Xiangfeng Bu, Yufan Wu, Yi Hong, Juping Shi, Jingdong Shao, Kai Jia, Qingli Dong, Xiang Wang
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引用次数: 0
摘要
肠炎沙门氏菌是一种主要的食源性病原体,耐多药(MDR)肠炎沙门氏菌的出现对公共卫生构成了严峻的挑战。在本研究中,我们报告了从临床中分离出的五株肠炎球菌的基因组特征。这些分离物表现出对七类抗菌药的耐药性,其中四种被鉴定为 MDR。分离株 33 A 对秋水仙素和多粘菌素 B 具有耐药性,但其基因组中未发现相关的抗菌药耐药基因(ARGs)。样本 21 A 和 44 A 能产生广谱β-内酰胺酶(ESBLs)。全基因组测序分析揭示了多种移动遗传元件(MGE)的存在,包括质粒、噬菌体和基因组岛,这可能促进了 ARGs 的获得和传播。值得注意的是,在质粒上发现了几个 ARGs,包括 blaCTX-M-55、blaTEM-141、blaTEM-1B、ahph(3')-IIa、ahph(3'')-Ib、ahph(6)-Id、tet(A)、floR、fosA3 和 sul2。此外,在每个分离株中还观察到 gyrA(D87G 和 D87Y)和 acrB(F28L 和 L40P)的染色体点突变。在沙门氏菌致病性岛(SPI)SPI-1 和 SPI-2 上发现了多个与 III 型分泌系统相关的毒力基因。系统发育分析表明,这五个分离株与数据库中的一个临床分离株和一个鸡源分离株聚类在一起,表明可能存在共同的感染源。我们的研究结果突显了肠杆菌 MDR 背后错综复杂的遗传机制,强调了持续监控和适当使用抗菌药物的必要性。这有助于我们了解肠炎双球菌在食物链中的传播。
Comparative genomics analysis of Salmonella Enteritidis isolated from clinical cases associated with chicken.
Salmonella Enteritidis is a major foodborne pathogen, and the emergence of multidrug-resistant (MDR) S. Enteritidis poses a serious public health challenge. In this study, we report the genomic characterization of five S. Enteritidis isolates from clinical. These isolates exhibited resistance to seven classes of antimicrobials with four of the five characterized as MDR. Isolate 33 A exhibited resistance to colistin and polymyxin B, while no associated antimicrobial resistance genes (ARGs) were identified in its genome. Isolate 21 A and 44 A were extended-spectrum beta-lactamases-producing (ESBLs). Whole genome sequencing analysis revealed the presence of multiple mobile genetic elements (MGEs), including plasmids, prophages, and genomic islands, which may have facilitated the acquisition and dissemination of ARGs. Notably, several ARGs, including blaCTX-M-55, blaTEM-141, blaTEM-1B, aph(3')-IIa, aph(3'')-Ib, aph(6)-Id, tet(A), floR, fosA3, and sul2, were identified on plasmids. In addition, chromosomal point mutations in gyrA (D87G and D87Y) and acrB (F28L and L40P) were also observed in each isolate. Multiple virulence genes associated with the type III secretion system were identified on Salmonella pathogenicity islands (SPIs) SPI-1 and SPI-2. Phylogenetic analysis revealed that the five isolates, along with a clinical and chicken origin isolates in the database, clustered together, suggesting a probable common source of infection. Our findings highlight the intricate genetic mechanisms behind MDR in S. Enteritidis, emphasizing the ongoing necessity for surveillance and appropriate antimicrobial usage. This contributes to our understanding of S. Enteritidis transmission within the food chain.
期刊介绍:
BMC Microbiology is an open access, peer-reviewed journal that considers articles on analytical and functional studies of prokaryotic and eukaryotic microorganisms, viruses and small parasites, as well as host and therapeutic responses to them and their interaction with the environment.