Balázs Bence, Tóth Zoltán, Nagy József Bálint, Majoros László, Tóth Ákos, Kardos Gábor
Department of Medical Microbiology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
Doctoral School of Pharmaceutical Sciences, University of Debrecen, 4032 Debrecen, Hungary.
Pathogens. 2022 Sep 2;11(9):1003. doi: 10.3390/pathogens11091003.
Increasing prevalence of A. baumannii was found in the faecal samples of inpatients without infection caused by A. baumannii (0.15%; 55/7806). The aim of the study was to determine whether there is a relationship between the clinical strains and the increased faecal occurrence. Characteristics of faecal and clinical isolates were compared between 2017 and 2019, and the direction of causality was assessed by Granger causality tests. In the case of the antibiotic resistance, faecal carriage of carbapenem-resistant Acinetobacter baumannii (CRAb) was Granger-caused by prevalence of CRAb in inpatients (F = 15.84, p < 0.001), but inpatient prevalence was not Granger-caused by CRAb faecal carriage (F = 0.03, p = 0.855). Whole genomes of 16 faecal isolates were sequenced by Illumina MiSeq; cgMLST types were determined. In faecal isolates, the occurrence of carbapenem resistance was lower than among the clinical isolates from the same period; only blaOXA-72 harbouring ST636 and ST492 were detected, and the blaOXA-23 harbouring ST2 and ST49 strains previously dominant in clinical isolates were absent. Carriage of blaOXA-72 was linked to pMAL-1-like and pA105-2-like plasmids in ST636 and ST492 isolates, respectively, both in clinical and faecal isolates. The new ST636 and ST492 strains may colonise the gut microbiota of the patients, which thus may play a role as a reservoir.
在没有鲍曼不动杆菌感染的住院患者粪便样本中发现鲍曼不动杆菌的流行率在增加(0.15%;55/7806)。本研究的目的是确定临床菌株与粪便中发生率增加之间是否存在关联。比较了2017年至2019年粪便和临床分离株的特征,并通过格兰杰因果检验评估因果关系方向。在抗生素耐药性方面,耐碳青霉烯鲍曼不动杆菌(CRAb)的粪便携带是由住院患者中CRAb的流行率格兰杰引起的(F = 15.84,p < 0.001),但住院患者的流行率不是由CRAb粪便携带格兰杰引起的(F = 0.03,p = 0.855)。通过Illumina MiSeq对16株粪便分离株的全基因组进行测序;确定了cgMLST类型。在粪便分离株中,碳青霉烯耐药性的发生率低于同期临床分离株;仅检测到携带blaOXA - 72的ST636和ST492,而之前在临床分离株中占主导地位的携带blaOXA - 23的ST2和ST49菌株不存在。在临床和粪便分离株中,blaOXA - 72的携带分别与ST636和ST492分离株中的pMAL - 1样和pA105 - 2样质粒相关。新的ST636和ST492菌株可能定殖于患者的肠道微生物群,因此可能起到储存库的作用。