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  7. Human Parasites, Micro-organisms And Zoonoses (UA_2008FBDBMW)

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Summary CHAPTER 2 - protozoa

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  • Human Parasites, Micro-organisms And Zoonoses (UA_2008FBDBMW)
  • Institución
  • Universiteit Antwerpen (UA)

The document consists of chapter 2: protozoa of the course Human parasites, micro-organisms and zoonoses of the master in biomedical sciences: tropical and infectious diseases given by prof. Guy Caljon. All information and important notes that were given during the classes were noted.

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Información del documento

  • 27 de diciembre de 2021
  • 46
  • 2021/2022
  • Resumen

Temas

  • parasitology
  • human parasites
  • zoonoses
  • protozoa
  • leishmania
  • malaria
  • toxoplasma
  • kinetoplasts
  • mucoflagellates
  • giardia

Escuela, estudio y materia

  • Universiteit Antwerpen (UA)
  • Biomedische Wetenschappen
  • Human Parasites, Micro-organisms And Zoonoses (UA_2008FBDBMW)
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CHAPTER 2: PROTOZOA
INTRODUCTION

GENERAL CHARACTERISTICS AND CLASSIFICATION


General characteristics
o Kingdom: protista, subkingdom: protozoa
o Can live in plants, invertebrates and vertebrates
o Some are free-living, some are parasites
o Subdivided in 7 phyla
 many of them are not pathogenic
 only 3 of them with human medical importance: sacromatogophora, apicomplexa and
ciliophoran
o structure:
 unicellular eukaryote cell structure
 specialized intracellular organelles: important for uptake of nutrients, metabolism,
locomotion etc.
o short generation time and high reproduction potential
 result: quickly adaptable organisms
 e.g. rapidly getting resistance  need for monitoring the resistance
o sexual and/or asexual multiplication
 asexual: very fast, used to colonize a host
 sexual: exchange of DNA material to get some variance in the DNA genome

General classification: 3 phyla of protozoa
In this course, we focus on the 3 phyla that are of human importance: sarcomastogophora, apicomplexa and
ciliophora.

o Sacromastogophora:
 Sarcodina:
 amoeboid with pseudopodia for moving and food uptake in a certain lifestage
 uptake of nutrients via phagocytosis
 extracellular
 heterotrophe
 Mastigophora:
 Eukaryotes with 1 or more flagellae in flagellar pocket in a certain lifestage
 Most are extracellular
o Apicomplexa: e.g. malaria, toxoplasma
 Eukaryotes with no flagellae (cannot move) but with apical organel complex in different
stages
 Intracellular
 heterotrophe
o Ciliophora:
 Oval cells with ciliated surface (smaller than flagella but higher amounts so can move)
 Presence of macro- and micronucleus, micro: important for sexual recombination
 Free-living or parasitic
 Heterotrophe

,SPECIFIC CHARACTERISTICS OF PROTOZOA




Explanation of the terminology
Endogeny: daughter cells inside mother cell before cell division (e.g. toxoplasma)
Schizogony: first multiple nuclear divisions followed by cytoplasmic incision, different processes
- merogony: give rise to merocytes which is a perfect target for drug treatment
- sporogony: give rise to sporozoites, proliferating/infectious stage of a parasite in a vector
- gametogony: give rise to gametocytes -> gametes, not a drug target
Cyst: protective stage of a parasite, can survive in certain conditions it which it otherwise won’t survive

,DETAILED CLASSIFICATION OF PROTOZOA




*only those indicated in blue are important to remember

- hemoflagellates: trypanosoma and leishmania
- mucoflagellates: trichomonas
 commensal, found in mucosa of GIT

Groups at risk for infections
- toxoplasma: risk during pregnancy
- isospora, cryptosporidium: risk for HIV patients
- plasmodium: risk for children (plasmodium falciparul, celebral malaria)
- babesia: risk for dogs, immunocomprimied people (no spleen)


Treatment of infections
- mucoflagellates: nitroimidazoles – induce ROS, cause DNA damage in the parasite
- hemoflagellates: different options depending on the location of the parasite
 if infection also in the brain: drug needs to able to cross the blood-brain barrier without being toxic

INTESTINAL AMOEBAE

Most entamoeba are located in the large intestine and will remain there, therefore the pathogenicity of these
parasites is very low as there are limited physiological processes in the large intestine with which the parasite
can interfere. As a result, most of entamoeba are commensal in the GI tract.
!Entamoeba histolytica: migration to liver  more pathogenic!

Entamoeba life stages
o Trophozoite stage: proliferating/feeding stage
o Cysts stage: survival stage outside of the host, metabolic reduced (e. gingivialis: no cysts!)
 Problem for disease control: decontamination of environment is impossible, only possible
to prevent exposure
 Problem for resistance: very resistant to chlorine: not useful to treat drinking water with
chlorine, better to boil and filter the water

,  1 cyst contains 4 nuclei so formation of 4 parasites out of 1 cyst

General morphology




Entamoebas have a cyst and trophozoite stage, the entamoeba will go from trophozoite to cyst when it goes
along in the GI tract. The entamoeba (trophozoites) feed on bacteria and will take these up by phagocytosis.

o Trophozoites:
 Pseudopodia: movement of parasite
 Nucleus: relaxed chromatin
 Karyosome: in centre of nucleus, with more condensed chromatin
o Cysts:
 Glycogen mass: food source/reserve
 2-4 nuclei in metacyst (precyst: only 1 nucleus)  1-4 parasites out of 1 cyst
 Chromidial bodies: aggregation of ribosomes in cytoplasm, contains RNA which are rapidly
translated to proteins when the entamoeba infects a host

Lot of entamoeba cysts and trophozoites are present in the intestine and thus in the feces (cysts: most in
normal feces, trophozoites: most in diarrhea). Therefore, making a differential diagnosis is sometimes hard.

 Major difference between E. histolytica and non-pathogenic specie E. dispar: morphologically identical
but E. histolytica feeds on RBC (haematophagous) , therefore RBC can be found in the cytoplasm or
vacuoles of the parasite

ENTAMOEBA HISTOLYTICA

E. histolytica has the capacity to become invasive under certain conditions. The parasite can produce a protein
cistolysin that will break down the barrier of the large intestine in the cryptes. The intestinal wall will start

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