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16S rRNA deep sequencing identifies Actinotignum schaalii as the major component of a polymicrobial intra-abdominal infection and implicates a urinary source

机译:16S rRNA深度测序将猕猴桃(Actinotignum schaalii)鉴定为多微生物腹腔内感染的主要成分并提示尿源

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摘要

>Introduction. It can be difficult to catalogue the individual organisms comprising polymicrobial patient infections, both because conventional clinical microbiological culture does not facilitate the isolation and enumeration of all members of a complex microbial community, and because fastidious organisms may be mixed with organisms that grow rapidly in vitro. Empiric antimicrobial treatment is frequently employed based on the anatomical site and the suspected source of the infection, especially when an appropriately collected surgical specimen is not obtained. >Case presentation. We present a case of an intra-abdominal infection in a patient with complex anatomy and recurrent urinary tract infections. Imaging did not reveal a clear source of infection, no growth was obtained from urine cultures and initial abdominal fluid cultures were also negative. In contrast, 16S rRNA deep sequencing of abdominal fluid samples revealed mixed bacterial populations with abundant anaerobes, including Actinotignum schaalii (Actinobaculum schaalii). Ultimately, only Enterobacter cloacae complex and meticillin-resistant Staphylococcus aureus, both of which were identified by sequencing, were recovered by culture. >Conclusion. The clinical application of 16S rRNA deep sequencing can more comprehensively and accurately define the organisms present in an individual patient's polymicrobial infection than conventional microbiological culture, detecting species that are not recovered under standard culture conditions or that are otherwise unexpected. These results can facilitate effective antimicrobial stewardship and help elucidate the possible origins of infections.
机译:>简介。由于传统的临床微生物培养不能促进复杂微生物群落的所有成员的分离和枚举,而且因为挑剔的微生物可能会难以对构成多微生物患者感染的单个生物进行分类。与在体外快速生长的生物混合。根据解剖部位和疑似感染源,经常采用经验性抗菌治疗,尤其是在没有获得适当收集的手术标本的情况下。 >病例介绍。我们介绍了一名解剖结构复杂且反复尿路感染的患者发生腹腔内感染的情况。影像学检查未发现明确的感染源,尿培养未见生长,最初的腹水培养也为阴性。相比之下,腹液样品的16S rRNA深度测序显示混合细菌种群具有丰富的厌氧菌,包括放线放线菌(Actintigcul schaalii)(Actinobaculum schaalii)。最终,仅通过测序鉴定出了阴沟肠杆菌复合物和耐甲氧西林金黄色葡萄球菌,两者均通过测序鉴定。 >结论。与常规微生物培养相比,16S rRNA深度测序的临床应用可以更全面,更准确地确定个体患者的微生物感染中存在的生物,从而检测在标准培养条件下未回收的物种或否则意外。这些结果可以促进有效的抗菌管理,并有助于阐明感染的可能来源。

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