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46                                         6  Malaria Parasites and Babesia

              from the body. It can prevent superinfection, but not reinfection. This type of
              immunity associated with asymptomatic infection is called premunition and
              disappears once the infection is eliminated.  Acquired antibody-mediated
              immunity is transferred from mother to foetus across the placenta and is evi-
              dent in endemic areas where infants below the age of 3 months are protected
              by passive maternal antibodies.  Young children are highly susceptible to
              malaria. As they grow up, they acquire immunity by subclinical or clinical
              infections. Incidence of malaria is low in older children and adults.


              Recrudescence

            Recrudescence occurs when parasites persist although the level of parasitaemia is
            below the fever or microscopic threshold. Erythrocytic schizogony continues in the
            body at low levels and parasitaemia gradually increase to cross the fever threshold.
            New malarial attacks then occur. These malaria attacks appear within 8 weeks after
            the primary attack. Recrudescence may be due to waning immunity of the host or to
            antigenic variation and is seen in all human malaria.


              Relapse

            It is seen in P. vivax and P. ovale infections, caused by the reactivation of hypnozoite
            stage in the liver. This leads to initiation of erythrocytic cycles and new attacks of
            malarial fever. Reactivation of hypnozoite stage usually occurs from 24 weeks to 5
            years after the primary attack.


              Diagnosis

              1.  Microscopic examination (Gold standard)
                 Demonstration of malarial parasite in the peripheral blood in thin and thick
              smears. Thin smear is used for detecting the parasites and determining the spe-
              cies by studying its morphological details. The thick smear is more sensitive and
              is used for detection of malarial parasite when there is low parasitaemia. Species
              identification is not easy in thick smear. Both thin and thick smears can be used
              to determine the parasitaemia level.
              2.  Rapid diagnostic tests (RDT)
                 The tests aid in the diagnosis of malaria by detecting malaria parasite antigens
              in human blood.
              3.  Molecular diagnosis
                 PCR on blood.
              4.  Serodiagnosis
                 It is used mainly for seroepidemiological survey and to identify the infected
              donors in transfusion malaria.
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