Carole Kowalewicz, Michael Timmermans, David Fretin, Pierre Wattiau, Cécile Boland
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引用次数: 1
摘要
鉴定抗微生物耐药性(AMR)基因并确定其在革兰氏阳性菌中的发生率,为了解这些细菌如何获得和维持耐药性提供了有用的数据。我们描述了一种针对革兰氏阳性菌AMR基因的内部珠阵列,并允许以降低的成本同时快速检测它们。共设计了41种AMR探针,靶向经常与四环素、大环内酯类、林可酰胺类、链菌素、胸膜菌素、氯霉素、糖肽、氨基糖苷类、二氨基嘧啶类、恶唑烷酮相关的基因,尤其是肠球菌和葡萄球菌共有的基因。使用该阵列研究了通过比利时官方AMR监测(2018-2020)从健康牲畜中分离的124株肠球菌和62株葡萄球菌,并通过全基因组测序进一步研究了其中的子样本。该阵列检测到与表型耐药性相关的AMR基因,分别占肠球菌和葡萄球菌个体耐药性表型的93.0%和89.2%。虽然利奈唑胺不用于兽医,但检测到了利奈唑啉耐药菌株。其特征是存在optrA和poxtA,提供对其他抗生素的交叉耐药性。更罕见的是,万古霉素耐药性是由vanA或vanL簇赋予的。通过该阵列检测到在肠球菌和葡萄球菌中循环的许多抗性基因,从而能够以负担得起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,以及表型和基因分型方法的互补性。该阵列现在可用于评估其他One Health AMR储层。
An in-house 45-plex array for the detection of antimicrobial resistance genes in Gram-positive bacteria
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.
期刊介绍:
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