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    28 February 1997, Volume 15 Issue 1
    论著
    MOLECULAR CLONING AND IDENTIFICATION OF GENES ENCODING MSP2 AND REGIONS 16- 17 IN MSP1 FROM TWO ISOLATES OF PLASMODIUM FALCIPARUM FROM CHINESE PATIENTS WITH CEREBRAL MALARIA
    BianZhongqi;SongGuanhong;GuanWeibin;YanWeiyao;ZhengZhaoxin
    1997, 15(1):  1-6. 
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    AIM: To provide a theoretical basis for designing safe and effective vaccines of human cerebral malaria. METHODS: Genomic DNA samples of two P. falciparum isolates were prepared directly from 5 cases of cerebral malaria patients’blood in Mengla County, Yunnan Province(CMH/YN ) and in Yingjiang County, Yunnan Province (CYJ/YN ). The samples were used for polymerase chain reaction (PCR) amplification and the two pairs of oligonucleotides for the highly conserved genes encoding of FC27 merozoite surface protein 2 (MSP2) and the regions 12- 17 in MAD20 merozoite surface protein 1 (MSP1) of Papua New Guinea strain of P. falciparum were used as primers. The PCR products were digested with EcoRI and KpnI, BamHI and HindIII, respectively, and the generated fragments were cloned into M13mp18 and M13mp19 vectors and transfected into Escherichia coli (E. coli) TG1. A single colorless plaque on the LB agar plate containing X-gal (5-bromo-4-chloro-3-indolyl-β-D-galactoside) and IPTG (isopropylthio-β-D-galactoside) was randomly picked and transformed into E. coli JM103. The replicative form (RF) DNA (RFDNA ) of M13 recombinant DNA extracted from E. coli by the method of alkali lysis were digested with EcoRI and KpnI, BamHI and Hind III, respectively, and the generated fragments were identical with inserted foreign DNA 0.918 kb and 0.8 kb designed by ourselves. RESULTS: It is proved that M13 recombinant DNA consists of M13 vectors with an insert of genes encoding MSP2 and the regions 16 - 17 in MSP1 from two isolates CMH/YN and CYJ/YN of P. falciparum from Chinese patients with cerebral malaria at its corresponding site. CONCLUSION: The results demonstrate for the first time that both isolates CMH/YN and CYJ/YN of P. falciparum from Chinese patients with cerebral malaria examined contain genes identical to those defined in known MAD20 MSP1 and FC27 MSP2 allelic dimorphic family. These findings provide valuable strategies both for the development of vaccines to prevent human cerebral malaria and for the establishment of a specific detection method of P.falciparum from patients with cerebral malaria.

    STUDIES ON DIAGNOSIS OF VISCERAL LEISHMANIASIS BASED ON PCR AMPLIFICATION OF LEISHMANIA DONOVANI kDNA FRAGMENT FROM BONE MARROW AND BLOOD SAMPLES OF VISCERAL LEISHMANIASIS PATIENTS
    HuXiaosu;YangWentian;MaYing;ChenJianping;HeShengquan;XuTingxi;XieXiaoquan
    1997, 15(1):  2-10. 
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    AIM: To develop a simple and accurate technique for the diagnosis of visceral leishmaniasis (VL) and identification of Leishmania pathogen. METHODS: Based on a set of oligonucleotide primers I and II designed by the authors with L. donovani specificity, a polymerase chain react ion (PCR ) was conducted to amplify a minicircle kDNA fragment (297 bp ) for identification and detection of L. donovani in the bone marrow , blood and serum samples from 22 confirmed VL patients and 4 bone marrow samples from 4 clinically diagnosed cases (59 samples collected from 26 cases). RESULTS: (1) The coincidence rate between PCR and bone marrow smear method was 96.2% (25/26) ; (2) The total positivity of PCR with the bone marrow , blood and serum was 95.4% (21/22) ; (3) The positive rate of PCR amplification with bone marrow , blood and serum specimens were 91.0% (20/22) , 68.8% (11/16)and 29.4% ( 5/17) , respectively. The controls included 15 bone marrow samples from 9 leukemia patients and 6 normal persons; 5 blood and 5 serum samples of normal persons. No amplification product was showed from all of the controls. CONCLUSION: The result shows that the diagnosis of visceral leishmaniasis based on detecting kDNA in blood by PCR amplification with primers I and II is promising.
    EFFECT OF ANTI-IDIOTYPIC ANTIBODY IMMUNIZATION ON PROTECTIVE IMMUNITY IN JIRDSAGAINST BRUGIA MALAYI
    ZhengHuijun;TangJunjie;LingTianyi;TaoZenghou;ChengWenfang;FangRenli
    1997, 15(1):  3-14. 
