Repeated expansions and fragmentations linked to Pleistocene climate changes shaped the genetic structure of a woody climber,Actinidia arguta(Actinidiaceae)

Botany ◽  
2018 ◽  
Vol 96 (1) ◽  
pp. 19-31 ◽  
Author(s):  
Jun-Wei Ye ◽  
Tao Jiang ◽  
Hong-Fang Wang ◽  
Tian-Ming Wang ◽  
Lei Bao ◽  
...  
Keyword(s):  
Genetic Structure ◽  
Climate Changes ◽  
Recent Common Ancestor ◽  
Niche Modelling ◽  
Analysis Of Molecular Variance ◽  
Molecular Variance ◽  
Actinidia Arguta ◽  
Most Recent Common Ancestor ◽  
Phylogeographic Break ◽  
Woody Climber

The genetic structure of temperate plants was extremely affected by climate changes during the Pleistocene. In East Asia, however, there are a limited number of phylogeography studies of widely distributed species. Actinidia arguta (Sieb. & Zucc.) Planch. ex Miq. (Actinidiaceae), a widely distributed woody climber, was chosen for this study. Twelve haplotypes were obtained using five chloroplast fragments. No haplotypes were shared on two sides of the Qinling–Dabie mountain ranges, indicating a phylogeographic break. The break was further revealed by analysis of molecular variance, spatial analysis of molecular variance, and ecological niche modelling. The most recent common ancestor of all haplotypes showed that global cooling and aridity of the Asian interior at the Pliocene–Pleistocene boundary may triggered this divergence. Two monophyletic lineages (north and south lineage) were revealed by Bayesian phylogeny and the maximum parsimony network. In the north lineage, mismatch analysis indicated an ancient spatial expansion. Distant distribution of closely related haplotypes indicated subsequent allopatric fragmentation. The widespread haplotype H2 implied another significant range expansion. In the south lineage, a considerable rise in sea level of the East China Sea may have triggered population fragmentation. The nested clade analysis also indicated that expansion and allopatric fragmentation were the main processes shaping the haplotype distributions. So, repeated range expansions and fragmentations have shaped the present genetic structure of A. arguta.

scholarly journals Recent and rapid colonization of the Lesser Sundas Archipelago from adjacent Sundaland by seven amphibian and reptile species

2019 ◽  
Author(s):  
Sean B. Reilly ◽  
Alexander L. Stubbs ◽  
Benjamin R. Karin ◽  
Evy Arida ◽  
Djoko T. Iskandar ◽  
...  
Keyword(s):  
Genetic Structure ◽  
Continental Shelf ◽  
Population Expansion ◽  
Phylogeographic Structure ◽  
Recent Common Ancestor ◽  
Stepping Stones ◽  
Terrestrial Vertebrate ◽  
Most Recent Common Ancestor ◽  
Short Time Span ◽  
Genetic Signatures

AbstractThe Lesser Sundas Archipelago is comprised of two parallel chains of islands that extend between the Asian continental shelf (Sundaland) and Australo-Papuan continental shelf (Sahul). These islands have served as stepping-stones for taxa dispersing between the Asian and Australo-Papuan biogeographic realms. While the oceanic barriers have prevented many species from colonizing the archipelago, a number of terrestrial vertebrate species have colonized the islands either by rafting/swimming or human introduction. Here we examine phylogeographic structure within the Lesser Sundas for three snake, two lizard, and two frog species that each have a Sunda Shelf origin. These species are suspected to have recently colonized the archipelago, though all have inhabited the Lesser Sundas for over 100 years. We sequenced mtDNA from 230 samples to test whether there is sufficiently deep genetic structure within any of these taxa to reject human-mediated introduction. Additionally, we tested for genetic signatures of population expansion consistent with recent introduction, and estimated the ages of Lesser Sundas clades, if any exist. Our results show little to no genetic structure between populations on different islands in five species, and moderate structure in two species. Nucleotide diversity is low for all species, and the ages of the most recent common ancestor for species with monophyletic Lesser Sundas lineages date to the Holocene or late Pleistocene. These results support the hypothesis that these species entered the archipelago relatively recently and either naturally colonized or were introduced by humans to most of the islands within the archipelago within a short time span.

