Literature DB >> 18374440

PCR assay for differentiating between Group I (proteolytic) and Group II (nonproteolytic) strains of Clostridium botulinum.

Elias Dahlsten1, Hannu Korkeala, Panu Somervuo, Miia Lindström.   

Abstract

Groups I (proteolytic) and II (nonproteolytic) C. botulinum are genetically and physiologically distinct groups of organisms, with both groups being involved with human botulism. Due to differences in spore heat resistance and growth characteristics, the two groups possess different types of human health risks through foods, drink, and the environment. The epidemiology of human botulism due to Groups I and II C. botulinum is poorly understood, largely due to insufficient characterization of disease isolates, and warrants thorough outbreak investigation with a particular attention to discrimination between the different physiological groups of C. botulinum. In this study, a PCR assay was developed to discriminate between Group I and Group II C. botulinum. The assay is based on the fldB associated with phenylalanine metabolism in proteolytic clostridia, and employs an internal amplification control targeted to conservative regions of 16S rrn in Groups I and II C. botulinum. The assay correctly identified all 36 Group I and 24 Group II C. botulinum strains, possessing a 100% exclusivity and inclusivity. The assay provides a substantial improvement in discriminating between the Groups I and II C. botulinum, which traditionally is based on a time-consuming and error-prone culture method. Differentiation between the physiological groups of C. botulinum is an essential step in investigation of human botulism outbreaks, and should be considered as a diagnostic corner-stone in order to improve our epidemiological understanding of human botulism.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18374440     DOI: 10.1016/j.ijfoodmicro.2008.02.018

Source DB:  PubMed          Journal:  Int J Food Microbiol        ISSN: 0168-1605            Impact factor:   5.277


  6 in total

1.  Novel structural elements within the nonproteolytic clostridium botulinum type F toxin gene cluster.

Authors:  N Dover; J R Barash; K K Hill; J C Detter; S S Arnon
Journal:  Appl Environ Microbiol       Date:  2010-12-23       Impact factor: 4.792

2.  Evaluation and Optimization of Microdrop Digital PCR for Detection of Serotype A and B Clostridium botulinum.

Authors:  Pengya Gao; Changde Wu; Jin Zhang; Shuping Wang; Ying Huang; Yinping Dong; Tingting Liu; Changyun Ye; Xuefang Xu; Wenwen Xin
Journal:  Front Microbiol       Date:  2022-05-09       Impact factor: 6.064

3.  Genetic diversity of the flagellin genes of Clostridium botulinum groups I and II.

Authors:  Cedric Woudstra; Dominic Lambert; Fabrizio Anniballi; Dario De Medici; John Austin; Patrick Fach
Journal:  Appl Environ Microbiol       Date:  2013-04-19       Impact factor: 4.792

4.  Differentiating Botulinum Neurotoxin-Producing Clostridia with a Simple, Multiplex PCR Assay.

Authors:  Charles H D Williamson; Adam J Vazquez; Karen Hill; Theresa J Smith; Roxanne Nottingham; Nathan E Stone; Colin J Sobek; Jill H Cocking; Rafael A Fernández; Patricia A Caballero; Owen P Leiser; Paul Keim; Jason W Sahl
Journal:  Appl Environ Microbiol       Date:  2017-08-31       Impact factor: 4.792

5.  Specific Isolation of Clostridium botulinum Group I Cells by Phage Lysin Cell Wall Binding Domain with the Aid of S-Layer Disruption.

Authors:  Zhen Zhang; François P Douillard; Hannu Korkeala; Miia Lindström
Journal:  Int J Mol Sci       Date:  2022-07-29       Impact factor: 6.208

6.  Two simultaneous botulism outbreaks in Barcelona: Clostridium baratii and Clostridium botulinum.

Authors:  S Lafuente; J Nolla; S Valdezate; C Tortajada; H Vargas-Leguas; I Parron; J A Sáez-Nieto; S Portaña; G Carrasco; E Moguel; S Sabate; R Argelich; J A Caylà
Journal:  Epidemiol Infect       Date:  2012-11-19       Impact factor: 4.434

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.