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    30 August 2018, Volume 36 Issue 4
    ORIGINAL ARTICLES
    Regulation of hepatic stellate cell membrane receptors by Hsp47-shRNA affects hepatic fibrosis in mice with Schistosoma japonicum infection
    Ju-hong DENG, Ran TAO, Qi-qin SONG, Hong-yan KONG, Yun-tao JIAO, Jia-quan HUANG
    2018, 36(4):  317-324. 
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    Objective To investigate the effect of hepatic stellate cell (HSC) membrane receptor regulation by heat shock protein 47 (HSP47)-shRNA on the Schistosoma japonicum-induced liver fibrosis in mice.Methods The mouse model of Schistosoma japonicum-induced liver fibrosis was established. Total RNA was extracted from liver tissues before infection and at weeks 4, 9 and 14 after infection (n = 5 mice in each group). The mRNA expression and protein levels of HSP47 were assessed by RT-PCR and Western blotting, respectively. The RM-6240BD multi-channel physiological signals were used to measure the portal vein pressure of mice, flow cytometry was used to detect the mean fluorescence intensity (MFI) of endothelin receptor (ETAR and ETBR) in HSC membranes, and immunohistochemistry was used to detect the expression of membrane receptors in liver before and at week 14 after infection. The relationships between the expression of HSP47 and portal vein pressure as well as expression of ETAR and ETBR in HSC were analyzed using the linear correlation analysis method. The NIH/3T3 cells and mouse model of Schistosoma japonicum-induced liver fibrosis (n = 12) were transfected with HSP47-shRNA expression plasmid, accompanied by a negative control group (control plasmid) and a blank control group (PBS group). RT-PCR was used to detect the mRNA expression of HSP47, type Ⅰ collagen and type Ⅲ collagen in NIH/3T3 cells at 0, 24 and 48 h after transfection and in the mouse model at week 14. Their protein levels were determined by Western blotting. MFI of the membrane receptors for ET, TGF-β and PDGF was detected by flow cytometry. Data were analyzed by student’s t-test for comparisons between groups, and by ANOVA for comparisons among groups. Results RT-PCT results showed that the relative expression levels of HSP47 mRNA were 0.592 ± 1.031, 1.253 ± 2.101 and 0.651 ± 1.532, respectively, in the mouse model at weeks 4, 9 and 14 after infection, all significantly increased compared with that before infection (0.253 ± 0.120) (P < 0.01). Western blotting revealed consistent changes of HSP47 protein level. The portal vein pressures were (3.010 ± 0.250), (8.850 ± 0.630), and (12.390 ± 0.830) mm Hg, respectively, significantly higher than that before infection [(2.350 ± 0.18) mm Hg; P < 0.01]. Flow cytometry showed that the MFI levels of ETAR were 3 245 ± 186, 6 108 ± 213 and 8 784 ± 257, all higher than that before infection (2 104 ± 232; P < 0.01). Similarly, the MFI levels of ETBR were also significantly higher at weeks 4, 9 and 14 after infection (3 812 ± 158, 4 524 ± 197 and 5 554 ± 156) than that before infection (2 091 ± 237) (P < 0.01). The relative expression of HSP47 mRNA was positively correlated with the portal vein pressure, relative MFI of ETAR, and relative MFI of ETBR (r = 0.750, 0.750 and 0.508, P < 0.05). Immunohistochemical results showed that at week 14 after infection, receptors for ETBR, TGF-β and PDGF were strongly expressed in the hepatic sites of fiber aggregation. RT-PCT results showed that the relative expression of HSP47 mRNA in the transfected NIH/3T3 cells 0.254 ± 2.358 was significantly lower than that in the negative control group (0.911 ± 1.391) (P < 0.01) at 48 h after transfection, and consistent protein changes were revealed by Western blotting. The relative expression levels of type Ⅰ and type Ⅲ procollagen mRNA were 0.656 ± 0.061 and 1.330 ± 0.155, significantly downregulated compared with the negative control group (1.521 ± 0.314 and 2.243 ± 0.142, P < 0.01). The relative MFI of ETBR measured by flow cytometry was 53.433 ± 5.243, significantly higher than that before transfection (30.825 ± 5.460, P < 0.05). There was no significant difference in TGF-β and PDGF receptors between cells before and after transfection (P > 0.05). RT-PCT results showed that the relative expression level of HSP47 mRNA was 2.686 ± 0.711, significantly lower than that of the negative control group (6.001 ± 0.458, P < 0.01) at week 14 after transfection. Western blotting showed consistent changes of the protein level. The mRNA expression of procollagentype Ⅰ and Ⅲ in the Hsp47-shRNA transfected group (10.956 ± 2.079, 14.071 ± 1.915) were both decreased compared with those in the blank control group (22.687 ± 1.478, 29.065 ± 2.537) (P < 0.01). Flow cytometry showed that the rate of ETAR positive expression in the transfected group [(51.48 ± 4.27)%] was significantly lower than that in the blank control group [(81.60 ± 6.07)%, P < 0.05]. The MFI values of ETAR and ETBR on the membrane of HSCs in the Hsp47-shRNA transfected group were 4 249 ± 344 and 3 706 ± 194, respectively, both lower than that of the blank control group (8 538 ± 494, 5 052 ± 213; P < 0.05). There was no significant difference in TGF-β or PDGF receptor between the transfection group and blank control group (P > 0.05) as measured by flow cytometry. Conclusion HSP47-shRNA has an effect on activated HSCs and in mice with Schistosoma japonicum-induced liver fibrosis. The change of ETR is one of the possible mechanisms of live fibrosis, especially portal hypertension.

