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不同宿主细菌中替加环素耐药基因(X6)引起的适应性代价的表征

Characterization of Fitness Cost Caused by Tigecycline-Resistance Gene (X6) in Different Host Bacteria.

作者信息

Jiang Lijie, Cai Wenhui, Tang Feifei, Wang Zhiqiang, Liu Yuan

机构信息

College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China.

Jiangsu Co-Innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Joint International Research Laboratory of Agriculture and Agri-Product Safety, The Ministry of Education of China, Yangzhou University, Yangzhou 225009, China.

出版信息

Antibiotics (Basel). 2021 Sep 27;10(10):1172. doi: 10.3390/antibiotics10101172.

Abstract

The emergence and prevalence of the (X) gene and its variants in the environment and in clinical settings constitute a growing concern for public health worldwide. Accordingly, the tigecycline resistance gene variant (X6) is widely detected in spp. and spp. rather than Enterobacteriaceae, while the underpinning behind this phenomenon is still unclear. To investigate the mechanisms underlying this distinct phenomenon, we assessed the fitness of the engineered plasmid pBAD-(X6) in different host bacteria by monitoring their growth curves, relative fitness and the ability of biofilm formation, as well as virulence in a model. MIC and qRT-PCR analysis indicated the successful expression of the (X6) gene in these strains in the presence of l-arabinose. Furthermore, we found that pBAD-(X6) displayed the lowest fitness cost in compared with that in or Enteritidis, suggesting the fitness difference of (X6)-bearing plasmids in different host bacteria. Consistently, the carriage of pBAD-(X6) remarkably reduced the biofilm production and virulence of or Enteritidis. These findings not only indicate that the fitness cost difference elicited by the (X6) gene may be responsible for its selectivity in host bacteria but also sheds new insight into the dissemination of antibiotic resistance genes (ARGs) in clinical and environmental isolates.

摘要

(X)基因及其变体在环境和临床环境中的出现与流行,已成为全球公共卫生领域日益关注的问题。相应地,替加环素耐药基因变体(X6)在[具体菌属1]和[具体菌属2]中广泛被检测到,而非肠杆菌科细菌,然而这一现象背后的原因仍不清楚。为了探究这一独特现象背后的机制,我们通过监测不同宿主细菌的生长曲线、相对适合度、生物膜形成能力以及在[动物模型名称]模型中的毒力,评估了工程质粒pBAD-(X6)在不同宿主细菌中的适合度。最低抑菌浓度(MIC)和定量逆转录聚合酶链反应(qRT-PCR)分析表明,在L-阿拉伯糖存在的情况下,(X6)基因在这些菌株中成功表达。此外,我们发现与[具体菌属3]或肠炎沙门氏菌相比,pBAD-(X6)在[具体菌属4]中表现出最低的适合度代价,这表明携带(X6)的质粒在不同宿主细菌中的适合度存在差异。一致地,携带pBAD-(X6)显著降低了[具体菌属3]或肠炎沙门氏菌的生物膜产生和毒力。这些发现不仅表明(X6)基因引发的适合度代价差异可能是其在宿主细菌中具有选择性的原因,还为临床和环境分离株中抗生素耐药基因(ARGs)的传播提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f979/8532885/705e8a69ab2d/antibiotics-10-01172-g001.jpg

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