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Table of Content

    28 February 2006, Volume 24 Issue 1
    述评
    Malaria Situation in the People's Republic of China in 2004
    ZHOUShui-sen;TANGLin-hua;SHENGHui-feng;WANGYi
    2006, 24(1):  1-3. 
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    论著
    National Surveillance of Schistosomiasis in China from 2000 to 2004
    ZHAOGen-ming;WANGLi-ying;ZHAOQi;CHENXian-yi;XIAODong-lou;HENa;WEIJian-guo;JIANGQing-wu
    2006, 24(1):  2-9. 
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    Objective To specify the trends of endemic situation among twenty one national surveillance sites for schistosomiasis from 2000 to 2004. Methods According to the national surveillance protocol, longitudinal surveillance on endemic situation of schistosomiasis was carried out at twenty-one sites since 2000. Results The infection rate of Schistosoma japonicum declined in six of the twenty-one surveillance sites. The density of living snails and of infected snails decreased in two sites but not well controlled in most other sites. The prevalence in cattle fluctuated yearly in most sites and maintained at a relatively high level. During the surveillance period, acute cases were found annually and the number of advanced patients did not increase significantly. No new case and infected snails were found in Jinshan, Shanghai, since 2000, where transmission of schistosomiasis was interrupted two decades ago. Conclusion Routine control strategies such as selective chemotherapy combined with livestock chemotherapy, snail control in risk areas have a positive impact on the control of schistosomiasis. However, these strategies should be lasted for longer time and the surveillance on snails and cattle should be continued.

    Mixed infection of Echinococcus granulosus and Echinococcus multilocularis in Dog
    WENHao;ZHANGYa-lou;Jean-MathieuBART;GiraudouxP;VuittonDA;MAXu-dong;ZOULin-yue;MIAOYu-qing;CraigPS
    2006, 24(1):  3-13. 
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    Objective To identify mixed infection of Echinococcus granulosus and E.multilocularis in a dog from Xinjiang. Methods Thirty dogs from the pasture area were dissected and over 10 000 Echinococcus adult worms were found from one dog. Morphological observation revealed possible mixed infection of the two Echinococcus species. Further identification was made by amplification of the target gene DNA fragment (mitochondrial 12S rRNA gene). Results The adult worms of E.granulosus showed a relatively longer and larger gravid proglottid, its genital pore situated near or below the middle-side of the segment. The uterus was in a sacculate shape with irregular branches and approximately over 200-800 eggs in it. Morphology of the adult worms of E.multilocularis was similar to E.granulosus, slightly smaller, consisting of 4 to 5 proglottids. The uterus was not sacculate and with no branch. Its lateral genital pore often situated in the anterior part of the segment. Sequence analysis of mitochondrial 12S rRNA gene showed that amplification with the Eg1f/r primers shared complete identity with E.granulosus G1 genotype (GenBank accession no. AY462129), while that with the EmH15/17 primers shared complete identity with E.multilocularis (GenBank accession no. AB031351). The presence of both E.granulosus and E.multilocularis was confirmed by microscopy and gene identification. Conclusion Mixed infection of the two species of Echinococcus has been confirmed in the dog by morphological observation and PCR technique.
    Study on Protective Immunity against Infection of Plasmodium yoelii 17XL in DBA/2 Mice
    ZHENGWei;LIUJun;MENGDong-ya;HUXiao-fang;CAOYa-ming
    2006, 24(1):  4-18. 
