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    30 June 2016, Volume 34 Issue 3
    Interferon-γ Induced by Toxoplasma gondii Excreted/Secreted Antigens Promotes Apoptosis of CD4+CD25+ Regulatory T Cells
    GE Ke1,QIU Xiao-yan2,WANG Li-juan1,CHEN Hui3,ZHANG Lu-yan3,
    2016, 34(3):  1-183-188. 
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    Objective To investigate the effect of excreted/secreted antigens(ESAs) from Toxoplasma gondii RH strain and TgCtwh3 strain on apoptosis of CD4+CD25+ regulatory T cells and interferon-γ(IFN-γ) secretion. Methods ESAs of Toxoplasma gondii RH strain and TgCtwh3 strain were prepared. Splenic mononuclear cells were isolated from C57BL/6 mice and randomly divided into RH ESA group(2×106 cells/well with addition of 10 μg/ml RH ESA), TgCtwh3 ESA group (2×106 cells/well with addition of 10 μg/ml TgCtwh3 ESA) and control group(2×106 cells/well with addition of 10 μg/ml ovalbumin). Flow cytometry was performed to examine the early apoptosis of CD4+CD25+ regulatory T cells after treatment for 48 h and 72 h. ELISA was conducted to determine the level of IFN-γ in the supernatant after treatment for 72 h. In another experiment, the 3 groups of splenic mononuclear cells were added with 10 μg/ml anti-IFN-γ antibody for 72 h and flow cytometry was performed to examine the early apoptosis of CD4+CD25+ regulatory T cells. Meanwhile, splenic mononuclear cells from IFN-γ knockout and wild-type C57BL/6 mice were also divided into the above-described 3 groups, and flow cytometry was performed to examine the early apoptosis of CD4+CD25+ regulatory T cells after treatment for 72 h. Results The concentrations of RH ESA and TgCtwh3 ESA were 0.54 mg/ml and 2.14 mg/ml, respectively. Flow cytometry showed that the early apoptosis rate of CD4+CD25+ regulatory T cells in the RH ESA group and the TgCtwh3 ESA group after 48 h treatment was (12.90±1.26)% and (9.71±1.04)%, respectively (P<0.05), both significantly higher than that in control group (4.48±0.48)% (P<0.01) . The early apoptosis rate of CD4+CD25+ regulatory T cells after 72 h in the RH ESA group was(15.21±1.11)%, significantly higher than that in the TgCtwh3 ESA group[(11.02±0.92)%] (P<0.05) and the control group[(10.10±1.49)%](P<0.01). ELISA showed that the level of interferon-γ in the RH ESA group and the TgCtwh3 ESA group after 72 h was(4 764.0±118.7) pg/ml and (3 629.0±33.6) pg/ml, respectively (P<0.01), both significantly higher than that in the control[(679.4±30.6) pg/ml](P<0.01). Flow cytometry revealed lower early apoptosis rate of CD4+CD25+ regulatory T cells in the RH ESA group added with anti-IFN-γ antibody[(10.44±1.44)%] compared with that without the addition of the antibody[(14.96±0.83)](P<0.05). But this difference was not observed for the TgCtwh3 ESA group. Moreover, the RH ESA-induced apoptosis rate of regulatory T cells from IFN-γ knockout mice[(10.64±0.55)%] was significantly lower than that from the wild-type mice [(15.21±1.11)%](P<0.01). But this difference was not found for the TgCtwh3 ESA treatment. Conclusion T. gondii RH ESA induces apoptosis of CD4+CD25+ regulatory T cells and IFN-γ secretion, and these effects are stronger than those of TgCtwh3 ESA. The T. gondii ESA-induced IFN-γ stimulates generation of anti-Toxoplasma immunity during acute Toxoplasma infection through mediation of regulatory T cell apoptosis.
    Secretion and Distribution of Rhoptry Protein 16 during Toxoplasma gondii Invasion into Host Cells
    JIANG Shi-chen, WEI Hai-xia, HE Cheng, DENG Sheng-qun, XIA Jing, PENG Hong-juan*
    2016, 34(3):  2-189-197. 
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    Objective To examine the secretion and localization of Toxoplasma gondii Rhoptry protein 16 (ROP16) during invasion of different strains of T. gondii into host cells. Methods The Tgrop16 gene was amplified by PCR on the cDNA of T. gondii RH strain, subcloned into the plasmid pET-32a(+), and expressed in Escherichia coli BL21(DE3) under the induction of isopropyl β-D-1-thiogalactopyranoside. New Zealand rabbit was immuned with the expressed recombinant protein TgROP16 to produce polyclonal anti-TgROP16 antibody. The specificity and sensitivity of the polyclonal antibody were examined by Western blotting and indirect ELISA, respectively. The transcriptional and protein levels of Tgrop16 in T. gondii RH strain and Pru strain were determined by real-time PCR and Western blotting, respectively. The secretion and distribution of TgROP16 in human foreskin fibroblasts(HFFs) during the invasion by T. gondii RH strain and Pru strain were examined by indirect immunofluorescence assay(IFA). Results Western blotting showed a specific band at Mr of ~100 000, indicating that the specific rabbit-derived anti-TgROP16 polyclonal antibody was capable of recognizing TgROP16. Indirect ELISA revealed a titer of 1:25 600 for the antibody. The relative expression level of Tgrop16 in Pru strain[(7.786±0.206)] was 7 times than that in RH strain[(1.000±0.110)](P<0.05) as detected by real-time PCR, and TgROP16 protein level was higher in RH strain than in Pru strain. IFA showed that TgROP16 was localized on the apical complex of the unrecruited tachyzoite of T. gondii before invasion and was secreted out of the recruited tachyzoite after invasion. Conclusion The anti-TgROP16 polyclonal antibody has high specificity and sensitivity. The TgROP16 protein level is higher in the RH strain than in the Pru strain. For both strains, TgROP16 is localized on the apical complex of the unrecruited tachyzoite before invasion and secreted out of the recruited tachyzoite during invasion.
