Professional Documents
Culture Documents
By:
Name : Dion Satrio Pambudi
Student ID : B1B015018
Group : 4
Entourage : II
Assistant : Wiwin Hadianti
2017
I. INTRODUCTION
A. Background
Parasites are organisms that live in or on another organism, the host, and live
at the expense of the host organisms. Parasites depends on their host for nutrients give
rise to the injury of the host. Some parasites might cause little harm to the host this
type of parasites called Opportunistic parasites. Some cause few or no symptoms in
healthy hosts, but may cause sever desease in immunocompomised host. Some
however may caue severe disease and even death if not properly treated, called
pathogenic parasites (Estridge, et al., 2000).
To complete their life cycles, the parasites own specific requirements. Some
parasites are mostly host-specific. In some ccases, if the conditions are right, the
parasites may survive or even thrive in unnatural host. There are types of hosts for
parasites. Definitive host, intermediate host, reservoir host, and vector. Some parasites
are required two or more different host to complete their life cycle (Estridge, et al.,
2000).
As we understand from previous paragraph that parasites can infect host in
other words another organisms including animals and human. Following this
statements, a useful parasite examination needed in order clarify if one organism is
infected by parasites or not (Estridge, et al., 2000). Diagnosis of parasites begins with
ova and parasite examination (Fischbach & Dunning, 2009). The two most common
parasitology laboratory requests are for blood and fecal examination. Other specimen
can be use such as tissue, fluid of organ, parts of organ can be use as specimen for
examination (Estridge, et al., 2000).
B. Purpose
A. Material
The tools used in the lab this time was microscope, object glass, cover glass,
surgery tools, camera, masker, latex glove.
The materials used are cow liver, cow gall, goat intestine, chiken intestine, and
snail (Lymnaea sp).
B. Methods
1. The examined snails are cut on the third circle or dorsal part. The water out is
dripped on the object glass and observed under microscope.
2. The examined cow liver and cow gall are firstly cut and split, then observed
whether there are worm in the preparation or not.
3. The examined chicken intestine are firstly sliced until it is clean from its dirt,
and then tested for the existence of worms among the dirt.
4. The examined duck intestine are firstly sliced, clean from the dirt, then tested
for the existence of worms.
5. The gall is immersed in the water until precipitated, then replace water after
precipitated, repeat until three times, then observe the precipitate resulted.
III. RESULT AND DISCUSSION
A. Result
Specimen Group
1 2 3 4 5
Cow Hepar Faciola Faciola
hepatica hepatica ()
(9)
Cow Gall Faciola hepatica (1)
Cow intestine
Goat intestine
Chicken intestine Ascaridiagalli
(20) &
Railietinate
tragona (9)
Snail - - 2 1 -
B. Discussion
1. Based on the result of observation, the average of albumin content for mice
feed with 0 gr dose of spirulina is 4.5235 g/dl, for 2 gr dose is 3,81875 g/dl, for
3 gr dose is 3,44775 g/dl, for 4 gr dose is 3,890175 g/dl, and for 5 gr dose is
3,046 g/dl.
2. To know the content of albumin content, we can use brom cresol method.
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