A novel high-resolution single locus sequence typing scheme for mixed populations of Propionibacterium acnes in vivo

PLoS One. 2014 Aug 11;9(8):e104199. doi: 10.1371/journal.pone.0104199. eCollection 2014.

Abstract

The Gram-positive anaerobic bacterium Propionibacterium acnes is a prevalent member of the normal skin microbiota of human adults. In addition to its suspected role in acne vulgaris it is involved in a variety of opportunistic infections. Multi-locus sequence-typing (MLST) schemes identified distinct phylotypes associated with health and disease. Being based on 8 to 9 house-keeping genes these MLST schemes have a high discriminatory power, but their application is time- and cost-intensive. Here we describe a single-locus sequence typing (SLST) scheme for P. acnes. The target locus was identified with a genome mining approach that took advantage of the availability of representative genome sequences of all known phylotypes of P. acnes. We applied this SLST on a collection of 188 P. acnes strains and demonstrated a resolution comparable to that of existing MLST schemes. Phylogenetic analysis applied to the SLST locus resulted in clustering patterns identical to a reference tree based on core genome sequences. We further demonstrate that SLST can be applied to detect multiple phylotypes in complex microbial communities by a metagenomic pyrosequencing approach. The described SLST strategy may be applied to any bacterial species with a basically clonal population structure to achieve easy typing and mapping of multiple phylotypes in complex microbiotas. The P. acnes SLST database can be found at http://medbac.dk/slst/pacnes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Typing Techniques / methods*
  • Genetic Loci / genetics*
  • Genomics
  • Humans
  • Microbiota / genetics
  • Propionibacterium acnes / classification*
  • Propionibacterium acnes / genetics*
  • Sequence Analysis
  • Species Specificity

Grants and funding

This study was supported by grant # DFF-1331-00241 to HB from the Danish Medical Research council and by an Aarhus University Health Faculty PhD stipend to CFPS. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.