scholarly journals Genetic Diversity and Dynamics of Sinorhizobium meliloti Populations Nodulating Different Alfalfa Cultivars in Italian Soils

2000 ◽  
Vol 66 (11) ◽  
pp. 4785-4789 ◽  
Author(s):  
Maria Carelli ◽  
Stefano Gnocchi ◽  
Silvia Fancelli ◽  
Alessio Mengoni ◽  
Donatella Paffetti ◽  
...  
Keyword(s):  
Genetic Diversity ◽  
Genetic Polymorphism ◽  
Genetic Structure ◽  
Sinorhizobium Meliloti ◽  
Dna Polymorphism ◽  
Random Amplified Polymorphic Dna ◽  
Analysis Of Molecular Variance ◽  
Molecular Variance ◽  
High Level ◽  
Rhizobium Population

ABSTRACT We analyzed the genetic diversity of 531 Sinorhizobium meliloti strains isolated from nodules of Medicago sativa cultivars in two different Italian soils during 4 years of plant growth. The isolates were analyzed for DNA polymorphism with the random amplified polymorphic DNA method. The populations showed a high level of genetic polymorphism distributed throughout all the isolates, with 440 different haplotypes. Analysis of molecular variance allowed us to relate the genetic structure of the symbiotic population to various factors, including soil type, alfalfa cultivar, individual plants within a cultivar, and time. Some of these factors significantly affected the genetic structure of the population, and their relative influence changed with time. At the beginning of the experiment, the soil of origin and, even more, the cultivar significantly influenced the distribution of genetic variability of S. meliloti. After 3 years, the rhizobium population was altered; it showed a genetic structure based mainly on differences among plants, while the effects of soil and cultivar were not significant.

scholarly journals Genetic structure of the endemic Papaver occidentale indicates survival and immigration in the Western Prealps

Alpine Botany ◽  
2020 ◽  
Vol 130 (2) ◽  
pp. 129-140 ◽  
Author(s):  
Loïc Pittet ◽  
Yann Fragnière ◽  
Sandra Grünig ◽  
Sébastien Bétrisey ◽  
Benoît Clément ◽  
...  
Keyword(s):  
Genetic Structure ◽  
Plant Species ◽  
Endemic Species ◽  
Climate Changes ◽  
Spatial Genetic Structure ◽  
Ecological Modelling ◽  
Conservation Priorities ◽  
Niche Modelling ◽  
Local Survival ◽  
History Of

Abstract Climatic oscillations of the Quaternary rapidly compelled plant species to shift their geographical range. How alpine plant species responded to climate change, however, remains elusive and remnants of the cold-adapted flora that currently strive in restricted ranges as small, isolated populations have been particularly overlooked. To address the evolutionary history of such a ‘glacial relict’, we here sampled and genotyped all known native populations of a narrow endemic species from the northwestern Alps, Papaver occidentale, as well as closely related taxa with double digest restriction-site Associated DNA (ddRAD) sequencing. Spatial patterns of genetic variation across populations coupled with insights from climatic niche modelling through time address underpinings of the long-term persistence of the species in face of climate changes. Evidence from population genetics and ecological modelling indicates that P. occidentale likely persisted through the last glacial maximum outside of the Western Prealps and that a major lineage recolonized the area from lower elevation, external regions. Differentiated lineages at the Northern margins of the species distribution range highlight highly divergent and geographically restricted populations that include considerable share of private markers and may indicate local glacial survival in isolated conditions. Our data thus imply that processes having shaped intraspecific spatial genetic structure within the Alps can be complex and lead to mosaic of populations with a mixed-history of local survival and immigration. A better understanding of spatio-temporal aspects of range contraction–expansion is crucial to shed light on processes underlying the evolution of remnant populations of such endemic species and set conservation priorities considering current climate changes.