    Prokaryotic Expression, Purification and Immunological Characterization of Micronemal Protein 16 of Toxoplama gondii
    LI Jin, CUI Yong, YIN Kun, LIU Gong-zhen, XIAO Ting, XU Chao,
    2016, 34(3):  3-198-202. 
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    Objective To prokaryotically express three gene fragments of micronemal protein 16 (TgMIC16) of Toxoplasma gondii, and analyze the immunoreactivity of the three recombinant protein products. Methods Primers were designed for three fragments of TgMIC16 gene which encode proteins within the functional domain. Reverse-transcription PCR was used to generate cDNA from RNA, and the three fragments were amplified on the cDNA by PCR using the designed primers. The PCR products were double-digested, inserted into the pET-32a(+) plasmid, and transformed into Escherichia coli TOP10 cells. Plasmids extracted from positive clones were confirmed by BamHⅠ/HindⅢ double digestion and sequencing, and further transformed into E. coli Rosetta cells. Protein expression was induced by IPTG, and confirmed by SDS-PAGE. The expressed recombinant proteins were purified with Ni-NTA affinity chromatography and their immunoreactivity analyzed with Western blotting. Results The amplified three fragments were 1 806, 1 290 and 855 bp in size. Double digestion and sequencing results confirmed the successful construction of the three recombinant plasmids. SDS-PAGE analysis showed successful expression of the three recombinant proteins(Mr 88 000, 68 000 and 52 000, respectively), in the form of inclusion bodies. Western blotting showed that the three purified recombinant proteins reacted with His monoclonal antibody and rabbit anti-T. gondii antibody. Conclusion The three fragments within the functional domain of TgMIC16 are successfully expressed in prokaryotic expression system and show immunoreactivity.
    In vitro Effect of Hypericin against Toxoplasma gondii Tachyzoites
    YANG Xiao-di1, SUN Xi-meng2, WANG Qi1, CUI Jie1, JI Yong-sheng3, XUE Hong-bao4,
    2016, 34(3):  4-203-207. 
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    Objective To investigate the killing effect of hypericin on tachyzoites of Toxoplasma gondii RH strain in vitro. Methods Normal saline (group A) and different concentrations of hypericin (5 μg/ml, group B; 50 μg/ml, group C; 500 μg/ml, group D) were added to T. gondii tachyzoites in 24-well plate(1×106/well). The tachyzoites were harvested after 2, 4 and 6 h, and underwent the following treatment: trypan blue staining to calculate the dyeing rate, Giemsa staining to observe the morphological and structural alterations of tachyzoites, and transmission electron microscopy to observe the ultrastructure of tachyzoites. In addition, flow cytometry was performed to calculate the survival rate of YFP-carrying Toxoplasma with the same treatment. Results The trypan blue dyeing rate at 2 h after treatment in groups B, C and D was(11.0±3.6)%, (25.0±6.3)% and(40.0±2.7)% respectively, with a significant difference of group D versus B and C (P<0.01), and groups C and D versus group A [(6.0±3.0)%)]. The dyeing rate at 4 h and 6 h in group D was(97.0±2.0)% and (98.0±1.7)%, respectively, both significantly higher than that of groups C [(30.0±7.2)%, (42.7±5.5)%], B [(20.0±3.0)%, (34.0±6.6)%] and A [(10.0±1.0)%, (19.3±4.9)%](P<0.01). Giemsa staining showed gradual end swelling and necrosis of tachyzoites with increased treatment duration and dosage. Transmission electron microscopy showed swelling of worm body, gap between cell membrane and matrix, increase and enlargement of vacuoles inside worm body, disruption of cell membrane, and dissolving of inner structures, with increased treatment duration. Flow cytometry showed significant difference of tachyzoite survival rate at 2, 4 and 6 h after hypericin treatment with that of the control group(P<0.01). The survival rate of group C at 2 h after hypericin treatment was(7.9±1.9)%, significantly lower than that of groups B [(38.1±5.5)%] and A [(81.8±6.0)%] (P<0.01). No tachyzoite was found to survive in group D at 2 h and in group C at 4 h. The survival rate of group B at 4 and 6 h after hypericin treatment was(14.3±7.9)% and (1.4±1.8)%, respectively, both significantly lower than that of group A[(73.8±11.3)% and(64.1±14.4)%, respectively] (P<0.01). Conclusion Hypericin has a remarkable killing effect on T. gondii tachyzoites, and the efficacy positively correlates with the dose and treatment duration.
    Cloning, Expression and Immungenicity Analysis of Antigen Eg-01883 Screened from Protoscoleces of Echinococcus granulosus
    ZHAO Yin-qi1,2,3,LI Zi-hua1,2,3,WANG Hao2,4,ZHU Ming-xing1,2,3,NIU Nan2,3,5,
    2016, 34(3):  5-208-214. 
