Feasibility of Using Multiple-Locus Variable-Number Tandem-Repeat Analysis for Epidemiology Study of Vibrio parahaemolyticus Infections

被引:2
|
作者
Jiang, Min [1 ]
Zhang, Jinjin [2 ]
Li, Yinghui [1 ]
Shi, Xiaolu [1 ]
Qiu, Yaqun [1 ]
Lin, Yiman [1 ]
Chen, Qiongcheng [1 ]
Jiang, Yixiang [1 ]
Hu, Qinghua [1 ]
机构
[1] Shenzhen Ctr Dis Control & Prevent, Shenzhen Major Infect Dis Control Key Lab, Longyuan Rd 8, Shenzhen 518055, Guangdong, Peoples R China
[2] Futian Dist Ctr Dis Control & Prevent, Shenzhen, Peoples R China
基金
中国国家自然科学基金;
关键词
FIELD GEL-ELECTROPHORESIS; SOUTHERN COASTAL REGION; ANALYSIS MLVA; CHINA; STRAINS; IDENTIFICATION; OUTBREAKS;
D O I
10.1089/fpd.2016.2141
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Vibrio parahaemolyticus causes foodborne gastroenteritis, which is often associated with the consumption of raw or undercooked shellfish. Molecular typing can provide critical information for detecting outbreaks and for source attribution. In this study, we describe the development and evaluation of an optimized multiple-locus variable-number tandem-repeat (VNTR) analysis (MLVA) for the characterization of V. parahaemolyticus isolates. The discriminatory power of MLVA was compared to that of pulsed-field gel electrophoresis (PFGE) by typing 73 sporadic isolates. Epidemiologic concordance was evaluated by typing 23 isolates from five epidemiologically well-characterized outbreaks. The optimized MLVA was applied in early warning, epidemiological surveillance, and source tracking for V. parahaemolyticus infections. There was no significant difference in the discriminatory power of PFGE and MLVA with six or eight VNTR loci for the sporadic isolates. All isolates within an outbreak were indistinguishable by MLVA with six loci, except for one outbreak. Typically, the epidemiological survey could be initiated according to PFGE clusters. We applied MLVA with six loci on 22 isolates in two PFGE clusters. Isolates in one PFGE cluster were distinguished by MLVA. Although a follow-up investigation showed that both clusters had no epidemiological concordance, MLVA decreased the frequency of initiation of epidemiological surveys, thereby reducing labor costs. The ability of MLVA to trace the source of infection was evaluated by isolates from two outbreaks and shrimp samples. The isolates from one of outbreaks and a shrimp had the same MLVA type, suggesting that an epidemiological survey was initiated. Data from the epidemiological investigation subsequently indicated that contaminated shrimp from a nearby city (Dongguan) might be the source of the outbreak. In conclusion, these results indicate that the optimized MLVA may be a promising tool for early warning and epidemiological surveillance of V. parahaemolyticus infections.
引用
收藏
页码:575 / 581
页数:7
相关论文
共 50 条
  • [21] Development of a Multiple-Locus Variable-Number Tandem-Repeat Typing Scheme for Genetic Fingerprinting of Burkholderia cenocepacia and Application to Nationwide Epidemiological Analysis
    Segonds, Christine
    Thouverez, Michelle
    Barthe, Antoine
    Bossuet-Greif, Nadege
    Tisseyre, Lenka
    Plesiat, Patrick
    Vergnaud, Gilles
    Chabanon, Gerard
    Pourcel, Christine
    JOURNAL OF CLINICAL MICROBIOLOGY, 2015, 53 (02) : 398 - 409
  • [22] Comparison of Multiple-Locus Variable-Number Tandem-Repeat Analysis with Pulsed-Field Gel Electrophoresis Typing of Acinetobacter baumannii in China
    Hu, Yuan
    Li, Boqing
    Jin, Dazhi
    Cui, Zhigang
    Tao, Xiaoxia
    Zhang, Binghua
    Zhang, Jianzhong
    JOURNAL OF CLINICAL MICROBIOLOGY, 2013, 51 (04) : 1263 - 1268
  • [23] Multiple-Locus Variable-Number Tandem Repeat Analysis of Vibrio cholerae in Comparison with Pulsed Field Gel Electrophoresis and Virulotyping
    Teh, Cindy Shuan Ju
    Chua, Kek Heng
    Thong, Kwai Lin
    JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY, 2010,
  • [24] Characterization of Escherichia coli O157:H7 in New Zealand using multiple-locus variable-number tandem-repeat analysis
    Dyet, K. H.
