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氟喹诺酮耐药. 携带者中的微生物组多样性

Microbiome diversity in carriers of fluoroquinolone resistant .

机构信息

Department of Urology, UT Health San Antonio Long School of Medicine, San Antonio, TX, USA.

South Texas Veterans Healthcare System, San Antonio, TX, USA.

出版信息

Investig Clin Urol. 2019 Mar;60(2):75-83. doi: 10.4111/icu.2019.60.2.75. Epub 2019 Feb 27.

Abstract

PURPOSE

Fluoroquinolone-resistant (FQR) causes transrectal prostate biopsy infections. In order to reduce colonization of these bacteria in carriers, we would like to understand the surrounding microbiome to determine targets for decolonization.

MATERIALS AND METHODS

We perform an observational study to investigate the microbiome differences in men with and without FQR organisms found on rectal culture. A rectal swab with two culturettes was performed on men before an upcoming prostate biopsy procedure as standard of care to perform "targeted prophylaxis." Detection of FQR was performed by the standard microbiology lab inoculates the swab onto MacConkey agar containing ciprofloxacin. The extra swab was sent for 16S rRNA amplicon sequencing (MiSeq paired-end) using the V1V2 primer. Alpha and beta-diversity analysis were performed using QIIME. We used PERMANOVA to evaluate the statistical significance of beta-diversity distances within and between groups of interest.

RESULTS

We collected 116 rectal swab samples before biopsy for 16S rRNA amplicon sequencing. We identified 18 isolates (15.5%, 18/116) that were positive and had relative reduced diversity profiles (p<0.05). Enterobacteriaceae were significantly over-represented in the FQR subjects (adjusted p=0.03).

CONCLUSIONS

Microbiome analysis determined that men colonized with FQR bacteria have less diverse bacterial communities (dysbiosis), higher levels of Enterobacteriaceae and reduced levels of . These results may have implications in pre/probiotic intervention studies.

摘要

目的

氟喹诺酮耐药(FQR)可引起经直肠前列腺活检感染。为了减少这些细菌在携带者中的定植,我们希望了解周围微生物组,以确定去定植的目标。

材料与方法

我们进行了一项观察性研究,以调查直肠培养中存在 FQR 菌和不存在 FQR 菌的男性之间的微生物组差异。在进行前列腺活检程序之前,按照标准护理对男性进行直肠拭子和两个培养管的检测,以进行“靶向预防”。通过标准微生物学实验室将拭子接种到含有环丙沙星的麦康凯琼脂上,来检测 FQR。额外的拭子用于 16S rRNA 扩增子测序(MiSeq 配对末端),使用 V1V2 引物。使用 QIIME 进行 alpha 和 beta 多样性分析。我们使用 PERMANOVA 来评估组内和组间 beta 多样性距离的统计显著性。

结果

我们在进行 16S rRNA 扩增子测序之前,收集了 116 例前列腺活检前的直肠拭子样本。我们鉴定出 18 个分离株(15.5%,18/116)为阳性,具有相对减少的多样性谱(p<0.05)。FQR 组中肠杆菌科的丰度显著增加(调整后的 p=0.03)。

结论

微生物组分析确定,定植 FQR 细菌的男性具有较少多样的细菌群落(失调),肠杆菌科水平较高,而水平降低。这些结果可能对预/益生菌干预研究具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c96/6397931/acb973de0dd8/icu-60-75-g001.jpg

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