The genetic structure of Atlantic cod (Gadus morhua) around Iceland: insight from microsatellites, the Pan I locus, and tagging experiments

2006 ◽  
Vol 63 (12) ◽  
pp. 2660-2674 ◽  
Author(s):  
Christophe Pampoulie ◽  
Daniel E Ruzzante ◽  
Valérie Chosson ◽  
Thóra Dögg Jörundsdóttir ◽  
Lorna Taylor ◽  
...  
Keyword(s):  
Genetic Structure ◽  
Microsatellite Loci ◽  
Gadus Morhua ◽  
Atlantic Cod ◽  
Allelic Variation ◽  
Scaling Analysis ◽  
Hierarchical Analysis ◽  
Multidimensional Scaling Analysis ◽  
Analysis Of Molecular Variance ◽  
Molecular Variance

Allelic variation at nine microsatellite loci and the Pan I locus provides evidence that Atlantic cod (Gadus morhua) around Iceland is genetically structured (FST = 0.003 and FST = 0.261, respectively). A total of 2534 cod were sampled at 22 spawning locations. For both types of markers, most of the significant pairwise FST resulted from northeastern–southwestern comparisons. A multidimensional scaling analysis based on FST, a spatial hierarchical analysis of molecular variance (SAMOVA) and a hierarchical analysis of molecular variance (AMOVA), conducted on both types of markers confirmed a genetic differentiation between cod from the northeastern and southwestern regions. Genetic discontinuities were revealed across two main current fronts in the southeast and northwest, where the cold and warm water masses meet. The AMOVA also detected genetic differences with depth. Expected and observed heterozygosity of microsatellite loci significantly decreased with depth, whereas the B allele frequency at the Pan I locus increased. A tagging experiment of spawning fish conducted during the same years as the genetic work revealed that tagged individuals released in the southwestern region seldom migrated to the northeastern region and vice versa, suggesting that the southwestern and northeastern populations of Atlantic cod around Iceland represent two distinct spawning components.

scholarly journals Allelic Genealogies in Sporophytic Self-Incompatibility Systems in Plants

Genetics ◽  
1998 ◽  
Vol 150 (3) ◽  
pp. 1187-1198 ◽  
Author(s):  
Mikkel H Schierup ◽  
Xavier Vekemans ◽  
Freddy B Christiansen
Keyword(s):  
Dominance Hierarchy ◽  
Common Ancestor ◽  
Recent Common Ancestor ◽  
Self Incompatibility ◽  
Most Recent Common Ancestor ◽  
Dominance Interactions ◽  
Turnover Process ◽  
Neutral Gene ◽  
Interspecific Comparisons ◽  
Coalescence Times

Abstract Expectations for the time scale and structure of allelic genealogies in finite populations are formed under three models of sporophytic self-incompatibility. The models differ in the dominance interactions among the alleles that determine the self-incompatibility phenotype: In the SSIcod model, alleles act codominantly in both pollen and style, in the SSIdom model, alleles form a dominance hierarchy, and in SSIdomcod, alleles are codominant in the style and show a dominance hierarchy in the pollen. Coalescence times of alleles rarely differ more than threefold from those under gametophytic self-incompatibility, and transspecific polymorphism is therefore expected to be equally common. The previously reported directional turnover process of alleles in the SSIdomcod model results in coalescence times lower and substitution rates higher than those in the other models. The SSIdom model assumes strong asymmetries in allelic action, and the most recessive extant allele is likely to be the most recent common ancestor. Despite these asymmetries, the expected shape of the allele genealogies does not deviate markedly from the shape of a neutral gene genealogy. The application of the results to sequence surveys of alleles, including interspecific comparisons, is discussed.

scholarly journals Molecular epidemiological characteristics of echovirus 6 in mainland China: extensive circulation of genotype F from 2007 to 2018