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    Objective To investigate the development and dynamic changes of host immune response in DBA/2 mice infected with Plasmodium yoelii 17XL. Methods Female DBA/2 mice were infected by intraperitoneal (i.p.) injection of 106 P.yoelii 17XL parasitized erythrocytes (PRBC). Levels of IL-12, IFN-γ, IL-4,IL-10 and P^yoelii 17XL-specific antibody in sera were measured by ELISA. Concentrations of NO in cell supernatants were measured by the Griess reaction. Parasitemia, percentage of mononuclear-macrophages of individual mice were monitored daily, and phagocytosis of mononuclear macrophages was also observed. Results Primary parasitemia in vein blood was developed on day 3 postinfection, which peaked with a level of 46.9% on day 9. Most mice cleared the infection and survived by day 20 postinfection. From day 6 to day 16, the phagocytosis of PRBC by rodent macrophages was observed on the blood smear. Infected mice had a continuously increased level of IL-12 in serum from day 1 post-infection. Accordingly, high level of IFN-γ was also detected in sera from day 1 postinfection, which peaked on day 6. Infected mice produced higher level of IL-4 and IL-10 in serum on day 6 postinfection, which peaked on day 9 and day 15 postinfection respectively. In addition, splenocytes from infected mice produced significantly higher level of NO on day 6 and 20 postinfection. Level of P.yoelii 17XL-specific IgG was determined in the sera of infected mice with a steadily increased trend after infection, which peaked on day 70 postinfection. Conclusions Effective polarizing of Th1 cells is significant in inhibition of parasitemia and eventual clearance of the Plasmodium parasites. Activated mononuclear-macrophages play a key role in inhibiting parasitemia in the early phase of infection with P.yoelii 17XL.
    Comparison of the role of dendritic cells and macrophages in inducing protective immunity against Schistosoma japonicum
    SHENDing-wen;LIYong-long;LIUWen-qi;LONGXiao-chun;LIUJuan;AndreasRuppel
    2006, 24(1):  5-22. 
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    Objective To compare a potential role of dendritic cells (DCs) and macrophages in inducing protective immunity against infection with Schistosoma japonicum. Methods DCs and macrophages were pulsed in vitro with soluble egg antigen (SEA) of S. japonicum. BALB/c mice were injected three times with DCs or macrophages, either antigen-pulsed or not,and challenged with 40 ± 2 cercariae of S. japonicum per mouse. Worms were collected 42 days later by portal perfusion of the mice and egg number of liver was calculated. To evaluate whether protective immunity had been induced by preparations of DCs or macrophages, the worm burden and fertility ( eggs per female per mouse liver) were compared between the groups of mice. The antibody level against SEA was detected by ELISA. Results With respect to mice injected with untreated cells, numbers of worms and eggs per female worms were significantly reduced in the groups of mice having received pulsed DCs (26. 3% and 37.9%, respectively), or pulsed macrophages (22. 0% and 30.7%). Untreated DCs and macrophages induced no significant effects. The antibody level against SEA rose in sera of all groups of mice up to 42 days after the challenge, but most pronounced in those immunized with pulsed DCs, although this was not significantly different from other groups. Conclusion The results suggest that the protective immunity against S. japonicum might be induced by DCs to a higher extent than by macrophages after in vitro pulsing with egg antigen.
    Effect of a Novel Drug———Enteric Coated Tribendimidine in the Treatment of Intestinal Nematode Infections
    WUZhong-xing;FANGYue-yi;LIUYi-sheng
    2006, 24(1):  6-26. 
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    Objective To study the therapeutic effect and possible adverse effects of tribendimidine enteric coated tablets in the treatment of infections due to hookworms, Ascaris lumbricoides, Trichuris trichiura, Enterobius vermicularis. Methods According to the standard clinical trial design and protocol, pearsons infected with hookworms, Ascaris lumbricoides, Trichuris trichiura, or Enterobius vermicularis respectively, were treated with tribendimidine enteric coated tablets in four counties of Guangdong and Jiangsu Provinces, albendazole was used as control. Results For hookworm infection, the curative rate (eggs negative in the faeces) were 89.5%(85/95) and 70.6%(60/85) with tribendimidine (400 mg) and albendazole(400 mg) respectively; for Ascaris infection, 97.4%(114/117) and 98.9%(91/92) with tribendimidine(300 mg) and albendazole(400 mg) respectively; for Trichuris infection,33.3%(25/75) and 56.1%(23/41) with tribendimidine(400 mg/day for 3 days) and albendazole(400 mg/day for 3 days) respectively; for Enterobius infection in children, 74.1%(60/81) and 93.0%(40/43) with tribendimidine(200 mg) and albendazole(200 mg) respectively. No considerable side effect was found. Conclusion Tribendimidine is highly active in the treatment of hookworm, Ascaris lumbricoides infections, free of major adverse effect and easy to administer. It is more effective than albendazole for the infection of Necator americanus.
