Department of Infectious Diseases, Central Clinical School, Monash University, Melbourne, Australia; Department of Infectious Diseases, Alfred Health, Melbourne, Australia.
Department of Infectious Diseases, Central Clinical School, Monash University, Melbourne, Australia; Department of Infectious Diseases, Alfred Health, Melbourne, Australia.
Clin Microbiol Infect. 2021 Dec;27(12):1856.e7-1856.e13. doi: 10.1016/j.cmi.2021.04.020. Epub 2021 Apr 26.
mcr-9.1 is a newly described mobile colistin resistance gene. We have noted its presence in multiple species of carbapenem-resistant Enterobacterales (CRE) from our institution. We aimed to determine the clinical features, genomic context and phenotypic impact of mcr-9.1 carriage in a series of patients between 2010 and 2019.
We identified 32 patients with mcr-9.1-carrying CRE isolates (mCRE) and collected demographic, antimicrobial exposure and infection data. Whole-genome sequencing (including short and long reads) was performed on 32 isolates. We assessed sequence similarity of mcr-9.1-harbouring plasmids, then compared our findings with plasmids for which sequence data were publicly available.
There was no colistin exposure in patients prior to isolation of mCRE. mcr-9.1 was identified on IncHI2 plasmids across four different bacterial species and was co-located with bla in 23/30 plasmids studied. mCRE isolates did not demonstrate phenotypic colistin resistance, either at baseline or following sublethal colistin exposure, thus showing that mcr-9.1 alone is not sufficient for resistance. Publicly available sequence data indicated the presence of carbapenemase genes in 236/619 mcr-9.1-carrying genomes (38%). IncHI2 plasmids carrying mcr-9.1 and carbapenemase genes were detected in genomes from North America, Europe, North Africa, Asia and Oceania.
Spread of mcr-9.1 in CRE from our institution was driven by IncHI2 'superplasmids', so termed because of their large size and their prolific carriage of resistance determinants. These were also detected in global CRE genomes. Phenotypic colistin resistance was not detected in our isolates but remains to be determined from global mCRE.
mcr-9.1 是一种新描述的移动多黏菌素耐药基因。我们在本机构的多种碳青霉烯类耐药肠杆菌科(CRE)物种中发现了它的存在。我们旨在确定 2010 年至 2019 年间一系列患者中 mcr-9.1 携带的临床特征、基因组背景和表型影响。
我们鉴定了 32 例携带 mcr-9.1 的 CRE 分离株(mCRE)的患者,并收集了人口统计学、抗菌药物暴露和感染数据。对 32 株分离株进行了全基因组测序(包括短读长和长读长)。我们评估了 mcr-9.1 携带质粒的序列相似性,然后将我们的发现与公开提供序列数据的质粒进行比较。
在 mCRE 分离之前,患者没有接触过多黏菌素。mcr-9.1 位于 4 种不同细菌种的 IncHI2 质粒上,在所研究的 30 个质粒中有 23 个质粒共定位bla。mCRE 分离株无论是在基线还是在亚致死浓度多黏菌素暴露后,均未表现出表型多黏菌素耐药性,因此表明 mcr-9.1 本身不足以产生耐药性。公开的序列数据表明,在 619 个携带 mcr-9.1 的基因组中,有 236 个(38%)存在碳青霉烯酶基因。从北美、欧洲、北非、亚洲和大洋洲的基因组中检测到携带 mcr-9.1 和碳青霉烯酶基因的 IncHI2 质粒。
本机构 CRE 中 mcr-9.1 的传播是由 IncHI2“超级质粒”驱动的,之所以这样命名,是因为它们的体积庞大,而且携带大量耐药决定因子。这些质粒也在全球 CRE 基因组中被检测到。我们的分离株未检测到表型多黏菌素耐药性,但仍需从全球 mCRE 中确定。