2021 ◽  
Author(s):  
Wenjun Cheng ◽  
Tianjiao Ji ◽  
Shuaifeng Zhou ◽  
Yong Shi ◽  
Lili Jiang ◽  
...  
Keyword(s):  
Common Ancestor ◽  
Mainland China ◽  
Recent Common Ancestor ◽  
Genetic Characteristics ◽  
Most Recent Common Ancestor ◽  
Significant Difference ◽  
Echovirus 6 ◽  
Epidemiological Characteristics ◽  
Highest Posterior Density ◽  
Genotype F

AbstractEchovirus 6 (E6) is associated with various clinical diseases and is frequently detected in environmental sewage. Despite its high prevalence in humans and the environment, little is known about its molecular phylogeography in mainland China. In this study, 114 of 21,539 (0.53%) clinical specimens from hand, foot, and mouth disease (HFMD) cases collected between 2007 and 2018 were positive for E6. The complete VP1 sequences of 87 representative E6 strains, including 24 strains from this study, were used to investigate the evolutionary genetic characteristics and geographical spread of E6 strains. Phylogenetic analysis based on VP1 nucleotide sequence divergence showed that, globally, E6 strains can be grouped into six genotypes, designated A to F. Chinese E6 strains collected between 1988 and 2018 were found to belong to genotypes C, E, and F, with genotype F being predominant from 2007 to 2018. There was no significant difference in the geographical distribution of each genotype. The evolutionary rate of E6 was estimated to be 3.631 × 10-3 substitutions site-1 year-1 (95% highest posterior density [HPD]: 3.2406 × 10-3-4.031 × 10-3 substitutions site-1 year-1) by Bayesian MCMC analysis. The most recent common ancestor of the E6 genotypes was traced back to 1863, whereas their common ancestor in China was traced back to around 1962. A small genetic shift was detected in the Chinese E6 population size in 2009 according to Bayesian skyline analysis, which indicated that there might have been an epidemic around that year.

scholarly journals Molecular epidemiology of coxsackievirus A16 circulating in children in Beijing, China from 2010 to 2019

2021 ◽  
Author(s):  
Ya-Fang Hu ◽  
Li-Ping Jia ◽  
Fang-Yuan Yu ◽  
Li-Ying Liu ◽  
Qin-Wei Song ◽  
...  
Keyword(s):  
Molecular Epidemiology ◽  
Evolutionary Rate ◽  
Foot And Mouth Disease ◽  
Recent Common Ancestor ◽  
Rt Pcr ◽  
Coxsackievirus A16 ◽  
Most Recent Common Ancestor ◽  
Etiological Agents ◽  
High Level ◽  
And Control

Abstract Background Coxsackievirus A16 (CVA16) is one of the major etiological agents of hand, foot and mouth disease (HFMD). This study aimed to investigate the molecular epidemiology and evolutionary characteristics of CVA16. Methods Throat swabs were collected from children with HFMD and suspected HFMD during 2010–2019. Enteroviruses (EVs) were detected and typed by real-time reverse transcription-polymerase chain reaction (RT-PCR) and RT-PCR. The genotype, evolutionary rate, the most recent common ancestor, population dynamics and selection pressure of CVA16 were analyzed based on viral protein gene (VP1) by bioinformatics software. Results A total of 4709 throat swabs were screened. EVs were detected in 3180 samples and 814 were CVA16 positive. More than 81% of CVA16-positive children were under 5 years old. The prevalence of CVA16 showed obvious periodic fluctuations with a high level during 2010–2012 followed by an apparent decline during 2013–2017. However, the activities of CVA16 increased gradually during 2018–2019. All the Beijing CVA16 strains belonged to sub-genotype B1, and B1b was the dominant strain. One B1c strain was detected in Beijing for the first time in 2016. The estimated mean evolutionary rate of VP1 gene was 4.49 × 10–3 substitution/site/year. Methionine gradually fixed at site-23 of VP1 since 2012. Two sites were detected under episodic positive selection, one of which (site-223) located in neutralizing linear epitope PEP71. Conclusions The dominant strains of CVA16 belonged to clade B1b and evolved in a fast evolutionary rate during 2010–2019 in Beijing. To provide more favorable data for HFMD prevention and control, it is necessary to keep attention on molecular epidemiological and evolutionary characteristics of CVA16.

