Department of Clinical Laboratory, Jinan Fourth People's Hospital, Jinan, Shandong 250031, P.R. China.
Department of Clinical Laboratory, Jinan Infectious Disease Hospital Affiliated to Shandong University, Jinan, Shandong 250021, P.R. China.
Mol Med Rep. 2018 Jun;17(6):8228-8236. doi: 10.3892/mmr.2018.8916. Epub 2018 Apr 23.
The aim of the present study was to investigate the correlation between the multi‑drug resistance of Shigella flexneri and the drug‑resistant gene cassette carried by integrons; in the meanwhile, to detect the associations between drug‑resistance and gene mutations of the active efflux pump acrAB‑tolC gene and its regulatory genes, including marOR, acrR and soxS. A total of 158 isolates were isolated from the stool samples of 1,026 children with diarrhoea aged 14 years old between May 2012 and October 2015 in Henan. The K‑B method was applied for the determination of drug resistance of Shigella flexneri, and polymerase chain reaction amplification was used for class 1, 2 and 3 integrase genes. Enzyme digestion and sequence analysis were performed for the variable regions of positive strains. Based on the drug sensitivity assessment, multi‑drug resistant strains that were resistant to five or more antibiotics, and sensitive strains were selected for amplification. Their active efflux pump genes, acrA and acrB, and regulatory genes, marOR, acrR and soxS, were selected for sequencing. The results revealed that 91.1% of the 158 strains were multi‑resistant to ampicillin, chloramphenicol, tetracycline and streptomycin, and 69.6% of the strains were multi‑resistant to sulfamethoxazole/trimethoprim. The resistance to ceftazidime, ciprofloxacin and levofloxacin was <32.9%. All strains (100%) were sensitive to cefoxitin, cefoperazone/sulbactam and imipenem. The rate of the class 1 integron positivity was 91.9% (144/158). Among these class 1 integron‑positive strains, 18 strains exhibited the resistance gene cassette dfrV in the variable region of the strain, four strains exhibited dfrA17‑aadA5 in the variable region and 140 strains exhibited blaOXA‑30‑aadA1 in the variable region. Four strains showed no resistance gene in the variable regions. The rate of class 2 integron positivity was 86.1% (136/158), and all positive strains harboured the dfrA1‑sat1‑aadA resistance gene cassette in the variable region. The class 3 integrase gene was not detected in these strains. The gene sequencing showed the deletion of base CATT in the 36, 37, 38, 39 site in the marOR gene, which is a regulatory gene of the active efflux pump, AcrAB‑TolC. Taken together, the multi‑drug resistance of Shigella flexneri was closely associated with gene mutations of class 1 and 2 integrons and the marOR gene.
本研究旨在探讨福氏志贺菌的多药耐药性与整合子携带的耐药基因盒之间的相关性;同时,检测主动外排泵 acrAB-tolC 基因及其调控基因 marOR、acrR 和 soxS 的基因突变与耐药性之间的关系。2012 年 5 月至 2015 年 10 月,从河南 1026 例 14 岁腹泻儿童的粪便标本中分离出 158 株福氏志贺菌。采用 K-B 法测定福氏志贺菌的耐药性,采用聚合酶链反应扩增 1 类、2 类和 3 类整合酶基因。对阳性菌株的可变区进行酶切和序列分析。基于药敏评估,选择对 5 种或 5 种以上抗生素耐药的多药耐药菌株和敏感菌株进行扩增。选择其主动外排泵基因 acrA 和 acrB 及其调控基因 marOR、acrR 和 soxS 进行测序。结果显示,158 株菌对氨苄西林、氯霉素、四环素和链霉素的多耐药率为 91.1%,对磺胺甲恶唑/甲氧苄啶的多耐药率为 69.6%。对头孢他啶、环丙沙星和左氧氟沙星的耐药率<32.9%。所有菌株(100%)对头孢西丁、头孢哌酮/舒巴坦和亚胺培南敏感。1 类整合子阳性率为 91.9%(144/158)。在这些 1 类整合子阳性菌株中,18 株在菌株的可变区显示出 dfrV 耐药基因盒,4 株在可变区显示出 dfrA17-aadA5,140 株在可变区显示出 blaOXA-30-aadA1。4 株在可变区没有耐药基因。2 类整合子阳性率为 86.1%(136/158),所有阳性菌株在可变区均携带 dfrA1-sat1-aadA 耐药基因盒。这些菌株中未检测到 3 类整合酶基因。基因测序显示,marOR 基因(主动外排泵 AcrAB-TolC 的调节基因)36、37、38、39 位碱基 CATT 缺失。综上所述,福氏志贺菌的多药耐药性与 1 类和 2 类整合子和 marOR 基因的基因突变密切相关。