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    Objective To screen for the Echinococcus granulosus 01883(Eg-01883) specifically expressed at the protoscolex period, clone and express this molecule as well as analyse its immunogenicity. Methods Eg-01883, which is highly expressed at the protoscolex period but not in oncosphere, was screened by analysing the published mRNA sequences of E. granuolosus. Total RNA of E. granuolosus was extracted, Eg-01883 was cloned by RT-PCR, and the recombinant plasmid pET28a-Eg-01883 was constructed. Expression of the recombinant protein rEg-01883 was induced by isopropyl-β-D-thiogalactoside (IPTG). ICR mice were randomized into 3 groups (n=12 in each group). Mice in the immunization group received subcutaneous injections of 10 μg rEg-01883 in 100 μl PBS emulsified in Freund’s adjuvant at multiple sites, followed by immune enhancement after 2 weeks. Mice in the adjuvant group were injected with PBS and adjuvant. Mice in the control group received no treatment. Blood was obtained through caudal vein before immunization, and at 1, 2, and 4 weeks after the first immunization, and through the eyeball at 6 weeks after immunization. Serum levels of IgG, IFN-γ and IL-4 were determined by ELISA. The immunogenicity of rEg-01883 was identified by Western blotting. Results Eg-01883 was screened, cloned, expressed and purified to obtain the recombinant protein rEg-01883, which mainly existed as the inclusion body. ELISA results showed that immunization with rEg-01883 induced production of specific IgG antibody. The serum IgG level in the immunization group increased from 1 week after the first immunization, peaked at 6 weeks(2.344±0.153), which was significantly higher than those of the adjuvant group(0.206 1±0.006) and the control group (0.241±0.01) (P<0.01). At 6 weeks after the first immunization, the serum levels of IFN-γ (43.23 pg/ml) and IL-4(24.88 pg/ml) in the immunization group were significantly higher than those in the adjuvant group(21.77 pg/ml, 13.27 pg/ml) and the control group(17.40 pg/ml, 12.25 pg/ml)(P<0.05). Western blot showed that the recombinant protein rEg-01883 could be recognized by His-Tag antibodies, serum of immunized mice, and serum of mice with secondary infection. Conclusion The recombinant protein rEg-01883 shows good immunogenicity in ICR mice.
    Immunotherapeutic Effect of Dermatophagoides pteronyssinus Group 1 Allergen T Cell Epitope Peptide Against Allergic Asthma in Mice
    LI Chao-pin*, ZHAO Bei-bei, ZHAN Xiao-dong
    2016, 34(3):  6-214-219. 
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    Objective To study the specific immunotherapeutic effect of Dermatophagoides pteronyssinus group 1 major allergen T-cell fusion epitope peptide vaccine TAT-IhC-DPTCE against allergic asthma. Methods One hundred and twenty SPF-grade BALB/c mice were randomized into PBS group(group A), asthma group (group B), and immune treatment groups respectively receiving intraperitoneal(i.p.) injections of ProDer p 1 allergen(group C), DPTCE (group D), TAT-DPTCE(group E) or TAT-IhC-DPTCE(group F) (n=20 in each group). In detail, PBS (group A) or allergen extract derived from Dermatophagoides pteronyssinus (groups B-F, 10 μg) was intraperitoneally injected on days 0, 7 and 14, and was continued by aerosol inhalation from day 21 for 7 consecutive days (0.5 μg/ml, once/day, 30 min each time). The mice in groups C-F received i.p. injections of 100 μg/ml ProDer p 1, DPTCE, TAT-DPTCE and TAT-IhC-DPTCE respectively 30 min prior to inhalation challenge on days 25-27 as a specific immunotherapy, while those in groups A and B received 200 μl PBS. Twenty-four hours after the last inhalation challenge, all the mice were sacrificed. The lung histopathological changes were examined by HE staining. The levels of IFN-γ, IL-13, IL-10 and TGF-β in the bronchoalveolar lavage fluid(BALF) was determined with ELISA, and eosinophils in the BALF were counted(n=20 mice in each group). The serum level of IgE, IgG1 and IgG2a in orbital blood was determined by ELISA(n=5 mice in each group). Results HE staining revealed increased BALF eosinophils and decreased pulmonary inflammation in group F compared with group B. The IFN-γ level in group F [(298.75±26.09) pg/ml] was significantly higher than those in groups B[(158.71±20.89) pg/ml], C[(210.38±18.92) pg/ml], D [(229.44±13.00) pg/ml] and E[(233.24±20.39) pg/ml] (all P<0.01). Similar results were also found for IL-10 and TGF-β, while the IL-13 levels in groups C [(47.35±4.71) pg/ml], D [(41.90±4.28) pg/ml], E[(41.05±6.50) pg/ml] and F[(18.53±5.67) pg/ml] were all significantly lower than that in group B [(66.68±6.63) pg/ml](all P<0.01). The number of BALF eosinophils in group B [5.65±0.91]×105/ml] was significantly higher than that in group A [(0.45±0.39)×105/ml] (P<0.01), while the BALF eosinophils in groups C [(4.00±0.59)×105/ml], D [(3.39±0.63)×105/ml], E [(3.24±0.69)×105/ml] and F [(1.42±0.49)×105/ml] decreased after immune treatment(all P<0.01). ELISA results showed that the serum IgE level in group F [(5.26±1.72) ng/ml] was significantly lower than those in group B [(32.81±2.98) ng/ml] and the other 3 treatment groups[group C, (20.06±3.17) ng/ml; D, (17.06±3.18) ng/ml; E, (16.23±3.61) ng/ml]. Similar results were also obtained for IgG1. In contrast, the serum IgG2a level in group F[(43.10±1.34) ng/ml] was significantly higher than those in group B[(12.61±1.87) ng/ml] and the other 3 treatment groups [group C, (23.37±2.67) ng/ml; D, (25.60±2.10) ng/ml; E, (25.91±1.33) ng/ml] (all P<0.01). Conclusion Immunotherapy with chimeric TAT-IhC-DPTCE can effectively ameliorate the allergic airway response and pulmonary inflammation in mice.
