Wang Wei, Peng Zixin, Baloch Zulqarnain, Hu Yujie, Xu Jin, Zhang Wenhui, Fanning Séamus, Li Fengqin
Key Laboratory of Food Safety Risk Assessment, Ministry of Health, China National Center for Food Safety Risk Assessment, Beijing, PR China.
College of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, PR China.
Microbiol Res. 2017 Nov;204:48-54. doi: 10.1016/j.micres.2017.07.006. Epub 2017 Jul 27.
The objective of this study was to genetically characterize the antimicrobial resistance mechanisms of Salmonella enterica serotype Indiana C629 isolated from a chicken carcass in China in 2014.
Antimicrobial susceptibility against a panel of 23 antimicrobial agents was carried out on Salmonella enterica serotype Indiana C629 and assessed according to CLSI standards. Whole-genome sequencing of this isolate was conducted to obtain the complete genome of S. Indiana.
Salmonella Indiana C629 expressed an XDR phenotype being resistant to more than 20 antimicrobial agents, including imipenem and meropenem. From the analysis of the resistance mechanisms, two mutations were identified in subunit A of DNA gyrase within the quinolone resistance determining region, in addition to the acquisition of mobile efflux pumps encoding oqxA/B/R. Additionally, four beta-lactamases resistance genes (bla, bla, bla, and bla), five aminoglycosides resistance genes (aac(3)-IV, aac(6')-Ib-cr, aadA2, aadA5, and aph(4)-Ia), two phenicol resistance genes (catB3 and floR), and five trimethoprim/sulfamethoxazole resistance genes (sul1/2/3 and dfrA12/17) were also identified. A total of 191 virulence genes were identified. Among them, 57 belonged to type-three secretion system (T3SS) encoding genes, 55 belonged to fimbrial adherence encoding genes, and 39 belonged to flagella-encoding genes CONCLUSIONS: This study demonstrated that multi-resistance mechanisms consistent with an XDR-phenotype, along with various virulence encoding genes of a S. Indiana strain in China These findings highlight the importance of cooperation among different sectors in order to monitor the spread of resistant pathogens among food animal, foods of animal origin and human beings that might further take measures to protect consumers' health.
本研究的目的是对2014年从中国一具鸡尸体中分离出的肠炎沙门氏菌印第安纳血清型C629的抗菌耐药机制进行基因特征分析。
对肠炎沙门氏菌印第安纳血清型C629进行了针对23种抗菌药物的药敏试验,并根据CLSI标准进行评估。对该分离株进行全基因组测序以获得印第安纳沙门氏菌的完整基因组。
沙门氏菌印第安纳C629表现出广泛耐药(XDR)表型,对20多种抗菌药物耐药,包括亚胺培南和美罗培南。通过对耐药机制的分析,除了获得编码oqxA/B/R的移动外排泵外,在喹诺酮耐药决定区域内的DNA促旋酶A亚基中鉴定出两个突变。此外,还鉴定出四个β-内酰胺酶耐药基因(bla、bla、bla和bla)、五个氨基糖苷类耐药基因(aac(3)-IV、aac(6')-Ib-cr、aadA2、aadA5和aph(4)-Ia)、两个氯霉素耐药基因(catB3和floR)以及五个甲氧苄啶/磺胺甲恶唑耐药基因(sul1/2/3和dfrA12/17)。共鉴定出191个毒力基因。其中,57个属于编码三型分泌系统(T3SS)的基因,55个属于编码菌毛黏附的基因,39个属于编码鞭毛的基因。结论:本研究表明,中国一株印第安纳沙门氏菌菌株存在与XDR表型一致的多重耐药机制以及各种毒力编码基因。这些发现凸显了不同部门之间合作的重要性,以便监测耐药病原体在食用动物、动物源性食品和人类之间的传播,进而采取措施保护消费者健康。