Examining the population structure and the influence of recombination and ecology on microbial populations makes great sense for understanding microbial evolution and speciation. Streptomycetes are a diverse group of bacteria that are widely distributed in nature and a rich source of useful bioactive compounds; however, they are rarely subjected to population genetic investigations. In this study, we applied a five-gene-based multilocus sequence analysis (MLSA) scheme to 41 strains of Streptomyces albidoflavus derived from diverse sources, mainly insects, sea, and soil. Frequent recombination was detected in S. albidoflavus, supported by multiple lines of evidence from the pairwise homoplasy index (⌽ w ) test, phylogenetic discordance, the Shimodaira-Hasegawa (SH) test, and network analysis, underpinning the predominance of homologous recombination within Streptomyces species. A strong habitat signal was also observed in both phylogenetic and Structure 2.3.3 analyses, indicating the importance of ecological difference in shaping the population structure. Moreover, all three habitat-associated groups, particularly the entomic group, demonstrated significantly reduced levels of gene flow with one another, generally revealing habitat barriers to recombination. Therefore, a combined effect of homologous recombination and ecology is inferred for S. albidoflavus, where dynamic evolution is at least partly balanced by the extent that differential distributions of strains among habitats limit genetic exchange. Our study stresses the significance of ecology in microbial speciation and reveals the coexistence of homologous recombination and ecological divergence in the evolution of streptomycetes.
Despite various currently available approaches to defining prokaryotic species and a growing recognition of their vast diversity in nature, the concept of microbial species has long been under dispute due to their widespread genomic heterogeneity and variable levels of gene exchange (1-3). Genetic clusters that emerge in molecular sequence analyses of populations are often regarded as bearing the status of species, and multiple theoretical models to resolve the evolutionary mechanisms that cause the creation and maintenance of the genetic clusters have been proposed (3, 4). Until now, two major parallel concepts of microbial species have been developed, focused on barriers to recombination and ecological divergence, respectively (4): the neutral model, raised by Fraser and colleagues (3, 5), highlights the role of recombination in converging and diverging clusters with various recombination rates, while the ecotype model, developed by Cohan and colleagues (6, 7), defines an ecotype as a group of ecologically similar strains which is purged of its diversity by periodic selection and/or genetic drift. Consequently, recombination and divergent selection have emerged as two key processes driving the increasing discussion concerning theoretical models of microbial speciation. Moreover, coexistence of these processes has been suggeste...