Genetic Analysis of Population Structure and Reproductive Mode of the Termite Reticulitermes chinensis Snyder

The subterranean termite Reticulitermes chinensis Snyder is an important pest of trees and buildings in China. Here, we characterized genetic structure and reproductive modes of R. chinensis from China for the first time. A total of 1,875 workers from 75 collection sites in Huanggang, Changsha and Chongqing cities were genotyped at eight microsatellite loci. Analysis of genetic clusters showed two subpopulations in Chongqing city. The Huanggang population showed a uniform genetic pattern and was separated from the other populations by the largest genetic distances (F _ST: 0.17–0.20). In contrast, smaller genetic distances (F _ST: 0.05–0.12) separated Changsha, Chongqing-1 and Chongqing-2 populations. Chongqing-1 was the only population showing a genetic bottleneck. Isolation by distance among colonies in the Huanggang population indicated limited alate dispersal or colony budding. Lack of isolation by distance among colonies within the populations of Changsha, Chongqing-1 and Chongqing-2, suggested long-range dispersal by alates and/or human-mediated transport. Overall, extended family colonies (73.91%) were predominant in all four populations, followed by simple (20.29%), and mixed family colonies (5.80%). Most simple families were headed by inbred related reproductive pairs in the Changsha population, while most simple families in the Chongqing-1 population were headed by outbred unrelated pairs. Simple families in the Huanggang population were a mixture of colonies headed by outbred or inbred reproductive pairs. The sample size of simple families in the Chongqing-2 population was too small to yield significant results. Extended families in all four populations were headed on the average by ≤10 neotenics. Mixed families likely originated from pleometrosis. Presence of heterozygote genotypes showed that all neotenic reproductives collected in addition from five field colonies in Wuhan city were sexually produced, suggesting that these colonies did not undergo parthenogenesis. This study contributes to better understanding of the variance of genetic structure and reproductive mode in the genus Reticulitermes.     

Molecular Diversity and Genetic Structure of Guineagrass (Panicum maximum Jacq.), a Tropical Pasture Grass

Guineagrass (Panicum maximum Jacq.) is a forage grass found in tropical and subtropical regions. It is an apomictic and tetraploid species from Africa. The objective of this study was to evaluate the genetic diversity of guineagrass accessions sampled from its regions of origin, which is in Tanzania and Kenya. In this study, a total of 396 accessions were analyzed, and a collection of reproducible and informative microsatellites was developed. Thirty microsatellites were employed to characterize these accessions. A total of 576 clones were sequenced from microsatellite-enriched libraries. Flanking primers were designed for 116 microsatellite loci and screened using a sample of 25 guineagrass accessions. The thirty selected polymorphic microsatellites employed in this study produced a total of 192 bands when evaluated in the 396 P. maximum accessions, with an average of 6.4 bands per microsatellite. Four genetic clusters were identified in the collection using STRUCTURE analysis, and these results were confirmed using AMOVA. The largest genetic variation was found within clusters (65.38%). This study revealed that the collection of accessions from the P. maximum region of origin was a rich source of genetic variability. The geographical distances and genetic similarities among accessions did not indicate a significant association between genetic and geographical variation, supporting the natural interspecific crossing between P. maximum, P. infestum and P. trichocladum as the origin of the high genetic variability and the existence of an agamic complex formed by these three species.     

Population Genetic Variation in the Tree Fern Alsophila spinulosa (Cyatheaceae): Effects of Reproductive Strategy

Background

Essentially all ferns can perform both sexual and asexual reproduction. Their populations represent suitable study objects to test the population genetic effects of different reproductive systems. Using the diploid homosporous fern Alsophila spinulosa as an example species, the main purpose of this study was to assess the relative impact of sexual and asexual reproduction on the level and structure of population genetic variation.