    The immunomodulatory effects of IL-18 against schistosome infection in mice with pVAX1/SjRPS4·CB plasmid vaccination
    Hong-bing CHENG, Yun-fei ZHOU, Shu-ju ZHANG, Shi-ping WANG, Qi-mei FENG, Yi-ping LIU, Guo-yan CUI, Hong WEI, Fen LI, Ming-she LIU
    2018, 36(4):  325-330. 
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    Objective To explore the immunoregulatory effect of pVAX1/IL-18 combined with pVAX1/SjRPS4·CB vaccine against schistosome infection in mice. Methods Seventy female BALB/c mice were divided into 5 groups: the normal saline (NS) group, pVAX1 plasmid group, pVAX1/IL-18 group, pVAX1/SjRPS4·CB group and pVAX1/SjRPS4·CB + pVAX1/IL-18 group. The mice were injected with 100 μg plasmid or an equal volume of NS at the quadriceps femoris of the left hind leg, once every other week, for a total of 3 vaccinations. Three weeks after the final vaccination, blood was collected from the tail, and the levels of IgG, IgG1 and IgG2a were determined by ELISA. The mice were then challenged with 20 ± 1 Schistosoma japonicum cercariae through abdominal patching and sacrificed 8 weeks later. Adult worms of S. japonicum were collected by portal vein perfusion to calculate the worm reduction rate. The liver tissue was collected to calculate the egg reduction rate in hepatic tissues under a microscope. Moreover, spleen was collected at a sterile condition, weighed, and the mouse spleen index was calculated. The splenic lymphocyte proliferation level in vitro was determined using MTT assay. Blood was collected from the tail before infection (at 3 weeks after the final vaccination) and at 2, 4, 6, and 8 weeks after infection, to assess the serum levels of IFN-γ and IL-4 by ELISA. Results At 3 weeks after the final vaccination, the A450 values of IgG, IgG1 and IgG2 in the pVAX1/SjRPS4·CB + pVAX1/IL-18 group were 1.03 ± 0.17, 0.32 ± 0.08, and 0.78 ± 0.12, respectively, and the IgG2a/IgG1 ratio was 2.44, all of which were significantly higher than those in the other 4 groups. The worm reduction rate and the egg decrease rate in the pVAX1/SjRPS4·CB + pVAX1/IL-18 group were 52.0% and 63.2%, respectively, both significantly higher than those in the other 3 groups (P < 0.05). The spleen index in the pVAX1/SjRPS4·CB + pVAX1/IL-18 group (3.32 ± 0.37) was also significantly higher than those in the other 4 groups (P < 0.05). MTT assay showed that the splenic lymphocyte proliferation level in vitro in the pVAX1/SjRPS4·CB + pVAX1/IL-18 group (A570 value, 4.45 ± 0.34) was significantly higher than those in the other 4 groups (P < 0.05). The IFN-γ levels in the pVAX1/SjRPS4·CB + pVAX1/IL-18 group before infection and at 2, 4, 6, and 8 weeks after infection were 569.07 ± 21.15 pg/ml, 560.66 ± 30.84 pg/ml, 577.46 ± 36.45 pg/ml, 605.03 ± 36.91 pg/ml and 636.33 ± 37.35 pg/ml, respectively, all significantly higher than those in the other 4 groups (P < 0.05). However, the IL-4 level was not altered either before versus after infection, or among different groups (P > 0.05). Conclusion IL-18 enhances the immunomodulatory effects of pVAX1/SjRPS4·CB against schistosome infection and induces Th1 type immune responses in mice.

    Analysis of transmission risk factors of schistosomiasis in a hilly demonstration plot of transmission interruption
    Chao LV, Li-yuan ZHOU, Xiao-ying XING, Dan-dan LIN, Tao CHEN, Rui CHEN, Han-chen KE, Zhou WANG, Wu PAN, Jing XU, Zhi-qiang QIN, Hong-qing ZHU, Shi-zhu LI
    2018, 36(4):  333-339. 
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    Objective To analyze the risk factors for schistosomiasis transmission in a hilly transmission interruption demonstration plot located at the south bank of Yangtze River. Methods The 2016-2017 schistosomiasis endemic information in local residents and livestock in a hilly transmission interruption demonstration plot located at the south bank of Yangtze River was collected. Field investigations were also carried out at benchland, cement ditch, field drain, flood discharge ditch, trunk canal, wasteland, desolate sands in the demonstration plot, where snails were surveyed through systematic sampling in combination with environmental sampling, and wild rodents were captured using cages or traps which were placed monthly, 3 days each time, for 3 consecutive months. The loop-mediated isothermal amplification (LAMP) method was used to detect the schistosome DNA in snails. The rodents captured were sacrificed and liver tissues were collected for egg examination in tissue homogenates. Feces from wild animals in the field were collected, and examined by the miracidium hatching method. Results A total of 12 232 (5 408/6 824) local residents were examined in 2016 and 2017 in the demonstration plot, of whom 152 showed positive serological test results and none showed positive fecal examination result. A total of 688 cattle were examined by serological test, of which only 1 showed positive result, and none showed positive fecal examination result. Meanwhile, 2 152 frames of snails were investigated in the 7 selected areas and 1 401 snails were obtained, including 1 398 live snails (427 frames), with an average density of 3.27 live snails/frame. The LAMP results showed that 5 out of 24 tubes of mixed DNA resulted in positive products, distributed at 3 sites. A total of 825 cages/traps were placed, and only 35 rodents were captured, distributed at 6 sites. None of the rodents were found to be infected with Schistosoma japonicun after stool hatching, while microscopic examination of the liver tissue revealed two rodents infected with Clonorchis sinensis. The purchased 2 samples of wild boar liver and one wild rabbit also showed negative results of microscopic examination and fecal hatching. A total of 137 fecal samples were collected, mainly from two spots (54 and 44 from each). The fecal samples were from cattle, goats, horses, swines and dogs, mostly from cattle (66 samples), and least from swines (4). Twenty-six were determined as positive by hatching, infection a positive rate of 19.0%, consisting of 15 cattle feces, 2 horse feces, 3 goat feces, 3 swine feces, and 3 dog feces. Conclusion No human cases of schistosomiasis were found in the demonstration plot. There has been a scenario of multiple livestock sources of infection in the demonstration plot, with an infection rate of 19.0% in livestock feces. The infected livestock feces are a crucial factor for the transmission of schistosomiasis in this area.