    Species Identification and Sequence Analysis of Plasmodium spp. in Border Areas of Yunnan Province by 18S rRNA-based Nested PCR
    ZHANG Cang-lin,ZHOU Hong-ning,NIE Ren-hua,LIU Hui,WANG Jian,
    2016, 34(3):  7-220-226. 
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    Objective To analyze blood samples from patients with falciparum malaria and vivax malaria in border areas of Yunnan Province, using 18S rRNA-based nested PCR, and compare 18S rRNA sequences. Methods Blood or filter blood samples with positive microscopic results for Plasmodium falciparum or P. vivax infection were collected from Laza, Nankajiang, Mangdong and Nawei of Myanmar, and from Mengla, Tengchong and Yingjiang of Yunnan Province between 2004 and 2011. 18S rRNA-based nested PCR was conducted on the samples, and PCR products were sequenced and blasted. Phylogenetic tree was constructed using the neighbor-joining method with MEGA software(version 6.06). Results Microscopic examination revealed P. falciparum infection in 256 samples and P. vivax infection in 219 samples. The 18S rRNA-based PCR further confirmed P. falciparum infection in 242 samples, P. vivax infection in 176 samples, and mixed infection in 57 samples. The consistency rate was 81.7% (388/475) between microscopic and PCR results. The inconsistency rate significantly correlated with parasite density (Spearman’s r=-0.408, P<0.05). Sequence alignment revealed 11 and 10 homologous sequences for P. falciparum and P. vivax 18S rRNA gene, comprising 2.9%(6/205) and 22.5%(27/120) variable sites, respectively. The 18S rRNA of P. falciparum clustered with that from Cameroon(GenBank accession number KC428742), but was distantly related with the S-type 18S rRNA from the Netherlands (U36465) and Brazil (U36466 and U36467). The 18S rRNA of P. vivax clustered with A-type 18S rRNA from Thailand (U07367), but was distantly related with the C-type 18S rRNA from Thailand(U07368). Conclusion Nested PCR revealed mixed infection in 57 samples among those identified with single infection by microscopy. There is no significant difference in 18S rRNA sequence in seven counties/cities in Yunnan Province.
    Polymorphism of 72-76 Coding Sequence within Exon 2 Region of Pfcrt in Yunnan Province
    ZHU Yao-ji1, CHEN Meng-ni2, XU Yan-chun2, MAO Xiang-hua2, DENG Yan2, DONG Ying2 *
    2016, 34(3):  8-227-234. 
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    Objective To understand the endemic situation of chloroquine-resistant falciparum malaria in Yunnan Province by analyzing the polymorphism of the 72-76 amino-acid coding sequence within exon 2 region of Plasmodium falciparum chloroquine resistant transporter(Pfcrt) gene (referred to as the 72-76 coding region) in malaria patients. Methods The filter paper blood samples and relative information of falciparum malaria cases were collected in 13 prefectures of Yunnan Province (excluding Diqing, Wenshan, Zhaotong prefectures) from August 2012 to September 2015. The source of infection was determined by epidemiological investigation and the place of case discovery was confirmed according to the endemic registration in the Infectious Diseases Reporting Manage System, Chinese Center for Disease Control and Prevention. The exon2 region of Pfcrt gene was amplified by nested PCR and sequenced. The polymorphism of the 72-76 coding region was analyzed with MEGA 5.04. The variable sites and genetic distance between sequences were calculated. The constituent ratio of the polymorphism in sub-populations was analyzed with IBM SPSS Statistics 21 software. Results Two hundred and thirty-two blood samples were collected in the period and source of infection included Yunnan of China, Africa and Myanma. Nested-PCR resulted in positive products in 210 samples. Sequence analysis showed the presence of chloroquine-sensitive genotype(CVMNK)(15.2%, 32/210) and mutated chloroquine-resistant genotype(CVIET, SVMNT and CVMNT)(76.2%, 160/210; 6.7%, 14/210; 1.9%, 4/210) 72-76 coding regions. The proportion of the CVMNK type was 100%(32/32) in cases with the range of 19-55 years, 46.9% (15/32) in farmers, and 59.4% (19/32) in patients with infection source in Southeast Asia, all significantly higher than those of other cases in the same groups(0; 31.3%, 10/32; and 37.5%, 12/32 respectively, χ2=13.674, 8.478, 6.292, P<0.05). The proportion of the CVIET and SVMNT genotypes in patients with infection source in Myanma and Cambodia was 81.3%(130/160) and 78.6%(11/14) respectively, significantly higher than those in patients with infection source in Yunnan Province(6.3%, 10/160; 21.4%, 3/14)(χ2=6.519 and 6.620, P<0.05). In samples with Africa infection source, the proportion of CVIET was 12.5%(20/160), with no detection of SVMNT. There was a 145 bp homologous locus among the 210 exon2 regions, of which the conservative sites accounted for 95.2%(138/145) and variable sites for 4.8%(7/145). The genetic distance between the 210 sequences ranged 0.000-0.036(0.012±0.005). The genetic distances from genotypes CVIET, SVMNT and CVMNT to the chloroquine-sensitive genotype CVMNK were(0.029±0.015), (0.021±0.013) and (0.014±0.001) respectively. 178 cases with chloroquine-resistant P. falciparum distributed in all the 13 prefectures. Among them, the regions with top detection rate of chloroquine-resistant genotypes were Dehong(51.7%, 92/178), Baoshan(24.7%, 44/178) and Lincang(5.6%, 10/178) bordering on Myanmar and Kunming(4.5%, 8/178). Conclusion There are three chloroquine-resistant genotypes of the 72-76 coding region in falciparum malaria cases in Yunnan Province, which distribute in 81.3%(13/16) of prefectures in the Province.
