Re-analysis of an outbreak of Shiga toxin-producing Escherichia coli O157:H7 associated with raw drinking milk using Nanopore sequencing

被引:2
|
作者
Greig, David R. [1 ,2 ,3 ,4 ]
Do Nascimento, Vivienne [1 ]
Gally, David L. [3 ,4 ]
Gharbia, Saheer E. [1 ,5 ]
Dallman, Timothy J. [6 ]
Jenkins, Claire [1 ,2 ]
机构
[1] United Kingdom Hlth Secur Agcy, Natl Infect Serv, London NW9 5EQ, England
[2] NIRH Hlth Protect Res Unit Gastrointestinal Pathog, Liverpool, England
[3] Univ Edinburgh, Div Infect & Immun, Roslin Inst, Edinburgh, Scotland
[4] Univ Edinburgh, Royal Dick Sch Vet Studies, Edinburgh, Scotland
[5] NIHR Hlth Protect Res Unit Genomes & Enabling Data, Warwick, England
[6] Univ Utrecht, Inst Risk Assessment Sci IRAS, Fac Vet Med, NL-3584 CL Utrecht, Netherlands
关键词
Foodborne outbreak; Genomic epidemiology; STEC O157:H7; WGS; Nanopore; Illumina; Prophage comparison; ENGLAND; IDENTIFICATION; ALIGNMENT; O157-H7; CATTLE;
D O I
10.1038/s41598-024-54662-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The aim of this study was to compare Illumina and Oxford Nanopore Technology (ONT) sequencing data to quantify genetic variation to assess within-outbreak strain relatedness and characterise microevolutionary events in the accessory genomes of a cluster of 23 genetically and epidemiologically linked isolates related to an outbreak of Shiga toxin-producing Escherichia coli O157:H7 caused by the consumption of raw drinking milk. There were seven discrepant variants called between the two technologies, five were false-negative or false-positive variants in the Illumina data and two were false-negative calls in ONT data. After masking horizontally acquired sequences such as prophages, analysis of both short and long-read sequences revealed the 20 isolates linked to the outbreak in 2017 had a maximum SNP distance of one SNP between each other, and a maximum of five SNPs when including three additional strains identified in 2019. Analysis of the ONT data revealed a 47 kbp deletion event in a terminal compound prophage within one sample relative to the remaining samples, and a 0.65 Mbp large chromosomal rearrangement (inversion), within one sample relative to the remaining samples. Furthermore, we detected two bacteriophages encoding the highly pathogenic Shiga toxin (Stx) subtype, Stx2a. One was typical of Stx2a-phage in this sub-lineage (Ic), the other was atypical and inserted into a site usually occupied by Stx2c-encoding phage. Finally, we observed an increase in the size of the pO157 IncFIB plasmid (1.6 kbp) in isolates from 2019 compared to those from 2017, due to the duplication of insertion elements within the plasmids from the more recently isolated strains. The ability to characterize the accessory genome in this way is the first step to understanding the significance of these microevolutionary events and their impact on the genome plasticity and virulence between strains of this zoonotic, foodborne pathogen.
引用
收藏
页数:12
相关论文
共 50 条
  • [21] Quantitative Detection of Shiga Toxin-Producing and Enteropathogenic Escherichia coli Serotypes O157 and O26 in Bulk Raw Milk
    Trevisani, Marcello
    Mancusi, Rocco
    Riu, Raffaela
    Serraino, Andrea
    FOOD ANALYTICAL METHODS, 2013, 6 (06) : 1750 - 1758
  • [22] Risk of Escherichia coli O157:H7, Non-O157 Shiga Toxin-Producing Escherichia coli, and Campylobacter spp. in Food Animals and Their Products in Qatar
    Mohammed, Hussni O.
    Stipetic, Korana
    Salem, Ahmed
    McDonough, Patrick
    Chang, Yung Fu
    Sultan, Ali
    JOURNAL OF FOOD PROTECTION, 2015, 78 (10) : 1812 - 1818
  • [23] An outbreak of Shiga toxin-producing Escherichia coli serogroup O157 linked to a lamb-feeding event
    Rowell, S.
    King, C.
    Jenkins, C.
    Dallman, T. J.
    Decraene, V.
    Lamden, K.
    Howard, A.
    Featherstone, C. A.
    Cleary, P.
    EPIDEMIOLOGY AND INFECTION, 2016, 144 (12) : 2494 - 2500
  • [24] Identification of shiga toxin producing Escherichia coli O157:H7 in raw cow milk samples from dairy farms in Mashhad using multiplex PCR assay
    Brenjchi, M.
    Jamshidi, A.
    Farzaneh, N.
    Bassami, M. R.
    IRANIAN JOURNAL OF VETERINARY RESEARCH, 2011, 12 (02) : 145 - 149
  • [25] stx genotype and molecular epidemiological analyses of Shiga toxin-producing Escherichia coli O157:H7/H- in human and cattle isolates
    Kawano, K.
    Ono, H.
    Iwashita, O.
    Kurogi, M.
    Haga, T.
    Maeda, K.
    Goto, Y.
    EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2012, 31 (02) : 119 - 127
  • [26] Comparative genomic analysis of Shiga toxin-producing and non-Shiga toxin-producing Escherichia coli O157 isolated from outbreaks in Korea
    Kwon, Taesoo
    Kim, Won
    Cho, Seung-Hak
    GUT PATHOGENS, 2017, 9 : 1 - 8
  • [27] Host range and lytic capability of four bacteriophages against bovine and clinical human isolates of Shiga toxin-producing Escherichia coli O157:H7
    Niu, Y. D.
    Johnson, R. P.
    Xu, Y.
    McAllister, T. A.
    Sharma, R.
    Louie, M.
    Stanford, K.
    JOURNAL OF APPLIED MICROBIOLOGY, 2009, 107 (02) : 646 - 656
  • [28] Escherichia coli O157:H7 and non-O157 Shiga toxin-producing E-coli in healthy cattle, sheep and swine herds in northern Spain
    Oporto, B.
    Esteban, J. I.
    Aduriz, G.
    Juste, R. A.
    Hurtado, A.
    ZOONOSES AND PUBLIC HEALTH, 2008, 55 (02) : 73 - 81
  • [29] Quantitative Risk Assessment of Haemolytic and Uremic Syndrome Linked to O157:H7 and Non-O157:H7 Shiga-Toxin Producing Escherichia coli Strains in Raw Milk Soft Cheeses
    Perrin, Frederique
    Tenenhaus-Aziza, Fanny
    Michel, Valerie
    Miszczycha, Stephane
    Bel, Nadege
    Sanaa, Moez
    RISK ANALYSIS, 2015, 35 (01) : 109 - 128
  • [30] Shiga toxin-producing Escherichia coli in Central Greece: prevalence and virulence genes of O157:H7 and non-O157 in animal feces, vegetables, and humans
    Pinaka, O.
    Pournaras, S.
    Mouchtouri, V.
    Plakokefalos, E.
    Katsiaflaka, A.
    Kolokythopoulou, F.
    Barboutsi, E.
    Bitsolas, N.
    Hadjichristodoulou, C.
    EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2013, 32 (11) : 1401 - 1408