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    30 June 1998, Volume 16 Issue 3
    述评
    MALARIA SITUATION IN THE PEOPLES REPUBLIC OF CHINA IN 1997
    AdvisoryCommitteeonMalaria;MOH
    1998, 16(3):  161-163. 
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    A cco rding to the case repo rt ing system , the number of malaria cases in Ch ina numbered
    34 645 (Taiw an P rovince and Hong Kong not included ) in 1997, with a mean incidence of
    2. 91 per a hundred thousand and lethal cases of 46. How ever, the estimated number of actualmalaria cases based on investigations at provincial level was 220 000- 250 000, showing a sligh t diminu t ion as compared with that in 1996.
    Yunnan and Hainan were continued to be the major provinces endemic fo r malaria,where the number of malaria cases amounted to 46% of the total in the whole country. In
    Yunnan Province, an increase of outbreak spots and resurgence of malaria incidence in border
    region were reported, while the incidence was stable or slight ly declined in most o ther
    provinces, but was fluctuated in provinces distributed with A nopheles anthropophagus
    Blood examination on febrile patients for 9 209 102 man/time in 1 294 counties of 18
    provinces/municipalit es/autonomous regions (P/M /A )with a population of 569 703 000 detected 26 816 cases positive for malaria parasite, showing a mean positive rate of 0. 29%; of which the number of falciparum malaria casesw ere 4 114 ( including mixed infections with vivax malaria, the same below ) , account ing for 15. 3% of the total parasite positives ; of the
    three quartan malaria cases detected, one was infected via blood transfusion. Totally 568 783 target-population and migratory people were surveyed, 2 861 were positive fo r malaria parasite, with a mean parasite rate of 0. 50%; and 586 falciparum malaria cases were among the posit ives. A s a whole, the endemicity of falciparum malaria was still confined to 44 counties
    of Hainan and Yunnan Provinces . Imported falciparum cases were reported in 74 counties located in 17 P/M /A , how ever, no introduced falciparum malaria cases were recorded.
    论著
    SENSITIVITY AND SPECIFICITY OF NESTED POLYMERASE CHAIN REACTION IN DETECTING PLASMODIUM VIVAX IN INFECTED MOSQUITOES
    LiFengwu;NiuChun;YeBinghui;ZhuXingping;ChenPeihui
    1998, 16(3):  164-167. 
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    AIM: To study the sensitivity and specificity of nested polymerase chain reaction for detection of
    Plasmodium vivax in infected mosquitoes. METHODS: Two pairs of primers specific to small subunit ribosomal DNA
    of P.vivax were used to amplify the specific SSUrDNA 121 bp fragment of P.vivax for detecting P.vivax infected
    mosquitoes with nested PCR. RESULTS: Nested PCR could detect as few as 3 sporozoites in one mosquito or 1
    infected mosquito mixed with a group of 99 normal ones. In contrast, no such specific 121bp DNA band was detected in P. falciparum , P. cynomolgi, P. yoeliiyoelii infected samples, nor in normal mosquito. CONCLUSION: The nested PCR technique we established showed high sensitivity and specificity
    APPLICATION OF IMMUNOCHROMATOGRAPHIC TEST FOR DIAGNOSIS AND SURVEILLANCE OF BANCROFTIAN FILARIASIS
    ZhengHuijun;TaoZenghou;FangRenli;ChangBaoyu;ZhangYulin;PaulTurner
    1998, 16(3):  168-171. 
