Loading...

Table of Content

    30 October 2015, Volume 33 Issue 5
    Malaria Situation in the People’s Republic of China in 2014
    ZHANG Li, ZHOU Shui-sen*, FENG Jun, FANG Wen, XIA Zhi-gui
    2015, 33(5):  1-319-326. 
    Asbtract ( )   PDF (1524KB) ( )  
    Related Articles | Metrics

    The 2014 malaria epidemiological data reported through the annual malaria statistics reporting system were collected and analyzed. A total of 3 078 malaria cases were reported in 680 counties of 30 Provinces/Municipalities/Autonomous Regions(P/M/A)(except Inner Mongolia) in 2014, decreased by 25.4% compared with the 4 128 cases in 2013. The incidence rate was 0.022 6/10 000. More cases distributed in Yunnan(17.3%, 533/3 078), Jiangsu (11.5%, 355/3 078), Sichuan(8.6%, 266/3 078), Henan(7.0%, 216/3 078) and Zhejiang(7.0%, 215/3 078) Provinces. Of all the cases, 56 (1.8%) were indigenous cases, mainly from the border area of Yunnan (comprising 9 counties) and the Tibet Autonomous Region(one county). Locally-infected falciparum malaria was only found in Yingjiang County (4 cases) and Cangyuan County (2 cases) of Yunnan. Indigenous malaria prevalence was of over 1/10 000 in Motuo County and Yingjiang County. There were 3 021 abroad-imported cases of malaria(98.1%), which widely distributed in the 30 P/M/As. In addition, one case of quartan malaria with long latency was reported in Guangdong Province. Of all the reported cases, 3 057 (99.3%) were further confirmed by plasmodium species, comprising 846 cases of vivax malaria(27.7%), 1 882 cases of falciparum malaria(61.6%), 3 cases of quartan malaria(1.7%), 231 cases of ovale malaria(7.6%), 44 cases of mixed infections, and one case of P. knowlesi malaria. Furthermore, 170 cases(5.5%) with severe conditions were reported in 16 P/M/As, and 25 deaths were reported in 15 P/M/As. In summary, remarkable achievements have been made in eliminating malaria in China, despite increases in imported cases. The border areas of Yunnan and Motuo County of Tibet Autonomous Region re-main the key regions for malaria elimination. Efforts are needed to reinforce the management of imported cases and the treatment of complicated malaria.

    Spatial Effect of the Dams and Sluices on the Risk of Schistosomiasis in Dongting Lake Region of Hunan Province
    ZHU Zheng1, HE Qing-yun2 *
    2015, 33(5):  2-328-337. 
    Asbtract ( )   PDF (3560KB) ( )  
    Related Articles | Metrics

    Objective  To determine the spatial effect of the dams and the sluices on the risk of schistosomiasis in Dongting Lake Region, and its mechanism, type and degree. Methods The positions, levels and types of the dams and the sluices in Dongting Lake Region of Hunan Province were marked on the base map. Epidemiological data of schistosomiasis among populations in 334 Townships in the Region were collected during March and July in each year of 2010-2014, and the 5-year average infection rate was calculated. A grid system composed of 1 220 hexagons was built to spatially quantify the effect of the dams and the sluices on the risk of schistosomiasis and the infection rates among populations. A two-step clustering was used to analyze the grid system, and the areas of infection peak were identified. The centrifugal model was used to simulate the degree and scope of the influence of these infection peak areas on the surrounding regions. The correlation coefficient model was used to determine the correlation coefficients between the dams and sluices and the spatial distribution of schistosomiasis. The correlation coefficients were then weighted, the integrated weighted risk of all grid cells calculated, and the weighted distribution figure for schistosomiasis risk produced. Results The results of two-step clustering revealed 15 areas of infection peak in the Region. The results of centrifugal model showed that the areas of infection peak significantly promoted the effect of the surrounding regions on the risk of infection. The correlation coefficients of the dams and the sluices with the infection rate among populations were 0.82 and 0.86, with the weights being 0.488 1 and 0.511 9,  respectively. The areas with high and relatively high risks of infection had a Crescent-shaped distribution along the Lishui River, West Dongting Lake, South Dongting Lake, East Dongting Lake and Chenglingji. The results were further verified by MAE testing. Conclusion The dams and sluices correlated strongly and positively with the risk of schistosomiasis. Fifteen areas of infection peak are identified to be determinant for schistosomiasis infection and spread, and have significant gradient spatial effect on schistosomiasis risk in surrounding areas.