    Analysis of Genetic Diversity of AFLP Marker among Populations of Oncomelania hupensis
    ZHOUYi-biao;ZHAOGen-ming;WEIJian-guo;JIANGQing-wu*
    2006, 24(1):  7-30. 
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    Objective To explore the degree of genetic diversity among populations of Oncomelania hupensis. Methods AFLP method was used to amplify the genomic DNA of thirteen snail populations from nine provinces (i.e. Yunnan, Sichuan, Guangxi, Fujian, Hunan, Hubei, Jiangxi, Anhui and Jiangsu) and the genetic diversities among snail populations were analyzed. Results The number of AFLP fragments amplified ranged from 403 to 472 for thirteen Oncomelania populations. Among the thirteen snail populations, the genetic diversity within the population from Xingzi County, Jiangxi Province, was most significant, and the percentage of polymorphic loci, Nei’s genetic diversity and Shannon’s information index were 93.22%, 0.345 and 0.510 respectively, while these indices for the snail population from Yizhou City, Guangxi Region, were the lowest, 55.80%, 0.191 and 0.287 respectively. The similarity between the in-group-individuals from Yizhou City, Guangxi Region, was most significant, and the average coefficient of similarity was 0.904, and that from Dantu County, Jiangsu Province, was the lowest (0.748). The genetic diversities among snail populations were significantly different for the thirteen snail populations ( P<0.01). Conclusion There is a certain genetic variation among Oncomelania snail populations from the mainland of China, and this variation is significantly different among snail populations from different areas.
    Preparation, Characterization and Preliminary Application of Recombinant Protein AP33 of Trichomonas vaginalis
    LIANGShao-hui;HUANGHui-cong;PANChang-wang*;XINGWen-luan;QINQian;ZHUGEQing-yun;TANFeng
    2006, 24(1):  8-34. 
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    Objective To clone ap33 gene of Trichomonas vaginalis(T.v), construct prokaryotic expression system of the gene and identify its antigenicity and immunogenicity. Methods The total RNA was extracted from a clinical isolate Tv317 and the cDNA was synthesized by reverse transcription. The ap33 gene from cDNA of Tv317 was amplified by PCR. The nucleotide sequence of the target DNA amplification fragment was sequenced after T-A cloning. The expression vector pET32a(+) with inserted ap33 gene was constructed. Recombinant fusion protein AP33 was expressed in E.coli strain BL21DE3 induced by IPTG at different dosages. Western blotting was applied to determine immunoreactivity of the recombinant fusion protein AP33 with antibody against whole cell of T.v. Double agar diffusion was applied to determine immunogenicity of the recombinant fusion protein AP33 with rabbit antiserum immunized with the recombinant fusion protein AP33, and ELISA with antigen of T.v, whole cell was applied to determine immunogenicity of the recombinant protein AP33. Positive human sera were tested by ELISA with the recombinant fusion protein AP33. Results High homology of nucleotide and amino acid sequences was revealed between the cloned ap33 and the corresponding gene. The recombinant protein showed a high expression level. The recombinant protein was recognized by anti-T.v polyclone antibody from rabbit, and showed a high titer. The clinical T.v isolates showed high ap33 expression level and stimulated the production of specific antibody. Antibody against AP33 was detected in 78% of the 50 patients infected with T.v by ELISA. Conclusion A prokaryotic expression system of T.v ap33 gene has been established. The expressed fusion protein AP33 shows satisfactory antigenicity and immunogenicity.
    Cloning and Identification of the cDNA and Genomic DNA Sequences of the Defensin Gene of Anopheles sinensis
    ZHANGYa-jing;CHENXiao-guang;ZHENGXue-li;WANGChun-mei
    2006, 24(1):  9-40. 