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    AIM: To evaluate the usefulness of immunochromatographic test (ICT) for rapid diagnosis and
    surveillance of Wuchereria bancrofti infection. METHODS: The monoclonal antibody based ICT assay was used to
    detect filarial antigens in the sera from bancroftian filariasis patients. RESULTS: 111 out of 116 bancroftian
    microfilarmia cases showed positive ICT reaction, giving a positive rate of 95.7%. Serum samples from 12
    malayian microfilaremia cases, 33 ascariasis cases, 20 schistosomiasis japonica cases and 6 trichinellosis cases were all found negative in ICT , demonstrating a specificity of 100%. In 73 chronic filariasis cases
    with elephantiasis, hydrocoele, and chyluria cases, 18 showed ICT positive, among whom 16 revealed microfilarem ia, suggesting that the ICT positive cases were with active infections. Of the 30 microfilaremia cases before single dose ivermectin treatment, 29 were ICT positive (96. 7% ). A negative conversion of microfilaremia was observed in all cases 8- 14 days post-treatment. Upon following up to 6 and 12 months, microfilaremia eappeared in 5 and 7 cases, respectively. 5 out of 13 ICT positive cases were found microfilaremic at 6 month post-treatment, while among the rest of 8 , 5 were found microfilaremic at 12 month post-treatment. Parallel use of ICT with routine blood film examination in Houda village,Zhecheng County, Henan Province for a post-control surveillance survey in 132 local individuals revealed 9 microfilaremia cases were also ICT positive. Of the 123 persons w th negative blood examination, only 1 was ICT positive. CONCLUSION: ICT is a rapid and simple method with high sensitivity and specificity, and might be used for the diagnosis, efficacy evaluation as well as a tool for post-control surveillance of bancroftian filarasis.

    DIFFERENTIATION OF CRYPTIC SPECIES A AND D OF ANOPHELES DIRUS COMPLEX BY POLYMERASE CHAIN REACTION
    XuXiaochun;XuJiannong;QuFengyi
    1998, 16(3):  172-175. 
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    AIM: To distinguish cryptic species A and D of Anopheles dirus complex using polymerase chain reaction (PCR). METHODS: A diagnostic PCR assay of species was developed by use of three primers, one derived from highly conservative 5.8 S coding sequences and two from different interspecies sequence in the second internal transcribed spacer (ITS2) of ribosomal DNA. RESULTS: Using the PCR method, specific fragments were amplified in both species, the size of fragments is 374 bp for species A and 663 bp for species D. Thirty
    samples of species A from AFRIMS and HN laboratory colony and seven samples of the species D from Yunnan Province were correctly identified by PCR. Satisfactory results were obtained from the amount of DNA as little as 1/1 600 of extracted DNA of a single mosquito or 1/5 of DNA derived from one leg of a mosquito triturated in water. A total of 148 field-collected specimens of Anopheles dirus from Heping (HP) , Baisha (BS) , Loukui(LK), and Maoyang (MY) in Hainan Province revealed fragment characteristic of species A, while 30 specimens from Mengla (ML) in Yunnan Province showed the specific fragment of species D. CONCLUSION: A simple and reliable Method was developed to identify cryptic species A and D of Anopheles dirus complex and it was further verified that Anopheles dirus from Hainan and Yunnan Provinces is the species A and the species D, respectively.

    IMMUNOSCREENING OF SCHISTOSOMA JAPONICUM EGG cDNA LIBRARY
    ZhouJinchun;YiXinyuan;ZengQingren;ZhangShunke;CaiChun
    1998, 16(3):  176-180. 
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    AIM: To screen and identify genes encoding vaccine candidates and molecules with diagnostic potential from S.japonicum(S.j) egg cDNA library. METHODS: S.j egg cDNA library was screened by sera from SEA immunized rabbits. Positive clones were identified after three rounds of screening and were excised automatically in vivo with helper phage. Products of PCR were used to detect insert sizes by agarose gel electrophoresis. DNA samples were obtained by purification using mini prep kit Automatic sequencing was carried out and the sequence data were analysed using GCG softw are. RESULTS: Twelve clones were identified as positive and the inserts were around 1. 2 kb in size. Compared with DNA sequences in GenBank, eight clones were homologous to a 70 kDa S. j heatshock protein (S. j H sP70). C18 exhibited 97. 8% homology with S. j 23. C22 and C23 shared 82. 4% and 89. 5% homology with S. j calreticulin, respectively. C12w as homologous to S. mansoni (S. m. ) immunophilin. CONCLUSION: This paper first reported the results of
    immuno screening S. j egg cDNA library by anti-SEA sera. Twelve positive clones were found to be related to protective immunity and/or immunodiagnosis of schistosomiasis.