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    AIM: To assess the protective immunity engendered by anti-filaria-anti-idiotypic antibody (anti-fil-anti-Id-Ab) in jirds (Meriones unguiculatus) against Brugia malayi. METHODS: Anti-fil-anti-Id-Ab was prepared from rabbits immunized with anti-fil-IgG separated from high-titer sera from bancroftian filariasis patients with chyluria or hydrocele. Twenty two healthy jirds were randomly allocated to 3 groups. Group 1 (7 jirds) were each immunized with a single intrasplenic administration of anti-fil-anti-Id-IgG (4 jirds) or B. malayi soluble antigen (3 jirds). Group 2 (10 jirds) were each immunized with 3 repeated sc and ip administration of anti-fil-anti-Id-IgG (5 jirds) at 7-10-day intervals or B. malayi soluble antigen (5 jirds). Group 3 ( 5 jirds) served as challenge controls. Ten days after the last immunization, each jird in all three groups were challenged by ip route with 200 B. malayi third stage larvae. RESULTS: Jirds immunized with a single administration or 3 repeated administration of anti-fil-anti-Id-IgG could induce 50% and 80% protective immunity, respectively. No microfilaria or adult worms could be found in these jirds. In control group using rabbit anti-human IgG or B. malayi adult worm soluble antigen, no apparent protective immunity was found. CONCLUSION: Immunization of jirds with anti-fil-anti-Id-IgG resulted in protected immunity (50% - 80%) against B. malayi third stage larvae infection.
    MOLECULAR CLONING OF cDNA ENCODING IMMUNODIAGNOSTIC ANTIGENS OF CYSTICERCOSIS
    SunShuhan;WangJunxia;ChenRuiwen;LuHuiping;PengYucong;WangZhaoxia
    1997, 15(1):  4-20. 
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    AIM: To clone and analyze the cDNA encoding immunodiagnostic antigen of cysticercosis. METHODS: Immunodiagnostic antigens of cysticercosis were obtained studied using recombinant DNA techniques. cDNA was synthesized from mRNA and a λgt11 expression library was constructed and immunoscreened with human and/or pig cysticercosis sera. RESULTS: Four positive cDNA clones (λcC1、λcC2、λcH1 and λcP1) were isolated. The λcC1 cDNA was 1 070 bp in length and consisted of a single open reading frame. The open reading frame of 747 bp encoded a polypeptide of 249 amino acids with a molecular weight of 27.36 kDa. The λcC1 fusion protein was identified as an common antigen for immunodiagnosis of both human and pig cysticercosis. CONCLUSION: The λcC1 fusion protein was highly sensitive and specific as compared to crude somatic antigen for the immunodiagnosis of cysticercosis.
    CONSTRUCTION AND PRIMARY CHARACTERIZATION OF ERYTHROCYTIC PLASMODIUM FALCIPARUM (FCC/HN) cDNA EXPRESSION LIBRARY
    WangYanni;XiaoGutian;BiHuixiang;JinLijuan;LiMing;LiYingjie;XieYi
    1997, 15(1):  5-25. 
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    AIM: To construct a cDNA expression library from erythrocytic Plasmodium falciparum (FCC/HN). METHODS: 1224 μg total RNA and 35.84 μg poly (A)+ mRNA have been successively obtained from the blood-stage Plasmodium falciparum mainly consisting of trophozoites using“single-step method”and by chromatography on oligo-(dT) cellulose. With the reverse transcriptase (M-MLV ) , 10 μg mRNA was synthesized into 1.75 μg blunt cDNA. After the cDNA was ligated to EcoRI (NotI, SalI) adapter and purified by fractionation, 200 ng cDNA of about 500 bp - 7 kb was collected. Of which 50 ng cDNA was ligated into λgt11 phage particles and was packaged with the packagen extract system in vitro. This library was characterized primarily by PCR. RESULTS: A cDNA library containing 106 recombinants has been constructed. CONCLUSION: The capacity of this library and the size of cDNA is suitable for further study.
    EXPLORATION ON ADJUVANT EFFECT OF SCHISTOSOMA JAPONICUM RIBOSOME PREPARATION
    WangJianjun;LiuShuxian
    1997, 15(1):  6-28. 
