ABSTRACT
Objective To summarize and analyze the epidemic situation and trend of animal plague in plague foci of Gansu section of Golmud-Dunhuang railway,and provide basic reference for prevention and control of the plague.Methods The quantity of Marmot,rate of carrying fleas and flea index,plague serological and etiology detection results,the cross analyzing results of the railway section and the animal plague foci in Gansu section of Dolmud-Dunhuang railway (Akesai and Subei counties) from 2010 to 2015 were analyzed via the retrospective analysis method.Results The total average density of Marmot of Golmud-Dunhuang railway crossing area Akesai and Subei counties was between 0.23-0.41 per hectare between 2010 and 2015.The rate of parasitic dye fleas in plague foci of Akesai was between 11.30％ and 32.65％,body flea index was 0.74-1.84.The rate of parasitic fleas dye fleas in plague foci of Subei was between 5.34％ and 14.07％,the flea index was 0.25-2.04.The etiology detection Marmot plague of Akesai and Subei was 2 049,142 of them were positive,the positive rate was 6.93％;592 groups of vector were detected,44 of them were positive;the positive rate was 7.43％.There was no statistically significant difference between inspection bacteria rate and parasitic vector inspection rate of Marmot (x2 =0.014,P ＞ 0.05).Totally 1 719 serums of Marmot were tested,132 of them were positive,the positive rate was 7.68％.Totally 421 serums of Canis lupus familiaris were detected,61 of them were positive,the positive rate was 14.49％.There was statistically significant difference between the serum positive rate of Marmot and Canis lupus familiaris (x2 =19.116,P ＜ 0.05).Totally 17 animal foci were found along the railway in 2013,the nearest distance of the foci of bid from construction was 0.5 km,popular area was 61.02 km2,and 1 360 people were directly threatened.Conclusions Animal plague in Akesai and Subei regions along Golmud-Dunhuang railway is highly active.So we must take effective measures to guarantee the smooth progress of railway construction.
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Objective To investigate clinical significance of the changes in the peripheral blood T lymphocytes subsets in patients with diseases related to HBV infection .Methods 257 cases of inpatients and outpatients were selected from Jan .to Dec .2013 ,and were divided into hepatitis B carriers (ASC)group ,chronic hepatitis B(CHB)group ,hepatocirrhosis(LC)group and primary liver cancer(PHC)group according to types of diseases related to HBV infection .Other 50 healthy individuals conducted physical exami‐nation were enro1led in the control group .The absolute CD3+ ,CD4+ and CD8+ T‐cell count ,and CD3+ ,CD4+ and CD8+ percent‐age and CD4+ /CD8+ value were detected in all subjects by using flow cytometer .These data were compared and analyzed .Results Compared with the control group ,there were no significant differences of the absolute CD3+ ,CD4+ and CD8+ T‐cell count ,and CD3+ ,CD4+ and CD8+ percentage and CD4+ /CD8+ value in ASC group ,CHB group and LC group(P>0 .05) .Compared with the control group ,the absolute CD4+ T‐cell count ,CD4+ percentage and the CD4+ /CD8+ value were decreased in the PHC group , while the CD8+ percentage were increased in the PHC group ,there were statistical significant differences between the two groups (P<0 .05) .Conclusion The peripheral blood T lymphocyte subsets could be monitor indexes of cell immune function in diseases related to HBV infection .
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Objective To detect amniotic fluid ABH blood group substances and ABO blood group genotype by the polymerase chain reaction with sequence-specific primers(PCR-SSP) to increase the prenatal diagnosis of fetal ABO blood group .Methods 53 pregnant women with gestational age 16 -25 weeks were selected .Amniotic fluid was extracted for detecting ABH blood group substances by the serological indirect agglutinating reaction ;the amniotic fluid cells were separated for extracting DNA .Then the PCR-SSP technique was adopted to analyze the ABO blood group genotypes .Results 16 specimens of amniotic fluid were non-se-creting type phenotype(30 .2% ) and 37 specimens of amniotic fluid were secreting type phenotype (69 .8% );48 specimens of amni-otic fluid were detected out the ABO blood group genotype by the PCR-SSP method .ABO blood group of fetal amniotic fluid cells by the gene identification was consistent to the detection results of amniotic fluid secreting type ABH blood group substances .Con-clusion The PCR-SSP technique can accurately detect the fetal amniotic fluid cells ABO blood group .
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Objective To establish the chip technology‐based real‐time PCR (RT‐PCR) platform and to apply it in the viral loads detection of HIV‐1 and HCV .Methods Based on the primers designed to aim at the conversed regions of HIV‐1 and HCV , The gene chip tube was prepared ,and the RT‐PCR reaction system was established for the simultaneous determination of viral loads .And the melting curves were used to distinguish viral species .The sensitivity and specificity of the method were estimated , and performance of the method was verified by using clinical samples .Results The specificity of the method was good .The lowest detectable limit of the detection method of HCV and HIV‐1 was 1 × 103 copy/mL .The clinical samples with viral loads around 1 × 103 -1 × 106 copy/mL could be detected accurately .Conclusion The method provides a new idea for the detection of HCV and HIV‐1 .