Nielsen Karen Leth, Olsen Markus Harboe, Pallejá Albert, Ebdrup Søren Røddik, Sørensen Nikolaj, Lukjancenko Oksana, Marvig Rasmus L, Møller Kirsten, Frimodt-Møller Niels, Hertz Frederik Boëtius
Department of Clinical Microbiology, Copenhagen University Hospital-Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen, Denmark.
Department of Neuroanaesthesiology, The Neuroscience Centre, Copenhagen University Hospital-Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen, Denmark.
Microorganisms. 2021 Dec 9;9(12):2542. doi: 10.3390/microorganisms9122542.
Hospitalization and treatment with antibiotics increase the risk of acquiring multidrug-resistant bacteria due to antibiotic-mediated changes in patient microbiota. This study aimed to investigate how broad- and narrow-spectrum antibiotics affect the gut microbiome and the resistome in antibiotic naïve patients during neurointensive care. Patients admitted to the neurointensive care unit were treated with broad-spectrum (meropenem or piperacillin/tazobactam) or narrow-spectrum antibiotic treatment (including ciprofloxacin, cefuroxime, vancomycin and dicloxacillin) according to clinical indications. A rectal swab was collected from each patient before and after 5-7 days of antibiotic therapy ( = 34), respectively. Shotgun metagenomic sequencing was performed and the composition of metagenomic species (MGS) was determined. The resistome was characterized with CARD RGI software and the CARD database. As a measure for selection pressure in the patient, we used the sum of the number of days with each antibiotic (antibiotic days). We observed a significant increase in richness and a tendency for an increase in the Shannon index after narrow-spectrum treatment. For broad-spectrum treatment the effect was more diverse, with some patients increasing and some decreasing in richness and Shannon index. This was studied further by comparison of patients who had gained or lost >10 MGS, respectively. Selection pressure was significantly higher in patients with decreased richness and a decreased Shannon index who received the broad treatment. A decrease in MGS richness was significantly correlated to the number of drugs administered and the selection pressure in the patient. Bray-Curtis dissimilarities were significant between the pre- and post-treatment of samples in the narrow group, indicating that the longer the narrow-spectrum treatment, the higher the differences between the pre- and the post-treatment microbial composition. We did not find significant differences between pre- and post-treatment for both antibiotic spectrum treatments; however, we observed that most of the antibiotic class resistance genes were higher in abundance in post-treatment after broad-spectrum treatment.
由于抗生素介导的患者微生物群变化,住院治疗并使用抗生素会增加获得多重耐药菌的风险。本研究旨在调查在神经重症监护期间,广谱和窄谱抗生素如何影响未使用过抗生素的患者的肠道微生物组和耐药基因组。根据临床指征,入住神经重症监护病房的患者接受了广谱(美罗培南或哌拉西林/他唑巴坦)或窄谱抗生素治疗(包括环丙沙星、头孢呋辛、万古霉素和双氯西林)。在抗生素治疗5 - 7天前后(n = 34),分别从每位患者采集直肠拭子。进行鸟枪法宏基因组测序并确定宏基因组物种(MGS)的组成。使用CARD RGI软件和CARD数据库对耐药基因组进行表征。作为患者选择压力的一种衡量指标,我们使用了每种抗生素使用天数的总和(抗生素天数)。我们观察到窄谱治疗后丰富度显著增加,香农指数有增加的趋势。对于广谱治疗,效果更为多样,一些患者的丰富度和香农指数增加,而一些患者则下降。通过分别比较获得或失去>10个MGS的患者进行了进一步研究。接受广谱治疗且丰富度降低和香农指数降低的患者的选择压力显著更高。MGS丰富度的降低与给药药物数量和患者的选择压力显著相关。窄谱组样本治疗前后的布雷 - 柯蒂斯差异显著,表明窄谱治疗时间越长,治疗前后微生物组成的差异越大。我们未发现两种抗生素谱治疗前后有显著差异;然而,我们观察到广谱治疗后,大多数抗生素类耐药基因在治疗后的丰度更高。