scholarly journals Paracoccidioides genomes reflect high levels of species divergence and little interspecific gene flow

2020 ◽  
Author(s):  
Heidi Mavengere ◽  
Katlheen Mattox ◽  
Marcus M Teixeira ◽  
Victoria E. Sepúlveda ◽  
Oscar M. Gomez ◽  
...  
Keyword(s):  
Gene Flow ◽  
Fungal Pathogens ◽  
Fungal Species ◽  
Species Boundaries ◽  
Whole Genome ◽  
Gene Exchange ◽  
Interspecific Gene Flow ◽  
Systematic Effort ◽  
Species Pairs ◽  
Show Evidence

ABSTRACTThe fungus Paracoccidioides spp. is a prevalent human pathogen endemic to South America. The genus is composed of five species. In this report, we use 37 whole genome sequences to study the allocation of genetic variation in Paracoccidioides. We tested three genome-wide predictions of advanced speciation, namely, that all species should be reciprocally monophyletic, that species pairs should be highly differentiated along the whole genome, and that there should be low rates of interspecific gene exchange. We find support for these three hypotheses. Species pairs with older divergences show no evidence of gene exchange, while more recently diverged species pairs show evidence of modest rates of introgression. Our results indicate that as divergence progresses, species boundaries become less porous among Paracoccidioides species. Our results suggest that species in Paracoccidioides are at different stages along the divergence continuum.IMPORTANCEParacoccidioides is the causal agent of the most frequent systemic mycosis in Latin America. Most of the inference of the evolutionary history of Paracoccidioides has used only a handful of molecular markers. In this report, we evaluate the extent of genome divergence among Paracoccidioides species and study the possibility of interspecific gene exchange. We find that all species are highly differentiated. We also find that the amount of gene flow between species is low and in some cases even completely absent in spite of geographic overlap. Our study constitutes a systematic effort to identify species boundaries in fungal pathogens, and determine the extent of gene exchange among fungal species.

scholarly journals Paracoccidioides Genomes Reflect High Levels of Species Divergence and Little Interspecific Gene Flow

mBio ◽  
2020 ◽  
Vol 11 (6) ◽  
pp. e01999-20
Author(s):  
Heidi Mavengere ◽  
Kathleen Mattox ◽  
Marcus M. Teixeira ◽  
Victoria E. Sepúlveda ◽  
Oscar M. Gomez ◽  
...  
Keyword(s):  
Gene Flow ◽  
Fungal Pathogens ◽  
Fungal Species ◽  
Species Boundaries ◽  
Whole Genome ◽  
Gene Exchange ◽  
Interspecific Gene Flow ◽  
Content Type ◽  
Species Pairs ◽  
Show Evidence

ABSTRACTThe fungus Paracoccidioides is a prevalent human pathogen endemic to South America. The genus is composed of five species. In this report, we use 37 whole-genome sequences to study the allocation of genetic variation in Paracoccidioides. We tested three genome-wide predictions of advanced speciation, namely, that all species should be reciprocally monophyletic, that species pairs should be highly differentiated along the whole genome, and that there should be low rates of interspecific gene exchange. We find support for these three hypotheses. Species pairs with older divergences show no evidence of gene exchange, while more recently diverged species pairs show evidence of modest rates of introgression. Our results indicate that as divergence progresses, species boundaries become less porous among Paracoccidioides species. Our results suggest that species in Paracoccidioides are at different stages along the divergence continuum.IMPORTANCEParacoccidioides is the causal agent of a systemic mycosis in Latin America. Most of the inference of the evolutionary history of Paracoccidioides has used only a few molecular markers. In this report, we evaluate the extent of genome divergence among Paracoccidioides species and study the possibility of interspecific gene exchange. We find that all species are highly differentiated. We also find that the amount of gene flow between species is low and in some cases is even completely absent in spite of geographic overlap. Our study constitutes a systematic effort to identify species boundaries in fungal pathogens and to determine the extent of gene exchange among fungal species.

scholarly journals Genomic signals of admixture and reinforcement between two closely related species of European sepsid flies

