Loading...

Table of Content

    30 October 2001, Volume 19 Issue 5
    论著
    Investigation on Genotype Constitution of Different Plasmodium vivax Isolates and its Geographical Distribution in China
    HUANGTianyi;HUANGYaming;WANGXiaoli;LIXueming;ZHANGZaixing;WANGShanqing;WANGGuangzhe;PANBo;HUANGZhibiao;FUWeizhong;LIUHui;GAOQi;ZHANGShaoqing;SHANGLeyuan;XUGuojun;SHENGYuzu0;LIIITao;LlPeng;ZENGFengxiu;CHEYing
    2001, 19(5):  2-264. 
    Asbtract ( )   PDF (336KB) ( )  
    Related Articles | Metrics

     Objective To investigate the population constitution and geographical distribution of Plasmodium vivax in China using molecular technique. Methods Blood spot filter paper samples with related epidemiological data were collected from vivax malaria patients living in malarious area of 10 provinces (autonomous region) in China. Semi nested or nested allelic specific PCR genotyping method was used to identify CSP genotypes, families and types of Plasmodium vivax of each isolate from these patients. Results Of 384 field isolates of Plasmodium vivax , 258 temperate zone family strains were identified,including 14 allelic variant genotypes spreading among 10 sampling provinces; allelic variants sized less than 731 bp were only seen in 5 provinces in southern China; 79 tropical zone family strains including 5 genotypes were also distributed in 5 provinces of southern China south to 25° N.lat; and 14 PV Type 2 strains including 2 genotypes were found in some areas of Hainan and Yunnan Provinces. In addition, 33 isolates from genotype-mixed infections were revealed. Conclusion At present, area north to 25° N.lat. of the country is the sole area prevalent for Plasmodium vivax family strains of temperate zone;there is overlapping distribution of P.v . of temperate zone family and tropical zone family of this parasite in the southern China south to 25° N.lat; where the most complex isolate constitution is in Yunnan and Hainan Provinces, and PV Type 2 strains have been found in some areas of the two provinces.Besides, there were 2 groups of genotype with distinct geographic distribution feature within the temperate zone family.

    A Study on the Recombinant 26 kDa Glutathione-S-Transferase as a Vaccine Candidate:Dynamics of Antibodies in Immunized Buffaloes and Protection against Schistosoma japonicum Infections
    HEYongkang;SONGGuancheng;LIUShuxian;LUOXinsong;ZHANGXinyue;XUYuxin;YUXinling;YANGRuiqing
    2001, 19(5):  3-267. 
    Asbtract ( )   PDF (202KB) ( )  
    Related Articles | Metrics
     ObjectiveTo observe the dynamics of antibodies and protection against Schistosoma japonicum infections in buffaloes after immunized with recombinant 26 kDa glutathione S transferase (reSjc26GST). Methods Buffaloes in 2 villages endemic for schistosomiasis japonica were selected as test and control groups, respectively.In test group initially 96 buffaloes were vaccinated with reSjc26GST, and 90 buffaloes in the control group did not experience vaccination. The indicators included levels of antibodies to reSjc26GST in buffaloes before and after infection with S japonicum and changes in infection rate. Results Specific antibodies, which showed a trend of trapezoid increase, were induced in buffaloes after immunized with reSjc26GST. Twenty months after immunization, the infection rate of the test group was decreased by 62 2% when compared with that before vaccination,and by 67 7% when compared with that of the control in the corresponding period.Conclusion Specific antibodies and a certain extent of protection were induced in buffaloes after immunized with reSjc26GST, which played an significant role in ameliorating morbidity.
    Immunity against Schistosoma japonicum Induced by Phage Display Peptides Mimicking Antigenic Epitopes of Trichinella spiralis
    ZHOUDong-ming;YIXin-yuan;ZENGXian-fang;WANGMin;LarryMcReynolds
    2001, 19(5):  4-271. 
