Comparative assessment of SSR and SNP markers for inferring the population genetic structure of the common fungus Armillaria cepistipes

• Published in: Heredity Vol. 119; no. 5; pp. 371 - 380
• Main Authors: Tsykun, T, Rellstab, C, Dutech, C, Sipos, G, Prospero, S
• Format: Journal Article
• Language: English
• Published: England Springer Nature B.V 01.11.2017; Nature Publishing Group
• Subjects: Armillaria - genetics; Divergence; Fungi; Genetic diversity; Genetic Markers; Genetic structure; Genetics, Population; Genomes; Genotype & phenotype; Life Sciences; Loci; Markers; Microsatellite Repeats; Microsatellites; Original; Polymorphism; Polymorphism, Single Nucleotide; Population genetics; Populations; Simple sequence repeats; Single-nucleotide polymorphism; Spatial distribution; Switzerland; Ukraine
• ISSN: 0018-067X; 1365-2540; 0018-067X
• DOI: 10.1038/hdy.2017.48

During the last years, simple sequence repeats (SSRs, also known as microsatellites) and single-nucleotide polymorphisms (SNPs) have become the most popular molecular markers for describing neutral genetic variation in populations of a wide range of organisms. However, only a limited number of studies has focused on comparing the performance of these two types of markers for describing the underlying genetic structure of wild populations. Moreover, none of these studies targeted fungi, the group of organisms with one of the most complex reproductive strategies. We evaluated the utility of SSRs and SNPs for inferring the neutral genetic structure of Armillaria cepistipes (basidiomycetes) at different spatial scales. For that, 407 samples were collected across a small (150 km ) area in the Ukrainian Carpathians and a large (41 000 km ) area in the Swiss Alps. All isolates were analyzed at 17 SSR loci distributed throughout the whole genome and at 24 SNP loci located in different single-copy conserved genes. The two markers showed different patterns of structure within the two spatial scales studied. The multi-allelic SSR markers seemed to be best suited for detecting genetic structure in indigenous fungal populations at a rather small spatial scale (radius of ~50-100 km). The pattern observed at SNP markers rather reflected ancient divergence of distant (~1000 km) populations that in addition are separated by mountain ranges. Despite these differences, both marker types were suitable for detecting the weak genetic structure of the two A. cepistipes populations investigated.