    The Effect of Lipopolysaccharide-Induced Mouse B Cell Activation on Schistosoma japonicum Development
    TANG Hong-bin1,CHENG La-ying1,XIONG Tao2,DONG Hui-fen2 *,JIANG Ming-sen2
    2015, 33(5):  3-338-345. 
    Asbtract ( )   PDF (3737KB) ( )  
    Related Articles | Metrics

    Objective  To investigate the effect of lipopolysaccharide(LPS)-induced B cell activation on the development of Schistosoma japonicum.  Methods  Eighteen BALB/c nude mice deficient in T cells and 23 BALB/c SCID mice deficient in T and B cells were used in this study. Each was infected with 30±1 S. japonicum cercariae. The nude (n=9, NL group) and SCID(n=12, SL group) mice then received 2-3(every two weeks) intraperitoneal injections with LPS (100 μg/mL, 0.2 mL for each mouse). The remaining nude(n=9, N group) and SCID(n=11, S group) mice received PBS injection as control. The mice were sacrificed on days 28 and 36 after infection(n=4/5, 4/5, 5/6, 6/6 for N, NL, S and SL groups, respectively), and adult worms were collected by hepatic portal vein perfusion. The collecting rate of the adult worms was calculated, the body-length measured, and pairs of worms recorded. The liver tissue was collected and digested with 5% KOH, and the number of eggs per gram of liver tissue was calculated. The levels of TGF-β, IFN-γ and IL-10 in peripheral blood were evaluated. Spleen cell suspension was prepared for detecting the proportion of regulatory B cells(Bregs) in splenic lymphocytes.  Results  On day 28 after infection, the body-lengths of male worms in NL and N groups were (7.65±2.85) mm and (5.28±1.64) mm (P<0.01), and those of female worms were (9.64±1.99) mm and (7.49±1.63) mm (P<0.01), respectively. On day 36 after infection, the number of eggs per gram of liver tissue was significantly higher in the NL group than in the N group(1 088±297 vs 715±404, P<0.05), and significantly lower in the SL group than in the S group(217±33 vs 573±160, P<0.01). The proportions of CD1dhiCD5+CD19+ Bregs in N group on days 28 and 36 after infection were(12.73±0.96)% and(37.15±3.04)% (P<0.05), respectively, with no significant difference with that of NL group. The serum levels of TGF-β and IFN-γ on day 28 after infection were significantly different between N and NL groups(TGF-β, 101.75±46.72 vs 260.90±45.34 pg/mL; IFN-γ, 7.91±1.62 vs 14.11±3.72 pg/mL, both P<0.01). Similarly, significant difference was found for the plasma level of IL-10 on day 36 after infection between the S and N groups (41.85±3.14 vs 66.25±4.16 pg/mL, P<0.01), and between the SL and NL groups (44.48±3.87 vs 72.22±17.76 pg/mL, P<0.01), but not between the LPS groups and the control groups.  Conclusion  LPS can induce the release of cytokines (e.g. TGF-β) from B cells of mice infected with S. japonium, to facilitate the early development of adult female and male worms.

