bioRxiv Science⌕ Search

bioRxiv · 10.1101/2021.08.12.456076

Analysis of wild plant pathogen populations reveals a signal of adaptation in genes evolving for survival in agriculture in the beet rust pathogen (Uromyces beticola)

Abstract

Improvements in crop resistance to pathogens can reduce yield losses and address global malnourishment today. Gene-for-gene -type interactions can identify new sources of resistance but genetic resistance is often short lived. Ultimately an understanding of how pathogens rapidly adapt will allow us to both increase resistance gene durability and more effectively target chemical treatments. Until recently all agricultural pathogens were living on wild hosts. To understand crop pathogen evolution, we compared genetic diversity in agricultural and wild populations. Wild reservoirs may be the source of emergent pathogen lineages, but here we outline a strategy for comparison of wild and agricultural pathogen populations to highlight genes adapting to agriculture. To address this, we have selected and developed the beet rust system (Beta vulgaris, Uromyces beticola, respectively) as our wild-agricultural model. Our hypothesis is that pathogen adaptation to agricultural crops will be evident as divergence in comparisons of wild and agricultural plant pathogen populations. We sampled isolates in both the wild and agriculture, sequenced and assembled and annotated a large fungal genome and analysed genetic diversity in 42 re-sequenced rust isolates. We found population differentiation between isolates in the wild compared to a predominantly agricultural group. Fungal effector genes are co-evolving with host resistance and are important for successful colonisation. We predicted (and found) that these exhibit a greater signal of diversification and adaptation and more importantly displayed increased wild agricultural divergence. Finding a signal of adaptation in these genes highlights this as an important strategy to identify genes which are key to pathogen success, that analysis of agricultural isolates alone cannot. Author SummaryAs quickly as we develop new strategies for crop defence, pathogens evolve to circumvent them. Novel crop pathogen strains emerge periodically and sweep through the agricultural system. However, because of the (often) clonal nature of these crop pathogens it is difficult to identify the trait that is key to their success. In other words, if there is a trait that is key for success in agriculture, all agricultural isolates will have it (or die without it). What we need is a case and control system where we identify genes important to pathogen success in agricultural by comparing them to pathogens that live in the wild. Here we exemplify this strategy by focussing on genes already known to specifically adapt for the successful colonisation of the host, the fungal effector genes. We find that these genes appear to be evolving quickly and that they are more different between the wild and agriculture than other non-effector genes. These differences between wild and agricultural pathogens suggest we are observing adaptation to agriculture. We do this work in the sugar beet rust system because of its tractability to sample but this understanding about how to identify genetic variation that is key to pathogen success in agriculture is applicable to crop systems where pathogen reservoirs exist as well as other pathogen reservoir systems (e.g. zoonoses).

Source connections

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

McMullan, M., Percival-Alwyn, L., Sawford, K., Kaithakottil, G., Grey, M., Yvanne, H., Low, R., Warring, S., Heavens, D., Peel, N., Kroboth, J., Stevens, M., Swarbreck, D., Clark, M., Hall, N.. 2021-08-13. Analysis of wild plant pathogen populations reveals a signal of adaptation in genes evolving for survival in agriculture in the beet rust pathogen (Uromyces beticola). https://doi.org/10.1101/2021.08.12.456076

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Both genetic and social inheritance influence female aggressive and submissive behavior in a wild primate

Agonistic interactions are important determinants of resource access in wild animals, but their genetic basis remains poorly understood. Here we use a quantitative genetics approach to estimate the heritability of aggressive and submissive behavior of wild female baboons, considering relative rates of both individual and dyadic aggression and submission. To control for the social inheritance that creates kin-based dominance hierarchies, we implemented a multi-matrix model that included a social status similarity matrix alongside the additive genetic matrix. Despite a substantial contribution of social inheritance, especially for submissive behavior, we found heritable components for both aggressive and submissive behavior (h2=0.21 and h2=0.09-0.11, respectively). In dyadic models, aggressive behavior was primarily influenced by the aggressor's genotype (a direct genetic effect), while submissive behavior was primarily affected by the social partner's genotype (an indirect genetic effect). Finally, we found evidence for a negative genetic (but not phenotypic) correlation between aggressive and submissive behavior within dyads, and a negative genetic correlation between submissive behavior and eliciting submissive behavior. Together, our results highlight how direct genetic, indirect genetic, and social inheritance effects combine to influence primate social behavior.

evolutionary biology↗

Genomic signatures of local adaptation in marram grass highlight the importance of provenance in dune restoration

Coastal sand dunes provide critical natural flood defences and key habitats for a range of threatened species. These systems are formed when shifting sands are stabilised by specialised coastal grasses. In Europe, marram grass (Calamagrostis arenaria) is the main dune building species. However, despite its ecological importance and its widespread use in dune restoration, little is known about the genomic innovations that facilitated the colonisation of the coast, the extent of local adaptation in current populations, or the genetic consequences of restoration practices. Using a chromosome-scale reference genome we generate here, we show that C. arenaria has significant expansions in several gene families relevant to coastal adaptation, including those associated with salinity, drought, and nutrient limitation. Using ddRAD-Seq data for over 200 individuals from 10 European populations, we identified strong genetic differentiation between northern and southern populations which corresponds to recognised subspecies. Within the northern european populations, the genetic structure is largely driven by isolation-by-distance. Although, we detected evidence of non-local planting in a restored Swedish dune system, where introduced plants were genetically distinct from the native population and both groups exhibited reduced genetic diversity. Genome-wide scans for local adaptation within the northern European marram grass individuals identified outlying genomic regions that were enriched for genes with functions associated with nutrient deficiency, drought, pathogen defence, and other environmental stressors characteristic of coastal dunes, potentially indicating local adaptation. Outlying regions also include genes associated with lignin biosynthesis and culm mechanical strength, potentially reflecting selection on the structural properties required to withstand different burial and wind exposure regimes. Overall, these findings show widespread local adaptation in C. arenaria, and support the use of local provenance in dune restoration and conservation.

evolutionary biology↗

Parallel Trajectories in the Evolution of C-class MADS-box Genes in Flowering Plants and Conifers

Gene duplication events frequently underpin phenotypic diversity due to the increase in genetic material that can be shaped by evolution. AGAMOUS (AG) genes are members of the MADS-box gene family that show conserved function in specifying reproductive organ identity in seed plants. While the function, expression, and evolution of these genes have been extensively studied in flowering plants, they remain understudied in gymnosperms. Consequently, little is known about how AG has contributed to reproductive diversity and evolution outside of the flowering plants. Here, we report that AG genes underwent two duplication events within conifers prior to the split between Cupressaceae and its sister family, Taxaceae. Further, we characterize the in situ expression pattern for each resulting paralog (AG1, AG2, and AG3) in seed cones of three Cupressaceae species, Metasequoia glyptostroboides, Taxodium distichum, and Juniperus virginiana. We discover gene expression patterns consistent with subfunctionalization: AG1 specialized in seed and sporangial development, AG2 in seed cone and seed coat development, and AG3 in ovuliferous scale development. This study provides an evolutionary mechanism for the development of unique seed cone reproductive traits in Cupressaceae. More broadly, our results uncover convergent patterns in the evolution of AG gene lineages across conifers and angiosperms.

evolutionary biology↗