2020 ◽  
Author(s):  
Athene Giesen ◽  
Wolf U. Blanckenhorn ◽  
Martin A. Schäfer ◽  
Kentaro K. Shimizu ◽  
Rie Shimizu-Inatsugi ◽  
...  
Keyword(s):  
Gene Flow ◽  
Dna Sequence ◽  
Species Boundaries ◽  
Adaptive Divergence ◽  
Sympatric Populations ◽  
Interspecific Gene Flow ◽  
Natural Systems ◽  
Sequence Identity ◽  
Interspecific Differences ◽  
Genome Wide

ABSTRACTInterspecific gene flow by hybridization may weaken species barriers and adaptive divergence, but can also initiate reinforcement of reproductive isolation trough natural and sexual selection. The extent of interspecific gene flow and its consequences for the initiation and maintenance of species barriers in natural systems remain poorly understood, however. To assess genome-wide patterns of gene flow between the two closely related European dung fly species Sepsis cynipsea and Sepsis neocynipsea (Diptera: Sepsidae), we tested for historical gene flow with the aid of ABBA-BABA test using whole-genome resequencing data from pooled DNA of male specimens originating from natural and laboratory populations. We contrasted genome-wide variation in DNA sequence differences between samples from sympatric populations of the two species in France and Switzerland with that of interspecific differences between pairs of samples involving allopatric populations from Estonia and Italy. In the French Cevennes, we detected a relative excess of DNA sequence identity, suggesting interspecific gene flow in sympatry. In contrast, at two sites in Switzerland, we observed a relative depletion of DNA sequence identity compatible with reinforcement of species boundaries in sympatry. Our results suggest that the species boundaries between S. cynipsea and S. neocynipsea in Europe depend on the eco-geographic context.

scholarly journals Genomic signals of admixture and reinforcement between two closely related species of European sepsid flies

2021 ◽  
Author(s):  
Athene Giesen ◽  
Wolf Blanckenhorn ◽  
Martin Schäfer ◽  
Kentaro K. Shimizu ◽  
Rie Shimizu-Inatsugi ◽  
...  
Keyword(s):  
Gene Flow ◽  
Dna Sequence ◽  
Species Boundaries ◽  
Adaptive Divergence ◽  
Sympatric Populations ◽  
Interspecific Gene Flow ◽  
Natural Systems ◽  
Sequence Identity ◽  
Interspecific Differences ◽  
Genome Wide

Interspecific gene flow by hybridization may weaken species barriers and adaptive divergence, but can also initiate reinforcement of reproductive isolation trough natural and sexual selection. The extent of interspecific gene flow and its consequences for the initiation and maintenance of species barriers in natural systems remain poorly understood, however. To assess genome-wide patterns of gene flow between the two closely related European dung fly species Sepsis cynipsea and Sepsis neocynipsea (Diptera: Sepsidae), we tested for historical gene flow with the aid of ABBA-BABA test using whole-genome resequencing data from pooled DNA of male specimens originating from natural and laboratory populations. We contrasted genome-wide variation in DNA sequence differences between samples from sympatric populations of the two species in France and Switzerland with that of interspecific differences between pairs of samples involving allopatric populations from Estonia and Italy. In the French Cevennes, we detected a relative excess of DNA sequence identity, suggesting interspecific gene flow in sympatry. In contrast, at two sites in Switzerland, we observed a relative depletion of DNA sequence identity compatible with reinforcement of species boundaries in sympatry. Our results suggest that the species boundaries between S. cynipsea and S. neocynipsea in Europe depend on the eco-geographic context.

scholarly journals The importance of intrinsic postzygotic barriers throughout the speciation process

2020 ◽  
Vol 375 (1806) ◽  
pp. 20190533 ◽  
Author(s):  
Jenn M. Coughlan ◽  
Daniel R. Matute
Keyword(s):  
Gene Flow ◽  
Reproductive Isolation ◽  
Rapid Evolution ◽  
Theoretical Work ◽  
Sympatric Species ◽  
Species Boundaries ◽  
Biological Models ◽  
Speciation Process ◽  
Species Pairs ◽  
Postzygotic Barriers

