Lu Xiuhui, He Jiaqi, Zheng Yali, Chen Fangzhou, Luo Jing, Ma Kejiao, Yang Fan, Wang Peng, Zhou Dongsheng, Gao Bo, Yin Zhe
State Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Sciences, Beijing, China.
Department of Clinical Laboratory, The First Affiliated Hospital of Henan University, Kaifeng, China.
Virulence. 2025 Dec;16(1):2512034. doi: 10.1080/21505594.2025.2512034. Epub 2025 Jun 19.
This study presents the genetic structure of two incompatibility (Inc) groups found in : the newly discovered IncFII and the newly designated Inc. An extensive genomic comparison was performed on all 14 plasmids (three IncFII plasmids and 11 Inc plasmids) from , including 12 newly sequenced in this study and two from GenBank. Three IncFII plasmids had similar conserved backbones but differed in accessory modules. The 11 Inc plasmids fell into two groups according to differences in the conserved genes of the plasmid backbone. The accessory modules of 11 Inc plasmids showed significant diversity, indicating numerous gene gains and losses, including in the Tnrelated region, in Tn, in a 17.3-kb region, and a 63.6-kb region. A minimum of 45 obtained antimicrobial resistance genes (ARGs) were identified in 13 of the 14 plasmids, covering resistance to 14 classes of antimicrobials and heavy metals. Five new mobile genetic elements (MGEs) were identified, including In2168, In1790, Tn, Tn, and Tn. Additionally, three MGEs, Tn, Tn, and Tn were newly designated. These two Inc group plasmids integrate abundant accessory modules that allow them to accumulate and distribute ARGs and improve the survivability of under the pressure of drug selection.
本研究展示了在[具体环境未提及]中发现的两个不相容性(Inc)组的遗传结构:新发现的IncFII和新指定的Inc。对来自[具体来源未提及]的所有14个质粒(3个IncFII质粒和11个Inc质粒)进行了广泛的基因组比较,包括本研究中新测序的12个和来自GenBank的2个。3个IncFII质粒具有相似的保守主干,但在辅助模块上有所不同。11个Inc质粒根据质粒主干保守基因的差异分为两组。11个Inc质粒的辅助模块显示出显著的多样性,表明有大量的基因得失,包括在Tn相关区域、Tn、一个17.3kb的区域和一个63.6kb的区域。在14个质粒中的13个中至少鉴定出45个获得性抗菌抗性基因(ARGs),涵盖对14类抗菌药物和重金属的抗性。鉴定出5个新的移动遗传元件(MGEs),包括In2168、In1790、Tn、Tn和Tn。此外,新指定了3个MGEs,即Tn、Tn和Tn。这两个Inc组质粒整合了丰富的辅助模块,使它们能够积累和分布ARGs,并在药物选择压力下提高[具体对象未提及]的生存能力。