    Preparation and Molluscicidal Effect of Chlorosalicylicamide Sustained-release Granules
    QIN Jie1,WEI Feng-hua2,TANG Qian1,YUAN Yi2,LI Gui-ling1,XU Xing-jian2,
    2016, 34(3):  9-235-238. 
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    Objective To prepare the 5% and 10% chlorosalicylicamide(quinoid-2’, 5-dichloro-4’-nitrosalicylanilide from niclosamide) sustained-release granules (LDS-SRG) and evaluate their molluscicidal effect. Methods The 5% and 10% LDS-SRG were prepared with screened carriers, surfactants, adhesives, defoamers and lubricants. Their bulk density, water content, repose angle, critical relative humidity, thermal stability and release rate were determined. Spraying method was used to test the molluscicidal effect of LDS-SRG at 1.6 g/m2. Meanwhile, 50% wettable powder of niclosamide ethanolamine salt(WPN) was applied as the positive control at 1.0 g/m2, and dechlorinated water was used as the blank control. The mortality of snails was calculated on days 3, 7 and 14 after administration. Results The 5% and 10% LDS-SRG were red brown in color, showed good fluidity, and had bulk density of 0.655 g/ml and 0.594 g/ml, moisture content of 1.15% and 1.28%, repose angle of 39.8° and 39.7°, and critical relative humidity of 64.98% and 61.63%, respectively. Moreover, both showed good thermal stability. The release curve was stable for both 5% and 10% LDS-SRG during day 1 to day 9, and faster release for 5% LDS-SRG than for 10% LDS-SRG. The burst release occurred on days 10 and 15, and the steady release occurred from days 14 and 20 for 5% and 10% LDS-SRG respectively. The snail mortality on day 7 after 5% LDS-SRG 1.6 g/m2 administration and on day 14 after 10% LDS-SRG 1.6 g/m2 administration was both higher than 95%, and higher than that of the 50% WPN 1.0 g/m2 control(P<0.05). Conclusion The 5% and 10% LDS-SRG show sustained-release potential and satisfactory molluscicidal effect by spraying, reaching the evaluation standard for molluscicidal agents.
    Imaging Analysis in Cases with Clonorchiasis-Associated Cholangiocarcinoma
    XU Shi-chang1,2,WEN Zhi-bo3*
    2016, 34(3):  10-239-244. 
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    Objective To investigate the magnetic resonance imaging (MRI) and computed tomography(CT) features of clonorchiasis-associated cholangiocarcinoma, and provide reference for its clinical diagnosis. Methods The CT and MRI (including magnetic resonance cholangiopancreatography, MRCP) data of 60 patients diagnosed to have cholangiocarcinoma(26 cases with clonorchiasis-associated cholangiocarcinoma, group A; 34 cases with simple cholangiocarcinomas, group B) by surgery or biopsy in two hospitals in Guangdong Province during July 2005 and June 2015 were collected. The tumor location, pathological types, imaging features, mode of enhancement, and the bile duct expansion were analyzed. Results Imaging results showed that the tumor tended to occur in the right liver in group A(46.2%, 12/26) and in the left hepatic duct and the liver explorer in group B (61.8%, 21/34)(P<0.05). The pathological types of tumor in both groups included the nodule/mass type(group A, 73.1%, 19/26; group B, 52.9%, 18/34), the infiltration type (15.4%, 4/26; 23.5%, 8/34), and the cavity growth type(11.5%, 3/26; 23.5%, 8/34)(P>0.05). Plain and enhanced CT and MRI results revealed no significant difference in tumor density, signal characteristics or the mode of enhancement between the two groups. MRCP results showed that the intrahepatic distal bile duct cystic dilatation, the intrahepatic bile duct cane soft tubular ectasia, the bile duct dilatation in the tumor, and the bile duct dilatation surrounding the tumor accounted for 61.5%(16/26), 19.2% (5/26), 50% (13/26) and 7.7%(2/26) in group A, and 8.8% (3/34), 64.8% (22/34), 20.6% (7/34) and 38.2% (13/34) in group B (P<0.05 for each of the four), respectively. Conclusion The clonorchiasis-associated cholangiocarcinoma has certain imaging characteristics. It is different from the simple cholangiocarcinomas in tumor location and intrahepatic bile duct dilatation.
    In Vitro Effects of Aminoalcohol-carbazole Compound BTB3 against Echinococcus granulosus
    LIU Cong-shan1,ZHANG Hao-bing1,XUE Jian1,TAO Yi1,HU Wei1,2*
    2016, 34(3):  11-245-248. 
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    Objective To evaluate the effects of a aminoalcohol-carbazole compound BTB3 against Echinococcus granulosus in vitro. Methods The protoscoleces from sheep and germinal cells from secondary-infected mice were cultured and treated with 1, 2, 4, 8, 10 and 20 μg/ml BTB3 for 3 days. The viability of protoscoleces and cells was determined by the methylene blue exclusion method and CCK-8 assay. Meanwhile, the effect of 10 μg/ml BTB3 on germinal cells was assessed by scanning electron microscopy(SEM). The metacestodes were treated with 1, 5 and 10 μg/ml BTB3 for two weeks, and the integrity of the metacestodes was evaluated by SEM. Results The 10 μg/ml and 20 μg/ml BTB3 caused a death rate of (100.0±0.0)% and (85.2±7.2)% respectively for protoscoleces. As the concentration decreased, the death rate remained below 10%. Moreover, the activity inhibition rate on germinal cells was about 100% for 8, 10 and 20 μg/ml BTB3, and was reduced with the decrease of BTB3 concentration other than the afore-mentioned three. SEM revealed detachment, shrinkage, and cavitation of germinal cells after BTB3 treatment. And the metacestodes all showed the loss of turgidity after BTB3 treatment for 14 days, which indicated cell detachment and uneven distribution of cells in internal cyst of metacestodes. Conclusion BTB3 has strong effects against Echinococcu granulosus protoscoleces, germinal cells and metacestodes in vitro, which make it a potential drug against hydatid diseases.