Intrinsic postzygotic barriers can play an important and multifaceted role in speciation, but their contribution is often thought to be reserved to the final stages of the speciation process. Here, we review how intrinsic postzygotic barriers can contribute to speciation, and how this role may change through time. We outline three major contributions of intrinsic postzygotic barriers to speciation. (i) reduction of gene flow : intrinsic postzygotic barriers can effectively reduce gene exchange between sympatric species pairs. We discuss the factors that influence how effective incompatibilities are in limiting gene flow. (ii) early onset of species boundaries via rapid evolution : intrinsic postzygotic barriers can evolve between recently diverged populations or incipient species, thereby influencing speciation relatively early in the process. We discuss why the early origination of incompatibilities is expected under some biological models, and detail how other (and often less obvious) incompatibilities may also serve as important barriers early on in speciation. (iii) reinforcement : intrinsic postzygotic barriers can promote the evolution of subsequent reproductive isolation through processes such as reinforcement, even between relatively recently diverged species pairs. We incorporate classic and recent empirical and theoretical work to explore these three facets of intrinsic postzygotic barriers, and provide our thoughts on recent challenges and areas in the field in which progress can be made. This article is part of the theme issue ‘Towards the completion of speciation: the evolution of reproductive isolation beyond the first barriers’.

scholarly journals Recurrent allopolyploidization events diversify eco-physiological traits in marsh orchids

2021 ◽  
Author(s):  
Thomas M. Wolfe ◽  
Francisco Balao ◽  
Emiliano Trucchi ◽  
Gert Bachmann ◽  
Wenjia Gu ◽  
...  
Keyword(s):  
Gene Flow ◽  
Whole Genome Duplication ◽  
Genome Duplication ◽  
Nutrient Transport ◽  
Ecological Niches ◽  
Whole Genome ◽  
Structural Reorganization ◽  
Interspecific Gene Flow ◽  
Ecological Barriers ◽  
Distinct Features

AbstractWhole-genome duplication, in particular allopolyploidy, has shaped the evolution of angiosperms and other organisms. Structural reorganization of chromosomes and repatterning of gene expression is frequently observed in early generation allopolyploids, with potential ecological consequences. The relative contributions of environmental and intrinsic drivers to these changes are unknown. We show here that in marsh orchids (Dactylorhiza, Orchidaceae), recurrently-formed allopolyploids are characterized by distinct eco-physiologies matching their respective environments, providing us with an excellent study system to address this question. Here we integrate eco-physiological and transcriptomic comparative studies to reveal a complex suite of intertwined, pronounced differences between sibling allopolyploids. We show that Dactylorhiza majalis that is distributed in Central and Southern Europe favors meadows with mesic soils. Its sibling allopolyploid D. traunsteineri occurs in fens, characterized by soils depleted by macro- and micronutrients, mainly in previously glaciated European areas. We further uncover distinct features in their nutrient transport, leaf elemental chemistry, light-harvesting, photoprotection, and stomata activity, that appear all linked to their distinct ecologies, in particular soil chemistry differences at their native sites. Recurrent polyploidization hence enriches biodiversity through eco-physiological diversification, providing the opportunity for sibling allopolyploids to evolve as distinct evolutionary units, despite pervasive interspecific gene flow.Significance StatementWhole-genome duplication resulting in polyploidy has underpinned the evolution of flowering plants and other organisms, and is important for many crops. However, the ecological implications of polyploidy remain little understood. Here, we demonstrate that two sibling allopolyploid marsh orchid species prefer distinct habitats, and have evolved a suite of distinctive ecophysiological characters (e.g. nutrient transport, energy harvesting and photoprotection). We argue that the divergence of these characters in the nascent polyploids drove adaptation into distinct ecological niches (low nutrient fens versus meadows with mesic soils), generating ecological barriers that maintains distinct, independent lineages, even in the presence of interspecific gene flow.

scholarly journals Natural selection maintains species despite widespread hybridization in the desert shrub Encelia

