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Comparison of Multilocus Variable-Number Tandem-Repeat Analysis and Whole-Genome Sequencing for Investigation of Clostridium difficile Transmission

机译:多位点可变数串联重复分析与全基因组测序研究艰难梭菌传播的比较

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摘要

No study to date has compared multilocus variable-number tandem-repeat analysis (MLVA) and whole-genome sequencing (WGS) in an investigation of the transmission of Clostridium difficile infection. Isolates from 61 adults with ongoing and/or recurrent C. difficile infections and 17 asymptomatic carriage episodes in children (201 samples), as well as from 61 suspected outbreaks affecting 2 to 41 patients in 31 hospitals in the United Kingdom (300 samples), underwent 7-locus MLVA and WGS in parallel. When the first and last samples from the same individual taken for a median (interquartile range [IQR]) of 63 days (43 to 105 days) apart were compared, the estimated rates of the evolution of single nucleotide variants (SNVs), summed tandem-repeat differences (STRDs), and locus variants (LVs) were 0.79 (95% confidence interval [CI], 0.00 to 1.75), 1.63 (95% CI, 0.00 to 3.59), and 1.21 (95% CI, 0.00 to 2.67)/called genome/year, respectively. Differences of >2 SNVs and >10 STRDs have been used to exclude direct case-to-case transmission. With the first serial sample per individual being used to assess discriminatory power, across all pairs of samples sharing a PCR ribotype, 192/283 (68%) differed by >10 STRDs and 217/283 (77%) by >2 SNVs. Among all pairs of cases from the same suspected outbreak, 1,190/1,488 (80%) pairs had concordant results using >2 SNVs and >10 STRDs to exclude transmission. For the discordant pairs, 229 (15%) had ≥2 SNVs but ≤10 STRDs, and 69 (5%) had ≤2 SNVs but ≥10 STRDs. Discordant pairs had higher numbers of LVs than concordant pairs, supporting the more diverse measure in each type of discordant pair. Conclusions on whether the potential outbreaks were confirmed were concordant in 58/61 (95%) investigations. Overall findings using MLVA and WGS were very similar despite the fact that they analyzed different parts of the bacterial genome. With improvements in WGS technology, it is likely that MLVA locus data will be available from WGS in the near future.
机译:迄今为止,尚无研究在艰难梭菌感染传播调查中比较多基因座可变数目串联重复分析(MLVA)和全基因组测序(WGS)。分离出儿童中持续存在和/或复发的艰难梭菌感染和儿童的17例无症状携带发作的成年人(201例),以及在英国31家医院中影响2至41例患者的61例疑似疫情(300例),同时接受了7位MLVA和WGS。比较来自同一个人的中值(四分位间距[IQR])相隔63天(43至105天)的第一个和最后一个样本时,单核苷酸变体(SNV)进化的估计速率(串联求和)重复差异(STRDs)和基因座变异(LVs)为0.79(95%置信区间[CI],0.00至1.75),1.63(95%CI,0.00至3.59)和1.21(95%CI,0.00至2.67) )/分别称为基因组/年份。大于2个SNV和大于10个STRD的差异已被用于排除直接的个案之间的传播。每个人的第一批连续样本用于评估鉴别力,在所有共有PCR核型的样本对中,192/283(68%)的差异大于10个STRD,而217/283(77%)的差异大于2个SNV。在来自同一可疑疫情的所有成对病例中,使用> 2个SNV和> 10个STRD排除传播,结果对为1,190 / 1,488(80%)对。对于不一致的对,有229个SNV≥2,但STRD≤10;有229个(15%)SNV≤2,但STRD≥10。不一致对具有比一致对更高的LV数,支持每种不一致对类型中更多样化的度量。在58/61(95%)的调查中,关于是否确认潜在爆发的结论是一致的。尽管它们分析了细菌基因组的不同部分,但使用MLVA和WGS的总体发现非常相似。随着WGS技术的改进,很可能在不久的将来可以从WGS获得MLVA基因座数据。

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