scholarly journals The Ancestry of a Sample of Sequences Subject to Recombination

Genetics ◽  
1999 ◽  
Vol 151 (3) ◽  
pp. 1217-1228 ◽  
Author(s):  
Carsten Wiuf ◽  
Jotun Hein
Keyword(s):  
Genetic Distance ◽  
Population Size ◽  
Upper Bound ◽  
Recombination Rate ◽  
Common Ancestor ◽  
Recent Common Ancestor ◽  
Sequence Length ◽  
Most Recent Common Ancestor ◽  
The Mean ◽  
Mean Time

Abstract In this article we discuss the ancestry of sequences sampled from the coalescent with recombination with constant population size 2N. We have studied a number of variables based on simulations of sample histories, and some analytical results are derived. Consider the leftmost nucleotide in the sequences. We show that the number of nucleotides sharing a most recent common ancestor (MRCA) with the leftmost nucleotide is ≈log(1 + 4N Lr)/4Nr when two sequences are compared, where L denotes sequence length in nucleotides, and r the recombination rate between any two neighboring nucleotides per generation. For larger samples, the number of nucleotides sharing MRCA with the leftmost nucleotide decreases and becomes almost independent of 4N Lr. Further, we show that a segment of the sequences sharing a MRCA consists in mean of 3/8Nr nucleotides, when two sequences are compared, and that this decreases toward 1/4Nr nucleotides when the whole population is sampled. A measure of the correlation between the genealogies of two nucleotides on two sequences is introduced. We show analytically that even when the nucleotides are separated by a large genetic distance, but share MRCA, the genealogies will show only little correlation. This is surprising, because the time until the two nucleotides shared MRCA is reciprocal to the genetic distance. Using simulations, the mean time until all positions in the sample have found a MRCA increases logarithmically with increasing sequence length and is considerably lower than a theoretically predicted upper bound. On the basis of simulations, it turns out that important properties of the coalescent with recombinations of the whole population are reflected in the properties of a sample of low size.

scholarly journals Genome Sequence Analysis of First Ross River Virus Isolate from Papua New Guinea Indicates Long-Term, Local Evolution

Viruses ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 482
Author(s):  
Alice Michie ◽  
John S. Mackenzie ◽  
David W. Smith ◽  
Allison Imrie
Keyword(s):  
Papua New Guinea ◽  
Large Scale ◽  
Solomon Islands ◽  
Febrile Illness ◽  
New Guinea ◽  
Recent Common Ancestor ◽  
Ross River Virus ◽  
Most Recent Common Ancestor ◽  
Mean Time

Ross River virus (RRV) is the most medically significant mosquito-borne virus of Australia, in terms of human morbidity. RRV cases, characterised by febrile illness and potentially persistent arthralgia, have been reported from all Australian states and territories. RRV was the cause of a large-scale epidemic of multiple Pacific Island countries and territories (PICTs) from 1979 to 1980, involving at least 50,000 cases. Historical evidence of RRV seropositivity beyond Australia, in populations of Papua New Guinea (PNG), Indonesia and the Solomon Islands, has been documented. We describe the genomic characterisation and timescale analysis of the first isolate of RRV to be sampled from PNG to date. Our analysis indicates that RRV has evolved locally within PNG, independent of Australian lineages, over an approximate 40 year period. The mean time to most recent common ancestor (tMRCA) of the unique PNG clade coincides with the initiation of the PICTs epidemic in mid-1979. This may indicate that an ancestral variant of the PNG clade was seeded into the region during the epidemic, a period of high RRV transmission. Further epidemiological and molecular-based surveillance is required in PNG to better understand the molecular epidemiology of RRV in the general Australasian region.

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