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    Objective To clone and identify the cDNA sequence and genomic DNA sequence of Anopheles sinensis defensin gene. Methods Referring to the published defenain gene sequences of Aedes aegypti and Anopheles gambiae, pairs of primers were designed to amplify the cDNA sequence and genomic DNA sequence of Anopheles sinensis defensin gene with template of Anopheles sinensis total RNA by RT-PCR and genomic DVA by nested PCR, respectively. These amplified fractions were cloned and sequenced, and were further identified and analyzed by relevant bioinformatics softwares. Results Complete genomic DNA sequence was cloned, including 5' and 3' UTR fraction and two exons separated by a 85 bp intron. Besides, the whole cDNA sequence of Anopheles sinensis defensin gene with 324 bp was also cloned, and its ORF encoded 107 amino acids. The mature peptide had 40 amino acids residues. Conclusion The whole cDNA sequence and complete genomic DNA
    sequence of the defensin gene of Anopheles sinensis have been cloned and identified for the first time.
    The Microfluorimetric Assay (MFA) in in vitro Testing the Sensitivity of Plasmodium falciparum to Antimalarial Drugs
    HUANGFang;TANGLin-hua;WANGQin-mei;HIYi-chang
    2006, 24(1):  10-44. 
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    Objective To determine the feasibility of the microfluorimetric assay (MFA) in screening antimalarial drugs. Methods The dose-response curves and effective concentration that resulted in a 50% inhibitory of parasitemia (IC50 ) of chloroquine, artemisinin, artemether and pyronaridine phosphate against Plasmodium falciparum strain FCC1/HN cultured in vitro were tested by microfluorimetric assay (MFA) and compared with those determined by microscopy-based assay. Results The IC50 of chloroquine, artemisinin, artemether and pyronaridine phosphate were 18.79, 6.32, 3.67 and 2.00 nmol/L by MFA and the IC50 of which were 19.65, 5.82, 4.38 and 2.83 nmol/L by microscopy-based technique respectively. The results from both techniques were similar or identical (P>0.05). Conclusion The microfluorimetric assay (MFA) is sensitive, rapid, easily interpreted and would be useful for testing the sensitivity of Plasmodium falciparum to antimalarials and for screening drugs.
    实验报道
    Construction of the Female Subtractive cDNA Library and Screening of the Specific Expressing Genes
    WANGYan-hai;PENGHong-juan*;CHENXiao-guang;SHENShu-man
    2006, 24(1):  11-50. 
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     Objective To screen the Schistosoma japonicum female specific expressing genes. Methods S.japonicum adult worms were collected from the rabbits’ vein after six-week infection by affusing method. The adult worms were stabilized by RNA-later liquid, the male and female worms were carefully separated with nipper. The high quality total RNA was extracted and mRNA was obtained after purification. Double stranded cDNAs were synthesized after reverse transcription. Female subtractive (female as tester, male as driver) and male subtractive (male as tester, female as driver) cDNA libraries were constructed. The differentially expressed genes were further screened by dot-blot hybridization. The clones were selected and sequenced, which showed apparently higher signals when hybridizing with the female subtracting male probes, than those signals when hybridizing with the male subtracting female probes. The homology of these sequences was searched with BLAST program. The semi-quantitative PCR was applied to test the differential gene expression in female and male adult worms. Result Female subtracting male and male subtracting female cDNA libraries were constructed with SSH technique. After dot-blot hybridization, 50 clones were tested to be the potential female differentially expressed genes and were sequenced. 42 expressing sequence tags (ESTs) were received. After bioinformatics analysis, 17 fragments (about 40.5%) showed high identity with the S.japonicum egg-shell protein genes, 17 sequences(about 40^5%) were highly homologous to unknown S.japoniucm genes and partly homologous to female specific 800 protein. 8 fragments (about 19^0%) showed high identity with other S.japonicum unknown genes. The fragments in clones of 577, 579, 668, 695, 720, and 708 were tested by RT-PCR to be the differentially expressed genes in female adult worms using S.japonicum actin gene as the internal standard. These fragments were highly homologous to S.japonicum egg shell protein gene AY222885, AY222895, AB017097, AF519182, M32281, and S.japonicum unknown gene AY813556 respectively. Conclusion SSH is essential to screen the differentially expressed genes of S.japonicum female worms. A number of female specific genes have been found by this method.
