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基因芯片技术对结核分枝杆菌耐药性检测的临床应用 被引量:7

Clinical application of gene chip technology in the detection of drug resistance of Mycobacterium tuberculosis
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摘要 目的评价基因芯片技术对结核分枝杆菌耐药性检测的效果。方法选取我院结核科2014年3月至2016年3月收治的涂片阳性的肺结核住院患者238例,取其痰标本,分别用基因芯片、传统的罗氏培养和药敏试验3种方法进行结核分枝杆菌的异烟肼耐药性检测和利福平耐药性检测;把罗氏培养和药敏试验的结果作为金标准,评价基因芯片技术的临床应用价值。结果基因芯片技术检测涂片阳性患者痰标本异烟肼耐药的情况与金标准无显著差异(P>0.05);利福平耐药的情况与金标准相比也无明显差异(P>0.05)。结论基因芯片能够快速、准确地检测结核分枝杆菌对利福平和异烟肼的耐药情况,是一种值得推广的临床实验室检测方法。 Objective To evaluate the effect of gene chip technology on the drug resistance of Mycobacterium tuberculosis. Methods 238 patients with smear positive pulmonary tuberculosis admitted to our hospital from March 2014 to March 2016 were selected as the subjects. Three methods were used to detect isoniazid resistance and rifampicin resistance of Mycobacterium tuberculosisin sputum samples: gene chip,traditional Roche culture and a drug sensitivity test. The results of Roche culture and drug sensitivity test were used as the gold standard to evaluate the value of gene chip technology. Results There was no significant difference in the resistance rate of smear positive patients with isoniazid detected with gene chip and the gold standard(P〉0.05). Similarly, there was no significant difference between the rifampin resistance rate determined by gene chip and the gold standard(P〉0.05). Conclusion Gene chip technology can rapidly and accurately detect the resistance of Mycobacterium tuberculosis to rifampicin and isoniazid, and it is a valuable clinical laboratory diagnostic method.
作者 陈瑶 吴英松 CHEN Yao WU Yingsong(School of Laboratory Medicine and Biotechnology, Southern Medical University, Guangzhou, Guangdong, China, 510515)
出处 《分子诊断与治疗杂志》 2017年第2期108-111,共4页 Journal of Molecular Diagnostics and Therapy
基金 重大传染病创新检测试剂的研制和应用研究(广州市协同创新重大专项 201400000004-1)
关键词 基因芯片技术 结核分枝杆菌 耐药性 检测 Gene chip technology Tuberculosis Drug resistance Detection
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  • 1雍刚,杨曦,廖巫山,喻林冲,麦涛,王有为.三种淋球菌培养基分离效果对比分析[J].实用医院临床杂志,2008,5(2):46-47. 被引量:2
  • 2王晓宏,熊正英.多重PCR-质谱联用技术在病原体检测中的应用及比较[J].微生物学免疫学进展,2011,39(4):81-83. 被引量:4
  • 3Lu Lu,Yang Gao,Miao Xu,Ru-Cun Ge,Lin Lu.Gene expression profiles associated with osteoblasts differentiated from bone marrow stromal cells[J].Asian Pacific Journal of Tropical Medicine,2014,7(5):344-351. 被引量:1
  • 4罗渊,刘伯华,祝庆余.悬浮芯片在核酸和蛋白质检测中的应用[J].微生物学杂志,2007,27(2):78-82. 被引量:9
  • 5Vanhee LM, Meersseman W, Laqrou K, et al. Rapid and direct quan- tification of viable Candida species in whole blood by use of immu- nomagnetic separation and solid - phase cytometry[ J]. J Clin Micro- biol,2010,48(4) :1126 - 1131.
  • 6Datta S, Janes ME, Simonson JG. Immunomagnetic separation and coagglutination of Vibrio parahaemolyticus with anti-flagellar protein monoclonal antibody [ J ]. Clin Vaccine Immunol, 2008,15 ( 10 ) : 1541 - 1546.
  • 7Yang ZY, Shim WB, Kim KY, et al. Rapid detection of enterotoxi- genic Clostridium perfringens in meat samples using immunomagnet- ic separation polymerase chain reaction( IMBS -PCR) [ J]. J Agric Food Chem,2010,58(12) :7135 -7140.
  • 8Tatavarthy A,Peak K, Vequilla W, et al. An accelerated method for isolation of Salmonella enterica serotype Typhimurium from artificial- ly contaminated foods, using a short preenrichment, immunomagnetic separation, and Xylose-lysine-desoxycholate agar( 6I × method) [ J ]. J Food Prot,2009,72 ( 3 ) :583 - 590.
  • 9Park Y, Cho YH, Jee Y, et al. Immunomagnetic separation combined with real-time reverse transcriptase PCR assays for detection of noro- virus in contaminated food [ J ]. Appl Environ Microbiol, 2008,74 ( 13 ) :4226 -4230.
  • 10Leon-Velarde CG,Zosherafatein L, Odumeru JA. Application of an au- tomated immunomagnetic separation-enzyme immunoassay for the de- tection of Salmonella enterica subspecies enterica from poultry envi- ronmental swabs [ J ]. J Microbiol Methods,2009,79 ( 1 ) : 13 - 17.

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