    ANALYSIS OF MOLECULAR KARYOTYPE OF LEISHMANIA ISOLATES FROM HILLY FOCI AND PLAIN FOCI OF CHINA
    LuFangli;HuXiaosu;TangHaimei;ZengFanya;ZhangYizheng;DaiBaomin
    1998, 16(3):  181-184. 
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    AIM: To analyse the molecular karyotypes of Leishmania isolates from
    hilly and plain foci of China. METHODS: Pulsed field gel electrophoresis(PFGE) was
    performed in 1% agarose at 6 V/cm in 0.5×TBE at 14℃ with a pulse time of 60 s for
    15 h and a pulse time 90 s for 9 h. RESULTS: Each isolate was resolved into 15
    different EtBr staining bands ranging in size from 200 to 2 200 kb, in which the
    karyotypes of 6 isolates from hilly foci were similar(including karyoptypes of
    canine isolates similar with those of human isolates), and they were partly similar with those of L. infantum. The karyo types of the two isolates from plain foci were similar, but the isolates from the two topographically different foci were different from each other. CONCLUSION: Homology exists between L. d. isolates from hilly foci and plain foci respectively, and exists in part between L. d. isolates from hilly foci and L. infantum ; while heterogeneity exist s between L. d. isolates from hilly foci and plain foci. The reservoir host, domestic dog, plays an important role as the infection source of leishmaniasis in the hilly foci of China.
    STUDY ON INVASIBILITY AND MULTIPLICATION OF TOXOPLASMA STRAINS WITH DIFFERENT VIRULENCE TOWARD VERO CELLS
    YangHuizhen;ZhangAimin;YangYang;QianZongli
    1998, 16(3):  185-188. 
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    AIM: To investigate the pathogenic mechanisms of Toxoplasma strains
    with different virulence. METHODS: Tachyzoites from 3 strains, Viz.RH, B 36 and
    Fukaya strains, were challenged to in vitro cultivated Vero cells. Systematic
    examinations on the earliest invasion time, the invasion rate and intracellular
    multiplication were performed under different cultivation conditions. RESULTS: The
    tachyzoites of all the 3 strains invaded the host cells wi thin a short period
    after inoculation. Invasion rates were all increased along with the prolonged duration of infection. The intracellular multiplication was found to be most active in RH strain, moderate in B36, and comparatively slow in Fukaya strain s. Using purified tachyzoites freed from host debris and proteins and adding sufficient FCS in the medium may facilitate the invasion and subsequent multiplication of the parasite. CONCLUSION: Strain differences in pathogenicity to the host may be correlated to the genetically predetermined multiplication capabilities of the parasites after being invaded to the host cell, and that environmental factors may give certain impact on the invasibility of the parasite.
    ACCUMULATION AND EFFLUXION OF CHLOROQUINE IN CHLOROQUINE SENSITIVE AND CHLOROQUINE RESISTANT PLASMODIUM BERGHEI
    WangQinmei;WangMingjie;ChangHuiling;YangBin
    1998, 16(3):  189-192. 
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    AIM:To explore whether the difference in the amount of chloroquine
    (CQ) accumulated in CQ resistant (CR) and in CQ sensitive (CS) P.berghei is
    involved in the infected erythrocytes (RBC) or in the parasites. METHODS:The
    concentration of CQ in infected RBC and parasites following ig administration of CQ
    to CS and CR infected mice was determined by HPLC method (extra standard).
    RESULTS:3 h after 4.06 mg/kg and 400 mg/kg administration, the accumulation of CQ
    in both infected RBC was similar, but in CR was 54. 0% and 42. 1% less than in CS
    (P < 0. 001) respect ively. The CQ accumulation in CS 3 h and 7 h after ig
    administration of CQ 400mg/kg was similar (0. 780±0. 128 nmol/protein and 0. 760±
    0. 180 nmol/mg protein), while in CR the CQ-accumulation was higher at 7 h than
    that at 3h after CQ administration (0. 452±0. 079 nmol/mg protein and 0. 559±0.
    124 nmol/mg protein P < 0. 02). CONCLUSION: The low CQ accumulation in CR is
    attributable to the parasite rather than to the infected RBC, and CR was not found
    to excrete CQ more rapidly than CS.