Methodology/Principal Findings

Inter-simple sequence repeats analysis was conducted on 140 individuals collected from seven populations (HSG, LCH, BPC, MPG, GX, LD, and ZHG) in China. Seventy-four polymorphic bands discriminated a total of 127 multilocus genotypes. Character compatibility analysis revealed that 50.0 to 70.0% of the genotypes had to be deleted in order to obtain a tree-like structure in the data set from populations HSG, LCH, MPG, BPC, GX, and LD; and there was a gradual decrease of conflict in the data set when genotypes with the highest incompatibility counts were successively deleted. In contrast, in population ZHG, only 33.3% of genotypes had to be removed to achieve complete compatibility in the data set, which showed a sharp decline in incompatibility upon the deletion of those genotypes. All populations examined possessed similar levels of genetic variation. Population ZHG was not found to be more differentiated than the other populations.

Conclusions/Significance

Sexual recombination is the predominant source of genetic variation in most of the examined populations of A. spinulosa. However, somatic mutation contributes most to the genetic variation in population ZHG. This change of the primary mode of reproduction does not cause a significant difference in the population genetic composition. Character compatibility analysis represents an effective approach to separate the role of sexual and asexual components in shaping the genetic pattern of fern populations.     

Genetic Variation at the MHC in a Population of Introduced Wild Turkeys

Genetic variation in the major histocompatibility complex (MHC) is known to affect disease resistance in many species. Investigations of MHC diversity in populations of wild species have focused on the antigen presenting class IIβ molecules due to the known polymorphic nature of these genes and the role these molecules play in pathogen recognition. Studies of MHC haplotype variation in the turkey (Meleagris gallopavo) are limited. This study was designed to examine MHC diversity in a group of Eastern wild turkeys (Meleagris gallopavo silvestris) collected during population expansion following reintroduction of the species in southern Wisconsin, USA. Southern blotting with BG and class IIβ probes and single nucleotide polymorphism (SNP) genotyping was used to measure MHC variation. SNP analysis focused on single copy MHC genes flanking the highly polymorphic class IIβ genes. Southern blotting identified 27 class IIβ phenotypes, whereas SNP analysis identified 13 SNP haplotypes occurring in 28 combined genotypes. Results show that genetic diversity estimates based on RFLP (Southern blot) analysis underestimate the level of variation detected by SNP analysis. Sequence analysis of the mitochondrial D-loop identified 7 mitochondrial haplotypes (mitotypes) in the sampled birds. Results show that wild turkeys located in southern Wisconsin have a genetically diverse MHC and originate from several maternal lineages.     

长江中游草鱼天然种群的生化遗传结构及变异

采用淀粉或聚丙烯酰胺凝胶电泳方法分析了长江中游武汉江段草鱼天然种群(n=81)中10种同工酶约28个基因座位的遗传变异型。该种群的多态座位比例为16.7%,平均杂合度为0.0739。而Utter和Folmar(1978)曾报道美国的5个草鱼人工繁殖种群的多态座位比例及平均杂合度分别为6%和0.021。比较结果表明,近交很可能是导致草鱼人工繁殖种群中遗传变异性降低的主要原因。我们认为生产上采用数量大、来源广的亲鱼进行人工繁殖,并定期用天然种群更换或补充繁殖用亲鱼很可能是保持或增加鱼类人工繁殖种群遗传变异性的一种有效手段。     

Genetic Diversity and Population Structure of Native and Introduced Date Palm (Phoenix dactylifera) Germplasm in the United Arab Emirates

Date palm (Phoenix dactylifera) has been cultivated since ancient times, but little is known about its genetic diversity and population structure. Examination of 80 date palm accessions grown in the United Arab Emirates, including a collection of varieties from around the world, using 21 microsatellite markers, indicated extensive genetic diversity, with many accessions heterozygous for most markers. The average number of alleles per locus (19), expected heterozygosity (0.7), observed heterozygosity (0.25) and fixation indices (Fst?=?0.6, Rst?=?0.72) demonstrated significant population structure. Analysis with a model-based Baysian method, STRUCTURE 2.4.1, indicated that the 80 accessions could be broadly divided into nine groups. Independent samples of genotypes with the same name, collected from different experimental stations, usually clustered together. The study was enriched for germplasm from the United Arab Emirates (UAE), and one STRUCTURE-derived grouping consisted mainly of UAE accessions. In a few other clusters, several genotypes from the UAE, Iraq and Oman grouped together. Two clusters included accessions from both North Africa and the Middle East. Many accessions in the STRUCTURE-derived populations appeared to be genetic admixtures. The results indicated a broad dissemination of related germplasms across date-palm growing regions of the world, with very few alleles that still correlate with particular regional germplasms.     