    Effect of siRNA interference with EgRad9 gene on DNA oxidative damage in protoscoleces of Echinococcus granulosus
    Xuan ZHENG, Shuai LU, Jun ZHAO, Guo-dong LV, Li-mei WEN, Ya-fen LI, Chun-yan TIAN, Jian-hua WANG
    2018, 36(4):  343-349. 
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    Objective To investigate the effect of siRNA interference with EgRad9 gene expression on DNA oxidative damage in protoscoleces of Echinococcus granulosus. Methods EgRad9-siRNA and scrambled iRNA were transfected into protoscoleces of Echinococcus granulosus by electroporation. It included EgRad9-siRNA-354, -614, and -971 interference groups, scrambled control and blank control groups. Three days after electroporation, the protoscoleces were treated with the maximum tolerated concentration of H2O2 for 1 h, stained by eosin, and observed under an inverted fluorescence microscope to calculate the survival rate of protoscoleces. The cultural medium in each group was collected for alkaline phosphatase activity assessment. RNA was extracted from protoscoleces using TRIzol, and EgRad9 mRNA expression was assessed by qRT-PCR. The single cell gel electrophoresis (comet assay) was used to detect DNA damage before and after transfection. The content of reactive oxygen species (ROS) in protoscoleces was assessed using an ROS detection kit. Data were analyzed using the SPSS 22.0 software. Results The maximum tolerated concentration of H2O2 for protoscoleces of Echinococcus granulosus was 0.4 mmol/L, and the intervention duration was 1 h. The siRNA sequences were effectively transfected by electroporation. Green fluorescent spots were clearly seen in the interference groups and scrambled control group, while none appeared in the blank control group. The survival rates of protoscoleces in the EgRad9-siRNA-354, -614, and -971 interference groups were (42.99 ± 4.03)%, (29.86 ± 5.87)% and (56.48 ± 4.64)%, respectively. Thus the EgRad9-siRNA-614 was considered as the most effective interfering sequence. The alkaline phosphatase activity in the EgRad9-siRNA-354, -614, and -971 interference groups was 0.024 ± 0.001, 0.004 ± 0.001, and 0.039 ± 0.002, respectively, with significant differences between EgRad9-siRNA-614 versus scrambled control (0.095 ± 0.001) and blank control groups (0.099 ± 0.001) (t = 10.227, 10.934, P < 0.01), which further supported the highest effectiveness of EgRad9-siRNA-614. The EgRad9 mRNA expression levels in the EgRad9-siRNA-354, -614, and -971 interference groups were 0.432 ± 0.055, 0.291 ± 0.079, and 0.612 ± 0.032, respectively, with significant differences between EgRad9-siRNA-614 versus scrambled control (1.001 ± 0.020) and blank control groups (1.001 ± 0.012) (t = 7.874, 7.663, P < 0.01), again verifying the highest effectiveness of EgRad9-siRNA-614. Under the same electrophoresis condition, the DNA fragments in the EgRad9-siRNA-614 group migrated from the nucleus to the anode, with a smearing tail. The Olive tail moment in the EgRad9-siRNA-614 group was 13.901 ± 2.263, significantly different from the scrambled control (0.074 ± 0.020) and blank control groups (0.047 ± 0.034) (t = 12.845, 13.251, P < 0.01). The ROS content in the EgRad9-siRNA-614 group was 13.024 ± 0.154, significantly different from the scrambled control (2.728 ± 0.083) and blank control groups (2.555 ± 0.007) (t = 9.296, 10.134, P < 0.01). Conclusion The EgRad9 gene plays an important role in DNA oxidative damage. The EgRad9-siRNA-614 can specifically interfere with the expression of EgRad9 in protoscoleces of Echinococcus granulosus, and reduce the ability of DNA oxidative damage repair in protoscoleces.

    In vitro effects of clorsulon and ornidazole against Echinococcus granulosus protoscoleces and E. multilocularis metacestodes
    Qi XIN, Hai-jun GAO, Xiao-xia SONG, Xu-dong SUN, Wei LV, PERVAIZ Nabil, Jun LU, Tao JING
    2018, 36(4):  352-356. 
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    Objective To evaluate the effects of clorsulon and ornidazole against Echinococcus granulosus protoscoleces and E. multilocularis metacestodes in vitro. Methods E. granulosus protoscoleces were isolated from livers of sheep infected with E. granulosus, and E. multilocularis metacestodes were isolated from the peritoneal cavity of infected Meriones unguiculatus. They were cultured in Dulbecco’s modified eagle medium (DMEM) seeded with human hepatoma cells for 2 months, then vesicles of 1-5 mm in diameter were collected. Four groups were set in the experiment: the clorsulon treatment group (experimental group), ornidazole group (experimental group), albendazole group (positive control), and 0.2% DMSO group (vehicle control group). The experiment was performed in duplicate, and repeated twice. All drugs were used at a final concentration of 40 μmol/L. Each well contained about 100 E. granulosus protoscoleces, or 25-35 E. multilocularis vesicles. After being treated for 24, 48, 72, 96, 120, 144 and 168 h, the protoscoleces were stained by trypan blue and observed by microscopy. The viability of protoscoleces was calculated and analyzed with analysis of chi-square test. The E. multilocularis vesicles were treated for 36 and 120 h, followed by morphological observation by microscopy and measurement of alkaline phosphatase activity in the culture supernatant. The results were analyzed with ANOVA. Result After treatment with clorsulon, ornidazole and albendazole, the protoscoleces showed a darkened color, decreased calcium precipitates, hook shedding, and scolex evagination and elongation, while 0.2% DMSO did not show such effects. After treatment with clorsulon, ornidazole or albendazole for 24, 48, 72, 96, 120, 144 and 168 h, the viability of protoscoleces was 79%, 70%, 56%, 42%, 33%, 16%, 15%; 86%, 67%, 63%, 48%, 32%, 28%, 21%; and 85%, 71%, 45%, 36%, 21%, 15%, 8%, respectively. In the 0.2% DMSO group, 100% of protoscoleces survived. The viability after clorsulon, ornidazole and albendazole treatment was significantly lower than that in the 0.2% DMSO group (χ2 = 147.83, 130.58, 170.37; P < 0.05). Compared to the intact vesicles after 0.2% DMSO treatment, clorsulon, ornidazole and albendazole all caused collapse and shrinkage of E. multilocularis vesicles. At 36 h of treatment with clorsulon, ornidazole, albendazole and 0.2% DMSO treatment, the A405 values of alkaline phosphatase were 0.196 ± 0.030, 0.186 ± 0.004, 0.244 ± 0.049 and 0.131 ± 0.020, respectively, and at 120 h, they were 0.431 ± 0.006, 0.271 ± 0.004, 0.423 ± 0.007 and 0.116 ± 0.004, respectively. There were significant differences in the alkaline phosphatase activity in the three drug treatment groups versus the 0.2% DMSO group (t = 0.006, 0.004, 0.007; P < 0.05). Conclusion Both clorsulon and ornidazole have strong effects against E. granulosus protoscoleces and E. multilocularis metacestodes in vitro, and are potential drugs for echinococcosis.

