https://li01.tci-thaijo.org/index.php/JTMP/issue/feedThe Journal of Tropical Medicine and Parasitology2015-02-12T22:04:58+07:00Jitra Waikaguljitra.wai@mahidol.ac.thOpen Journal SystemsThe Parasitology and Tropical Medicine Association of Thailandhttps://li01.tci-thaijo.org/index.php/JTMP/article/view/30805Role of Cathepsin B in Schistosoma japonicum Infection2015-02-12T22:04:57+07:00Saiwasan Buathongpeerapan.tan@mahidol.ac.thSaovanee Leelayoovajparasit@gmail.comMathirut Mungthinjparasit@gmail.comPeerapan Tan-ariyapeerapan.tan@mahidol.ac.th<p>Proteases, including cysteine-, serine-, threonine-, aspartate-, and metallo-proteases, are a group of enzymes that have the catalytic ability to hydrolyze or digest peptide bonds of proteins. Proteases play important roles in host invasion, hemoglobin degradation, transformation and immune invasion of schistosomes. The gut cathepsin B of all schistosomes including <em>S. japonicum</em>, <em>S. mansoni </em>and <em>S. haematobuim </em>is involved in hemoglobinolysis. Since <em>Schistosoma japonicum </em>cercariae show quicker migration through host skin as compared to <em>S. mansoni </em>and <em>S. haematobium</em>, it has been proposed that cathepsin B residing in the acetabular gland of <em>S. japonicum </em>might be one of the factors that facilitates its rapid skin penetration. This review focuses on the potential roles of cathepsin B for hemoglobin degradation and skin penetration of schistosomes. Defining the role of cathepsin B might be useful in identifying the drug target for schistosomiasis.</p>Copyright (c) 2015 The Journal of Tropical Medicine and Parasitologyhttps://li01.tci-thaijo.org/index.php/JTMP/article/view/30807Prevalence of hair follicle mites, Demodex folliculorum and Demodex brevis, on the facial skin of Chiang Mai University Students, and the relationship with acne vulgaris2015-02-12T22:04:57+07:00Atipat Manoyanajparasit@gmail.comUdom Chaithonguchaitho@yahoo.comSiri Chiewchanvitjparasit@gmail.com<p>The hair follicle mites, <em>Demodex folliculorum </em>and <em>D. brevis </em>are asymptomatic parasites of humans. To date, the genus <em>Demodex </em>has been implicated in the occurrence of many skin diseases. Thus, the main aim of this study was to determine the infestation rate of <em>Demodex </em>spp. in young adults and study the relationship between <em>Demodex </em>density and acne vulgaris. Furthermore, the mean densities of <em>Demodex </em>mites between clindamycin users and a control group were also observed in this study. Studied population consisted of 280 healthy volunteers from Chiang Mai University (age 20-22 years old). Skin samples were collected by a skin scraping technique and were examined for the parasite by direct microscopic examination. Both species were found in the resulting skin samples. The overall prevalence of <em>Demodex </em>mites on the facial skin of Chiang Mai University students was 40.36%. The mite prevalence in males (44.20%) was significantly higher than in female (36.62%) (<em>P </em>= 0.024). <em>Demodex folliculorum </em>had a higher prevalence (31.1%) than <em>D. brevis </em>(26.1%). The mite density in males (0.89 <em>Demodex</em>/cm2) was also significantly higher than in female (0.49 <em>Demodex</em>/cm2) (<em>P </em>= 0.035). We also found that males were approximately twice as likely to have acne vulgaris as females. Although <em>Demodex </em>has been involved in the etiology of many skin diseases, the parasite does not appear to be related to acne vulgaris in young adults (<em>P </em>= 0.313). Thus, the eradication of <em>Demodex </em>mites is not necessary for the therapeutic treatment of acne vulgaris. The mites were found on all facial sites, the highest density being in the area of the nose followed by the forehead and cheeks, but there was no significant difference among these 3 areas. This study also determined the effect of clindamycin on <em>Demodex </em>mites. The results revealed that the use of clindamycin was not related to the density of <em>Demodex </em>mites. However, additional sample sizes for the clindamycin study are needed.