Molecular epidemiology of Salmonella enterica serovar Kottbus isolated in Germany from humans, food and animals

被引:12
|
作者
Toboldt, Anne [1 ,2 ]
Tietze, Erhard [3 ]
Helmuth, Reiner [1 ]
Junker, Ernst [1 ]
Fruth, Angelika [3 ]
Malorny, Burkhard [1 ]
机构
[1] Fed Inst Risk Assessment, Natl Reference Lab Salmonella, D-10589 Berlin, Germany
[2] Free Univ Berlin, Dept Biol Chem & Pharm, D-14195 Berlin, Germany
[3] Natl Reference Ctr Salmonellae & Other Bacterial, Div Enteropathogen Bacteria & Legionella, Wernigerode Branch, Robert Koch Inst, D-38855 Wernigerode, Germany
关键词
Salmonella enterica serovar Kottbus; Poultry; Infection source; Multilocus sequence typing; Pulsed-field gel electrophoresis; Antimicrobial resistance; RESISTANCE; INTEGRONS; INFECTION;
D O I
10.1016/j.vetmic.2014.01.020
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Salmonella enterica serovar Kottbus has been continuously isolated from poultry and poultry meat, especially from turkey. We investigated by comparative molecular typing 95 S. Kottbus isolates obtained in Germany between 2000 and 2011 from poultry/poultry meat, pig/pork, cattle, reptiles, the environment as well as from human cases to identify potential infection sources for humans, especially the role of poultry and poultry products as vehicle in transmission of S. Kottbus isolates to humans. Multilocus sequence typing analysis detected three main genetic lineages. Most human isolates belonged to lineage 1 represented by sequence types ST212 and ST808. Part of the isolates isolated from cattle and pork were also linked to this lineage. Nevertheless, human isolates and especially isolates from poultry/poultry meat, and with less extend from other livestock, grouped in lineage 2 represented by ST582. Four additional isolates from reptiles and humans belonging to ST1669 represented the third lineage. The three lineages were also reflected by pulsed-field gel electrophoresis typing data and DNA microarray analysis of 102 pathogenicity genes. Antimicrobial resistance especially to nalidixic acid and ciprofloxacin was predominantly observed in isolates assigned to lineage 2, which contains predominantly resistant isolates compared to lineage 1 and 3. Sequencing of the quinolone resistance-determining region of gyrA revealed a point mutation in codon 83 or 87 responsible for nalidixic acid resistance and MIC values for ciprofloxacin between 0.125 and 0.25 mg/l. Overall, this study showed that in Germany a specific S. Kottbus lineage (ST582), which is well-established in poultry, can be transmitted to humans by poultry meat and, consequently, poses a risk for human health. (c) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:97 / 108
页数:12
相关论文
共 50 条
  • [41] Characterization of class I integrons among Salmonella enterica serovar Enteritidis isolated from humans and poultry
    Firoozeh, Farzaneh
    Zahraei-Salehi, Taghi
    Shahcheraghi, Fereshteh
    Karimi, Vahid
    Aslani, Mohammad M.
    FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 2012, 64 (02): : 237 - 243
  • [42] Changing Patterns of Salmonella enterica Serovar Rissen From Humans, Food Animals, and Animal-Derived Foods in China, 1995-2019
    Elbediwi, Mohammed
    Shi, Daiwei
    Biswas, Silpak
    Xu, Xuebin
    Yue, Min
    FRONTIERS IN MICROBIOLOGY, 2021, 12
  • [43] Genetic Relationships among Multidrug-Resistant Salmonella enterica Serovar Typhimurium Strains from Humans and Animals
    Hong, Yu-Ping
    Wang, You-Wun
    Huang, I-Hsiu
    Liao, Yu-Chieh
    Kuo, Hung-Chih
    Liu, Yen-Yi
    Tu, Yueh-Hua
    Chen, Bo-Han
    Liao, Ying-Shu
    Chiou, Chien-Shun
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2018, 62 (05)
  • [44] Emerging high-level ciprofloxacin resistance and molecular basis of resistance in Salmonella enterica from humans, food and animals
    Kuang, Dai
    Zhang, Jianmin
    Xu, Xuebin
    Shi, Weimin
    Chen, Sheng
    Yang, Xiaowei
    Su, Xudong
    Shi, Xianming
    Meng, Jianghong
    INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2018, 280 : 1 - 9
  • [45] Characterization of Antimicrobial Resistance in Salmonella enterica Serotype Heidelberg Isolated from Food Animals
    Lynne, Aaron M.
    Kaldhone, Pravin
    David, Donna
    White, David G.
    Foley, Steven L.
    FOODBORNE PATHOGENS AND DISEASE, 2009, 6 (02) : 207 - 215
  • [46] Antimicrobial Resistance Profiles and Molecular Characteristics of Salmonella enterica Serovar Agona Isolated from Food-Producing Animals During 2010-2020 in South Korea
    Song, Hyun-Ju
    Ali, Sekendar
    Moon, Bo-Youn
    Kang, Hee Young
    Noh, Eun Jeong
    Kim, Tae-Sun
    Kim, Su-Jeong
    Kim, Ji-In
    Lee, Yun Jin
    Yoon, Soon-Seek
    Lim, Suk-Kyung
    FOODBORNE PATHOGENS AND DISEASE, 2025, 22 (03) : 210 - 218
  • [47] Molecular follow-up of Salmonella enterica subsp enterica serovar Agona infection in cattle and humans
    Lindqvist, N
    Sittonen, A
    Pelkonen, S
    JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (10) : 3648 - 3653
  • [48] Isolation and molecular characterization of Salmonella enterica serovar Javiana from food, environmental and clinical samples
    Mezal, Ezat H.
    Stefanova, Rossina
    Khan, Ashraf A.
    INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2013, 164 (01) : 113 - 118
  • [49] Clonal Dissemination of Salmonella enterica Serovar Infantis in Germany
    Hauser, Elisabeth
    Tietze, Erhard
    Helmuth, Reiner
    Junker, Ernst
    Prager, Rita
    Schroeter, Andreas
    Rabsch, Wolfgang
    Fruth, Angelika
    Toboldt, Anne
    Malorny, Burkhard
    FOODBORNE PATHOGENS AND DISEASE, 2012, 9 (04) : 352 - 360
  • [50] Molecular epidemiology of antimicrobial resistance among Salmonella enterica serovar Infantis from poultry in Kagoshima, Japan
    Shahada, Francis
    Chuma, Takehisa
    Tobata, Takayuki
    Okamoto, Karoku
    Sueyoshi, Masuo
    Takase, Kozo
    INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2006, 28 (04) : 302 - 307