    Feasibility assessment of using parasitic species-specific genes to detect plerocercoid infection in worm-free pathological tissue of mice
    Yue HU, Yan CHEN, Jin-fu LI, Xing-hui MENG, Qiao-xia LIU, Jian LIU
    2018, 36(4):  357-361. 
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    Objective To assess the feasibility of using specific sequences of cytochrome C oxidase 1 gene(cox1) and internal transcribed spacer 1 (ITS-1) to detect plerocercoid infection in worm-free pathological tissue of mice. Methods Twenty Kunming mice aged 6-8 weeks were randomly divided into the infection group (15 mice) and the uninfected group (5 mice). Mice in the infected group were orally infected with plerocercoids from snake (5 plecerocoids/mouse), while the uninfected mice received no treatment. The mice were sacrificed on day 14 after infection. Subcutaneous muscle tissues containing plerocercoids (worm-containing tissue), worm-stripped tissues (worm-free tissue) and their correspondant of the uninfected group were taken and cut into sections. A portion of these sections were processed for hematoxylin-eosin (HE) staining, while the other portion was used for DNA extraction with a modified proteinase K digestion method. The cox1 (using 2 pairs of primers, resulting in cox1-1 and cox1-2) and ITS-1 (1 pair of primers) were amplified by PCR, and PCR products from DNA of the worm-free tissues in the infection group were cloned, sequenced and aligned with gene sequences of KJ418421, KF990161 and GQ999947 of plerocercoid. The same method was used to prepare muscle tissues from mice infected with cysticercus cellulosae from pigs and the DNA preparation. The species specificity of cox1 and ITS-1 was verified by PCR. Results PCR amplification on DNA of the worm-containing tissue produced specific bands of 822 bp (ITS-1), 414 bp (cox1-1), and 151 bp (cox1-2) after the first round of PCR. No bands were produced from DNA of the worm-free tissue under the same condition but a further round of PCR using the products of the first round resulted in three bands of the same sizes as above. No bands were seen in the uninfected group, either after the first or the second round of PCR. The cox1-1 sequence in the worm-free tissue shared 98.2%, 99.1% and 99.12% homology with KJ418421, KF990161 and GQ999947 of plerocercoid, respectively. No specific bands were amplified from DNA of cysticercus-infected tissue of pigs. Conclusion Repeated PCR amplification using cox1 and ITS-1 gene sequences as the target can identify plerocercoid infection in worm-free pathological tissues of mice.

    The role of TLR4/NF-κB signaling pathway in Cryptosporidim parvum infection
    Rui JI, Rui-wen LIANG, Zhi-yu GUAN, Rui-fang LI, Yu-rong FU, Hong-yan WANG
    2018, 36(4):  361-366. 
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    Objective To explore the role of the Toll-like receptor 4/ nuclear factor κB(TLR4/NF-κB)pathway in intestinal mucosal damage induced by Cryptosporidium parvum infection in mice. Methods Thirty 4-week-old BALB/c male mice were randomly divided into 1-week infection group and 2-week infection group and the non-infection group (n = 10 in each group). The mouse model of Cryptosporidium parvum infection was established intragastrically with 1×105 oocysts. Uninfected mice have normal diet and drinking water. Ten infected mice were sacrificed at 7 days after infection (1-week infection group) and 14 days after infection (2-week infection group), respectively. The normal control mice were sacrificed at 14 days after infection. The intestinal tissue was collected for observing pathological alterations of intestinal mucosa. The relative expression of TLR4 mRNA and NF-κB p65 mRNA in intestinal mucosa was detected by qRT-PCR. The relative expression of TLR4 and NF-κB p65 in intestinal mucosa was detected by Western blotting. The expression of interleukin 1β (IL-1β) and tumor necrosis factor α (TNF-α) in intestinal mucosa was detected by ELISA. Result HE staining showed atrophy and shedding of intestinal villi in the infection group, with submucosal edema and a significant gap between muscle layers, while the intestinal villi were intact in the non-infection group. qRT-PCR showed that the relative expression of TLR4 mRNA in the intestinal mucosa in infection group at week 1 and week 2 was 2.3 ± 0.4 and 3.5 ± 0.1, respectively, higher than the non-infection group (1.0 ± 0.0) (P < 0.05, P < 0.01), and the relative expression of NF-κB p65 mRNA in the intestinal mucosa in infection group at week 1 and week 2 was 2.6 ± 0.3 and 3.6 ± 0.2, higher than the non-infection group (1.1 ± 0.1) (P < 0.05, P < 0.01). Western blotting showed that the protein level of TLR4 in the intestinal mucosa in infection group at week 1 and week 2 was 0.4 ± 0.0 and 0.6 ± 0.0, higher than the non-infection group (0.2 ± 0.0) (P < 0.05, P < 0.01), and that of NF-κB p65 in infection group at week 1 and week 2 was and 0.6 ± 0.0 and 0.8 ± 0.1, higher than the non-infection group (0.4 ± 0.0) (P < 0.05, P < 0.01). ELISA results showed that the expression level of IL-1β in the intestinal mucosa in infection group at week 1 and week 2 was 33.4 ± 2.2 and 46.1 ± 2.5, higher than the non-infection group (22.3 ± 5.0) (P < 0.01), and that of TNF-α in infection group at week 1 and week 2 was 45.7 ± 2.0 and 55.4 ± 3.6, higher than the non-infection group (25.7 ± 9.3) (P < 0.01). Conclusion Cryptosporidium parvum infection may activate the TLR4/NF-κB signaling pathway, up-regulate the expression of TLR4 and NF-κB p65, and promote the release of inflammatory factors TNF-α and IL-1β, thus inducing intestinal mucosal inflammation.