    Expression of Tim-3 on Peripheral CD56+ NK Cells and Its Correlation with Liver Fibrosis in Patients with Advanced Schistosomiasis
    WU Qi-wen1, ZHU Xiang1, FU Xia1, YANG Jin-sun2, CAO Zhi-guo3, PU Chun1 *
    2015, 33(5):  4-346-350. 
    Asbtract ( )   PDF (1048KB) ( )  
    Related Articles | Metrics

    Objective To explore the expression of T cell immunoglobulin and mucin domain protein 3 (Tim-3) on CD56+ NK cells in peripheral blood and its correlation with liver fibrosis indicators in patients with advanced schistosomiasis. Methods Tim-3 expression on CD56+ NK cells from 28 patients with advanced schistosomiasis and 30 healthy controls was determined by flow cytometry. The serum levels of IFN-γ and IL-4 were detected by enzyme-linked immunosorbent assay (ELISA). Fibroscan analyzer was used for liver stiffness measurement (LSM)to determine the extent of liver fibrosis. Four serological indicators of liver fibrosis, collagen type III N-peptide (PIIIP N-P), Laminin (LN), collagen IV (CIV) and hyaluronic acid (HA) were measured by the Automated Chemiluminescence Immunoassay Analyzer. Results Flow cytometry analysis showed that Tim-3 expression on CD56+ NK cells in advanced schistosomiasis patients was (62.3±11.4)%, significantly higher than that (52.1±6.5)% (P<0.01). In patients with advanced schistosomiasis and the healthy controls, the levels of PIIIP N-P were (86.5±29.5) ng/mL and (22.0±7.8) ng/mL, LN (49.3±21.5) ng/mL and (20.4±6.3) ng/mL, CIV (67.5±22.3) ng/mL and (22.0±3.9) ng/mL, HA (645.9±483.1) ng/mL and (54.7± 27.7) ng/mL, respectively. There were significant differences in all these indicators between the two groups (P<0.05). The levels of IFN-γ were (93.9±20.1) ng/L and (107.7±24.6) ng/L, and those of IL-4 were (46.6±11.8) ng/L and (28.9±8.9) ng/L respectively in patients with advanced schisto-somiasis and the healthy controls, both with significant differences (P<0.05). Spearman nonparametric correlation analysis showed that Tim-3 expression on CD56+ NK cells in patients was positively correlated with the levels of LSM, PIIIP N-P, LN, CIV and IL-4 (r=0.528-0.834, P<0.01), but negatively with serum IFN-γ (r=-0.501, P<0.01). No correlation was found with the HA level (r=0.352, P>0.05). Conclusion The expression of Tim-3 on peripheral CD56+ NK cells increases in patients with advanced schistosomiasis compared with the healthy controls, and it positively correlates with the levels of LSM, PIIIP N-P, LN, CIV and IL-4, four indicators of liver fibrosis.

    Endemic Situation of Echinococcosis in Gannan Tibetan Autonomous Prefecture
    MA Yu-an, SHANG Wen-jie*
    2015, 33(5):  5-352-356. 
    Asbtract ( )   PDF (453KB) ( )  
    Related Articles | Metrics

