Malaria Diagnosis & Life Cycle: Parasitemia & Plasmodium Species, Study notes of Biology

An in-depth look into the laboratory diagnosis of malaria, focusing on the determination of parasitemia using thick and thin smears. Additionally, it explains the life cycle of plasmodium spp., from the initial infection in the human host to the transmission to a new host via a mosquito bite.

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Laboratory diagnosis of malaria
Plasmodium spp.
Determination of Parasitemia
Determination of parasitemia can be done using both thick and thin smears.
Thick smears:
The number of parasites/µl of blood is determined by enumerating the number of parasites
in relation to the standard number of WBCs/µl (8000).
No. Parasites × (8000 ÷ No. WBCs counted)
= No. parasites per µL of blood
Thin smears:
The percent of infected RBCs is determined by enumerating the number of infected
RBCs in relation to the number of uninfected RBCs. A minimum of 500 RBCs total
should be counted.
(No. infected RBCs ÷ Total No. RBCs counted) × 100
= Percent Infected RBCs
Notes:
Multiply-infected RBCs are counted as one.
Gametocytes are not figured in calculations.
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Laboratory diagnosis of malaria

Plasmodium spp.

Determination of Parasitemia

Determination of parasitemia can be done using both thick and thin smears.

Thick smears:

The number of parasites/μl of blood is determined by enumerating the number of parasites

in relation to the standard number of WBCs/μl (8000).

No. Parasites × (8000 ÷ No. WBCs counted)

= No. parasites per μL of blood

Thin smears:

The percent of infected RBCs is determined by enumerating the number of infected

RBCs in relation to the number of uninfected RBCs. A minimum of 500 RBCs total

should be counted.

(No. infected RBCs ÷ Total No. RBCs counted) × 100

= Percent Infected RBCs

Notes:

  • Multiply-infected RBCs are counted as one.
  • Gametocytes are not figured in calculations.

Laboratory diagnosis of malaria

Plasmodium spp.

Life Cycle of Plasmodium spp.

The malaria parasite life cycle involves two hosts. During a blood meal, a malaria-infected female Anopheles mosquito inoculates sporozoites into the human host. Sporozoites infect liver cells and mature into schizonts , which rupture and release merozoites. (Of note, in P. vivax and P. ovale a dormant stage [hypnozoites] can persist in the liver and cause relapses by invading the bloodstream weeks, or even years later.) After this initial replication in the liver (exo-erythrocytic schizogony ), the parasites undergo asexual multiplication in the erythrocytes (erythrocytic schizogony ). Merozoites infect red blood cells. The ring stage trophozoites mature into schizonts, which rupture releasing merozoites. Some parasites differentiate into sexual erythrocytic stages (gametocytes). Blood stage parasites are responsible for the clinical manifestations of the disease.

The gametocytes, male (microgametocytes) and female (macrogametocytes), are ingested by an Anopheles mosquito during a blood meal. The parasites’ multiplication in the mosquito is known as the sporogonic cycle. While in the mosquito's stomach, the microgametes penetrate the macrogametes generating zygotes. The zygotes in turn become motile and elongated (ookinetes) which invade the midgut wall of the mosquito where they develop into oocysts. The oocysts grow, rupture, and release sporozoites , which make their way to the mosquito's salivary glands. Inocula- tion of the sporozoites into a new human host perpetuates the malaria life cycle.