    Epidemiological Survey of Echinococcosis in Xinjiang Uygur Autonomous Region in 2012
    Maimaitijiang WUMAIER1,2, Adili SIMAYI1, Yisilayin OSMAN1, Yalikun MAIMAITIYIMING1,
    2016, 34(3):  12-249-254. 
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    Objective To understand the endemic status of echinococcosis in Xinjiang Uygur Autonomous Region, to provide scientific basis for planning and promoting control measures in this region. Methods Eight hundred people of all age ranges were examined in each of the selected agricultural area, pastoral area, pastoral-agricultural area, and township area of 92 counties in 14 prefectures in Xinjiang during March and October of 2012, resulting in a total of 3 200 people surveyed in each county. B ultrasonic abdominal scan was performed, accompanied by serum antibody detection for suspected cases. Results A total of 293 140 people were examined. The overall morbidity was 0.14%(407/293 140). The morbidity in the north region was 0.18%(290/158 985, 71.25%of all the cases), and that in the south region was 0.09%(117/134 155, 28.75% of all the cases)(P<0.05 between the regions). The cases were mainly distributed in Urumqi City(19.90%, 81/407), Tarbagatai Prefecture(13.27%, 54/407), Yili Kazak Autonomous Prefecture(13.02%, 53/407) and Changji Hui Autonomous Prefecture(9.83%, 40/407). The prevalence was higher in Mongolian[0.42%(21/5 045)] and Kirgiz [0.35%(32/9 045)] than in other ethnic groups(0.07%-0.22%)(P<0.05). There was no significant difference in prevalence between males[0.13%(195/144 715)] and females[0.14%(212/148 425)] (P>0.05). The prevalence was lowest in the 0-9 year group[0.07%(7/10 754)], and higher in the the age groups of 70-79[0.27%(33/12 310)] and 80-99 years[0.28%(7/2 461)], showing a trend of elevation with ageing. Further, the cases were mainly in the population of 30-49 years(43%, 175/407). The prevalence was higher in the uneducated[0.25%, 39/15 470] than in the educated populations(0.06%-0.14%)(P<0.05), and higher in pastoralists[0.29%, 63/22 074] than in populations with other occupations(0.00%-0.13%)(P<0.05). The prevalence in pastoral area, agricultural area, pastoral-agricultural area, and township area was 0.16%(70/44 247), 0.16%(181/113 016), 0.12%(88/70 610) and 0.10%(68/65 267), respectively. The township area had the lowest prevalence, which was significantly different from both the pastoral area and the agricultural area(P<0.05). Conclusion Echincoccosis is widely distributed in Xinjiang, with more cases in the north.
    Risk Assessment for Malaria Transmission in the Border Area of Yunnan Province
    YIN Shou-qin1,XIA Shang2,ZHOU Xing-wu3,YANG Ya-ming3,XIA Zhi-gui2,
    2016, 34(3):  13-255-260. 
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    Objective To assess the malaria transmission risk in the border area of Yunnan Province and provide evidence for adjustment of malaria intervention and elimination strategies. Method Data concerning malaria prevalence, vector distribution, and institutional intervention capacity were collected in 197 towns of 20 counties in the border area of Yunnan Province during 2012-2014. The malaria transmission potential index (TPI), intervention capacity index(ICI) and malaria risk index(MRI) were calculated for each town, based on the criteria formulated by a professional committee. The towns were categorized according to the indices aforementioned. The risk map was created with GIS software. Results Based on the TPI, the 197 towns comprised of 2 grade-I towns(including Nabang in Yingjiang and Banlao in Cangyuan) with high transmission potential, 11 grade-II towns with moderate transmission potential and 184 grade-III towns with low transmission potential. Based on the ICI, the 197 towns comprised of 4 grade-III towns(including Zhongke in Ximen, Zhonghe and Diantan in Tengchong, and Menghan in Jinghong) with a weak control capacity, 20 grade-II towns with a moderate control capacity and 173 grade-I towns with a strong control capacity. Based on the MRI, the 197 towns comprised of 2 grade-I towns(including Nabang in Yingjiang, and Banlao in Cangyuan) with a high transmission risk level, 12 grade-II towns with a moderate level and 183 grade-III towns with a low level distributed in 20 counties. Conclusion The grade I or II towns with moderate and high transmission risk constitute <5% of the 197 towns in the border area, suggesting a relatively low level of malaria transmission risk in most counties.
    Genetic Variation of Oncomelania hupensis in Weishan Lake of Shandong Province Using Microsatellite DNA Markers
    HE Jian1, MIAO Feng2, YANG Kun1, ZHAO Chang-lei2, LIU Xin2*
    2016, 34(3):  14-261-265. 