    A SURVEY OF ECHINOCOCCUS GRANULOSUS INFECTION IN CAMELUS BACTRIANUS IN NORTH XINJIANG
    ChaiJunjie;JiaoWei;IsrainOsman;QuQun;WangHongbin;Yusupujiang
    1998, 16(3):  193-196. 
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    AIM: To determine the situation and characteristics of Echinococcus
    granulosus infection in camels ( Camelus bactrianus ) in our country.METHODS:The
    camels slaughtered in abattoir were examined for visceral infection of larval
    cestode of Echinococcus. The number and diameter of cysts were recorded and the
    content of cysts were examined microscopically to detect the protoscoleces.
    RESULTS:185 out of 375 camels were positive, the infection rate was 49.3%. The
    metacestodes parasitized mainly in the liver and lung, the ratio between liver and lung involved was 1∶0. 64. The fertile cyst rate was 39. 2% , the fertile cyst-carrying rate of camels was 4. 8% , the cyst index was 7. 53. The cyst wall was relatively thin and the cysts located singly on the surface of liver. There was no daughter cyst seen in fertile cysts. The average diameter of fertile cysts was 5. 6±2. 65 cm in liver and 4. 83±2. 03 cm in lung. The percentage of animals harboring calcified cysts was 64. 3%. CONCLUSION: The infection rate of metacestodes of Echinococcus granulosus in Bactrian camel was very high in north Xin jiang and the characteristics of infection differ in some aspects from the local sheep and cattle and from dromedaries in Africa as well. Further study is needed to elucidate the significance of the infection of E. granulosus in Bactrian camels.
    THE MORBIDITY INVESTIGATION OF RESIDENTS IN A HIGHLY ENDEMIC VILLAGE OF SCHISTOSOMIASIS IN POYANG LAKE REGION
    LiuJianxiang;ZhaoGenming;WuZhongdao;TaoBo;JiangQingwu
    1998, 16(3):  197-200. 
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    AIM: To investigate the morbidity of residents in a highly endemic village of
    schistosomiasis, and to evaluate the usefulness of ultrasound in morbidity study. METHODS:
    Morbidity induced by Schistosoma japonicum was evaluated and compared in target population by
    using parasitological examination, ultrasound investigation and medical history questionnaire.RESULTS: The schistosome infection rate was 22.9% in the study population and the
    prevalence of abnormal ultrasound findings in the liver and spleen was high. The abnormal ultrasound findings correlated with sex significantly, the abnormality of liver parenchyma correlated with age, sex, infection status, occupation and the number of treatment after multiple logistic regression analysis. CONCLUSION: The ultrasound examination could find out the direct pathological changes resulting from schistosome infection.
    APPLICATION OF IMPROVED WESTERN BLOT METHOD IN DIAGNOSIS OF CYSTICERCOSIS
    WangMin;GuoYingjun;ChenRuiwen;XuZhijie;SunShuhan
    1998, 16(3):  201-203. 
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    AIM:To evaluate the diagnostic value of four specific antigens from cDNA of
    Cysticercus cellulosae . cC1,cC2,and cP1 and cH1 ( 28 kDa, 18 kDa, 14 kDa and 34 kDa ), mixing in equal proportions for the diagnosis of cysticercosis. METHODS:Taking the FP (fusion proteins) as antigen to make IWB (improved Western blot ) analysis basing on the detection of antibody
    responses against FP,and making ELISA / IHA crude antigen(CA) analysis.They were evaluated
    comparatively while using l07 infected sera of cysticerco sis cases, 40 infected sera of clonorchiasis cases, 24 infected sera of ech inococcosis cases and 34 sera of healthy persons. The FP are encoded by cDNAs of β-galacto sidase-specific antigens of Cysticercus cellulosae isolated from the cDNA library. RESULTS: 94 (87. 9% ) sera from l07 cysticercosis cases recognized FP in IWB and could not cross-react with the sera of echinococcosis cases, clonorchiasis cases and healthy persons, the specific rates were 100%, whereas ELISA, IHA using CA were 84. 1%and 74. 8%, respectively and could cross-react with the sera of echinococcosis cases, the false positive rates were 2. 5% and 12. 5% respectively; CA 2EL ISA/IHA could cross-react with the sera of clonorchiasis patients, the false positive rates were 8.3% and 16. 7%, respectively; and they could also cross-react with the sera of healthy persons, the false positive rates were 8. 8% and 11. 8% , respectively. CONCLUSION: The recombinant FP used in the immunodiagnosis of cysticercosis is specific and sensitive.