    Asbtract ( )   PDF (277KB) ( )  
    Related Articles | Metrics
     Objective To obtain the short peptides mimicking antigenic epitopes of Trichinella spiralis ( T.s. ), and explore their cross protective immunity against Schistosoma japonicum ( S.j. ) in mice. Methods IgG antibodies were purified from sera of mice infected with T.s. . The purified IgG was used to immunoscreen a phage random peptide library of 7 amino-acid residues displayed as a fusion to protein of filamentous phage. Positive clones were obtained by affinity selection, the reactivity of each clone binding to specific IgG was detected by ELISA. Kunming mice were immunized subcutaneously three times with mixed phage clones. The mice were sacrificed 45 days after challenge. The worms and the liver eggs were counted. Results After three rounds of panning, the relevant phages had been enriched approximately 150 times in production as compared to those from the first round. Of 24 phage clones randomly selected from the third round biopanning, 21 clones were shown to actually bind to the specific IgG. As compared with the control group, the worm and the liver egg reduction rates in vaccination group were 42.8% and 66.3% ( P <0.001), respectively. Conclusion The above results demonstrate that antigenic epitopes of T.s. can be prepared by immunoscreening phage random peptide library and a significant protective immunity against S.j. can be induced by these epitopes in mice.
    Clonning and Identification of the Gene Encoding Specific IgE Antibody-Related Antigen of Schistosoma japonicum
    WANGYong;SUChuan;ZHANGZhao-song;HUXue-mei;SHENLei;LIUFeng;WANGRong-zhi;CHENShu-zhen;LIChun-lin;WUGuan-ling
    2001, 19(5):  5-275. 
    Asbtract ( )   PDF (264KB) ( )  
    Related Articles | Metrics
     Objective To obtain the gene encoding specific IgE-related antigen of Schistosoma japonicum from the cDNA library of adult Schistosoma japonicum . Methods The pooled sera from 15 individuals with high levels of specific IgE antibody against SWAP were absorbed with Protein-G and used for screening of IgE-related antigen from the adult worm cDNA library of Schistosoma japonicum . The inserted cDNA was amplified by PCR and sequenced. According to the first reading frame of the sequence, a pair of new probes, in which Eco R Ⅰ and Not Ⅰsites were incorporated respectively,were designed and used to amplify the target gene. Then,the gene was cloned into vector pGEM-T and subcloned into expression vector pGEX-6p-1. The fusion protein was expressed, analysed by SDS-PAGE and identified by Western blotting with the specific IgE antibody, respectively. Results The inserted cDNA fragment from the positive clone was about 1 200 bp,with the ORF of 507 bp which encoded 169 amino acids. The deduced molecular weight of the recombinant protein was 19.3 kDa. The homology between the target gene(Sj43B) and other known DNA sequences was less than 40%. The fusion protein expressed by the recombinant vector pGEX-6p-1/Sj43B could be recognized by schistosome specific IgE antibody. Conclusion Sj43B may encode the specific IgE-related antigen of Schistosoma japonicum . The successful construction of recombinant plasmid pGEX-6p-1/Sj43B lay the groundwork for further studies on immunological characteristics and protection immunity of the recombinant protein.
    Studies on Antagonism between Exorchis ovariolobularis and Schistosoma japonicum in Oncomelania hupensis
    YEXiangqun
    2001, 19(5):  6-281. 
    Asbtract ( )   PDF (433KB) ( )  
    Related Articles | Metrics
     Objective To examine the antagonistic interactions between Schistosoma japonicum and Exorchis ovariolobularis in the snail host, Oncomelania hupensis . Methods The infection rate and average number of cercariae of S japonicum were examined in O hupensis which had been superinfected with S japonicum and E ovariolobularis .The experimental snails were histologically observed by paraffin section. Results When snails were fed with eggs of E ovariolobularis 37 days later than S japonicum infection, the infection rate of S japonicum (52 9%) was significantly lower than that of the single S japonicum infected control (75 9%). When E ovariolobularis infected snails were exposed to S japonicum miracidia at different intervals, the infection rates of S japonicum were 64%, 66 7%, 65 2%, 56 4% and 57 1%, respectively. On the other hand, the infection rate of S japonicum in the single infected control was 90 5%. There existed significant differences. Furthermore, the average number of S japonicum cercariae shed from superinfected snails were significantly less than that of single S japonicum infected control. The histological observation showed that the larvae of S japonicum in superinfected snails were sluggish in development, irregular, shrunken, deformed, relatively small in number as compared with the control. The sporocysts contained few germ balls or immature cercariae and most of the digestive glands of superinfected snails were atrophied. Conclusion There is antagonism between E ovariolobularis and S japonicum in O hupensis , and E ovariolobularis is dominant in this situation.