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    Objective To identify the genetic variation of Oncomelania hupensis between Weishan Lake population and Yangtze River population. Methods O. hupensis snails were collected from Jiangdu District of Yangzhou City, Yizheng City, Danyang City, and Liuhe District of Nanjing City in Jiangsu Province, as well as Weishan Lake of Jining City in Shandong Province. Four polymorphic microsatellite DNA loci(A18, C22, T4-33 and T6-17) were amplified by using microsatellite PCR to analyze the number of alleles (Na), the expected heterozygosity (He), the observed heterozygosity (Ho) and the average number of pairwise differences between populations. Analyses of molecular variance(AMOVA) and cluster analysis were performed to find the genetic variation between O. hupensis snail populations. Unweighted pair group method with arithmetic mean (UPGMA) and neighbour joining(NJ) method were used to construct the phylogenetic tree to describe genetic variation and clustering among populations. Mantel test was carried out to detect the correlation between the genetic distance and geographical distance. Results A total of 103 snails were collected. The snail populations of Jiangdu, Yizheng, Danyang, Liuhe, and Weishan Lake had Na of 7.50, 12.50, 10.00, 11.50; Ho of 0.16, 0.27, 0.17, 0.30, 0.22; and He of 0.81, 0.91, 0.84, 0.90, 0.92, respectively. The Weishan Lake population showed relatively higher levels of the three indicators, indicating a higher genetic diversity, but with no significant difference with the other four populations. The average number of pairwise differences was lowest between the Weishan Lake and Jiangdu populations(0.79), and it was higher between Danyang population and the others(0.87-0.97). AMOVA result showed the inter-individual genetic variation accounted for 92.50% of the total variations. NJ and UPGMA analysis showed Jiangdu and Weishan Lake populations gathered together in one branch, Yizheng and Liuhe populations formed another relatively independent branch, and then was Danyang population. Genetic distance and geographical distance showed no correlation by Mantel test. Conclusion There is a high genetic diversity of O. hupensis in Weishan Lake and Yangtze River populations, and no significant genetic divergence between Weishan Lake snail population and its original Yangtze River population.
    In vitro Killing Effect of Eucalyptus robusta Leaves Extract on Echinococcus granulosus Protoscolices
    ZHAO Yu-ning,ZHANG Hao-bing*
    2016, 34(3):  15-266-271. 
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    Objective To investigate the effect of Eucalyptus robusta leaves extract against Echinococcus granulosus protoscolices in vitro. Methods Mature leaves of Eucalyptus robusta were collected on 24th day in each month from January to December 2012, and air-dried in the room. Ultrasonic extraction of the leaves was done with 4 solvents with different polarity, petroleum ether, dichloromethane, ethyl acetate and anhydrous ethanol. Protoscolices were incubated with the extract at various concentrations for 72 h, and mortality and median lethal dose(LC50) was calculated. Results The extracts were different in characteristics and yield. The petroleum ether extract was in the form of black oil, while dichloromethane, ethyl acetate and anhydrous ethanol extracts were in the form of dark green, pink and white powder respectively. The average yields by petroleum ether, dichloromethane, ethyl acetate, and anhydrous ethanol were 4.4%, 2.1%, 2.3% and 2.3%, respectively. The extract yield was highest for petroleum ether, with a yield of 5.4% in May. The mortality of protoscoleces in all monthly groups of petroleum ether and dichloromethane extracts reached 100% with the concentration of 100 μg/ml and the same mortality reached in most groups of petroleum ether extracts with the concentration of 50 μg/ml. The effects of dichloromethane extracts were less than petroleum ether extracts, but significantly stronger than those of ethyl acetate and ehanol extracts. Further studies conducted on petroleum ether and dichloromethane extracts showed, the lethal effect of petroleum ether extract ranked in month of preparation from strong to weak as June>March>November>April>February>May>October>August>December>July>January>September. In June, the LC50 was 2.577 μg/ml and 95% confidence interval was 0.85-6.22 μg/ml. The lethal effect of dichlorom ethane extract ranked in month of preparation from strong to weak as November>May>October>April>July>December>June>September>August>February>March>January. In November, the LC50 was 21.85 μg/ml, and 95% confidence interval was 12.38-36.28 μg/ml. Conclusion The Eucalyptus robusta leaves contain potential compounds against Echinococcus granulosus. Further experiments of isolation, analysis and identification are needed.
    Blastocystis Infection in Pet Dogs in Selected Areas of Anhui and Zhejiang Provinces
    LI Wen-chao, WANG Kai, QIN Mian, LIU Zong-hua, YUAN Gan, LIU De-yi, GU You-fang*
    2016, 34(3):  16-272-276. 
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    Objective To determine the prevalence and subtypes of Blastocystis in pet dogs in Anhui and Zhejiang Provinces. Methods Pet dog fecal samples were collected from veterinary clinics in Baohe District of Hefei City, Xuanzhou District of Xuancheng City, Fengyang County and Mingguang City of Chuzhou City, Longzihu District of Bengbu City, Si County of Suzhou City in Anhui Province, as well as in Yuhang District of Hangzhou City in Zhejiang Province from April to December, 2013. Blastocystis was detected by microscopic examination as well as nested PCR and single-step PCR based on small subunit ribosomal DNA sequences. The PCR products were sequenced, and Blastocystis subtypes were assigned. Results A total of 315 pet dog fecal samples were collected. The incidence of Blastocystis infection determined by microscopic examination, nested PCR and single-step PCR was 1.3%(4/315), 1.9%(6/315) and 1.9%(6/315), respectively. In addition, the two PCR methods both revealed Blastocystis infection only in Chuzhou City(3.4%, 1/29) and Hefei City(5.6%, 4/72). The pet dogs in Chuzhou City carried ST1 and ST2 subtypes while those in Hefei carried only ST1. There was no significant difference in infection rate between adult and young dogs and between male and female dogs. Conclusion Blastocystis infection exists in pet dogs in Chuzhou City and Hefei City.
    Research Progress on the Role of Small Non-coding RNA in Schistosoma Infection
    YANG Jie1, QIN Zhi-qiang2 *, XU Jing2, QIAN Ying-jun2, ZHOU Dong-ming3
    2016, 34(3):  17-277-281. 
