沙门氏菌对氟喹诺酮类药物的耐药性:机制、适应性和毒力

Jun Li, H. Hao, A. Sajid, Heying Zhang, Zonghui Yuan
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引用次数: 4

摘要

氟喹诺酮类药物是非常有效的广谱抗生素,通常用于治疗人类和动物感染,包括沙门氏菌病。氟喹诺酮类药物通过抑制沙门氏菌的DNA复制来对抗沙门氏菌。然而,沙门氏菌的几种人畜共患血清型已产生耐药性或对氟喹诺酮类药物不太敏感。沙门氏菌通过取代拓扑异构酶亚基内的氨基酸、过度表达多药外排泵或减少外膜孔蛋白的表达来表现其耐药性。质粒介导的喹诺酮类耐药基因进一步提高了耐药水平,可在菌株间水平传递耐药。沙门氏菌耐药的发生是一个多因素的过程,氟喹诺酮类药物耐药性的获得可能对细菌的适应度和毒力有重要影响。由于在沙门氏菌中观察到对氟喹诺酮类药物的高度耐药性,需要注意避免误用和过度使用这类重要抗生素,以尽量减少耐药性的发生和传播。
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Fluoroquinolone Resistance in Salmonella: Mechanisms, Fitness, and Virulence
Fluoroquinolones are highly effective broad-spectrum antibiotics usually used for the treatment of human and animal infections, including salmonellosis. Fluoroquinolones act against Salmonella by inhibiting their DNA replication. However, several zoonotic serotypes of Salmonella have developed resistance or are less susceptible to fluoroquinolones. Salmonella presents its resistance by substituting amino acids within the topoisomerase subunits, overexpression of multidrug efflux pumps, or decreasing the expression of outer membrane porins. The resistance level is further increased with the plasmid-mediated quinolone resistance genes which could horizontally transfer the resistance from strain to strain. The development of resistance in Salmonella shows that it is a multifactorial process and the acquisition of fluoroquinolone resistance might have significant influences on the bacterial fitness and virulence. Due to the high level resistance against fluoroquinolones that has been observed in Salmonella, care needs to be taken to avoid misuse and overuse of this important class of antibiotics to minimize the occurrence and dissemination of resistance.
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