Evaluation of multiple-locus variable number of tandem repeats analysis for typing livestock-associated methicillin-resistant Staphylococcus aureus

PLoS One. 2013;8(1):e54425. doi: 10.1371/journal.pone.0054425. Epub 2013 Jan 21.

Abstract

Background: The increasing occurrence of livestock-associated (LA) methicillin-resistant Staphylococcus aureus (MRSA) associated with the clonal complex (CC) 398 within the past years shows the importance of standardized and comparable typing methods for the purposes of molecular surveillance and outbreak detection. Multiple-locus variable number of tandem repeats analysis (MLVA) has recently been described as an alternative and highly discriminative tool for S. aureus. However, until now the applicability of MLVA for the typing of LA-MRSA isolates from different geographic origin has not been investigated in detail. We therefore compared MLVA and S. aureus protein A (spa) typing for characterizing porcine MRSA from distinct Dutch and German farms.

Methodology/principal findings: Overall, 134 MRSA isolates originating from 21 different pig-farms in the Netherlands and 36 farms in Germany comprising 21 different spa types were subjected to MLVA-typing. Amplification and subsequent automated fragment sizing of the tandem repeat loci on a capillary sequencer differentiated these 134 isolates into 20 distinct MLVA types. Whereas overall MLVA and spa typing showed the same discriminatory power to type LA-MRSA (p = 0.102), MLVA was more discriminatory than spa typing for isolates associated with the prevalent spa types t011 and t034 (Simpson's Index of Diversity 0.564 vs. 0.429, respectively; p<0.001).

Conclusion: Although the applied MLVA scheme was not more discriminatory than spa typing in general, it added valuable information to spa typing results for specific spa types (t011, t034) which are highly prevalent in the study area, i.e. Dutch-German border area. Thus, both methods may complement each other to increase the discriminatory power to resolute highly conserved clones such as CC398 (spa types t011, t034) for the detection of outbreaks and molecular surveillance of zoonotic MRSA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Typing Techniques
  • Disease Outbreaks
  • Germany
  • Livestock / genetics
  • Livestock / microbiology
  • Methicillin-Resistant Staphylococcus aureus / genetics*
  • Methicillin-Resistant Staphylococcus aureus / isolation & purification
  • Methicillin-Resistant Staphylococcus aureus / pathogenicity
  • Minisatellite Repeats / genetics*
  • Molecular Epidemiology
  • Netherlands
  • Phylogeny
  • Staphylococcal Infections / epidemiology
  • Staphylococcal Infections / genetics
  • Staphylococcal Infections / veterinary
  • Staphylococcal Protein A / genetics*
  • Swine / genetics
  • Swine / microbiology*

Substances

  • Staphylococcal Protein A

Grants and funding

This work was supported in part by grants from the Bundesministerium für Bildung und Forschung (BMBF, http://www.bmbf.de/), Germany “Interdisciplinary Research Network MedVet-Staph” to R.K. and K.B. (01KI1014A), by the INTERREG IVa project SafeGuard (MRSA vet-net) to R.K., P.v.d.W. and K.B. (III-2-03 = 025) and by the BMBF (01KI1020) and the Medical Faculty Münster (BD9817044) to A.M. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.