我国盾叶薯蓣居群遗传结构分析

利用随机扩增多态DNA(RAPD)标记,分析研究了中国11个盾叶薯蓣居群82个个体的遗传多样性与遗传结构,15个寡聚核苷酸引物扩增共得到108条带,其中96条为多态带,占88．89％。Shannon多样性指数(I)为0．3093,居群水平的变异从0．1564到0．3098,物种水平的Nei基因多样度(h)为0．2499,居群水平的变化范围为0．1607到0．2137。遗传变异分析表明,物种水平的基因分化系数Gst为0．3415,居群间的基因流Nm为0．9641,居群间遗传交换小。分子方差分析(AMOVA)表明,居群内变异为68．96％,地区间变异为19．45％,居群问变异为11．58％。聚类结果以长江为界,将盾叶薯蓣分为南北两个大类群。研究结果对盾叶薯蓣种质的迁地保护有重要意义。     

Genetic Structure of the Population of Alternaria solani in Brazil

Understanding the genetic structure of the population of Alternaria solani (AS) is an important component of epidemiological studies of early blight, a severe disease that affects potato (Po) and tomato (To) worldwide. Up to 150 isolates obtained from both hosts were analysed with RAPD and AFLP markers to estimate the amount and distribution of genetic variability of AS in Brazil. Using RAPD, gene diversity (h = 0.20) and scaled indices of diversity of Shannon (H′ = 0.66) and Stoddart and Taylor’s (G = 0.31) for the Po population were higher than those of the To (h = 0.07, H′ = 0.34, G = 0.17). For AFLP, the statistics for the Po (h = 0.17, H′ = 0.86, G = 0.49) and To (h = 0.17, H′ = 0.85, G = 0.36) populations were similar. For each RAPD and AFLP locus, the allele frequency for the overall population ranged from 0.006 to 0.988, and 0.007 to 0.993, respectively. Genetic differentiation was high (G_ST = 0.41 and θ = 0.59) and moderately high (G_ST = 0.23 and θ = 0.37) when estimated with RAPD and AFLP, respectively. Based on cluster analyses, there was strong evidence of association of pathogen haplotypes with host species. The null hypothesis of random association of alleles was rejected in the analysis of both RAPD (I_A = 13.1, P < 0.001) and AFLP (I_A = 2.2, P < 0.001) markers. The average number of migrants was estimated to be around one and two individuals per generation, using RAPD and AFLP, respectively. There was no correlation between genetic distance and geographical origin of AS haplotypes for RAPD (r = ?0.07, P = 0.84) and AFLP (r = ?0.03, P = 0.70). The AS population is clonal with high genetic variability, and there is genetic differentiation between the populations that affect To and Po.     

Relationship between the Reproductive Capability of a Subdivided Population and Its Genetic Structure: Computer Simulation,the Simplest Multilocus Model

An original computer model, simulating joint genetic and demographic dynamics of subdivided populations, is proposed. The model accounts for the reverse effect of the genetic structure on the reproductive capability of a population, which is based on a postulated limited set of biallelic loci, controlling variation in an adaptive quantitative trait. The model allows to simulate spreading of the population, originating from a single small colony, resulting in establishment of involves genetic and demographic equilibrium (a normal population-genetic process) and reorganization of the genetic structure of the subdivided population under anthropogenic pressure, associated with a decrease in its reproductive capability (an adverse population-genetic process).     