    Protective Efficacy of Co-immunization with Sj26 DNA and Recombinant Protein Vaccine Against Schistosoma japonicum in Mice
    YUGuang-qing;LIUWen-qi;LEIJia-hui;MOHong-mei;CHENYu-li;LIYong-long+*
    2006, 24(1):  12-55. 
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    Objective To study the protective efficacy of co-immunization with Schistosoma japonicum glutathione S-transferase (Sj26) DNA and recombinant Sj26 protein (rSj26 GST) vaccine against Schistosoma japonicum in BALB/c mice. Methods The Sj26 gene was cloned into eukaryotic expression vector pEGFP-N3 with enhanced green fluorescence protein. The recombinant plasmid pEGFP-Sj26 was transfected into baby hamster kidney (BHK) cells, fluorescent microscope and Western blotting were employed to identify the expressed products. Each mouse in co-immunization group was primed with plasmid pEGFP-Sj26, boosted 2 weeks later and immunized with rSj26 GST 4 weeks later. While each mouse in pEGFP-Sj26 group and rSj26 GST group was primed and boosted with pEGFP-Sj26 or rSj26 GST independently. Two weeks after last immunization, each mouse was challenged with 40±1 cercariae of S.japonicum Chinese strain. At the 45th day post-infection, mice were sacrificed and the worms were perfused from portal vein and the number of worms and eggs in liver tissue were counted. Results In BHK cells transfected with the recombinant plasmid pEGFP-Sj26,the expression of Sj26-EGFP fusion protein was confirmed by fluorescent microcopy and Western blotting. The worm reduction rate in co-immunized group was 50.8%, significantly higher than that in pEGFP-Sj26 group (28.0%,P<0.01) and rSj26 GST group (25.5%, P<0.01). Liver egg reduction rate in co-immunized group, pEGFP-Sj26 group and rSj26 GST group were 32.7%, 20.6% and 33^0% respectively. The number of eggs per female in liver of co-immunized mice and rSj26 GST group were significantly higher than that in control group (P<0.01). Conclusion Compared to the immunization with pEGFP-Sj26 or rSj26 GST alone,the co-immunization with pEGFP-Sj26 and rSj26 GST can enhance protective efficacy in BALB/c mice.
    In vitro Effect of Combined Traditional Chinese Medicine (Changqing Capsule) on The Tachyzoites of Toxoplasma gondii
    ZHANGWei;FANGFu-rong*;LIUYuan-jiao;YANGLian-di;LUORuo-yu;GONGFei;LUHui;XUXiao-xia
    2006, 24(1):  13-58. 
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     Objective To detect the in vitro effect of the traditional Chinese medicine on the tachyzoites of Toxoplasma gondii. Methods Supernatant (1.5 ml) of different doses of the traditional Chinese medicine (Changqing capsule) was collected by normal saline immersion and 2.5×104 Toxoplasma gondii tachyzoites were added in each paste well for 8 hours. Spiramycin, pyrimethamine and azithromycin in different doses were used as controls. Normal saline was used as negative control. Mice were inoculated with drug-treated tachyzoites intraperitoneally or intragastrically. The normal mice were subcultured after 8 days for 3 generations. Results The incident number of the infected mice was significantly different among groups with different drugs and doses: 2/60, 16/60, 10/60 and 10/60 in the groups of Changqing capsule, spiramycin, pyrimethamine and azithromycin respectively (P<0.05). No mice were found incident in groups of high and medium dose Changqing capsule while 2 out of 20 found sick in the low dose group (P<0.05). The subculture observation showed that 2 and 1 mice in the first generation of the low dose Changqing capsule group inoculated intraperitoneally and intragastrically were found infected respectively. 2 mice of the second generation in low dose spiramycin group and 1 mouse of the third generation in low dose pyrimethamine group were also found infected. Conclusion The in vitro killing effect of the Changqing capsule on the tachyzoites of Toxoplasma gondii is better than the current clinical drugs and shows a positive correlation with the dosages.
