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Objective: To investigate phytochemicals present in the essential oil from aerial parts of eastern red cedar, Juniperus virginiana (J. virginiana) L. (Cupressaceae) and to determine its killing and repellent activities against larvae, pupae, and adults of the Asian malaria mosquito, Anopheles stephensi (Diptera: Culicidae). Methods: J. virginiana essential oil was extracted by hydrodistillation, and its chemical composition was determined by gas chromatography-mass spectrometry. Seven different logarithmic concentrations of J. virginiana essential oils were used in larvicidal and pupicidal assays. J. virginiana essential oils-impregnated bed nets were applied in a designed animal module to test excito-repellent activity against adult mosquitoes. Results: Fourteen constituents corresponding to 99.98% of J. virginiana essential oils were identified. Five main components were terpinen-4-ol (25.21%), camphor (19.89%), E-3-hexen-1-ol (13.30%), γ-terpinene (7.86%), and l-menthone (2.27%). The LC
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Objective: Ilam is a border province and a high risk zone for zoonotic cutaneous leishmaniasis [ZCL]. Identification of Leishmania parasite species in clinical infections is a prerequisite for planning appropriate control measures. This study investigates the demographic characteristics of patients and molecular epidemiology of Leishmania parasites in the skin lesions of patients from Ilam Province
Methods: A total of 106 cases of suspected cutaneous leishmaniasis were detected passively and microscopic slides prepared from their active skin lesions. We randomly selected 50 slides. A fragment of the rDNA-ITS1 gene was amplified after which the PCR products digested with HaeIII restriction enzyme. There were 18 samples sequenced and their phylogenetic relationships compared with sequences retrieved from GenBank
Results: Leishmania amastigotes were detected in 100 slides. The highest and lowest distribution of cases was from the Moosian and Dehloran districts, respectively. There were 68.9% males and 31.1% of cases were women. The RFLP pattern of all samples was similar to Leishmania major. Phylogenetic relationships displayed great similarity between our sequences and those of Leishmania major parasites from sandflies trapped in Ilam and South Khorasan Provinces and human hosts from Esfarayen, Mahshahr and Afghanistan plus Leishmania mexicana of Venezuelan origin classified together in the same clade
Conclusion: Due to homogeneous morphology, problems associated with the cultivation of Leishmania and the two-step molecular identification process, the rDNA-ITS1-RFLP method has gained considerable attention in recent years. This method could be used as a very sensitive, simple, rapid and inexpensive method to detect Leishmania parasites in a variety of clinical and non-clinical samples
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Myiasis, the invasion of live human tissue by larva of Diptera, is reported in the nasal cavity of a 5.5-year-old Iranian girl. She was referred from Golestan Province to the Shaheed Rajaei Heart Center in Tehran. In the 41[th] day after admission, a live parasite was found in her nasal secretions suction identified presumably as a second instar larvae of a facultative myiasis, Woholfartia nuba [Diptera: Sarcophagidae], on the basis of mtDNA-COI and morphological characteristics. Since presence of the larva was recorded after hospitalization, by definition, this infestation is considered a nosocomial myiasis
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Relapsing fever caused by Borrelia persica is an acute tick-borne disease which is transmitted by soft ticks of Ornithodoros tholozani to human. The disease is reported from Middle East and many regions of Iran. Detection of infection is problematic since the suspected infected ticks should be fed on animal hosts such as guinea pigs and subsequently after 7-14 days, the animal blood should be microscopically investigated for Borellia spirochetes on a Giemsa stainined thick smear. This classic method named xenodiagnosis is hard, time consuming, and less reliable. In this study, the application of PCR technique has been examined for detection of Borellia persica in soft ticks of O. tholozani. Tick specimens were collected from northwestern Iran and were fed on Borellia persica infected guinea pigs. DNA of the animal blood were extracted and used as target for PCR amplification of 16rDNA gene. Subsequently the products were subjected to sequencing. The effect of tick sex and post digestion as well as the minimum nyjcrilper of spirochetes on the efficiency of PCR were also tested. The xenodiagnosis assay was able to detect infection in only 13.3% of the tick-bitten animal bloods whereas all of these blood specimens were PCR positive against the 16rDNA gene. There was no difference in results of PCR for male and female of the ticks. Post digestion of infected blood meal in ticks did not affect the efficacy of PCR and the recently-fed samples showed similar results to those of completely gravid ones. A test on the threshold sensitivity of PCR assay indicated that only one spirochete is enough for the primers to anneal and to amplify the target gene. This study describes the first molecular assay for diagnosis of B. persica infected ticks in Iran and due to its high speed, accuracy, and applicability is a substitution method for diagnostic purposes inTBRF foci
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Molecular epidemiology of Visceral Leishmaniasis [VL] is currently used widely for different objectives such as vector incrimination studies. In this study three different loci including kinetoplast DNA [kDNA], ribosomal DNA [rDNA], cystein protease B [CPB[ of Leishmania parasite genome were used for detection and identification of natural infection of sand flies of Germi district of Ardebil province, the most important VL or Kala-azar foci in Iran. The results showed that the three loci of kDNA, rDNA and CPBs are respectively more appropriate for leptomonad infection/initial screening, identification of the L.donovani complex, and discrimination of the species complex. It was also verified that both members of the complex, L.donovani and L.infantum, are present in the study area and are transmitted to the hosts by Phlebotomus perfiliewi transcaucasicus sandflies. This is the first report on natural infection of sand flies to L.donovani in the country and since the ecology and biology of L.donovani differs extensively from L.infantum, it is necessary to perform further studies to highlight the role of L.donovani in epidemiology of VL in the region and country