Lecture 5 Protozoa-Trypanosomatids Flashcards

1
Q

Protozoa

A

-eukaryotic, single cell organisms that can be free living or parasitic in nature

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2
Q

Protozoa move by three basic types of organelles

A

-pseudopodia
-flagella
-cilia

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3
Q

Flagella are composed of

A

-a central axoneme formed by nine peripheral and one central pair of microtubules
-an outer sheath that is the continuation of the outer membrane
¤ a kinetosome (basal body), that gives origin to
the axoneme, lies at the bottom of flagellar
pocket
¤ the flagellum may bend back along and loosely
attached to the lateral cell surface, forming a
finlike undulating membrane

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4
Q

Protozoa Reproduction

A

-either asexual or sexual

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5
Q

What are the different patterns that asexua reproduction follows?

A

-Binary fission: in which one divides into two.
-The plane of fission is random in amebas
-longitudinal in flagellates
-transverse in ciliates

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6
Q

Multiple fission

A

-occurs in some amebas and in apicomplexa.
-in this type of division the nucleus and other essential organelles divide repeatedly before cytokinesis. Thus a large of daughter cells are produced simultaneously

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7
Q

Amphimictic

A

Involving the union of gametes from two parents

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8
Q

Automictic

A

One parent give rise to both gametes

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9
Q

Encystation

A

¤ Many protozoa can secrete a resistant covering and enter a resting
stage, or cyst.
¤ Cyst formation is particularly common among parasitic protozoa as
well as among free-living protozoa found in temporary bodies of
water that are subject to drying or other harsh conditions.
¤ Cysts provide protection against unfavorable conditions and serve as
sites for reorganization and nuclear division, followed by
multiplication after excystation.
¤ Conditions favoring encystation are not fully understood, but in most
cases they involve adverse environmental events such as food
deficiency, desiccation, increased tonicity, decreased oxygen
concentration, pH or temperature change.
¤ In species in which the cyst is a resistant stage, a return of favorable
conditions stimulates excystation.

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10
Q

Protozoans metabolism are divided between

A

-photosynthetic: they synthesize carbohydrates in chloroplasts
-Nonphotosynthetic or heterotrophic: require their energy in the form of complex carbon molecules and their nitrogen int the form of a mixture or preformed amino acids.

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11
Q

In what conditions do protozoans live in?

A

-live in tissues with low oxygen and glucose availability and have adapted their metabolism to such conditions

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12
Q

Protozoan Flagellates

A

-flagellates are protozoans
over 50,000 and a small number are pathogenic to humans
-are very small
-have one or more flagellates that propel them their the host

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13
Q

Trypanosomatids

A

-trypanosomes are unicellular hero flagellates which belong to the class kinetoplastea
-kinetoplastea are parasitic that have a single nucleus, mitochondria, and flagella
-have a prominent accumulation of mitochondrial DNA
-They show a variety of forms varying from long, thin, motile spindle shapes
to spherical organisms in which the flagellum is reduced to a tiny stub.

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14
Q

Trypanosomes are classified in 2 groups

A

-¤ Salivarian: salivarian trypanosomes replicate extracellularly in the blood and
tissue fluids of mammals and in the digestive system of tsetse flies. Their
distribution is restricted to Sub-Saharan Africa.
¤ There are several species that are host-specific.
¤ Trypanosoma congolense and Trypanosoma vivax are the major
pathogens of cattle and goats.
¤ Trypanosoma brucei brucei is a parasite of cattle
¤ Trypanosoma brucei rhodesiense and Trypanosoma brucei gambiense
these are the causative agents of sleeping sickness in humans
¤ Stercorarian: multiply extracellularly in the digestive system of various
Rhodnius, Triatoma and Panstrongylus species – reduviid bugs. Infection of
mammalian hosts occurs when infected bug faeces are rubbed into the bite
site, and in this host, the parasites multiply intracellularly

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15
Q

Trypanosomatids Morphology

A

-show a variety of forms varying from long thin ,motile spindle shapes to spherical organisms to which the flagellum is reduced to a tiny stub.

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16
Q

Amastigotes

A

-contains a nucleus, basal body structure called a blepharoplast and a damsel paranasal body.
-the large single nucleus id usually located off center
- blepharoplast gives rise to and is attached to an axoneme

17
Q

Promastigote morphology

A

¤ The large single nucleus is located in or near the center of the long slender body.
¤ The kinetoplast is located in the anterior end of the organism.
¤ A single free flagellum extends anteriorly from the axoneme.

18
Q

Epimastigote Morphology

A

-the body is wider than the promastigote
-the large single nucleus is located in the posterior end of the organism
-the kinetoplast is located anterior to the nucleus.
-an undulating membrane, measuring half the body length, forms into a free flagellum at the anterior end of the epimastigote.

19
Q

Tryposmastigote Morphology

A

¤ The typical trypomastigote measures 12 to 35 μm long by 2 to 4 μm wide, and may often
assume the shape of the letters C, S or U in stained blood films
¤ The long slender trypomastigote is characterized by a posteriorly located kinetoplast from
which emerges a full body length undulating membrane.
¤ The single large nucleus is located anterior to the kinetoplast.
¤ An anterior free flagellum may or may not be present.

20
Q

How is the shape of parasites maintained

A

maintained by a corset of microtubles which spiral around the parasite

21
Q

Three organelles are important in cellular metabolism

A
  • The mitochondrion: they possess only
    one that changes depending on the
    metabolic state of the parasites.
  • The glycosomes: contain most enzymes
    of glycolysis and parts of several additional
    pathways.
  • Acidocalcisomes: acidic compartment
    that stores polyphosphates and calcium.
22
Q

Cell surface protein variation

A

-* African trypanosome parasites are
densely coated in a single Variant
Surface Glycoprotein (VSG).
* While growing in the bloodstream of
humans and other mammals
Trypanosoma brucei species evade
the host immune response by
switching from the expression of one
VSG coat to another.
* This requires selection and activation
of a single new VSG gene from a
huge number of possible VSG
variants encoded throughout the
genome.
* Switching VSG expression is based in
DNA recombination events that result
in chromosome translocations drawn
from more than 2,000 VSGs.