    Laboratory diagnosis of an imported case of African trypanosomiasis
    Yao-ying LIN, Shan-ying ZHANG, Han-guo XIE, Rong OUYANG, Zhu-yun CHEN, Qing-sheng LIU
    2018, 36(4):  366-369. 
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    Objective To diagnose an imported case of suspected African trypanosomiasis by laboratory tools. Methods Clinical information of the patient was collected. The blood and cerebrospinal fluid samples were examined by microscopy after Giemsa staining. DNA of Trypanosoma brucei was extracted from the patient blood sample, and amplified by PCR using primers for T. brucei genus expression site-associated gene(ESAG), T. brucei gambiense-specific glycoprotein(TgsGP) and T. brucei rhodesiense serum resistance-associated (SRA) gene. The PCR products underwent electrophoresis, sequencing, and the sequences were blasted in GenBank. Results The patient was a 41-year-old female from Fuzhou, Fujian Province. She was bitten by an unknown insect in Serengeti National Park of Tanzania (July 28-29, 2018). After returning to China on August 6, she began to develop symptoms of fever, fatigue, and coughing on August 8. She visited a class A hospital in Fuzhou City, where he was disgnosed with infectious fever. The symptoms were not improved after treatment with efdinir (for anti-infection) and Saridon (for fever). The patient was transferred to another class A hospital in the city on August 9, but the fever was still not effectively ameliorated after a combination of anti-infective eftizoxime, anti-viral Tamiflu, phlegm-resolving Mucosolvin and Shiwei Longdanhua Capsule, liver-protective Tianxing and diisopropylamine chloroacetate, and nutrition support, accompanied by progressive increases of liver enzymes. On August 14, the blood and cerebrospinal fluid samples of the patient were sent to Fujian Provincial Center for Disease Control and Prevention for Plasmodium examination. Microscopy of the Giemsa-stained samples showed suspected African trypanosome trypomastigotes in the blood sample, but failed to find Plasmodium. No Trypanosoma was found in the cerebrospinal fluid. PCR results showed a product of 260 bp with the primers for ESAG, no specific product with the primers for TgsGP but a product of 266 bp with the primers for SRA. Results of sequence alignment revealed that the EASG amplified sequence had a 95% homology with AY682003.1, and the SRA amplified sequence had a 99% homology with AJ345058.1. After confirmation of T. brucei rhodesiense infection, the patient was intravenously injected with 20 mg/kg suramin (provided by WHO) on days 1, 3, 7, 14 and 21, with dosage no more than 1 g at each injection. After one treatment course, the patient basically recovered, and was not detected with Trypanosoma at regular checkups in the hospital. Conclusion The case is confirmed to be T. brucei rhodesiense infection by the laboratory diagnosis.

    Clinical features and diagnosis of an imported loiasis patient in Shanghai
    Qi CAI, Nai-fang YE, Lin AI, Jia-xu CHEN, Jian-biao WANG
    2018, 36(4):  370-374. 
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    Objective To analyze the clinical features and diagnosis of an imported loiasis patient in Shanghai. Methods Epidemiological data were collected and patient’s clinical signs and symptoms were studied. Blood and bone marrow sample smears were prepared and stained with Wright’s solution for parasitological analysis under a light microscope. The internal transcribed spacer 1(ITS-1) region of the parasite was sequenced after PCR amplification and were analyzed using basic local alignment search tool (BLAST) program of GenBank. The patient was treated with properly. Result The patient worked in Congo from May to November 2015 and developed with swellings and darkening of the skin in distal left upper extremity after he returned to China in January 2016. He went to a local hospital and in Zhejiang Province the examination results showed elevated number of eosinophiles as well as inflammation in the left upper limb as revealed by magnetic resonance, then was diagonsed as eosinophilic fasciitis. The symptoms were not improved after over 1 year treatment with oral medrol. The patient then went to the dermatology department of Shanghai Ruijin Hospital for further treatment on Febuary 27, 2018. Physical examination concluded dark skin, no swellings, no lumps, no lymphadenopathy or other abnormalities. Eosinophils count was 8.2 × 109/L. Microfilariae were found in blood and marrow smears. More microfilariae were found in blood smear of 8 ml peripheral blood after centrifugation. PCR amplification resulted in a band of ~457 bp, sequence of which had 100% homology to that of Loa loa (GenBank Accession No: DQ995497). The microfilariae were identified as Loa loa microfilariae by morphological observation and gene sequencing. The patient was diagnosed as loiasis and treated with single oral ivermectin at 150 μg/(kg·d). After 2 weeks of treatment, no microfilaria was found in the peripheral blood, and only 12 microfilariae were found in concentrated blood smear of 8 ml peripheral blood. The number of eosinophils was 6.39 × 109/L. These results suggested the effectiveness of ivermection. Conclusion This is an imported loasis case diagnosed by parasitological examination and molecular detection.

    Screening and identification of primers for internal control used in ACT1-qPCR analysis of Toxoplasma gondii
    Hai-ting GUO, Zhi-bao CHEN, Zhong-yuan LI
    2018, 36(4):  375-380. 
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    Objective PCR was performed on DNA extracted from tachyzoites of Toxoplasma gondii RH, PRU and VEG strains, HFF and Vero cell lines, and brain tissues of SPF-grade Kunming mice, in order to identify primers for internal control used to quantify Toxoplasma gondii by quantitative PCR (qPCR). Methods Genomic DNA was extracted from in vitro cultured HFF and Vero cells and tachyzoites of T. gondii RH, PRU and VEG strains. A SPF-grade Kunming mouse was sacrificed by cervical dislocation and the brain tissue was isolated for DNA extraction. The P1/P2 primer specific for T. gondii MIC6 gene (ToxoDB: TGME49_218520) was synthesized according to previous reports, and used for PCR amplification using the extracted DNA samples as template. The presence of T. gondii DNA was examined based on the PCR product bands. PCR with omission of DNA template was used as a blank control. Primers for T. gondii ACT1 gene (ToxoDB: TGME49_209030) were designed, underwent NCBI Primer-BLAST alignment, and synthesized as P3/P4, P5/P6, P7/P8, P9/P10 and P11/P12, with an expected band size of 121 bp. Using T. gondii RH DNA as the template, the annealing temperatures of the primers were optimized by gradient PCR. The optimized PCR conditions were used to amplify the DNA samples, and agarose gel electrophoresis was performed to identify the suitable internal control primers for qPCR of T. gondii. Results As expected, a single band of ~1 050 bp was seen after PCR amplification of T. gondii MIC6 gene using DNA samples from T. gondii RH, PRU and VEG strains, while no band was seen in the blank control group and on other samples, suggesting that the obtained DNA samples can be used in the following examinations. Optimization of PCR annealing temperatures revealed that all primer candidates except the P7/P8 performed comparably at different annealing temperatures, and 56 ℃ was selected as the annealing temperature to amplify ACT1 gene by PCR and qPCR. As expected, using this temperature, all primers resulted in a band of ~121 bp, while no band was seen in the blank control group. In addition, non-target bands were seen after amplification of Vero DNA using primers P7/P8 and P9/P10, and after amplification of Kunming mouse brain DNA using primers P3/P4, P5/P6 and P9/P10, some of which were ~121 bp. Notably, primer P11/P12 was specific and no non-target band was seen after amplification of the Toxoplasma negative samples. Conclusion Primers P11 (5′-TCGGTGACGAAGCCCAAA-3′)/P12 (5′-AGTTCGTTGTAGAAGGTGTGA-3′) are suitable as forward and reverse primers used in qPCR analysis of T. gondii ACT1 gene.