    The Construction of Recombinant Plasmids of Toxoplasma gondii P30 and the Immunoprotective Activity of the P30 Constructs
    GONGYa*;CHENXiaoguang;FENGMingzhao
    2001, 19(5):  7-286. 
    Asbtract ( )   PDF (349KB) ( )  
    Related Articles | Metrics
     Objective To identify the potential DNA vaccine candidate which can induce the protective immune response to Toxoplasma gondii by inoculating mice with plasmid DNAs encoding three different forms of P30 antigen (membranous secretory,and intracellular). Methods Three forms of recombinant plasmid: pcDNA3 P30Mb(contain the whole P30 gene sequence,including the gene encoding signal peptide and hydrophobic tail),pcDNA3 P30Se(contain the whole P30 gene sequence, without the gene encoding hydrophobic tail) and pcDNA3 P30In(contain the whole P30 gene sequence,without the gene encoding signal peptide) were constructed by PCR and subcloning technique. The mice were immunized with different forms of recombinant plasmids and IgG antibodies in the mice were detected by ELISA and Western blotting. Results Three forms of expression recombinant plasmid of Toxoplasma gondii P30 gene were successfully constructed. The P30 inserts were identified by restrictive enzyme digestion and sequencing. ELISA and Western blotting analysis demonstrated that specific IgG antibody could be induced in three immunized groups, but there was some difference in appearence time and intensity of IgG.Conclusion Genetically immunization of mice with the recombinant plasmids could elicit specific IgG antibodies. In respect to IgG response, the immune efficiency of the three forms of recombinant plasmids was different at the beginning (2 wk),but 4 wk later approximately same.
    Studies on Ultrastructure and Histochemistry of Trichomonas vaginalis Adhering to Vaginal Mucosa of Rats
    CHENWenlie;CHENJinfu;ZHONGXiurong;TANGChangrong;CHENXi;LINXi
    2001, 19(5):  8-289. 
    Asbtract ( )   PDF (233KB) ( )  
    Related Articles | Metrics
     Objective To study interaction between Trichomonas vaginalis and epithelium of genital tract of host as well as the pathogenesis of T vaginalis . Methods Immunohistochemical technique was used to observe the adhering process of T vaginalis to vaginal mucosa in rats by transmission and scanning microscopy. Results T vaginalis were shown to be PAS positive and clusters of T vaginalis were found to adhere to columnar epithelium rich in mucopolysaccharide on the surface of vaginal mucosa as viewed in sections of the middle and upper parts of the orgen. T vaginalis was positive for cathepsin. And the membrane of epithelial cells was often damaged by the released hydrolase.The parasite was also positive for actin;the microfilament bundles were arranged in reticular form in ameboid T vaginalis . The latter would penetrate between epithelial cells,and its filiform pseudopodia would invade the interspace of microvilli of the epithelium,to encircle and gradually phagocytize microvilli. Digitiform pseudopodia would insert between epithelial cells and encircle part of them.A few T vaginalis were found to adhere to the keratinized epithelium between mucosal folds as shown in the sections of the lower part of vagina. Conclusion T vaginalis is inclined to parasitise vaginal fornix because the superficial epithelial cells there are rich in mucinogen granules and abundant microvilli exist. After adhering, T vaginalis releases hydrolase to digest and phagocytize epithelium,which may directly damage the epithelium of the genital canal. Moreover, T vaginalis would take in mucopolysaccharide to affect the normal clearance process of vagina,resulting in inflammation of parasitized tissue.The cytoskeleton,cell coat,polymorphism of pseudopodia and lysosome of T vaginalis play an important role in the courses of movement,adhesion, encirclement,phagocytosis and digestion.
    Analysis of Leishmania Species and Strains from China by RAPD Technique
    LUdian-mei;HUXiao-su*;QIAOZhong-dong
    2001, 19(5):  9-293. 
