Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Department of Biomedicine, Aarhus University, Aarhus, Denmark.
Front Cell Infect Microbiol. 2023 May 17;13:1165017. doi: 10.3389/fcimb.2023.1165017. eCollection 2023.
Orthopaedic implant-associated infections (OIAIs) due to can be difficult to diagnose. The aim of this pilot study was to determine if metagenomic next-generation sequencing (mNGS) can provide additional information to improve the diagnosis of OIAIs. mNGS was performed on sonication fluid (SF) specimens derived from 24 implants. These were divided into three groups, based on culture results: group I, culture-negative (n = 4); group II, culture-positive for (n = 10); and group III, culture-positive for other bacteria (n = 10). In group I, sequence reads from were detected in only one SF sample, originating from a suspected case of OIAIs, which was SF and tissue culture-negative. In group II, sequences were detected in 7/10 samples. In group III, sequence reads were found in 5/10 samples, in addition to sequence reads that matched the bacterial species identified by culture. These samples could represent polymicrobial infections that were missed by culture. Taken together, mNGS was able to detect DNA in more samples compared to culture and could be used to identify cases of suspected OIAIs, in particular regarding possible polymicrobial infections, where the growth of might be compromised due to a fast-growing bacterial species. However, since SF specimens are usually low-biomass samples, mNGS is prone to DNA contamination, possibly introduced during DNA extraction or sequencing procedures. Thus, it is advisable to set a sequence read count threshold, taking into account project- and NGS-specific criteria.
骨植入物相关感染(OIAIs)由于 可能难以诊断。本初步研究旨在确定宏基因组下一代测序(mNGS)是否可以提供额外信息以改善 OIAIs 的诊断。对来自 24 个植入物的超声液(SF)标本进行了 mNGS。这些标本根据培养结果分为三组:I 组,培养阴性(n=4);II 组,培养阳性 (n=10);III 组,培养阳性其他细菌(n=10)。在 I 组中,仅在一个 SF 样本中检测到来自疑似 OIAIs 的一个 SF 和组织培养阴性样本的 序列读取。在 II 组中,在 7/10 个样本中检测到 序列。在 III 组中,在 5/10 个样本中发现了 序列读取,此外还有与培养鉴定的细菌种类匹配的序列读取。这些样本可能代表了培养遗漏的混合感染。总之,与培养相比,mNGS 能够检测到更多样本中的 DNA,并且可用于识别疑似 OIAIs 的病例,特别是对于可能的混合感染,由于快速生长的细菌种类, 的生长可能受到影响。然而,由于 SF 标本通常是低生物量样本,mNGS 容易受到 DNA 污染,可能是在 DNA 提取或测序过程中引入的。因此,建议根据项目和 NGS 的具体标准设置序列读取计数阈值。