    CHARACTERISTICS OF DEVELOPMENT AND MORPHOLOGY OF ECHINOCOCCUS GRANULOSUS OF CAMEL ORIGIN IN NORTH XINJIANG
    JiaoWei;ChaiJunjie;IsrainOsman;QuQun
    1998, 16(3):  204-208. 
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    AIM: To study the characteristics of development and morphology of E. granulosus of
    camel origin in north Xinjiang. METHODS:Six dogs were infected with protoscolices and then
    purged with arecoline at days 35 and 45 p.i.RESULTS:Six dogs were heavily infected, the worm
    burden were 14 780 to 135 900 at days 35 and 45 p.i. At day 35 p.i. 77% of the had developed
    three segments, 10% contained mature eggs with fully developed “thick shelled” embryophores.
    Morphological studies revealed the following characteristics for 35-day-old worms: the mean
    length of the terminal segment accounted for 56% of the total worm length: the position of the
    sexually mature segment was always terminal (77% ) ; the female reproductive system possessed an
    enlongated ovary with compact lobules; the Mehlis gland was covered by the vitelline gland and
    the testes were distributed throughout the segment arranging in a row posterior to the vitelline
    gland. CONCLUSION: The E. granulosus of camel isolate in north Xin jiang can readily be
    distinguished from the horse, sheep , cattle and pig strains, but is similar to the camel (
    Camelus drom edarius ) strain distributed in North Africa.
    ULTRASTRUCTURAL OBSERVATION ON SPERMATOCYTOGENESIS IN TAENIID CESTODES
    TianXifeng;YuanLijie;LiYihong;HuoXiaoqing;HanXiuling;XuMin;LuMinjie;DaiJianjun;DongLu
    1998, 16(3):  209-213. 
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    AIM: To study the spermatocytogenesis of taeniid cestodes at the ultrastructural leaves. METHODS: Transmission electron microscopy. RESULTS: The ultrastructural observation on spermatocytogenesis in Taenia solium, T. saginata and T. pisiformis were made by TEM. Two types of spermatogonia; type A and B, as well as the supporting cells surrounding the peripheral of spermatogonia are recognized. The type A spermatogonia are stem cells and the type B are mother cells which produce 16 primary spermatocytes by mitosis for 4 times with the cells unseparated. The primary spermatocytes are characterized by the ribosome masses in the cytoplasm. 32 secondary spermatocytes arranged in roselike were produced by reductive division of primary spermatocytes. The secondary spermatocytes become the spermatid quickly by short time development. CONCLUSION: The dividing mode of spermatogonia in Taeniid cestodes is mitosis with cells unseparated.

    实验研究
    EFFECT OF RNA AGAINST HEPATIC FIBROSIS IN RABBITS INFECTED WITH SCHISTOSOMAJAPONICUM
    PengYanzhong;HuangQitong;YanShaonan;DengBin;HuJijun
    1998, 16(3):  214-218. 
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    AIM: To study the effect of ribonucleic acid (RNA) against schistosomal hepatic
    fibosis in rabbits. METHODS: 54 rabbits were randomly and equally divided into normal group,
    infected group, and RNA group. On the 40,70,100th day after RNA i.m. injection, 6 rabbits from
    each of the above 3 groups were killed and their plasma and liver were examined by way of
    biochemistry and pathology. RESULTS: Compared with the infected group the collagen fiber of
    liver in RNA group was less produced, the hepatic cellular nucleolus was enlarged, the number of
    rough endoplasmic reticulum (RER) and the granules on the RER were increased, the collagen fiber
    around fat-storing cell was decreased, the content of hyaluronic acid in plasma, the hydroxyp
    roline level in liver tissue, the percentage of collagen fiber distribution and the collagen
    fiber level in liver tissue of RNA group were significantly reduced.CONCLUSION: RNA might play a
    role in the prevention of schistosomal hepatic fibrosis.