    Immunological Regulation and Treatment of Brucea javanica and Fructus Psoraleae on Rats with Pneumocystis carinii Pneumonia
    QINYuan-hua;CUIYu*;RENYi-xin;ZHANGXiao-lin;WANGYan;ZHENGXiao-yu;CHENXu-wei;SUNMin
    2006, 24(1):  14-62. 
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    Objective To study the imumunological regulation and treatment of Brucea javanica and fructus psoraleae, traditional Chinese medicine, on rats with Pneumocystis carinii pneumonia (PCP). Methods Rats were injected subcutaneously by dexamethasone. When the rats got Pc infected, they were divided into two groups: rats in one group were treated with the mixture of Brucea javanica and fructus psoraleae and another group was used as infected control. Control with normal rats was also established. Observations were made on the number of cysts in lungs and the changes of CD4+ T cells, CD8+ T cells and TNF-α in the serum to demonstrate the imumunological regulation and killing effect of the medicine on cysts in the infected rats. Results The body weight of the rats treated with Brucea javanica and fructus psoraleae increased considerably than that of immunosuppressed rats and the normal control. The damaged lung got improved and repaired, and a significant cyst reduction was shown in the treated group. The CD4+ T cells, CD8+ T cells and level of TNF-α in serum also increased in the treated group significantly. Conclusion The mixture of Brucea javanica and fructus psoraleae plays an imumunological regulation on rats with Pneumocystis carinii pneumonia and shows certain killing effect on the cysts.
    综述
    Defense Mechanisms of Taeniidae against Host Immune Response
    ZHENGYa-dong;LUOXue-nong;HUZhi-min;CAIXue-peng*
    2006, 24(1):  15-66. 
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    The defense mechanisms of Taeniidae against host immune reaction were reviewed. The parasites may defend themselves from the host’s immune attack by: ① producing specific biochemicals as barriers against the damage caused by immune reactions, ② changing surface antigens and secret?鄄ing some active substances that interfere and deconstruct host’s immune system and other hazards, ③ self-disguising through synthesizing homologies to host’s substances in structure or function in order to avoid the immune surveillance of the host.
    研究简报
    Coartem and Fansimef in the Treatment of Falciparum Malaria
    SHENWen-juan;MoulayeThiero
    2006, 24(1):  16-26. 
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    From 2001 to 2003, anti-malarial combination coartem and fansimef, recommended by WHO, were used to treat falciparum malaria in Mali, 28 cases in each group. The mean fever clearance time, mean asexual parasite clearance time and the cure rate in 28 days were 35.3±6.4, 34.7±6.9 hours and 100% respectively in coartem group, and 32.6±5.8, 36.8±5.3 hours and 96.4% respectively in the fansimef group, with no significant difference between the two groups (P>0.05).
    Human Parasitology Teaching in the 21st Century
    TIANXi-feng;HANXiu-ling;HEBao-ling;ZHAOLi-na;HUOXiao-qing
    2006, 24(1):  17-58. 
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    Multimedia techniques were applied in parasitological teaching and experimental practices. In order to strengthen the practical ability of the undergraduate students, reform was conducted including a prioritization of the teaching content, use of series micro-slides and video show, etc.
    Study on the Methods for Detection of Toxoplasma Antigen
    LIHui;XUBian-li;DENGYan;ZHAOXu-dong;LINXi-meng;YANXu-xia
    2006, 24(1):  18-69. 
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    A sandwich ELISA was established with monoclonal antibody as detecting antibody and rabbit anti- Toxoplasma polyclonal antibody as capturing antibody. ABC(avidin-biotin-peroxidase complex)-ELISA and immuno-PCR were also used to detect different concentrations of Toxoplasma antigen. The lowest concentration of antigen to be detected by sandwich ELISA, ABC-ELISA and immuno-PCR was 0.6 μg/ml, 0.075 μg/ml and 0.1 ng/ml respectively. The immuno-PCR shows a much higher sensitivity than the other two methods.