<strong></strong></p>Copyright (c) 2015 The Journal of Tropical Medicine and Parasitologyhttps://li01.tci-thaijo.org/index.php/JTMP/article/view/30808Refractoriness of the natural malaria vector Culex quinquefasciatus to Plasmodium gallinaceum2015-02-12T22:04:58+07:00Mintra Pruck-Ngernjparasit@gmail.comSittiporn Pattaradilokratjparasit@gmail.comKamlang Chumpolbanchornjparasit@gmail.comSuntorn Pimnonjparasit@gmail.comPongchai Harnyuttanakornjparasit@gmail.comPrayute Buddhirakkuljparasit@gmail.comTawee Saiwichaitawee.sai@mahidol.ac.thDevelopment of effective strategies to control malaria transmission is an important issue in malaria research. This study aimed to investigate refractoriness of laboratory and field strains of the malaria vector <em>Culex quinquefasciatus </em>to the avian malaria parasite <em>Plasmodium gallinaceum</em>, a model of the human malaria disease. Transmission potential was determined by feeding batches of <em>Cx. quinquefasciatus </em>on <em>P. gallinaceum </em>infected chickens with 10% and 30% parasitemia. The mosquitoes were examined for percent infectivity and numbers of oocysts. Our study showed that when the mosquitoes were fed on the infected chickens with high parasitemia, the laboratory isolate of <em>Cx. quinquefasciatus </em>was more susceptible to <em>P. gallinaceum </em>transmission and produced significantly higher oocyst numbers than the field isolate. There were, however, no differences in term of the transmission potential and infectivity of the malaria parasite when the mosquitoes were allowed to feed on the <em>P. gallinaceum</em>-infected chickens with low parasitemia. In conclusion, our study demonstrated the differences in refractoriness of the natural vector <em>Cx. quinquefasciatus </em>to the transmission of the avian malaria <em>P. gallinaceum</em>, implying the existence of the natural pathogen resistance mechanisms in the <em>Culex </em>mosquito.Copyright (c) 2015 The Journal of Tropical Medicine and Parasitologyhttps://li01.tci-thaijo.org/index.php/JTMP/article/view/30811Intestinal parasites in captive mugger crocodiles (Crocodylus palustris) in south India2015-02-12T22:04:58+07:00NV Rajeshmgjayathangaraj@gmail.comR Kalpana Devikalpanafern@gmail.comMG Jayathangarajmgjayathangaraj@gmail.comM Ramanramapara@gmail.comR Sridharsri_ramaswamy@yahoo.com<p>Coprological samples of captive mugger crocodiles (<em>Crocodylus palustris</em>) were randomly collected (N=102) from Snake Park, Guindy (N=36), Arignar Anna Zoological Park, Vandalur (N=44) and Amaravathy Crocodile farm (N=22) and screened for evidence of intestinal parasites using fecal sedimentation and flotation technique. Quantitative analysis of fecal samples was not performed for this study. The fecal samples collected were on random sampling basis under captive environment condition, irrespective of their sex, since both male and female are reared in the confined area. The samples were collected among the adult group of crocodiles (> 8 ft) in length bearing an average weight of 500 pounds. Parasitic fauna evidenced trematode eggs including Renifers which were predominant in Snake Park, Guindy (36.1%) and Amaravathy Crocodile farm (22.7%), and nematode eggs, <em>Dujardinascaris </em>sp., in Arignar Anna Zoological Park, Vandalur (36.4%). There were mixed infection between <em>Dujardinascaris </em>sp., (11.4%) and Renifers (5.6%). <em>Ophiotaenia </em>sp. was also found in a few samples. <em>Polydelphis </em>sp. was found in Amaravathy farm (13.7%). Renifers (19.6%) and <em>Dujardinascaris </em>sp. (21.6%) were found in mugger crocodiles from all these three locations. Mixed infection of sporulated coccidian oocyst (4.9%) <em>Isospora </em>sp. and <em>Eimeria </em>sp. were found in Snake Park Guindy and Amaravathy Crocodile farm. Snake Park, Guindy and Amaravathy Crocodile farm had the habit of feeding fishes to this crocodile resulting in the transmission of trematode and cestode.<em></em></p>Copyright (c) 2015 The Journal of Tropical Medicine and Parasitology