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    AIM: To investigate the adjuvant effect and protective activity of Schistosoma japonicum ribosome preparation (SRP). METHODS: Mice were immunized with SRP, SWA and SRP+SWA, respectively. Humoral immunity levels of mice were detected by ELISA and protective immunity of mice were indicated by worm reduction rate. RESULTS: Mice immunized with SRP or SRP + SWA produced higher specific antibody titer than mice immunized with SWA. However, mice immunized with SRP or SRP+ SWA failed to exhibit higher worm reduction rate than mice immunized with SWA. CONCLUSION: SRP could enhance the humoral response of mice to SWA, but did not result in protective immunity of mice against the schistosomes.
    STUDIES ON EXPERIMENTAL INFECTION AND HOST TRANSFER OF FOWLS AND FROGS WITH PARAGONIMUS WESTERMANI AND PAGUMOGONIMUS SKRJABINI
    YanTao;GuoEping;ZhanXimei;LiGuiyun
    1997, 15(1):  8-33. 
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    AIM: To explore the distribution and development of Paragonimus westermani and Pagumogonimus skrjabini in fowls and frogs in addition to the invasiveness of the juveniles recovered from the above animals to cats or dogs. METHODS: Chickens, ducks, quails and parrots were infected orally each with 30 - 200 metacercariae of Paragonimus westermani and Pagumogonimus skrjabini, respectively. Dogs or cats were infected with juveniles obtained from the above animals. RESULTS: Juveniles were obtained from body cavities, livers, lungs and muscles of fowls and frogs 60 days after infection. Most of the juveniles were detected from the muscles but their development retarded. In 60 frogs infected with metacercariae of Paragonimus westermani, no worm was found. Infection rate of frogs infected with Pagumogonimus skrjabini was1.7% - 40.0%. After host transfer, juveniles developed well and matured in the thoracic cavities or lung worm cysts of dogs or cats, but some prematured worms were also detected. CONCLUSION: Attention should be given to the role of fowls or frogs in the transmission of human paragonimiasis in endemic area.
    EFFECT OF ALCOHOLIC EXTRACT OF SCORPION ON CYSTICERCUS CELLULOSAE IN VITRO
    ZhangGuijun;ZhangLihua;ToshihiroTanaka
    1997, 15(1):  10-37. 
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    AIM: To demonstrate the effect of alcoholic extract of Buthus martensii against Cysticercus cellulosae in vitro. METHODS: Fresh Cysticercus cellulosae were cultured in 15% swine bile medium containing scorpio alcoholic extract. RESULTS: The scorpio extract at 26mg/ml exerted profound effect in destroying cysticerci as assessed by the morphological changes and loss of vitality. After of the Cysticercus cellulosae were cultured in medium containing scorpio extract for 4, 6 and 8 hours, evident pathological changes were revealed. The main microscopic features were peeling of microtriches, swelling, and deformity of rostellum and suckers of evaginated cysticerci. CONCLUSION: Scorpion extract exerts damage effect on both the tegument and scolex of Cysticercus celluosae.
    EVALUATION OF A SHORT-TERM HEALTH EDUCATION PROGRAMME IN A SCHISTOSOMIASIS HIGHLY ENDEMIC AREA
    LiuJianxiang;YuanHongchang;HuangJingheng;ZhangShaoji;HuGuanghan;LinDandan;JiangQingwu
    1997, 15(1):  12-41. 
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    AIM: To assess the effect of health education on the control of schistosomiasis. METHODS: A high dam-circle marsh subtype endemic village named Fanhu in Jiangxi Province near Poyang Lake was chosen for carrying out a short-term mass communication health education programme. The effect was evaluated through investigations on knowledge in schistosomiasis control, water-contact frequency and schistosome infection rate pre-and post-education. RESULTS: The results showed that such an education programme could improve the target residents’ knowledge, but the water-contact behavior and schistosome infection rate had not been significantly changed. CONCLUSION: Short-term health education could enhance the residents’ understanding of schistosomiasis control and decrease the frequency of contacting infested water and the infection rate in women. However, the reinfection rate in men remain high because of high frequency of fishing.
    COMPUTED TOMOGRAPHY ANALYSISOF160 CASES OF CEREBRAL CYSTICERCOSIS
    LianChen;ZhengWanzhong;LiXuesong;ChenJingqi
    1997, 15(1):  13-44. 
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    AIM: To provide more evidence for the precise diagnosis and suitable treatment of cerebral cysticercosis cases. METHODS: Computed tomography (CT) was performed on 160 cases of cerebral cysticercosis. RESULTS: According to CT findings, cerebral cysticercosis is divided into four types, namely: cerebral parenchyma, cerebral ventricle, cerebral membrane and mixed type. CONCLUSION: The location and amount of the foci of cerebral cysticercosis bear close relation with the status and prognosis of the disease.