    Asbtract ( )   PDF (261KB) ( )  
    Related Articles | Metrics
     Objective To analyze genetic relationship of Leishmania species and strains from China by RAPD technique. Methods DNAs from Leishmania strains, including L donovani(L d.) isolates from patients, dogs and sandflies of three different foci in China and international reference strains, were amplified by seven random primers. The DNA polymorphic bands detected were analyzed by clustering analysis with SPSS software. Results ① L d . isolates from hill and plain foci in China were divided into two groups. The genetic distance of L d .isolates is distant between them. ② L d .XJ771, L d .XJ901, L d .XJ801 from desert, vicinity of desert, and plain regions in Xinjiang were in the same group.It indicated that the genetic distance among L d .isolates from the three regions is close. ③ L d .isolated from VL patients and dogs in hill foci could not be discriminated distintly, showing high homology between them. ④ L d .DD8 from India,the reference strain of plain type,was clustered with L d .isolates from plain foci in China.It provided scientific basis for the viewpoint "Kala Azar from east area of China is similar to that from India". ⑤ L infantum and L d .isolates from hill foci in China were clustered into different groups. ⑥ The genetic distance is close between L d .isolates from plain foci in China and L d .Jed;⑦ L infantum and L tropica showed the closest genetic distance. Conclusion Differences at genetic level exist in Leishmania isolates from different foci in China.
    ON Cleanliness of Hands in Diminution of Ascaris lumbricoides Infection in Children
    XULongqi;XIAODonghua;ZHOUChanghai;ZHANGXueqiang;LANShuigen;ZHENXiuxiang;ZHANGWenling;FUJieping;YEBo;DANGHui;ZHUXianzu;HUANGShilan
    2001, 19(5):  10-297. 
    Asbtract ( )   PDF (251KB) ( )  
    Related Articles | Metrics
     Objective To study the relationship between cleanliness of children′s hands and diminution of Ascaris lumbricoides infection. Methods Before the study all persons positive for ascaris eggs in the preliminary survey were treated with albendazole. Hand washing habit before meal and after defecation was kept in children of experimental group, but not in the control group. Kato thick smear stool examination was done once every two months for one year to compare the new infection rates in children without ascaris infection in the two groups, and the reinfection rates in the cured negative cases were also compared between them in half a month after chemotherapy. Results All the new infection rates as well as reinfection rates of each reexamination in the experimental group were significantly lower than that of the control group ( P <0 001). Reexamination one year later showed that the ascaris infection rate of the experimental group was 35 2%, reducing by 48 5% as compared with 68 3% before the operation of the project; while ascaris infection rate of the control group was 73 7%,increasing by 78 0% as compared with 41 4% before the operation of the project. Conclusion Washing hands with toilet soap to keep hands clean can significantly reduce ascaris infection rate.
    Immunostimulatory Activity Elicited by CpG Sequences in Cysticercus Cellulosae Paramyosin cDNA
    SUNShuhan;GUOYingjun;WANGQingmin;CHENRuiwen
    2001, 19(5):  11-299. 
    Asbtract ( )   PDF (128KB) ( )  
    Related Articles | Metrics
     Objective To analyse the immunostimulatory activity of CpG sequences in cysticercus cellulosae paramyosin (also named Antigen B,AgB)cDNA. Methods C57BL/6 mice were immunized with pcDNA3 AgB plasmid,pcDNA3 AgB′(CpG sequences were mutated),pcDNA3 or AgB protein and two weeks later,immune response was assayed by ELISA. Results IgG and IgG 2a were detectable at week 2 after immunization and continually increased until week 4.The antibody levels elicited by pcDNA3 AgB were significantly higher( P <0 05) than those elicited by others. Conclusion After pcDNA3 AgB plasmid inoculation,the immune response of mouse was elicited not only by the AgB protein but also by the CpG immunostimulatory sequences in the AgB cDNA.
    AN Approach to the Morphology of Buccal Armature of Sergentomyia nankingensis
    XIONGGuanghua;JINChangfa
    2001, 19(5):  12-302. 
    Asbtract ( )   PDF (167KB) ( )  
    Related Articles | Metrics
     ObjectiveTo describe the morphological variation of pointed teeth of buccal armature of Sergentomyia nankingensis in a supplementary study. Methods The morphology of Sergentomyia nankingensis was observed and the specimens included S nankingensis captured from the field as well as the female ones bred in the laboratary and their offspring of first generation. Results The buccal armature of females and males, consists of about 10-19 and 8-15 pointed teeth and the pigmented plate is polymorphous. In the nature,the number of pointed teeth of buccal armature of Sergentomyia is unstable,varying in more than 10 teeth in the same species sometimes. Conclusion Identification of species needs large amount of specimens for comparative observation. Sergentomyia sandfly should be raised separately and individually for morphological observation of its newly emerged offspring, especially when the sandfly specimens and data collected in the field were not sufficient.
