Division for Infection Control and Environmental Health, Norwegian Institute of Public Health (NIPH), Oslo, Norway.
European Program for Public Health Microbiology Training (EUPHEM), European Centre for Disease Prevention and Control (ECDC), Stockholm, Sweden.
Euro Surveill. 2019 Jan;24(4). doi: 10.2807/1560-7917.ES.2019.24.4.1800186.
IntroductionDuring summer 2016, Norway observed an increase in subsp. serovar Chester cases among travellers to Greece.AimOur aim was to investigate genetic relatedness of Chester for surveillance and outbreak detection by core genome multilocus sequence typing (cgMLST) and compare the results to genome mapping.MethodsWe included Chester isolates from 51 cases of salmonellosis between 2000 and 2016. Paired-end sequencing (2 × 250 bp) was performed on Illumina MiSeq. Genetic relatedness by cgMLST for subsp. including 3,002 genes and seven housekeeping genes, was compared by reference genome mapping with CSI Phylogeny version 1.4 and conventional MLST.ResultsConfirmed travel history was available for 80% of included cases, to Europe (n = 13), Asia (n = 12) and Africa (n = 16). Isolates were distributed into four phylogenetic clusters corresponding to geographical regions. Sequence type (ST) ST411 and a single-locus variant ST5260 (n = 17) were primarily acquired in southern Europe, ST1954 (n = 15) in Africa, ST343 (n = 11) and ST2063 (n = 8) primarily in Asia. Part of the European cluster was further divided into a Greek (n = 10) and a Cypriot (n = 4) cluster. All isolates in the African cluster displayed resistance to ≥ 1 class of antimicrobials, while resistance was rare in the other clusters.ConclusionWhole genome sequencing of Chester in Norway showed four geographically distinct clusters, with a possible outbreak occurring during summer 2016 related to Greece. We recommend public health institutes to implement cgMLST-based real-time surveillance for early and accurate detection of future outbreaks and further development of cluster cut-offs.
引言
2016 年夏季,挪威观察到前往希腊旅行的人群中副伤寒血清型切斯特亚种病例有所增加。
目的
我们旨在通过核心基因组多位点序列分型(cgMLST)调查切斯特氏菌的遗传相关性,用于监测和暴发检测,并将结果与基因组图谱进行比较。
方法
我们纳入了 2000 年至 2016 年间 51 例沙门氏菌病的切斯特分离株。在 Illumina MiSeq 上进行了配对末端测序(2×250 bp)。通过参考基因组图谱与 CSI Phylogeny version 1.4 和传统 MLST 对包括 3002 个基因和 7 个管家基因的副伤寒血清型 cgMLST 的遗传相关性进行比较。
结果
纳入病例中有 80%(n=41)可确认旅行史,前往欧洲(n=13)、亚洲(n=12)和非洲(n=16)。分离株分为四个与地理区域相对应的系统发育群。序列型(ST)ST411 和单一位点变异 ST5260(n=17)主要在南欧获得,ST1954(n=15)在非洲,ST343(n=11)和 ST2063(n=8)主要在亚洲。部分欧洲群进一步分为希腊(n=10)和塞浦路斯(n=4)群。非洲群中的所有分离株均对≥1 类抗生素表现出耐药性,而其他群中耐药性罕见。
结论
挪威对切斯特氏菌的全基因组测序显示了四个具有地理差异的群,2016 年夏季可能与希腊有关的暴发。我们建议公共卫生机构实施基于 cgMLST 的实时监测,以早期、准确地检测未来的暴发,并进一步制定群集截止值。