ATLASBLOOD, BONE MARROW, SPLEEN PARASITES
      SPOROZOEA Order: Eucoccidiida

      PLASMODIUM OVALE

      Adapted and redrawn from NCDC

      pf1-ic

      Plasmodium sp.: life cycle


      Geographic distribution of Malaria infection

      pf2-ic

      Plasmodium sp.: geographic distribution.

      (Adapted and redrawn from: World Malaria Situation in 1993,
      Weekly Epidemiological Record, 1996, 71, 33-40).


      By Prof. Christopher F.Curtis BA PhD, Stefania Vergnano, Anna Lucchini,MD.

      pf2a-ic

        Plasmodium sp.: the genus Anopheles includes more than 400 species of mosquitoes.
        Many may act as vectors of human diseases such as malaria,
        filariasis and some arbovirus.
        Eggs present a pair of lateral floats and are laid singly on the water surface,
        while larvae lay in a horizontal position under the water surface.

      By Prof. Christopher F.Curtis BA PhD, Stefania Vergnano,MD, Anna Lucchini,MD.

      pf2b-ic

        Plasmodium sp.: the resting position of the adult is characteristic
        with the proboscid, head and abdomen in a straight line
        at an angle of about 45° with the surface on which they rest.
        Only about 60 species can transmit malaria and they greatly
        differ in their efficiency as vectors according to man
        biting behaviour, survival, fertility, adaptation to different breeding place.
        The most efficient vectors belong to the A.gambiae complex,
        widely distributed in tropical Africa, where also important is A.funestus.
        In Asia important vectors are A.culicifaciens, A.dirus, A.sinensis and A.miminus;
        in the Pacific area A.farauti and A.maculatus play a predominant role
        in malaria transmission. The main vector in South America in A.albimanus.

      By Mr Graham Icke and Dr Richard Davis.

      poT-ic

      P.ovale: species identification is possible on the basis
      of the appearance of parasites of each of the four malaria species.
      Shape and size of asexual parasites and of macro- and microgametocytes,
      developmental stages in peripheral blood, modifications of infected erythrocytes,
      presence of dots or clefts on the red blood cells are the main differential characteristics.

      Courtesy of Mr Graham Icke
      MSc MIBiol FIBMS Grad Dip Bus
      A/Principal Scientist, Laboratory Services, Royal Perth Hospital.
      and Dr Richard Davis
      PhD MSc FAACB FIBMS MASM
      Emeritus Consultant Haematologist, Royal Perth Hospital.

      Image taken from "The Microscopic Diagnosis of Tropical Diseases",
      Published by BAYER in 1955 (Now Public Domain).


      po1a-ic

      Malaria diagnosis relies on observation of parasites in
      Giemsa-stained thin or thick smears (G-TS).
      Alternative techniques for identification of malaria parasites
      are based on fluorochromes such as Acridine Orange (AO), DAPI-PI or BCP.
      With these dyes malaria parasites are easily recognized under UV light,
      reducing the time spent reading the slides.
      Another method, based on fluorochromes, the quantitative buffy coat (QBC)
      (Becton-Dickinson) analysis wich uses AO staining of centrifuged parasites
      in a capillary tube containing a float, has been shown to be rapid and accurate.

      By doctor Juan Cabezos

      pf-qbc-es-ic

      P.falciparum: gametocytes of P.falciparum. QBC technique (60X).

      Courtesy of doctor Juan Cabezos 
      Laboratorio de Parasitologia, 
      Unidad de Medicina Tropical y Enfermedades Importadas. 
      Avda. Drassanes 17-21 08001 Barcelona, Spain

      Recently different immunochromatographic tests such as the ParaSight F
      (Becton Dickinson) and the Malaquick (ICT) wich capture and detect
      the histidine rich protein 2 (HRP-2) antigen, and the OPTIMAL wich detects
      Plasmodium lactate dehydrogenase (pLDH) have been developed and distributed.
      The tests are highly sensitive and specific and are now able to distinguish
      P.falciparum infections from non-falciparum infections.
      P.ovale, thin smear, Giemsa stain.

      By Mr Graham Icke and Dr Richard Davis.

      pITT-ic

      Malaria diagnosis:
      whereas thin film gives more informations on parasite morphology
      and permits an easier morphologic differentiation,
      G-TS is more sensitive allowing a concentration of plasmodia (10-15 folds)
      and it is the standard reference diagnostic test.

      Courtesy of Mr Graham Icke
      MSc MIBiol FIBMS Grad Dip Bus
      A/Principal Scientist, Laboratory Services, Royal Perth Hospital.
      and Dr Richard Davis
      PhD MSc FAACB FIBMS MASM
      Emeritus Consultant Haematologist, Royal Perth Hospital.


      po1b-ic

      Malaria diagnosis: G-TS needs careful stain
      (2% Giemsa) and experience in examining slides;
      reasonable sensitivity is reached by observing at least 500-1.000 White Blood Cells (WBC).
      Quantification of baseline parasitemia is necessary
      for monitoring the response to therapy.
      Parasites must be counted in parallel with leucocyte
      and parasitemia expressed as parasites/µl.

      N. of parasites counted x N. of WBC/µl
      Separ.gif (941 byte)

      N. of WBC counted

      = N. of parasites/µl

      P.ovale, thick smear, Giemsa stain.


      By Dr. Marc Lontie.

      poLon-ic

      po1c-ic

                        poLon-ic Plasmodium ovale: trophozoite

      po1c-ic P.ovale: all stages are seen in blood films; prominent Shuffner's
      dots are present at all stages.
      Trophozoites appear as rings with, usually, a compact cytoplasm;
      they do not have ameboid cytoplasm.
      The parasites are smaller than P.vivax.


      By Dr. Marc Lontie
      po2-ic P_ovale1-ic

      P.ovale: red blood cells are enlarged, ovalized and distorted with fimbriae at poles.
      Schizonts have usually 8-10 merozoites.

      P_ovale1: P.ovale: enlarged oval red cell with one trophozoite
      (Giemsa, thin film).

      P_ovale1: Courtesy of Dr. Marc Lontie:
      Director of the laboratory of the
      Medisch Centrum voor Huisartsen,
      Maria Theresiastraat 63a; B-3000 Leuven, Belgium.


      po3-ic

      P.ovale: micro- and macrogametocytes are sometimes difficult
      to differentiate from late trophozoites;
      they are round and occupy almost the entire erythrocyte.
      Microgametocytes have a more scattered chromatin.