1.Ertapenem for the treatment of bacterial liver abscess
Tiemin PEI ; Zhiyang HAN ; Keyan Lü ; Yong MA ; Dalong YIN ; Lianxin LIU
Chinese Journal of General Surgery 2012;27(5):367-369
ObjectiveTo explore the efficacy of an antibiotic ertapenem for the treatment of bacterial liver abscess. MethodThe clinical data of 134 hospitalized bacterial liver abscess patients were retrospectively analyzed to evaluate the clinical and bacteriological efficacy of ertapenem from March 2009-2011in our hospital. ResultFever was present in 122 (91%)cases,abdominal pain was complained in 70 (52.2% ) cases and rigor in 66 (49.3% ) cases.In 92(68.7% ) cases the abscess was located in the right lobe of the liver.Leukocytosis and liver dysfunction were found in 73 cases(54.8% ) and 84 cases (62.7% ),respectively.Ultrasonography was the most effective diagnostic means for liver abscess.Fortyone cases(30.6% )were treated conservatively with ertapenem and 82(61.2% )were treated with ertapenem associated with percutaneous liver puncture aspiration and 11cases (8.2% )were treated with ertapenem associated with surgery.The clinical success rate was respectively 89%,87.8%,90.9%.The average duration of medication and length of stay were respectively ( 7.0 ± 2.4 ) d and 14.2 d.Ninety-seven pathogens were isolated from samples and predominant strains were Klebsiella species.Bacterial eradication rate was 92.8%.The sensitivities of isolated bacteria to ertapenem were 94.8%.ConclusionsErtapenem administration is effective therapy for bacterial liver abscess.
2.Application of CRISPR/Cas9 genome editing technology for inhibition of hepatitis B virus replication
Tao WU ; Xiaojuan ZHU ; Lunbiao CUI ; Huan FAN ; Yin CHEN ; Xiling GUO ; Kangchen ZHAO ; Zhiyang SHI ; Fengcai ZHU
Chinese Journal of Microbiology and Immunology 2015;(8):600-605
Objective To evaluate the practicability of using CRISPR/Cas9 genome editing tech-nology for inhibition of hepatitis B virus ( HBV) replication. Methods Two sgRNA targeting sites were de-signed for the S region of HBV genome. The CRISPR/Cas9 expression plasmids specific for HBV were con-structed and then transfected into a cell line expressing HBV genome(HepG2-N10). The cytotoxicity of cells transfected with different expression plasmids were detected by MTT assay. The levels of hepatitis B surface antigen ( HBsAg ) were determined by using chemiluminescent immunoassay ( CLIA ) . The expression of HBV at mRNA level was analyzed by quantitative real-time PCR ( qRT-PCR) . The qPCR was performed for the detection of extracellular and intracellular HBV DNA. The next-generation sequencing ( NGS) Illumina MiSeq Platform was used to analyze HBV genome editing. Results No significant cytotoxic effects were de-tected in HepG2-N10 cells transfected with different expression plasmids. Compared with the cells carrying pCas-Guide-GFP-Scramble, the levels of HBsAg in the supernatants of transfected cell culture harboring pCas-Guide-GFP-G1 and pCas-Guide-GFP-G2 were decreased by 24. 2% (P<0. 05) and 16. 9% (P>0. 05), respectively. The levels of HBsAg in cells transfected with pCas-Guide-GFP-G1 and pCas-Guide-GFP-G2 were respectively decreased by 16. 4% (P>0. 05) and 32. 1% (P>0. 05) as compared with that of pCas-Guide-GFP-Scramble transfected group. The expression of HBV at mRNA level was inhibited as indica-ted by the results of qRT-PCR. Moreover, the levels of extracellular HBV DNA were respectively suppressed by 23% (P>0. 05) and 35% (P<0. 05), and the levels of intracellular HBV DNA were respectively sup-pressed by 7. 2% (P>0. 05) and 18% (P>0. 05). Different types of insertion/deletion mutation were de-tected in HBV genome by high-throughput sequencing. Conclusion HBV-specific CRISPR/Cas9 system could inhibit the expression of HBV gene and the replication of virus. Therefore, the CRISPR/Cas9 genome editing technology might be used as a potential tool for the treatment of persistent HBV infection.