    Objective To understand the endemic status of echinococcosis in Gannan Tibetan Autonomous Prefecture. Methods The 2007-2013 survey data on hydatid disease prevention and control were collected from 8 counties/cities in Gannan Tibetan Autonomous Prefecture and analyzed. Ultrasound scanning was used to detect echinococcosis infection, ELISA was performed to detect anti-Echinococcus IgG in serum of children under 12 years, and double-antibody sandwich ELISA method was used to detect Echinococcus antigen in dog’s feces. Visceral dissection was performed to examine hydatid infection in domestic ruminants. Results The prevalence of echinococcosis in residents was 225/100 000(810/360 440), comprising 224/10 0000(807/360 440) for cystic echinococcosis and 1/100 000(3/360 440) for alveolar echinococcosis. The prevalence was 2.3/100 000(340/151 280) in males and 2.3/100 000(470/209 160) in females, with no significant difference(χ2=6.41,P>0.05). Among different age populations, the 30-40 age group had the highest proportion (44.2%, 358/810) to all detected infections. Besides, the prevalence was the highest in herdsmen, followed by farmers. Echinococcosis was detected in 372 administrative villages in the Prefecture. The positive rate for serum anti-Echinococcus IgG was 4.0%(1 921/47 841) in children under 12 years. The positive rate for Echinococcus antigen in dog’s feces was 5.5%(3 523/64 521). The rate of hydatid infection in domestic ruminants was 3.3%(1 148/35 134). After seven years’ comprehensive control, the prevalence of echinococcosis in residents dropped from 440/100 000(97/21 938) in 2007 to 290/100 000(160/55 954) in 2013(χ2=11.69,P<0.05). The positive rate for serum anti-Echinococcus IgG in children also dropped from 7.9%(150/1 902) in 2007 to 2.1%(151/7 100) in 2013. Consistently, the positive rate for Echinococcus antigen in dog’s feces dropped from 11.9% (335/2 819) in 2007 to 3.3%(466/13 608) in 2013 (χ2=338.52,P<0.05); and the rate of hydatid infection in domestic ruminants dropped from 8.8%(235/2 658) in 2007 to 1.5%(107/7 271) in 2013(χ2=317.86, P<0.05). Conclusion The control activities during 2007-2013 has shown significant achievements in reducing echinococcosis in Gannan Tibetan Autonomous Prefecture.

    Investigation on the Outbreak of Visceral Leishmaniasis in 2014 in Jiashi County of Xinjiang
    OSMAN Yisilayin1 *, SIMAYI Adili1, KEYUMU Kaisuer2, ABLIMIT Maimaitiaili3, JI Fang4,
    2015, 33(5):  6-357-361. 
    Asbtract ( )   PDF (800KB) ( )  
    Related Articles | Metrics

     Objective To understand the epidemiological characteristics of visceral leishmaniasis(VL) outbreak in Jiashi County of Xinjiang Uygur Autonomous Region in 2014, and provide basis for VL prevention and control strategies.  Methods Data on VL epidemic situation in Xinjiang from July 1, 2009 to June 30, 2015 were collected from Chinese CDC Infectious Disease Reporting Information Management System (reporting system). On-site epidemiological investigation was conducted in October, 2014, among children under 3 years in 23 villages in Gholtoghrak Township and Koxawat Township in Jiashi County, regions that had dramatically increased reports of VL cases from July 1. For suspected cases who showed symptoms such as fever and hepato-splenomegaly, blood (20 μl) was collected through fingerstick (with parental guardian consent) for rk39 immunochromatographic strip testing. Children with positive results were given sodium stibogluconate treatment (6×200 mg/kg, intravenously). Results A total of 637 VL cases were reported in Xinjiang from July 1, 2009 to June 30, 2015. Among the 192 cases reported from July 1, 2014 to June 30, 2015 in Xinjiang, cases from Jiashi County occupied 86.46% (166/192) of the cases. The number of VL cases in Jiashi County showed a trend of increase since the first report in August, with a total number of 114 in October, November and December. The 166 cases in Jiashi County had an age range of 23 days-8 years, with those under one year accounting for 95.18%(158/166). The 113 cases in Gholtoghrak Township of the County had an age range of 23 days-3 years, with those under one year accounting for 96.46% (109/113). The age-distribution of VL casess in the County accorded with the characteristic of the desert type. On-site investigation of 833 children in the 23 villiages revealed 11 children with positive results of rk39 immunochromatographic strip testing out of 14 suspected cases, all recovered after one course of sodium stibogluconate treatment. Conclusion In 2014, VL outbreak occurs in Jiashi County with 95% of the cases being children under one year old. This outbreak was identified to be the desert type.