    Establishment and application of multiplex PCR for co-detection of genus- and species-specific malaria parasites
    Li JIANG, Yao-guang ZHANG, Li CAI, Zhen-yu WANG, min ZHU, Xiao-jiang MA, Huan-yu WU
    2018, 36(4):  380-387. 
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    Objective To establish an efficient malaria parasite detection method with genus- and species-specificity. Methods Specific primers were designed, including 4 pairs for 18S rRNA ribosomes which were species specific and 1 pair for mitochondrial gene which was genus specific. They were connected to the universal primer (5′-CGAGTCCTGCGGTCTCAAATT-3′) to generate 5 pairs of chimeric primers. PCR reaction was performed to determine the optimal annealing temperature and primer concentrations. Multiple PCR was performed to optimize the reaction condition of the 5 primer pair mix to establish the new method named P5-mPCR. Patient blood samples, which contained different densities of parasites of Plasmodium vivax (Pv), P. malariae (Pm), P ovale (Po), and P falciparum (Pf), and simulated mixed infection samples were examined by P5-mPCR to determine the sensitivity of P5-mPCR. A variety of blood samples infected by other parasites or worm DNA were examined to evaluate the specificity of the method. The 212 malaria blood samples were tested to evaluate the application value of P5-mPCR in comparison to the nested PCR. Results The optimized reaction system of P5-mPCR consisted of (volume ratio): 10% of DNA template, 5% of primers mix, 35% of distilled water and 50% of Taq polymerase pre-mixed solution. The optimal condition for P5-mPCR system was as follows: 95 ℃ for 5 min, 5 cycles of 94 ℃ for 15 s, 58 ℃ for 20 s, and 72 ℃ for 20 s; 10 cycles of 94 ℃ for 15 s, 62 ℃ for 20 s, and 72 ℃ for 20 s; 25 cycles for 94 ℃ for 15 s, 68 ℃for 20 s, and 72 ℃ for 20 s; 72 ℃ for 3 min; 10 ℃ for 5 min. The amplified products were 778, 582, 400, 256 and 334 bp for Pv, Pm, Po, Pf, and genus Plasmodium, respectively, with a detection sensitivity of 4.49, 5.45, 6.39, 4.07 parsites/μl blood (average of 4.85 parsites/μl blood for species-specific detection), and 0.10-1.07 parasites/μl blood (mean value, 0.41 for genus-specific detection). Specific amplification bands were clearly seen in testing mixed blood sample containing 50-200 parsites/μl blood. No specific bands were seen for Schistosoma japonicum, Toxoplasma gondii, Leishmania donovani, Cysticercus cellulosae, Paragonimus westermani and Cryptosporidium. For the 212 clinically-suspected malaria blood samples, the consistency of the testing results was higher between the nested PCR and P5-mPCR(Kappa = 0.866, P < 0.01), and the positive rate by nested PCR and P5-mPCR was 75.0% (159/212) and 79.7% (169/212), respectively, with a significant difference (χ2 = 8.100,P < 0.01). From the point of species-specificity diagnosis, the differences were mainly derived from the Pf (P < 0.01) and Po (P < 0.05) samples. While for samples with Pv, Pm, and mixed infections, there was no statistical difference between the two methods (P > 0.05). Conclusion The P5-mPCR detection system has a high sensitivity and good specificity, is simple to perform, fast and efficient, and can simultaneously identify 4 species of malaria parasites.

    Current status of key parasitic infections of humans in Heilongjiang Province in 2015
    Lei TANG, Zhi-feng XING, Tao GE, Shi-hui YIN, Shuang YUAN
    2018, 36(4):  388-392. 
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    Objective To understand the status of key parasitic infections of humans in Heilongjiang Province, and provide scientific basis for formulating the prevention and control measures for key parasites in the province. Methods The study was performed from April to June 2015, in accordance with the National Survey Program and Implementation Rules for the status of human key parasites. A stratified cluster random sampling method was used to extract 104 rural survey sites and 15 town survey points from 40 counties (cities and districts) in the Province. The number of persons examined at each survey point was no less than 250. Fecal samples were collected from subjects, and worm eggs of nematode, Taenia tapeworm and Clonorchis sinensis were examined by a modified thick smear method and counted. The direct smear method was used to detect intestinal protozoan cysts and trophozoites, while the cellophane and swab method was used to detect pinworm eggs and the eggs of Taenia solium. Results A total of 30 280 people were examined, of whom the total intestinal parasite infection rate was 2.5% (751/30 280), while no intestinal protozoa were found. Three kinds of intestinal worms were detected: Ascaris lumbricoides, Trichuris trichiura and C. sinensis, with infection person of 3, 1 and 747, respectively. The infected population was predominated by C. sinensis infection (99.5%, 747/751). Both A. lumbricoides and T. trichura showed mild infection. The proportion with light, medium or heavy infections of C. sinensis was 82.3% (615/747), 16.9%(126/747), and 0.8%(6/747), respectively. The infection rate in rural areas was 2.8%(737/26 456), significantly higher than that in urban areas (0.4%, 14/3 824) (χ2 = 80.875, P < 0.05). There were also significant differences in infection rate between males and females [3.1% (464/15 171) versus 1.9% (287/15 109), χ2 = 42.037, P < 0.05), among different age groups (χ2 = 121.628, P < 0.05) [being highest in the 30-39 group which was 3.3% (148/4 430)], among different occupations (χ2 = 165.864, P < 0.05) [being highest in the famers (herdsmen and fishermen) which was 3.2% (695/21 914)], among different ethnic groups (χ2 = 8.482, P < 0.05)[being highest in the Han population which was 2.5% (743/29 487)], and among different educational levels (χ2 = 123.031, P < 0.05) [being highest in those with a middle high school level which was 3.5% (500/14 425)]. Conclusion Three species of key parasites in humans are found in Heilongjiang Province, predominated by Clonorchis sinensis infection (99.5%), most of which showed a light degree of infection. The infection rate varied by factors of gender, age, occupation, ethnicity and education level.

