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25 June 2008, Volume 3 Issue 2
    

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    Review
  • WENG Xin-hua
    Journal of Microbes and Infections. 2008, 3(2): 0-72.
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  • 论著
  • YU Chun-hua; LI Qiong; HUANG Rui
    Journal of Microbes and Infections. 2008, 3(2): 67-69.
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    Objective To identify the antibiotic sensitivity of multi-drug resistant Salmonella typhi and detect its resistant genes. Methods 5 resistant Salmonella typhi strains and 1 sensitive strain was selected randomly, then antibiotic susceptibility to 12 different antibiotics were tested by K-B method. Reserpine inhibition test was also performed to find the drug excretion system. TEM type of β-lactamase gene, aminoglycosides modifying enzyme gene aac(6′)-Ⅰb, aac3-Ⅱ, qacEΔ1-sul1 gene, catA, catB gene, and cmlA gene were detected by PCR process. Results 5 multi-drug resistant strains were resistant to ampicillin, piperacillin, cefuroxime, ceftazidime, kanamycin, gentamycin, trimesulf and chloramphenicol, and they were all sensitive to meropenem, cefoperazone and cefepime; they showed an intermediate sensitivity to cafalotin. The strain which doesn’t carry pRST98 was sensitive to all of the antibiotics. All strains were negative in reserpine inhibition test. 5 drug-resistant strains carried aac3-Ⅱ、qacEΔ1-sul1 and catA gene, 4 of them harbored TEM type of β-lactamase gene, but none of the 5 strains carried aac(6′)-Ⅰb, catB or cmlA. Conclusion The multi-drug resistant Salmonella typhi strains carrying pRST98 contained an array of drug resistant genes, which lead to the resistance to different antibiotics.

  • ZHOU Qian-yi; ZHANG Jian-lei; WEI Jing-ping

    Journal of Microbes and Infections. 2008, 3(2): 70-72.
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    Objective To investigate the antimicrobial resistance of enterococcus faecalis and enterococcus faecium in our hospital for the rational use of antibiotic. Methods GPI plate was applied for bacterial identification and susceptibility testing.Whonet5 software was used for data analysis. Results Less than 50% of enterococcus faecalis and enterococcus faecium isolates were resistant to chloramphenicol and nitrofurantoin. Less than 1% of enterococcus faecalis and enterococcus faecium isolates were resistant to vancomycin. The resistance rate of enterococcus faecalis to penicillin G, high concentration gentamicin, ciprofloxacin, rifampicin and erythromycin descend year by year, and that of enterococcus faecium to ciprofloxacin, rifampicin and nitrofurantoin was opposite. In addition, the resistance rate of enterococcus faecium to most antibiotic was higher than enterococcus faecalis. Conclusions The enterococcus faecalis and enterococcus faecium is becoming multi-resistant bacteria. Antimicrobial therapy should be decided according to the results of susceptibility testing.
  • ZHAO Su-ying; LI Min; LI Ke-juan
    Journal of Microbes and Infections. 2008, 3(2): 73-74.
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    Object To study the etiology of COPD sufferer and compare the drug sensitivity with whole hospital. Method Identify the bacterium by VITEK,detect the drug sensitivity、ESBLs and MRS with K-B method according to NCCLS, statistic analysis with WHONET 5.4. Result In positive samples, Klebsiella pneumoniae、Pseudomonas aeruginosa and Escherichia coli are responsible for the first、second and the third,Gram-positive bacterium are mostly consisted of Staphylococcus and Enterococcus,ESBLs and MRS are respectively 78.5%,76.1%. Fisher probabilities shows the drug resistance ratio of Gram-negative bacterium is higher than the whole hospital evidently. Conclusion In COPD sufferer,Gram-negative bacterium are in the ascendant and the drug resistance ratio is higher than whole hospital;high detection of ESBLs and MRS means the high drug resistance of the bacterium.
  • LI Xiao-xiao1; REN Jun1; WANG Long2; MA Zhang-mei1; WANG Zhu-gang2; XIE You-hua1.3; Wen Yu-mei1.3

