Institute of Tropical Medicine, Department of Clinical Sciences, STI Unit, Antwerp, Belgium.
University of Antwerp, Laboratory of Medical Microbiology, Vaccine and Infectious Disease Institute, Antwerp, Belgium.
J Antimicrob Chemother. 2021 Jun 18;76(7):1752-1758. doi: 10.1093/jac/dkab084.
The prevalence of azithromycin resistance in Neisseria gonorrhoeae is increasing in numerous populations worldwide.
To characterize the genetic pathways leading to high-level azithromycin resistance.
A customized morbidostat was used to subject two N. gonorrhoeae reference strains (WHO-F and WHO-X) to dynamically sustained azithromycin pressure. We tracked stepwise evolution of resistance by whole genome sequencing.
Within 26 days, all cultures evolved high-level azithromycin resistance. Typically, the first step towards resistance was found in transitory mutations in genes rplD, rplV and rpmH (encoding the ribosomal proteins L4, L22 and L34 respectively), followed by mutations in the MtrCDE-encoded efflux pump and the 23S rRNA gene. Low- to high-level resistance was associated with mutations in the ribosomal proteins and MtrCDE efflux pump. However, high-level resistance was consistently associated with mutations in the 23S ribosomal RNA, mainly the well-known A2059G and C2611T mutations, but also at position A2058G.
This study enabled us to track previously reported mutations and identify novel mutations in ribosomal proteins (L4, L22 and L34) that may play a role in the genesis of azithromycin resistance in N. gonorrhoeae.
全球许多人群中淋病奈瑟菌对阿奇霉素的耐药率正在上升。
描述导致高水平阿奇霉素耐药的遗传途径。
使用定制的病态恒化器对 2 株淋病奈瑟菌参考株(WHO-F 和 WHO-X)进行动态持续阿奇霉素压力处理。我们通过全基因组测序跟踪耐药性的逐步演变。
在 26 天内,所有培养物均进化出高水平的阿奇霉素耐药性。通常,第一步是在编码核糖体蛋白 L4、L22 和 L34 的 rplD、rplV 和 rpmH 基因中发现短暂突变,随后是 MtrCDE 编码的外排泵和 23S rRNA 基因的突变。低水平至高水平耐药与核糖体蛋白和 MtrCDE 外排泵的突变有关。然而,高水平耐药始终与 23S 核糖体 RNA 的突变有关,主要是众所周知的 A2059G 和 C2611T 突变,但也与 A2058G 位置有关。
本研究使我们能够追踪先前报道的突变,并鉴定核糖体蛋白(L4、L22 和 L34)中的新突变,这些突变可能在淋病奈瑟菌阿奇霉素耐药的发生中起作用。