A complete profile of the 20-hydroxyecdysone (20-HE) titer, development and endocrine events from 1st instar to pupation of the larvae of non-diapause-destined (NDD) and diapause-destined (DD) tasar silkworm, Antheraea mylitta Drury (Lepidoptera: Saturniidae) was studied. Diapause is induced by short days of 11 hr photophase coupled with <= 24°C prevailing in September-November. Diapausing pupae produce adults in July (>= 12h light, >= 26°C) and one generation is completed by August. The growth rate during the course of development of larval instars decreases and instar durations are inversely related to the body weight at the time of initiation of a larval instar. A growth compensation mechanism operates during the development of the larval instars. The growth rate was higher in early instars (1st to 4th) in both generations. The DD larvae complete the final instar in 16 days followed by a spinning stage of 13 days. The NDD larvae complete the final larval instar in 9 days followed by spinning stage of 6 days and spend 14 days in the pupal stage. The signal to release the prothoracicotropic hormone (PTTH) is related to critical body weight of larvae. From 1st to 4th instar, pre-ecdysial peaks of 20-HE were recorded in both NDD and DD generations. The programme for undergoing diapause was initiated during 3rd instar and induced by a sudden decrease in the level of 20-HE in the DD generation. Two peaks of 20-HE are required for the larval-pupal transformation, first at the wandering stage and the second at cuticle formation.
The present study evaluates the performance of OptiMAL-IT® test and nested PCR assay in detection of malaria parasites. A total of 76 randomly selected blood samples collected from two malaria endemic areas were tested for malaria parasites using microscopy and OptiMAL-IT® test in the field. PCR assays were performed in the laboratory using DNA extracted from blood spots of the same samples collected on the FTA™ classic cards. Of the total of 61 field confirmed malaria positive samples, only 58 (95%) were detected positive using microscopy in the laboratory. Sensitivity, specificity, positive predictive value, negative predictive value and false discovery rate of OptiMal-IT® in comparison to the microscopy were 93%, 83%, 95%, 79% and 5%, respectively. On the other hand, the sensitivity and specificity of PCR assay were 97% and 100 %, respectively, whereas positive predictive value, negative predictive value and false discovery rate were 100%, 90% and 0%, respectively. The overall performance of OptiMal-IT® and PCR assays for malaria diagnosis was 76% and 97%, respectively. PCR assay enabled the identification of infection with Plasmodium malariae Laveran, 1881 in four samples misidentified by microscopy and Plasmodium-specific antigen (PAN) identified by the OptiMAL-IT® test. In addition to the standard methods, such PCR assay could be useful to obtain the real incidence of each malaria parasite species for epidemiological perspectives.