    Journal of Microbes and Infections. 2008, 3(2): 75-79.
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    Objective To verify the changes of a circadian gene dbp ( coding for the D site albumin promoter binding protein) in liver tissues of HBsAg positive transgenic mice. Methods Real-time fluorescent quantitative PCR was used to compare the transcriptional levels of dbp in male and female HBsAg positive transgenic mice versus their controls. Individual transgenic mouse and mice at different time points were used to study the regulation of dbp. Results In the liver tissues from both #59 and #10 lineages of HBsAg positive transgenic mice, dbp was up-regulated, compared to their control counterparts, but there was marked individual variability. Preliminary results showed that in HBsAg negative female mice, the transcriptional level of dbp was higher than that in male mice. This difference was more marked in HBsAg positive female transgenic mice. At 8:00 and 2:00, dbp was up-regulated in HBsAg positive transgenic mice, compared to the controls. However, at 8:00 and 2:00, the dbp transcriptional levels were similar between HBsAg positive transgenic mice and the controls. Conclusions For the first time it is reported that dbp was up-regulated in HBsAg positive transgenic mice, which provided evidence that HBV protein expression could be associated with changes in a circadian gene. Further studies are needed to confirm whether this up-regulation can also be found in patients, and clarify the implications of this observation.
  • GONG Kuang-long; YOU Yong-yan; ZHANG Jin-ping; SUN Huo-hua; SHA Zhong; GONG Xiang-dong
    Journal of Microbes and Infections. 2008, 3(2): 80-83.
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    Objective Chlamydia trchomatis and Neisserria gonorrhoeae are the primary bacterial pathogens causing urethral infection in men.Methlend blue stain is used to detect urethral inflammation, suggestive of infection, in men and guide threapeutic dicisions. In the absence of signs, symptoms or polymorphonuclear leukocyte on methlend blue stain(PMNLs).The tctreatment is deferred on management. Studing relation about Chlamydia-infected,Gonorrhea-infeced and PMNLs who compare their clical characteristics of urethral inflammation in men. Metholds 3,000 were presenting for routine sexually transmitted disease care with uethral PMNLS count, the direct qualitive detection of Chlamydia trachomatis antigen and culture. Results: Among 3,000 eligible men,387(12.0%) had chlamydia and 415(13.8%)had gonorrhea. Among chlamydia-infected men,PMNLS per oil-immersion field were ≥5 in 242(62.5%), 1 to 4 in 59(15.2%),and none in 86(22.2%),36(9.3%) and 141(36.4%) in men were asympomati or signs at that stage oa their infection. Among gonorrhea-infected, PMNs per oil-immersion field were ≥5 in 397(95.7%), 1 to 4 in 10(2.4%), none in 8(1.9%), 5(1.2%) and 46(11.1%) in men were asympomati or signs at that stage oa their infection. And an additional 86 were coinfeced with both organisms. PMNLs were≥5 in 76,1 to 4 in 5,none in 5. Conclusions:The paper used to analyze the ralationship of urethral inflammation PMNs,Chlamydia trachomatis and Neisseria gonorrhoeae infetion.The pations of chlamydia、gonorrhea and PMNLs in men infected have obvious difference(P<0.001). 86(22.2%) of chlamydial and 8(1.2%)of gonococcal infection had no evidence of PMNLs. It is strenuous that both of clical and testing teehnicality is important to increase dignosis for urthral inflammation in men and control sexually transmitted disease.
  • LIU Hua , CHEN Zhiao , CHENG Yu-ming, YUAN Zheng-hong
    Journal of Microbes and Infections. 2008, 3(2): 84-89.
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    Objective To investigate the role of Hepatitis B surface antigen (HBsAg) in the immune escape of innate immunity by Hepatitis B virus (HBV). Methods After treated with PMA, THP-1 was differentiated into macrophage- like cells. Macrophage- like cells were treated further with LPS and the pam3csk4 in the presence or absence of HBsAg. Cytokine IL-10 , IL-12 protein, IL-10, IL-12 mRNA levels , NF-κB p65 protein nuclear translocation as well as IκB-α degradation and ERK protein phosphorylation were detected to monitor the activation of the TLR signaling pathway. Results LPS and the pam3csk4 induced production of cytokine IL-10 , IL-12 protein, NF-κB p65 protein nuclear translocation as well as IκB-α degradation and ERK protein phosphorylation were inhibited by HBsAg in a dose-dependent manner. Conclusion HBsAg inhibit the activation of TLR2 and TLR4 signaling pathway.
  • WANG Qing-zhong1,2; ZHANG Lu1; XU Ying1; CHEN Jia-zhen1; ZHU Bing-dong1; QIE Ya-qing1; WANG Jiu-ling1; WANG Hong-hai1
    Journal of Microbes and Infections. 2008, 3(2): 90-93.
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    Objective To detect the subcellular location of Rv2629 in Mycobactrium tuberculosis, and the drug susceptibility testing of transformed M. smegmatis. Methods Different component of Mycobacterium tuberculosis were separated by differential velocity centrifugation, and subcellular location of Rv2629 was examined by Western-Blot. pMV261 plasmid was used to transformed the Rv2629 gene to M. smegmatis. RIF resistant was assayed by BACTEC MGIT 960 instrument. Results The subcellular location of Rv2629 was major at cell wall and cell membrane. The MIC of RIF for M. smegmatis transformed with mutated Rv2629 was 160μg/mL. While the MIC for wild type Rv2629 gene was 20μg/mL similar to the parental strain. Conclution These results indicate that the 191A/C mutation of Rv2629 gene is associated with RIF resistance.
  • 病例分析
  • LIU Li1; LU Hong-zhou1,2
    Journal of Microbes and Infections. 2008, 3(2): 94-96.
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  • 综述
  • ZHANG Yuan-yuan; ZHONG Jiang
    Journal of Microbes and Infections. 2008, 3(2): 97-99.
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  • WANG Yin-chun
    Journal of Microbes and Infections. 2008, 3(2): 100-102.
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  • WU Da-lei; SHEN Xu
    Journal of Microbes and Infections. 2008, 3(2): 103-106.
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  • ZHANG Yi-bo; NI Yu-xing
    Journal of Microbes and Infections. 2008, 3(2): 107-110.
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  • ZHANG Kuo; WEI Yu-xiang; LI Jin-ming
    Journal of Microbes and Infections. 2008, 3(2): 111-114.
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  • WANG Xu; SHEN Xu
    Journal of Microbes and Infections. 2008, 3(2): 115-117.
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  • JU Chang-yan; LIU Heng-chuan
    Journal of Microbes and Infections. 2008, 3(2): 118-120.
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