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一种用于检测革兰氏阳性菌中抗菌药物耐药基因的内部 45 重阵列。

An in-house 45-plex array for the detection of antimicrobial resistance genes in Gram-positive bacteria.

机构信息

Veterinary Bacteriology, Sciensano, Ixelles, Belgium.

出版信息

Microbiologyopen. 2023 Feb;12(1):e1341. doi: 10.1002/mbo3.1341.

Abstract

Identifying antimicrobial resistance (AMR) genes and determining their occurrence in Gram-positive bacteria provide useful data to understand how resistance can be acquired and maintained in these bacteria. We describe an in-house bead array targeting AMR genes of Gram-positive bacteria and allowing their rapid detection all at once at a reduced cost. A total of 41 AMR probes were designed to target genes frequently associated with resistance to tetracycline, macrolides, lincosamides, streptogramins, pleuromutilins, phenicols, glycopeptides, aminoglycosides, diaminopyrimidines, oxazolidinones and particularly shared among Enterococcus and Staphylococcus spp. A collection of 124 enterococci and 62 staphylococci isolated from healthy livestock animals through the official Belgian AMR monitoring (2018-2020) was studied with this array from which a subsample was further investigated by whole-genome sequencing. The array detected AMR genes associated with phenotypic resistance for 93.0% and 89.2% of the individual resistant phenotypes in enterococci and staphylococci, respectively. Although linezolid is not used in veterinary medicine, linezolid-resistant isolates were detected. These were characterized by the presence of optrA and poxtA, providing cross-resistance to other antibiotics. Rarer, vancomycin resistance was conferred by the vanA or by the vanL cluster. Numerous resistance genes circulating among Enterococcus and Staphylococcus spp. were detected by this array allowing rapid screening of a large strain collection at an affordable cost. Our data stress the importance of interpreting AMR with caution and the complementarity of both phenotyping and genotyping methods. This array is now available to assess other One-Health AMR reservoirs.

摘要

鉴定抗微生物药物耐药性 (AMR) 基因并确定其在革兰氏阳性菌中的存在,为了解耐药性如何在这些细菌中获得和维持提供了有用的数据。我们描述了一种针对革兰氏阳性菌的 AMR 基因的内部珠子阵列,可同时以较低的成本快速检测所有基因。总共设计了 41 个 AMR 探针,以靶向与四环素、大环内酯类、林可酰胺类、糖肽类、氨基糖苷类、二氨基嘧啶类、恶唑烷酮类耐药相关的基因,这些基因在肠球菌和葡萄球菌中广泛存在。通过官方比利时 AMR 监测(2018-2020 年)从健康家畜中分离的 124 株肠球菌和 62 株葡萄球菌用该阵列进行了研究,其中一部分通过全基因组测序进行了进一步研究。该阵列检测到与肠球菌和葡萄球菌个体耐药表型相关的 AMR 基因,分别为 93.0%和 89.2%。尽管利奈唑胺未在兽医学中使用,但仍检测到耐利奈唑胺的分离株。这些分离株的特征是存在 optrA 和 poxtA,对其他抗生素具有交叉耐药性。较少见的是,万古霉素耐药性由 vanA 或 vanL 簇赋予。该阵列检测到在肠球菌和葡萄球菌中循环的许多耐药基因,允许以可承受的成本快速筛选大量菌株。我们的数据强调了谨慎解释 AMR 的重要性以及表型和基因型方法的互补性。该阵列现在可用于评估其他 One-Health AMR 储库。

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