    Robertson, I.
    Turbitt, E.
    Carter, P. E.
    EPIDEMIOLOGY AND INFECTION, 2011, 139 (03) : 464 - 471
  • [25] Identification of the Source of Francisella tularensis Infection by Multiple-Locus Variable-Number Tandem Repeat Analysis
    Fujita, Osamu
    Hotta, Akitoyo
    Uda, Akihiko
    Yamamoto, Yoshie
    Fujita, Hiromi
    Shinya, Fumiaki
    Asano, Shigeyuki
    Morikawa, Shigeru
    Tanabayashi, Kiyoshi
    Yamada, Akio
    JAPANESE JOURNAL OF INFECTIOUS DISEASES, 2013, 66 (06) : 543 - 545
  • [26] A Single-Tube Multiple-Locus Variable-Number Tandem-Repeat Analysis of Mycoplasma pneumoniae Clinical Specimens by Use of Multiplex PCR-Capillary Electrophoresis
    Yan, Chao
    Sun, Hongmei
    Xue, Guanhua
    Zhao, Hanqing
    Wang, Liqiong
    Feng, Yanling
    Li, Shaoli
    JOURNAL OF CLINICAL MICROBIOLOGY, 2014, 52 (12) : 4168 - 4171
  • [27] Multiple-Locus Variable-Number Tandem-Repeat Analysis of 201 Mycoplasma pneumoniae Isolates from Beijing, China, from 2008 to 2011
    Zhao, Fei
    Liu, Gang
    Cao, Bin
    Wu, Jiang
    Gu, Yixin
    He, Lihua
    Meng, Fanliang
    Zhu, Liang
    Yin, Yudong
    Lv, Min
    Zhang, Jianzhong
    JOURNAL OF CLINICAL MICROBIOLOGY, 2013, 51 (02) : 636 - 639
  • [28] Utilizing Rapid Multiple-Locus Variable-Number Tandem-Repeat Analysis Typing To Aid Control of Hospital-Acquired Clostridium difficile Infection: a Multicenter Study
    Hardy, Katherine
    Manzoor, Susan
    Marriott, Claire
    Parsons, Helen
    Waddington, Claire
    Gossain, Savita
    Szczepura, Ala
    Stallard, Nigel
    Hawkey, Peter M.
    JOURNAL OF CLINICAL MICROBIOLOGY, 2012, 50 (10) : 3244 - 3248
  • [29] Multiple-locus variable-number tandem-repeat analysis for discriminating within Salmonella enterica serovar Typhimurium definitive types and investigation of outbreaks
    Dyet, K. H.
    Turbitt, E.
    Carter, P. E.
    EPIDEMIOLOGY AND INFECTION, 2011, 139 (07) : 1050 - 1059
  • [30] Identification of Variable-Number Tandem-Repeat (VNTR) Sequences in Acinetobacter baumannii and Interlaboratory Validation of an Optimized Multiple-Locus VNTR Analysis Typing Scheme
    Pourcel, Christine
    Minandri, Fabrizia
    Hauck, Yolande
    D'Arezzo, Silvia
    Imperi, Francesco
    Vergnaud, Gilles
    Visca, Paolo
    JOURNAL OF CLINICAL MICROBIOLOGY, 2011, 49 (02) : 539 - 548