    Molecular Detection of Giardia lamblia and Cryptosporidium Species in Pet Dogs
    GU You-fang, WANG Kai, LIU De-yi, MEI Nan, CHEN Cheng, CHEN Tao, HAN Min-min, ZHOU Li, CAO Jia-tong, ZHANG Heng, ZHANG Xue-liang, FAN Zi-lai, LI Wen-chao*
    2015, 33(5):  7-362-367. 
    Asbtract ( )   PDF (724KB) ( )  
    Related Articles | Metrics

    Objective  To determine the prevalence of Giardia lamblia and Cryptosporidium species infection in pet dogs, and identify the G. lamblia assemblages and Cryptosporidium species. Methods A total of 315 fresh fecal samples were collected from pet clinics in five counties of Anhui Province and in Hangzhou of Zhejiang Province. Hemi-nested-PCR targeting the GDH gene of G. lamblia and nested-PCR targeting the SSU rRNA gene of Cryptosporidium were performed in all the fecal samples. The PCR products were sequenced and analyzed using bioinformatics methods to identify the G. lamblia assemblages and Cryptosporidium species. Results The positive rates of G. lamblia and Cryptosporidium spp. infections in the 315 fecal samples were 3.2% (10/315) and 1.6% (5/315), respectively. Specifically, the two indicators were both significantly higher in dogs ≤12 months (17.8% and 11.1%, respectively) than in adult dogs (0.7% and 0.0%) (P<0.05). However, there was no significant difference in the two indicators between male and female dogs. In addition, two G. lamblia assemblages were identified, assemblages B(n=6) and D(n=4). Sequence analysis of PCR products of the SSU rRNA gene showed that the five Cryptosporidium isolates were C. canis(n=5). Conclusion The prevalences of G. lamblia and Cryptosporidium infection in pet dogs in Anhui and Zhejiang Provinces were 3.2 % and 1.6 %, respectively. The assemblages of G. lamblia in this study are of types B and D.

    Expression of Cocktail DNA Vaccine Comprising Toxoplasma gondii SAGl, MIC3 and ROP2 Using Fluorescent Protein-Reporting Vectors and Evaluation of Its Immunogenicity
    WANG Yan-juan, CAO Jian-ping, SUN Ya-wen, XU Yu-xin, SHEN Yu-juan*
    2015, 33(5):  8-368--371. 
    Asbtract ( )   PDF (882KB) ( )  
    Related Articles | Metrics

    Objective  To construct a cocktail DNA vaccine that expresses multiple genes of Toxoplasma gondii and investigate its immunogenicity in mice. Methods Genes for surface antigens(SAG), microneme(MIC), and rhoptry protein(ROP) were amplified from genomic DNA of T. gondii and then cloned separately into eukaryotic fluorescent protein expression vectors pShuttle-CMV-MCS-EF1α-AmCyan, pLVX-IRES-Zsgreen and pLVX-IRES-rfp, to construct expression plasmids pShuttle-SAG1, pLVX-Zsgreen-MIC3 and pLVX-rfp-ROP2. 293F cells were transfected with a combination of the three plasmids using the polyethylenimine(PEI) method. Forty-eight hours later, the expression of the three genes was observed under a fluorescence microscope. In addition, 30 C57BL/6 mice were randomized to receive intramuscular injection of saline(50 μl, group A), pShuttle+pLVX?鄄Zsgreen+pLVX-rfp empty plasmids(2 μg/μL, 17 μL of each, group B) and  pShuttle-SAG1+pLVX-Zsgreen-MIC3+ pLVX-rfp-ROP2 recombinant plasmid(2 μg/μL, 17 μL of each, group C). After 28 days, anti-T. gondii antibody in mouse serum was detected by ELISA, to evaluate the immunogenicity of the vaccine. Results  The SAG1, MIC3 and ROP2 genes were amplified from the genomic DNA, with product sizes of 1, 1.1 and 1.7 kb. The eukaryotic expression plasmids pShuttle-SAG1, pLVX-Zsgreen-MIC3 and pLVX-rfp-ROP2 were constructed, and the corresponding fluorescences(blue, green and red) were observed after transfection. On day 28 after mouse vaccination, ELISA showed that the mean A450 values for serum IgG in groups A, B and C were(0.620±0.029),(0.741±0.040) and(1.561±0.131), respectively, with the group C value being significantly higher than the others(P<0.01). Conclusion The cocktail DNA vaccine comprising T. gondii SAGl, MIC3 and ROP2 shows promising immunogenicity in mice, and the fluorescent protein expression vectors are reliable tools for expression of the target genes.