    Human Natural Infection of Plasmodium knowlesi
    ZHUHuai-min;LIJun;ZHENGHui
    2006, 24(1):  19-71. 
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    A blood film slide taken from a patient previously diagnosed as vivax malaria in Mojiang County, Yunnan Province, showing atypical forms. The ring forms had multinuclei, and the late trophozoites trended to form band. The schizonts and gametocytes were somewhat alike to Plasmodium vivax. PCR amplification confirmed that the patient was infected by P.knowlesi.

    Construction of Eukaryotic Expression Recombinant Plasmid of Trichomonas vaginalis Ferredoxin Gene
    XIEHui;WANGYa-jing*;TIEChao-nan;BIShi-liang;LIUPei-na
    2006, 24(1):  20-73. 
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    Total DNA was extracted from T. vaginalis with Chelex-100 method and used as templates for PCR. The ferredoxin gene was directionally cloned into plasmid pMD-18T vector and subcloned into eukaryotic expression vector pcDNA3.1(+). The transformants were screened and identified by PCR and restriction analysis. The size of amplified ferredoxin gene was 306bp and the DNA sequence of cloned gene was same with that published.
    Survey on Natural Nidus of Metorchis orientalis in Huaihe River Basin
    ZHUYu-xia;SUNEn-tao;LIChao-pin*;QINZhi-hui
    2006, 24(1):  21-75. 
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    Parafossarulus striatulus, Pseudorasbora parva and brood ducks are involved in the lifecycle of Metorchis orientalis. Natural nidi of M.orientalis are confirmed in Huaihe River Basin.
    Comparison on the In vitro Hatching Methods for Taenia solium Eggs
    ZHAOYan-bing
    2006, 24(1):  22-76. 
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    Sodium hypochlorite digestion(NaClo) method and enzyme method were compared in the hatching of Taenia solium eggs. Both methods are effective, but the sodium hypochlorite digestion shows higher hatching rate (96.4%) and viability (89.0%) in a shorter reaction time (< 5 min) without needing expensive reagents.
    Study on the Expression of Immune Function in Cases Infected by Cyclospora cayetanensis
    XULi-fa;LIChao-pin*
    2006, 24(1):  23-78. 
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    In Cyclospora cayetanensis oocyst-positiv patients, T cell subsets in peripheral mononuclear cell and membrane interleukin-2 receptor (mIL-2R) were detected with the method of biotin-streptavidin(BSA) and soluble interleukin-2 receptor(sIL-2R) as well as special IgG, IgM in serum was detected by ELISA. Results showed that there is a significant difference between the infected and uninfected individuals.
    Pigment Deposit in Liver of BALB/c Mice Infected by Schistosoma japonicum and its Relation to the Effect of Praziquantel Treatment
    TAOJun;CAIWei-min;ZhangBin-bin;HuangYan;XiangQuan;LIURong-hua
    2006, 24(1):  24-80. 
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    Pigment is a kind of metabolite excreted by schistosome after erythrocyte ingestion. It deposited first in liver sinusoid, then outside and inside of granuloma, and around eggs. The level of pigment was in parallel with the degree of liver fibrosis(P<0.01). After chemotherapy with praziquantel, the level of pigment decreased considerably(P<0.01) and the size of granuloma shrinked obviously too(P<0.01). Therefore, the degree of liver fibrosis in mice with schistosome infection and the effect of praziquantel can be recognized by the level and distribution of pigment.
    Morphological Observation and Measurement for Synthetic Micrograph of Phthirus pubis
    ZHAOGuang-ming;ZHAOJi-chao;ZHAOLian-hua;HANGui-fu;WANGXiang-ze;CHENQi-ke
    2006, 24(1):  25-Ⅱ. 
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    Larva and adult of Phthirus pubis were dehydrated and transparentized. Photos were taken separately and synthesized to integrated photograph with computer for morphological observation and measurement.