    Epidemiological characteristics of malaria in Guizhou Province during 2005-2016
    Li-dan LU, Dong AN, Jian-jun XU, Yan GENG, Dan-cheng YAO, Shan CAI
    2018, 36(4):  392-398. 
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    Objective To analyze the malaria monitoring data in Guizhou Province from 2005 to 2016 and understand epidemiological characteristics, in order to provide reference for formulating and adjusting strategies and measures for malaria prevention. Methods Data on malaria cases and epidemiological investigations in Guizhou Province from 2005 to 2016 were collected and analyzed with regard to the incidence and distribution of malaria, diagnosis of cases, Plasmodium species constitution, and sources of infection for imported cases. Results During 2005-2016, a total of 4 578 malaria cases were reported in the Province, of whom 4 429 (96.7%) were indigenous cases, 16 (0.3%) were imported from other places in China, and 133 (2.9%) from other countries. These cases consisted of 2 965 (64.8%) vivax malaria, 89 (1.9%) falciparum malaria, 9 (0.2%) ovale malaria, 2 (0.1%) quartan malaria, 2 (0.1%) mixed infections, and 1 511 (33%) unclassified cases. Among all the cases, 3 217 (73%) were clinically diagnosed, all reported during 2005-2011; and 1 361 cases (29.7%) were diagnosed with laboratory tests. The laboratory diagnosis rate has been reaching 100% since 2012. Specifically, the cases reported during 2005-2011 were mainly indigenous cases, distributed mostly in South Qian Autonomous Prefecture, Southeast Qian Autonomous Prefecture, and Southwest Qian Autonomous Prefecture (92.2%, 4 085/4 429). From 2012 on, no indigenous cases were reported, the 106 cases reported were all imported from other countries, and mainly distributed in Guiyang and Zunyi cities (60.2%, 80/133). They were mainly from African countries (86, 64.7%), followed by Southeast Asia (40, 30.1%). Most of the cases were males (3 101, 67.7%). For the occupation distribution, the indigenous cases were predominated by farmers (3 357, 75.8%), followed by students (478, 10.8%); while the imported cases from other countries were mainly farmers (35, 26.3%) and workers (34, 25.6%). The malaria incidence among indigenous cases peaked from July to September, a time coinciding with the endemic season of malaria, and the cases imported from other countries occurred throughout the year, with no significant seasonal variation. Conclusion The endemic situation of indigenous malaria cases has been effectively controlled in Guizhou Province, achieving the goal of malaria elimination. Control of malaria imported from other countries will be the focus of the project in the future.

    REVIEWS
    The role of type Ⅰ interferon in protozoan infections
    Yuan-lin MA, Fang-li LYU
    2018, 36(4):  399-404. 
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    Plasmodium spp., Toxoplasma gondii, Leishmania spp., and Trypanosoma spp. are protozoa that pose a serious health threat to humans. There has been accumulating evidence for an important role of type Ⅱ interferon (IFN-Ⅱ) against parasite infection. However, little is known on the role of IFN-Ⅰ in host defense against parasites. The IFN-Ⅰ responses induced by protozoal infection may vary according to the parasite species/strain, parasite burder, parasite develpmental stage, and the host genetic background. In addition, there are interactions between IFN-Ⅰ and IFN-Ⅱ during protozoan infection. This review summarizes recent findings on the role of IFN-Ⅰ and its regulatory mechanisms during protozoan infection.

    miRNA functions in parasite-related immune regulation in hosts
    Ke LIU, Hai-bin HUANG, Gui-lian YANG
    2018, 36(4):  405-408. 
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    MicroRNAs (miRNAs) are endogenous small-molecule RNAs that participate in the regulation of physiological and pathological processes through post-transcriptional regulation of gene expression. Exploring the functions of miRNAs in host-parasite interactions has become a research focus these years, with topics including the transmission of miRNAs from parasites, the miRNA-mediated regulation of host immune responses, the intermediate host responses, and the immunopathological effects induced by parasite infection. In this review we summarize the latest studies on these topics in order to provide new insights for further research on pathogenesis mechanisms of the parasites.

    Research development on non-coding RNA of Plasmodium falciparum
    Zhi-hua WANG, Chun-yan WEI, Heng WANG
    2018, 36(4):  409-413. 
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    Malaria remains among the top three infectious diseases in the world and poses a serious threat to human health. Among the five Plasmodium species that cause human malaria, Plasmodium falciparum has the highest virulence and is the most lethal one. It has been shown that the immune evasion of parasites is closely related to the mutually exclusive expression of antigen-coding genes in P. falciparum, which depends on the precise gene regulatory mechanism. There are a large number of non-coding RNAs (ncRNAs) in P. falciparum, and some of them have been found to play a vital role in gene expression during parasite development and in pathogenesis. In this review we summarize recent findings on functions of P. falciparum-related ncRNAs, in order to advance our understanding of the regulation of Plasmodium gene expression and provide a theoretical basis for studies on molecular mechanism of Plasmodium pathogenesis.

    Extracellular vesicles of parasites: research development and prospect
    Hui SHEN, Chun-ying LIU, Yu-min ZHAO
    2018, 36(4):  413-417. 
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    Extracellular vesicles(EVs) are vesicles released by cells. Almost all types of cells can produce and release EVs. Exosomes (Exo) and microvesicles (MVs) are two types of EVs. As an important approach for cell-cell signaling through fusion with target cells, the EVs have received much attention in recent years. Secretion of EVs has been identified in a wide range of parasites, and participates in parasitic infections. EVs may serve as a biomarker for disease diagnosis, and therapeutic targets or tools. In this review, we provide an overview on the parasite-associated EVs and their physiological functions.

    Leishmaniasis and its control
    Li-ren GUAN, Chun-hua GAO
    2018, 36(4):  418-425. 
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    Leishmaniasis is an ancient parasitic disease. It can be divided into 3 types: visceral leishmaniasis(VL), cutaneous leishmaniasis(CL) and mucocutaneous leishmaniasis(MCL) according to clinical manifestations. Leishmaniasis is widely distributed in Asia, Africa, Europe, and central and south America. The control of leishmaniasis is challenging and thus a long-run task. There are two types of leishmaniasis in China, including the VL and CL types. The human VL, which once had a prevalence in plain areas of 7 provinces in eastern and central China, was reported to be eliminated in 1983, but is still occurring in some ancient oasis plain areas of southern Xinjiang. The VLs in the mountainous and desert regions in the west are of the zoonotic type and are difficult to control, and these areas are the main endemic foci of the disease. The CL type was found in Karamay, Xinjiang in the 1980s, and its distribution in other areas of China has yet to be investigated. In recent years, CL cases imported from abroad have been reported in Sichuan, Anhui, Xinjiang and Henan provinces/autonomous regions. It remains to be determined if the disease can spread in western China. The prevalence of AIDS and the increased numbers of HIV infections in the population offer possibilities of co-infection with Leishmania and HIV. This will have an impact on the endemic trend of leishmaniasis in China.

