No single genealogical reconstruction or typing method currently encompasses all levels of bacterial diversity, from domain to strain. We propose ribosomal multilocus sequence typing (rMLST), an approach which indexes variation of the 53 genes encoding the bacterial ribosome protein subunits (rps genes), as a means of integrating microbial genealogy and typing. As with multilocus sequence typing (MLST), rMLST employs curated reference sequences to identify gene variants efficiently and rapidly. The rps loci are ideal targets for a universal characterization scheme as they are: (i) present in all bacteria; (ii) distributed around the chromosome; and (iii) encode proteins which are under stabilizing selection for functional conservation. Collectively, the rps loci exhibit variation that resolves bacteria into groups at all taxonomic and most typing levels, providing significantly more resolution than 16S small subunit rRNA gene phylogenies. A web-accessible expandable database, comprising whole-genome data from more than 1900 bacterial isolates, including 28 draft genomes assembled de novo from the European Bioinformatics Institute (EBI) sequence read archive, has been assembled. The rps gene variation catalogued in this database permits rapid and computationally non-intensive identification of the phylogenetic position of any bacterial sequence at the domain, phylum, class, order, family, genus, species and strain levels. The groupings generated with rMLST data are consistent with current nomenclature schemes and independent of the clustering algorithm used. This approach is applicable to the other domains of life, potentially providing a rational and universal approach to the classification of life that is based on one of its fundamental features, the translation mechanism.

National-scale genotyping was a practical and efficient methodology for the quantification of the contributions of different sources to human Campylobacter infection. Combined with the knowledge that retail chicken is routinely contaminated with Campylobacter, these results are consistent with the view that the largest reductions in human campylobacteriosis in industrialized countries will come from interventions that focus on the poultry industry.

Genome-wide association studies have the potential to identify causal genetic factors underlying important phenotypes but have rarely been performed in bacteria. We present an association mapping method that takes into account the clonal population structure of bacteria and is applicable to both core and accessory genome variation. Campylobacter is a common cause of human gastroenteritis as a consequence of its proliferation in multiple farm animal species and its transmission via contaminated meat and poultry. We applied our association mapping method to identify the factors responsible for adaptation to cattle and chickens among 192 Campylobacter isolates from these and other host sources. Phylogenetic analysis implied frequent host switching but also showed that some lineages were strongly associated with particular hosts. A seven-gene region with a host association signal was found. Genes in this region were almost universally present in cattle but were frequently absent in isolates from chickens and wild birds. Three of the seven genes encoded vitamin B 5 biosynthesis. We found that isolates from cattle were better able to grow in vitamin B 5 -depleted media and propose that this difference may be an adaptation to host diet.evolution | genomics | host adaptation | transmission ecology C olonization of multiple host species increases the number of transmission opportunities for animal pathogens and symbionts but depends on making rapid adjustments to each new host (1). For organisms such as Campylobacter, relatively small genome size (1.6 Mb) limits the phenotypic flexibility of each bacterium. Single clones can multiply to large numbers within hosts, and genetic variation arising among these bacteria increases the range of available phenotypes. This might allow a bacterial lineage to passage successfully through multiple hosts by repeatedly evolving host adaptive traits.Experimental work has shown that a large proportion of adaptations to new environments incur an equal or greater cost in other environments (2). This cost of adaptation might make a strategy of continuous evolution unstable by causing a progressive loss of fitness in the course of repeated host switching. Three factors that could reduce this cost of readaptation are canalization of genetic change via contingency loci (3, 4); coordinated genetic regulation of host-specific factors (5, 6); and import of DNA by recombination from other, already adapted, lineages in each new host species (7). The relative importance of these mechanisms for host specificity in Campylobacter remains unknown.Campylobacter jejuni and Campylobacter coli are common components of the gut microbiota in numerous wild and domesticated animal species, as well as, together, being one of the most common causes of food poisoning in humans. The characterization of large numbers of C. jejuni and C. coli isolates from diverse sources and locations by multilocus sequence typing (MLST) has shown that there is genetic differentiation among sequence types (STs) associated with diffe...

The nature of species boundaries in bacteria remains controversial. In particular, the mechanisms of bacterial speciation and maintenance in the face of frequent genetic exchange are poorly understood. Here, we report patterns of genetic exchange that show two closely related zoonotic pathogenic species, Campylobacter jejuni and Campylobacter coli, are converging as a consequence of recent changes in gene flow. Population expansion into a novel ecological niche generated by human activity is the most probable explanation for the increase in genetic exchange between these species. Bacterial speciation can therefore occur by mechanisms analogous to those seen in metazoans, where genetic diversification and incipient speciation caused by ecological factors have been reported in several genera.