Population Genetic Structure of Wild Boars in Poland

The analysis involved wild boars from the Lublin region, Warmia and Mazury, and Wielkopolska. The study material comprised muscle tissue samples collected from 100 wild boars. We analysed loci S0008, SW1129, SW986, SW1465, SW1492, SW1514, SW2532, SW461, SW841, SW2021, and SW2496 [1, 2]. The largest number of specific alleles, i.e. in six loci, was observed in wild boars from Warmia and Mazury; in turn, there were only two alleles in the group of wild boars from Lublin, and no alleles in individuals from Wielkopolska. The average value of the observed heterozygosity was H_o = 0.51, and the average value of expected heterozygosity was H_e = 0.63. PIC was another analysed indicator, with its lowest value determined for wild boars from the Wielkopolska region (0.53), and the highest value (0.62) was found for the animals from Warmia and Mazury. In the study population of wild boars, we also determined the F_ST index, which was 0.073, and N_m had a value greater than 3 (3.15); therefore, it can be concluded that the number of migrants per generation was 3. Both coefficients confirm the possibility of gene transfer and reproduction within and between the analysed populations of the wild boars. In our study, we observed a greater genetic distance between the wild boar populations from Wielkopolska and the Lublin and Warmia and Mazury regions in spite of the smaller geographical distance of these lands. This may be caused the less extensive network of ecological corridors as well as the occurrence of anthropogenic barriers e.g. large urban centres, an extensive network of roads, and the high volume of traffic in the direction of the capital.     

Hitchhiking and the Population Genetic Structure of Avian Influenza Virus

Previous studies have revealed a major difference in the phylogenetic structure, extent of genetic diversity, and selection pressure between the surface glycoproteins and internal gene segments of avian influenza viruses (AIV) sampled from wild birds. However, what evolutionary processes are responsible for these strikingly different evolutionary patterns is unclear. To address this issue, we estimated the rate of evolutionary change and time of origin of each segment of AIV sampled globally. Strikingly, the internal segments of the sampled AIV strains possess common ancestors that existed less than 200 years ago. Similarly recent times of origin were observed for each of the individual subtypes within the HA, NA, and NS gene segments. Such a shallow history of genetic diversity suggests an evolutionary model in which the genetic structure of AIV is shaped by a combination of occasional selective sweeps in the HA and NA (and possibly NS) segments, coupled with transient genetic linkage to the internal gene segments.     

Genetic Structure of the Ancestral Population of Modern Humans

Neutral DNA polymorphisms from an 8-kb segment of the dystrophin gene, previously ascertained in a worldwide sample (n= 250 chromosomes), were used to characterize the population ancestral to the present-day human groups. The ancestral state of each polymorphic site was determined by comparing human variants with their orthologous sites in the great apes. The ``age before fixation' of the underlying mutations was estimated from the frequencies of the new alleles and analyzed in the context of these polymorphisms' distribution among 13 populations from Africa, Europe, Asia, New Guinea, and the Americas (n= 860 chromosomes in total). Seventeen polymorphisms older tan 100,000–200,000 years, which contributed ∼90% to the overall nucleotide diversity, were common to all human groups. Polymorphisms endemic to human groups or continentally restricted were younger than 100,000–200,000 years. Africans (six populations) with 13 such sites stood out from the rest of the world (seven populations), where only 2 population-specific variants were observed. The similarity of the frequencies of the old polymorphisms in Africans and non-Africans suggested a similar profile of genetic variability in the population before the modern human's divergence. This ancestral population was characterized by an effective size of about 10,000 as estimated from the nucleotide diversity; this size may describe the number of breeding individuals over a long time during the Middle Pleistocene or reflect a speciation bottleneck from an initially larger population at the end of this period. Received: 3 February 1998 / Accepted: 9 February 1998     

Genetic Diversity and Population Structure of the Brachiaria brizantha Germplasm

Brachiaria brizantha (Hochst. ex A. Rich.) Stapf. (syn. Urochloa brizantha (Hochst. ex A. Rich.) R.D. Webster) is a species used primarily as forage in tropical America and Southeast Asia. B. brizantha has been extensively researched since the 1980s with the initiation of the Tropical Forages Breeding Program conducted by the Brazilian Agricultural Research Corporation (Empresa Brasileira de Pesquisa Agropecuária; EMBRAPA), holding one of the largest germplasm collections in the world. This work has identified 15 new microsatellite markers for this species, which have been used in addition to five previously reported markers, to estimate the genetic similarities among 172 accessions and six cultivars of this species. Similarity index values ranged from 0.40 to 1.00. Two duplications were found in the germplasm. A Bayesian analysis performed using the STRUCTURE 2.3.3 program revealed the presence of three clusters with different allelic pools. This analysis is valuable for the performance of crosses to explore heterosis; however, the mode of reproduction of the accessions and ploidy barriers must be observed for effective exploration. A grouping analysis using the neighbor-joining method was consistent with the STRUCTURE analysis, and a combination approach suggested that this germplasm collection does not exhibit considerable genetic variability despite the presence of three distinct allelic pools. The lack of correlation between the genetic and geographic distances is also discussed.     

