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沙门氏菌中同时编码对环丙沙星和头孢曲松耐药性的可接合质粒的进化和传播。

Evolution and transmission of a conjugative plasmid encoding both ciprofloxacin and ceftriaxone resistance in Salmonella.

机构信息

a Shenzhen Key Lab for Food Biological Safety Control, Food Safety and Technology Research Center, Hong Kong PolyU Shen Zhen Research Institute , Shenzhen , People's Republic of China.

b Department of Applied Biology and Chemical Technology , State Key Lab of Chirosciences, The Hong Kong Polytechnic University , Kowloon , Hong Kong.

出版信息

Emerg Microbes Infect. 2019;8(1):396-403. doi: 10.1080/22221751.2019.1585965.

Abstract

Ceftriaxone and ciprofloxacin are the drugs of choice in treatment of invasive Salmonella infections. This study discovered a novel type of plasmid, pSa44-CIP-CRO, which was recovered from a S. London strain isolated from meat product and comprised genetic determinants that encoded resistance to both ciprofloxacin and ceftriaxone. This plasmid could be resolved into two daughter plasmids and co-exist with such daughter plasmids in a dynamic form in Salmonella; yet it was only present as a single plasmid in Escherichia coli. One daughter plasmid, pSa44-CRO, was found to carry the bla gene, which encodes resistance to ceftriaxone, whereas the other plasmid, pSa44-CIP, carried multiple PMQR genes such as qnrB6-aac(6')-Ib-cr, which mediated resistance to ciprofloxacin. These two daughter plasmids could be integrated into one single plasmid through ISPa40 mediated homologous recombination. Mouse infection and treatment experiments showed that carriage of plasmid, pSa44-CIP-CRO by S. typhimurium led to the impairment of treatment by ciprofloxacin or cefitiofur, a veterinary drug with similar properties as ceftriaxone. In conclusion, dissemination of such conjugative plasmids impairs current choices of treatment for life-threatening Salmonella infection and hence constitutes a serious public health threat.

摘要

头孢曲松和环丙沙星是治疗侵袭性沙门氏菌感染的首选药物。本研究从一种从肉类产品中分离出的 S. London 菌株中发现了一种新型质粒 pSa44-CIP-CRO,该质粒包含编码对环丙沙星和头孢曲松耐药的遗传决定簇。该质粒可被分解为两个子质粒,并以动态形式与沙门氏菌中的子质粒共存;然而,在大肠杆菌中,它仅以单个质粒的形式存在。一个子质粒 pSa44-CRO 携带 bla 基因,该基因编码对头孢曲松的耐药性,而另一个质粒 pSa44-CIP 则携带多种 PMQR 基因,如 qnrB6-aac(6')-Ib-cr,介导对环丙沙星的耐药性。这两个子质粒可以通过 ISPa40 介导的同源重组整合到一个单一的质粒中。小鼠感染和治疗实验表明,鼠伤寒沙门氏菌携带质粒 pSa44-CIP-CRO 会导致对环丙沙星或头孢噻呋(一种与头孢曲松性质相似的兽用药物)治疗的效果受损。总之,这种可接合质粒的传播会损害目前对危及生命的沙门氏菌感染的治疗选择,因此构成了严重的公共卫生威胁。

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