    Detection of Anti-Spirometra erinaceieuropaei Antibody Using ELISA
    DingYue-xinGuoLiliLiuDianwuZhangPuhongLiuShuxian
    2001, 19(5):  13-304. 
    Asbtract ( )   PDF (129KB) ( )  
    Related Articles | Metrics
     Objective To study specific diagnosis of Spirometra erinaceieuropaei . Methods An enzyme linked immunosorbent assay (ELISA) was studied using highly pure gene engineering antigen expressed by the recombination of the cloned cysteine proteinase gene of Spirametra erinaceieuropaei with expression vector pMAL TM c2. Six sera from patient infected with Spirometra erinaceieuropaei were detected using this method. Results and Conclusion The results showed that the gene engineering antigen reacted strongly with the sera from Spirometra erinaceieuropaei infected patients, but did not with the sera from Cysticercus cellulosae infected patients.
    临床报道
    A Clinical Trial of Triclabendazole in the Treatment of Human Paragonimiasis skrjabini
    HUPeng;LIUYuehan
    2001, 19(5):  14-307. 
    Asbtract ( )   PDF (196KB) ( )  
    Related Articles | Metrics
     Objective To observe the therapeutic effect of triclabendazole in patients with paragonimiasis skrjabini. Methods Four patients were treated with triclabendazole at dosage of 10 mg/kg bid for 3 days and were followed up for 6~10 months. The clinical symptoms, chest X ray, hemogram and liver function tests were observed before and after treatment. Results Migratory subcutaneous nodules in three patients all disappeared. Small amount of pleural effusion were absorbed in two patients. Severe headache subsided in a patient with cerebral lesion. MRI showed a bean sized calcified spot in the right frontal region. Chest X ray in 2 patients showed that pulmonary lesions were markedly absorbed and disappeared. There was no adverse effect of the drug.Conclusion Triclabendazole has marked therapeutic effect on paragonimiasis skrjabini. It is safe in administration and well tolerated.
    A Study of Artemether Combined with Primaquine in the Treatment of Falciparum malaria
    HUANGJianrong;GAOYingqi;NganaweiElie
    2001, 19(5):  15-309. 
    Asbtract ( )   PDF (137KB) ( )  
    Related Articles | Metrics
     Objective To evaluate the efficacy and side effects of artemether combined with primaquine in the treatment of falciparum malaria. Methods Randomization and comparison methods were used in 121 falciparum malaria cases in the Republic of Central Africa.Sixty one cases were treated with artemether combined with primaquine(Group A used artemether orally,Group B used artemether intramuscularly).And 60 cases received single artemether (Group C used artemether orally,Group D used artemether intramuscularly ) were taken as control. Results In Group A and B the mean fever clearance time were 47 6±15 7 and 36 9±10 7 hours, clinical cure rates 84 4% and 100%, relapse rates 6 3% and 3 4% ,respectively.In Group C and D the mean fever clearance time were 48 2±18 4 and 42 2±9 5 hours,clinical cure rates 90 1% and 96 3%, relapse rates 21 2% and 18 5%,respectively.Side effects in cases of all groups were mild. Conclusion Artemether combined with primaquine and single artemether(via both routes) showed good therapeutic effects in falciparum malaria cases, while artemether combined with primaquine was more effective than single artemether in reducing relapes rate of malaria.
    Three Lethal Cases of Angiostrongylus cantonensis Infected Children
    LIDaoning;HEAi;WANGYi;LIANGYu;LIZhuoya;MENJinxiu;ZHANXimei
    2001, 19(5):  16-311. 
    Asbtract ( )   PDF (162KB) ( )  
    Related Articles | Metrics
     Objective To offer approaches to diagnosis and treatment of Angiostrongylus cantonensis infection on the basis of analyzing three lethal cases of the disease. Methods Clinical manifestations, pathological changes and species identification were pursued. Results Angiostrongyliasis is usually neglected in medical departments.The three cases here reported were all misdiagnosed and had not receiced anthelmintic treatment hence fatality ensued. Conclusion Early examination of CSF,bronchial lavage fluid and feces is urged so as to secure accurate diagnosis and conduct efficacious anthelmintic therapy to cure the patients.