Genetic Diversity and Population Structure of Theileria annulata in Oman

Background

Theileriosis, caused by a number of species within the genus Theileria, is a common disease of livestock in Oman. It is a major constraint to the development of the livestock industry due to a high rate of morbidity and mortality in both cattle and sheep. Since little is currently known about the genetic diversity of the parasites causing theileriosis in Oman, the present study was designed to address this issue with specific regard to T. annulata in cattle.

Methods

Blood samples were collected from cattle from four geographically distinct regions in Oman for genetic analysis of the Theileria annulata population. Ten genetic markers (micro- and mini-satellites) representing all four chromosomes of T. annulata were applied to these samples using a combination of PCR amplification and fragment analysis. The resultant genetic data was analysed to provide a first insight into the structure of the T. annulata population in Oman.

Results

We applied ten micro- and mini-satellite markers to a total of 310 samples obtained from different regions (174 [56%] from Dhofar, 68 [22%] from Dhira, 44 [14.5%] from Batinah and 24 [8%] from Sharqia). A high degree of allelic diversity was observed among the four parasite populations. Expected heterozygosity for each site ranged from 0.816 to 0.854. A high multiplicity of infection was observed in individual hosts, with an average of 3.3 to 3.4 alleles per locus, in samples derived from Batinah, Dhofar and Sharqia regions. In samples from Dhira region, an average of 2.9 alleles per locus was observed. Mild but statistically significant linkage disequilibrium between pairs of markers was observed in populations from three of the four regions. In contrast, when the analysis was performed at farm level, no significant linkage disequilibrium was observed. Finally, no significant genetic differentiation was seen between the four populations, with most pair-wise F_ST values being less than 0.03. Slightly higher F_ST values (G_ST’ = 0.075, θ = 0.07) were detected when the data for T. annulata parasites in Oman was compared with that previously generated for Turkey and Tunisia.

Conclusion

Genetic analyses of T. annulata samples representing four geographical regions in Oman revealed a high level of genetic diversity in the parasite population. There was little evidence of genetic differentiation between parasites from different regions, and a high level of genetic diversity was maintained within each sub-population. These findings are consistent with a high parasite transmission rate and frequent movement of animals between different regions in Oman.     

Introduced Plant Viruses and the Invasion of a Native Grass Flora

Weed and native grasses from the South Island of New Zealand were surveyed for virus infection. Cocksfoot mottle virus (CfMV) and Ryegrass mosaic virus (RgMV) were restricted to a few introduced species; however, Barley yellow dwarf viruses (BYDVs) have invaded native grasses in New Zealand. Virus incidence was significantly lower in the native species (2%) than in the introduced species (12%). Four different serotypes (RMV, RPV, PAV, MAV) were detected in the introduced grass flora but only two (RMV, PAV) were detected in native species. In experimental transmission tests the aphid vector Rhopalosiphum padi's survival was variable on the 20 native species tested but this was not due to the presence or absence of endophytic fungi as none were detected in the New Zealand species. Aphid numbers increased and plants were killed when R. padi fed on Agrostis muelleriana and Festuca multinodis. R. padi transmitted a PAV isolate to these and six other native species. BYDVs infected 4/5 of the subfamilies tested. Virus incidence in native Arundinoideae and Pooideae was significantly lower than in introduced Pooideae and Panicoideae. One species of Bambusoideae collected from the field was not infected but was found susceptible in glasshouse tests. Agrostis capillaris, Dactylis glomerata and Lolium perenne were identified as the most likely reservoirs of infection for the native flora. Anthoxanthum odoratum was not infected but if the SGV serotype and its vector Schizaphis graminum were ever introduced, A. odoratum could form an effective reservoir from near sea level into alpine areas. This revised version was published online in July 2006 with corrections to the Cover Date.