2020 ◽  
Author(s):  
Christopher D DiVittorio ◽  
Sonal Singhal ◽  
Adam B Roddy ◽  
Felipe Zapata ◽  
David D Ackerly ◽  
...  
Keyword(s):  
Gene Flow ◽  
Natural Selection ◽  
Field Experiments ◽  
Population Genomics ◽  
Coastal Dunes ◽  
Species Boundaries ◽  
Hybrid Zones ◽  
Desert Shrubs ◽  
Species Complexes ◽  
Species Pairs

ABSTRACTNatural selection is an important driver of genetic and phenotypic differentiation between species. A powerful way to test the role of natural selection in the formation and maintenance of species is to study species complexes in which potential gene flow is high but realized gene flow is low. For a recent radiation of New World desert shrubs (Encelia: Asteraceae), we use fine-scale geographic sampling and population genomics to determine patterns of gene flow across two hybrid zones formed between two independent pairs of species with parapatric distributions. After finding evidence for extremely strong selection at both hybrid zones, we use a combination of field experiments, high-resolution imaging, and physiological measurements to determine the ecological basis for selection at one of the hybrid zones. Our results identify multiple ecological mechanisms of selection (drought, salinity, herbivory, and burial) that together are sufficient to maintain species boundaries despite high rates of hybridization. Given that multiple pairs of species hybridize at ecologically divergent parapatric boundaries in the adaptive radiation of Encelia, such mechanisms may maintain species boundaries throughout this group.SIGNIFICANCE STATEMENTIn Baja California, the deserts meet the coastal dunes in a narrow transition visible even from satellite images. We study two species pairs of desert shrubs (Encelia) that occur across this transition. Although these species can interbreed, they remain distinct. Using a combination of genetics, field experiments, 3D-imaging, and physiological measurements, we show that natural selection counteracts the homogenizing effects of gene exchange. The different habitats of these species create multiple mechanisms of selection - drought, salinity, herbivory, and burial, which together maintain these species in their native habitats and their hybrids in intermediate habitats. This study illustrates how environmental factors influence traits and fitness and how this in turn maintain species, highlighting the importance of natural selection in speciation.

scholarly journals Diversification, disparification, and hybridization in the desert shrubs Encelia

2020 ◽  
Author(s):  
Sonal Singhal ◽  
Adam B. Roddy ◽  
Christopher DiVittorio ◽  
Ary Sanchez-Amaya ◽  
Claudia L. Henriquez ◽  
...  
Keyword(s):  
Gene Flow ◽  
Environmental Gradients ◽  
Phenotypic Traits ◽  
List Type ◽  
Phenotypic Evolution ◽  
Interspecific Gene Flow ◽  
Desert Shrubs ◽  
Geographic Ranges ◽  
Species Pairs ◽  
Adaptive Radiations

SummaryThere are multiple hypotheses for the spectacular plant diversity found in deserts. We explore how different factors, including the roles of ecological opportunity and selection, promote diversification and disparification in Encelia, a lineage of woody plants in the deserts of the Americas.Using a nearly complete species-level phylogeny along with a broad set of phenotypic traits, we estimate divergence times and diversification rates, identify instances of hybridization, quantify trait disparity, and assess phenotypic divergence across environmental gradients.We show that Encelia originated and diversified recently (mid-Pleistocene) and rapidly, with rates comparable to notable adaptive radiations in plants. Encelia probably originated in the hot deserts of North America, with subsequent diversification across steep environmental gradients. We uncover multiple instances of gene flow between species. The radiation of Encelia is characterized by fast rates of phenotypic evolution, trait lability, and extreme disparity across environments and between species-pairs with overlapping geographic ranges.Encelia exemplifies how interspecific gene flow in combination with high trait lability can enable exceptionally fast diversification and disparification across steep environmental gradients.

scholarly journals Hybrid asexuality as a primary reproductive barrier: on the interconnection between asexuality and speciation

