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伤寒沙门氏菌和甲型副伤寒沙门氏菌对环丙沙星高水平耐药的分子分析:是否需要扩大喹诺酮耐药决定区?

Molecular analysis of high-level ciprofloxacin resistance in Salmonella enterica serovar Typhi and S. Paratyphi A: need to expand the QRDR region?

作者信息

Capoor M R, Nair D, Walia N S, Routela R S, Grover S S, Deb M, Aggarwal P, Pillai P K, Bifani P J

机构信息

Department of Microbiology, Vardhman Mahaveer Medical College and Safdarjung Hospital, New Delhi, India.

出版信息

Epidemiol Infect. 2009 Jun;137(6):871-8. doi: 10.1017/S0950268808001076. Epub 2008 Aug 8.

Abstract

Fourteen strains of S. Typhi (n=13) and S. Paratyphi A (n=1) resistant to ciprofloxacin were compared with 30 ciprofloxacin decreased-susceptibility strains on the basis of qnr plasmid analysis, and nucleotide substitutions at gyrA, gyrB, parC and parE. In ciprofloxacin-resistant strains, five S. Typhi and a single S. Paratyphi A showed triple mutations in gyrA (Ser83-->Phe, Asp87-->Asn, Glu133-->Gly) and a novel mutation outside the quinolone resistance determining region (QRDR) (Met52-->Leu). Novel mutations were also discovered in an isolate (minimum inhibitory concentration 8 microg/ml) in gyrA gene Asp76-->Asn and outside the QRDR Leu44-->Ile. Out of 30 isolates with reduced susceptibility, single mutation was found in 12 strains only. Genes encoding qnr plasmid (qnr A, qnr B, AAC1-F) were not detected in ciprofloxacin-resistant or decreased-susceptibility strains. Antimicrobial surveillance coupled with molecular analysis of fluoroquinolone resistance is warranted for reconfirming novel and established molecular patterns of resistance, which is quintessential for reappraisal of enteric fever therapeutics.

摘要

基于qnr质粒分析以及gyrA、gyrB、parC和parE的核苷酸替换情况,将14株对环丙沙星耐药的伤寒沙门氏菌(n = 13)和甲型副伤寒沙门氏菌(n = 1)与30株对环丙沙星敏感性降低的菌株进行了比较。在对环丙沙星耐药的菌株中,5株伤寒沙门氏菌和1株甲型副伤寒沙门氏菌在gyrA基因上出现三重突变(Ser83→Phe、Asp87→Asn、Glu133→Gly),并在喹诺酮耐药决定区(QRDR)之外出现一个新突变(Met52→Leu)。在一株分离株(最低抑菌浓度为8μg/ml)中还发现了gyrA基因的新突变Asp76→Asn以及QRDR之外的Leu44→Ile。在30株敏感性降低的分离株中,仅12株发现了单个突变。在对环丙沙星耐药或敏感性降低的菌株中未检测到编码qnr质粒的基因(qnr A、qnr B、AAC1-F)。有必要将抗菌监测与氟喹诺酮耐药性的分子分析相结合,以重新确认新的和已确定的耐药分子模式,这对于重新评估肠热病治疗方法至关重要。

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