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    Small non-coding RNA controls the expression of target genes and is related with mRNA degradation, chromatin modification and genome stability. Recent studies showed that small non-coding RNA is not only associated with the incidence of schistosomiasis, but also acts as a potential biomarker. In this article, we will review the applications of small non-coding RNA in schistosomiasis diagnosis and its potential role in schistosome development and pathogenesis, in the aim to provide hints for developing detection methods and vaccines for schistosomiasis and for drug development.
    Diapause of Aedes albopictus and the Related Molecular Mechanisms
    XIA Dan,TENG Ping-ying,CHEN Xiao-guang,ZHOU Xiao-hong*
    2016, 34(3):  18-282-289. 
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    Aedes albopictus is an important transmitting vector of a wide range of arboviruses such as Dengue virus and Chikungunya virus. The rapid and aggressive global spread of Aedes albopictus contributes to the rapid expansion of Dengue virus. The diapause of Aedes albopictus provides a crucial ecological basis for its adaptation to a wide range of climatic and geographical conditions. This review gives an update on research progress on diapause of Aedes albopictus and the related molecular mechanisms.
    Risk Assessment of Malaria in Libo County, Guizhou Province
    ZHOU Xue-mei, MO Hai-liang, LIANG Qi-min
    2016, 34(3):  19-195-197. 
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    Data concerning malaria endemic situation during 2006-2012 and data concerning malaria transmission risk and malaria elimination capacity during 2010-2012 were collected. The results showed that during 2006-2012, malaria in Libo County was predominated by vivax malaria with the transmission vector of Anopheles sinensis, and malaria incidence declined year by year(3.72/10 000, 3.56/10 000, 5.76/10 000, 4.34/10 000, 2.54/10 000, 1.14/10 000, and 0, respectively). In the residents surveyed during 2010-2012, >2% received blood test, 82.9%(29/35) received standard therapy, 93.3%(651/698)had usage of insect-resistant facilities, and 440 received medical training, with an awareness rate of 92.3%(738/800)in the residents. The malaria transmission risk index of Anopheles mosquito was 2, the area risk value was 10, and the malaria transmission risk index was 20, indicating a moderately-low level of risk.
    An Imported Case of Vivax Malaria with Co-occurrence of Different Stages of Plasmodium vivax in Erythrocyte
    WANG Jia-zhi1, YIN Xue-mei1, LI Xi-shang1, YIN Shou-qin1, FENG Jun2 *
    2016, 34(3):  20-290-292. 
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    The blood sample from a case of vivax malaria in Tengchong City, Yunnan Province, was tested with CareStartTM malaria rapid diagnostic test, Giemsa staining and nested PCR in 2012. The case was determined to be infected with Plasmodium vivax, P. malariae or P. ovale other than P. falciparum by CareStartTM malaria rapid diagnostic test. Microscopic results revealed multinuclear P. vivax ring form and multi-infections with P. vivax in blood slides, with occurrence of two or more nuclei in one ring form accounting for 14.68%(188/1 280), and parasitism of two or more P. vivax rings in one erythrocyte accounting for 22.50%(288/1 280). In addition, co-occurrence of ring form and trophozoite, and ring form and gametophyte was found in erythrocytes. Nested PCR revealed P. vivax-specific amplification products. Combining the results with epidemiological information and clinical symptoms, this case was finally diagnosed as imported vivax malaria, and the erythrocytes of the case harbored different stages of P. vivax parasites.
    A Retrospective Analysis on 47 Children with Paragonimiasis in Ningbo City
    XU Hui-qing1*,ZHANG Xin-gang2
    2016, 34(3):  21-293-294. 
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    A retrospective analysis was performed on 47 children diagnosed with paragonimiasis in Ningbo Women and Children’s Hospital from January 2004 to December 2014. The 47 children comprised 32 boys (68.1%) and 15 girls (48.9%), and 24 cases(51.1%) in urban areas and 23 (48.9%) in rural areas (P>0.05). There was a trend of increase in paragonimiasis occurrence in preschoolers since 2010. Forty-three cases had a history of eating raw or wine-preserved crabs and 4 cases had a history of drinking raw stream water. There were 2 cases of paragonimus encephalopathy and one case accompanied by subcutaneous nodules. Thirty-nine cases showed increases in eosinophil number and proportion in peripheral blood, and 29 cases showed increased serum IgE level. Forty-seven cases had negative results for detection of paragonimus eggs in sputum and stool. The dot immuno-gold filtration-assay and ELISA showed a 100% positive rate for paragonimus serum antibody. All the 47 cases were administered with praziquantel after diagnosis, and no adverse effect was reported during the treatment.
    Pathogen Identification in an Imported Case of Cutaneous Leishmaniasis
    LAI De-hua1, WU Na1, XIE Yi-ting1, HONG Xiao-kun1, CHEN Yun-fu1,
    2016, 34(3):  22-295-296,封三. 
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    In this study, immune and molecular biological methods were used to identify the pathogen in a blood sample from a patient with dermatosis. Venous blood was collected and tested with Leish rK39 dipsticks. The lesion sample was collected and fixed in 75% ethanol, and DNA was extracted. The internal transcribed spacer 1 of rDNA and N-acetylglucosamine-1-phosphate transferase of Leishmania were amplified with PCR using primers LITSR-L5.8S and NAGTL1s-NAGTL4, respectively. The amplified products were sequenced and analyzed by BLAST. Weakly positive results were obtained for the gold-labeled Leish rK39 dipstick serological test. PCR resulted in products of 404 bp and 1 405 bp with primers LITSR-L5.8S and NAGTL1-NAGTL4, respectively. Both were 99.7% homologous to the corresponding sequence of Leishmania major. The accession number of the two sequences were KU975160 and KX150476. The case of dermatosis is diagnosed as imported cutaneous leishmaniasis and the pathogen is L. major.