Ceyssens Pieter-Jan, Mattheus Wesley, Vanhoof Raymond, Bertrand Sophie
Unit Bacterial Diseases, Scientific Institute of Public Health (WIV-ISP), Brussels, Belgium.
Unit Bacterial Diseases, Scientific Institute of Public Health (WIV-ISP), Brussels, Belgium
Antimicrob Agents Chemother. 2015 Jan;59(1):544-52. doi: 10.1128/AAC.04203-14. Epub 2014 Nov 10.
The Belgian National Reference Centre for Salmonella received 16,544 human isolates of Salmonella enterica between January 2009 and December 2013. Although 377 different serotypes were identified, the landscape is dominated by S. enterica serovars Typhimurium (55%) and Enteritidis (19%) in a ratio which is inverse to European Union averages. With outbreaks of Salmonella serotypes Ohio, Stanley, and Paratyphi B variant Java as prime examples, 20 serotypes displayed significant fluctuations in this 5-year period. Typhoid strains account for 1.2% of Belgian salmonellosis cases. Large-scale antibiotic susceptibility analyses (n = 4,561; panel of 12 antibiotics) showed declining resistance levels in S. Enteritis and Typhimurium isolates for 8 and 3 tested agents, respectively. Despite low overall resistance to ciprofloxacin (4.4%) and cefotaxime (1.6%), we identified clonal lineages of Salmonella serotypes Kentucky and Infantis displaying rising resistance against these clinically important drugs. Quinolone resistance is mainly mediated by serotype-specific mutations in GyrA residues Ser83 and Asp87 (92.2% not wild type), while an additional ParC_Ser80Ile mutation leads to ciprofloxacin resistance in 95.5% S. Kentucky isolates, which exceeds European averages. Plasmid-mediated quinolone resistance (PMQR) alleles qnrA1 (n = 1), qnrS (n = 9), qnrD1 (n = 4), and qnrB (n = 4) were found in only 3.0% of 533 isolates resistant to nalidixic acid. In cefotaxime-resistant isolates, we identified a broad range of Ambler class A and C β-lactamase genes (e.g., bla(SHV-12), blaTEM-52, bla(CTX-M-14), and bla(CTX-M-15)) commonly associated with members of the family Enterobacteriaceae. In conclusion, resistance to fluoroquinolones and cefotaxime remains rare in human S. enterica, but clonal resistant serotypes arise, and continued (inter)national surveillance is mandatory to understand the origin and routes of dissemination thereof.
2009年1月至2013年12月期间,比利时国家沙门氏菌参考中心接收了16544株人源肠炎沙门氏菌分离株。尽管鉴定出377种不同血清型,但肠炎沙门氏菌血清型鼠伤寒沙门氏菌(55%)和肠炎沙门氏菌(19%)占主导地位,其比例与欧盟平均水平相反。以沙门氏菌血清型俄亥俄、斯坦利和副伤寒B变种爪哇的暴发为例,20种血清型在这5年期间出现了显著波动。伤寒菌株占比利时沙门氏菌病病例的1.2%。大规模抗生素敏感性分析(n = 4561;12种抗生素检测组)显示,肠炎沙门氏菌和鼠伤寒沙门氏菌分离株对8种和3种检测药物的耐药水平分别下降。尽管对环丙沙星(4.4%)和头孢噻肟(1.6%)的总体耐药率较低,但我们鉴定出沙门氏菌血清型肯塔基和婴儿沙门氏菌的克隆谱系对这些临床重要药物的耐药性正在上升。喹诺酮耐药性主要由GyrA残基Ser83和Asp87的血清型特异性突变介导(92.2%非野生型),而额外的ParC_Ser80Ile突变导致95.5%的肯塔基沙门氏菌分离株对环丙沙星耐药,这超过了欧盟平均水平。在533株对萘啶酸耐药的分离株中,仅3.0%发现了质粒介导的喹诺酮耐药性(PMQR)等位基因qnrA1(n = 1)、qnrS(n = 9)、qnrD1(n = 4)和qnrB(n = 4)。在对头孢噻肟耐药的分离株中,我们鉴定出广泛的安布勒A类和C类β-内酰胺酶基因(如bla(SHV-12)、blaTEM-52、bla(CTX-M-14)和bla(CTX-M-15)),这些基因通常与肠杆菌科成员相关。总之,人源肠炎沙门氏菌对氟喹诺酮和头孢噻肟的耐药性仍然罕见,但出现了克隆耐药血清型,必须持续进行(国际)监测以了解其起源和传播途径。