    STANDARD INTERPRETATION
    Interpretation of the Criteria for Diagnosis of Fascioliasis
    Yan ZHOU, Yan-hong XIONG, Xue-nian XU
    2018, 36(4):  425-428. 
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    The Criteria for Diagnosis of Fascioliasis (WS/T 566-2017) (referred to as the Criteria) was compiled in accord with the Management Measures for Health Criteria and GB/T 1.1-2009 Standardization Work Guidelines. The Criteria is composed of six chapters, including the range of application, terms and definitions, diagnostic basis, diagnostic principle, diagnosis and differential diagnosis. Three informative appendices (etiology, epidemiology and clinical manifestation, as well as differential diagnosis) and one normative appendix (laboratory examination) are appended. The Criteria was issued by the former National Health and Family Planning Commission of China ([2017] No. 11) and was implemented on February 1, 2018. The Criteria provides for the first time technical reference for fascioliasis diagnosis in medical institutions and disease control institutions in China, and also fills the gap of diagnosis criteria of fascioliasis in China. Combined with the current enidemic situation of fascioliasis in China, this paper interprets the main contents of the Criteria so as to promote its publicity and implementation.

    SHORT COMMUNICATIONS
    A survey on intestinal nematodes in primary and middle school students in Baise City from 2006 to 2016
    Ji-guang DENG, Shui-lan YU, Zhi NONG, Yi-chao YANG
    2018, 36(4):  330-332. 
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    A survey was performed on intestinal nematodes among primary and middle school students in Baise city from 2006 to 2016, using the modified Kato thick smear (Kato-Katz) method to examine worm eggs under microscope. The positive fecal samples were further used to culture hookworm larvae using the tube filter method, to identify the species of hookworms. Meanwhile, pinworms were examined by the transparent paper anal swab method for students under 12 years. A total of 10 273 students were examined, of whom 385 (3.75%) were infected with intestinal nematodes. The infection rate of intestinal nematodes was highest in 2006 (17.22%, 36/709) and lowest in 2016 (1.15%, 11/956). The infection rates of whipworm, roundworm, pinworm and hookworms were 2.25% (231/10 273), 0.79% (80/10 273), 0.67% (69/10 273) and 0.05% (5/10 273), respectively. The hookworms detected were all identified to be Ancylostoma duodenale. The four species all showed mild infection, and no mixed infection was found. The infection rate of intestinal parasites was 3.36% (180/5 361) in boys and 4.17% (205/4 912) in girls (χ2 = 4.722, P < 0.005). The infection rate of intestinal nematodes was highest in the 6-year-old group (6.4%, 95/1485). Among different areas of residence, the infection rate of intestinal nematodes was highest in rural areas (13.11%, 110/839), and lowest in urban areas (2.44%, 212/8 692), with the rural-urban fringe areas in-between (8.49%, 63/742) (χ2 = 291.445, P < 0.01). Those detected with intestinal nematode infection received deworming treatment with the compound albendazole. The results suggest a trend of decrease for intestinal nematode infections, and whipworm is the most common intestinal nematode.

    Diagnosis and analysis of an imported case of cutaneous leishmaniasis in Henan Province
    Su-hua LI, Li-jun GAO, Ya-lan ZHANG, Rui-min ZHOU, Cheng-yun YANG, Dan QIAN, Ying LIU, Yu-ling ZHAO, De-ling LU, Hong-wei ZHANG, Bian-li XU
    2018, 36(4):  339-342. 
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    The male patient who went to Uzbekistan in June 2017 and found two small red rashes on the left thoracic arm on July 2 returned to China in October. The rashes became larger with a small amount of pus. A rapid strip test for leishmaniasis showed that the patient serum was negative for anti-Leishmania antibody. Microscopic examination of the lesioned tissue revealed no Leishmania amastigotes. The lesioned tissue was cultured in NNN medium and a large number of promastigotes were found in culture on day 8. The promastigote DNA was extracted and underwent PCR amplification using Leishmania-specific primers K13A/K13B and L5.8S/LITSR, producing fragments of 120 and 350 bp. The two products were 90% and 98% homologous to the corresponding sequences of L. major (GenBank accession number: EU370906.1 and FN677342.1). The patient was diagnosed as imported cutaneous leishmaniasis and the pathogen was identified to be L. major. The disease was controlled after 2 treatment courses with sodium stibogluconate at a total dosage of 7.2 g (6 days for each course, with a 1-week interval between them). The patient had recovered by the end of the study.

    Epidemiological investigation on hydatidosis in students of Guluo Tibetan Autonomous Prefecture in Qinghai Province
    Shi-lei CHENG, Hui-xia CAI, Xiao MA, Jing-xiao ZHANG, Na LIU, Xiong-ying ZHANG, Ke-mei SHI, Yu-fang LIU
    2018, 36(4):  349-351. 
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    To understand the prevalence of hydatidosis in students of Guluo Tibetan Autonomous Prefecture, Qinghai Province, (referred to as Guluo Prefecture hereafter), ELISA and B-ultrasonography were performed in students of 6 to 19-year from 50 schools in 40 towns of 6 counties in the Prefecture in 2012. The results showed that the hydatidosis prevalence by ultrasound was 2.9% (247/8 597) and the positive rate of serum antibody was 16.1% (1 218/7 552) among the students. Both indices were highest in Dari county (5.6%, 124/2 225; 23.0%, 428/1 861, respectively), and were significantly different among counties (χ2 = 228.314 and 100.449, P < 0.05). The prevalence in males and females was 2.7% (116/4 232) and 3.0% (131/4 365), respectively (P > 0.05). The serum antibody positive rates in males and females were 15.7% (579/3 698) and 16.6% (639/3 854), respectively (P > 0.05). Among different age groups, the group of 13-19 years had the highest prevalence (7.6%, 57/750), while the group of 8-9 years had the highest serum antibody positive rate (18.5%, 214/1 159), both showed significant difference among age groups (χ2 = 75.088, 27.994, P < 0.05). These results show a high prevalence of hydatidosis in Guluo Prefecture.