2016 ◽  
Author(s):  
Karel Janko ◽  
Jan Pačes ◽  
Hilde Wilkinson-Herbots ◽  
Rui J Costa ◽  
Jan Röslein ◽  
...  
Keyword(s):  
Gene Flow ◽  
Reproductive Barrier ◽  
Published Data ◽  
Gene Pools ◽  
Hybrid Zones ◽  
Interspecific Gene Flow ◽  
Species Pairs ◽  
History Of ◽  
Gradual Accumulation ◽  
Fish Hybrids

Speciation usually proceeds in a continuum from intensively hybridizing populations until the formation of irreversibly isolated species. Restriction of interspecific gene flow may often be achieved by gradual accumulation of intrinsic postzygotic incompatibilities with hybrid infertility typically evolving more rapidly than inviability. A reconstructed history of speciation in European loaches (Cobitis) reveals that accumulation of postzygotic reproductive incompatibilities may take an alternative, in the literature largely neglected, pathway through initiation of hybrids' asexuality rather than through a decrease in hybrids' fitness. Combined evidence shows that contemporary Cobitis species readily hybridize in hybrid zones, but their gene pools are isolated as hybridization produces infertile males and fertile but clonally reproducing females that cannot mediate introgressions. Nevertheless, coalescent analyses indicated intensive historical gene flow during earlier stages of Cobitis diversification, suggesting that non-clonal hybrids must have existed in the past. The revealed patterns imply that during the initial stages of speciation, hybridization between little diverged species produced recombinant hybrids mediating gene flow, but growing divergence among species caused disrupted meiosis in hybrids resulting in their clonality, which acts as a barrier to gene flow. Comparative analysis of published data on other fish hybrids corroborated the generality of our findings; the species pairs producing asexual hybrids were more genetically diverged than those pairs producing fertile sexual hybrids but less diverged than species pairs producing infertile hybrids. Hybrid asexuality therefore appears to evolve at lower divergence than other types of postzygotic barriers and might thus represent a primary reproductive barrier in many taxa.

scholarly journals Post-translational regulation of autophagy is involved in intra-microbiome suppression of fungal pathogens

Microbiome ◽  
2021 ◽  
Vol 9 (1) ◽  
Author(s):  
Jing Wang ◽  
Chaoyun Xu ◽  
Qiming Sun ◽  
Jinrong Xu ◽  
Yunrong Chai ◽  
...  
Keyword(s):  
Translational Regulation ◽  
Fungal Pathogens ◽  
Fungal Growth ◽  
Fungal Species ◽  
26S Proteasome ◽  
Healthy Plant ◽  
Autophagy Induction ◽  
Histone Acetyltransferase Gcn5 ◽  
Plant Microbiota ◽  
Autophagic Process

Abstract Background Microbiome interactions are important determinants for ecosystem functioning, stability, and health. In previous studies, it was often observed that bacteria suppress potentially pathogenic fungal species that are part of the same plant microbiota; however, the underlying microbe-microbe interplay remains mostly elusive. Here, we explored antagonistic interactions of the fungus Fusarium graminearum and bacterium Streptomyces hygroscopicus at the molecular level. Both are ubiquitous members of the healthy wheat microbiota; under dysbiosis, the fungus causes devastating diseases. Results In co-cultures, we found that Streptomyces alters the fungal acetylome leading to substantial induction of fungal autophagy. The bacterium secrets rapamycin to inactivate the target of rapamycin (TOR), which subsequently promotes the degradation of the fungal histone acetyltransferase Gcn5 through the 26S proteasome. Gcn5 negatively regulates fungal autophagy by acetylating the autophagy-related protein Atg8 at the lysine site K13 and blocking cellular relocalization of Atg8. Thus, degradation of Gcn5 triggered by rapamycin was found to reduce Atg8 acetylation, resulting in autophagy induction in F. graminearum. Conclusions Autophagy homeostasis plays an essential role in fungal growth and competition, as well as for virulence. Our work reveals a novel post-translational regulation of autophagy initiated by a bacterial antibiotic. Rapamycin was shown to be a powerful modulator of bacteria–fungi interactions with potential importance in explaining microbial homeostasis in healthy plant microbiomes. The autophagic process provides novel possibilities and targets to biologically control pathogens.

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