Literature DB >> 22488053

Novel genomic tools for specific and real-time detection of biothreat and frequently encountered foodborne pathogens.

Abdela Woubit1, Teshome Yehualaeshet, Tsegaye Habtemariam, Temesgen Samuel.   

Abstract

The bacterial genera Escherichia, Salmonella, Shigella, Vibrio, Yersinia, and Francisella include important food safety and biothreat agents. By extensive mining of the whole genome and protein databases of diverse, closely and distantly related bacterial species and strains, we have identified novel genome regions, which we utilized to develop a rapid detection platform for these pathogens. The specific genomic targets we have identified to design the primers in Francisella tularensis subsp. tularensis, F. tularensis subsp. novicida, Shigella dysenteriae, Salmonella enterica serovar Typhimurium, Vibrio cholerae, Yersinia pestis, and Yersinia pseudotuberculosis contained either known genes or putative proteins. Primer sets were designed from the target regions for use in real-time PCR assays to detect specific biothreat pathogens at species or strain levels. The primer sets were first tested by in silico PCR against whole-genome sequences of different species, subspecies, or strains and then by in vitro PCR against genomic DNA preparations from 23 strains representing six biothreat agents (Escherichia coli O157:H7 strain EDL 933, Shigella dysenteriae, S. enterica serovar Typhi, F. tularensis subsp. tularensis, V. cholerae, and Y. pestis) and six foodborne pathogens (Salmonella Typhimurium, Salmonella Saintpaul, Shigella sonnei, F. tularensis subsp. novicida, Vibrio parahaemolyticus, and Y. pseudotuberculosis). Each pathogen was specifically identifiable at the genus and species levels. Sensitivity assays performed with purified DNA showed the lowest detection limit of 128 fg of DNA/μl for F. tularensis subsp. tularensis. A preliminary test to detect Shigella organisms in a milk matrix also enabled the detection of 6 to 60 CFU/ml. These new tools could ultimately be used to develop platforms to simultaneously detect these pathogens.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22488053      PMCID: PMC3524339          DOI: 10.4315/0362-028X.JFP-11-480

Source DB:  PubMed          Journal:  J Food Prot        ISSN: 0362-028X            Impact factor:   2.077


  27 in total

1.  Rapid detection of Escherichia coli O157:H7 with multiplex real-time PCR assays.

Authors:  Narayanan Jothikumar; Mansel W Griffiths
Journal:  Appl Environ Microbiol       Date:  2002-06       Impact factor: 4.792

Review 2.  Real-time nucleic acid-based detection methods for pathogenic bacteria in food.

Authors:  John L McKillip; Maryanne Drake
Journal:  J Food Prot       Date:  2004-04       Impact factor: 2.077

Review 3.  The polymerase chain reaction: miracle or mirage? A critical review of its uses and limitations in diagnosis and research.

Authors:  P A Wright; D Wynford-Thomas
Journal:  J Pathol       Date:  1990-10       Impact factor: 7.996

4.  Primers are decisive for sensitivity of PCR.

Authors:  Q He; M Marjamäki; H Soini; J Mertsola; M K Viljanen
Journal:  Biotechniques       Date:  1994-07       Impact factor: 1.993

5.  Parallel evolution of virulence in pathogenic Escherichia coli.

Authors:  S D Reid; C J Herbelin; A C Bumbaugh; R K Selander; T S Whittam
Journal:  Nature       Date:  2000-07-06       Impact factor: 49.962

Review 6.  Multiplex polymerase chain reaction: a practical approach.

Authors:  P Markoulatos; N Siafakas; M Moncany
Journal:  J Clin Lab Anal       Date:  2002       Impact factor: 2.352

7.  Simultaneous Screening of 24 Target Genes of Foodborne Pathogens in 35 Foodborne Outbreaks Using Multiplex Real-Time SYBR Green PCR Analysis.

Authors:  Hiroshi Fukushima; Jun Kawase; Yoshiki Etoh; Kumiko Sugama; Shunshuke Yashiro; Natsuko Iida; Keiji Yamaguchi
Journal:  Int J Microbiol       Date:  2010-09-28

8.  Complete genome sequence of Yersinia pestis strain 91001, an isolate avirulent to humans.

Authors:  Yajun Song; Zongzhong Tong; Jin Wang; Li Wang; Zhaobiao Guo; Yanpin Han; Jianguo Zhang; Decui Pei; Dongsheng Zhou; Haiou Qin; Xin Pang; Yujun Han; Junhui Zhai; Min Li; Baizhong Cui; Zhizhen Qi; Lixia Jin; Ruixia Dai; Feng Chen; Shengting Li; Chen Ye; Zongmin Du; Wei Lin; Jun Wang; Jun Yu; Huanming Yang; Jian Wang; Peitang Huang; Ruifu Yang
Journal:  DNA Res       Date:  2004-06-30       Impact factor: 4.458

Review 9.  Bacillus anthracis, Francisella tularensis and Yersinia pestis. The most important bacterial warfare agents - review.

Authors:  M Pohanka; P Skládal
Journal:  Folia Microbiol (Praha)       Date:  2009-10-14       Impact factor: 2.629

10.  The complete genome sequence of Yersinia pseudotuberculosis IP31758, the causative agent of Far East scarlet-like fever.

Authors:  Mark Eppinger; M J Rosovitz; Wolfgang Florian Fricke; David A Rasko; Galina Kokorina; Corinne Fayolle; Luther E Lindler; Elisabeth Carniel; Jacques Ravel
Journal:  PLoS Genet       Date:  2007-07-10       Impact factor: 5.917

View more
  3 in total

Review 1.  Applications of polymerase chain reaction-based methods for the diagnosis of plague (Review).

Authors:  Yanan Zhang; Zhanli Wang; Wenrui Wang; Hui Yu; Min Jin
Journal:  Exp Ther Med       Date:  2022-06-14       Impact factor: 2.751

2.  Customizable PCR-microplate array for differential identification of multiple pathogens.

Authors:  Abdela Woubit; Teshome Yehualaeshet; Sherrelle Roberts; Martha Graham; Moonil Kim; Temesgen Samuel
Journal:  J Food Prot       Date:  2013-11       Impact factor: 2.077

3.  A New Generation Microarray for the Simultaneous Detection and Identification of Yersinia pestis and Bacillus anthracis in Food.

Authors:  Noriko Goji; Trevor Macmillan; Kingsley Kwaku Amoako
Journal:  J Pathog       Date:  2012-10-18
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.