首页> 外文期刊>Diagnostic microbiology and infectious disease >Analysis of multilocus sequence typing schemes for 35 different bacteria revealed that gene loci of 10 bacteria could be replaced to improve cost-effectiveness.
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Analysis of multilocus sequence typing schemes for 35 different bacteria revealed that gene loci of 10 bacteria could be replaced to improve cost-effectiveness.

机译:对35种不同细菌的多基因座序列分型方案的分析表明,可以替换10种细菌的基因座以提高成本效益。

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摘要

Although multilocus sequence typing (MLST) has been widely used for bacterial typing, the contribution of the gene loci to the discriminatory power of each MLST scheme is unknown. We analyzed the discriminatory powers of 36 MLST schemes using all combinations of the 7 loci and contributions of each locus to the schemes. In 10 schemes, sequencing 6 loci can achieve the discriminatory powers of 7 loci. For the other 26 schemes, the median marginal increase in discriminatory power when 7 instead of 6 loci were used is 0.0004. Sequencing the 7 loci of 50 strains each of Pseudomonas aeruginosa and Acinetobacter baumannii revealed that the discriminatory power for P. aeruginosa was 0.9861 when either 6 (without trp) or 7 loci were used and that for A. baumannii was 0.9363 when 5, 6, or 7 loci were used. Genes that have no additional or minimal contribution to the overall discriminatory powers should be replaced.
机译:尽管多基因座序列分型(MLST)已广泛用于细菌分型,但基因位点对每种MLST方案的鉴别能力的贡献尚不清楚。我们使用7个基因座的所有组合以及每个基因座对方案的贡献,分析了36种MLST方案的鉴别力。在10个方案中,对6个基因座进行测序可以实现7个基因座的区分能力。对于其他26个方案,当使用7个而不是6个基因座时,判别力的边际中位数增加为0.0004。分别对铜绿假单胞菌和鲍曼不动杆菌的50个菌株的7个基因座进行测序,结果表明,当使用6个基因座(不使用trp)或7个基因座时,铜绿假单胞菌的鉴别力为0.9861,而当5、6、5、6、5和6时,对鲍曼不动杆菌的鉴别力为0.9363。或使用了7个基因座。对总的歧视能力没有其他贡献或贡献最小的基因应该被替换。

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