria is the method of
choice for treated dogs.
Feline dirofilariasis cannot be reliably diagnosed by microfilaremia or antigenemia tests, because
heartworm numbers are typically too low; antibody titers to D immitis are used to detect prior exposure
and possible current infection in cats.