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Table 1: Protozoans Spp. "CYSTS" Size Number OF Nuclei Karyosome Peripheral Chromatin Cytoplas M and Inclusion

1. The document provides information on 10 protozoan species including their size, number of nuclei, karyosome features, cytoplasmic inclusions, and pathogenicity. 2. It describes morphological characteristics like size, motility, nuclear features, and cytoplasmic contents that can be used to identify different protozoan species under the microscope. 3. Certain species like Entamoeba histolytica and Naegleria fowleri are identified as pathogenic parasites while others such as Entamoeba hartmanii are typically non-pathogenic.

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Joshua Trinidad
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0% found this document useful (0 votes)
224 views3 pages

Table 1: Protozoans Spp. "CYSTS" Size Number OF Nuclei Karyosome Peripheral Chromatin Cytoplas M and Inclusion

1. The document provides information on 10 protozoan species including their size, number of nuclei, karyosome features, cytoplasmic inclusions, and pathogenicity. 2. It describes morphological characteristics like size, motility, nuclear features, and cytoplasmic contents that can be used to identify different protozoan species under the microscope. 3. Certain species like Entamoeba histolytica and Naegleria fowleri are identified as pathogenic parasites while others such as Entamoeba hartmanii are typically non-pathogenic.

Uploaded by

Joshua Trinidad
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© © All Rights Reserved
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TABLE 1:

PROTOZOANS SIZE NUMBER KARYOSOME PERIPHERAL CYTOPLAS


spp. “CYSTS” OF CHROMATIN M AND
NUCLEI INCLUSION
15-60 4 small fine, uniform, RBC
1. E. histolytica µm and evenly
distributed
-2.0 µm 2-4 large no peripheral insulin
2. E. coli chromatin proteins

5-10 µm 4 small, compact, uniform cyst


3. E. hartmanii centrally or
eccentrically
6–12 µm 4 large karyosome no peripheral present
4. E. nana chromatin

20-150 1 prominent clumped finely


5. E. gingivalis µm central nucleus granular

9 - 15μ 1 large coarse, RBC


6. I. butschlii granular

13-17 1 large coarse, clumped bright to dark


7. B. hominis mm uneven red

8-15 µm 1 large, dense lack numerous


8. Naegleria fowleri

15 to 25 1 large no peripheral prominent


9. Acanthamoeba spp. μm chromatin contractile
vacuole
50-70 μm 2 small, central granule ciliated
10. B. coli

PROTOZOANS SIZE MOTILITY KARYOSOME PERIPHERAL CYTOPLASM PATHOGENECITY U


spp. CHROMATIN & F
“TROPHOZOITE INCLUSION

15-60 sluggish small fine, RBC  pathogenic ame
1. E. µm uniform, and ba la
histolytica evenly
distributed
50 µm sluggish large no peripheral insulin not
2. E. coli chromatin proteins considered path e
ogenic ka

15 µm less rapid small, uniform cyst not


3. E. hartmanii compact considered path w
ogenic t
p

6–12  sluggish large no peripheral present non-pathogenic  g


4. E. nana µm karyosome chromatin amoeba

10-20 pseudopod prominent clumped finely not


5. E. µm central granular considered path k
gingivalis nucleus ogenic

8-20 sluggish large coarse, RBC not


6. I. butschlii µm granular considered path s
ogenic
n
50-70 Rotary, large coarse, coarse, unclear pathoge p
7. B. hominis mm boring clumped clumped nic te
uneven uneven
10-35 lobopodia large, dense lack lack pathogenic D
8. Naegleria µm l
fowleri

15 to cytoskeleto large no peripheral no pathogenic


9. 25 μm n-based chromatin peripheral n
Acanthamoeba chromatin
spp.

50-100 “like a small, granule granule opportunistic pat


10. B. coli μm thrown central hogen la
football”

TABLE 2:
REFERENCES:

Centers for Disease Control and Prevention


Laboratory Diagnosis of Amebiasis by Mehmet Tanyuksel, William A. Petri Jr.
Global Health, Division of Parasitic Diseases and Malaria

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