    Extraction Method of Malaria Parasite DNA from Preserved Positive Blood Smears
    XU Chao,WEI Qing-kuan,LI Jin,XIAO Ting,JIA Feng-Ju,WANG Wei-yan,YIN Kun,FU Ting-Xia,ZHAO Gui-hua,LIU Gong-zhen,HUANG Bing-cheng*
    2015, 33(5):  9-372-376. 
    Asbtract ( )   PDF (546KB) ( )  
    Related Articles | Metrics

     Objective  To develop a method for DNA extraction from malaria parasites on preserved blood smears, to provide basis for research on malaria genetic traceability.  Methods  The improved DNA extraction kit(QIAamp DNA Mini Kit) was used to extract plasmodium DNA from 41 giemsa-stained blood smears, and the extraction was compared with that using the Chelex-100 and Na2HPO4 methods. Nested PCR was used to amplify small subunit ribosomal RNA to identify Plasmodium parasite. The PCR products underwent sequencing and sequence alignment, to analyze the difference in PCR positive rates between blood smears prepared in the 1980s and in recent 10 years, between blood smears with and without deoil/decoloration, and between blood smears with different qualities.  Results  The total PCR positive rate for the improved kit method was 70.7% (29/41). The PCR positive rate for blood smears prepared in the 1980s and in recent 10 years was 78.6% (11/14) and 66.7% (18/27) respectively, with no significant difference (χ2=0.63, P>0.05). The PCR positive rate for blood smears with and without deoil/decoloration was 62.5% (15/24) and 82.4% (14/17) respectively, also with no significant difference (χ2=1.89, P>0.05). However, the PCR positive rate was significantly higher in blood smears with high quality [93.3%(28/30)] than those with low quality[9.1%(1/11)](χ2=27.59, P<0.01). Sequence alignment showed that the PCR products were consistent with the target DNA fragments. However, DNA extracted using the Chelex-100 and Na2HPO4 methods showed negative PCR results.  Conclusions  DNA extracted from blood smears prepared in the 1980s using the improved Kit  (QIAamp DNA Mini Kit) shows a high PCR positive rate. Besides, blood smear staining and use of oil for microscopic examination do not affect DNA extraction.

    SWOT Analysis of the National Survey on Current Status of Major Human Parasitic Diseases in China
    ZHU Hui-hui,ZHOU Chang-hai,CHEN Ying-dan*,ZANG Wei,XIAO Ning,ZHOU Xiao-nong
    2015, 33(5):  10-377-381. 
    Asbtract ( )   PDF (478KB) ( )  
    Related Articles | Metrics

    The National Survey on Current Status of Major Human Parasitic Diseases in China has been carried out since 2014 under the organization of the National Health and Family Planning Commission of the People’s Republic of China. The National Institute of Parasitic Diseases, Chinese Center for Disease Control and Prevention(NIPD, China CDC) provided technical support and was responsible for quality control in this survey. This study used SWOT method to analyze the strengths, weaknesses, opportunities and threats that were encountered by the NIPD, China CDC during the completion of the survey. Accordingly, working strategies were proposed to facilitate the future field work. 