3.Resting state functional connectivity analysis of the frontal lobe-amygdala in different age paragraph female patients with bipolar disorder
Yinzhu MA ; Shengnan WEI ; Zhiyang YIN ; Xuesheng FAN ; Dahai WANG ; Yanqing TANG ; Fei WANG
Chinese Journal of Nervous and Mental Diseases 2017;43(12):710-714
Objective To find frontal lobe-amygdala functional connections in different age paragraph female patients with bipolar disorder. Methods The FMRI date were acquired from 30 patients with bipolar disorder aged 13 to 25 years old and 30 age-and education level-and gender-matched health controls.FMRI was also conducted on 30 patients with bipolar disorder aged 26 to 45 years old and 30 age-and education level-and gender-matched health controls.The date was calculated by using MATLAB based DPARSF software. Results Compared with corresponding health controls, the lobe-amygdala functional connections significantly decreased in patients aged 13 to 25 years but remained unchanged in patients aged 26 to 45 years old. Conclusions The decrease in the frontal lobe-amygdala functional connections decreased in female patients aged 13 to 25 years old may be related to the underdevelopment in vulnerable immature brain.In contrast, the frontal lobe-amygdala functional connections in female patients aged 26 to 45 years old remain intact.
4. Rapid detection of human adenovirus by recombinase polymerase amplification assay and lateral flow dipstick
Kangchen ZHAO ; Yiyue GE ; Lunbiao CUI ; Yin CHENG ; Zhiyang SHI ; Fengcai ZHU ; Minghao ZHOU
Chinese Journal of Experimental and Clinical Virology 2017;31(4):357-361
Objective:
To establish a rapid and sensitive isothermal amplification assay for the detection of human Adenovirus.
Methods:
Primers and probe used for recombinase polymerase amplification(RPA)were designed based on the conserved region of the adenoviruses hexon gene. After optimizing the reaction temperature and times, the products of RPA were detected by capillary electrophoresis and lateral flow dipstick(LFD). Sensitivity and specicity of the assay were evaluated. The diagnostic value of the RPA-LFD assay was verified using clinical samples which were simultaneously tested by real time PCR assay.
Results:
The analytical sensitivity of RPA-LFD assay was 2 copies DNA molecules per reaction and no cross reaction with other pathogens was observed. Compared with real-time PCR assay, the sensitivity, and specificity of the present assay were all 100%.
Conclusions
The RPA-LFD assay developed in this study has the characteristics of high specificity, sensitivity, rapid and no requirement of expensive equipment which provided a new tool for rapid detection of human adenovirus.
5.Spontaneous Regional Brain Activity in Healthy Individuals is Nonlinearly Modulated by the Interaction of ZNF804A rs1344706 and COMT rs4680 Polymorphisms.
Lingling CUI ; Fei WANG ; Miao CHANG ; Zhiyang YIN ; Guoguang FAN ; Yanzhuo SONG ; Yange WEI ; Yixiao XU ; Yifan ZHANG ; Yanqing TANG ; Xiaohong GONG ; Ke XU
Neuroscience Bulletin 2019;35(4):735-742
ZNF804A rs1344706 has been identified as one of the risk genes for schizophrenia. However, the neural mechanisms underlying this association are unknown. Given that ZNF804A upregulates the expression of COMT, we hypothesized that ZNF804A may influence brain activity by interacting with COMT. Here, we genotyped ZNF804A rs1344706 and COMT rs4680 in 218 healthy Chinese participants. Amplitudes of low-frequency fluctuations (ALFFs) were applied to analyze the main and interaction effects of ZNF804A rs1344706 and COMT rs4680. The ALFFs of the bilateral dorsolateral prefrontal cortex showed a significant ZNF804A rs1344706 × COMT rs4680 interaction, manifesting as a U-shaped modulation, presumably by dopamine signaling. Significant main effects were also found. These findings suggest that ZNF804A affects the resting-state functional activation by interacting with COMT, and may improve our understanding of the neurobiological effects of ZNF804A and its association with schizophrenia.