Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
New South Wales Public Health Bulletin New South Wales Public Health Bulletin Society
Supporting public health practice in New South Wales
RESEARCH ARTICLE

Using MLVA to type strains of Salmonella Typhimurium in New South Wales

Gwendolyn L. Gilbert
+ Author Affiliations
- Author Affiliations

Centre for Infectious Diseases and Microbiology, Institute of Clinical Pathology and Medical Research, Westmead Hospital, Westmead. Email: l.gilbert@usyd.edu.au

NSW Public Health Bulletin 19(2) 29-31 https://doi.org/10.1071/NB07116
Published: 28 February 2008

Abstract

Summary: Phage typing has been the traditional strain typing (or ‘fingerprinting’) method used in Australia for surveillance of common salmonella serovars (such as Salmonella Typhimurium) and outbreak investigations. The need for more accessible, discriminatory and objective methods has been recognised but, until now, none has been widely accepted. Recently, the molecular typing method, known as MLVA (multilocus variable number tandem repeat analysis), has been applied to several Salmonella serovars and promises to provide faster strain typing and cluster identification than phage typing, with comparable or better sensitivity. The present article is intended as a short primer on MLVA typing, which has recently been introduced into routine use at the New South Wales Enteric Reference Laboratory at the Centre for Infectious Diseases and Microbiology, Institute of Clincial Pathology and Medical Research, Westmead.


Acknowledgements

I would like to thank Qinning Wang, Vitali Sintchenko, Peter Howard, Peter Jelfs and Robert Chiew for their contributions to the work described in the present study. Qinning Wang kindly provided images and data for the figures.


References


[1] Hyytia-Trees E,  Smole SC,  Fields PA,  Swaminathan B,  Ribot EM. Second generation subtyping: a proposed PulseNet protocol for multiple-locus variable-number tandem repeat analysis of Shiga toxin-producing Escherichia coli O157 (STEC O157). Foodborne Pathog Dis 2006; 3(1): 118–31.
Crossref | GoogleScholarGoogle Scholar | PubMed |

[2] Lindstedt BA,  Vardund T,  Aas L,  Kapperud G. Multiple-locus variable-number tandem-repeats analysis of Salmonella enterica subsp. enterica serovar Typhimurium using PCR multiplexing and multicolor capillary electrophoresis. J Microbiol Methods 2004; 59(2): 163–72.
Crossref | GoogleScholarGoogle Scholar | PubMed |

[3] Ramisse V,  Houssu P,  Hernandez E,  Denoeud F,  Hilaire V,  Lisanti O, et al. Variable number of tandem repeats in Salmonella enterica subsp. enterica for typing purposes. J Clin Microbiol 2004; 42(12): 5722–30.
Crossref | GoogleScholarGoogle Scholar | PubMed |

[4] Boxrud D,  Pederson-Gulrud K,  Wotton J,  Medus C,  Lyszkowicz E,  Besser J, et al. Comparison of multiple-locus variable-number tandem repeat analysis, pulsed-field gel electrophoresis, and phage typing for subtype analysis of Salmonella enterica serotype Enteritidis. J Clin Microbiol 2007; 45(2): 536–43.
Crossref | GoogleScholarGoogle Scholar | PubMed |

[5] Lindstedt BA,  Torpdahl M,  Nielsen EM,  Vardund T,  Aas L,  Kapperud G. Harmonization of the multiple-locus variable-number tandem repeat analysis method between Denmark and Norway for typing Salmonella Typhimurium isolates and closer examination of the VNTR loci. J Appl Microbiol 2007; 102(3): 728–35.
Crossref | GoogleScholarGoogle Scholar | PubMed |

[6] Torpdahl M,  Sorensen G,  Lindstedt BA,  Nielsen EM. Tandem repeat analysis for surveillance of human Salmonella Typhimurium infections. Emerg Infect Dis 2007; 13(3): 388–95.
PubMed |