    Recombinase Polymerase Amplification and its Applications in Parasite Detection
    ZHENG Wen-bin1,2, WU Yao-dong1, MA Jian-gang1,2, ZHU Xing-quan1, ZHOU Dong-hui1 *
    2015, 33(5):  11-382-386. 
    Asbtract ( )   PDF (741KB) ( )  
    Related Articles | Metrics

    Recombinase polymerase amplification(RPA) is a recently-developed isothermal nucleic-acid-amplification technology that is based on the nucleic acid replication mechanism in T4 bacteriophage. With this technique, nucleic-acid templates can be amplified to measurable levels within 20 min at 37-42 ℃. The RPA process has high sensitivity and specificity, and is simple to operate,  thus nucleic acids can be detected rapidly in non-laboratory conditions. Since its development in 2006, the RPA technique has been applied in agriculture, food safety, medicine, transgene detection, etc. In this review, we will give an overview on the research progress of RPA and its application in parasite detection.

    Research Progress on Genetic Diversity in Animal Parasitic Nematodes
    YIN Fang-yuan1,2, LI Fa-cai1,2, ZHAO Jun-long1, HU Min1 *
    2015, 33(5):  12-387-392. 
    Asbtract ( )   PDF (467KB) ( )  
    Related Articles | Metrics

    The development of molecular genetic markers for parasitic nematodes has significant implications in fundamental and applied research in Veterinary Parasitology. Knowledge on genetic diversity of nematodes would not only provide a theoretical basis for understanding the spread of drug-resistance alleles, but also have implications in the development of nematode control strategies. This review discusses the applications of molecular genetic markers(RFLP, RAPD, PCR-SSCP, AFLP, SSR and mitochondrial DNA) in research on the genetic diversity of parasitic nematodes.

    The Anatomical Method of Isolating Central Ganglia from Oncomelania hupensis
    TAN Ping*,YU Zhi-jun
    2015, 33(5):  13-350-351. 
    Asbtract ( )   PDF (481KB) ( )  
    Related Articles | Metrics

    In this experiment the soft tissue of Oncomelania hupensis was obtained by breaking the shell with a hemostat. The central ganglia of O. hupensis were then collected from the fresh soft tissue under a dissecting microscope. This method lays a base for studying the effects of molluscicides or various biological and physicochemical factors on the central ganglia of O. hupensis.

    Malaria Epidemic Situation in Rudong County of Jiangsu Province during 1999-2014
    MIAO Ping,Chen Hong-xin
    2015, 33(5):  14-393-394. 
    Asbtract ( )   PDF (295KB) ( )  
    Related Articles | Metrics

    From 1999 to 2014 a total of 23 cases of malaria were reported in Rudong County, Jiangsu Province, comprising one indigenous case of vivax malaria, 9 imported cases of vivax malaria, and 13 imported cases of falciparum malaria. The imported cases accounted for 95.7%(22/23) of all cases. The first diagnosis was mainly made in town hospitals and village clinics, accounting for 60.9%. There was no obvious seasonal variation in disease onset, and all cases reported in 2004 were imported.

    Investigation of Soil-Transmitted Nematode Infections in Xuchang City of Henan Province in 2012
    PENG Jin-hua*
    2015, 33(5):  15-395-396. 
    Asbtract ( )   PDF (364KB) ( )  
    Related Articles | Metrics

    The Weidu District, Yanling County and Yuzhou City were selected in Xuchang City for investigation of the status of soil-transmitted nematode infections in 2012, in accordance with the National Monitoring Program for Soil-Transmitted Nematodiasis(2011 Revised Edition). Kato-Katz technique was used to detect soil-transmitted nematodes in feces of residents over 3 years old, and the cellophane tape peri-anal swab method was used to detect pinworm eggs in children between 3-12 years. A total of 2 991 fecal samples were examined. The total infection rate of soil-transmitted nematodiasis was 4.3%(128/2 991), decreased by 63.0% and 55.1% when compared with that in 2010(11.6%) and that in Henan Province in 2004(9.5%) respectively. The infection rates of roundworms, whipworms, hookworms and pinworms were 3.7%(110/2 991), 0.3%(9/2 991), 0.1%(3/2 991), and 0.2%(6/2 991), respectively, all showing mild intensity of infection. The infection rate of soil-transmitted nematodiasis was highest in farmers (5.5%,113/2 059), followed by children (3.1%,3/98).